Kári Stefánsson
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Icelandic neurologist
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Kári Stefánssonmedical Degrees
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Kári Stefánsson's Degrees
- PhD Neurology University of Chicago
Why Is Kári Stefánsson Influential?
(Suggest an Edit or Addition)According to Wikipedia, Kári Stefánsson is an Icelandic neurologist and founder and CEO of Reykjavik-based biopharmaceutical company deCODE genetics. In Iceland he has pioneered the use of population-scale genetics to understand variation in the sequence of the human genome. His work has focused on how genomic diversity is generated and on the discovery of sequence variants impacting susceptibility to common diseases. This population approach has served as a model for national genome projects around the world and contributed to the realization of several aspects of precision medicine.
Kári Stefánsson's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Biological Insights From 108 Schizophrenia-Associated Genetic Loci (2014) (6445)
- Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (2010) (3485)
- Discovery and Refinement of Loci Associated with Lipid Levels (2013) (2475)
- Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes (2006) (2206)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
- Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
- Variant of TREM2 associated with the risk of Alzheimer's disease. (2013) (2004)
- Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (2012) (2002)
- Hundreds of variants clustered in genomic loci and biological pathways affect human height (2010) (1961)
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) (1882)
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) (1839)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2018) (1816)
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) (1801)
- Large recurrent microdeletions associated with schizophrenia (2008) (1790)
- A high-resolution recombination map of the human genome (2002) (1763)
- Rate of de novo mutations and the importance of father’s age to disease risk (2012) (1720)
- Common variants in ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer’s disease (2011) (1701)
- Genome-wide association study identifies five new schizophrenia loci (2011) (1680)
- Neuregulin 1 and susceptibility to schizophrenia. (2002) (1657)
- Common variants conferring risk of schizophrenia (2009) (1653)
- Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease (2014) (1591)
- A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline (2012) (1519)
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) (1507)
- A variant associated with nicotine dependence, lung cancer and peripheral arterial disease (2008) (1503)
- Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia (2013) (1455)
- Corrigendum: Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer (2009) (1432)
- Genetics of gene expression and its effect on disease (2008) (1345)
- Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity (2009) (1344)
- Association between microdeletion and microduplication at 16p11.2 and autism. (2008) (1338)
- Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2018) (1248)
- Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2019) (1232)
- New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
- Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
- Spread of SARS-CoV-2 in the Icelandic Population (2020) (1170)
- Identification of common genetic risk variants for autism spectrum disorder (2019) (1140)
- Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) (1124)
- Genome-wide association study identifies 74 loci associated with educational attainment (2016) (1114)
- Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants (2009) (1100)
- A variant in CDKAL1 influences insulin response and risk of type 2 diabetes (2007) (1066)
- Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture (2012) (1045)
- Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (1028)
- A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction (2007) (1013)
- Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
- Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
- A mega-analysis of genome-wide association studies for major depressive disorder (2013) (979)
- The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke (2004) (960)
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
- Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2018) (914)
- Variants conferring risk of atrial fibrillation on chromosome 4q25 (2007) (910)
- Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24 (2007) (904)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
- Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease (2011) (894)
- Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies (2011) (873)
- Humoral Immune Response to SARS-CoV-2 in Iceland (2020) (808)
- A common variant on chromosome 9p21 affects the risk of myocardial infarction. (2007) (795)
- Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction (2009) (790)
- Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer (2007) (787)
- De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia (2011) (768)
- Common variants associated with plasma triglycerides and risk for coronary artery disease (2013) (767)
- The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm (2008) (765)
- Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes (2007) (765)
- A common inversion under selection in Europeans (2005) (760)
- Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) (758)
- Mapping cis- and trans-regulatory effects across multiple tissues in twins (2012) (754)
- Variants in MTNR1B influence fasting glucose levels (2009) (742)
- Seven New Loci Associated with Age-Related Macular Degeneration (2013) (741)
- Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (2019) (724)
- Genetic determinants of hair, eye and skin pigmentation in Europeans (2007) (709)
- Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma (2007) (690)
- Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma (2015) (690)
- Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior (2010) (688)
- Twenty bone mineral density loci identified by large-scale meta-analysis of genome-wide association studies (2009) (687)
- Many sequence variants affecting diversity of adult human height (2008) (664)
- Large-scale whole-genome sequencing of the Icelandic population (2015) (638)
- Multiple genetic loci for bone mineral density and fractures. (2008) (632)
- A common variant associated with prostate cancer in European and African populations (2006) (630)
- The nature of nurture: Effects of parental genotypes (2017) (618)
- Sequence variants at the TERT-CLPTM1L locus associate with many cancer types (2009) (613)
- The gene encoding phosphodiesterase 4D confers risk of ischemic stroke (2003) (602)
- CNVs conferring risk of autism or schizophrenia affect cognition in controls (2013) (585)
- Association of neuregulin 1 with schizophrenia confirmed in a Scottish population. (2003) (581)
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) (578)
- Parental origin of sequence variants associated with complex diseases (2009) (573)
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
- Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses (2016) (563)
- Fine-scale recombination rate differences between sexes, populations and individuals (2010) (551)
- An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) (547)
- Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database (2012) (546)
- The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
- A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. (2009) (532)
- Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis (2010) (530)
- Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma (2011) (526)
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
- Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (516)
- Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution (2007) (515)
- Rare and low-frequency coding variants alter human adult height (2016) (511)
- Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche (2014) (511)
- Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly. (2017) (493)
- Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer (2008) (490)
- Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies (2010) (477)
- Disruption of the neurexin 1 gene is associated with schizophrenia. (2009) (469)
- A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke (2009) (466)
- Mapping the human genetic architecture of COVID-19 (2021) (455)
- Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies (2012) (446)
- Detection of sharing by descent, long-range phasing and haplotype imputation (2008) (441)
- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus (2011) (428)
- Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure (2011) (424)
- A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci (2010) (423)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
- Erratum: Detection and interpretation of shared genetic influences on 42 human traits (2016) (417)
- Sequence variant on 8q24 confers susceptibility to urinary bladder cancer (2008) (410)
- FTO genotype is associated with phenotypic variability of body mass index (2012) (407)
- Loss-of-function mutations in SLC30A8 protect against type 2 diabetes (2014) (405)
- Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture (2015) (399)
- Biobank-driven genomic discovery yields new insight into atrial fibrillation biology (2018) (398)
- Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations (2009) (393)
- Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke (2012) (392)
- Several common variants modulate heart rate, PR interval and QRS duration (2010) (391)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction (2006) (383)
- Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study (2012) (382)
- Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits (2013) (365)
- S-100 protein in soft-tissue tumors derived from Schwann cells and melanocytes. (1982) (363)
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) (361)
- Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility (2009) (360)
- Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk (2017) (359)
- Seventy-five genetic loci influencing the human red blood cell (2012) (357)
- Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes (2017) (353)
- Mutations in BRIP1 confer high risk of ovarian cancer (2011) (350)
- Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1 (2010) (350)
- Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (2015) (349)
- Two newly identified genetic determinants of pigmentation in Europeans (2008) (349)
- Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders (2016) (348)
- The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals (2016) (347)
- New sequence variants associated with bone mineral density (2009) (345)
- Multiancestry association study identifies new asthma risk loci that colocalize with immune cell enhancer marks (2017) (337)
- Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer (2008) (337)
- Genome-wide meta-analysis identifies new susceptibility loci for migraine (2013) (336)
- ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma (2008) (335)
- Parental influence on human germline de novo mutations in 1,548 trios from Iceland (2017) (325)
- Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2014) (322)
- New common variants affecting susceptibility to basal cell carcinoma (2009) (321)
- Polygenic risk scores for schizophrenia and bipolar disorder predict creativity (2015) (317)
- Identification of an imprinted master trans-regulator at the KLF14 locus related to multiple metabolic phenotypes (2011) (316)
- Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile (2011) (313)
- Sequence variants at CHRNB 3 – CHRNA 6 and CYP 2 A 6 affect smoking behavior (2010) (312)
- A direct characterization of human mutation based on microsatellites (2012) (310)
- Large-scale genomic analyses link reproductive ageing to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair (2015) (308)
- Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease: A Genome-Wide Analysis of Common Variants (2014) (303)
- Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis (2012) (302)
- Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia (2017) (301)
- The impact of low-frequency and rare variants on lipid levels (2015) (300)
- Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
- An Icelandic example of the impact of population structure on association studies (2005) (298)
- Variant of TREM 2 Associated with the Risk of Alzheimer ’ s Disease (2012) (296)
- Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma (2010) (296)
- A genetic risk factor for periodic limb movements in sleep. (2007) (295)
- Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes (2014) (294)
- A rare variant in MYH6 is associated with high risk of sick sinus syndrome (2011) (294)
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) (294)
- S-100 protein in human chondrocytes (1982) (292)
- Familial aggregation of Parkinson's disease in Iceland. (2000) (292)
- Familial aggregation of atrial fibrillation in Iceland. (2006) (291)
- Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure (2020) (288)
- Interferon-γ-Induced Oligodendrocyte Cell Death: Implications for the Pathogenesis of Multiple Sclerosis (1995) (286)
- Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. (2011) (286)
- Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke (2008) (284)
- Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus (2013) (279)
- Cancer as a Complex Phenotype: Pattern of Cancer Distribution within and beyond the Nuclear Family (2004) (278)
- Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease (2017) (278)
- Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease (2015) (275)
- Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (2011) (270)
- Collaborative Meta-analysis: Associations of 150 Candidate Genes With Osteoporosis and Osteoporotic Fracture (2009) (267)
- Mapping of a familial essential tremor gene, FET1, to chromosome 3q13 (1997) (264)
- Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration (2011) (264)
- Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases (2012) (263)
- Linkage of Osteoporosis to Chromosome 20p12 and Association to BMP2 (2003) (263)
- Common variants at 19p13 are associated with susceptibility to ovarian cancer (2010) (262)
- Genome-Wide Association Study Using Extreme Truncate Selection Identifies Novel Genes Affecting Bone Mineral Density and Fracture Risk (2011) (262)
- Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome (2015) (262)
- A germline variant in the TP53 polyadenylation signal confers cancer susceptibility (2011) (261)
- Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization (2014) (260)
- Crystal structure of the heterodimeric complex of LXRα and RXRβ ligand‐binding domains in a fully agonistic conformation (2003) (259)
- Rate of de novo mutations, father’s age, and disease risk (2012) (258)
- Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density (2009) (256)
- Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer (2009) (253)
- Copy number variations of chromosome 16p13.1 region associated with schizophrenia (2011) (253)
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) (252)
- Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) (250)
- Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits (2013) (249)
- mtDna and the islands of the North Atlantic: estimating the proportions of Norse and Gaelic ancestry. (2001) (247)
- Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population. (2005) (245)
- Common variants on 8p12 and 1q24.2 confer risk of schizophrenia (2011) (243)
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria (2018) (241)
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) (240)
- CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD (2005) (238)
- Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age (2014) (238)
- The mutation rate in the human mtDNA control region. (2000) (236)
- Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization (2013) (236)
- HLA-Cw6-positive and HLA-Cw6-negative patients with Psoriasis vulgaris have distinct clinical features. (2002) (235)
- Assessing population differentiation and isolation from single‐nucleotide polymorphism data (2002) (234)
- Inheritance of human longevity in Iceland (2000) (230)
- Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease (2011) (228)
- A susceptibility gene for late‐onset idiopathic Parkinson's disease (2002) (222)
- mtDNA and the origin of the Icelanders: deciphering signals of recent population history. (2000) (222)
- Distribution of S-100 protein outside the central nervous system (1982) (221)
- Effects of a 5-lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction: a randomized trial. (2005) (221)
- Localization of a susceptibility gene for common forms of stroke to 5q12. (2002) (219)
- Genetic factors contribute to the risk of developing endometriosis. (2002) (218)
- Distinct clinical differences between HLA-Cw*0602 positive and negative psoriasis patients--an analysis of 1019 HLA-C- and HLA-B-typed patients. (2006) (217)
- Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets (2017) (217)
- Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits (2017) (215)
- Estimating Scandinavian and Gaelic ancestry in the male settlers of Iceland. (2000) (214)
- Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche (2009) (213)
- Genome-wide analysis of multiethnic cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma (2014) (212)
- A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22. (2010) (210)
- Common variants at VRK2 and TCF4 conferring risk of schizophrenia. (2011) (210)
- Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism (2017) (209)
- A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13. (1999) (208)
- A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) (207)
- Discovery of common variants associated with low TSH levels and thyroid cancer risk (2012) (207)
- Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2. (2003) (206)
- Variant in the sequence of the LINGO1 gene confers risk of essential tremor (2009) (204)
- Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-Wide Association Meta-analysis Involving More Than 22 000 Cases and 60 000 Controls (2010) (203)
- Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination Rate (2008) (203)
- Large-scale analysis of association between GDF5 and FRZB variants and osteoarthritis of the hip, knee, and hand. (2009) (203)
- Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease (2016) (202)
- Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes (2009) (199)
- Genetic evidence of assortative mating in humans (2017) (199)
- The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis (2013) (199)
- Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium. (2010) (198)
- Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm (2010) (197)
- S‐100 protein in granular cell tumors. (Granular cell myoblastomas) (1982) (197)
- The Scientific Foundation for Personal Genomics: Recommendations from a National Institutes of Health–Centers for Disease Control and Prevention Multidisciplinary Workshop (2009) (196)
- Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls (2012) (196)
- Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure underpinning obesity (2017) (193)
- Genomewide scan for hand osteoarthritis: a novel mutation in matrilin-3. (2003) (193)
- Identification of a large set of rare complete human knockouts (2015) (192)
- Recombination rate and reproductive success in humans (2004) (191)
- Single-Tissue and Cross-Tissue Heritability of Gene Expression Via Identity-by-Descent in Related or Unrelated Individuals (2011) (189)
- Proligodendroblast Antigen (POA), a Developmental Antigen Expressed by A007/O4‐Positive Oligodendrocyte Progenitors Prior to the Appearance of Sulfatide and Galactocerebroside (1992) (186)
- A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer (2012) (185)
- Neuregulin1 (NRG1) Signaling through Fyn Modulates NMDA Receptor Phosphorylation: Differential Synaptic Function in NRG1+/− Knock-Outs Compared with Wild-Type Mice (2007) (184)
- Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium☆ (2017) (183)
- Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels (2019) (183)
- Characterizing mutagenic effects of recombination through a sequence-level genetic map (2019) (181)
- A susceptibility gene for psoriatic arthritis maps to chromosome 16q: evidence for imprinting. (2003) (180)
- Patients with myasthenia gravis and thymoma have in their sera IgG autoantibodies against titin (1990) (179)
- Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. (2010) (178)
- Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1. (2011) (177)
- Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis (2018) (176)
- A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer (2010) (174)
- A Polymorphism in IRF4 Affects Human Pigmentation through a Tyrosinase-Dependent MITF/TFAP2A Pathway (2013) (174)
- Brain age prediction using deep learning uncovers associated sequence variants (2019) (173)
- Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. (2018) (171)
- Expanding the range of ZNF804A variants conferring risk of psychosis (2011) (169)
- Multiple novel transcription initiation sites for NRG1. (2004) (164)
- The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts (2007) (163)
- Common genetic variants associated with open-angle glaucoma. (2011) (161)
- Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype (2004) (160)
- Profiling of genes expressed in peripheral blood mononuclear cells predicts glucocorticoid sensitivity in asthma patients. (2005) (160)
- Microwave-hydrothermal processing for synthesis of electroceramic powders (1993) (159)
- Variants in the fetal genome near FLT1 are associated with risk of preeclampsia (2017) (159)
- Weighting sequence variants based on their annotation increases power of whole-genome association studies (2016) (159)
- Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. (2012) (158)
- Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22 (2010) (156)
- Common variants at 6p21.1 are associated with large artery atherosclerotic stroke (2012) (156)
- Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels (2010) (154)
- The oligodendrocyte-myelin glycoprotein belongs to a distinct family of proteins and contains the HNK-1 carbohydrate (1990) (153)
- Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. (2019) (153)
- An Association Between the Kinship and Fertility of Human Couples (2008) (150)
- Tracking Five Millennia of Horse Management with Extensive Ancient Genome Time Series (2019) (150)
- Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways (2012) (150)
- Meta-analyses identify 13 novel loci associated with age at menopause and highlights DNA repair and immune pathways (2011) (149)
- Identification of low-frequency variants associated with gout and serum uric acid levels (2011) (149)
- An alternatively spliced region of the human hexabrachion contains a repeat of potential N-glycosylation sites. (1989) (148)
- A genome-wide scan for preeclampsia in the Netherlands (2001) (147)
- A populationwide coalescent analysis of Icelandic matrilineal and patrilineal genealogies: evidence for a faster evolutionary rate of mtDNA lineages than Y chromosomes. (2003) (146)
- Physical and neurobehavioral determinants of reproductive onset and success (2016) (146)
- Graphtyper enables population-scale genotyping using pangenome graphs (2017) (145)
- Neuregulin 1 and schizophrenia (2004) (144)
- Rejection of fetal neocortical neural transplants by H-2 incompatible mice. (1987) (144)
- Ischemic Stroke Is Associated with the ABO Locus: The EuroCLOT Study (2013) (142)
- Protection of privacy by third-party encryption in genetic research in Iceland (2000) (140)
- The genetic spectrum of a population-based sample of familial hemiplegic migraine. (2007) (139)
- A variant in MCF2L is associated with osteoarthritis. (2011) (137)
- A sequence variant on 17q21 is associated with age at onset and severity of asthma (2010) (137)
- Genome-wide association study identifies multiple susceptibility loci for multiple myeloma (2016) (136)
- Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci (2017) (135)
- On the replication of genetic associations: timing can be everything! (2008) (135)
- Variants in DENND1A are associated with polycystic ovary syndrome in women of European ancestry. (2012) (133)
- European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene. (2011) (133)
- A major susceptibility gene for asthma maps to chromosome 14q24. (2002) (133)
- A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip (2013) (132)
- Loss-of-function variants in ATM confer risk of gastric cancer (2015) (132)
- Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study (2010) (131)
- Genetic predisposition to mosaic Y chromosome loss in blood (2019) (131)
- Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases (2010) (131)
- The power of genetic diversity in genome-wide association studies of lipids (2021) (129)
- Selection against variants in the genome associated with educational attainment (2017) (129)
- A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration (2013) (129)
- Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM (2011) (127)
- Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (127)
- A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration). (2004) (127)
- Psoriasis patients who are homozygous for the HLA‐Cw*0602 allele have a 2·5‐fold increased risk of developing psoriasis compared with Cw6 heterozygotes (2003) (125)
- Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31 (2014) (125)
- Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease (2015) (124)
- Genetic overlap between Alzheimer’s disease and Parkinson’s disease at the MAPT locus (2015) (124)
- Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits (2008) (122)
- Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality (2016) (121)
- Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition (2018) (121)
- Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption. (2011) (121)
- Circulating autoantibodies to the 200,000-dalton protein of neurofilaments in the serum of healthy individuals. (1985) (120)
- Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms (2014) (120)
- Personalized genomic information: preparing for the future of genetic medicine (2010) (120)
- A variant in FTO shows association with melanoma risk not due to BMI (2013) (120)
- Relatedness disequilibrium regression estimates heritability without environmental bias (2018) (119)
- Familial risk of lung carcinoma in the Icelandic population. (2004) (118)
- Expression of the Oligodendrocyte‐Myelin Glycoprotein by Neurons in the Mouse Central Nervous System (1998) (117)
- HLA class II sequence variants influence tuberculosis risk in populations of European ancestry (2016) (117)
- Assessment of Osteoarthritis Candidate Genes in a Meta-Analysis of Nine Genome-Wide Association Studies (2014) (117)
- Male-pattern baldness susceptibility locus at 20p11 (2008) (117)
- DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis (2018) (116)
- A phosphatidylinositol-linked peanut agglutinin-binding glycoprotein in central nervous system myelin and on oligodendrocytes (1988) (116)
- Genetic Architecture of Vitamin B12 and Folate Levels Uncovered Applying Deeply Sequenced Large Datasets (2013) (115)
- Contribution of ADAM33 polymorphisms to the population risk of asthma (2005) (113)
- The complete cDNA sequence of human hexabrachion (Tenascin). A multidomain protein containing unique epidermal growth factor repeats. (1991) (113)
- Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus (2010) (113)
- Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness (2017) (113)
- Focal brain injury and upregulation of a developmentally regulated extracellular matrix protein. (1995) (112)
- Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene (2010) (110)
- Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease. (2016) (108)
- Common and rare variants associated with kidney stones and biochemical traits (2015) (108)
- Genetic correlation between amyotrophic lateral sclerosis and schizophrenia (2017) (107)
- Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis (2015) (106)
- Common risk variants identified in autism spectrum disorder (2017) (106)
- Population Genomics: Laying the Groundwork for Genetic Disease Modeling and Targeting (1998) (106)
- Common and low-frequency variants associated with genome-wide recombination rate (2013) (106)
- Linkage of Essential Hypertension to Chromosome 18q (2002) (105)
- A large-scale genome-wide association study meta-analysis of cannabis use disorder (2020) (104)
- The inheritance of hip osteoarthritis in Iceland. (2000) (104)
- A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma (2017) (104)
- A Reassessment of Genetic Diversity in Icelanders: Strong Evidence from Multiple Loci for Relative Homogeneity Caused by Genetic Drift (2003) (104)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
- Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci (2017) (103)
- The Impact of Divergence Time on the Nature of Population Structure: An Example from Iceland (2009) (103)
- Association of Folate-Pathway Gene Polymorphisms with the Risk of Prostate Cancer: a Population-Based Nested Case-Control Study, Systematic Review, and Meta-analysis (2009) (102)
- Large-scale integration of the plasma proteome with genetics and disease (2021) (102)
- mtDNA variation in Inuit populations of Greenland and Canada: migration history and population structure. (2006) (101)
- Common variant at 16p11.2 conferring risk of psychosis (2014) (100)
- Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis (2018) (100)
- Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence (2017) (100)
- A genome-wide association study of early menopause and the combined impact of identified variants (2013) (99)
- The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
- Maintenance of isolated oligodendrocytes in long-term culture (1980) (99)
- Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2015) (98)
- GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes (2018) (98)
- Localization of a gene for migraine without aura to chromosome 4q21. (2003) (97)
- Multi-nucleotide de novo Mutations in Humans (2016) (97)
- Sharing of antigenic determinants between the nicotinic acetylcholine receptor and proteins in Escherichia coli, Proteus vulgaris, and Klebsiella pneumoniae. Possible role in the pathogenesis of myasthenia gravis. (1985) (97)
- Mechanism of oxyhemoglobin-induced release of endothelin-1 from cultured vascular endothelial cells and smooth-muscle cells. (1993) (97)
- Recommendations for standardization and phenotype definitions in genetic studies of osteoarthritis: the TREAT-OA consortium. (2010) (96)
- Anxiety with panic disorder linked to chromosome 9q in Iceland. (2003) (96)
- Nitric oxide synthase and guanylate cyclase levels in canine basilar artery after subarachnoid hemorrhage. (1995) (96)
- Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders (2015) (95)
- Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility (2017) (95)
- A genome-wide association study yields five novel thyroid cancer risk loci (2017) (95)
- Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. (2011) (94)
- A Mouse Model that Recapitulates Cardinal Features of the 15q13.3 Microdeletion Syndrome Including Schizophrenia- and Epilepsy-Related Alterations (2014) (93)
- The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease. (2010) (93)
- Complement genes contribute sex-biased vulnerability in diverse illnesses (2020) (92)
- Allelic frequencies and patterns of single-nucleotide polymorphisms in candidate genes for asthma and atopy in Iceland. (2001) (92)
- A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm. (2013) (92)
- Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes (2018) (91)
- Early Spread of SARS-Cov-2 in the Icelandic Population (2020) (91)
- Genome-wide association study implicates CHRNA2 in cannabis use disorder (2017) (91)
- A role for the acetylcholine receptor-inducing protein ARIA in oligodendrocyte development. (1994) (91)
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases (2012) (90)
- Whole genome characterization of sequence diversity of 15,220 Icelanders (2017) (90)
- Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes. (2019) (90)
- Shared genetic basis for migraine and ischemic stroke (2015) (89)
- Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. (2010) (89)
- Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation (2020) (88)
- A population‐based familial aggregation analysis indicates genetic contribution in a majority of renal cell carcinomas (2002) (88)
- The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms (2014) (87)
- Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. (2016) (87)
- Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium (2017) (87)
- Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction (2017) (87)
- Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria (2019) (86)
- Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing (2017) (85)
- A large Icelandic family with early osteoarthritis of the hip associated with a susceptibility locus on chromosome 16p. (2001) (84)
- Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2 (2017) (83)
- Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations (2021) (83)
- Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility. (2016) (83)
- Association Study of Nonsynonymous Single Nucleotide Polymorphisms in Schizophrenia (2012) (82)
- Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. (2012) (81)
- Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits (2021) (81)
- Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (2018) (81)
- Multiple transmissions of de novo mutations in families (2018) (81)
- Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis (2018) (81)
- The Y-chromosome point mutation rate in humans (2015) (81)
- European Bone Mineral Density Loci Are Also Associated with BMD in East-Asian Populations (2010) (80)
- Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals (2022) (80)
- Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology. (2013) (79)
- A Variant in LDLR Is Associated With Abdominal Aortic Aneurysm (2013) (79)
- Association Between IL-1 β /TNF- α –Induced Glucocorticoid-Sensitive Changes in Multiple Gene Expression and Altered Responsiveness in Airway Smooth Muscle (2001) (78)
- The inheritance of rheumatoid arthritis in Iceland. (2001) (78)
- The Icelandic Healthcare Database and informed consent. (2000) (77)
- Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence (2015) (76)
- Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process (2014) (75)
- Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis (2017) (75)
- Identification of sequence variants influencing immunoglobulin levels (2017) (75)
- The BARD1 Cys557Ser Variant and Breast Cancer Risk in Iceland (2006) (75)
- A Missense Variant in PTPN22 is a Risk Factor for Drug-induced Liver Injury. (2019) (75)
- Genome-wide analysis yields new loci associating with aortic valve stenosis (2017) (74)
- Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation (2015) (72)
- A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease (2018) (72)
- Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (2019) (72)
- The sequences of 150,119 genomes in the UK Biobank (2021) (72)
- A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation (2017) (72)
- Inhibition of T cell activation by the extracellular matrix protein tenascin. (1994) (72)
- The rate of meiotic gene conversion varies by sex and age (2016) (72)
- GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs (2019) (69)
- Associations of autozygosity with a broad range of human phenotypes (2019) (68)
- A sequence variant in ZFHX 3 on 16 q 22 associates with atrial fibrillation and ischemic stroke (2009) (68)
- Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women (2020) (67)
- PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION (2018) (67)
- Genetic evidence for a family-based Scandinavian settlement of Shetland and Orkney during the Viking periods (2005) (67)
- Sequence variants from whole genome sequencing a large group of Icelanders (2015) (67)
- Shared heritability and functional enrichment across six solid cancers (2018) (67)
- Localization of a gene for peripheral arterial occlusive disease to chromosome 1p31. (2002) (66)
- A saturated map of common genetic variants associated with human height (2022) (65)
- Structure of the human hexabrachion (tenascin) gene. (1991) (65)
- DG-041 inhibits the EP3 prostanoid receptor—A new target for inhibition of platelet function in atherothrombotic disease (2008) (65)
- Identification of Gal(β1–3)GalNAc bearing glycoproteins at the nodes of ranvier in peripheral nerve (1994) (65)
- Truncating mutations in RBM12 are associated with psychosis (2017) (65)
- Genome-wide association study identifies 48 common genetic variants associated with handedness (2019) (65)
- Correction: Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases (2010) (64)
- Sequences From First Settlers Reveal Rapid Evolution in Icelandic mtDNA Pool (2009) (64)
- Polymorphisms in hypocretin/orexin pathway genes and narcolepsy (2001) (64)
- Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles (2021) (64)
- Antagonists of the EP3 receptor for prostaglandin E2 are novel antiplatelet agents that do not prolong bleeding. (2009) (64)
- Lessons from the past: Familial aggregation analysis of fatal pandemic influenza (Spanish flu) in Iceland in 1918 (2008) (64)
- Immunohistochemistry of retinoblastomas in humans. (1984) (64)
- Genome-wide association study of migraine implicates a common susceptibility variant on 8 q 22 . 1 (2010) (64)
- deCODE genetics, Inc. (2003) (63)
- Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase (2016) (63)
- A Genome-Wide Association Study Identifies an Osteoarthritis Susceptibility Locus on Chromosome 7 q 22 (2010) (63)
- Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder (2019) (63)
- Insights into imprinting from parent-of-origin phased methylomes and transcriptomes (2018) (62)
- A common variant at 8q24.21 is associated with renal cell cancer (2013) (62)
- 15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia (2017) (62)
- Familial predisposition and cosegregation analysis of adult obstructive sleep apnea and the sudden infant death syndrome. (2002) (61)
- Genetic variation at 16q24.2 is associated with small vessel stroke (2017) (61)
- PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity (2018) (61)
- Meta-analysis of Alzheimer’s disease on 9,751 samples from Norway and IGAP study identifies four risk loci (2018) (60)
- Nationwide Study on Hypertrophic Cardiomyopathy in Iceland: Evidence of a MYBPC3 Founder Mutation (2014) (60)
- A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts (2020) (60)
- Corrigendum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes (2011) (60)
- Prion susceptibility and protective alleles exhibit marked geographic differences (2003) (59)
- Molecular Evolution of τ Protein: Implications for Alzheimer's Disease (1996) (59)
- A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape (2016) (59)
- New basal cell carcinoma susceptibility loci (2015) (58)
- Structure and chromosomal localization of the human gene for a brain form of prostaglandin D2 synthase. (1992) (58)
- Diversity in non-repetitive human sequences not found in the reference genome (2017) (58)
- Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2020) (58)
- Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease (2018) (57)
- A Missense Variant in PLEC Increases Risk of Atrial Fibrillation. (2017) (57)
- GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures (2019) (56)
- Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures (2016) (56)
- A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis (2019) (56)
- Cerebral small vessel disease genomics and its implications across the lifespan (2020) (56)
- The natural history of untreated multiple sclerosis in Iceland. A total population-based 50 year prospective study (2002) (55)
- Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis (2017) (55)
- Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits (2018) (55)
- Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (55)
- The nature of Neanderthal introgression revealed by 27,566 Icelandic genomes (2020) (54)
- Genome-wide association meta-analysis yields 20 loci associated with gallstone disease (2018) (54)
- Impact of Genetics on Low Bone Mass in Adults (2008) (54)
- Screen for CACNA1A and ATP1A2 Mutations in Sporadic Hemiplegic Migraine Patients (2008) (54)
- Differences between germline genomes of monozygotic twins (2021) (54)
- Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (53)
- Genes contributing to risk for common forms of stroke. (2005) (52)
- Clinical characteristics of patients with colorectal cancer with double somatic mismatch repair mutations compared with Lynch syndrome (2019) (51)
- Ancient genomes from Iceland reveal the making of a human population (2018) (51)
- Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (2018) (50)
- PDE4D and ALOX5AP genetic variants and risk for Ischemic Cerebrovascular Disease in Sweden (2007) (50)
- Using quality measures to facilitate allele calling in high-throughput genotyping. (1999) (49)
- Epigenetic and genetic components of height regulation (2016) (49)
- Composition of the founding population of Iceland: biological distance and morphological variation in early historic Atlantic Europe. (2004) (49)
- Rare mutations associating with serum creatinine and chronic kidney disease. (2014) (48)
- Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. (2020) (47)
- Blocking the EP3 receptor for PGE2 with DG-041 decreases thrombosis without impairing haemostatic competence. (2014) (47)
- The OMgp gene, a second growth suppressor within the NF1 gene (1998) (47)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depressive disorder (2017) (47)
- Causal Effect of Genetic Variants Associated With Body Mass Index on Multiple Sclerosis Susceptibility (2017) (47)
- Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis (2020) (46)
- Support for involvement of the AHI1 locus in schizophrenia (2007) (46)
- TCF4 (e2‐2; ITF2): A schizophrenia‐associated gene with pleiotropic effects on human disease (2013) (46)
- Genetics of psoriasis in Iceland: evidence for linkage of subphenotypes to distinct Loci. (2005) (46)
- FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease (2020) (46)
- Long read sequencing of 1,817 Icelanders provides insight into the role of structural variants in human disease (2019) (45)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (45)
- Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease (2020) (45)
- Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene (2014) (45)
- Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's disease. (2015) (45)
- Distribution of S-100 protein and glial fibrillary acidic protein in normal and gliotic human retina. (1984) (45)
- Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants (2021) (45)
- A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis (2015) (44)
- GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer (2020) (44)
- GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study (2019) (44)
- Gene-based pleiotropy across migraine with aura and migraine without aura patient groups (2016) (44)
- Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders (2016) (43)
- The inheritance of hand osteoarthritis in Iceland. (2003) (43)
- A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta (2018) (43)
- Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation (2018) (42)
- Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma (2014) (42)
- Large-scale genome-wide association meta-analysis of endometriosis reveals 13 novel loci and genetically-associated comorbidity with other pain conditions (2018) (42)
- Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions (2017) (41)
- Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer. (2014) (41)
- Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimer’s disease risk (2018) (41)
- Assessment of gene‐by‐sex interaction effect on bone mineral density (2012) (41)
- A common biological basis of obesity and nicotine addiction (2013) (41)
- Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2018) (40)
- β-Trace Gene Expression Is Regulated by a Core Promoter and a Distal Thyroid Hormone Response Element* (1997) (40)
- A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis (2021) (40)
- Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA (2018) (39)
- Human genetics as a foundation for innovative drug development (2013) (39)
- Neuregulin 1 in schizophrenia: out of Iceland (2003) (39)
- Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (39)
- The Adult Reading History Questionnaire (ARHQ) in Icelandic (2014) (39)
- The genealogic approach to human genetics of disease. (2001) (38)
- Two Rare Mutations in the COL1A2 Gene Associate With Low Bone Mineral Density and Fractures in Iceland (2016) (38)
- A new subclade of mtDNA haplogroup C1 found in Icelanders: evidence of pre-Columbian contact? (2011) (38)
- The Crystal Structure of Guinea Pig 11β-Hydroxysteroid Dehydrogenase Type 1 Provides a Model for Enzyme-Lipid Bilayer Interactions* (2005) (38)
- Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus (2017) (38)
- Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction (2019) (38)
- Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 (2018) (37)
- Association of polygenic score for major depression with response to lithium in patients with bipolar disorder (2020) (37)
- Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2016) (37)
- COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA (2017) (37)
- Evaluation of Association of HNF1B Variants with Diverse Cancers: Collaborative Analysis of Data from 19 Genome-Wide Association Studies (2010) (37)
- Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas (2016) (36)
- No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder (2011) (36)
- Rare coding variants and X-linked loci associated with age at menarche (2015) (36)
- The influence of genetic constitution on migraine drug responses (2016) (36)
- Association of Vitamin D Binding Protein Variants with Chronic Mucus Hypersecretion in Iceland (2004) (36)
- The role of linkage studies for common diseases. (2001) (35)
- Large Scale Replication Study of the Association between HLA Class II/BTNL2 Variants and Osteoarthritis of the Knee in European-Descent Populations (2011) (34)
- Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity (2013) (34)
- A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus (2013) (34)
- A whole genome association study in Icelandic multiple sclerosis patients with 4804 markers (2003) (34)
- Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort (2016) (34)
- Myelin-associated glycoprotein in human retina (1984) (34)
- The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects. (2009) (34)
- Molecular evolution of tau protein: implications for Alzheimer's disease. (1996) (33)
- Commentary: gene-environment interactions and smoking-related cancers. (2010) (33)
- Structure and chromosomal localization of the gene for the oligodendrocyte-myelin glycoprotein (1990) (33)
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) (33)
- Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry. (2016) (33)
- PARK10 Candidate RNF11 Is Expressed by Vulnerable Neurons and Localizes to Lewy Bodies in Parkinson Disease Brain (2007) (32)
- Largest GWAS (N=1,126,563) of Alzheimer's Disease Implicates Microglia and Immune Cells (2020) (32)
- Rare and Common Variants Conferring Risk of Tooth Agenesis (2018) (32)
- Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients (2017) (32)
- Genome-wide linkage screen of a consanguineous multiple sclerosis kinship (2003) (32)
- Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis (2016) (32)
- Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study (2019) (32)
- Genetic risk information for common diseases may indeed be already useful for prevention and early detection (2010) (32)
- Two large glycosylated polypeptides found in myelinating oligodendrocytes but not in myelin. (1986) (32)
- Association between IL-1beta/TNF-alpha-induced glucocorticoid-sensitive changes in multiple gene expression and altered responsiveness in airway smooth muscle. (2001) (31)
- A polygenic resilience score moderates the genetic risk for schizophrenia (2019) (31)
- Chromosomal localization of the human hexabrachion (tenascin) gene and evidence for recent reduplication within the gene. (1990) (31)
- Geographic atrophy in age-related macular degeneration and TLR3. (2009) (31)
- Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation (2017) (31)
- CDKN2A mutations and melanoma risk in the Icelandic population (2008) (31)
- Familiality of kidney stone disease in Iceland (2009) (30)
- Trial of a Selective Acetylcholinesterase Inhibitor, Galanthamine Hydrobromide, in the Treatment of Chronic Fatigue Syndrome (1996) (29)
- Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies (2015) (29)
- Gangliosides of human spinal cord: Aberrant composition of cords from patients with amyotrophic lateral sclerosis (1984) (29)
- Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour (2021) (29)
- PARANEOPLASTIC MYELOPATHY: ANTIBODIES AGAINST PROTEIN IN NORMAL SPINAL CORD AND UNDERLYING NEOPLASM (1985) (29)
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- An in vivo and in vitro analysis of systemic immune function in mice with histologic evidence of neural transplant rejection (1987) (26)
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- The oligodendrocyte-myelin glycoprotein of mouse: primary structure and gene structure. (1993) (25)
- Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) (25)
- Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2016) (25)
- Complement genes contribute sex-biased vulnerability in diverse disorders (2020) (25)
- Meta‐Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry (2019) (25)
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- Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density (2019) (24)
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- Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin (2018) (23)
- Ethics of population genomics research (1999) (23)
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- A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease (2015) (23)
- Impact of Selection Bias on Estimation of Subsequent Event Risk (2017) (23)
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- Genome-wide association study identifies 30 loci associated with bipolar disorder (2019) (22)
- Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death (2018) (22)
- Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (22)
- Association Analysis of 29,956 Individuals Confirms That a Low-Frequency Variant at CCND2 Halves the Risk of Type 2 Diabetes by Enhancing Insulin Secretion (2015) (22)
- Sequence variants associating with urinary biomarkers (2018) (22)
- A systematic evaluation of 151 candidate genes for their association with osteoporosis and osteoporotic fracture in a meta-analysis of genome-wide association data (2009) (22)
- Genetic insight into sick sinus syndrome (2021) (21)
- Adiposity-Dependent Regulatory Effects on Multi-tissue Transcriptomes (2016) (21)
- Large genome-wide association study identifies three novel risk variants for restless legs syndrome (2020) (21)
- Discussion on the meeting on ‘Statistical modelling and analysis of genetic data’ (2002) (21)
- GORpipe: a query tool for working with sequence data based on a Genomic Ordered Relational (GOR) architecture (2016) (21)
- MAP1B mutations cause intellectual disability and extensive white matter deficit (2018) (21)
- Prevention of neural allograft rejection in the mouse following in vivo depletion of L3T4+ but not LYT-2+ T-lymphocytes. (1990) (21)
- Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression (2020) (20)
- 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans (2021) (20)
- Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms (2016) (20)
- Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2017) (20)
- Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
- Sequence variants with large effects on cardiac electrophysiology and disease (2019) (19)
- A Variant in MCF 2 L Is Associated with Osteoarthritis (19)
- Peripheral neuropathy, high serum IgM, and paraproteinemia in mother and son (1985) (19)
- Sharing of Epitopes by Bacteria and the Nicotinic Acetylcholine Receptor: A Possible Role in the Pathogenesis of Myasthenia Gravis (1987) (19)
- Long PCR detection of the C4A null allele in B8-C4AQ0-C4B1-DR3. (2000) (19)
- Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis (2020) (19)
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- Genetic diversity fuels gene discovery for tobacco and alcohol use (2022) (18)
- Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters (2017) (18)
- Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer (2016) (18)
- Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank (2019) (18)
- SAG: a Schwann cell membrane glycoprotein (1992) (18)
- Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder (2012) (18)
- Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes (2022) (18)
- The past, present, and future of direct-to-consumer genetic tests (2010) (18)
- The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis (2021) (18)
- Genetic homogeneity of Icelanders (2000) (17)
- Meta-analysis fine-mapping is often miscalibrated at single-variant resolution (2022) (17)
- Association of a novel functional promoter variant (rs2075533 C>T) in the apoptosis gene TNFSF8 with risk of lung cancer--a finding from Texas lung cancer genome-wide association study. (2011) (17)
- Is multiple sclerosis an autoimmune disease? (1994) (17)
- Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults. (2019) (17)
- Common Sequence Variants Associated With Coronary Artery Disease Correlate With the Extent of Coronary Atherosclerosis (2015) (17)
- Distinction between the effects of parental and fetal genomes on fetal growth (2021) (17)
- Dinucleotide repeat polymorphism for the hexabrachion gene (HXB) on chromosome 9q32-34. (1992) (16)
- GPC5 rs2352028 variant and risk of lung cancer in never smokers. (2010) (16)
- Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry (2017) (16)
- Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs (2021) (16)
- Roadmap for a precision-medicine initiative in the Nordic region (2019) (16)
- Genome-wide TDT analysis in a localized population with a high prevalence of multiple sclerosis indicates the importance of a region on chromosome 14q (2003) (16)
- A polygenic and phenotypic risk prediction for Polycystic Ovary Syndrome evaluated by Phenome-wide association studies. (2020) (16)
- The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large‐Scale Proteomics Scan in Iceland (2021) (15)
- Identification of genetic loci associated with nocturnal enuresis: a genome-wide association study. (2021) (15)
- Reconstructing an African haploid genome from the 18th century (2018) (15)
- Developmental Changes in the Molecular Weights of Polypeptides in the Human CNS That Carry the HNK‐1 Epitope and Bind Phaseolus vulgaris Lectins (1988) (15)
- Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma (2020) (15)
- Model-based assessment of replicability for genome-wide association meta-analysis (2021) (15)
- Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2011) (15)
- Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank (2020) (15)
- A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease (2017) (14)
- Distribution of the neuronal specific protein, 14-3-2, in central nervous system lesions of tuberous sclerosis (2004) (14)
- Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming (2020) (14)
- Sequence variant at 4q25 near PITX2 associates with appendicitis (2017) (14)
- A genetic contribution to inflammatory bowel disease in Iceland: a genealogic approach. (2004) (14)
- Neuropathy accompanying IgMλ monoclonal gammopathy (2004) (13)
- Identification of 22 susceptibility loci associated with testicular germ cell tumors (2021) (13)
- Predicting facial characteristics from complex polygenic variations. (2015) (13)
- Genome-wide association study of 1 million people identifies 111 loci for atrial fibrillation (2018) (13)
- Distribution of glial fibrillary acidic protein in central nervous system lesions of tuberous sclerosis (2004) (13)
- Multiomics study of nonalcoholic fatty liver disease (2022) (13)
- Description of the EuroTARGET cohort: A European collaborative project on TArgeted therapy in renal cell cancer-GEnetic- and tumor-related biomarkers for response and toxicity. (2017) (13)
- Comparing migraine with and without aura to healthy controls using RNA sequencing (2019) (13)
- MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk (2020) (13)
- Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations (2017) (13)
- Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes (2019) (12)
- Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability (2017) (12)
- Eleven genomic loci affect plasma levels of chronic inflammation marker soluble urokinase-type plasminogen activator receptor (2021) (12)
- A Method for Detecting Long Non-Coding RNAs with Tiled RNA Expression Microarrays (2014) (12)
- Paraneoplastic syndromes of the nervous system (1988) (12)
- Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2019) (12)
- Developmental alterations in molecular weights of proteins in the human central nervous system that react with antibodies against myelin- associated glycoprotein (1984) (12)
- Data Resource Profile: The Copenhagen Hospital Biobank (CHB). (2020) (12)
- Identification of Genetic Loci Shared Between Attention-Deficit/Hyperactivity Disorder, Intelligence, and Educational Attainment (2019) (11)
- Sequence variants at CYP 1 A 1 – CYP 1 A 2 and AHR associate with coffee consumption (2011) (11)
- Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk (2021) (11)
- A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma. (2011) (11)
- A phenotypic analysis of T lymphocytes isolated from the brains of mice with allogeneic neural transplants. (1988) (10)
- Genetic approaches to assessing evidence for a T helper type 1 cytokine defect in adult asthma. (2004) (10)
- A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin (2018) (10)
- Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (10)
- Genetic Risk of Coronary Artery Disease, Features of Atherosclerosis, and Coronary Plaque Burden (2020) (10)
- Monoclonal antibodies and lectins as probes for investigation of the cell biology of human trabecular meshwork: a preliminary report. (1989) (10)
- PopDel identifies medium-size deletions jointly in tens of thousands of genomes (2019) (10)
- Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology (2022) (10)
- Autosomal dominant cerebrovascular amyloidosis: Properties of peripheral blood lymphocytes (1980) (10)
- Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche DTU Orbit (05/11/2017) (2014) (10)
- Deep learning based brain age prediction uncovers associated sequence variants (2019) (10)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (10)
- Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus (2020) (9)
- A genome wide linkage disequilibrium screen in Parkinson’s disease (2005) (9)
- A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo (2021) (9)
- Clinical risk factors, DNA variants, and the development of type 2 diabetes. (2009) (9)
- The genetic structure of Norway (2020) (9)
- Erratum: Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (Neuron (2018) 98(4) (743–753.e4), (S0896627318303222) (10.1016/j.neuron.2018.04.014)) (2018) (9)
- Erratum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes (Nature Genetics (2011) 43 (561-564)) (2011) (9)
- Using genome-Wwide complex trait analysis to quantify 'missing heritability' in Parkinson's disease (2012) (8)
- The mother’s risk of premature death after child loss across two centuries (2019) (8)
- Generation Scotland (2015) (8)
- Twenty loci associated with bone mineral density identified by large-scale meta-analysis of genome-wide association datasets (2009) (8)
- Observation¶HLA class II alleles and haplotypes in Icelandic Type I diabetic patients: comparison of Icelandic and Norwegian populations (2002) (8)
- Population Genomics of Drug Response (2004) (8)
- Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (8)
- Response to Comments on "An Association Between the Kinship and Fertility of Human Couples" (2008) (8)
- Experimental allergic neuritis in the SJL/J mouse: dysfunction of peripheral nerve without clinical signs (1991) (8)
- Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2020) (8)
- A truncated analogue of CCL2 mediates anti-fibrotic effects on murine fibroblasts independently of CCR2. (2012) (8)
- Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland (2021) (8)
- Corrigendum: The genomic landscape of juvenile myelomonocytic leukemia (2015) (8)
- Corrigendum: The gene encoding phosphodiesterase 4D confers risk of ischemic stroke (2005) (8)
- Neuroimaging Findings in Neurodevelopmental Copy Number Variants: Identifying Molecular Pathways to Convergent Phenotypes (2022) (8)
- Discovering patterns of pleiotropy in genome-wide association studies (2018) (7)
- Genetic Associations and Architecture of Asthma-COPD Overlap (2022) (7)
- TREM2 and neurodegenerative disease. (2013) (7)
- Neuropathy accompanying IgM lambda monoclonal gammopathy. (1983) (7)
- A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy (2019) (7)
- Reconstruction of a large-scale outbreak of SARS-CoV-2 infection in Iceland informs vaccination strategies (2021) (7)
- Generation of Monoclonal Antibodies Recognizing Neuronal Elements in Formalin‐fixed Paraffin‐embedded Human Tissue (1985) (7)
- Elevated Common Variant Genetic Risk for Tourette Syndrome in a Densely Affected Pedigree (2021) (7)
- PopDel identifies medium-size deletions simultaneously in tens of thousands of genomes (2021) (7)
- HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry (2021) (7)
- A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids (2021) (6)
- Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood (2019) (6)
- The CRP and GDNF genes do not contribute to apnea-hypopnea index or risk of obstructive sleep apnea. (2011) (6)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (6)
- Role of pharmacogenomics in drug development (2004) (6)
- Identification of Lynch syndrome risk variants in the Romanian population (2018) (6)
- Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011) (2011) (6)
- Analysis of Diffusion Tensor Imaging Data From the UK Biobank Confirms Dosage Effect of 15q11.2 Copy Number Variation on White Matter and Shows Association With Cognition (2021) (6)
- A rare missense variant in NR1H4 associates with lower cholesterol levels (2018) (6)
- Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset (2022) (6)
- CCR5-del32 is not deleterious in the homozygous state in humans (2019) (6)
- Random glucose GWAS in 493,036 individuals provides insights into diabetes pathophysiology, complications and treatment stratification (2021) (6)
- Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition (2018) (6)
- Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (Proceedings of the National Academy Sciences of the United States of America (2011) 108, 17, (7119-7124)) (2011) (6)
- Reply to “Many hypotheses but no replication for the association between PDE4D and stroke” (2006) (6)
- The population genomic legacy of the second plague pandemic (2022) (6)
- Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer (2022) (6)
- Genetic effects on the timing of parturition and links to fetal birth weight (2022) (6)
- 370 A GENOME-WIDE ASSOCIATION STUDY IDENTIFIES A LOCUS ON CHROMOSOME 7Q22 TO INFLUENCE SUSCEPTIBILITY FOR OSTEOARTHRITIS (2009) (6)
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- Lifelong Reduction in LDL Cholesterol Due to a Gain-of-Function Mutation in LDLR. (2020) (6)
- deCODE: A Genealogical Approach to Human Genetics in Iceland (2006) (5)
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- A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy (2021) (5)
- The Hexabrachion Gene as a Candidate for a Tuberous Sclerosis Gene (1991) (5)
- Genome Wide Association Metanalysis Of Skull Bone Mineral Density Identifies Loci Relevant For Osteoporosis And Craniosynostosis (2021) (5)
- A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome (2022) (5)
- Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure (2019) (5)
- Estimating heritability without environmental bias (2017) (5)
- A rare missense mutation in MYH6 confers high risk of coarctation of the aorta (2017) (5)
- A peanut agglutinin-binding glycoprotein in CNS myelin and oligodendrocytes (1987) (5)
- Molecular mimicry and microorganisms: a role in the pathogenesis of myasthenia gravis? (1989) (5)
- Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts (2023) (5)
- Myelin-associated glycoprotein in the developing human retina. (1986) (5)
- Segmental duplication density decrease with distance to human-mouse breaks of synteny (2006) (4)
- Effect of booster vaccination against Delta and Omicron variants in Iceland (2022) (4)
- The genetic architecture of osteoarthritis: insights from UK Biobank (2017) (4)
- Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (2019) (4)
- Correction: Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria (2019) (4)
- An epitope shared by central nervous system myelin and peripheral blood macrophages (1986) (4)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (4)
- Correction: Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer (2016) (4)
- 356 COMMON VARIANTS IN SKELETAL DYSPLASIA GENES ARE ASSOCIATED WITH OSTEOARTHRITIS (2011) (4)
- A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam (2022) (4)
- Predicting the probability of death using proteomics (2021) (4)
- Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals (2022) (4)
- Positional cloning: complex cardiovascular traits. (2006) (4)
- A Peanut Agglutinin Binding Glycoprotein in CNS Myelin and Oligodendrocytes (1988) (4)
- Genome-wide association study identifies 48 common genetic variants associated with handedness (2020) (4)
- Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program (2021) (4)
- Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies (2022) (4)
- DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis (2018) (4)
- Pattern of reactivity of IgM from the sera of eight patients with IgM monoclonal gammopathy and neuropathy with components of neural tissues: Evidence for interaction with more than one epitope (2004) (4)
- Germline variants at SOHLH2 influence multiple myeloma risk (2021) (4)
- Corrigendum: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma (2008) (4)
- Publisher Correction: Shared heritability and functional enrichment across six solid cancers (2019) (4)
- Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2017) (4)
- Erroneous claims about the impact of mitochondrial DNA sequence database errors. (2003) (4)
- Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity (2017) (4)
- Genetic risk score and cardiovascular events in women. (2010) (4)
- Disclosure of Genetic Risk Revealed in a Research Study. (2020) (4)
- A common variant at 8 q 24 . 21 is associated with renal cell cancer (2017) (4)
- Abstract 942: Imputation from The 1000 Genomes Project identifies rare large effect variants of BRCA2-K3326X and CHEK2-I157T as risk factors for lung cancer; a study from the TRICL consortium (2014) (4)
- The Norwegian Mother, Father, and Child cohort study (MoBa) genotyping data resource: MoBaPsychGen pipeline v.1 (2022) (4)
- Comment on the phosphodiesterase 4D replication study by Bevan et al. (2005) (4)
- Genetic variants associated with platelet count are predictive of human disease and physiological markers (2021) (3)
- Syddansk Universitet Association analysis of 29 , 956 individuals confirms that a low-frequency variant at CCND 2 halves the risk of type 2 diabetes by enhancing insulin secretion (2015) (3)
- Mendelian Randomization Study of ACLY and Cardiovascular Disease. (2020) (3)
- Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures (2019) (3)
- 83 ANALYSIS OF CANDIDATE OSTEOARTHRITIS GENES IN A META-ANALYSIS OF 8 GENOME-WIDE ASSOCIATION STUDIES (2011) (3)
- The genomics of heart failure: design and rationale of the HERMES consortium (2021) (3)
- Reply to “A call for accurate phenotype definition in the study of complex disorders” (2004) (3)
- Supplementary Material 3 (2015) (3)
- Supplementary Material 5 (2014) (3)
- Supplementary Material 6 (2014) (3)
- Monday, 27 August 2012 (2012) (3)
- Correction for Schumann et al., Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (2011) (3)
- INGE GRUNDKE-IQBAL LECTURE FOR ALZHEIMER'S RESEARCH: A MUTATION IN APP PROTECTS AGAINST ALZHEIMER'S DISEASE AND AGE-RELATED COGNITIVE DECLINE (2014) (3)
- Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (3)
- Determination of contiguity of subclones using the polymerase chain reaction. (1988) (3)
- 14GENETIC META-ANALYSIS IDENTIFIES 9 NOVEL LOCI AND FUNCTIONAL PATHWAYS FOR ALZHEIMER'S DISEASE RISK (2019) (3)
- Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing (2017) (3)
- Profile of common prostate cancer risk variants in an unscreened Romanian population (2017) (3)
- Data Related to Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) (3)
- Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis (2018) (3)
- A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank (2020) (3)
- Functional dissection of inherited non-coding variation influencing multiple myeloma risk (2022) (3)
- Supplementary Material 7 (2014) (3)
- Evaluating differences in linkage disequilibrium between populations (2010) (3)
- Interferon-y-Induced Oligodendrocyte Cell Death: Implications for the Pathogenesis of Multiple Sclerosis (2007) (3)
- Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome. (2022) (3)
- Polygenic Risk Score–Enhanced Risk Stratification of Coronary Artery Disease in Patients With Stable Chest Pain (2021) (3)
- Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database (2021) (3)
- Increased absorption of phytosterols is the simplest and most plausible explanation for coronary artery disease risk not accounted for by non-HDL cholesterol in high cholesterol absorbers (2020) (3)
- Mutations in RPL3L and MYZAP increase risk of atrial fibrillation (2017) (3)
- Augustine Kong Recombination Rate Gene Associate with Genome-Wide RNF 212 Sequence Variants in the (3)
- Sequence variant at 8 q 24 . 21 associates with sciatica caused by lumbar disc herniation (2017) (3)
- Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism (2023) (3)
- Author Correction: GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study (2019) (3)
- Comprehensive population-wide detection of Lynch syndrome in Iceland. (2016) (3)
- Genetic variants associated with syncope implicate neural and autonomic processes. (2023) (2)
- Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample (2022) (2)
- Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility (2016) (2)
- Recurrence of de novo mutations in families (2017) (2)
- An Anniversary Party (2011) (2)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
- Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis (2016) (2)
- Identification of genetic loci shared between ADHD, intelligence and educational attainment (2020) (2)
- Genealogy certainly matters for multifactorial genetic disease (1999) (2)
- Tuberous sclerosis. (1991) (2)
- Immunohistochemical staining of cells in the brain of a patient with acquired immune deficiency syndrome (AIDS) with a monoclonal antibody to visna virus (2004) (2)
- Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2022) (2)
- Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency (2021) (2)
- The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions (2023) (2)
- Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene (2022) (2)
- 291 LINKAGE ANALYSIS FOR HAND HYPERMOBILITY SUGGESTS A SUSCEPTIBILITY GENE ON CHROMOSOME 19P (2007) (2)
- Identification of 64 new risk loci for major depression, refinement of the genetic architecture and risk prediction of recurrence and comorbidities (2022) (2)
- Whole genome sequencing finds rare high-risk genotypes for hip osteoarthritis in the COMP and CHADL genes (2017) (2)
- The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions (2023) (2)
- Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci. (2022) (2)
- HLA alleles, disease severity, and age associate with T-cell responses following infection with SARS-CoV-2 (2022) (2)
- HUMORAL IMMUNE RESPONSE TO MAJOR MYELIN PROTEINS IN EXPERIMENTAL ALLERGIC NEURITIS (1984) (2)
- Comment on “Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics” (2021) (2)
- GWAS of Hematuria (2022) (2)
- The Epidermal Growth Factor Receptor Associates with and Recruits Phosphatidylinositol 3-Kinase to the Platelet-derived Growth Factor b Receptor* (1998) (2)
- On Sequence Variants that Influence the Risk of Common Diseases (2008) (2)
- Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases (2021) (1)
- Genetics & Genomics and Epigenetics 370 A GENOME-WIDE ASSOCIATION STUDY IDENTIFIES A LOCUS ON CHROMOSOME 7 Q 22 TO INFLUENCE SUSCEPTIBILITY FOR OSTEOARTHRITIS (2009) (1)
- Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2019) (1)
- Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 (2018) (1)
- The role of adiposity in cardiometabolic traits (2013) (1)
- Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution (2019) (1)
- Large-scale comparison of immunoassay- and aptamer-based plasma proteomics through genetics and disease (2022) (1)
- Effect of booster vaccination against Delta and Omicron SARS-CoV-2 variants in Iceland (2022) (1)
- Supplementary Material 9 (2013) (1)
- Estimating robustness of the tileShuffle method with repeated probes (2014) (1)
- A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease (2018) (1)
- Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2020) (1)
- 2017 William Allan Award. (2018) (1)
- Polygenic overlap between C-reactive protein , plasma lipids and Alzheimer ’ s disease 1 2 (2017) (1)
- Genome-Wide Association Study to Identify Genetic Determinants of Atopy (2010) (1)
- A genome-wide association study of asthma-COPD overlap syndrome (ACOS) (2020) (1)
- Title Convergent lines of evidence support CAMKK 2 as a schizophrenia susceptibility gene (2014) (1)
- Abstract 1171: Risk Variants for Atrial Fibrillation on Chromosome 4q25 Associate with Non-Cardiogenic Stroke Suggesting that AF is a Much Greater Cause of Stroke than Previously Recognized (2008) (1)
- Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) (1)
- The genetic history of Scandinavia from the Roman Iron Age to the present (2023) (1)
- Identification of a PTPN22 missense variant as a general genetic risk factor for drug-induced liver injury (2018) (1)
- Genome-wide association for major depression through age at onset stratificationGenomic analysis of age at onset in depression (2016) (1)
- Thirty novel sequence variants impacting human intracranial volume (2022) (1)
- Supplementary Material 15 (2013) (1)
- Genome-Wide Association Study of Over One Million Participants Identifies 49 Novel Loci Associated With Coronary Artery Disease (2019) (1)
- Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement (2022) (1)
- Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies | NOVA. The University of Newcastle's Digital Repository (2012) (1)
- OSTEOARTHRITIS PATIENTS ARE NOT ALL CAST IN THE SAME MOULD: GENETIC ASSOCIATIONS OF KNEE AND HIP OSTEOARTHRITIS DIFFER BETWEEN PATIENTS WHO HAVE UNDERGONE JOINT REPLACEMENT AND PATIENTS WHO HAVE NOT (2022) (1)
- Graphtyper: Population-scale genotyping using pangenome graphs (2017) (1)
- Author Correction: The rate of meiotic gene conversion varies by sex and age (2018) (1)
- Cartilage Acidic Protein 1 in Plasma Associates With Prevalent Osteoarthritis and Predicts Future Risk as Well as Progression to Joint Replacements: Results From the UK Biobank Resource (2022) (1)
- Abstract 19235: Rare Missense Mutations of ABCG5/ABCG8 Raise Cholesterol and Phytosterol Levels and Increase the Risk of Coronary Artery Disease (2016) (1)
- Abstract 2318: The Type 2 Diabetes Gene CDKAL1 Discovered by Genome-wide Association is Expressed in Beta Cells and Modulated by Glucose Concentration (2007) (1)
- Genetic Variability in the Uptake of Dietary Sterols Affects the Risk of Coronary Artery Disease (2019) (1)
- Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2021) (1)
- Questions about genetic variation in 9p21 as a predictor of cardiovascular risk. (2009) (1)
- Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility (2017) (1)
- Corrigendum: Rare coding variants and X-linked loci associated with age at menarche (2015) (1)
- Icelandic genetic database not at risk from bankruptcy (2010) (1)
- Discovery and Refinement Supplementary (2015) (1)
- Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (1)
- Sequence variants in the PTCH 1 gene associate with spine bone mineral density and osteoporotic fractures U (2016) (1)
- Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology (2022) (1)
- Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (2020) (1)
- Abstract #LB-139: A comprehensive genome-wide association study of lung cancer (2009) (1)
- Analysis of diffusion tensor imaging data from UK Biobank confirms dosage effect of 15q11.2 copy-number variation on white matter and shows association with cognition (2020) (1)
- Exome-chip meta-analysis identifies novel loci, including ADAMTS6 associated with cardiac conduction (2018) (1)
- Multi-polygenic scores in psychiatry: from disorder-specific to transdiagnostic perspectives (2022) (1)
- Cell-free fetal DNA for genetic evaluation in Copenhagen Pregnancy Loss Study (COPL): a prospective cohort study (2023) (1)
- Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program (2022) (1)
- Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (2018) (1)
- Cloning of cDNA for Two Large Polypeptides Found in Myelinating Oligodendrocytes (1988) (1)
- Corrigendum: Variant in the sequence of the LINGO1 gene confers risk of essential tremor (2009) (1)
- PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity (2018) (1)
- Exposure of binding sites for antibodies and concanavalin A on collagen by solubilization in hot urea. An immunoblot analysis. (1986) (1)
- A 180 kD Glycoprotein Found in Ventral Horn Neurons of Spinal Cord (1987) (1)
- Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (1)
- Supplementary Material 4 (2015) (1)
- Genetic propensities for verbal and spatial ability have opposite effects on body mass index and risk of schizophrenia (2021) (1)
- A 70‐Kd Polypeptide Secreted by Human Peripheral Blood Mononuclear Cells That Suppresses Proliferation of a Human Glioblastoma Cell Line (1988) (1)
- Crystal Structure of Guinea Pig 11beta-Hydroxysteroid Dehydrogenase Type 1 (2004) (1)
- Genome-wide analysis yields new loci associating with aortic valve stenosis (2018) (1)
- THE OLIGODENDROCYTE MYELIN GLYCOPROTEIN (OMgp): AN ADHESION MOLECULE IN THE OLIGODENDROCYTE-MYELIN UNIT (1990) (1)
- Meta-analysis of Alzheimer’s disease on 9,751 samples from Norway and IGAP study identifies four risk loci (2018) (1)
- Molecular benchmarks of a SARS-CoV-2 epidemic (2021) (1)
- Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity (2018) (1)
- 162 S-100 IN AN INSULINOMA ACCOMPANIED BY PERIPHERAL NEUROPATHY (1981) (0)
- Running Head : GWAS Meta-Analysis of Alzheimer ’ s Disease 1 Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimer ’ s disease risk (2019) (0)
- Haplotype analysis of rs9275224, rs2856717, rs9275424, and rs9275596 at the HLA-DQB1/DRB1 locus. (2012) (0)
- A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy (2019) (0)
- Molecular mimicry between the autoantigen Anoctamin 2 and Epstein Barr virus nuclear antigen 1 associates with increased risk for multiple sclerosis (2018) (0)
- Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2021) (0)
- Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits (2018) (0)
- Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles - A Mendelian randomization analysis. (2022) (0)
- Biobank-driven genomic discovery yields new insight into atrial fibrillation biology (2018) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (0)
- Abstract 2921: Genome-wide Association Reveals Sequence Variants on 4q25 that Affect the Risk of Atrial Fibrillation and Stroke (2007) (0)
- F122WHOLE GENOME SEQUENCING OF SCHIZOPHRENIA IN IRELAND (2019) (0)
- 101 Genetics of atopy and asthma in the founder population of Iceland: Lack of evidence of IgE regulating genes (2000) (0)
- Predicting the probability of death using proteomics (2021) (0)
- Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer (2021) (0)
- A potential role for genes in asthma independent of atopy (2002) (0)
- Abstract 1964: A Genome-Wide Association Study in Icelanders Identifies a Novel Sequence Variant on Chromosome 16q22 That is Additive to 4q25 Variants for Atrial Fibrillation Risk (2009) (0)
- Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk (2022) (0)
- 27. GENOME-WIDE CROSS-DISORDER ANALYSES OF ADHD AND CANNABIS USE DISORDER AND CANNABIS USE (2022) (0)
- Established risk loci for systemic lupus erythematosus at NCF2, STAT4, TNPO3, IRF5 and ITGAM associate with distinct clinical manifestations: a Danish genome-wide association study. (2022) (0)
- Titin is a major autoantigen in MG (1994) (0)
- A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy (2021) (0)
- Abstract 826: Large-scale genome-wide association study identifies multiple novel germline susceptibility variants associated with bladder cancer risk (2021) (0)
- Coronary heart disease The chromosome 9 p 21 risk locus is associated with angiographic severity and progression of coronary artery disease (2010) (0)
- Molecular genetic overlap between migraine and major depressive disorder (2018) (0)
- Erratum: Ischemic stroke is associated with the ABO locus: The EuroCLOT study (2014) (0)
- Genetic architecture of band neutrophil fraction in Iceland (2022) (0)
- Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2019) (0)
- A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine (2020) (0)
- Reactivity of human monoclonal immunoglobulins (HMI) with autoantigens (1987) (0)
- Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
- The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis (2021) (0)
- Genotype score associated with the risk of androgenetic alopecia. (2012) (0)
- Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. (2017) (0)
- Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains (2023) (0)
- Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA (2018) (0)
- Abstract 15504: The Effect of Sequence Variants on the Presence of Coronary Artery Disease Also Predicts Effect on Angiographic Severity (2013) (0)
- Fluorescent polymers as integrated light sources The Icelandic Student Innovation Fund September (2012) (0)
- A biochemically distinct sub-population of neurons in the human substantia gelatinosa Study with G-6-PD histochemistry (1982) (0)
- 16 GENOME-WIDE LINKAGE SCAN ON A LARGE ICELANDIC COHORT WITH HIP AND KNEE OSTEOARTHRITIS (2007) (0)
- Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas (2016) (0)
- Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications (2023) (0)
- In vitro transcription analysis of the β-trace gene promoter in cell line TE671 (1996) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
- A genome-wide meta-analysis identi es 53 sequence variants associating with carpal tunnel syndrome (2022) (0)
- Identifi cation of new susceptibility loci for osteoarthritis ( arcOGEN ) : a genome-wide association study (2012) (0)
- Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease (2020) (0)
- Crystal structure of the LXRalfa-RXRbeta LBD heterodimer (2004) (0)
- First Rounders Podcast: Kari Stefansson (2015) (0)
- Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels (2019) (0)
- Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks (2017) (0)
- Erratum (2012) (0)
- Identification of five novel osteoarthritis susceptibility loci through the UK biobank resourse of five novel osteoarthritis susceptibility loci through the UK biobank resourse (2017) (0)
- A sequence variant associating with educational attainment also affects childhood cognition (2016) (0)
- Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans (2023) (0)
- Characterization of EAN in the SJL/J mouse (1987) (0)
- Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma (2020) (0)
- Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis (2020) (0)
- Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study. (2023) (0)
- Abstract 18777: The Low-Density Lipoprotein Cholesterol and Body Mass Index/Type-2 Diabetes Signals in the HMGCR Region Are Not Explained by a Single Variant (2016) (0)
- ReplicationStudyandMeta-AnalysisinEuropean SamplesSupportsAssociationofthe3p21.1Locuswith (2012) (0)
- Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (0)
- Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (0)
- Author response: The mother’s risk of premature death after child loss across two centuries (2019) (0)
- Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals (2018) (0)
- A 70kd polypeptide secreted by human peripheral blood mononuclear cells that suppresses proliferation of a human glioblastoma cell line (1987) (0)
- Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction (2020) (0)
- Diversity in non-repetitive human sequences not found in the reference genome (2017) (0)
- Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation (2018) (0)
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) (0)
- Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome (2022) (0)
- Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition (2018) (0)
- Research highlights (2007) (0)
- Role of TNC in Wound-Healing in the CNS: 34 (1995) (0)
- GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study (2019) (0)
- Corrigendum to “A genome-wide association study identifies a common variant near the GPR22 gene as a new locus involved in prevalence and progression of osteoarthritis” [Bone. 44S2 (2009) S224] (2010) (0)
- Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years (2017) (0)
- Abstract 4405: Sequence Variant for Atrial Fibrillation on Chromosome 4q25 near the PITX2 Gene Increases Risk for Recurrent AF (2008) (0)
- Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene (2022) (0)
- Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) (0)
- Clinical Connections (2023) (0)
- Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality (2020) (0)
- A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis (2021) (0)
- Cognition in Schizophrenia (2021) (0)
- Severe osteoarthritis of the hand associates with markers within the ALDH1A2 gene and with very rare variants at 1p31 (2017) (0)
- Peer Review Status: Peer reviewed Citation for item: (2012) (0)
- Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2019) (0)
- Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure (2020) (0)
- Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations (2017) (0)
- The clinical utility of genetic risk variants in type 2 diabetes. (2008) (0)
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2018) (0)
- Shared heritability and functional enrichment across six solid cancers (2019) (0)
- 1227Familiality of fatal measles infections in Iceland, 1882. Analysis of a reconstructed patient cohort from a major epidemic (2014) (0)
- Whole-genome sequencing and deep imputation identifies non-coding variants near Engrailed-1 with large effects on bone mineral density and fracture (2015) (0)
- Shared antigens on acetylcholine receptor and bacterial proteins. (1985) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
- Genome-wide meta-analysis results for AGA in MAAN. (2012) (0)
- Multiple transmissions of de novo mutations in families (2018) (0)
- Reconstructing an African haploid genome from the 18th century (2018) (0)
- Effect of Schizophrenia Risk Variants On Mating and Fecundity (2019) (0)
- The effect of SNPs on expression levels in Nimblegen RNA expression microarrays (2015) (0)
- Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2018) (0)
- MAP1B mutations cause intellectual disability and extensive white matter deficit (2018) (0)
- Title European bone mineral density loci are also associated withBMD in East-Asian populations (2010) (0)
- Identification of common genetic risk variants for autism spectrum disorder (2019) (0)
- Relatedness disequilibrium regression estimates heritability without environmental bias (2018) (0)
- Errata (2011) (0)
- Genome-wide association meta-analysis yields 20 loci associated with gallstone disease (2018) (0)
- The Development of an Infrastructure to Facilitate the Use of Whole Genome Sequencing for Population Health (2022) (0)
- Cross-cancer genome-wide association analysis of lung, ovary, breast, prostate and colon cancer identifies a novel cancer locus at 1q22 (2015) (0)
- Insights into imprinting from parent-of-origin phased methylomes and transcriptomes (2018) (0)
- Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes (2018) (0)
- Decoding Diversity from a “Small Rock” in the North Atlantic: An Interview with Kari Stefansson (2022) (0)
- To see the final version of this paper please visit the publisher's website. Access to the published version may require a subscription. (2010) (0)
- Genome-wide association analysis of coffee drinking suggests association with CYP1A1CYP1A2 and NRCAM (2012) (0)
- SMAD3 as a novel osteoarthritis risk locus (2020) (0)
- A genome-wide meta-analysis identifies 53 sequence variants associating with carpal tunnel syndrome (2022) (0)
- Author Correction: Germline variants at SOHLH2 influence multiple myeloma risk (2021) (0)
- Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis (2018) (0)
- Abstract 889: An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for theXRCC4SNPs (2011) (0)
- Mendelian Randomization Studies of the Role of Biomarkers in Type 2 Diabetes (2009) (0)
- Supplementary Material (nature09270-s1) (2012) (0)
- Variants in the LRP5 gene influence BMD both through common variants of small effect and rare mutations of large effect in osteoporotic families (2009) (0)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture ofmajor depressive disorder (2018) (0)
- Abstract 20276: Variants in the CDNK2B Gene on Chromosome 9p21 are Associated with Coronary Artery Disease Events in African American High Risk Families (2010) (0)
- P0085 - Generalized anxiety disorder in the anxiety/depression spectrum (2008) (0)
- Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis (vol 50, pg 1072, 2018) (2018) (0)
- Author Correction: The rate of meiotic gene conversion varies by sex and age (2018) (0)
- Adult Reading History Questionnaire--Icelandic Version (2015) (0)
- Genetics of coarctation of the aorta in Iceland (2016) (0)
- Research Explorer A large-scale genome-wide association study meta-analysis of cannabis use disorder (2020) (0)
- GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes (2018) (0)
- S.26.03 Schizophrenia genes identified by positional cloning affect the glutamatergic system (2003) (0)
- Rare sequence variants that disrupt ASGR 1 function lower non-HDL cholesterol and protect against coronary artery disease (2016) (0)
- The genetics of common diseases (2020) (0)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression (2018) (0)
- Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT. (2022) (0)
- Genome-wide association study on 13,167 individuals identifies regulators of hematopoietic stem and progenitor cell levels in human blood (2021) (0)
- Causal relationships between migraine and microstructural white matter: a Mendelian randomization study (2023) (0)
- Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis (2018) (0)
- Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis (2018) (0)
- Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (0)
- Roadmap for a precision-medicine initiative in the Nordic region (2019) (0)
- Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes (2019) (0)
- Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures (2019) (0)
- GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures (2019) (0)
- Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis (2018) (0)
- Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (2019) (0)
- HAPMIX results of chromosome 6 in chiptyped Icelanders (2017) (0)
- Genetic predisposition to mosaic Y chromosome loss in blood (2019) (0)
- 133 Evidence of heritability of the common form of atrial fibrillation (2005) (0)
- A rare missense variant in NR1H4 associates with lower cholesterol levels (2018) (0)
- Correction: Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (2017) (0)
- Sequence variant at 4q25 near PITX2 associates with appendicitis (2017) (0)
- Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns (2019) (0)
- Asthmatic patients exhibit different gene expression profiles, depending on their sensitivity to glucocorticoids (2002) (0)
- Cloning of cDNA coding for two large polypeptides (gps150/225) found in myelinating oligodendrocytes (1987) (0)
- Variants in the CDNK2B Gene on Chromosome 9p21 are Associated with Coronary Artery Disease Events in African American High Risk Families (2010) (0)
- Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry (2017) (0)
- A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis (2019) (0)
- Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density (2019) (0)
- 992 GENETIC CORRECTION OF PSA LEVELS AND PROSTATE CANCER RISK MARKERS IMPROVE POSITIVE PREDICTIVE VALUE OF THE PSA TEST (2011) (0)
- 95. GENOME-WIDE ASSOCIATION STUDY OF 14,000 CASES IDENTIFIES FOUR NEW RISK GENES AND IMPLICATES CALCIUM SIGNALING IN TOURETTE SYNDROME AND CHRONIC TIC DISORDERS (2022) (0)
- Eleven genomic loci affect plasma levels of chronic inflammation marker soluble urokinase-type plasminogen activator receptor (2021) (0)
- Correction: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (0)
- Genome-wide association and HLA fine mapping studies identify risk loci and genetic 1 pathways of allergic rhinitis (2018) (0)
- S.15.03 Neuregulin 1 and schizophrenia (2004) (0)
- Eleven genomic loci affect plasma levels of chronic inflammation marker soluble urokinase-type plasminogen activator receptor (2021) (0)
- The Epigenetics of common diseases (2017) (0)
- Functional characterization of GWAS loci associated with fracture risk (2013) (0)
- Abstract 19040: Different SCARB1 Locus Variants Associate With Hdl-Cholesterol and the Risk of Coronary Artery Disease (2016) (0)
- The nature of Neanderthal introgression revealed by 27,566 Icelandic genomes (2020) (0)
- Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing (2019) (0)
- Differences between germline genomes of monozygotic twins (2021) (0)
- ibration ) rates when added to conventional risk factors (2009) (0)
- Title : Ancient genomes from Iceland reveal the making of a human population One (2017) (0)
- Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank (2020) (0)
- Genome-wide meta-analysis identifies new loci and functional pathways influencing 1 Alzheimer ’ s disease risk 2 3 (2020) (0)
- A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin (2018) (0)
- Publisher Correction: Identification of 371 genetic variants for age at first sex and birth linked to externalising behavior (2021) (0)
- Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition (2018) (0)
- Prostate Cancer in Special Populations (2010) (0)
- The genetic basis of cross-phenotype correlation with bone fracture risk: the GEFOS consortium (2013) (0)
- University of Groningen Genome-wide analysis yields new loci associating with aortic valve stenosis (2018) (0)
- Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect (2023) (0)
- Abstract PR-7: A European genome-wide association study of urinary bladder cancer (2008) (0)
- Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2019) (0)
- Genetic insight into sick sinus syndrome. (2021) (0)
- Syddansk Universitet Variant ASGR1 associated with a reduced risk of coronary artery disease (2016) (0)
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