Cornelia M. Van Duijn
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Cornelia M. Van Duijnbiology Degrees
Biology
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Genetics
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Biology
Cornelia M. Van Duijn's Degrees
- PhD Genetics University of Amsterdam
- Masters Biomedical Sciences University of Amsterdam
- Bachelors Biomedical Sciences University of Amsterdam
Why Is Cornelia M. Van Duijn Influential?
(Suggest an Edit or Addition)Cornelia M. Van Duijn'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
- Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
- Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease (2013) (3484)
- Effects of Age, Sex, and Ethnicity on the Association Between Apolipoprotein E Genotype and Alzheimer Disease: A Meta-analysis (1997) (3245)
- Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) (1801)
- Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 (2006) (1377)
- Genome-wide association study of blood pressure and hypertension (2009) (1371)
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) (1107)
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
- Identification of seven loci affecting mean telomere length and their association with disease (2013) (761)
- A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance (2012) (756)
- New loci associated with kidney function and chronic kidney disease (2010) (754)
- Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene (1992) (752)
- Variants in MTNR1B influence fasting glucose levels (2009) (742)
- Common genetic variants influence human subcortical brain structures (2015) (731)
- Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior (2010) (688)
- Genome-wide association analyses identify 18 new loci associated with serum urate concentrations (2012) (678)
- Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study (2008) (661)
- Whole-genome sequence variation, population structure and demographic history of the Dutch population (2014) (650)
- Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function (2010) (605)
- Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility (2019) (589)
- Multiple loci associated with indices of renal function and chronic kidney disease (2009) (583)
- Alcohol consumption and risk of dementia: the Rotterdam Study (2002) (570)
- Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma (2011) (526)
- A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis (2001) (515)
- Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies (2010) (477)
- Apolipoprotein E4 allele in a population–based study of early–onset Alzheimer's disease (1994) (455)
- 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)
- DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism (2003) (419)
- FTO genotype is associated with phenotypic variability of body mass index (2012) (407)
- Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture (2015) (399)
- Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (379)
- Meta-analysis of telomere length in 19 713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect (2013) (375)
- Sequence variants at CHRNB 3 – CHRNA 6 and CYP 2 A 6 affect smoking behavior (2010) (312)
- Large-scale genomic analyses link reproductive ageing to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair (2015) (308)
- Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
- Variant of TREM 2 Associated with the Risk of Alzheimer ’ s Disease (2012) (296)
- Genome-wide association analysis identifies susceptibility loci for migraine without aura (2012) (286)
- Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies (2006) (284)
- Susceptibility loci for intracranial aneurysm in European and Japanese populations (2008) (283)
- Metabolic network failures in Alzheimer's disease: A biochemical road map (2017) (280)
- Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus (2013) (279)
- Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report (2011) (271)
- The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression (2009) (211)
- A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14 (2010) (208)
- A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25 (2010) (207)
- Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis (2008) (203)
- Estimating human age from T-cell DNA rearrangements (2010) (173)
- Convergent genetic and expression data implicate immunity in Alzheimer's disease (2014) (172)
- The vast complexity of primary open angle glaucoma: Disease genes, risks, molecular mechanisms and pathobiology (2013) (162)
- The dopamine D4 receptor gene 48-base-pair-repeat polymorphism and mood disorders: A meta-analysis (2005) (159)
- Glucocorticoid Receptor Gene-Based SNP Analysis in Patients with Recurrent Major Depression (2006) (156)
- Altered bile acid profile in mild cognitive impairment and Alzheimer's disease: Relationship to neuroimaging and CSF biomarkers (2018) (151)
- Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways (2012) (150)
- Linkage disequilibrium in young genetically isolated Dutch population (2004) (146)
- A genome-wide association study of aging (2011) (146)
- The effect of APOE and other common genetic variants on the onset of Alzheimer's disease and dementia: a community-based cohort study (2018) (139)
- Amyloid precursor protein gene mutation in early-onset Alzheimer's disease (1991) (132)
- Genetic risk of primary open angle glaucoma (1998) (121)
- Sex-specific genetic effects influence variation in body composition (2008) (118)
- The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility (2017) (113)
- Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies (2018) (113)
- Refining genetic associations in multiple sclerosis (2008) (108)
- Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval (2002) (107)
- A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression (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)
- Genetics of cortisol secretion and depressive symptoms: A candidate gene and genome wide association approach (2011) (103)
- Alzheimer's Disease Genes and Cognition in the Nondemented General Population (2013) (91)
- An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype (2017) (89)
- Mutations in the hemochromatosis gene (HFE), Parkinson's disease and parkinsonism (2003) (88)
- Genetic risk of neurodegenerative diseases is associated with mild cognitive impairment and conversion to dementia (2015) (81)
- EVI5 is a risk gene for multiple sclerosis (2008) (80)
- Association of Alzheimer's disease GWAS loci with MRI markers of brain aging (2015) (79)
- Serum levels of interleukin-6 are not elevated in patients with Alzheimer's disease (1990) (77)
- Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (2015) (75)
- Epidemiology of the dementias: recent developments and new approaches. (1996) (73)
- Genetic polymorphisms and heart failure (2004) (66)
- Serum apolipoprotein E level is not increased in Alzheimer's disease: the Rotterdam study (1998) (66)
- ACE gene is associated with Alzheimer's disease and atrophy of hippocampus and amygdala (2005) (65)
- The apolipoprotein E gene and its age-specific effects on cognitive function (2010) (65)
- A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism (2003) (59)
- Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project (2012) (58)
- The Consortium on Health and Ageing: Network of Cohorts in Europe and the United States (CHANCES) project—design, population and data harmonization of a large-scale, international study (2014) (56)
- Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (55)
- Epistatic effect of genes from the dopamine and serotonin systems on the temperament traits of Novelty Seeking and Harm Avoidance (2002) (51)
- Erratum: Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence (2017) (50)
- The impact of apolipoprotein E on dementia in persons with Down's syndrome (2008) (50)
- Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt–Jakob Disease phenotype (2001) (50)
- Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (2018) (50)
- Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample (1999) (49)
- PLD3 variants in population studies (2015) (49)
- Common DNA variants predict tall stature in Europeans (2014) (48)
- PARK 7 , a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism , on Chromosome 1 p 36 (2001) (47)
- Mutation screening of the tau gene in patients with early-onset Alzheimer's disease (1999) (47)
- The expression of type III hyperlipoproteinemia: involvement of lipolysis genes (2009) (45)
- Heritability of fasting glucose levels in a young genetically isolated population (2006) (44)
- Cathepsin D gene and the risk of Alzheimer's disease: A population-based study and meta-analysis (2011) (44)
- Amyloid β secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease (2001) (44)
- The −491 A/T polymorphism in the regulatory region of the Apolipoprotein E gene and early-onset Alzheimer's disease (1998) (42)
- Hormone replacement therapy and Alzheimer's disease. (1999) (42)
- Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt–Jakob disease (2004) (41)
- Distinguishing true from false positives in genomic studies: p values (2013) (39)
- Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction (2019) (38)
- Genes, pathways, and animal models in primary open-angle glaucoma (2015) (37)
- Genetic epidemiology of Creutzfeldt-Jakob disease in Europe. (2001) (36)
- The GAB2 Gene and the Risk of Alzheimer's Disease: Replication and Meta-Analysis (2009) (36)
- Comparison of participant information and informed consent forms of five European studies in genetic isolated populations (2010) (35)
- Epidemiology of neurological diseases in elderly people: what did we learn from the Rotterdam Study? (2006) (35)
- Disentangling the biological pathways involved in early features of Alzheimer's disease in the Rotterdam Study (2018) (35)
- Association of cyclin-dependent kinase 5 and neuronal activators p35 and p39 complex in early-onset Alzheimer's disease (2005) (33)
- APOE genotyping in differential diagnosis of Alzheimer's disease (1996) (33)
- Epigenome-wide Association Study of Attention-Deficit/Hyperactivity Disorder Symptoms in Adults (2019) (32)
- Strong linkage on 2q33.3 to familial early-onset generalized osteoarthritis and a consideration of two positional candidate genes (2006) (32)
- Common variants in Alzheimer’s disease: Novel association of six genetic variants with AD and risk stratification by polygenic risk scores (2019) (30)
- Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies (2015) (29)
- Discovery by the Epistasis Project of an epistatic interaction between the GSTM3 gene and the HHEX/IDE/KIF11 locus in the risk of Alzheimer's disease (2013) (29)
- Cerebrovascular risk factors do not contribute to genetic variance of cognitive function The ERF study (2007) (29)
- A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15 q 25 (2010) (29)
- Genetic variants in RBFOX3 are associated with sleep latency (2016) (29)
- Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study (2020) (29)
- HFE variants, APOE and Alzheimer's disease: Findings from the population-based Rotterdam Study (2009) (28)
- A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration (2020) (28)
- The UBQLN1 polymorphism, UBQ-8i, at 9q22 is not associated with Alzheimer's disease with onset before 70 years (2006) (28)
- Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia (vol 99, pg 13675, 2002) (2002) (28)
- Genes predict village of origin in rural Europe (2010) (28)
- Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide (2017) (28)
- Mutation analysis of candidate genes within the 2q33.3 linkage area for familial early-onset generalised osteoarthritis (2007) (27)
- Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium (2018) (26)
- Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population (2017) (25)
- Serum apolipoprotein E is associated with long-term risk of Alzheimer’s disease: The Rotterdam Study (2016) (25)
- Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2016) (25)
- Fine-mapping the effects of Alzheimer's disease risk loci on brain morphology (2016) (25)
- Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations (1999) (23)
- Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions (2012) (23)
- TMEM106B Influences Volume of Left-Sided Temporal Lobe and Interhemispheric Structures in the General Population (2014) (23)
- Association of adiponectin and leptin with relative telomere length in seven independent cohorts including 11,448 participants (2014) (23)
- Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (22)
- Age-related maculopathy: Its genetic basis (2001) (22)
- Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population (2009) (22)
- The molecular genetics of early-onset Alzheimer's disease (2004) (22)
- Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European Populations (2017) (21)
- Linkage analysis of adult height in a large pedigree from a Dutch genetically isolated population (2009) (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)
- A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease (2018) (20)
- A Genome-Wide Association Study in isolated populations reveals new genes associated to common food likings (2016) (18)
- Relationship of the Ubiquilin 1 gene with Alzheimer's and Parkinson's disease and cognitive function (2007) (18)
- VEGF Polymorphisms Are Associated With Endocardial Cushion Defects: A Family-Based Case-Control Study (2010) (17)
- 315 Estrogen, apolipoprotein E and the risk of Alzheimer's Disease (1996) (16)
- Menopause and the Brain (1997) (16)
- Familial aggregation of preeclampsia and intrauterine growth restriction in a genetically isolated population in The Netherlands (2008) (16)
- The impact of genetic testing on complex diseases (2005) (16)
- Is Parental Age Related to the Risk of Alzheimer's Disease? (1990) (16)
- UvA-DARE ( Digital Academic Repository ) Four Novel Loci ( 19 q 13 , 6 q 24 , 12 q 24 , and 5 q 14 ) Influence the Microcirculation In Vivo (2010) (15)
- Decreased DNA repair capacity in familial, but not in sporadic Alzheimer's disease (1991) (15)
- Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2011) (15)
- Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits (2011) (15)
- Towards predictive genetic testing of complex diseases (2006) (14)
- Neopterin and the risk of dementia in persons with Down syndrome (2009) (14)
- How to kickstart a national biobanking infrastructure – experiences and prospects of BBMRI-NL (2012) (13)
- Erratum: Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia (Proceedings of the National Academy of Sciences of the United States of America (October 15, 2002) 99:21 (13675-13680)) (2002) (13)
- Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking (2015) (13)
- Association of 5 0 estrogen receptor alpha gene polymorphisms with bone mineral density, vertebral bone area and fracture risk (2003) (13)
- Plasma β amyloid and impaired CO2-induced cerebral vasomotor reactivity (2007) (12)
- Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360) (2017) (12)
- Low-density lipoprotein receptor mutations generate synthetic genome-wide associations (2012) (12)
- CDH6 and HAGH protein levels in plasma associate with Alzheimer’s disease in APOE ε4 carriers (2019) (12)
- Multi-trait genome-wide association study identifies new loci associated with optic disc parameters (2019) (12)
- IS ALZHEIMER'S DISEASE DISTINCT FROM NORMAL AGEING? (1988) (12)
- Does bilirubin protect against hemochromatosis gene (HFE) related mortality? (2004) (11)
- Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies (2020) (11)
- Role of APOE in dementia: A critical reappraisal. (1998) (11)
- PLASMA AMYLOID BETA LEVELS, CEREBRAL SMALL-VESSEL DISEASES AND COGNITION: THE ROTTERDAM STUDY (2017) (10)
- The GAB2 gene and the risk of Alzheimer's disease: Replication and meta-analysis (2009) (10)
- Mutation analysis of the chromosome 14q24.3 dihydrolipoyl succinyltransferase (DLST) gene in patients with early-onset Alzheimer disease (1995) (10)
- Associations between the deletion polymorphism of the angiotensin 1-converting enzyme gene and ocular signs of primary open-angle glaucoma (2005) (9)
- GENESTAT: an information portal for design and analysis of genetic association studies (2009) (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)
- A deletion in DJ-1 and the risk of dementia—a population-based survey (2004) (9)
- Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation (2019) (9)
- The dystrophin gene and cognitive function in the general population (2014) (9)
- Erratum: Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis (American Journal of Human Genetics (2016) 99(2) (481–488)(S0002929716302208)(10.1016/j.ajhg.2016.06.016)) (2016) (8)
- Apolipoprotein E ϵ4 allele is associated with left ventricular systolic dysfunction (2004) (8)
- miLD and booLD Programs for Calculation and Analysis of Corrected Linkage Disequilibrium (2003) (8)
- Evidence for major gene inheritance of Alzheimer disease in families of patients with and without APOE ε4 (1996) (8)
- Apolipoprotein E genotype and concomitant clinical features in early-onset Alzheimer's disease (2004) (8)
- COMPREHENSIVE GENE-GENE INTERACTION META-ANALYSIS OF IGAP GWA STUDIES (2014) (7)
- 3 Population-specific genotype imputations using minimac or IMPUTE 2 (2018) (7)
- Genetic Factors in Early- and Late-Onset Alzheimer’s Disease (1999) (7)
- Increased High Density Lipoprotein-levels associated with Age-related Macular degeneration. Evidence from the EYE-RISK and E3 Consortia (2018) (7)
- The ERCC 6 Gene and Age-related Macular Degeneration (2010) (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)
- No evidence for prion protein gene locus multiplication in Creutzfeldt-Jakob disease (2010) (6)
- Prospects of genetic research of mild cognitive impairment (2004) (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)
- Association of the IGF1 gene with fasting insulin levels (2016) (5)
- Anticipation in familial amyotrophic lateral sclerosis with SOD 1G 93 S mutation (2002) (5)
- Exome sequencing identifies rare damaging variants in the ATP8B4 and ABCA1 genes as novel risk factors for Alzheimer’s Disease (2020) (5)
- METABOLITES ASSOCIATED WITH COGNITIVE FUNCTION IN THE ROTTERDAM STUDY AND ERASMUS RUCPHEN FAMILY STUDY (2016) (4)
- Genome-wide association study of plasma triglycerides, phospholipids and relation to cardio-metabolic risk factors (2019) (4)
- ASSOCIATION OF ALZHEIMER DISEASE GWAS LOCI WITH MRI-MARKERS OF BRAIN AGING (2014) (4)
- EXOME CHIP META-ANALYSIS OF ALZHEIMER'S DISEASE IN THE IGAP CONSORTIUM (2014) (4)
- Erratum: Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (Proc Natl Acad Sci USA (2014) 111 (13790-13794) DOI: 10.1073/pnas.1404623111) (2015) (4)
- 749 Evidence for major gene inheritance of Alzheimer disease in families of patients with and without APOE ε4. VS Rao (1996) (4)
- Association study between a promoter polymorphism in the presenilin 1 gene and late-onset Alzheimer's disease (2000) (3)
- Telomere length variation reduces with age: evidence of survivor effect (2014) (3)
- Supplementary Material 5 (2014) (3)
- Gut microbiome-wide association study of depression (2021) (3)
- Effects of Age and Ethnicity on the Link Between APOE ∊4 and Alzheimer Disease—Reply (1998) (3)
- Supplementary Material 3 (2015) (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)
- Supplementary Material 6 (2014) (3)
- Supplementary Material 7 (2014) (3)
- Apolipoprotein E genotype modifies the association between smoking and early-onset Alzheimer's disease (1995) (3)
- PLD3 ASSOCIATES TO PROLINE A PROPOSED BIOMARKER IN MAPSTONE ET AL (2014) (3)
- Reply to “Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis” (2010) (2)
- Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis Reply (2010) (2)
- University of Groningen Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk (2011) (2)
- Behavioral and psychological signs and symptoms in patients with dementia of the Alzheimer type (DAT) and frontotemporal dementia (FTD): No effect of APOE genotype (2002) (2)
- P4-154 Genomic sequencing of MAPT provides an extended SNP map and identifies >30 H1 subhaplotypes (2004) (2)
- The alpha-2 macroglobulin gene in Alzheimer's disease: A population-based study and meta-analysis (2000) (2)
- Risk factors for Alzheimer's disease : a genetic-epidemiologic study (1992) (2)
- The apolipoprotein E gene and the risk of early-onset Alzheimer's disease (1995) (2)
- CYP 1 A 2 and coffee intake and the modifying effect of sex , age , and smoking 1 – 3 (2012) (2)
- Reply to — Alzheimer's disease and the family effect (1994) (2)
- EIF 2 AK 3 variants in Dutch patients with Alzheimer ' s disease (2018) (2)
- GENOME-WIDE META-ANALYSIS OF LATE-ONSET ALZHEIMER’S DISEASE USING RARE VARIANT IMPUTATION IN 64,859 SUBJECTS IDENTIFIES RISK LOCI WITH ROLES IN INNATE IMMUNITY AND CARDIOVASCULAR TRAITS: THE INTERNATIONAL GENOMICS OF ALZHEIMER’S PROJECT (IGAP) (2019) (1)
- polymorphisms with bone mineral density, vertebral bone area and fracture risk (2003) (1)
- In vitro analysis of Alzheimer's disease-related presenilin 1 and 2 mutations: effect on beta-amyloid processing (2002) (1)
- Genetic Diagnosis of Age-RMacular Degeneration: The Role of Molecular Genetics in the Identification of High Risk Eyes (2008) (1)
- Can Dietary Antioxidants Reduce the Genetic Risk of Early Age-Related Macular Degeneration? (2009) (1)
- Identification of novel rare genetic variants associated with COPD in the general population (2018) (1)
- ALDH2 and Head and Neck Cancer: a Meta-analysis implementing a Mendelian Randomization approach (2009) (1)
- Supplementary Material 4 (2015) (1)
- A study of ADHD in a genetic isolate (2000) (1)
- GENETIC RISK OF NEURODEGENERATIVE DISEASES IS ASSOCIATED WITH MILD COGNITIVE IMPAIRMENT AND CONVERSION TO DEMENTIA: THE ROTTERDAM STUDY (2014) (1)
- WHOLE-GENOME SEQUENCING IN FAMILIAL LATE-ONSET ALZHEIMER’S DISEASE IDENTIFIES RARE VARIATION IN AD CANDIDATE GENES (2017) (1)
- EVALUATION OF THE ABSOLUTE GENETIC RISK OF ALZHEIMER'S DISEASE IN THE AGING POPULATION (2016) (1)
- Supplementary Material 15 (2013) (1)
- Genome-wide Association Studies From Four Cohorts Reveal Multiple Novel Loci Related To Pulmonary Function (2010) (1)
- Alzheimer's disease, genetic and environmental factors (1998) (1)
- A genome-wide SNP-by-NO2 interaction study on lung function in the LifeLines study (2017) (1)
- Nicastrin significantly modifies risk for familial early-onset Alzheimer's disease in a Dutch population based sample (2002) (1)
- Abstract 1967: Genome-wide Association Analysis of 25,330 Individuals Identifies Multiple Loci Associated With Resting Heart Rate (2009) (1)
- Erratum: Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology (The American Journal of Human Genetics (2019) 105(1) (15–28), (S0002929719301880), (10.1016/j.ajhg.2019.05.002)) (2019) (1)
- Supplementary Material 9 (2013) (1)
- A genome-wide search for novel early-onset Alzheimer disease genes (2000) (1)
- Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile (2019) (1)
- An International Genome-Wide Association Study of Glaucoma-Related Optic Disc Parameters in 18,000 Caucasians: the International Glaucoma Genetics Consortium (2013) (1)
- Polygenic overlap between C-reactive protein , plasma lipids and Alzheimer ’ s disease 1 2 (2017) (1)
- Low-frequency variant imputation identifies rare variant candidate loci in a gwas of late-onset Alzheimer’s disease in the igap consortium (2015) (1)
- Two-octapeptide repeat deletion of the prion protein gene associated with a rapidly progressive dementia (2001) (1)
- Heritability and genetics of personality in healthy families and families with affective disorders from Sweden (2002) (1)
- Heritability and Determinants of Intraocular Pressure in an Isolated Population in the Netherlands (2006) (1)
- DNA methylation mediates the association between occupational exposures and lung function (2017) (1)
- A genome-wide association study identifies a susceptibility 1 locus for refractive errors and myopia at 15 q 14 2 3 (2010) (1)
- Identification of Biomarkers for the Prevention of Chronic Disease (2020) (1)
- Exome-chip meta-analysis identifies novel loci, including ADAMTS6 associated with cardiac conduction (2018) (1)
- Phosphosphingolipid levels are associated with cognitive function and level of education in healthy subjects (2012) (1)
- The First Genome-Wide Association Meta-Analysis of Borderline Personality Disorder Features (2017) (1)
- Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration (2006) (1)
- Discovery and Refinement Supplementary (2015) (1)
- Whole exome sequence analysis of white matter hyperintensities on cranial MRI (2015) (1)
- A genome-wide linkage study for COPD in a Dutch genetic isolate (2017) (0)
- PATHWAY-SPECIFIC GENETIC RISK SCORE ASSOCIATED WITH ALZHEIMER’S DISEASE AND WHITE MATTER LESIONS IN COGNITIVELY NORMAL SUBJECTS (2017) (0)
- Metabolomics Prediction of Future Type 2 Diabetes (2016) (0)
- Development of algorithms and software for high-performance computing in genetic analysis of complex human traits (2004) (0)
- Abstract 2074: Association of Hypertension Drug Target Genes With Blood Pressure and Hypertension: Results From a Genome-wide Association Study in 29,136 Individuals (2009) (0)
- Contents Vol. 61, 2006 (2006) (0)
- Delft University of Technology EIF2AK3 variants in Dutch patients with Alzheimer's disease (2018) (0)
- THE INFLUENCE OF GENETIC AND ENVIRONMENTAL FACTORS ON BLOOD PRESSURE VARIANCE IN A GENETICALLY ISOLATED POPULATION: P2.224 (2004) (0)
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- Abstract 150: Trans-ethnic GWAS of Mri-defined Brain Infarcts: Charge Consortium (2015) (0)
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