Cristen Willer
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American-Canadian bioinformatician and geneticist
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Cristen Willerbiology Degrees
Biology
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Bioinformatics
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#97
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Genetics
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Biology
Cristen Willer's Degrees
- PhD Genetics Stanford University
- Bachelors Bioinformatics University of California, Berkeley
Why Is Cristen Willer Influential?
(Suggest an Edit or Addition)According to Wikipedia, Cristen Jennifer Willer is an American-Canadian bioinformatician and geneticist. She is an associate professor of Internal Medicine, Human Genetics, and Computational Medicine and Bioinformatics at the University of Michigan.
Cristen Willer'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
- METAL: fast and efficient meta-analysis of genomewide association scans (2010) (3721)
- 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)
- A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants (2007) (2840)
- Discovery and Refinement of Loci Associated with Lipid Levels (2013) (2475)
- LocusZoom: regional visualization of genome-wide association scan results (2010) (2373)
- Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
- MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes (2010) (2008)
- 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)
- 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)
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (2009) (1735)
- Newly identified loci that influence lipid concentrations and risk of coronary artery disease (2008) (1626)
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) (1507)
- Common variants at 30 loci contribute to polygenic dyslipidemia (2009) (1380)
- Common variants near MC4R are associated with fat mass, weight and risk of obesity (2008) (1307)
- New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
- Genome-wide association study identifies eight loci associated with blood pressure (2009) (1225)
- Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
- Genotype imputation. (2009) (1013)
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2018) (914)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
- Loss-of-function mutations in APOC3, triglycerides, and coronary disease. (2014) (799)
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) (785)
- Common variants associated with plasma triglycerides and risk for coronary artery disease (2013) (767)
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
- Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (516)
- Rare and low-frequency coding variants alter human adult height (2016) (511)
- Twin concordance and sibling recurrence rates in multiple sclerosis (2003) (502)
- Timing of birth and risk of multiple sclerosis: population based study (2004) (461)
- Genomic inflation factors under polygenic inheritance (2011) (456)
- Mapping the human genetic architecture of COVID-19 (2021) (455)
- Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease (2016) (434)
- Exome-wide association study of plasma lipids in >300,000 individuals (2017) (428)
- Common variants in the GDF5-UQCC region are associated with variation in human height (2008) (400)
- Biobank-driven genomic discovery yields new insight into atrial fibrillation biology (2018) (398)
- Genetics of Blood Lipids Among ~300,000 Multi-Ethnic Participants of the Million Veteran Program (2018) (387)
- Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology (2017) (357)
- The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals (2016) (347)
- Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. (2016) (309)
- Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) (294)
- Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample (2006) (264)
- Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk (2014) (263)
- Exome sequencing and characterization of 49,960 individuals in the UK Biobank (2020) (244)
- New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (2016) (242)
- Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance. (2005) (240)
- Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension (2016) (234)
- Genetically determined height and coronary artery disease. (2015) (220)
- A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) (207)
- Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease (2017) (204)
- Genetic evidence of assortative mating in humans (2017) (199)
- Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. (2014) (197)
- Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure underpinning obesity (2017) (193)
- Meta-Analysis of Gene Level Tests for Rare Variant Association (2013) (183)
- Biological and clinical insights from genetics of insomnia symptoms (2018) (175)
- Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. (2008) (170)
- Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels. (2016) (164)
- Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease (2017) (135)
- Screening of 134 Single Nucleotide Polymorphisms (SNPs) Previously Associated With Type 2 Diabetes Replicates Association With 12 SNPs in Nine Genes (2007) (132)
- GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approach (2015) (131)
- The power of genetic diversity in genome-wide association studies of lipids (2021) (129)
- Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses (2020) (128)
- Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses (2020) (128)
- Whole exome sequencing and characterization of coding variation in 49,960 individuals in the UK Biobank (2019) (126)
- Deep-coverage whole genome sequences and blood lipids among 16,324 individuals (2017) (124)
- Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms (2014) (120)
- The power of meta-analysis in genome-wide association studies. (2013) (115)
- Comprehensive Association Study of Type 2 Diabetes and Related Quantitative Traits With 222 Candidate Genes (2008) (114)
- Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps (2021) (114)
- Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
- Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants contributing to lipid levels and coronary artery disease (2017) (103)
- Causal relationships between NAFLD, T2D and obesity have implications for disease subphenotyping. (2020) (102)
- Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts (2019) (101)
- A meta-analysis of genomic screens in multiple sclerosis. The Transatlantic Multiple Sclerosis Genetics Cooperative. (2001) (96)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale (2020) (93)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale (2020) (93)
- Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (2020) (92)
- Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes (2018) (91)
- Exploring and visualizing large-scale genetic associations by using PheWeb (2020) (91)
- Eight blood pressure loci identified by genome-wide association study of 34,433 people of European ancestry (2009) (88)
- Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes (2019) (88)
- Common Variants in Maturity-Onset Diabetes of the Young Genes Contribute to Risk of Type 2 Diabetes in Finns (2006) (87)
- Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese (2015) (84)
- Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations (2021) (83)
- Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve (2017) (82)
- Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development. (2018) (82)
- Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals. (2016) (81)
- Evidence of linkage with HLA-DR in DRB1*15-negative families with multiple sclerosis. (2001) (78)
- Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations (2008) (78)
- Genome-wide analysis yields new loci associating with aortic valve stenosis (2017) (74)
- Within-family studies for Mendelian randomization: avoiding dynastic, assortative mating, and population stratification biases (2019) (74)
- Perhexiline activates KLF14 and reduces atherosclerosis by modulating ApoA-I production. (2015) (72)
- Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database (2006) (71)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2017) (68)
- PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION (2018) (67)
- An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group. (2004) (65)
- A saturated map of common genetic variants associated with human height (2022) (65)
- Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. (2014) (64)
- Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease (2017) (64)
- Hepatic Transmembrane 6 Superfamily Member 2 Regulates Cholesterol Metabolism in Mice. (2016) (63)
- Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data (2022) (60)
- Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects (2022) (59)
- Within-sibship GWAS improve estimates of direct genetic effects (2021) (58)
- Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections. (2016) (55)
- Cardiometabolic Traits, Sepsis, and Severe COVID-19 (2020) (53)
- No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study (2002) (53)
- Common Variants Show Predicted Polygenic Effects on Height in the Tails of the Distribution, Except in Extremely Short Individuals (2011) (53)
- Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (53)
- Finding genes and variants for lipid levels after genome-wide association analysis (2012) (53)
- Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals (2020) (53)
- New Blood Pressure–Associated Loci Identified in Meta-Analyses of 475 000 Individuals (2017) (50)
- Genetic susceptibility to MS: a second stage analysis in Canadian MS families (2001) (47)
- Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations (2008) (46)
- The emerging landscape of health research based on biobanks linked to electronic health records: Existing resources, statistical challenges, and potential opportunities (2019) (45)
- Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants (2021) (45)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (45)
- GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer (2020) (44)
- Receptor-Mediated ER Export of Lipoproteins Controls Lipid Homeostasis in Mice and Humans. (2020) (43)
- Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation (2018) (42)
- Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program (2020) (41)
- Association of exome sequences with plasma C-reactive protein levels in >9000 participants. (2015) (40)
- Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis (2018) (39)
- Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (39)
- Association between microchimerism and multiple sclerosis in Canadian twins (2006) (36)
- Genetic variants in CETP increase risk of intracerebral hemorrhage (2016) (36)
- Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. (2016) (34)
- Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use (2019) (33)
- Electronic health records: the next wave of complex disease genetics. (2018) (33)
- Largest GWAS (N=1,126,563) of Alzheimer's Disease Implicates Microglia and Immune Cells (2020) (32)
- A genome-wide scan in forty large pedigrees with multiple sclerosis (2007) (32)
- A multigenerational family with multiple sclerosis. (2002) (32)
- Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort (2020) (29)
- A first update on mapping the human genetic architecture of COVID-19 (2022) (27)
- Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (26)
- Lower Extremity Function Is Independently Associated With Hospitalization Burden in Heart Failure With Preserved Ejection Fraction. (2019) (24)
- Recent developments in genome and exome-wide analyses of plasma lipids (2015) (24)
- Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association (2022) (23)
- Microchimerism in autoimmunity and transplantation: potential relevance to multiple sclerosis (2002) (23)
- Accurate local-ancestry inference in exome-sequenced admixed individuals via off-target sequence reads. (2013) (22)
- A genome scan in a single pedigree with a high prevalence of multiple sclerosis (2007) (22)
- Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease (2020) (22)
- Narrow-sense heritability estimation of complex traits using identity-by-descent information (2017) (22)
- Cardiometabolic Traits, Sepsis, and Severe COVID-19: A Mendelian Randomization Investigation (2020) (21)
- Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2020) (21)
- Genetic insight into sick sinus syndrome (2021) (21)
- Age-of-onset information helps identify 76 genetic variants associated with allergic disease (2020) (21)
- Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2017) (20)
- Methods for Association Analysis and Meta‐Analysis of Rare Variants in Families (2015) (20)
- Genome sequencing unveils a regulatory landscape of platelet reactivity (2019) (18)
- Genetic diversity fuels gene discovery for tobacco and alcohol use (2022) (18)
- Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels (2017) (18)
- Meta-analysis fine-mapping is often miscalibrated at single-variant resolution (2022) (17)
- Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans. (2014) (16)
- A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers (2018) (16)
- 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)
- The HUNT study: A population-based cohort for genetic research (2021) (15)
- Cardiopulmonary Exercise Testing Following Open Repair for a Proximal Thoracic Aortic Aneurysm or Dissection (2020) (14)
- No large-effect low-frequency coding variation found for myocardial infarction. (2014) (14)
- A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors (2017) (14)
- Complex and Potentially Harmful Medication Patterns in Heart Failure with Preserved Ejection Fraction. (2020) (13)
- Genome-wide association study of 1 million people identifies 111 loci for atrial fibrillation (2018) (13)
- Higher admission rates and in-hospital mortality for acute type A aortic dissection during Influenza season: a single center experience (2020) (13)
- MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk (2020) (13)
- Mitochondrial genome-wide association study of migraine – the HUNT Study (2020) (13)
- Genome-scale CRISPR screening for modifiers of cellular LDL uptake. (2021) (12)
- Competitive enzyme-linked immunosorbent assay for the determination of zinc bacitracin in animal feedingstuffs. (1994) (12)
- Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools (2021) (11)
- Cardiometabolic traits, sepsis and severe covid-19 with respiratory failure: a Mendelian randomization investigation (2020) (11)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (10)
- TCR beta polymorphisms and multiple sclerosis. (2004) (10)
- Exposure and risk factors for COVID-19 and the impact of staying home on Michigan residents (2020) (10)
- Aortic progression and reintervention in patients with pathogenic variants after a thoracic aortic dissection. (2020) (10)
- Use of a Polygenic Risk Score Improves Prediction of Myocardial Injury After Non-Cardiac Surgery (2020) (9)
- Maternal - offspring HLA-DRB1 compatibility in multiple sclerosis. (2005) (9)
- Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes (2021) (9)
- Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux. (2021) (8)
- Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm. (2021) (8)
- The Emerging Landscape of Epidemiological Research Based on Biobanks Linked to Electronic Health Records: Existing Resources, Analytic Challenges and Potential Opportunities (2018) (8)
- Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes (2020) (8)
- Genetic associations with temporal shifts in obesity and severe obesity during the obesity epidemic in Norway: A longitudinal population-based cohort (the HUNT Study) (2020) (8)
- Genome-scale CRISPR screening for modifiers of cellular LDL uptake (2020) (7)
- Robust meta‐analysis of biobank‐based genome‐wide association studies with unbalanced binary phenotypes (2019) (7)
- Development and Validation of a Polygenic Risk Score for Stroke in the Chinese Population (2021) (7)
- Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices (2021) (7)
- An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels (2018) (7)
- Effects of the coronary artery disease associated LPA and 9p21 loci on risk of aortic valve stenosis. (2019) (7)
- Whole genome sequence analysis of blood lipid levels in >66,000 individuals (2021) (7)
- Polygenic risk score from a multi-ancestry GWAS uncovers susceptibility of heart failure (2021) (7)
- A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study (2022) (6)
- Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children with asthma. (2019) (6)
- A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids (2021) (6)
- Meta-Analysis of Gene Level Association Tests (2013) (6)
- Genetic mutations associated with susceptibility to perioperative complications in a longitudinal biorepository with integrated genomic and electronic health records. (2020) (6)
- Genome-wide association study of cardiac troponin I in the general population (2021) (6)
- A first stage genome‐wide screen for regions shared identical‐by‐descent in hutterite families with multiple sclerosis (2008) (6)
- Cardiorespiratory Fitness After Open Repair for Acute Type A Aortic Dissection - A Prospective Study. (2021) (6)
- Disclosure of clinically actionable genetic variants to thoracic aortic dissection biobank participants (2021) (6)
- Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts (2023) (5)
- The causal effects of serum lipids and apolipoproteins on kidney function: multivariable and bidirectional Mendelian-randomization analyses (2021) (5)
- Genome-wide association meta-analysis identifies novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation (2021) (5)
- Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk (2017) (5)
- Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts (2023) (5)
- Gait speed is a preoperative indicator of postoperative events after elective proximal aortic surgery. (2020) (5)
- Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT (2021) (5)
- Multi-ancestry GWAS for venous thromboembolism identifies novel loci followed by experimental validation in zebrafish (2022) (5)
- Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors (2022) (5)
- Variation in Serum PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9), Cardiovascular Disease Risk, and an Investigation of Potential Unanticipated Effects of PCSK9 Inhibition: A Genome-Wide Association Study and Mendelian Randomization Study in the HUNT, Norway (2019) (5)
- Mendelian Randomization Analysis Dissects the Relationship between NAFLD, T2D, and Obesity and Provides Implications to Precision Medicine (2019) (5)
- Identification of ACE2 modifiers by CRISPR screening (2021) (4)
- Exome sequencing and characterization of 49,960 individuals in the UK Biobank (2020) (4)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (4)
- Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease (2019) (4)
- Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits (2022) (4)
- Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals (2022) (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)
- Incorporating family disease history and controlling case–control imbalance for population-based genetic association studies (2021) (4)
- Identification of cell type specific ACE2 modifiers by CRISPR screening (2022) (4)
- A survey of aortic disease biorepository participants’ preferences for return of research genetic results (2020) (4)
- Insights into blood lipids from rare variant discovery. (2015) (4)
- Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies (2022) (4)
- A novel homozygous ABCA1 variant in an asymptomatic man with profound hypoalphalipoproteinemia. (2018) (4)
- An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. (2021) (4)
- Genome-Wide Association Study Identifies LINC01184/SLC12A2 As Risk Locus for Skin and Soft Tissue Infections. (2021) (3)
- Coding variants in RPL 3 L and MYZAP increase risk of atrial fi brillation (2018) (3)
- Differences in Inflammation, Treatment, and Outcomes Between Black and Non-Black Patients Hospitalized for COVID-19: A Prospective Cohort Study (2021) (3)
- Multi-ancestry meta-analysis identifies 2 novel loci associated with ischemic stroke and reveals heterogeneity of effects between sexes and ancestries (2022) (3)
- Sex-Specific Survival Bias and Interaction Modeling in Coronary Artery Disease Risk Prediction (2021) (3)
- Type 2 diabetes sex-specific effects associated with E167K coding variant in TM6SF2 (2021) (3)
- Variants associated with HHIP expression have sex-differential effects on lung function. (2020) (3)
- Genome-wide association analysis of excessive daytime sleepiness identifies 42 loci that suggest phenotypic subgroups (2018) (3)
- Translating genetic association of lipid levels for biological and clinical application (2021) (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)
- WikiGWA: an open platform for collecting and using genome-wide association results (2012) (3)
- Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals (2022) (3)
- Exposure and Risk Factors for COVID-19 and the Impact of Staying Home on 8,047 Biorepository Participants (2020) (2)
- Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk (2023) (2)
- Using Genomic Structural Equation Modeling to Partition the Genetic Covariance Between Birthweight and Cardiometabolic Risk Factors into Maternal and Offspring Components in the Norwegian HUNT Study (2022) (2)
- A genome-scan in a single pedigree with a high prevalence of MS (2007) (2)
- Clinical, genetic, and experimental increase in soluble urokinase plasminogen activator receptor levels promotes atherosclerosis. (2022) (2)
- Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease. (2023) (2)
- Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2022) (2)
- Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis (2022) (2)
- Genome-wide association scans identify novel loci that influence lipid levels and risk of coronary artery disease (2007) (2)
- Types and Causes of Injuries in a Youth Ice Hockey Program Over Three Seasons (2006) (2)
- Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program (2021) (1)
- Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (1)
- POLYPHARMACY AND POTENTIALLY INAPPROPRIATE MEDICATION USE ARE UNIVERSAL AMONG PATIENTS WITH HEART FAILURE WITH PRESERVED EJECTION FRACTION (2019) (1)
- Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution (2019) (1)
- Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (2020) (1)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility (2022) (1)
- Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (1)
- Identification of heart rate-associated loci and genes (2013) (1)
- Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) (1)
- Genome-wide analysis yields new loci associating with aortic valve stenosis (2018) (1)
- ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma (2022) (1)
- Author Correction: Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits (2022) (1)
- Variants associated with HHIP expression have sex-differential effects on lung function (2021) (1)
- Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (1)
- Do maternal intrauterine environmental influences that lower offspring birthweight causally increase offspring cardiometabolic risk factors in later life? A Mendelian randomization study of 45,849 genotyped parent offspring pairs in the HUNT study (2020) (1)
- Meta-analysis of Genetic Associations in up to 339,224 Individuals Identify 66 New Loci for Bmi, Confirming a Neuronal Contribution to Body Weight Regulation and Implicating Several Novel Pathways (2013) (1)
- A Genome Scan for Genes Underlying Adult Body Size Differences between Central African Pygmies and their Non-Pygmy Neighbors (2017) (1)
- Discovery and Refinement Supplementary (2015) (1)
- Genome-Wide Association Study of Over One Million Participants Identifies 49 Novel Loci Associated With Coronary Artery Disease (2019) (1)
- A Novel Variant in APOB Gene Causes Extremely Low LDL-C Without Known Adverse Effects (2020) (1)
- A fast linkage method for population GWAS cohorts with related individuals (2023) (0)
- Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2021) (0)
- Polygenic Risk Score Identifies Patients at Increased Risk for Abdominal Aortic Aneurysm and May Benefit from Ultrasound Screening (2020) (0)
- Abstract 452: Low Rates of Influenza Vaccine and Higher Occurrence of Acute Type A Aortic Dissection in the Winter Months- a Call for Action to Incorporate Influenza Vaccine Into Preventive Strategies for High Risk Patients (2019) (0)
- Confirmation of linkage between the HLA-DR locus and multiple sclerosis in two unusually large MS families. (1999) (0)
- Higher admission rates and in-hospital mortality for acute type A aortic dissection during Influenza season: a single center experience (2020) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
- Title : Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (0)
- Supplementary Material (nature09270-s1) (2012) (0)
- Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program (2018) (0)
- A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors (2017) (0)
- A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers (2018) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2020) (0)
- Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (0)
- SNPs associated with HHIP expression have differential effects on lung function in males and females (2019) (0)
- Genetic and Functional Characterization of ANGPTL7 as a Therapeutic Target for Glaucoma (2021) (0)
- Biological and clinical insights from genetics of insomnia symptoms (2019) (0)
- Exploring and visualizing large-scale genetic associations by using PheWeb (2020) (0)
- Biological and clinical insights from genetics of insomnia symptoms (2019) (0)
- Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts (2020) (0)
- Biobank-driven genomic discovery yields new insight into atrial fibrillation biology (2018) (0)
- Title Exome-wide association analysis reveals novel codingsequence variants associated with lipid traits in Chinese (2015) (0)
- Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium (2021) (0)
- Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries (2018) (0)
- Forty multiplex families with MS: Linkage analysis of chromosome 6 and HLA-DRB1 (2002) (0)
- Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies (2018) (0)
- Clonal haematopoiesis and risk of chronic liver disease (2023) (0)
- Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (2020) (0)
- Genome-wide association study of skin and soft tissue infection susceptibility (2020) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
- Genetic insight into sick sinus syndrome. (2021) (0)
- Bicuspid Aortic Valve–Associated Regulatory Regions Reveal GATA4 Regulation and Function During Human-Induced Pluripotent Stem Cell–Based Endothelial-Mesenchymal Transition—Brief Report (2022) (0)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale (2020) (0)
- MEASURING THE LEVELS OF THE CARDIAC BIOMARKER SUPAR (SOLUBLE UROKINASE PLASMINOGEN ACTIVATOR RECEPTOR) TO PREDICT THE RISK OF AORTIC ANEURYSMS (2023) (0)
- Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale (2020) (0)
- Title: Biological and clinical insights from genetics of insomnia symptoms Short Title: Insights from genetics of insomnia symptoms (2018) (0)
- University of Groningen Genome-wide analysis yields new loci associating with aortic valve stenosis (2018) (0)
- Utility of family history in disease prediction in the era of polygenic scores (2021) (0)
- POLYPHARMACY, MULTIMORBIDITY, AND THERAPEUTIC COMPETITION IN HEART FAILURE WITH PRESERVED EJECTION FRACTION (2020) (0)
- The MHC and multiple sclerosis susceptibility - several levels of complexity (2004) (0)
- Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer (2021) (0)
- Integrating large scale genetic and clinical information to predict cases of heart failure (2022) (0)
- 743 HUNTing for genes that affect inflammatory skin disease in 4,071 cases and 40,430 controls (2018) (0)
- Analysis plan for primary cohort GWAS for blood lipid levels for the Global Lipids Genetics Consortium (2021) (0)
- Variant-specific inflation factors for assessing population stratification at the phenotypic variance level (2021) (0)
- Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes (2018) (0)
- Disclosure of clinically actionable genetic variants to thoracic aortic dissection biobank participants (2021) (0)
- Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation (2018) (0)
- A genome-wide scan for regions shared identical by descent in Hutterite MS families (2002) (0)
- Abstract 154: Genetic Variants in CETP That Increase HDL Levels also Increase Risk of Intracerebral Hemorrhage (2017) (0)
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2018) (0)
- Trans-ancestry meta-analysis improves performance of genetic scores for multiple adiposity-related traits in East Asian populations (2022) (0)
- Genotyping and imputation (2018) (0)
- Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (0)
- Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease (2021) (0)
- Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis (2019) (0)
- Using human genetics to understand the causes and consequences of circulating cardiac troponin I in the general population (2020) (0)
- New insights into the genetic etiology of 57 essential and non-essential trace elements in humans (2023) (0)
- Acknowledgement to the Reviewers (2006) (0)
- Rare loss of function variants in candidate genes and risk of colorectal cancer (2018) (0)
- Deep-coverage whole genome sequences and blood lipids among 16,324 individuals (2018) (0)
- Deep-coverage whole genome sequences and blood lipids among 16,324 individuals (2018) (0)
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