Jerome I Rotter

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Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction

Udo Hoffmann, David M Herrington, Eric Boerwinkle, 2011, Circulation.

Trans-ethnic meta-analysis of white blood cell phenotypes.

Yusuke Nakamura, Ming-Huei Chen, Rehan Qayyum, 2014, Human molecular genetics.

Impact of rare and common genetic variants on diabetes diagnosis by hemoglobin A1c in multi-ancestry cohorts: The Trans-Omics for Precision Medicine Program

James A Perry, Eric Boerwinkle, Josée Dupuis, 2019, bioRxiv.

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Eden R Martin, Seth Love, Brian Lawlor, 2019, Nature Genetics.

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.

Christian Gieger, Thomas Meitinger, Paul Mitchell, 2013, Human molecular genetics.

Evaluating gene × gene and gene × smoking interaction in rheumatoid arthritis using candidate genes in GAW15

Xiuqing Guo, Xiaohui Li, J. Rotter, 2007, BMC proceedings.

Genetic architecture of subcortical brain structures in 38,851 individuals

Benjamin S Aribisala, Tien Yin Wong, Wiro J Niessen, 2019, Nature Genetics.

Nature Genetics Advance Online Publication Genetic Association Study of Qt Interval Highlights Role for Calcium Signaling Pathways in Myocardial Repolarization

Michael J Ackerman, Christian Gieger, Thomas Meitinger, 2022 .

Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.

Mengmeng Du, Charles Kooperberg, Eric Boerwinkle, 2014, Human molecular genetics.

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

Judy H Cho, Dan L Nicolae, Mark J Daly, 2007, Nature Genetics.

Genome-wide association analysis identifies multiple loci related to resting heart rate.

Christian Gieger, Thomas Meitinger, Henry Völzke, 2010, Human molecular genetics.

Genome-wide association identifies multiple ulcerative colitis susceptibility loci

Kathryn Roeder, Judy H Cho, Chun Li, 2010, Nature Genetics.

Application of Bayesian classification with singular value decomposition method in genome-wide association studies

Soonil Kwon, Xiuqing Guo, J. Rotter, 2009, BMC proceedings.

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

Inês Barroso, Jiyoung Heo, Beverley Balkau, 2015, Nature communications.

Pleiotropic genes for metabolic syndrome and inflammation.

Eric Boerwinkle, Josée Dupuis, Sharon L R Kardia, 2014, Molecular genetics and metabolism.

A genome-wide association study of chronic obstructive pulmonary disease in Hispanics.

Qi Yan, Wei Chen, Edwin K Silverman, 2015, Annals of the American Thoracic Society.

Minimal model-based insulin sensitivity has greater heritability and a different genetic basis than homeostasis model assessment or fasting insulin.

Daniel J Zaccaro, Richard M Watanabe, Richard N Bergman, 2003, Diabetes.

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects.

Constantin Polychronakos, David C Wilson, Joseph T. Glessner, 2010, Human molecular genetics.

Individualizing therapies in type 2 diabetes mellitus based on patient characteristics: what we know and what we need to know.

David M Nathan, Leif Groop, Robert A Rizza, 2010, The Journal of clinical endocrinology and metabolism.

CUBN is a gene locus for albuminuria.

Sylvia Stracke, Ming-Huei Chen, Luigi Ferrucci, 2011, Journal of the American Society of Nephrology : JASN.

Serum Immune Responses Predict Rapid Disease Progression among Children with Crohn's Disease: Immune Responses Predict Disease Progression

Dennis Christie, Iwona Wrobel, Ying-Chao Lin, 2006, The American Journal of Gastroenterology.

Admixture Mapping of Subclinical Atherosclerosis and Subsequent Clinical Events Among African Americans in 2 Large Cohort Studies

Jasmin Divers, Degui Zhi, Wendy S Post, 2017, Circulation. Cardiovascular genetics.

A genome-wide association study of central corneal thickness in Latinos.

Paul Marjoram, W James Gauderman, Talin Haritunians, 2013, Investigative ophthalmology & visual science.

Novel genetic loci associated with hippocampal volume

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2017, Nature Communications.

Systemic soluble tumor necrosis factor receptors 1 and 2 are associated with severity of diabetic retinopathy in Hispanics.

Xiuqing Guo, Eli Ipp, B. Klein, 2012, Ophthalmology.

Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.

Thomas Meitinger, Uwe Völker, Reinhold Schmidt, 2009, JAMA.

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.

He Gao, Tim Kacprowski, Andres Metspalu, 2016, American journal of human genetics.

Edinburgh Research Explorer Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies

Jean-François Dartigues, Reinhold Schmidt, Sudha Seshadri, 2022 .

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Tin Aung, Paul Mitchell, Ching-Yu Cheng, 2013, Nature Genetics.

Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

Jie Huang, Uwe Völker, Ming-Huei Chen, 2017, PloS one.

52 Genetic Loci Influencing Myocardial Mass.

Christian Gieger, Thomas Meitinger, Manolis Kellis, 2016, Journal of the American College of Cardiology.

Novel Genetic Loci Associated With Retinal Microvascular Diameter

Paul Mitchell, Ching-Yu Cheng, Eric Boerwinkle, 2016, Circulation. Cardiovascular genetics.

Novel Associations of Multiple Genetic Loci With Plasma Levels of Factor VII, Factor VIII, and von Willebrand Factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium

Ming-Huei Chen, Qiong Yang, Nicole Soranzo, 2010, Circulation.

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2016, Nature Neuroscience.

Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos.

W James Gauderman, Mina Torres, Rohit Varma, 2016, Human molecular genetics.

Statin-induced changes in gene expression in EBV-transformed and native B-cells.

Eugene Bolotin, Kyungpil Kim, Kelan Tantisira, 2014, Human molecular genetics.

Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk

Christian Gieger, Xiaofeng Zhu, Paolo Vineis, 2011, Nature.

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

Jianwen Cai, Tao Wang, Charles Kooperberg, 2019, PLoS genetics.

Variation in the 3-Hydroxyl-3-Methylglutaryl Coenzyme A Reductase Gene Is Associated With Racial Differences in Low-Density Lipoprotein Cholesterol Response to Simvastatin Treatment

Deborah A Nickerson, David Waters, Xiuqing Guo, 2008, Circulation.

Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis

Christian Gieger, Sanghoon Moon, Tien Yin Wong, 2017, PLoS Medicine.

Phenotypic predictors of response to simvastatin therapy among African-Americans and Caucasians: the Cholesterol and Pharmacogenetics (CAP) Study.

Feng Lin, Deborah A Nickerson, David Waters, 2006, The American journal of cardiology.

Common genetic variants and subclinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis (MESA).

David A Bluemke, Wendy S Post, Stephen S Rich, 2016, Atherosclerosis.

Prospective study of particulate air pollution exposures, subclinical atherosclerosis, and clinical cardiovascular disease: The Multi-Ethnic Study of Atherosclerosis and Air Pollution (MESA Air).

Thomas Lumley, Lianne Sheppard, Ana V Diez Roux, 2012, American journal of epidemiology.

Variants in ZNF365 isoform D are associated with Crohn's disease

Talin Haritunians, Dermot P B McGovern, S. Targan, 2011, Gut.

Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

Steve Epstein, Chih-Cheng Hsu, Peng Chen, 2017, Nature Genetics.

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Christian Gieger, Alex Doney, Inês Barroso, 2010, Nature Genetics.

Genome‐Wide Family‐Based Linkage Analysis of Exome Chip Variants and Cardiometabolic Risk

Carl D Langefeld, Jirong Long, Nicholette D. Palmer, 2014, Genetic epidemiology.

Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosis.

Vilmundur Gudnason, Tamara B Harris, Kathleen F Kerr, 2014, JAMA.

Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.

Edwin K Silverman, Vilmundur Gudnason, Thomas Lumley, 2012, American journal of respiratory and critical care medicine.

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.

Tom R. Gaunt, Fotios Drenos, Meena Kumari, 2012, American journal of human genetics.

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Tariq Ahmad, Albert Cohen, Judy H Cho, 2010, Nature Genetics.

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Christian Gieger, Gonçalo Abecasis, He Gao, 2018, Nature Genetics.

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.

Fernando Pires Hartwig, Claude Bouchard, Christian Gieger, 2018, American journal of human genetics.

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

Claude Bouchard, Uwe Völker, Todd L Edwards, 2016, Nature Genetics.

IL‐23 receptor (IL‐23R) gene protects against pediatric Crohn's disease

Iwona Wrobel, S. Targan, M. Dubinsky, 2007, Inflammatory bowel diseases.

Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology

Andrew Carroll, Eric Boerwinkle, Andrew D. Johnson, 2017, Nature Genetics.

Genome‐wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans

Nicholette D. Palmer, Chuan Gao, Adolfo Correa, 2018, Genetic epidemiology.

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

Avni Santani, Steven Joffe, Michael J Bamshad, 2015, Genome research.

Discovery and fine mapping of serum protein loci through transethnic meta-analysis.

Christian Gieger, Yusuke Nakamura, Luigi Ferrucci, 2012, American journal of human genetics.

Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

Jie Huang, Uwe Völker, Ming-Huei Chen, 2017, The Journal of clinical investigation.

Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.

Xiaofeng Zhu, Todd L Edwards, Dana C Crawford, 2016, American journal of human genetics.

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

Claude Bouchard, Beverley Balkau, Bengt Sennblad, 2012, Nature Genetics.

Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations

Xiaofeng Zhu, Tamar Sofer, Joshua C Denny, 2017, PLoS genetics.

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Christian Gieger, Gonçalo Abecasis, He Gao, 2017, bioRxiv.

Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family‐Based Linkage and Association in the IRAS Family Study

John Blangero, Carl D Langefeld, Jirong Long, 2017, Annals of human genetics.

Elevated plasma free fatty acids are associated with sudden death: a prospective community-based evaluation at the time of cardiac arrest.

Naser Ahmadi, K. Reinier, J. Jui, 2014, Heart rhythm.

Inactivating mutations in NPC1L1 and protection from coronary heart disease.

John Spertus, Thomas Meitinger, Joshua C Denny, 2014, The New England journal of medicine.

Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis From the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

Eric Boerwinkle, Thomas Lumley, Wolfgang Lieb, 2010, Circulation. Cardiovascular genetics.

Genome-wide association and large scale follow-up identifies 16 new loci influencing lung function

Christian Gieger, Inês Barroso, Florian Kronenberg, 2011, Nature Genetics.

Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans.

Xiaofeng Zhu, Tamar Sofer, Raanan Arens, 2016, American journal of respiratory and critical care medicine.

Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos.

W James Gauderman, Mina Torres, Rohit Varma, 2016, Human molecular genetics.

Large-Scale Candidate Gene Analysis in Whites and African Americans Identifies IL6R Polymorphism in Relation to Atrial Fibrillation: The National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) Project

Sudha Seshadri, Thomas H Mosley, Martina Müller-Nurasyid, 2011, Circulation. Cardiovascular genetics.

Genome-wide analysis of genetic loci associated with Alzheimer disease.

Sudha Seshadri, Vilmundur Gudnason, Thomas Lumley, 2010, JAMA.

Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

Jia Jia, Ming-Huei Chen, Eric Boerwinkle, 2016, Nature Genetics.

Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection.

Xiaofeng Zhu, Ingo Ruczinski, Swapan Mallick, 2011, American journal of human genetics.

A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes.

Yan Zhang, Henri-Jean Garchon, Robert H Podolsky, 2004, Nature genetics.

Common variants at ten loci influence QT interval duration in the QTGEN Study

Thomas Lumley, Fernando Rivadeneira, Christopher J O'Donnell, 2009, Nature Genetics.

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.

Christian Gieger, Ingo Ruczinski, Tom R. Gaunt, 2012, American journal of human genetics.

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.

Uwe Völker, Tim Kacprowski, Ming-Huei Chen, 2015, Blood.

Genetic architecture of gene expression traits across diverse populations

Hae Kyung Im, Xiuqing Guo, Lauren S. Mogil, 2018, bioRxiv.

Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium.

Dana C Crawford, Florian Kronenberg, Eric Boerwinkle, 2012, Atherosclerosis.

Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

Hynek Pikhart, Tom R. Gaunt, Meena Kumari, 2014, BMJ : British Medical Journal.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

Claude Bouchard, William Wheeler, Peter Kraft, 2014 .

Novel Loci Associated With PR Interval in a Genome-Wide Association Study of 10 African American Cohorts

Wei Chen, Luigi Ferrucci, Yun Li, 2012, Circulation. Cardiovascular genetics.

Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.

Dror Berel, Talin Haritunians, Xiuqing Guo, 2010, Human molecular genetics.

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.

Xiaofeng Zhu, Todd L Edwards, Wei Guo, 2013, American journal of human genetics.

Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

Joshua C Denny, Wei-Qi Wei, Fredrik Nyberg, 2016, Journal of Medical Genetics.

Predicting Stroke Through Genetic Risk Functions: The CHARGE Risk Score Project

Sudha Seshadri, Eric Boerwinkle, Martin Dichgans, 2014, Stroke.