Leslie A Lange

发表

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.

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

Philippe Froguel, Nicholas J Timpson, Dirkje S Postma, 2010, Nature Genetics.

Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals.

Yiran Guo, Hakon Hakonarson, H. Hakonarson, 2013, Human molecular genetics.

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.

Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ.

Yun Li, Karen L Mohlke, E. Lange, 2010, Human molecular genetics.

A Variational Bayes Discrete Mixture Test for Rare Variant Association

Benjamin A. Logsdon, Deborah A Nickerson, Christopher J O'Donnell, 2014, Genetic epidemiology.

Association of exome sequences with plasma C-reactive protein levels in >9000 participants.

Pierre Fontanillas, Charles Kooperberg, Eric Boerwinkle, 2015, Human molecular genetics.

Autosomal Genome-Wide Scan for Coronary Artery Calcification Loci in Sibships at High Risk for Hypertension

Patrick Royston, Eric Boerwinkle, Stephen T Turner, 2002, Arteriosclerosis, thrombosis, and vascular biology.

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

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

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

Hynek Pikhart, Fernando Pires Hartwig, Joshua C Denny, 2017, The lancet. Diabetes & endocrinology.

Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults.

Yun Li, Kyle J. Gaulton, Shawn Levy, 2010, Human molecular genetics.

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.

Comparison of ENCODE region SNPs between Cebu Filipino and Asian HapMap samples

Karen L Mohlke, E. Lange, K. Mohlke, 2007, Journal of Human Genetics.

Population-specific coding variant underlies genome-wide association with adiponectin level.

Yun Li, Karen L Mohlke, Jingchun Luo, 2012, Human molecular genetics.

Genome- and exome-wide association study of serum lipoprotein (a) in the Jackson Heart Study

William Valdar, Yun Li, Qing Duan, 2015, Journal of Human Genetics.

Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.

Sudha Seshadri, Deborah A Nickerson, Wei-Min Chen, 2015, JAMA neurology.

Single-nucleotide polymorphisms at five loci are associated with C-reactive protein levels in a cohort of Filipino young adults

Karen L Mohlke, E. Lange, K. Mohlke, 2011, Journal of Human Genetics.

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.

Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array

Tom R. Gaunt, Shah Ebrahim, Jie Zheng, 2015, European Journal of Human Genetics.

Inactivating mutations in NPC1L1 and protection from coronary heart disease.

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

Common variants in the CRP gene in relation to longevity and cause-specific mortality in older adults: the Cardiovascular Health Study.

Bruce M Psaty, Lucia A Hindorff, Elad Ziv, 2008, Atherosclerosis.

Loss-of-function mutations in APOC3, triglycerides, and coronary disease.

He Zhang, Thomas Meitinger, Raimund Erbel, 2014, The New England journal of medicine.

HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials

Hynek Pikhart, Bengt Sennblad, Tom R. Gaunt, 2015, The Lancet.

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.