Guillaume Lettre

发表

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

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

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Thomas Meitinger, Inês Barroso, Peter Kraft, 2010, Nature Genetics.

Genetic regulation of adult stature

G. Lettre, Guillaume Lettre, 2009, Current opinion in pediatrics.

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.

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

Christian Gieger, Thomas Meitinger, Inês Barroso, 2009, Nature Genetics.

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia

Gonçalo R. Abecasis, Stuart H. Orkin, Ramaiah Nagaraja, 2008, Proceedings of the National Academy of Sciences.

Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation

Joel N Hirschhorn, Cameron D. Palmer, J. Hirschhorn, 2010, Nature Genetics.

A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry

Xiaofeng Zhu, Olufunmilayo I. Olopade, Alex P. Reiner, 2013, Nature Genetics.

Multiple Loci Are Associated with White Blood Cell Phenotypes

Christian Gieger, Yusuke Nakamura, Kazuhiko Yamamoto, 2011, PLoS genetics.

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Thomas Meitinger, Inês Barroso, Peter Kraft, 2011, Nature Genetics.

A Variational Bayes Discrete Mixture Test for Rare Variant Association

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

FTO genotype is associated with phenotypic variability of body mass index

Joel Eriksson, Joseph E. Powell, Andres Metspalu, 2012, Nature.

Common variants in the GDF5-UQCC region are associated with variation in human height

Shah Ebrahim, Debbie A Lawlor, Yoav Ben-Shlomo, 2008, Nature Genetics.

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

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

Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits

Uwe Völker, Marie-Pierre Dubé, Alexander Teumer, 2014, Nature Genetics.

Genomic inflation factors under polygenic inheritance

Mark I McCarthy, Reedik Mägi, Nicholas G Martin, 2011, European Journal of Human Genetics.

Lp-PLA2, scavenger receptor class B type I gene (SCARB1) rs10846744 variant, and cardiovascular disease

David M Herrington, Walter Palmas, Mary Cushman, 2018, PloS one.

Human genetic variation alters CRISPR-Cas9 on- and off-targeting specificity at therapeutically implicated loci

Jean-Claude Tardif, Matthew C. Canver, Daniel G. MacArthur, 2017, Proceedings of the National Academy of Sciences.

Developmental cell biology: Developmental apoptosis in C. elegans: a complex CEDnario

Michael O. Hengartner, G. Lettre, M. Hengartner, 2006, Nature Reviews Molecular Cell Biology.

Frameshift indels introduced by genome editing can lead to in-frame exon skipping

Adam Lavertu, M. Rivas, A. Lavertu, 2017, PloS one.

Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT)

Yusuke Nakamura, Yukinori Okada, David Couper, 2011, PLoS genetics.

Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project

Donald W. Bowden, Eric Boerwinkle, Christopher A. Haiman, 2011, PLoS genetics.

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

Yadav Sapkota, Thomas Meitinger, Andres Metspalu, 2017, Nature Communications.

Strategies to fine-map genetic associations with lipid levels by combining epigenomic annotations and liver-specific transcription profiles.

Karen L Mohlke, K. Mohlke, G. Lettre, 2014, Genomics.

European Ancestry as a Risk Factor for Atrial Fibrillation in African Americans

Kathleen F. Kerr, Eric Vittinghoff, E. Vittinghoff, 2010, Circulation.

Rare variant association studies: considerations, challenges and opportunities

G. Lettre, P. Auer, Guillaume Lettre, 2015, Genome Medicine.

Comparison of DNA methylation profiles in human fetal and adult red blood cell progenitors

Karim Benkirane, G. Lettre, S. Lessard, 2015, Genome Medicine.

A common variant of HMGA2 is associated with adult and childhood height in the general population

Richa Saxena, Leena Peltonen, Eleftheria Zeggini, 2007, Nature Genetics.

Variants at the APOE/C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High‐Density Lipoprotein Cholesterol

Robert A. Hegele, Amina Barhdadi, G. Lettre, 2018, Journal of the American Heart Association.

A Meta-Analysis and Genome-Wide Association Study of Platelet Count and Mean Platelet Volume in African Americans

Rehan Qayyum, Benjamin A. Logsdon, Tamara B. Harris, 2012, PLoS 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.

Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans

Walter Palmas, Steven A. McCarroll, Struan F. A. Grant, 2011, Human 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.

Genome-wide association of anthropometric traits in African- and African-derived populations.

Xiaofeng Zhu, Charles Rotimi, Kristin Ardlie, 2010, Human molecular genetics.