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Recent progress in the study of the genetics of height

Human genetics, 2011-05, Vol.129 (5), p.465-472

Lettre, Guillaume

2011

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Fetal haemoglobin in sickle-cell disease: from genetic epidemiology to new therapeutic strategies

The Lancet (British edition), 2016-06, Vol.387 (10037), p.2554-2564

2016

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Rare variant association studies: considerations, challenges and opportunities

Genome medicine, 2015-02, Vol.7 (1), p.16-16

2015

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Multimodal CRISPR perturbations of GWAS loci associated with coronary artery disease in vascular endothelial cells

PLoS genetics, 2023-03, Vol.19 (3), p.e1010680-e1010680

2023

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Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically

Arteriosclerosis, thrombosis, and vascular biology, 2016-12, Vol.36 (12), p.2439

2016

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

Proceedings of the National Academy of Sciences - PNAS, 2017-12, Vol.114 (52), p.E11257-E11266

2017

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Genome partitioning of genetic variation for complex traits using common SNPs

Nature genetics, 2011-06, Vol.43 (6), p.519-525

2011

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Major cell-types in multiomic single-nucleus datasets impact statistical modeling of links between regulatory sequences and target genes

Scientific reports, 2023-03, Vol.13 (1), p.3924-3924, Article 3924

2023

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Polygenic determinants in extremes of high-density lipoprotein cholesterol

Journal of lipid research, 2017-11, Vol.58 (11), p.2162-2170

2017

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

PloS one, 2017-06, Vol.12 (6), p.e0178700-e0178700

2017

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One step closer to linking GWAS SNPs with the right genes

Nature genetics, 2022-06, Vol.54 (6), p.748-749

Lettre, Guillaume

2022

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Importance of genetic testing in unexplained cardiac arrest

European heart journal, 2022-08, Vol.43 (32), p.3071-3081

2022

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The genetics of platelet count and volume in humans

Platelets (Edinburgh), 2018-02, Vol.29 (2), p.125-130

2018

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Genetic model testing and statistical power in population-based association studies of quantitative traits

Genetic epidemiology, 2007-05, Vol.31 (4), p.358-362

2007

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Pleiotropic effects for Parkin and LRRK2 in leprosy type-1 reactions and Parkinson’s disease

Proceedings of the National Academy of Sciences - PNAS, 2019-07, Vol.116 (31), p.15616-15624

2019

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Variant-aware saturating mutagenesis using multiple Cas9 nucleases identifies regulatory elements at trait-associated loci

Nature genetics, 2017-04, Vol.49 (4), p.625-634

2017

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DNA polymorphisms at the BCL11A, HBS1L-MYB, and β-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease

Proceedings of the National Academy of Sciences - PNAS, 2008-08, Vol.105 (33), p.11869-11874

2008

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An erythroid-specific ATP2B4 enhancer mediates red blood cell hydration and malaria susceptibility

The Journal of clinical investigation, 2017-08, Vol.127 (8), p.3065-3074

2017

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Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon

PloS one, 2014-03, Vol.9 (3), p.e92506-e92506

2014

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

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (5), p.1620-1625

2008

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Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA)

BMJ open, 2022-03, Vol.12 (3), p.e059021-e059021

2022

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Blocking HbS Polymerization in SCD

Cell, 2020-03, Vol.180 (5), p.819-819

Lettre, Guillaume

2020

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

Circulation (New York, N.Y.), 2010-11, Vol.122 (20), p.2009-2015

2010

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Optimal sequencing strategies for identifying disease-associated singletons

PLoS genetics, 2017-06, Vol.13 (6), p.e1006811-e1006811

2017

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Integrative analysis of vascular endothelial cell genomic features identifies AIDA as a coronary artery disease candidate gene

Genome Biology, 2019-07, Vol.20 (1), p.133-133, Article 133

2019

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Recent progress in the study of the genetics of height

Fetal haemoglobin in sickle-cell disease: from genetic epidemiology to new therapeutic strategies

Rare variant association studies: considerations, challenges and opportunities

Multimodal CRISPR perturbations of GWAS loci associated with coronary artery disease in vascular endothelial cells

Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically

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

Genome partitioning of genetic variation for complex traits using common SNPs

Major cell-types in multiomic single-nucleus datasets impact statistical modeling of links between regulatory sequences and target genes

Polygenic determinants in extremes of high-density lipoprotein cholesterol

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

One step closer to linking GWAS SNPs with the right genes

Importance of genetic testing in unexplained cardiac arrest

The genetics of platelet count and volume in humans

Genetic model testing and statistical power in population-based association studies of quantitative traits

Pleiotropic effects for Parkin and LRRK2 in leprosy type-1 reactions and Parkinson’s disease

Variant-aware saturating mutagenesis using multiple Cas9 nucleases identifies regulatory elements at trait-associated loci

DNA polymorphisms at the BCL11A, HBS1L-MYB, and β-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease

An erythroid-specific ATP2B4 enhancer mediates red blood cell hydration and malaria susceptibility

Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon

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

Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA)

Blocking HbS Polymerization in SCD

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

Optimal sequencing strategies for identifying disease-associated singletons

Integrative analysis of vascular endothelial cell genomic features identifies AIDA as a coronary artery disease candidate gene

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