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2018 William Allan Award Introduction: Eric S. Lander

American journal of human genetics, 2019-03, Vol.104 (3), p.373-374

Daly, Mark J.

2019

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Eric Lander and David Botstein on Mapping Quantitative Traits

Genetics (Austin), 2016-05, Vol.203 (1), p.1-3

Churchill, Gary A

2016

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2018 William Allan Award: Discovering the Genes for Common Disease: From Families to Populations

American journal of human genetics, 2019-03, Vol.104 (3), p.375-383

Lander, Eric S.

2019

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Pedigree likelihood formulae based on founder and founder couple symmetry and validation of DNA testing software

Forensic science international : genetics, 2023-01, Vol.62, p.102782-102782, Article 102782

Yang, Da

2023

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Genomewide analysis of PRC1 and PRC2 occupancy identifies two classes of bivalent domains

PLoS genetics, 2008-10, Vol.4 (10), p.e1000242-e1000242

2008

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Identification of cancer driver genes based on nucleotide context

Nature genetics, 2020-02, Vol.52 (2), p.208-218

2020

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A molecular signature of metastasis in primary solid tumors

Nature genetics, 2003-01, Vol.33 (1), p.49-54

2003

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Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

Nature genetics, 2003-02, Vol.33 (2), p.177-182

2003

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Activity-by-contact model of enhancer-promoter regulation from thousands of CRISPR perturbations

Nature genetics, 2019-12, Vol.51 (12), p.1664-1669

2019

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PedStr Software for Cutting Large Pedigrees for Haplotyping, IBD Computation and Multipoint Linkage Analysis

Annals of human genetics, 2009-09, Vol.73 (5), p.527-531

2009

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Nipbl and mediator cooperatively regulate gene expression to control limb development

PLoS genetics, 2014-09, Vol.10 (9), p.e1004671-e1004671

2014

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A novel Ruminococcus gnavus clade enriched in inflammatory bowel disease patients

Genome medicine, 2017-11, Vol.9 (1), p.103-103, Article 103

2017

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Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome

PLoS genetics, 2009-09, Vol.5 (9), p.e1000650-e1000650

2009

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Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations

Nature genetics, 2018-09, Vol.50 (9), p.1219-1224

2018

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High-resolution haplotype structure in the human genome

Nature genetics, 2001-10, Vol.29 (2), p.229-232

2001

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Fast Linkage Analysis with MOD Scores Using Algebraic Calculation

Human heredity, 2014-01, Vol.78 (3/4), p.179-194

2014

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RNA antisense purification (RAP) for mapping RNA interactions with chromatin

Methods in molecular biology (Clifton, N.J.), 2015, Vol.1262, p.183

2015

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Paired exome analysis of Barrett's esophagus and adenocarcinoma

Nature genetics, 2015-09, Vol.47 (9), p.1047-1055

2015

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Large intergenic non-coding RNA-RoR modulates reprogramming of human induced pluripotent stem cells

Nature genetics, 2010-12, Vol.42 (12), p.1113-1117

2010

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Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel

European journal of human genetics : EJHG, 2017-06, Vol.25 (7), p.869-876

2017

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Whole-genome and multisector exome sequencing of primary and post-treatment glioblastoma reveals patterns of tumor evolution

Genome research, 2015-03, Vol.25 (3), p.316

2015

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The Genetic Landscape of Diamond-Blackfan Anemia

American journal of human genetics, 2018-12, Vol.103 (6), p.930-947

2018

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Characterization of single-nucleotide polymorphisms in coding regions of human genes

Nature genetics, 1999-07, Vol.22 (3), p.231-238

1999

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Assessing the impact of population stratification on genetic association studies

Nature genetics, 2004-04, Vol.36 (4), p.388-393

2004

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2018 William Allan Award Introduction: Eric S. Lander

Eric Lander and David Botstein on Mapping Quantitative Traits

2018 William Allan Award: Discovering the Genes for Common Disease: From Families to Populations

Pedigree likelihood formulae based on founder and founder couple symmetry and validation of DNA testing software

Genomewide analysis of PRC1 and PRC2 occupancy identifies two classes of bivalent domains

Identification of cancer driver genes based on nucleotide context

A molecular signature of metastasis in primary solid tumors

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

Activity-by-contact model of enhancer-promoter regulation from thousands of CRISPR perturbations

PedStr Software for Cutting Large Pedigrees for Haplotyping, IBD Computation and Multipoint Linkage Analysis

Nipbl and mediator cooperatively regulate gene expression to control limb development

A novel Ruminococcus gnavus clade enriched in inflammatory bowel disease patients

Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations

A mutational signature reveals alterations underlying deficient homologous recombination repair in breast cancer

High-resolution haplotype structure in the human genome

Fast Linkage Analysis with MOD Scores Using Algebraic Calculation

RNA antisense purification (RAP) for mapping RNA interactions with chromatin

Paired exome analysis of Barrett's esophagus and adenocarcinoma

Large intergenic non-coding RNA-RoR modulates reprogramming of human induced pluripotent stem cells

Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel

Whole-genome and multisector exome sequencing of primary and post-treatment glioblastoma reveals patterns of tumor evolution

The Genetic Landscape of Diamond-Blackfan Anemia

Characterization of single-nucleotide polymorphisms in coding regions of human genes

Assessing the impact of population stratification on genetic association studies

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