Gonçalo R Abecasis

发表

An evaluation of the replicate pool method: quick estimation of genome‐wide linkage peak p‐values

Janis E Wigginton, Gonçalo R Abecasis, G. Abecasis, 2006, Genetic epidemiology.

Ancestry estimation and control of population stratification for sequence-based association studies

Chaolong Wang, Hyun Min Kang, Sebastian Zöllner, 2014, Nature 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.

Fine Mapping Major Histocompatibility Complex Associations in Psoriasis and Its Clinical Subtypes

Vinod Chandran, Buhm Han, Proton Rahman, 2014, American journal of human genetics.

Genome-wide scan reveals association of psoriasis with IL-23 and NFB pathways

Pui-Yan Kwok, Sampath Prahalad, Dafna Gladman, 2016 .

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 .

Gene Expression in Skin and Lymphoblastoid Cells: Refined Statistical Method Reveals Extensive Overlap in Cis-eqtl Signals

Wei Chen, Andre Franke, Liming Liang, 2022 .

Blood pressure loci identified with a gene-centric array.

Jean Tichet, Tom R. Gaunt, Jackie A Cooper, 2011, American journal of human genetics.

Accurate local-ancestry inference in exome-sequenced admixed individuals via off-target sequence reads.

Hyun Min Kang, Xiaowei Zhan, Cristen Willer, 2013, American journal of human 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.

Molecular dissection of psoriasis: integrating genetics and biology.

Andrew Johnston, Gonçalo R Abecasis, Trilokraj Tejasvi, 2010, The Journal of investigative dermatology.

Efficient study designs for test of genetic association using sibship data and unrelated cases and controls.

Michael Boehnke, Gonçalo R Abecasis, G. Abecasis, 2006, American journal of human genetics.

Correcting for Sample Contamination in Genotype Calling of DNA Sequence Data.

Hyun Min Kang, Michael Boehnke, Gonçalo R Abecasis, 2015, American journal of human genetics.

Meta-analysis and imputation refines the association of 15q25 with smoking quantity

Tariq Ahmad, Inês Barroso, Lowell Satler, 2010, Nature Genetics.

Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis

Gianmauro Cuccuru, Carlo Sidore, Francesco Cucca, 2010, Nature 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.

Genotype Imputation from Large Reference Panels.

Brian L Browning, Gonçalo R Abecasis, G. Abecasis, 2018, Annual review of genomics and human genetics.

Unraveling a multifactorial late-onset disease: from genetic susceptibility to disease mechanisms for age-related macular degeneration.

Anand Swaroop, Gonçalo R Abecasis, Emily Y Chew, 2009, Annual review of genomics and human genetics.

Methods for Association Analysis and Meta‐Analysis of Rare Variants in Families

Francesco Cucca, Dajiang J Liu, Matthew Zawistowski, 2015, Genetic epidemiology.

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.

The benefits of using genetic information to design prevention trials.

Li Li, Meena Kumari, Hyun Min Kang, 2013, American journal of human genetics.

52 Genetic Loci Influencing Myocardial Mass.

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

Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration.

Jurg Ott, Josephine Hoh, Sapna Shah, 2005, American journal of human genetics.

Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.

Christian Gieger, Andres Metspalu, Christopher G Mathew, 2012, American journal of human genetics.

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

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

Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Christian Gieger, Jason Carey, Steven Wiltshire, 2016 .

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

Christian Gieger, Thomas Meitinger, Raimund Erbel, 2009, Nature Genetics.

Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2

Christian Gieger, Mario Albrecht, Yun Li, 2010, Nature Genetics.

Genomewide Scan Reveals Association of Psoriasis with IL-23 and NF-κB Pathways

Pui-Yan Kwok, Sampath Prahalad, Yun Li, 2008, Nature Genetics.

Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease

Inês Barroso, Michael Inouye, Panagiotis Deloukas, 2010, Arteriosclerosis, thrombosis, and vascular biology.

Genome-wide physical activity interactions in adiposity. A meta-analysis of 200,452 adults

Claude Bouchard, Christian Gieger, Tuija Tammelin, 2017 .

The impact of genotyping error on family-based analysis of quantitative traits

Stacey S Cherny, Gonçalo R Abecasis, Lon R Cardon, 2001, European Journal of Human Genetics.

Genotype calling and haplotyping in parent-offspring trios

Wei Chen, Yun Li, Hyun Min Kang, 2013, Genome research.

Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans

Gonçalo R Abecasis, Maria Karayiorgou, G. Abecasis, 2009, Proceedings of the National Academy of Sciences.

Corrigendum: Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

Michael Boehnke, Gonçalo R Abecasis, Laura J Scott, 2006, Nature Genetics.

Population and individual-specific regulatory variation in Sardinia

Alexis Battle, John Novembre, Xin Li, 2017, Nature Genetics.

Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry

Pierre Fontanillas, Sandra Sanchez-Roige, Anita Pandit, 2017, Nature Neuroscience.

Meta-analysis and imputation refines the association of 15q25 with smoking quantity

Inês Barroso, Lowell Satler, Paul Scheet, 2010, Nature Genetics.

The influence of genomic context on mutation patterns in the human genome inferred from rare variants

John Novembre, Daniel Wegmann, Sebastian Zöllner, 2013, Genome research.

Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits

Rasool Tahmasbi, Jian Yang, Peter M Visscher, 2017, Nature Genetics.

Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences

Maria Cerezo, Paul Flicek, Yaniv Erlich, 2016, Nature Genetics.

Genome-wide analysis of disease progression in age-related macular degeneration

Lars G Fritsche, Lai Wei, Qi Yan, 2018, Human molecular genetics.

A comparison of approaches to account for uncertainty in analysis of imputed genotypes

Paul Scheet, Yun Li, Gonçalo R Abecasis, 2011, Genetic epidemiology.

Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1.

Gonçalo R Abecasis, Maria Karayiorgou, Kimberly F Doheny, 2004, American journal of human genetics.

Powerful regression-based quantitative-trait linkage analysis of general pedigrees.

Shaun Purcell, Pak C Sham, Stacey S Cherny, 2002, American journal of human genetics.

Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits

James Strait, Wei-Min Chen, Ramaiah Nagaraja, 2007, PLoS genetics.

Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs

Carlo Sidore, Francesco Cucca, David Schlessinger, 2014, European Journal of Human Genetics.

Ancestry-agnostic estimation of DNA sample contamination from sequence reads

Fan Zhang, Hyun Min Kang, Michael Boehnke, 2020, Genome research.

Sequence features in regions of weak and strong linkage disequilibrium.

Gonçalo R Abecasis, G. Abecasis, Daryl J. Thomas, 2005, Genome research.

CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration

Yun Li, Liming Liang, Anand Swaroop, 2006, Nature Genetics.

Genotype‐based matching to correct for population stratification in large‐scale case‐control genetic association studies

Weihua Guan, Michael Boehnke, Liming Liang, 2009, Genetic epidemiology.

Shigeo Yoshida, Anand Swaroop, Gonçalo R Abecasis, 2004, American journal of human genetics.

Genes for Good: Engaging the Public in Genetics Research via Social Media.

Lars G Fritsche, Alan M. Kwong, Anita Pandit, 2019, American journal of human genetics.

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

John Spertus, Markus Perola, Eric Boerwinkle, 2012, The Lancet.

Sequence and haplotype analysis supports HLA-C as the psoriasis susceptibility 1 gene.

Stefan Jenisch, Michael Weichenthal, Gonçalo R Abecasis, 2006, American journal of human genetics.

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

Christian Fuchsberger, Tanya M. Teslovich, Johanna Kuusisto, 2012, Nature Genetics.

Variants in MTNR1B influence fasting glucose levels

Inês Barroso, Paul Scheet, Nicole Soranzo, 2009, Nature Genetics.

Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function.

Ramaiah Nagaraja, David Schlessinger, Andrea Maschio, 2008, American journal of human genetics.