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Characterization of ADME gene variation in 21 populations by exome sequencing

autore

Gonçalo Abecasis

1976 -

pubblicato in: Pharmacogenetics and Genomics

data di pubblicazione: 2016-12-15

Cita articoli 41

Data

Titolo

Autori

2015-04-16

An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data

Goo Jun
2015-02-01

Polymorphism in CYP2D6 and CYP2C19, members of the cytochrome P450 mixed-function oxidase system, in the metabolism of psychotropic drugs

Julia C Stingl, Roberto Viviani
2015-02-12

Impact of ABCG2 and SLCO1B1 polymorphisms on pharmacokinetics of rosuvastatin, atorvastatin and simvastatin acid in Caucasian and Asian subjects: a class effect?
2014-02-11

Association between copy number variation losses and alcohol dependence across African American and European American ethnic groups

Vince D. Calhoun
2013-11-26

Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset

Bruce M. Psaty, John P. A. Ioannidis, Themistocles L. Assimes, Jerome I Rotter, Ulrike Peters, Deborah A Nickerson, David M Herrington
2013-08-01

Effects of polymorphisms in ABCG2, SLCO1B1, SLC10A1 and CYP2C9/19 on plasma concentrations of rosuvastatin and lipid response in Chinese patients
2013-07-09

Pharmacogenomics, ancestry and clinical decision making for global populations

Daniel Shriner, Adebowale A. Adeyemo, Charles Rotimi, Jinyan Huang
2012-11-20

Multi-ethnic cytochrome-P450 copy number profiling: novel pharmacogenetic alleles and mechanism of copy number variation formation

Robert J. Desnick
2012-11-01

An integrated map of genetic variation from 1,092 human genomes

Gilean McVean, Gonçalo Abecasis, Richard M. Durbin, Adam Auton, Robert E Handsaker, Vineet Bafna, Klaudia Walter, Andrew G. Clark, Andrea Angius, Matthew Hurles, Gabor T Marth
2012-10-01

Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth

Michael C. O'Donovan, George Kirov, Menachem Fromer, Douglas M. Ruderfer, Sarah E. Bergen, Jennifer L. Moran, Christina M. Hultman, Patrick F Sullivan, Pamela Sklar
2012-07-22

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

Christian Fuchsberger, Gonçalo Abecasis
2012-07-20

Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data

Gaelle Marenne, Francisco X Real, Benjamín Rodríguez-Santiago, Emmanuelle Génin, Nuria Malats, Nathaniel Rothman, Debra T. Silverman, Stephen Chanock, Luis A Perez-Jurado, Montse Garcia-Closas
2012-05-17

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

Jun Wang, Gonçalo Abecasis, Dana Fraser, Simon Topp, John Whittaker, Matthew D. Hall, Daniel Wegmann
2011-07-05

Demographic history and rare allele sharing among human populations

Carlos D. Bustamante, Andreas Dahl, Andrew G. Clark, Klaudia Walter, Simon Gravel
2011-08-01

The variant call format and VCFtools

Richard M. Durbin, Klaudia Walter, Andreas Dahl, Vineet Bafna
2011-03-31

Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel

Núria López-Bigas, Abel Gonzalez-Perez
2011-11-29

Population differences in major functional polymorphisms of pharmacokinetics/pharmacodynamics-related genes in Eastern Asians and Europeans: implications in the clinical trials for novel drug development
2011-11-23

CYP2D6, SULT1A1 and UGT2B17 copy number variation: quantitative detection by multiplex PCR.
2010-10-27

Dindel: accurate indel calls from short-read data

Gerton Lunter, Richard M. Durbin, Willem H. Ouwehand, Gilean McVean
2010-09

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

David Altshuler, Kristian Cibulskis, Stacey Gabriel, Aaron McKenna, Mark Joseph Daly, Andrey Sivachenko, Eric Banks, Andrew Kernytsky, Mark DePristo
2010-06-18

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

William M. McLaren, Paul Flicek, Fiona Cunningham, Bethan Pritchard
2010-04-01

The Human Cytochrome P450 (CYP) Allele Nomenclature website: a peer-reviewed database of CYP variants and their associated effects

Magnus Ingelman-Sundberg
2010-02-19

Genetic variation in metabolizing enzyme and transporter genes: comprehensive assessment in 3 major East Asian subpopulations with comparison to Caucasians and Africans
2010-11-16

Global patterns of genetic diversity and signals of natural selection for human ADME genes

Mark Stoneking
2009-07-15

Fast and accurate short read alignment with Burrows-Wheeler transform

Richard M. Durbin, Heng Li
2009-05-01

Simultaneous localized feature selection and model detection for gaussian mixtures
2009-09-01

Copy-number variations (CNVs) of the human sex steroid metabolizing genes UGT2B17 and UGT2B28 and their associations with a UGT2B15 functional polymorphism

Chantal Guillemette
2008-01-01

Sulfotransferase gene copy number variation: pharmacogenetics and function
2008-03-19

Pharmacokinetics/genotype associations for major cytochrome P450 enzymes in native and first- and third-generation Japanese populations: comparison with Korean, Chinese, and Caucasian populations

Yasushi Fujio
2007-09

PLINK: a tool set for whole-genome association and population-based linkage analyses

Shaun Purcell, Julian Maller, Mark Joseph Daly, Pamela Sklar, Benjamin M. Neale
2007-02-01

CYP2D6 worldwide genetic variation shows high frequency of altered activity variants and no continental structure

Antti Sajantila, Oscar Lao, Guido Barbujani
2006-12-15

Safety and efficacy of statins in Asians

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