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 TitleAuthors / EditorsDate
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Transcriptome and genome sequencing uncovers functional variation in humans Lappalainen, Tuuli Emilia; Giger, Thomas; Padioleau, Ismael; Ongen, Halit; ... Dermitzakis, Emmanouil 2013
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Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia BELNEU Consortium, EU EOD Consortium 2018
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mtDNA analysis of Nile River Valley populations : a genetic corridor or a barrier to migration? Krings, Matthias; Salem, Abd-el Halim; Bauer, Karin; Geisert, Helga; ... Stoneking, Mark 1999
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Molecular analysis of the beta-globin gene cluster in the Niokholo Mandenka population reveals a recent origin of the beta(S) Senegal mutation Currat, Mathias; Trabuchet, Guy; Rees, David; Perrin, Pascale; ... Excoffier, Laurent Georges Louis 2002
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Insights into hominid evolution from the gorilla genome sequence Scally, Aylwyn 2012
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Initial sequencing and comparative analysis of the mouse genome Mouse Genome Analysis Group 2002
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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies Nalls, Michael A; Plagnol, Vincent; Hernandez, Dena G; Sharma, Manu; ... Wood, Nicholas W 2011
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Identification of VPS35 mutations replicated in French families with Parkinson disease Lesage, S; Condroyer, C; Klebe, S; Honoré, A; ... Brice, A 2012
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Identification of low frequency knockout mutants in Dictyostelium discoideum created by single or double homologous recombination Charette, Steve; Cornillon, Sophie Marie; Cosson, Pierre 2006
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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project Birney, Ewan 2007
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Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls Brenner, Darren R; Brennan, Paul; Boffetta, Paolo; Amos, Christopher I; ... Hung, Rayjean J 2013
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Guidelines for investigating causality of sequence variants in human disease MacArthur, D G; Manolio, T A; Dimmock, D P; Rehm, H L; ... Gunter, C 2014
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GSTA1 Genetic Variants and Conditioning Regimen: Missing Key Factors in Dosing Guidelines of Busulfan in Pediatric Hematopoietic Stem Cell Transplantation Nava, Tiago; Rezgui, Mohamed A; Uppugunduri Satyanarayana, Chakradhara Rao; Curtis, Patricia; ... Bittencourt, Henrique 2017
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Genetic structure of Mediterranean populations revealed by Y-chromosome haplotype analysis Quintana-Murci, Lluís; Veitia, Reiner; Fellous, Marc; Semino, Ornella; Poloni, Estella S. 2003
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Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies Nguyen, Khanh-Dung H; Pihur, Vasyl; Ganesh, Santhi K; Rakha, Ankit; ... Chakravarti, Aravinda 2013
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Defining the role of common variation in the genomic and biological architecture of adult human height Wood, Andrew R; Esko, Tonu; Yang, Jian; Vedantam, Sailaja; ... Goddard, Michael E 2014
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Comparison of human chromosome 21 conserved nongenic sequences (CNGs) with the mouse and dog genomes shows that their selective constraint is independent of their genic environment Dermitzakis, Emmanouil; Kirkness, Ewen; Schwarz, Scott; Birney, Ewan; ... Antonarakis, Stylianos 2004
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Comparative architectures of mammalian and chicken genomes reveal highly variable rates of genomic rearrangements across different lineages Bourque, Guillaume; Zdobnov, Evgeny; Bork, Peer; Pevzner, Pavel A; Tesler, Glenn 2005
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An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium 2012
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An integrated encyclopedia of DNA elements in the human genome ENCODE Project Consortium 2012
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A worldwide analysis of AG molecular diversity inferred from serology Sanchez-Mazas, Alicia; Bütler-Brunner, E.; Bütler, R.; Calderón, R.; ... Langaney, André 2001
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A map of human genome variation from population-scale sequencing 1000 Genomes Project Consortium 2010
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A cSNP map and database for human chromosome 21 Deutsch, Samuel; Iseli, C.; Bucher, P.; Antonarakis, Stylianos; Scott, Hamish Steele 2001