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 TitleAuthors / EditorsDate
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International Lung Cancer Consortium: pooled analysis of sequence variants in DNA repair and cell cycle pathways International Lung Cancer Consortium 2008
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Genomic determinants of the efficiency of internal ribosomal entry sites of viral and cellular origin Kazadi, Kayole; Loeuillet, Corinne; Deutsch, Samuel; Ciuffi, Angela; ... Telenti, Amalio 2008
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Genetics. Life after GWA studies Dermitzakis, Emmanouil; Clark, A. G. 2009
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Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry Benjamin, Emelia J.; Ehret, Georg Benedikt 2009
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Contribution of genome-wide significant single-nucleotide polymorphisms and antiretroviral therapy to dyslipidemia in HIV-infected individuals: a longitudinal study Rotger, Margalida; Bayard, Cornelia; Taffe, Patrick; Martinez, Raquel; ... Tarr, P. E. 2009
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A map of human genome variation from population-scale sequencing 1000 Genomes Project Consortium 2010
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Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study Rauch, Andri; Kutalik, Zoltan; Descombes, Patrick; Cai, Tao; ... Bochud, Pierre-Yves 2010
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The genetics of affective disorder and suicide McGuffin, Peter; Perroud, Nader Ali; Uher, R.; Butler, A.; ... Farmer, A. 2010
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New loci associated with kidney function and chronic kidney disease Kottgen, Anna; Pattaro, Cristian; Boger, Carsten A. 2010
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An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits Hsu, Yi-Hsiang; Zillikens, M Carola; Wilson, Scott G.; Farber, Charles R.; ... Kiel, D. P. 2010
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Type 2 diabetes susceptibility gene expression in normal or diabetic sorted human alpha and beta cells: correlations with age or BMI of islet donors Kirkpatrick, Clare; Marchetti, Piero; Purrello, Francesco; Piro, Salvatore; ... Wollheim, Claes 2010
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Follow-up study of the GIGYF2 gene in French families with Parkinson's disease Lesage, Suzanne; Condroyer, Christel; Lohman, Ebba; Troiano, André; ... Brice, Alexis 2010
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Mendelian disorders and multifactorial traits: the big divide or one for all? Antonarakis, Stylianos; Chakravarti, Aravinda; Cohen, J. C.; Hardy, John 2010
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Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian family Layouni, Samia; Salzmann, Annick; Guipponi, Michel; Mouthon, Dominique; ... Malafosse, Alain 2010
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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Jacquemont, Sébastien 2011
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A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium McKay, James D 2011
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Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes Small, Kerrin S; Hedman, Asa K; Grundberg, Elin; Nica, Alexandra; ... Dermitzakis, Emmanouil 2011
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Genome-wide association study identifies a common variant associated with risk of endometrial cancer Montgomery, Stephen; Dermitzakis, Emmanouil 2011
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From expression QTLs to personalized transcriptomics Montgomery, Stephen; Dermitzakis, Emmanouil 2011
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Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts Borel, Christelle; Deutsch Escalante, Samuel; Letourneau, Audrey; Migliavacca Voeffray, Eugenia Linda; ... Antonarakis, Stylianos 2011
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