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Impact of CD14 Polymorphisms on Anti-Apolipoprotein A-1 IgG-Related Coronary Artery Disease Prediction in the General Population Antiochos, Panagiotis; Marques-Vidal, Pedro; Virzi, Julien; Pagano, Sabrina; ... Vuilleumier, Nicolas 2017
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Standard Genotyping Overestimates Transmission of Mycobacterium tuberculosis among Immigrants in a Low-Incidence Country Stucki, David; Ballif, Marie; Egger, Matthias; Furrer, Hansjakob; ... Fenner, Lukas 2016
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An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis Marchetti, Giovanna; Girelli, Domenico; Zerbinati, Carlotta; Lunghi, Barbara; ... Martinelli, Nicola 2015
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Quantitative variability of 342 plasma proteins in a human twin population Liu, Yansheng; Buil Demur, Alfonso Alberto; Collins, Ben C; Gillet, Ludovic C J; ... Aebersold, Ruedi 2015
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The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study Winkler, Thomas W; Justice, Anne E; Graff, Mariaelisa; Barata, Llilda 2015
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Post-Transcriptional Regulation of Renalase Gene by miR-29 and miR-146 MicroRNAs: Implications for Cardiometabolic Disorders Kalyani, Ananthamohan; Sonawane, Parshuram J; Khan, Abrar Ali; Subramanian, Lakshmi; ... Mahapatra, Nitish R 2015
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Human genomics. The human transcriptome across tissues and individuals Melé, Marta; Ferreira, Pedro G; Reverter, Ferran; DeLuca, David S; ... Guigó, Roderic 2015
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Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins Buil Demur, Alfonso Alberto; Brown, Andrew Anand; Lappalainen, Tuuli Emilia; Viñuela, Ana; ... Dermitzakis, Emmanouil 2015
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Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome International Chromosome 22q11.2 Consortium 2015
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P < 5 × 10(-8) has emerged as a standard of statistical significance for genome-wide association studies Jannot Berthier, Anne-Sophie; Ehret, Georg Benedikt; Perneger, Thomas 2015
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Variant GADL1 and response to lithium in bipolar I disorder Hou, Liping; Heilbronner, Urs; Rietschel, Marcella; Kato, Tadafumi; ... Aubry, Jean-Michel 2014
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Cigarette smoking reduces DNA methylation levels at multiple genomic loci but the effect is partially reversible upon cessation Tsaprouni, Loukia G; Yang, Tsun-Po; Bell, Jordana; Dick, Katherine J; ... Deloukas, Panos 2014
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Allelic mapping bias in RNA-sequencing is not a major confounder in eQTL studies Panousis, Nikolaos; Gutierrez Arcelus, Maria; Dermitzakis, Emmanouil; Lappalainen, Tuuli Emilia 2014
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High-allelic variability in HLA-C mRNA expression: association with HLA-extended haplotypes Bettens, F; Brunet, L; Tiercy, Jean-Marie 2014
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Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome Nikolaev, Sergey Igorievich; Santoni, Federico; Vannier, Anne; Falconnet, Emilie; ... Antonarakis, Stylianos 2013
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Pharmacogenetic study on risperidone long-acting injection: influence of cytochrome P450 2D6 and pregnane X receptor on risperidone exposure and drug-induced side-effects Choong, Eva; Polari, Andrea; Kamdem, Rigobert Hervais; Gervasoni, Nicola Gérard; ... Eap, Chin B 2013
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A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease Holmans, Peter; Moskvina, Valentina; Jones, Lesley; Sharma, Manu; ... Morris, Huw R 2013
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Loci influencing blood pressure identified using a cardiovascular gene-centric array Ganesh, Santhi K; Tragante, Vinicius; Guo, Wei 2013
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Lack of strong effect modification by NFE2L2/CYP3A5/ABO of the risk of venous thrombosis associated with oral hormone therapy Blondon, Marc; Wiggins, K L; Harrington, L B; Psaty, B M; Smith, N L 2013
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Influence of CRTC1 polymorphisms on body mass index and fat mass in psychiatric patients and the general adult population Choong, Eva; Quteineh, Lina; Cardinaux, Jean-René; Gholam-Rezaee, Mehdi; ... Eap, Chin Bin 2013
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Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcription Kilpinen, Leena Helena; Waszak, Sebastian M; Gschwind, Andreas R; Raghav, Sunil K; ... Dermitzakis, Emmanouil 2013
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A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A. Lane, Jérôme; Boehlen, Françoise 2013
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Fine Mapping and Identification of BMI Loci in African Americans Ehret, Georg Benedikt 2013
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Integrative annotation of variants from 1092 humans: application to cancer genomics Lappalainen, Tuuli Emilia; Dermitzakis, Emmanouil 2013
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Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression Trudu, Matteo; Janas, Sylvie; Lanzani, Chiara; Debaix, Huguette; ... Rampoldi, Luca 2013
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Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations O'Seaghdha, Conall M; Guessous, Idris; Köttgen, Anna; Wallaschofski, Henri; ... Bochud, Murielle 2013
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IL28B polymorphisms do not predict response to therapy in chronic hepatitis C with HCV genotype 5 Antaki, Nabil; Bibert, Stéphanie; Kebbewar, Kamel; Asaad, Fouad; ... Negro, Francesco 2012
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IL28B alleles associated with poor hepatitis C virus (HCV) clearance protect against inflammation and fibrosis in patients infected with non-1 HCV genotypes Bochud, Pierre-Yves; Bibert, Stéphanie; Kutalik, Zoltán; Patin, Etienne; ... Negro, Francesco 2012
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Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection Patin, Etienne; Kutalik, Zoltán; Guergnon, Julien; Bibert, Stéphanie; ... Abel, Laurent 2012
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Genomic variation and its impact on gene expression in Drosophila melanogaster Massouras, Andreas; Waszak, Sebastian M; Albarca-Aguilera, Monica; Hens, Korneel; ... Deplancke, Bart 2012
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Sex-biased genetic effects on gene regulation in humans Dima, Antigoni; Nica, Alexandra; Montgomery, Stephen; Stranger, Barbara E; ... Dermitzakis, Emmanouil 2012
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Extensive natural variation for cellular hydrogen peroxide release is genetically controlled Attar Cohen, Homa; Bedard, Karen; Migliavacca Voeffray, Eugenia Linda; Gagnebin, Maryline; ... Antonarakis, Stylianos 2012
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Genotype-based test in mapping cis-regulatory variants from allele-specific expression data Lefebvre, Jean Francois; Vello, Emilio; Ge, Bing; Montgomery, Stephen; ... Labuda, Damian 2012
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Extent, causes, and consequences of small RNA expression variation in human adipose tissue Parts, Leopold; Hedman, Åsa K; Keildson, Sarah; Knights, Andrew J; ... Lindgren, Cecilia M 2012
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Tandem repeat sequence variation as causative cis-eQTLs for protein-coding gene expression variation: the case of CSTB. Borel, Christelle; Migliavacca Voeffray, Eugenia Linda; Letourneau, Audrey; Gagnebin, Maryline; ... Antonarakis, Stylianos 2012
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The Brisbane Systems Genetics Study: genetical genomics meets complex trait genetics Powell, Joseph E; Henders, Anjali K; McRae, Allan F; Caracella, Anthony; ... Montgomery, Grant W 2012
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Analysis of case-control association studies with known risk variants Zaitlen, Noah; Pasaniuc, Bogdan; Patterson, Nick; Pollack, Samuela; ... Price, Alkes L 2012
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Patterns of cis regulatory variation in diverse human populations Stranger, Barbara E; Montgomery, Stephen; Dima, Antigoni; Parts, Leopold; ... Dermitzakis, Emmanouil 2012
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A multi-SNP locus-association method reveals a substantial fraction of the missing heritability Ehret, Georg Benedikt; Lamparter, David; Hoggart, Clive J.; Whittaker, John C.; ... Kutalik, Zoltán 2012
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Risky communication in atherosclerosis and thrombus formation Meens, Merlijn; Pfenniger, Anna; Kwak, Brenda 2012
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Replication of association of the interleukin 23 receptor rs1343151 variant with rheumatoid arthritis in Caucasian sample sets Chen-Xu, Michael; Topless, Ruth; McKinney, Cushla; Merriman, Marilyn E; ... Merriman, Tony R 2012
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A single-nucleotide substitution mutator phenotype revealed by exome sequencing of human colon adenomas Nikolaev, Sergey Igorievich; Sotiriou, Sotirios K; Pateras, Ioannis S; Santoni, Federico; ... Halazonetis, Thanos 2012
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Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele Radhakrishna, Uppala; Nath, Swapan K; McElreavey, Ken; Ratnamala, Uppala; ... Butler, Merlin G 2012
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Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities Mittag, Florian; Büchel, Finja; Saad, Mohamad; Jahn, Andreas; ... Sharma, Manu 2012
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Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis Paternoster, Lavinia; Standl, Marie 2012
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Large-scale replication and heterogeneity in Parkinson disease genetic loci Sharma, Manu 2012
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Mapping cis- and trans-regulatory effects across multiple tissues in twins Nica, Alexandra; Buil Demur, Alfonso Alberto; Dima, Antigoni; Montgomery, Stephen; Dermitzakis, Emmanouil 2012
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A systematic survey of loss-of-function variants in human protein-coding genes MacArthur, Daniel G; Montgomery, Stephen; Dermitzakis, Emmanouil 2012
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KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron Collaboration 2012
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Clinical and genetic correlates of suicidal ideation during antidepressant treatment in a depressed outpatient sample Perroud, Nader Ali; Bondolfi, Guido; Uher, Rudolf; Gex-Fabry, Marianne; ... Kosel, Markus Mathaus 2011
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