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 TitleAuthors / EditorsDate
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[What's new in internal medicine?] Laffitte, Emmanuel Alexis 2014
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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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A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium McKay, James D 2011
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A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease Krüger, Rejko; Sharma, Manu 2011
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A map of open chromatin in human pancreatic islets Gaulton, Kyle J.; Nammo, Takao; Pasquali, Lorenzo; Simon, Jeremy M.; ... Ferrer, Jorge 2010
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A novel locus regulates both retroviral glycoprotein 70 and anti-glycoprotein 70 antibody production in New Zealand mice when crossed with BALB/c Rigby, R. J.; Rozzo, S. J.; Gill, Herpreet; Fernandez-Hart, Timothy; ... Vyse, T. J. 2004
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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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A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study Peters, Ulrike; North, Kari E; Sethupathy, Praveen; Buyske, Steve; ... Kooperberg, Charles 2013
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A two-stage meta-analysis identifies several new loci for Parkinson's disease French Parkinson's Disease Genetics Study Group 2011
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Alcohol-related cancers and genetic susceptibility in Europe: the ARCAGE project: study samples and data collection Lagiou, Pagona; Georgila, Christina; Minaki, Ploumitsa; Ahrens, Wolfgang; ... Brennan, Paul J. 2009
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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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Analysis of MHC class II genes in the susceptibility to lupus in New Zealand mice Rozzo, S. J.; Vyse, T. J.; David, C. S.; Palmer, E.; ... Kotzin, B. L. 1999
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APOE and modulation of Alzheimer's and frontotemporal dementia Boccardi, Marina; Sabattoli, F; Testa, C; Beltramello, A; ... Frisoni, Giovanni 2004
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Are abdominal wall defects and external genitalia anomalies randomly expressed in some families? Wonkam, Ambroise; Extermann, Philipe; Birraux, Jacques Maurice; Fokstuen, Siv 2011
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Arterial smooth muscle cell heterogeneity: implications for atherosclerosis and restenosis development Hao, Hiroyuki; Gabbiani, Giulio; Bochaton-Piallat, Marie-Luce 2003
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Association Between Oxytocin Receptor Genotype, Maternal Care, and Eating Disorder Behaviours in a Community Sample of Women Micali, Nadia; Crous-Bou, Marta; Treasure, Janet; Lawson, Elizabeth A 2017
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Association of a common vitamin D-binding protein polymorphism with inflammatory bowel disease Eloranta, Jyrki J; Wenger, Christa; Mwinyi, Jessica; Hiller, Christian; ... Kullak-Ublick, Gerd A 2011
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Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals Johnson, Andrew D; Newton-Cheh, Christopher; Chasman, Daniel I; Ehret, Georg Benedikt; ... Levy, Daniel 2011
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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study Ross, Owen A 2011
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ATM gene and lymphoid malignancies Gumy Pause, Fabienne; Wacker, Pierre; Sappino, Pascal 2004
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ATM variants and predisposition to childhood T-lineage acute lymphoblastic leukaemia Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, D R; Sappino, Pascal 2006
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Attitudes of future lawyers and psychologists to the use of genetic testing for criminal behavior Elger, Bernice Simone 2005
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Autoantigen glycoprotein 70 expression is regulated by a single locus, which acts as a checkpoint for pathogenic anti-glycoprotein 70 autoantibody production and hence for the corresponding development of severe nephritis, in lupus-prone PXSB mice Haywood, M. E.; Vyse, T. J.; McDermott, Aileen; Thompson, E. M.; ... Morley, B. J. 2001
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BARD1, a possible biomarker for breast and ovarian cancer Irminger, Irmgard 2010
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Breast cancer prognosis is inherited independently of patient, tumor and treatment characteristics Verkooijen, Helena M; Hartman, Mikael; Usel, Massimo; Benhamou, Simone; ... Rapiti Aylward, Elisabetta 2012
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BXSB/long-lived is a recombinant inbred strain containing powerful disease suppressor loci Haywood, M. E.; Gabriel, Luisa; Rose, S. J.; Rogers, N. J.; ... Morley, B. J. 2007
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Caractéristiques et suivi prospectif sur deux ans des enfants atteints d'hypertension artérielle pulmonaire Fraisse, Alain; Jais, Xavier; Schleich, Jean-Marc; di Filippo, S.; ... Bonnet, D. 2010
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Cardiovascular risk in patients with rheumatoid arthritis Lauper, Kim; Gabay, Cem 2017
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CFH, C3 and ARMS2 are significant risk loci for susceptibility but not for disease progression of geographic atrophy due to AMD. Scholl, Hendrik P N; Fleckenstein, Monika; Fritsche, Lars G; Schmitz-Valckenberg, Steffen; ... Weber, Bernhard H F 2009
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Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology Ripperger, Tim; Von Bueren, André 2017
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Chronic active gastritis in X-linked lymphoproliferative disease Rougemont, Anne-Laure; Fournet, Jean-Christophe; Martin, Steven R.; de Saint-Basile, Geneviève; ... Le Deist, Françoise 2008
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Clinical classification of pulmonary hypertension Simonneau, Gerald; Galiè, Nazzareno; Rubin, Lewis J; Langleben, David; ... Fishman, Alfred 2004
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CNVs and genetic medicine (excitement and consequences of a rediscovery) Beckmann, J. S.; Sharp, A. J.; Antonarakis, Stylianos 2008
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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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Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation Hutter, Pierre; Couturier, A.; Scott, R. J.; Alday, P.; ... Buerstedde, J. M. 1996
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COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome Gothelf, Doron; Eliez, Stéphan; Thompson, Tracy; Hinard, Christine; ... Reiss, A. L. 2005
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Connexin37: a potential modifier gene of inflammatory disease Chanson, Marc; Kwak, Brenda 2007
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Contributions of Ea(z) and Eb(z) MHC genes to lupus susceptibility in New Zealand mice Vyse, T. J.; Rozzo, S. J.; Drake, C. G.; Appel, V. B.; ... Kotzin, B. L. 1998
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Control of multiple autoantibodies linked with a lupus nephritis susceptibility locus in New Zealand black mice Vyse, T. J.; Rozzo, S. J.; Drake, C. G.; Izui, Shozo; Kotzin, B. L. 1997
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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy Korff, Christian 2015
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Diagnosis of nonalcoholic fatty liver disease in children and adolescents: position paper of the ESPGHAN Hepatology Committee Vajro, Pietro; Lenta, Selvaggia; Socha, Piotr; Dhawan, Anil; ... Nobili, Valerio 2012
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Diagnostic utility of 18F-Fluorodeoxyglucose positron emission tomography (FDG-PET) in asymptomatic subjects at increased risk for Alzheimer's disease Drzezga, Alexander; Altomare, Daniele; Festari, Cristina; Arbizu, Javier; ... Boccardi, Marina 2018
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Differential role of three major New Zealand Black-derived loci linked with Yaa-induced murine lupus nephritis Kikuchi, Shuichi; Fossati-Jimack, Liliane; Moll, Thomas; Amano, Hirofumi; ... Izui, Shozo 2005
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Discovery and refinement of loci associated with lipid levels Global Lipids Genetics Consortium 2013
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Do allelic variants of the connexin37 1019 gene polymorphism differentially predict for coronary artery disease and myocardial infarction? Wong Christen, Cindy Wai Yin; Christen, Thomas; Pfenniger, Anna; James, Richard William; Kwak, Brenda 2007
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Does chasing selected 'Fox' to the nucleus prevent diabetes? Wang, Haiyan; Wollheim, Claes 2005
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Double frameshift mutations in APC and MSH2 in the same individual Soravia, Claudio; DeLozier, Celia; Dobbie, Zuzana; Berthod, Claudine Rey; ... Hutter, Pierre 2006
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Double frameshift mutations in APC and MSH2 in the same individual Soravia, Claudio; De Lozier, Celia; Dobbie, Zuzana; Berthod, Claudine; ... Hutter, Pierre 2005
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Effects of single genetic variants and polygenic obesity risk scores on disordered eating in adolescents - The HUNT study Sardahaee, Farzaneh Saeedzadeh; Holmen, Turid Lingaas; Micali, Nadia; Kvaløy, Kirsti 2017
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Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes Delio, Maria; Schneider, Maude; Dahoun, Sophie; Eliez, Stéphan; Armando, Marco 2013
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