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 TitleAuthors / EditorsDate
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Year in review in Intensive Care Medicine 2010: I. Acute renal failure, outcome, risk assessment and ICU performance, sepsis, neuro intensive care and experimentals Antonelli, Massimo; Azoulay, Elie; Bonten, Marc; Chastre, Jean; ... Zhang, Haibo 2011
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Whole exome sequencing of a dominant retinitis pigmentosa family identifies a novel deletion in PRPF31 Villanueva, Adda; Willer, Jason R; Bryois, Julien; Dermitzakis, Emmanouil; ... Davis, Erica E 2014
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When information can save lives: the duty to warn relatives about sudden cardiac death and environmental risks Elger, Bernice Simone; Michaud, Katarzyna; Mangin, Patrice 2010
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War exposure, 5-HTTLPR genotype and lifetime risk of depression Artero, Sylvaine; Touchon, Jacques; Dupuy, Anne-Marie; Malafosse, Alain; Ritchie, Karen 2011
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Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations North, Kari E.; Franceschini, Nora; Avery, Christy L.; Baird, Lisa; ... Hunt, Steven C. 2010
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Variants in DNA double-strand break repair and DNA damage-response genes and susceptibility to lung and head and neck cancers Danoy, Patrick; Michiels, Stefan; Dessen, Philippe; Pignat, Cécile; ... Benhamou, Simone 2008
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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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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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Transcriptional profiling of type 1 diabetes genes on chromosome 21 in a rat beta-cell line and human pancreatic islets Bergholdt, R; Karlsen, A E; Hagedorn, P H; Aalund, M; ... Pociot, F 2007
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Transcript Expression Data from Human Islets Links Regulatory Signals from Genome-Wide Association Studies for Type 2 Diabetes and Glycemic Traits to Their Downstream Effectors van de Bunt, Martijn; Manning Fox, Jocelyn E; Dai, Xiaoqing; Barrett, Amy; ... Gloyn, Anna L 2015
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Toward a NOTCH1/FBXW7/RAS/PTEN-based oncogenetic risk classification of adult T-cell acute lymphoblastic leukemia: a Group for Research in Adult Acute Lymphoblastic Leukemia study Trinquand, Amélie; Tanguy-Schmidt, Aline; Ben Abdelali, Raouf; Lambert, Jérôme; ... Asnafi, Vahid 2013
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The Yaa gene model of systemic lupus erythematosus Izui, Shozo; Iwamoto, Masahiro; Fossati-Jimack, Liliane; Merino, Ramon; ... Ibnou-Zekri, Nabila 1995
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The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminoma Gimelli, Stefania; Beri, Silvana; Drabkin, Harry A.; Gambini, Claudio; ... Gimelli, Giorgio 2009
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The Sgp3 locus on mouse chromosome 13 regulates nephritogenic gp70 autoantigen expression and predisposes to autoimmunity Laporte, Catherine; Ballester, Benoit; Mary, Charles; Izui, Shozo; Reininger, Luc 2003
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The Johns Hopkins University Collaborative Schizophrenia Study: an epidemiologic-genetic approach to test the heterogeneity hypothesis and identify schizophrenia susceptibility genes Pulver, A. E.; Wolyniec, P. S.; Housman, D.; Kazazian, H. H.; ... Kempf, L. 1996
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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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The Elephant in the Room: The Role of Microtubules in Cancer Cirillo, Luca; Gotta, Monica; Meraldi, Patrick 2017
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The diagnosis and management of gastric cancer: expert discussion and recommendations from the 12th ESMO/World Congress on Gastrointestinal Cancer, Barcelona, 2010 Van Cutsem, E; Dicato, M; Geva, R; Arber, N; ... Zalcberg, J 2011
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Specific BACE1 genotypes provide additional risk for late-onset Alzheimer disease in APOE epsilon 4 carriers Gold, Gabriel; Blouin, Jean-Louis; Herrmann, François; Michon, Agnès; ... Antonarakis, Stylianos 2003
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SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension Won, Joong-Ho; Ehret, Georg Benedikt; Chakravarti, Aravinda; Olshen, Richard A 2011
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Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study Pichler, Irene; Del Greco M, Fabiola; Gögele, Martin; Lill, Christina M; ... Pramstaller, Peter 2013
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Schizophrenia and chromosomal deletions within 22q11.2 Lindsay, E. A.; Morris, Michael Andréw; Gos, A.; Nestadt, G.; ... Pulver, A. E. 1995
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SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia Marelli, Cecilia; van de Leemput, Joyce; Johnson, Janel O; Tison, Francois; ... Brice, Alexis 2011
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Role of the major histocompatibility complex class II Ea gene in lupus susceptibility in mice Ibnou-Zekri, Nabila; Iwamoto, Masahiro; Fossati-Jimack, Liliane; McConahey, P. J.; Izui, Shozo 1997
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Role of mitofusin 2 mutations in the physiopathology of Charcot-Marie-Tooth disease type 2A Cartoni, Romain; Martinou, Jean-Claude 2009
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Resistance to cerebral ischemic injury in UCP2 knockout mice: evidence for a role of UCP2 as a regulator of mitochondrial glutathione levels De Bilbao, Fabienne; Arsenijevic, Denis; Vallet, Philippe; Hjelle, O. P.; ... Giannakopoulos, Panteleimon 2004
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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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Prothrombin G20210A mutation and lower extremity peripheral arterial disease: a systematic review and meta-analysis Vazquez, F; Rodger, M; Carrier, M; Le Gal, G; ... Gandara, E 2015
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Primary care physicians' knowledge and attitudes towards genetic testing for breast-ovarian cancer predisposition Escher, Monica; Sappino, Pascal 2000
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Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family Neerman Arbez, Marguerite; Vu, Dung; Abu-Libdeh, Bassam; Bouchardy, Isabelle; Morris, Michael Andréw 2003
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Prédispositions génétiques dans l'allergie médicamenteuse : importance du HLA Bergmann, Marcel; Villard, Jean; Caubet, Jean-Christoph Roger J-P 2014
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Predicting stroke through genetic risk functions: the CHARGE Risk Score Project Ehret, Georg Benedikt 2014
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Polymorphisms in the Cd22 gene of inbred mouse strains Lajaunias, Frédéric; Ibnou-Zekri, Nabila; Fossati-Jimack, Liliane; Chicheportiche, Yves; ... Izui, Shozo 1999
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Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers Anheim, M; Elbaz, A; Lesage, S; Durr, A; ... Brice, A 2012
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Overexpression of plasminogen activator inhibitor type 2 in basal keratinocytes enhances papilloma formation in transgenic mice Zhou, Hong-Ming; Bolon, Isabelle; Nichols, Anthony; Wohlwend, Annelise Isabelle; Vassalli, Jean-Dominique 2001
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Non-alcoholic fatty liver disease and insulin resistance: from bench to bedside Gariani, Karim; Philippe, Jacques; Jornayvaz, François 2013
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No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome Glaser, Bronwyn; Debbané, Martin; Hinard, Christine; Morris, Michael Andréw; ... Eliez, Stéphan 2006
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No association between DUP25 and anxiety disorders Henrichsen, C. N.; Delorme, Richard; Boucherie, Maria; Marelli, Dominique; ... Dahoun, Sophie 2004
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NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects Lu, Weining; Quintero-Rivera, Fabiola; Fan, Yanli; Alkuraya, Fowzan S; ... Maas, Richard L 2007
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Multiple ADH genes are associated with upper aerodigestive cancers Hashibe, Mia; Benhamou, Simone; Bouchardy Magnin, Christine 2008
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Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration Michaud, Katarzyna; Fellmann, Florence; Abriel, Hugues; Beckmann, Jacques S.; ... Elger, Bernice Simone 2009
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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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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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Marked hemiatrophy in carriers of Duchenne muscular dystrophy Rajakulendran, Sanjeev; Kuntzer, Thierry; Dunand, Murielle; Yau, Shu C.; ... Hanna, Michael G. 2010
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Lymphoid enhancer factor-1 links two hereditary leukemia syndromes through core-binding factor alpha regulation of ELA2 Li, Feng-Qian; Person, Richard E; Takemaru, Ken-Ichi; Williams, Kayleen; ... Horwitz, Marshall 2004
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LRP5 gene polymorphisms and idiopathic osteoporosis in men Ferrari, Serge Livio; Deutsch, Samuel; Baudoin, C.; Cohen-Solal, M.; ... de Vernejoul, M. C. 2005
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Loss of Insl3: a potential predisposing factor for testicular torsion Sozubir, Selami; Barber, Theodore; Wang, Yi; Ahn, Chul; ... Baker, Linda A. 2010
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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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LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromes Mehenni, Hamid; Lin-Marq, Nathalie; Buchet-Poyau, Karine; Reymond, Alexandre; ... Antonarakis, Stylianos 2005
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Lessons from BXSB and related mouse models Izui, Shozo; Ibnou-Zekri, Nabila; Fossati-Jimack, Liliane; Iwamoto, Masahiro 2000
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