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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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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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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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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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Cardiovascular risk in patients with rheumatoid arthritis Lauper, Kim; Gabay, Cem 2017
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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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The Elephant in the Room: The Role of Microtubules in Cancer Cirillo, Luca; Gotta, Monica; Meraldi, Patrick 2017
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Interleukin-33 and RANK-L Interplay in the Alveolar Bone Loss Associated to Periodontitis Lapérine, Olivier; Cloitre, Alexandra; Caillon, Jocelyne; Huck, Olivier; ... Lesclous, Philippe 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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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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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy Korff, Christian 2015
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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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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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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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High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms Kurki, Mitja I; Gaál, Emília Ilona; Kettunen, Johannes; Lappalainen, Tuuli Emilia; ... Jääskeläinen, Juha E 2014
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HLA-DRB1 and HLA-DQB1 allele associations in an Albanian patient population with rheumatoid arthritis: correlations with the specific autoantibody markers and inter-population DRB1 allele frequency variability Prifti-Kurti, Margarita; Nunes, Jose Manuel; Shyti, Erkena; Ylli, Zamira; ... Sulcebe, Genc 2014
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Predicting stroke through genetic risk functions: the CHARGE Risk Score Project Ehret, Georg Benedikt 2014
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Genetic implication of a novel thiamine transporter in human hypertension International Consortium for Blood Pressure Genome-Wide Association Studies 2014
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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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[What's new in internal medicine?] Laffitte, Emmanuel Alexis 2014
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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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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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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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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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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 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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Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations Franceschini, Nora 2013
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Fine Mapping and Identification of BMI Loci in African Americans Ehret, Georg Benedikt 2013
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Discovery and refinement of loci associated with lipid levels Global Lipids Genetics Consortium 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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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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Non-alcoholic fatty liver disease and insulin resistance: from bench to bedside Gariani, Karim; Philippe, Jacques; Jornayvaz, François 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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Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers Anheim, M; Elbaz, A; Lesage, S; Durr, A; ... Brice, A 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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Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction Borel, Christelle; Cheung, Fanny; Stewart, Helen; Koolen, David A; ... Sharp, Andrew J 2012
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Large-scale replication and heterogeneity in Parkinson disease genetic loci Sharma, Manu 2012
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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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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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Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndrome Friese, Ryan S; Ye, Chun; Nievergelt, Caroline M; Schork, Andrew J; ... O'Connor, Daniel T 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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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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Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorder Carrard, Anthony; Trachsler-Salzmann, Annick; Malafosse, Alain; Karege, Félicien 2011
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Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population Saad, Mohamad; Lesage, Suzanne; Saint-Pierre, Aude; Corvol, Jean-Christophe; ... Brice, Alexis 2011
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Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease Lesage, Suzanne; Anheim, Mathieu; Condroyer, Christel; Pollak, Pierre; ... Brice, Alexis 2011
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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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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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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study Ross, Owen A 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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