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A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22) Gill, M.; Vallada, H.; Collier, D.; Sham, P.; ... Read, C. M. 1996
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A new HLA-DR4 allele, DRB1*0474, with an unusual residue at position 77 Desaules, Claire-Anne; Villard, Jean; Tiercy, Jean-Marie 2008
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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 PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset Lalioti, M. D.; Scott, Hamish Steele; Genton, P.; Grid, D.; ... Antonarakis, Stylianos 1998
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A shared HLA-DRB1 epitope in the DR beta first domain is associated with Vogt-Koyanagi-Harada syndrome in Indian patients Tiercy, Jean-Marie; Rathinam, Sivakumar R.; Gex-Fabry, Marianne; Baglivo, Edoardo 2010
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A study of Gm allotypes and immunoglobulin heavy gamma IGHG genes in Berbers, Arabs and sub-Saharan Africans from Jerba Island, Tunisia Loveslati, B Y.; Sanchez-Mazas, Alicia; Ennafaa, H.; Marrakchi, R.; ... Elgaaied, A B. 2001
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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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ADME pharmacogenetics: investigation of the pharmacokinetics of the antiretroviral agent lopinavir coformulated with ritonavir Lubomirov, Rubin; di Iulio, J.; Fayet, A.; Colombo, Sara; ... Telenti, A. 2010
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African diversity from the HLA point of view: influence of genetic drift, geography, linguistics, and natural selection Sanchez-Mazas, Alicia 2001
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An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree Radhakrishna, U.; Senol, S.; Herken, H.; Gucuyener, K.; ... Antonarakis, Stylianos 2001
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An apportionment of human HLA diversity Sanchez-Mazas, Alicia 2007
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An integrated encyclopedia of DNA elements in the human genome ENCODE Project Consortium 2012
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An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium 2012
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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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Arg16 homozygosity of the beta2-adrenergic receptor improves the outcome after beta2-agonist tocolysis for preterm labor Landau, Ruth; Morales, M. A.; Antonarakis, Stylianos; Blouin, Jean-Louis; Smiley, R. M. 2005
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Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome Deutsch, Samuel; Rideau, Alexandra; Bochaton-Piallat, Marie-Luce; Merla, Giuseppe; ... Beris, Photis 2003
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Assessing allele-specific expression across multiple tissues from RNA-seq read data Pirinen, Matti; Lappalainen, Tuuli Emilia; Zaitlen, Noah A; Dermitzakis, Emmanouil; ... Rivas, Manuel A 2015
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Association between brain-derived neurotrophic factor gene and a severe form of bipolar disorder, but no interaction with the serotonin transporter gene Vincze, Ilona; Perroud, Nader; Buresi, Catherine; Baud, Patrick; ... Malafosse, Alain 2008
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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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Balancing selection and heterogeneity across the classical human leukocyte antigen loci: a meta-analytic review of 497 population studies Solberg, Owen D.; Mack, Steven J.; Lancaster, Alex K.; Single, Richard M.; ... Thomson, Glenys 2008
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Biased allelic expression in human primary fibroblast single cells Borel, Christelle; Ferreira Marinheiro, Pedro; Santoni, Federico; Delaneau, Olivier; ... Antonarakis, Stylianos 2015
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Biological effect of increased maintenance dose of clopidogrel in cardiovascular outpatients and influence of the cytochrome P450 2C19*2 allele on clopidogrel responsiveness Fontana, Pierre; Senouf, David; Mach, François 2008
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Both transmembrane domains of SecG contribute to signal sequence recognition by the Escherichia coli protein export machinery Bost, S.; Silva, Filo; Rudaz, C.; Belin, Dominique 2000
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Characterization of mouse Dactylaplasia mutations: a model for human ectrodactyly SHFM3 Friedli, Marc; Nikolaev, Sergey Igorievich; Lyle, Robert; Arcangeli, Mélanie; ... Antonarakis, Stylianos 2008
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Chronic graft dysfunction in renal transplant patients: potential role of plasminogen activator inhibitor type 1 Lahlou, Anis; Peraldi, Marie-Noelle; Thervet, Eric; Flahault, Antoine; ... Rondeau, Eric 2002
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Clinical characteristics of frontotemporal patients with symmetric brain atrophy Boccardi, Marina; Laakso, Mikko P; Bresciani, Lorena; Geroldi, Cristina; ... Frisoni, Giovanni 2002
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Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping Kibar, Z.; Dube, M. P.; Powell, J.; McCuaig, C.; ... Rouleau, G. A. 2000
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Common genetic variation and the control of HIV-1 in humans Fellay, Jacques; Ge, Dongliang 2009
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Conditional gene targeting in macrophages and granulocytes using LysMcre mice Clausen, B. E.; Burkhardt, C.; Reith, Walter; Renkawitz, R.; Forster, I. 1999
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Contribution of NZB autoimmunity 2 to Y-linked autoimmune acceleration-induced monocytosis in association with murine systemic lupus Kikuchi, Shuichi; Santiago-Raber, Marie-Laure; Amano, Hirofumi; Amano, Eri; ... Izui, Shozo 2006
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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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Cord blood banks collect units with different HLA alleles and haplotypes to volunteer donor banks: a comparative report from Swiss Blood stem cells Meyer-Monard, S.; Passweg, Jakob; Troeger, C.; Eberhard, H-P; ... Tiercy, Jean-Marie 2009
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Coupling of termination, 3' processing, and mRNA export Hammell, C M; Gross, Stefan; Zenklusen, Daniel; Heath, Catherine V; ... Cole, C N 2002
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Detection of polymorphisms in the human urokinase-type plasminogen activator gene Conne, Béatrice; Berczy, M.; Belin, Dominique 1997
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Dimorphism of TAP-1 gene in Caucasian with juvenile myoclonic epilepsy and in Tunisian with idiopathic generalized epilepsies Layouni, S.; Chouchane, L.; Malafosse, Alain; Dogui, M. 2010
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Discrepancies in reporting the CAG repeat lengths for Huntington's disease Quarrell, Oliver W; Handley, Olivia; O'Donovan, Kirsty; Dumoulin, Christine; ... Landwehrmeyer, G Bernhard 2012
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Disentangling human tolerance and resistance against HIV. Regoes, Roland R; McLaren, Paul J; Battegay, Manuel; Bernasconi, Enos; ... Fellay, Jacques 2014
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Divergent adaptation of hepatitis C virus genotypes 1 and 3 to human leukocyte antigen-restricted immune pressure Rauch, Andri; James, Ian; Pfafferott, Katja; Nolan, David; ... Gaudieri, Silvana 2009
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DNA sequence variability of IGHG3 alleles associated to the main G3m haplotypes in human populations Dard, Patricia; Lefranc, Marie-Paule; Osipova, Ludmilla; Sanchez-Mazas, Alicia 2001
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DNA typing by microbead arrays and PCR-SSP: apparent false-negative or -positive hybridization or amplification signals disclose new HLA-B and -DRB1 alleles Rahal, M.; Kervaire, B.; Villard, Jean; Tiercy, Jean-Marie 2008
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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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Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy Lalioti, M. D.; Scott, Hamish Steele; Buresi, C.; Rossier, Colette; ... Antonarakis, Stylianos 1997
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Effective T-cell responses select human immunodeficiency virus mutants and slow disease progression Frater, A. John; Brown, H.; Oxenius, A.; Gunthard, Huldrych; ... Phillips, R. E. 2007
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Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1 Cironi, Luisa; Provero, Paolo; Riggi, Nicola; Janiszewska, Michalina; ... Stamenkovic, Ivan 2009
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Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung disease de Pontual, L.; Pelet, A.; Clement-Ziza, M.; Trochet, D.; ... Amiel, J. 2007
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Expression of aberrant forms of CD22 on B lymphocytes in Cd22a lupus-prone mice affects ligand binding Nitschke, Lars; Lajaunias, Frédéric; Moll, Thomas; Ho, Liza; ... Izui, Shozo 2006
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Formation of stable epialleles and their paramutation-like interaction in tetraploid Arabidopsis thaliana Mittelsten Scheid, Ortrun; Afsar, Karin; Paszkowski, Jerzy 2003
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Frequency and determinants of pregnancy-induced child-specific sensitization Hönger, G; Fornaro, I; Granado, C; Tiercy, Jean-Marie; ... Schaub, S 2013
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Gene cluster lock after pheromone receptor gene choice Roppolo, Daniele; Vollery, Sarah; Kan, C. D.; Luescher, Christian; ... Rodriguez, Ivan 2007
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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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