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 TitleAuthors / EditorsDate
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Interethnic genetic differentiation : GM polymorphism in Eastern Senegal Blanc, Madeleine; Sanchez-Mazas, Alicia; Hubert Van Blyenburgh, Ninian; Sevin, André; ... Langaney, André 1990
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A worldwide population study of the Ag-system haplotypes, a genetic polymorphism of human low-density lipoprotein Breguet, Georges; Bütler, R.; Bütler-Brunner, E.; Sanchez-Mazas, Alicia 1990
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Characterization of cDNA clones containing CCA trinucleotide repeats derived from human brain Margolis, R. L.; Breschel, T. S.; Li, S. H.; Kidwai, A. S.; ... Ross, C. A. 1995
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Nuclear DNA polymorphism in a Mandenka population from Senegal: comparison with eight other human populations Poloni, Estella S.; Excoffier, Laurent Georges Louis; Mountain, J.L.; Langaney, André; Cavalli-Sforza, LL. 1995
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Molecular characterization of HLA-C incompatibilities in HLA-ABDR-matched unrelated bone marrow donor-recipient pairs. Sequence of two new Cw alleles (Cw*02023 and Cw*0707) and recognition by cytotoxic T lymphocytes Grundschober, C; Rufer, Nathalie; Sanchez-Mazas, Alicia; Madrigal, A; ... Tiercy, Jean-Marie 1997
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HLA class II DRB1, DQA1 and DQB1 polymorphisms in the Polish population from Wielkopolska Jungerman, M; Sanchez-Mazas, Alicia; Fichna, P; Ivanova, R; ... Djoulah, S 1997
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HLA class II DNA polymorphism in a Moroccan population from the Souss, Agadir area Izaabel, H; Garchon, H J; Caillat-Zucman, S; Beaurain, G; ... Sanchez-Mazas, Alicia 1998
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Maternal and paternal lineages in Albania and the genetic structure of Indo-European populations Belledi, M.; Poloni, Estella S.; Casalotti, R.; Conterio, F.; ... Excoffier, Laurent Georges Louis 2000
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Genetic differentiation of Yemeni people according to rhesus and Gm polymorphisms Chaabani, H.; Sanchez-Mazas, Alicia; Sallami, S. F. 2000
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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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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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HLA class II polymorphism in Aka Pygmies and Bantu Congolese and a reassessment of HLA-DRB1 African diversity Renquin, Johan; Sanchez-Mazas, Alicia; Halle, L.; Rivalland, S.; ... Kaplan, C. 2001
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ATM gene alterations in childhood acute lymphoblastic leukemias Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, David; Sappino, Pascal 2003
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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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Genetic diversity in Tunisia: a study based on the GM polymorphism of human immunoglobulins Fadhlaoui-Zid, Karima; Dugoujon, Jean-Michel; Elgaaied, Amel; Ben Amor, Mohamed; ... Sanchez-Mazas, Alicia 2004
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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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Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with variation in vertebral bone mass, vertebral bone size, and stature in whites Ferrari, Serge Livio; Deutsch, Samuel; Choudhury, Urmila; Chevalley, Thierry; ... Antonarakis, Stylianos 2004
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The effect of the Neolithic expansion on European molecular diversity Currat, Mathias; Excoffier, Laurent Georges Louis 2005
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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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HLA class II genetic diversity in southern Tunisia and the Mediterranean area Abdennaji Guenounou, B.; Loueslati, B Yacoubi; Buhler, Stéphane; Hmida, S.; ... Sanchez-Mazas, Alicia 2006
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HLA-C molecular characterization of a Lebanese population and genetic structure of 39 populations from Europe to India-Pakistan Buhler, Stéphane; Megarbane, A.; Lefranc, G.; Tiercy, J-M.; Sanchez-Mazas, Alicia 2006
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Influence of serotonin receptor 2A His452Tyr polymorphism on brain temporal structures: a volumetric MR study Filippini, Nicola; Scassellati, Catia; Boccardi, Marina; Pievani, Michela; ... Gennarelli, Massimo 2006
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Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation Everman, D. B.; Morgan, C. T.; Lyle, Robert; Laughridge, M. E.; ... Schwartz, C. E. 2006
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An apportionment of human HLA diversity Sanchez-Mazas, Alicia 2007
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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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Sequence variation in ultraconserved and highly conserved elements does not cause X-linked mental retardation Bottani, Armand; Chelly, Jamel; de Brouwer, A. P.; Pardo, Bruno; ... Conrad, Bernard 2007
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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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Worldwide distribution of NAT2 diversity: implications for NAT2 evolutionary history Sabbagh, Audrey; Langaney, André; Darlu, Pierre; Gérard, Nathalie; ... Poloni, Estella S. 2008
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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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Candidate genes for temporal lobe epilepsy: a replication study Trachsler-Salzmann, Annick; Perroud, Nader; Crespel, Arielle; Lambercy, Carmen; Malafosse, Alain 2008
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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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Interaction between BDNF Val66Met and childhood trauma on adult's violent suicide attempt Perroud, N.; Courtet, P.; Vincze, Ilona; Jaussent, I.; ... Malafosse, Alain 2008
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Effect of the XbaI polymorphism of estrogen receptor alpha on postmenopausal gray matter Boccardi, Marina; Scassellati, Catia; Ghidoni, Roberta; Testa, Cristina; ... Frisoni, Giovanni 2008
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Common regulatory variation impacts gene expression in a cell type-dependent manner Dimas, Antigone S.; Deutsch, Samuel; Stranger, Barbara E.; Montgomery, Stephen; ... Antonarakis, Stylianos 2009
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Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease Lesage, S; Condroyer, C; Lannuzel, A; Lohmann, E; ... Brice, A 2009
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Genetic structure of Europeans: a view from the North-East Nelis, Mari; Esko, Tonu; Antonarakis, Stylianos; Borel, Christelle; Gagnebin, Maryline 2009
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HOXA1 A218G polymorphism is associated with smaller cerebellar volume in healthy humans Canu, Elisa; Boccardi, Marina; Ghidoni, Roberta; Benussi, Luisa; ... Frisoni, Giovanni 2009
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Polymorphisms in multidrug resistance-associated protein gene 4 is associated with outcome in childhood acute lymphoblastic leukemia Ansari Djaberi, Marc Georges; Sauty, Géraldine; Labuda, Malgorzata; Gagné, Vincent; ... Krajinovic, Maja 2009
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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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The AmpliChip CYP450 test: cytochrome P450 2D6 genotype assessment and phenotype prediction Rebsamen, M C.; Desmeules, Jules Alexandre; Daali, Youssef; Chiappe, A.; ... Rossier, M. F. 2009
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Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorder Perroud, Nader Ali; Salzmann, Annick; Saiz, Pilar A.; Baca-Garcia, Enrique; ... Malafosse, Alain 2010
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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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BRD2 and TAP-1 genes and juvenile myoclonic epilepsy Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed 2010
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Telomere length and ApoE polymorphism in mild cognitive impairment, degenerative and vascular dementia Zekry Berger, Dina Selma; Herrmann, François; Irminger-Finger, Irmgard; Graf, Cristophe; ... Krause, Karl-Heinz 2010
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Epistatic selection between coding and regulatory variation in human evolution and disease Lappalainen, Tuuli Emilia; Montgomery, Stephen; Nica, Alexandra; Dermitzakis, Emmanouil 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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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 genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium McKay, James D 2011
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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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IL28B polymorphisms predict reduction of HCV RNA from the first day of therapy in chronic hepatitis C. Bochud, Pierre-Yves; Bibert, Stéphanie; Negro, Francesco; Haagmans, B; ... Lagging, M 2011
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