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Arylamine N-Acetyltransferases in Anthropology Sabbagh, Audrey; Darlu, Pierre; Vangenot, Christelle; Poloni, Estella S. 2018
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Multifactorial genetic divergence processes drive the onset of speciation in an Amazonian fish Jardim De Queiroz, Luiz; Torrente-Vilara, Gislene; Quilodran, Claudio; Rodrigues da Costa Doria, Carolina; Montoya Burgos, Juan Ignacio 2017
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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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HLA-A-B-C-DRB1-DQB1 phased haplotypes in 124 Nigerian families indicate extreme HLA diversity and low linkage disequilibrium in Central-West Africa Testi, M; Battarra, M; Lucarelli, G; Isgro, A; ... Sanchez-Mazas, Alicia 2015
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Protection From Varicella Zoster in Solid Organ Transplant Recipients Carrying Killer Cell Immunoglobulin-Like Receptor B Haplotypes Schmied, Laurent; Terszowski, Grzegorz; Gonzalez, Asensio; Schmitter, Karin; ... Stern, Martin 2015
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High-allelic variability in HLA-C mRNA expression: association with HLA-extended haplotypes Bettens, F; Brunet, L; Tiercy, Jean-Marie 2014
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Potential and limitation of HLA-based banking of human pluripotent stem cells for cell therapy De Rham, Casimir; Villard, Jean 2014
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The distribution of MICA alleles in an Austrian population: evidence for increasing polymorphism Wenda, Sabine; Faé, Ingrid; Sanchez-Mazas, Alicia; Nunes, Jose Manuel; ... Fischer, Gottfried F 2013
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Haplotype diversity generated by ancient recombination-like events in the MHC of Indian rhesus macaques Doxiadis, Gaby G M; de Groot, Nanine; Otting, Nel; de Vos-Rouweler, Annemiek J M; ... Bontrop, Ronald E 2013
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Glutathione S-transferase gene variations influence BU pharmacokinetics and outcome of hematopoietic SCT in pediatric patients Ansari Djaberi, Marc Georges; Rezgui, MA; Théoret, Y; Uppugunduri Satyanarayana, Chakradhara Rao; ... Krajinovic, M 2013
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Genotype-based test in mapping cis-regulatory variants from allele-specific expression data Lefebvre, Jean Francois; Vello, Emilio; Ge, Bing; Montgomery, Stephen; ... Labuda, Damian 2012
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Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele Radhakrishna, Uppala; Nath, Swapan K; McElreavey, Ken; Ratnamala, Uppala; ... Butler, Merlin G 2012
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Identification of VPS35 mutations replicated in French families with Parkinson disease Lesage, S; Condroyer, C; Klebe, S; Honoré, A; ... Brice, A 2012
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Polymorphism in multidrug resistance-associated protein gene 3 is associated with outcomes in childhood acute lymphoblastic leukemia Ansari Djaberi, Marc Georges; Sauty, G; Labuda, M; Gagné, V; ... Krajinovic, M 2012
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Haplotype-based banking of human pluripotent stem cells for transplantation: potential and limitations Zimmermann, Anna; Preynat-Seauve, Olivier; Tiercy, Jean-Marie; Krause, Karl-Heinz; Villard, Jean 2012
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Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing Ratnamala, Uppala; Lyle, Robert; Rawal, Rakesh; Singh, Raminder; ... Radhakrishna, Uppala 2011
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Rare and common regulatory variation in population-scale sequenced human genomes Montgomery, Stephen; Lappalainen, Tuuli Emilia; Gutierrez Arcelus, Maria; Dermitzakis, Emmanouil 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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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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Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study Rauch, Andri; Kutalik, Zoltan; Descombes, Patrick; Cai, Tao; ... Bochud, Pierre-Yves 2010
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Lack of evidence for HLA-linked patterns of odorous carboxylic acids released from glutamine conjugates secreted in the human axilla Natsch, Andreas; Kuhn, Fabian; Tiercy, Jean-Marie 2010
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HMOX1 and GST variants modify attenuation of FEF25-75% decline due to PM10 reduction Curjuric, I.; Imboden, M.; Schindler, C.; Downs, S. H.; ... Probst-Hensch, N. M. 2010
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Modulation of anger control in suicide attempters by TPH-1 Baud, Patrick; Perroud, N.; Courtet, P.; Jaussent, I.; ... Malafosse, Alain 2009
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Gene expression levels are a target of recent natural selection in the human genome Kudaravalli, Sridhar; Veyrieras, Jean-Baptiste; Stranger, Barbara E.; Dermitzakis, Emmanouil; Pritchard, Jonathan K. 2009
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Three common polymorphisms in the CYBA gene form a haplotype associated with decreased ROS generation Bedard, Karen; Attar Cohen, Homa; Bonnefont, Jérôme; Jaquet, Vincent; ... Krause, Karl-Heinz 2009
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PAX5 mutations occur frequently in adult B-cell progenitor acute lymphoblastic leukemia and PAX5 haploinsufficiency is associated with BCR-ABL1 and TCF3-PBX1 fusion genes: a GRAALL study Familiades, J; Bousquet, M; Lafage-Pochitaloff, M; Béné, M-C; ... Delabesse, E 2009
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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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Large-scale population study of human cell lines indicates that dosage compensation is virtually complete Johnston, Colette M.; Lovell, Frances L.; Leongamornlert, Daniel A.; Stranger, Barbara E.; ... Ross, Mark T. 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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Influence of ABCB1 gene polymorphisms and P-glycoprotein activity on cyclosporine pharmacokinetics in peripheral blood mononuclear cells in healthy volunteers Ansermot, Nicolas; Rebsamen, Michela; Chabert, Jocelyne; Fathi, Marc; ... Desmeules, Jules Alexandre 2008
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An apportionment of human HLA diversity Sanchez-Mazas, Alicia 2007
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A whole-genome association study of major determinants for host control of HIV-1 Fellay, Jacques; Shianna, K. V.; Ge, Dongliang; Colombo, Sara; ... Goldstein, D. B. 2007
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The probability of identifying a 10/10 HLA allele-matched unrelated donor is highly predictable Tiercy, Jean-Marie; Nicoloso, G; Passweg, Jakob; Schanz, U; ... Gratwohl, Alois 2007
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Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1 Naveed, Mohammed; Nath, S. K.; Gaines, Mathew; Al-Ali, M. T.; ... Radhakrishna, Uppala 2007
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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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DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects Hornef, Nada; Olbrich, Heike; Horvath, Judit; Zariwala, M. A.; ... Omran, Heymut 2006
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Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis Naveed, Mohammed; Al-Ali, M. T.; Murthy, S. K.; Al-Hajali, Sarah; ... Radhakrishna, Uppala 2006
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Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34 Radhakrishna, Uppala; Ratnamala, Uppala; Gaines, Mathew; Beiraghi, Soraya; ... Nath, S. K. 2006
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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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Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains Adams, D. J.; Dermitzakis, Emmanouil; Cox, Tony; Smith, James; ... Bradley, Allan 2005
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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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A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein Wattenhofer, Marie; Sahin-Calapoglu, Nilufer; Andreasen, Ditte; Kalay, Ersan; ... Antonarakis, Stylianos 2005
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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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Knobloch syndrome: novel mutations in COL18A1, evidence for genetic heterogeneity, and a functionally impaired polymorphism in endostatin Menzel, Olivier; Bekkeheien, R. C.; Reymond, Alexandre; Fukai, Naomi; ... Guipponi, Michel 2004
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The genome sequence of the malaria mosquito Anopheles gambiae Holt, Robert A 2002
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In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis Michaud, Joelle; Wu, Feng; Osato, Motomi; Cottles, G. M.; ... Scott, Hamish Steele 2002
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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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