| Title | Authors / Editors | Date |
unige:144661 |
Expression estimation and eQTL mapping for HLA genes with a personalized pipeline |
Aguiar, Vitor; César, Jônatas; Delaneau, Olivier; Dermitzakis, Emmanouil; Meyer, Diogo |
2019 |
unige:143934 |
Clinical and biological features of PTPN2-deleted adult and pediatric T-cell acute lymphoblastic leukemia |
Alcantara, Marion; Simonin, Mathieu; Lhermitte, Ludovic; Touzart, Aurore; ... Asnafi, Vahid |
2019 |
unige:135503 |
Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31 |
Wang, Heming; Nandakumar, Priyanka; Tekola-Ayele, Fasil; Tayo, Bamidele O; ... Zhu, Xiaofeng |
2019 |
unige:108546 |
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 |
unige:102916 |
Mapping the HLA diversity of the Iberian Peninsula |
Romòn, Iñigo; Montes, Carmen; Ligeiro, Dario; Trindade, Hélder; ... Buhler, Stéphane |
2016 |
unige:88214 |
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 |
unige:90262 |
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 |
unige:79657 |
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 |
unige:102917 |
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 |
unige:83343 |
αIIbβ3 variants defined by next-generation sequencing: predicting variants likely to cause Glanzmann thrombasthenia |
Buitrago, Lorena; Rendon, Augusto; Liang, Yupu |
2015 |
unige:90276 |
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 |
unige:74398 |
Disentangling human tolerance and resistance against HIV. |
Regoes, Roland R; McLaren, Paul J; Battegay, Manuel; Bernasconi, Enos; ... Fellay, Jacques |
2014 |
unige:80001 |
HLA variation reveals genetic continuity rather than population group structure in East Asia |
Di, Da; Sanchez-Mazas, Alicia |
2014 |
unige:102920 |
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 |
unige:89078 |
Lack of strong effect modification by NFE2L2/CYP3A5/ABO of the risk of venous thrombosis associated with oral hormone therapy |
Blondon, Marc; Wiggins, K L; Harrington, L B; Psaty, B M; Smith, N L |
2013 |
unige:77652 |
Frequency and determinants of pregnancy-induced child-specific sensitization |
Hönger, G; Fornaro, I; Granado, C; Tiercy, Jean-Marie; ... Schaub, S |
2013 |
unige:102921 |
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 |
unige:102923 |
HLA in anthropology: the enigma of Easter Island |
Sanchez-Mazas, Alicia; Thorsby, Erik |
2013 |
unige:43412 |
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders |
Travaglini, Lorena; Brancati, Francesco; Silhavy, Jennifer; Iannicelli, Miriam; ... Gleeson, Joseph G |
2013 |
unige:43643 |
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 |
unige:32178 |
A systematic survey of loss-of-function variants in human protein-coding genes |
MacArthur, Daniel G; Montgomery, Stephen; Dermitzakis, Emmanouil |
2012 |
unige:45222 |
Large-scale replication and heterogeneity in Parkinson disease genetic loci |
Sharma, Manu |
2012 |
unige:32201 |
Epistatic selection between coding and regulatory variation in human evolution and disease |
Lappalainen, Tuuli Emilia; Montgomery, Stephen; Nica, Alexandra; Dermitzakis, Emmanouil |
2011 |
unige:24639 |
A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium |
McKay, James D |
2011 |
unige:25376 |
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 |
unige:25737 |
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 |
unige:45235 |
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study |
Ross, Owen A |
2011 |
unige:45244 |
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease |
Krüger, Rejko; Sharma, Manu |
2011 |
unige:21404 |
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 |
unige:21209 |
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 |
unige:21077 |
BRD2 and TAP-1 genes and juvenile myoclonic epilepsy |
Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed |
2010 |
unige:21078 |
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 |
unige:9227 |
Genetic structure of Europeans: a view from the North-East |
Nelis, Mari; Esko, Tonu; Antonarakis, Stylianos; Borel, Christelle; Gagnebin, Maryline |
2009 |
unige:5537 |
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 |
unige:1680 |
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 |
unige:45251 |
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 |
unige:19966 |
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 |
unige:43455 |
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 |
unige:114068 |
HOXA1 A218G polymorphism is associated with smaller cerebellar volume in healthy humans |
Canu, Elisa; Boccardi, Marina; Ghidoni, Roberta; Benussi, Luisa; ... Frisoni, Giovanni |
2009 |
unige:2538 |
Candidate genes for temporal lobe epilepsy: a replication study |
Trachsler-Salzmann, Annick; Perroud, Nader; Crespel, Arielle; Lambercy, Carmen; Malafosse, Alain |
2008 |
unige:2540 |
Interaction between BDNF Val66Met and childhood trauma on adult's violent suicide attempt |
Perroud, N.; Courtet, P.; Vincze, Ilona; Jaussent, I.; ... Malafosse, Alain |
2008 |
unige:1720 |
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 |
unige:1633 |
Worldwide distribution of NAT2 diversity: implications for NAT2 evolutionary history |
Sabbagh, Audrey; Langaney, André; Darlu, Pierre; Gérard, Nathalie; ... Poloni, Estella S. |
2008 |
unige:1878 |
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 |
unige:114072 |
Effect of the XbaI polymorphism of estrogen receptor alpha on postmenopausal gray matter |
Boccardi, Marina; Scassellati, Catia; Ghidoni, Roberta; Testa, Cristina; ... Frisoni, Giovanni |
2008 |
unige:33304 |
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 |
unige:8707 |
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 |
unige:8654 |
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 |
unige:1964 |
An apportionment of human HLA diversity |
Sanchez-Mazas, Alicia |
2007 |
unige:8740 |
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 |