| | Title | Authors / Editors | Date |
|
unige:8756 |
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 |
|
unige:129001 |
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease |
Scott, Robert A; Freitag, Daniel F; Li, Li; Ehm, Margaret G; ... Waterworth, Dawn M |
2016 |
|
unige:2415 |
A new HLA-DR4 allele, DRB1*0474, with an unusual residue at position 77 |
Desaules, Claire-Anne; Villard, Jean; Tiercy, Jean-Marie |
2008 |
|
unige:128592 |
A new mutation in the C-terminal end of TTC37 leading to a mild form of syndromic diarrhea/tricho-hepato-enteric syndrome in seven patients from two families |
Fabre, Alexandre; Petit, Laëtitia Marie; Hansen, Lars F; Wewer, Anne V; ... Paerregaard, Anders |
2018 |
|
unige:45249 |
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 |
|
unige:8848 |
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 |
|
unige:21341 |
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 |
|
unige:2008 |
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 |
|
unige:40634 |
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 |
|
unige:136230 |
Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects |
Fontana, Pierre; Dupont, Annabelle; Gandrille, Sophie; Bachelot-Loza, Christilla; ... Gaussem, Pascale |
2003 |
|
unige:21098 |
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 |
|
unige:2011 |
African diversity from the HLA point of view: influence of genetic drift, geography, linguistics, and natural selection |
Sanchez-Mazas, Alicia |
2001 |
|
unige:8981 |
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 |
|
unige:1964 |
An apportionment of human HLA diversity |
Sanchez-Mazas, Alicia |
2007 |
|
unige:37818 |
An integrated encyclopedia of DNA elements in the human genome |
ENCODE Project Consortium |
2012 |
|
unige:45216 |
An integrated map of genetic variation from 1,092 human genomes |
1000 Genomes Project Consortium |
2012 |
|
unige:114083 |
APOE and modulation of Alzheimer's and frontotemporal dementia |
Boccardi, Marina; Sabattoli, F; Testa, C; Beltramello, A; ... Frisoni, Giovanni |
2004 |
|
unige:8851 |
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 |
|
unige:8725 |
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 |
|
unige:90259 |
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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