| Title | Authors / Editors | Date |
unige:127659 |
Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry |
Nandakumar, Priyanka; Lee, Dongwon; Richard, Melissa A; Tekola-Ayele, Fasil; ... Chakravarti, Aravinda |
2017 |
unige:127790 |
Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations |
Yoneyama, S; Yao, J; Guo, X; Fernandez-Rhodes, L; ... North, K E |
2017 |
unige:127636 |
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals |
Ehret, Georg Benedikt; Ferreira, Teresa; Morris, Andrew P; Newton-Cheh, Christopher; Munroe, Patricia B |
2016 |
unige:89655 |
Alternative Splicing QTLs in European and African Populations |
Ongen, Halit; Dermitzakis, Emmanouil |
2015 |
unige:40637 |
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations |
Franceschini, Nora |
2013 |
unige:40644 |
Discovery and refinement of loci associated with lipid levels |
Global Lipids Genetics Consortium |
2013 |
unige:32171 |
Patterns of cis regulatory variation in diverse human populations |
Stranger, Barbara E; Montgomery, Stephen; Dima, Antigoni; Parts, Leopold; ... Dermitzakis, Emmanouil |
2012 |
unige:32235 |
Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency |
Sosa, Maria Ximena; Sivakumar, I K Ashok; Maragh, Samantha; Veeramachaneni, Vamsi; ... Chakravarti, Aravinda |
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:32203 |
Rare and common regulatory variation in population-scale sequenced human genomes |
Montgomery, Stephen; Lappalainen, Tuuli Emilia; Gutierrez Arcelus, Maria; Dermitzakis, Emmanouil |
2011 |
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: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:1633 |
Worldwide distribution of NAT2 diversity: implications for NAT2 evolutionary history |
Sabbagh, Audrey; Langaney, André; Darlu, Pierre; Gérard, Nathalie; ... Poloni, Estella S. |
2008 |
unige:84389 |
Rapidly expanding lesion in a giant congenital melanocytic nevus |
Bajwa, Nadia Masood; Mostow, Eliot N; Schwartz, Richard M |
2003 |
unige:2011 |
African diversity from the HLA point of view: influence of genetic drift, geography, linguistics, and natural selection |
Sanchez-Mazas, Alicia |
2001 |
unige:2012 |
Genetic differentiation of Yemeni people according to rhesus and Gm polymorphisms |
Chaabani, H.; Sanchez-Mazas, Alicia; Sallami, S. F. |
2000 |
unige:13238 |
Y-chromosome specific YCAII, DYS19 and YAP polymorphisms in human populations: a comparative study |
Quintana-Murci, L.; Semino, O.; Poloni, Estella S.; Liu, A.; ... Santachiara-Benerecetti, A S. |
1999 |