Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: OR5V1[original query] |
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Systematic association mapping identifies NELL1 as a novel IBD disease gene.
PloS one 2007 2 (8): e691. Franke Andre, Hampe Jochen, Rosenstiel Philip, Becker Christian, Wagner Florian, Häsler Robert, Little Randall D, Huse Klaus, Ruether Andreas, Balschun Tobias, Wittig Michael, Elsharawy Abdou, Mayr Gabriele, Albrecht Mario, Prescott Natalie J, Onnie Clive M, Fournier Hélène, Keith Tim, Radelof Uwe, Platzer Matthias, Mathew Christopher G, Stoll Monika, Krawczak Michael, Nürnberg Peter, Schreiber Stef |
Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.
Journal of lipid research 2018 Aug . Hebbar Prashantha, Nizam Rasheeba, Melhem Motasem, Alkayal Fadi, Elkum Naser, John Sumi Elsa, Tuomilehto Jaakko, Alsmadi Osama, Thanaraj Thangavel Alphon |
Exome-wide analysis identify multiple variations in olfactory receptor genes (OR12D2 and OR5V1) associated with autism spectrum disorder in Saudi females. Frontiers in medicine 2023 2 10 1051039. Almandil Noor B, Alismail Maram Adnan, Alsuwat Hind Saleh, AlSulaiman Abdulla, AbdulAzeez Sayed, Borgio J Franc |
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