Center-Authored Papers

Filters: Author is Bamshad, Michael  [Clear All Filters]
2014
Santos-Cortez RLP, Lee K, Giese AP, Ansar M, Amin-Ud-Din M, Rehn K, Wang X, Aziz A, Chiu I, Hussain Ali R et al..  2014.  Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish.. Human molecular genetics. Abstract
Rehman AU, Santos-Cortez RLP, Morell RJ, Drummond MC, Ito T, Lee K, Khan AA, Basra MAR, Wasif N, Ayub M et al..  2014.  Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86.. American journal of human genetics. 94(1):144-52. Abstract
Bigham AW, Mackelprang RD, Celum C, de Bruyn G, Beima-Sofie K, John-Stewart G, Ronald A, Mugo NR, Buckingham K, Bamshad M et al..  2014.  Variants in host viral replication cycle genes are associated with heterosexual HIV-1 acquisition in Africans.. Journal of acquired immune deficiency syndromes (1999). Abstract
2015
Sudmant PH, Mallick S, Nelson BJ, Hormozdiari F, Krumm N, Huddleston J, Coe BP, Baker C, Nordenfelt S, Bamshad M et al..  2015.  Global diversity, population stratification, and selection of human copy number variation.. Science (New York, N.Y.). Abstract
Regalado ES, Guo D-chuan, Santos-Cortez RLP, Hostetler E, Bensend TA, Pannu H, Estrera A, Safi H, Mitchell AL, Evans JP et al..  2015.  Pathogenic FBN1 Variants in Familial Thoracic Aortic Aneurysms and Dissections.. Clinical genetics. Abstract
Ullah R, Ansar M, Durrani ZU, Lee K, Santos-Cortez RLP, Muhammad D, Ali M, Zia M, Ayub M, Khan S et al..  2015.  Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosis.. International journal of dermatology. Abstract