Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns

by Coughlin, Curtis R, Scharer, Gunter H, Shaikh, Tamim H
Published 2012

Flame Retardant and Antimicrobial Jute Textile Using Sodium Metasilicate Nonahydrate

by Basak S., Samanta Kartick K., Chattopadhyay S.K., Das S., Narkar R., Dsouza C., Shaikh A.H.
Published 2014-06-01

Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease...

by Yu, Hung-Chun, Coughlin, Curtis R., Geiger, Elizabeth A., Salvador, Blake J., Elias, Ellen R., Cavanaugh, Jean L., Chatfield, Kathryn C., Miyamoto, Shelley D., Shaikh, Tamim H.
Published 2016

Evaluating Familial Essential Tremor with Novel Genetic Approaches: Is it a Genotyping or Phenotyping Issue?

by Gonzalez-Alegre, Pedro, Di Paola, Jorge, Wang, Kai, Fabbro, Shay, Yu, Hung-Chun, Shaikh, Tamim H., Darbro, Benjamin W., Bassuk, Alexander G.
Published 2014

Assessment of low vitamin D among Saudi Arabians: Did we overshoot the runway?

by Sadat-Ali, Mir, Al-Elq, Abdulmohsen H., Al-Shaikh, Iman H., Al-Turki, Haifa A., Al-Ali, Amein K., Al-Othman, Abdallah A.
Published 2014

A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population

by Imtiaz, Faiqa, Taibah, Khalid, Ramzan, Khushnooda, Bin-Khamis, Ghada, Kennedy, Shelley, Al-Mubarak, Bashayer, Trabzuni, Daniah, Allam, Rabab, Al-Mostafa, Abeer, Sogaty, Sameera, Al-Shaikh, Abdulmoneem H, Bamukhayyar, Saeed S, Meyer, Brian F, Al-Owain, Mohammed
Published 2011

Rare structural variation of synapse and neurotransmission genes in autism

by Gai, X, Xie, H M, Perin, J C, Takahashi, N, Murphy, K, Wenocur, A S, D'arcy, M, O'Hara, R J, Goldmuntz, E, Grice, D E, Shaikh, T H, Hakonarson, H, Buxbaum, J D, Elia, J, White, P S
Published 2012