Mary C Whitman

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 3

Top Topics

Minimally Invasive

Percutaneous Coronary Intervention

Top Venues

Nature genetics

Journal of binocular vision and ocular motility

This page only lists publications with an associated author ORCID identifier.

Publications

Alan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, Wai-Man Chan, Elke de Boer, Sarah J Garnai, Brenda J Barry, Tammy Ray, Michael Kosicki, Caroline D Robson, Zhongyang Zhang, Thomas E Collins, Alon Gelber, Brandon M Pratt, Yuko Fujiwara, Arushi Varshney, Monkol Lek, Peter E Warburton, Carol Van Ryzin, Tanya J Lehky, Christopher Zalewski, Kelly A King, Carmen C Brewer, Audrey Thurm, Joseph Snow, Flavia M Facio, Narisu Narisu, Lori L Bonnycastle, Amy Swift, Peter S Chines, Jessica L Bell, Suresh Mohan, Mary C Whitman, Sandra E Staffieri, James E Elder, Joseph L Demer, Alcy Torres, Elza Rachid, Christiane Al-Haddad, Rose-Mary N Boustany, David A Mackey, Angela F Brady, María Fenollar-Cortés, Melanie Fradin, Tjitske Kleefstra, George W Padberg, Salmo Raskin, Mario Teruo Sato, Stuart H Orkin, Stephen C J Parker, Tessa A Hadlock, Lisenka E L M Vissers, Hans van Bokhoven, Ethylin Wang Jabs, Francis S Collins, Len A Pennacchio, Irini Manoli, Elizabeth C Engle
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis. Nature genetics (2023)
Jamaji C Nwanaji-Enwerem, Taylor Gateman, Sarah Whitecross, Mary C Whitman
First Visit Characteristics Associated with Future Surgery in Intermittent Exotropia. Journal of binocular vision and ocular motility 72 (1) (2022)
Mary C Whitman, Brenda J Barry, Caroline D Robson, Flavia M Facio, Carol Van Ryzin, Wai-Man Chan, Tanya J Lehky, Audrey Thurm, Christopher K Zalewski, Kelly A King, Carmen Brewer, Konstantinia Almpani, Janice S Lee, Angela Delaney, Edmond J FitzGibbon, Paul R Lee, Camilo Toro, Scott M Paul, Omar A Abdul-Rahman, Bryn D Webb, Ethylin Wang Jabs, Hans Ulrik Moller, Dorte Ancher Larsen, Jayne H Antony, Christopher Troedson, Alan Sl Ma, Glad Ragnhild, Katrine V Wirgenes, Emma Tham, Malin Kvarnung, Timothy James Maarup, Sarah MacKinnon, David G Hunter, Francis S Collins, Irini Manoli, Elizabeth C Engle
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy. Human genetics 140 (12) (2021)