Mir Reza Bekheirnia

Publication Activity (10 Years)

Years Active: 2016-2019
Publications (10 Years): 2

Top Topics

Gene Expression

Top Venues

Genetics in medicine : official journal of the American College of Medical Genetics

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

Publications

Alexandria T M Blackburn, Nasim Bekheirnia, Vanessa C Uma, Mark E Corkins, Yuxiao Xu, Jill Anne Rosenfeld, Matthew N Bainbridge, Yaping Yang, Pengfei Liu, Suneeta Madan-Khetarpal, Mauricio R Delgado, Louanne Hudgins, Ian Krantz, David Rodriguez-Buritica, Patricia G Wheeler, Lihadh Al-Gazali, Aisha Mohamed Saeed Mohamed Al Shamsi, Natalia Gomez-Ospina, Hsiao-Tuan Chao, Ghayda M Mirzaa, Angela E Scheuerle, Mary K Kukolich, Fernando Scaglia, Christine Eng, Helen Rankin Willsey, Michael C Braun, Dolores J Lamb, Rachel K Miller, Mir Reza Bekheirnia
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract. Genetics in medicine : official journal of the American College of Medical Genetics 21 (12) (2019)
Mir Reza Bekheirnia, Nasim Bekheirnia, Matthew N Bainbridge, Shen Gu, Zeynep Hande Coban Akdemir, Tomasz Gambin, Nicolette K Janzen, Shalini N Jhangiani, Donna M Muzny, Mini Michael, Eileen D Brewer, Ewa Elenberg, Arundhati S Kale, Alyssa A Riley, Sarah J Swartz, Daryl A Scott, Yaping Yang, Poyyapakkam R Srivaths, Scott E Wenderfer, Joann Norma Bodurtha, Carolyn D Applegate, Milen Velinov, Angela Myers, Lior Borovik, William J Craigen, Neil A Hanchard, Jill Anne Rosenfeld, Richard Alan Lewis, Edmond T Gonzales, Richard A Gibbs, John W Belmont, David R Roth, Christine Eng, Michael C Braun, James R Lupski, Dolores J Lamb
Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene. Genetics in medicine : official journal of the American College of Medical Genetics 19 (4) (2016)