Susan M Hiatt (Susan Hiatt)

Years Active: 2019-2020
Publications (10 Years): 2

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

Publications

Tiana M Scott, Hui Guo, Evan E Eichler, Jill Anne Rosenfeld, Kaifang Pang, Zhandong Liu, Seema Lalani, Weimin Bi, Yaping Yang, Carlos A Bacino, Haley Streff, Andrea M Lewis, Mary K Koenig, Isabelle Thiffault, Allison Bellomo, David B Everman, Julie R Jones, Roger E Stevenson, Raphael Bernier, Christian Gilissen, Rolph Pfundt, Susan M Hiatt, Gregory M Cooper, Jimmy L Holder, Daryl A Scott
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder. Human mutation 41 (5) (2020)
Mathilde Nizon, Vincent Laugel, Kevin M Flanigan, Matthew Pastore, Megan A Waldrop, Jill A Rosenfeld, Ronit Marom, Rui Xiao, Amanda Gerard, Olivier Pichon, Cédric Le Caignec, Marion Gérard, Klaus Dieterich, Megan Truitt Cho, Kirsty McWalter, Susan M Hiatt, Michelle L Thompson, Stéphane Bézieau, Alexandrea Wadley, Klaas J Wierenga, Jean-Marc Egly, Bertrand Isidor
Variants in MED12L, encoding a subunit of the mediator kinase module, are responsible for intellectual disability associated with transcriptional defect. Genetics in medicine : official journal of the American College of Medical Genetics 21 (12) (2019)

Susan M Hiatt.css-eqlu8i{font-size:small;padding-left:4px;} (Susan Hiatt)