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This is a list of publications by this organization, listed chronologically starting with the most recent first. The source of publications may be a combination of Scopus and manually entered data from a user. New publications from Scopus appear in this list weekly and publications entered by a user appear instantly. Citation counts start from 1996 and come directly from Scopus.
Jillian Lee Wiggins; Jirair K. Bedoyan; Melisa Carrasco; Johnna R. Swartz; Donna M. Martin; Christopher S. Monk
Age-related effect of serotonin transporter genotype on amygdala and prefrontal cortex function in adolescence
Joseph A. Micucci; Wanda S. Layman; Elizabeth A. Hurd; Ethan D. Sperry; Sophia F. Frank; Mark A. Durham; Donald L. Swiderski; Jennifer M. Skidmore; Peter C. Scacheri; Yehoash Raphael; et al.
CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome
Thor Thorsson; William W. Russell; Nour El-Kashlan; Rachel Soemedi; Jonathan Levine; Sarah B. Geisler; Todd Ackley; Aoy Tomita-Mitchell; Jill A. Rosenfeld; Ana Töpf; et al.
Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development
Mark W. Russell; Maide O. Raeker; Sarah B. Geisler; Peedikayil E. Thomas; Tracy A. Simmons; John A. Bernat; Thor Thorsson; Jeffrey W. Innis
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations
Morgan Jones; Gail Osawa; Joshua A. Regal; Daniel N. Weinberg; James Taggart; Hande Kocak; Ann Friedman; David O. Ferguson; Catherine E. Keegan; Ivan Maillard
Hematopoietic stem cells are acutely sensitive to Acd shelterin gene inactivation
Morgan Jones; Gail Osawa; Joshua A Regal; Daniel N Weinberg; James Taggart; Hande Kocak; Ann Friedman; David O Ferguson; Catherine E Keegan; Ivan Maillard
Hematopoietic stem cells are acutely sensitive to Acd shelterin gene inactivation.
Shane C. Quinonez; Jeffrey W. Innis
Human HOX gene disorders
Andrea H. Seeley; Mark A. Durham; Mark A. Micale; Jeffrey Wesolowski; Bradley R. Foerster; Donna M. Martin
Macrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1-q24.2 contiguous gene deletion
Jillian Lee Wiggins; Johnna R. Swartz; Donna M. Martin; Catherine Lord; Christopher S. Monk
Serotonin transporter genotype impacts amygdala habituation in youth with autism spectrum disorders
Ethan D. Sperry; Elizabeth A. Hurd; Mark A. Durham; Elyse N. Reamer; Adam B. Stein; Donna M. Martin
The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development
Heon Yung Gee; Edgar A Otto; Toby W Hurd; Shazia Ashraf; Moumita Chaki; Andrew Cluckey; Virginia Vega-Warner; Pawaree Saisawat; Katrina A Diaz; Humphrey Fang; et al.
Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies