Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11.2 deletion syndrome.

by Erica Hasten, Bernice E Morrow
Published 2019-08-01

Tbx1 and Jag1 act in concert to modulate the fate of neurosensory cells of the mouse otic vesicle

by Stephania Macchiarulo, Bernice E. Morrow
Published 2017-10-01

Mammalian TBX1 preferentially binds and regulates downstream targets via a tandem T-site repeat.

by Raquel Castellanos, Qing Xie, Deyou Zheng, Ales Cvekl, Bernice E Morrow
Published 2014-01-01

Integrated rare variant-based risk gene prioritization in disease case-control sequencing studies.

by Jhih-Rong Lin, Quanwei Zhang, Ying Cai, Bernice E Morrow, Zhengdong D Zhang
Published 2017-12-01

A Pedigree-Based Map of Recombination in the Domestic Dog Genome

by Christopher L. Campbell, Claude Bhérer, Bernice E. Morrow, Adam R. Boyko, Adam Auton
Published 2016-11-01

Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects.

by Anshuman Sewda, A J Agopian, Elizabeth Goldmuntz, Hakon Hakonarson, Bernice E Morrow, Deanne Taylor, Laura E Mitchell, Pediatric Cardiac Genomics Consortium
Published 2019-01-01

Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects.

by Anshuman Sewda, A J Agopian, Elizabeth Goldmuntz, Hakon Hakonarson, Bernice E Morrow, Fadi Musfee, Deanne Taylor, Laura E Mitchell, Pediatric Cardiac Genomics Consortium
Published 2020-01-01

Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome.

by Silvia E Racedo, Erica Hasten, Mingyan Lin, Gnanapackiam Sheela Devakanmalai, Tingwei Guo, Ertugrul M Ozbudak, Chen-Leng Cai, Deyou Zheng, Bernice E Morrow
Published 2017-03-01

Correction: A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family.

by Kunjan Patel, Arnaud P Giese, J M Grossheim, Rashmi S Hegde, Maria Delio, Joy Samanich, Saima Riazuddin, Gregory I Frolenkov, Jinlu Cai, Zubair M Ahmed, Bernice E Morrow
Published 2015-01-01

A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family.

by Kunjan Patel, Arnaud P Giese, J M Grossheim, Rashmi S Hegde, Maria Delio, Joy Samanich, Saima Riazuddin, Gregory I Frolenkov, Jinlu Cai, Zubair M Ahmed, Bernice E Morrow
Published 2015-01-01

Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects

by Fadi I. Musfee, A. J. Agopian, Elizabeth Goldmuntz, Hakon Hakonarson, Bernice E. Morrow, Deanne M. Taylor, Martin Tristani-Firouzi, W. Scott Watkins, Mark Yandell, Laura E. Mitchell
Published 2021-04-01

Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States

by Omobola O. Oluwafemi, Fadi I. Musfee, Laura E. Mitchell, Elizabeth Goldmuntz, Hongbo M. Xie, Hakon Hakonarson, Bernice E. Morrow, Tingwei Guo, Deanne M. Taylor, Donna M. McDonald-McGinn, Beverly S. Emanuel, A. J. Agopian
Published 2021-07-01

Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36.

by Hitisha P Zaveri, Tyler F Beck, Andrés Hernández-García, Katharine E Shelly, Tara Montgomery, Arie van Haeringen, Britt-Marie Anderlid, Chirag Patel, Himanshu Goel, Gunnar Houge, Bernice E Morrow, Sau Wai Cheung, Seema R Lalani, Daryl A Scott
Published 2014-01-01