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

por Macchiarulo, Stephania, Morrow, Bernice E.
Publicado 2017

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

por Hasten, Erica, Morrow, Bernice E.
Publicado 2019

Mammalian TBX1 Preferentially Binds and Regulates Downstream Targets Via a Tandem T-site Repeat

por Castellanos, Raquel, Xie, Qing, Zheng, Deyou, Cvekl, Ales, Morrow, Bernice E.
Publicado 2014

Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice

por Freyer, Laina, Nowotschin, Sonja, Pirity, Melinda K, Baldini, Antonio, Morrow, Bernice E
Publicado 2013

Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis

por Braunstein, Evan M, Monks, Dennis C, Aggarwal, Vimla S, Arnold, Jelena S, Morrow, Bernice E
Publicado 2009

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

por Campbell, Christopher L., Bhérer, Claude, Morrow, Bernice E., Boyko, Adam R., Auton, Adam
Publicado 2016

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

por Lin, Jhih-Rong, Zhang, Quanwei, Cai, Ying, Morrow, Bernice E., Zhang, Zhengdong D.
Publicado 2017

Spatiotemporal Gene Coexpression and Regulation in Mouse Cardiomyocytes of Early Cardiac Morphogenesis

por Liu, Yang, Lu, Pengfei, Wang, Yidong, Morrow, Bernice E., Zhou, Bin, Zheng, Deyou
Publicado 2019

Single-cell transcriptomics uncovers a non-autonomous Tbx1-dependent genetic program controlling cardiac neural crest cell development

por De Bono, Christopher, Liu, Yang, Ferrena, Alexander, Valentine, Aneesa, Zheng, Deyou, Morrow, Bernice E.
Publicado 2023

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

por Sewda, Anshuman, Agopian, A. J., Goldmuntz, Elizabeth, Hakonarson, Hakon, Morrow, Bernice E., Taylor, Deanne, Mitchell, Laura E.
Publicado 2019

Crk and Crkl Are Required in the Endocardial Lineage for Heart Valve Development

por Wu, Bingruo, Wu, Brian, Benkaci, Sonia, Shi, Lijie, Lu, Pengfei, Park, Taeju, Morrow, Bernice E., Wang, Yidong, Zhou, Bin
Publicado 2023

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

por Sewda, Anshuman, Agopian, A. J., Goldmuntz, Elizabeth, Hakonarson, Hakon, Morrow, Bernice E., Musfee, Fadi, Taylor, Deanne, Mitchell, Laura E.
Publicado 2020

Genetic analysis of nonalcoholic fatty liver disease within a Caribbean–Hispanic population

por Edelman, Deborah, Kalia, Harmit, Delio, Maria, Alani, Mustafa, Krishnamurthy, Karthik, Abd, Mortadha, Auton, Adam, Wang, Tao, Wolkoff, Allan W., Morrow, Bernice E.
Publicado 2015

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

por Racedo, Silvia E., Hasten, Erica, Lin, Mingyan, Devakanmalai, Gnanapackiam Sheela, Guo, Tingwei, Ozbudak, Ertugrul M., Cai, Chen-Leng, Zheng, Deyou, Morrow, Bernice E.
Publicado 2017

The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder

por Wenger, Tara L., Kao, Charlly, McDonald-McGinn, Donna M., Zackai, Elaine H., Bailey, Alice, Schultz, Robert T., Morrow, Bernice E., Emanuel, Beverly S., Hakonarson, Hakon
Publicado 2016

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

por Patel, Kunjan, Giese, Arnaud P., Grossheim, J. M., Hegde, Rashima S., Delio, Maria, Samanich, Joy, Riazuddin, Saima, Frolenkov, Gregory I., Cai, Jinlu, Ahmed, Zubair M., Morrow, Bernice E.
Publicado 2015

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

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

Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects

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

An optimized approach for multiplexing single-nuclear ATAC-seq using oligonucleotide-conjugated antibodies

por Bera, Betelehem Solomon, Thompson, Taylor V., Sosa, Eric, Nomaru, Hiroko, Reynolds, David, Dubin, Robert A., Maqbool, Shahina B., Zheng, Deyou, Morrow, Bernice E., Greally, John M., Suzuki, Masako
Publicado 2023

Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome

por McGinn, Daniel E., Crowley, T. Blaine, Heung, Tracy, Tran, Oanh, Moss, Edward, Zackai, Elaine H., Emanuel, Beverly S., Chow, Eva W. C., Morrow, Bernice E., Swillen, Ann, Bassett, Anne S., McDonald-McGinn, Donna M.
Publicado 2022