Dgcr8 functions in the secondary heart field for outflow tract and right ventricle development in mammals

Authors: Racedo, Silvia E. ^a, Liu, Yang ^d, Shi, Lijie ^a, Zheng, Deyou ^{a, b, c}, Morrow, Bernice E. ^{a, e, ∗}

Source: In Developmental Biology February 2024 506:72-84

Tbx2 and Tbx3 regulate cell fate progression of the otic vesicle for inner ear development

Authors: Song, Hansoo, Morrow, Bernice E.

Source: In Developmental Biology February 2023 494:71-84

scDAPP: a comprehensive single-cell transcriptomics analysis pipeline optimized for cross-group comparison.

Authors: Ferrena, Alexander, Zheng, Xiang Yu, Jackson, Kevyn, Hoang, Bang, Morrow, Bernice E, Zheng, Deyou

Source: NAR Genomics & Bioinformatics; Dec2024, Vol. 6 Issue 4, p1-9, 9p

Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects

Authors: Antonarakis, Stylianos E., Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, María Angeles, Epstein, Michael P., Evers, Rens, Fernandez, Luis, Fritsch, Rosemarie, Algas, Fernando García, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S., Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Teresa, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther D.A., Vergaelen, Elfi, Warren, Steve T., Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong, Zwick, Michael, Zhao, Yingjie, Diacou, Alexander, Johnston, H. Richard, Musfee, Fadi I., McDonald-McGinn, Donna M., McGinn, Daniel, Crowley, T. Blaine, Repetto, Gabriela M., Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Kates, Wendy R., Digilio, M. Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne, Moss, Hayley, Owen, Michael J., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J., Shprintzen, Robert J., Campbell, Linda, Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Bearden, Carrie E., Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob A.S., Gothelf, Doron, Zackai, Elaine, Agopian, A.J., Gur, Raquel E., Bassett, Anne S., Emanuel, Beverly S., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Morrow, Bernice E.

Source: In The American Journal of Human Genetics 2 January 2020 106(1):26-40

NOTCH maintains developmental cardiac gene network through WNT5A

Authors: Wang, Yidong, Lu, Pengfei, Wu, Bingruo, Morrow, Bernice E., Zhou, Bin

Source: In Journal of Molecular and Cellular Cardiology December 2018 125:98-105

Mouse and Human CRKL Is Dosage Sensitive for Cardiac Outflow Tract Formation

Authors: Racedo, Silvia E., McDonald-McGinn, Donna M., Chung, Jonathan H., Goldmuntz, Elizabeth, Zackai, Elaine, Emanuel, Beverly S., Zhou, Bin, Funke, Birgit, Morrow, Bernice E.

Source: In The American Journal of Human Genetics 5 February 2015 96(2):235-244

Copy Number Variation of the glucose transporter gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome

Authors: Mlynarski, Elisabeth E., Sheridan, Molly B., Xie, Michael, Guo, Tingwei, Racedo, Silvia E., McDonald McGinn, Donna M., Gai, Xiaowu, Chow, Eva W.C., Vorstman, Jacob, Swillen, Ann, Devriendt, Koen, Breckpot, Jeroen, Digilio, Maria Cristina, Marino, Bruno, Dallapiccola, Bruno, Philip, Nicole, Simon, Tony J., Roberts, Amy E., Piotrowicz, Małgorzata, Bearden, Carrie E., Eliez, Stephan, Gothelf, Doron, Coleman, Karlene, Kates, Wendy R., Devoto, Marcella, Zackai, Elaine, Heine-Suñer, Damian, Shaikh, Tamim H., Bassett, Anne S., Goldmuntz, Elizabeth, Morrow, Bernice E., Emanuel, Beverly S.

Source: In The American Journal of Human Genetics March 2015

Genetic Modifiers of the Physical Malformations in Velo-Cardio-Facial Syndrome/DiGeorge Syndrome

Authors: Aggarwal, Vimla S., Morrow, Bernice E.

Source: Developmental Disabilities Research Reviews. 2008 14(1):19-25.

Peer Reviewed: Y

Page Count: 7

Descriptors: Patients, Genetics, Etiology, Genetic Disorders, Human Body, Animals, Symptoms (Individual Disorders), Research, Physical Disabilities, Anatomy

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

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

Source: Journal of the American Heart Association; 9/19/2023, Vol. 12 Issue 18, p1-15, 28p

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

Authors: Hasten, Erica¹, Morrow, Bernice E.¹ Bernice.morrow@einstein.yu.edu

Source: PLoS Genetics. 8/14/2019, Vol. 15 Issue 8, p1-30. 30p.

Subject Terms: *ENDODERM, *SUBCLAVIAN artery, *EXTRACELLULAR matrix proteins, *NOTCH genes, *THYMUS, *PARATHYROID glands

Cleft palate, retrognathia and congenital heart disease in velo-cardio-facial syndrome: A phenotype correlation study

Authors: Friedman, Marcia A., Miletta, Nathanial, Roe, Cheryl, Wang, Dongliang, Morrow, Bernice E., Kates, Wendy R., Higgins, Anne Marie, Shprintzen, Robert J.

Source: In International Journal of Pediatric Otorhinolaryngology 2011 75(9):1167-1172

Chapter 2 - Genetics, mechanism, and pathophysiology of 22q11.2 deletion syndrome

Authors: Morrow, Bernice E.

Source: In The Chromosome 22q11.2 Deletion Syndrome 2022:34-52

Mutational analysis of HOXA2 and SIX2 in a Bronx population with isolated microtia

Authors: Monks, Dennis C., Jahangir, Arthee, Shanske, Alan L., Samanich, Joy, Morrow, Bernice E., Babcock, Melanie

Source: In International Journal of Pediatric Otorhinolaryngology 2010 74(8):878-882

GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent

Authors: Shan, Jidong, Chobot-Rodd, Janie, Castellanos, Raquel, Babcock, Melanie, Shanske, Alan, Parikh, Sanjay R., Morrow, Bernice E., Samanich, Joy

Source: In International Journal of Pediatric Otorhinolaryngology 2010 74(6):611-618

Mesodermal Tbx1 is required for patterning the proximal mandible in mice

Authors: Aggarwal, Vimla S., Carpenter, Courtney, Freyer, Laina, Liao, Jun, Petti, Marilena, Morrow, Bernice E.

Source: In Developmental Biology 2010 344(2):669-681

Genetic evaluation of American minority pediatric cochlear implant recipients

Authors: Fischer, Tova C., Samanich, Joy, Morrow, Bernice E., Chobot-Rodd, Janie, Shanske, Alan, Parikh, Sanjay R.

Source: In International Journal of Pediatric Otorhinolaryngology 2009 73(2):195-203

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

Authors: 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

Source: Epigenetics & Chromatin; 4/28/2023, Vol. 16 Issue 1, p1-13, 13p

Subject Terms: BIOLOGICAL assay, Y chromosome, DEMULTIPLEXING, IMMUNOGLOBULINS, CHROMATIN, CHROMOSOMES

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

Authors: De Bono, Christopher, Liu, Yang, Ferrena, Alexander, Valentine, Aneesa, Zheng, Deyou, Morrow, Bernice E.

Source: Nature Communications; 3/21/2023, p1-20, 20p

Subject Terms: NEURAL crest, DIGEORGE syndrome, VASCULAR smooth muscle, CARDIOVASCULAR development, THORACIC aorta, CELL communication

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Identification of downstream genetic pathways of Tbx1 in the second heart field

Authors: Liao, Jun, Aggarwal, Vimla S., Nowotschin, Sonja, Bondarev, Alexei, Lipner, Shari, Morrow, Bernice E.

Source: In Developmental Biology 15 April 2008 316(2):524-537