Bernice E Morrow (Bernice Morrow)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 16

Top Venues

Nature communications

Science (New York, N.Y.)

American journal of medical genetics. Part A

PloS one

Albert Einstein College of Medicine, Yeshiva University

Albert Einstein College of Medicine, Yeshiva University (PHD)

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

Affiliation History

Albert Einstein College of Medicine, Yeshiva University Jul 01 1995

United States

Professor :: Genetics

Education History

Albert Einstein College of Medicine, Yeshiva University Sep 01 1979 - Dec 01 1985

United States

PHD :: Molecular Pharmacology

Publications

Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, Terrence Blaine Crowley, Valeria Capra, Jeremiah Martino, Meade Haller, Camila Araújo, Hélio R Machado, Renee George, Bryn Gerding, Kiely N James, Valentina Stanley, Nan Jiang, Kameron Alu, Naomi Meave, Anna S Nidhiry, Fiza Jiwani, Isaac Tang, Ashna Nisal, Ishani Jhamb, Arzoo Patel, Aakash Patel, Jennifer McEvoy-Venneri, Chelsea Barrows, Celina Shen, Yoo-Jin Ha, Robyn Howarth, Madison Strain, Allison Elizabeth Ashley-Koch, Matloob Azam, Sara Mumtaz, Gyang Markus Bot, Richard H Finnell, Zoha Kibar, Ahmed I Marwan, Gia Melikishvili, Hal S Meltzer, Osvaldo M Mutchinick, David A Stevenson, Henry J Mroczkowski, Betsy Ostrander, Erica Schindewolf, Julie Moldenhauer, Elaine H Zackai, Beverly S Emanuel, Sixto García-Miñaúr, Sebastian Kwiatkowski, Roger E Stevenson, Maha Saad Zaki, Hope Northrup, Hanna K McNamara, Kimberly A Aldinger, Ian G Phelps, Mei Deng, Ian A Glass, null null, Bernice E Morrow, Donna M McDonald-McGinn, Simone Sanna-Cherchi, Dolores J Lamb, Joseph G Gleeson
Risk of meningomyelocele mediated by the common 22q11.2 deletion. Science (New York, N.Y.) 384 (6695) (2024)
Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, Terrence Blaine Crowley, Valeria Capra, Jeremiah Martino, Meade Haller, Camila Araújo, Hélio R Machado, Renee George, Bryn Gerding, Kiely N James, Valentina Stanley, Nan Jiang, Kameron Alu, Naomi Meave, Anna S Nidhiry, Fiza Jiwani, Isaac Tang, Ashna Nisal, Ishani Jhamb, Arzoo Patel, Aakash Patel, Jennifer McEvoy-Venneri, Chelsea Barrows, Celina Shen, Yoo-Jin Ha, Robyn Howarth, Madison Strain, Allison Elizabeth Ashley-Koch, Matloob Azam, Sara Mumtaz, Gyang Markus Bot, Richard H Finnell, Zoha Kibar, Ahmed I Marwan, Gia Melikishvili, Hal S Meltzer, Osvaldo M Mutchinick, David A Stevenson, Henry J Mroczkowski, Betsy Ostrander, Erica Schindewolf, Julie Moldenhauer, Elaine H Zackai, Beverly S Emanuel, Sixto García-Miñaúr, Sebastian Kwiatkowski, Roger E Stevenson, Maha Saad Zaki, Hope Northrup, Hanna K McNamara, Kimberly A Aldinger, Ian G Phelps, Mei Deng, Ian A Glass, null null, Bernice E Morrow, Donna M McDonald-McGinn, Simone Sanna-Cherchi, Dolores J Lamb, Joseph G Gleeson, Allison Elizabeth Ashley Koch, Hal S Meltzer, Joan Le, Kit Sing Au, Hope Northrup, Gyang Markus Bot, Valeria Capra, Richard H Finnell, Zoha Kibar, Philip J Lupo, Helio R Machado, Camila Araújo, Tony Magana, Ahmed I Marwan, Gia Melikishvili, Osvaldo M Mutchinick, Roger E Stevenson, Anna Yurrita, Maha S Zaki, Sara Mumtaz, José Ramón Medina-Bereciartu, Caroline M Kolvenbach, Shirlee Shril, Friedhelm Hildebrandt, Mahmoud M Noureldeen, Aida Ms Salem, Yukitoshi Takahashi, Hormos Salimi-Dafsari, H Westley Phillips, Brian Hanak, Bülent Kara, Ayfer Sakarya Güneş, David D Gonda, Salman Kirmani, Tinatin Tkemaladze, Joseph G Gleeson
Risk of meningomyelocele mediated by the common 22q11.2 deletion. Science (New York, N.Y.) 384 (6695) (2024)
Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, Terrence Blaine Crowley, Valeria Capra, Jeremiah Martino, Meade Haller, Camila Araújo, Hélio R Machado, Renee George, Bryn Gerding, Kiely N James, Valentina Stanley, Nan Jiang, Kameron Alu, Naomi Meave, Anna S Nidhiry, Fiza Jiwani, Isaac Tang, Ashna Nisal, Ishani Jhamb, Arzoo Patel, Aakash Patel, Jennifer McEvoy-Venneri, Chelsea Barrows, Celina Shen, Yoo-Jin Ha, Robyn Howarth, Madison Strain, Allison Elizabeth Ashley-Koch, Matloob Azam, Sara Mumtaz, Gyang Markus Bot, Richard H Finnell, Zoha Kibar, Ahmed I Marwan, Gia Melikishvili, Hal S Meltzer, Osvaldo M Mutchinick, David A Stevenson, Henry J Mroczkowski, Betsy Ostrander, Erica Schindewolf, Julie Moldenhauer, Elaine H Zackai, Beverly S Emanuel, Sixto García-Miñaúr, Sebastian Kwiatkowski, Roger E Stevenson, Maha Saad Zaki, Hope Northrup, Hanna K McNamara, Kimberly A Aldinger, Ian G Phelps, Mei Deng, Ian A Glass, null null, Bernice E Morrow, Donna M McDonald-McGinn, Simone Sanna-Cherchi, Dolores J Lamb, Joseph G Gleeson
Risk of meningomyelocele mediated by the common 22q11.2 deletion. Science (New York, N.Y.) 384 (6695) (2024)
Yingjie Zhao, Yujue Wang, Lijie Shi, Donna M McDonald-McGinn, T Blaine Crowley, Daniel E McGinn, Oanh T Tran, Daniella Miller, Jhih-Rong Lin, Elaine H Zackai, H Richard Johnston, Eva W C Chow, Jacob A S Vorstman, Claudia Vingerhoets, Therese van Amelsvoort, Doron Gothelf, Ann Swillen, Jeroen Breckpot, Joris Robert Vermeesch, Stephan Eliez, Maude Schneider, Marianne B M van den Bree, Michael J Owen, Wendy R Kates, Gabriela M Repetto, Vandana Shashi, Kelly Schoch, Carrie E Bearden, M Cristina Digilio, Marta Unolt, Carolina Putotto, Bruno Marino, Maria Pontillo, Marco Armando, Stefano Vicari, Kathleen Angkustsiri, Linda Campbell, Tiffany Busa, Damian Heine-Suñer, Kieran C Murphy, Declan G M Murphy, Sixto García-Miñaúr, Luis Fernández, null null, Zhengdong D Zhang, Elizabeth Goldmuntz, Raquel E Gur, Beverly S Emanuel, Deyou Zheng, Christian R Marshall, Anne Susan Bassett, Tao Wang, Bernice E Morrow
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. NPJ genomic medicine 8 (1) (2023)
Christopher De Bono, Yang Liu, Alexander Ferrena, Aneesa Valentine, Deyou Zheng, Bernice E Morrow
Single-cell transcriptomics uncovers a non-autonomous Tbx1-dependent genetic program controlling cardiac neural crest cell development. Nature communications 14 (1) (2023)
Bingruo Wu, Brian Wu, Sonia Benkaci, Lijie Shi, Pengfei Lu, Taeju Park, Bernice E Morrow, Yidong Wang, Bin Zhou
Crk and Crkl Are Required in the Endocardial Lineage for Heart Valve Development. Journal of the American Heart Association (2023)
Christopher De Bono, Yang Liu, Alexander Ferrena, Aneesa Valentine, Deyou Zheng, Bernice E Morrow
Single-cell transcriptomics uncovers a non-autonomous Tbx1-dependent genetic program controlling cardiac neural crest cell development. Nature communications 14 (1) (2023)
Christopher De Bono, Yang Liu, Alexander Ferrena, Aneesa Valentine, Deyou Zheng, Bernice E Morrow
Single-cell transcriptomics uncovers a non-autonomous Tbx1-dependent genetic program controlling cardiac neural crest cell development. Nature communications 14 (1) (2023)
Hiroko Nomaru, Yang Liu, Christopher De Bono, Dario Righelli, Andrea Cirino, Wei Wang, Hansoo Song, Silvia E Racedo, Anelisa G Dantas, Lu Zhang, Chen-Leng Cai, Claudia Angelini, Lionel A Christiaen, Robert G Kelly, Antonio Baldini, Deyou Zheng, Bernice E Morrow
Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm. Nature communications 12 (1) (2021)
Lijie Shi, Silvia E Racedo, Alexander Diacou, Taeju Park, Bin Zhou, Bernice E Morrow
Crk and Crkl have shared functions in neural crest cells for cardiac outflow tract septation and vascular smooth muscle differentiation. Human molecular genetics (2021)
Anshuman Sewda, A J Agopian, Elizabeth Goldmuntz, Hakon Hakonarson, Bernice E Morrow, Fadi I Musfee, Deanne M Taylor, Laura E Mitchell, null null
Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects. PloS one 15 (6) (2020)
Anshuman Sewda, A J Agopian, Elizabeth Goldmuntz, Hakon H Hakonarson, Bernice E Morrow, Deanne M Taylor, Laura E Mitchell, null null
Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects. PloS one 14 (7) (2019)
Bernice E Morrow, Donna M McDonald-McGinn, Beverly S Emanuel, Joris R Vermeesch, Peter J Scambler
Molecular genetics of 22q11.2 deletion syndrome. American journal of medical genetics. Part A 176 (10) (2019)
Erica Hasten, Bernice E Morrow
Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11.2 deletion syndrome. PLoS genetics 15 (8) (2019)
Yingjie Zhao, Tingwei Guo, Ania M Fiksinski, Elemi Breetvelt, Donna M McDonald-McGinn, Terrence B Crowley, Alexander Diacou, Maude Schneider, Stephan Eliez, Ann Swillen, Jeroen Breckpot, Joris Vermeesch, Eva W C Chow, Doron Gothelf, Sasja Duijff, Rens Evers, Thérèse A van Amelsvoort, Marianne van den Bree, Michael Owen, Maria Niarchou, Carrie E Bearden, Claudia Ornstein, Maria Pontillo, Antonino Buzzanca, Stefano Vicari, Marco Armando, Kieran C Murphy, Clodagh Murphy, Sixto Garcia-Minaur, Nicole Philip, Linda Campbell, Jaume Morey-Cañellas, Jasna Raventos, Jordi Rosell, Damian Heine-Suner, Robert J Shprintzen, Raquel E Gur, Elaine Zackai, Beverly S Emanuel, Tao Wang, Wendy R Kates, Anne Susan Bassett, Jacob A S Vorstman, Bernice E Morrow, null null
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects. American journal of medical genetics. Part A 176 (10) (2018)
Stephania Macchiarulo, Bernice E Morrow
Tbx1 and Jag1 act in concert to modulate the fate of neurosensory cells of the mouse otic vesicle. Biology open 6 (10) (2017)

Bernice E Morrow.css-eqlu8i{font-size:small;padding-left:4px;} (Bernice Morrow)

Publication Activity (10 Years)

Top Topics

Top Venues

Bernice E Morrow (Bernice Morrow)