Bernice E. Morrow

ScholarGPS® ID: 26582663734443

Affiliation
Albert Einstein College of Medicine, The Bronx, New York City, United States
Affiliation History

Field
Life Sciences
Discipline
Genetics
Top Specialties
Human Genetics | Chromosomal Deletion Syndrome | Molecular Genetics | Medical Genetics | Chromosome | Morphogenesis | Inner Ear | Birth Defect | Congenital Heart Defect | Mutation | Genomics | Mammal | Binding Protein | DNA | Yeast
Metrics Summary
Publication Count
150
Predicted Citations
12,393
Predicted h-index
55
Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

  • Publications
  • Books
  • Patents
  • NIH/NSF
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Dgcr8 functions in the secondary heart field for outflow tract and right ventricle development in mammals (journal article)
Racedo, Silvia E. | Liu, Yang | Shi, Lijie | Zheng, Deyou | Morrow, Bernice E.
Developmental Biology, volume 506 (2024).
10.1016/j.ydbio.2023.12.005
Cited by (2) | Cite | Source
Crk and Crkl Are Required in the Endocardial Lineage for Heart Valve Development (journal article)
Wu, Bingruo | Wu, Brian | Benkaci, Sonia | Shi, Lijie | Lu, Pengfei | Park, Taeju | Morrow, Bernice E. | Wang, Yidong | Zhou, Bin
Journal of the American Heart Association, volume 12, issue 18 (2023).
10.1161/JAHA.123.029683
Cited by (1) | Cite | Source
An optimized approach for multiplexing single-nuclear ATAC-seq using oligonucleotide-conjugated antibodies (journal article)
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
Epigenetics & Chromatin, volume 16, issue 1 (2023).
10.1186/s13072-023-00486-7
Cite | Source
Single-cell transcriptomics uncovers a non-autonomous Tbx1-dependent genetic program controlling cardiac neural crest cell development (journal article)
De Bono, Christopher | Liu, Yang | Ferrena, Alexander | Valentine, Aneesa | Zheng, Deyou | Morrow, Bernice E.
Nature Communications, volume 14, issue 1 (2023).
10.1038/s41467-023-37015-9
Cited by (9) | Cite | Source
Tbx2 and Tbx3 regulate cell fate progression of the otic vesicle for inner ear development (journal article)
Song, Hansoo | Morrow, Bernice E.
Developmental Biology, volume 494 (2023).
10.1016/j.ydbio.2022.12.003
Cited by (2) | Cite | Source
Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression (journal article)
Campbell, Ian M. | Crowley, T. Blaine | Jobaliya, Chintan | Bailey, Alice | McGinn, Daniel E. | Gaiser, Kimberly | Bassett, Anne | Gur, Raquel E. | Morrow, Bernice | Emanuel, Beverly S. | ... | Lambert, Michele P.
Clinical Genetics, volume 103, issue 1, pages 109-113 (2023).
10.1111/cge.14227
Cited by (2) | Cite | Source
Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome (journal article)
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 | ... | McDonald-McGinn, Donna M.
Genes, volume 13, issue 10, pages 1800- (2022).
10.3390/genes13101800
Cited by (2) | Cite | Source
Crk and Crkl have shared functions in neural crest cells for cardiac outflow tract septation and vascular smooth muscle differentiation (journal article)
Shi, Lijie | Racedo, Silvia E | Diacou, Alexander | Park, Taeju | Zhou, Bin | Morrow, Bernice E
Human Molecular Genetics, volume 31, issue 8, pages 1197-1215 (2022).
10.1093/hmg/ddab313
Cited by (4) | Cite | Source
Genetics, mechanism, and pathophysiology of 22q11.2 deletion syndrome (book chapter)
In The Chromosome 22q11.2 Deletion Syndrome
Morrow, Bernice E.
Elsevier (2022)
10.1016/B978-0-12-816047-3.00017-4
Cite | Source
Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm (journal article)
Nomaru, Hiroko | Liu, Yang | De Bono, Christopher | Righelli, Dario | Cirino, Andrea | Wang, Wei | Song, Hansoo | Racedo, Silvia E. | Dantas, Anelisa G. | Zhang, Lu | ... | Morrow, Bernice E.
Nature Communications, volume 12, issue 1 (2021).
10.1038/s41467-021-26966-6
Cited by (24) | Cite | Source
Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States (journal article)
Oluwafemi, Omobola O. | Musfee, Fadi I. | Mitchell, Laura E. | Goldmuntz, Elizabeth | Xie, Hongbo M. | Hakonarson, Hakon | Morrow, Bernice E. | Guo, Tingwei | Taylor, Deanne M. | McDonald-McGinn, Donna M. | ... | Agopian, A. J.
Genes, volume 12, issue 7, pages 1030- (2021).
10.3390/genes12071030
Cite | Source
Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects (journal article)
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.
Genes, volume 12, issue 5, pages 655- (2021).
10.3390/genes12050655
Cited by (2) | Cite | Source
Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR) (journal article)
Pastor, Steven | Tran, Oanh | Jin, Andrea | Carrado, Danielle | Silva, Benjamin A. | Uppuluri, Lahari | Abid, Heba Z. | Young, Eleanor | Crowley, T. Blaine | Bailey, Alice G. | ... | Emanuel, Beverly S.
Scientific Reports, volume 10, issue 1 (2020).
10.1038/s41598-020-69134-4
Cited by (19) | Cite | Source
Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects (journal article)
Sewda, Anshuman | Agopian, A. J. | Goldmuntz, Elizabeth | Hakonarson, Hakon | Morrow, Bernice E. | Musfee, Fadi | Taylor, Deanne | Mitchell, Laura E.
PLOS ONE, volume 15, issue 6, pages e0234357- (2020).
10.1371/journal.pone.0234357
Cited by (7) | Cite | Source
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins (journal article)
Vervoort, Lisanne | Demaerel, Wolfram | Rengifo, Laura Y | Odrzywolski, Adrian | Vergaelen, Elfi | Hestand, Matthew S | Breckpot, Jeroen | Devriendt, Koen | Swillen, Ann | McDonald-McGinn, Donna M | ... | Vermeesch, Joris R
Human Molecular Genetics, volume 28, issue 22, pages 3724-3733 (2019).
10.1093/hmg/ddz166
Cited by (8) | Cite | Source
The 22q11 low copy repeats are characterized by unprecedented size and structural variability (journal article)
Demaerel, Wolfram | Mostovoy, Yulia | Yilmaz, Feyza | Vervoort, Lisanne | Pastor, Steven | Hestand, Matthew S. | Swillen, Ann | Vergaelen, Elfi | Geiger, Elizabeth A. | Coughlin, Curtis R. | ... | Vermeesch, Joris R.
Genome Research, volume 29, issue 9, pages 1389-1401 (2019).
10.1101/gr.248682.119
Cited by (27) | Cite | Source
Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11.2 deletion syndrome (journal article)
Hasten, Erica | Morrow, Bernice E.
PLOS Genetics, volume 15, issue 8, pages e1008301- (2019).
10.1371/journal.pgen.1008301
Cited by (26) | Cite | Source
Spatiotemporal Gene Coexpression and Regulation in Mouse Cardiomyocytes of Early Cardiac Morphogenesis (journal article)
Liu, Yang | Lu, Pengfei | Wang, Yidong | Morrow, Bernice E. | Zhou, Bin | Zheng, Deyou
Journal of the American Heart Association, volume 8, issue 15 (2019).
10.1161/JAHA.119.012941
Cited by (8) | Cite | Source
Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion status (journal article)
Xie, Hongbo M. | Taylor, Deanne M. | Zhang, Zhe | McDonald‐McGinn, Donna M. | Zackai, Elaine H. | Stambolian, Dwight | Hakonarson, Hakon | Morrow, Bernice E. | Emanuel, Beverly S. | Goldmuntz, Elizabeth
Birth Defects Research, volume 111, issue 13, pages 888-905 (2019).
10.1002/bdr2.1534
Cited by (4) | Cite | Source
Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects (journal article)
Sewda, Anshuman | Agopian, A. J. | Goldmuntz, Elizabeth | Hakonarson, Hakon | Morrow, Bernice E. | Taylor, Deanne | Mitchell, Laura E.
PLOS ONE, volume 14, issue 7, pages e0219926- (2019).
10.1371/journal.pone.0219926
Cited by (15) | Cite | Source