Projects per year
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Dive into the research topics where Bernice E. Morrow is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Grants
- 13 Finished
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Tbx1 and canonical Wnt signaling in the second heart field
Morrow, B. E. & Chenleng, C.
9/15/15 → 8/31/16
Project: Research project
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Genetic Basis of Syndromic and Non-Syndromic Congential Heart Defects
Morrow, B. E., Emanuel, B. & Goldmuntz, E.
Eunice Kennedy Shriver National Institute of Child Health and Human Development
9/24/11 → 6/30/21
Project: Research project
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Developmental mechanisms of human congenital heart disease
9/24/11 → 6/30/20
Project: Research project
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Developmental Genetics of the Pharyngeal Apparatus
Morrow, B. E. & Rose, S. A.
7/1/09 → 6/30/12
Project: Research project
Publications
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Common variation in cytoskeletal genes is associated with conotruncal heart defects
Musfee, F. I., Agopian, A. J., Goldmuntz, E., Hakonarson, H., Morrow, B. E., Taylor, D. M., Tristani-Firouzi, M., Watkins, W. S., Yandell, M. & Mitchell, L. E., 2021, In: Genes. 12, 5, 655.Research output: Contribution to journal › Article › peer-review
Open Access -
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
International 22q11.2 Brain and Behavior Consortium, Jan 2 2020, In: American Journal of Human Genetics. 106, 1, p. 26-40 15 p.Research output: Contribution to journal › Article › peer-review
12 Scopus citations -
Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects
Pediatric Cardiac Genomics Consortium, Jun 2020, In: PloS one. 15, 6, e0234357.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
International 22q11.2DS Brain and Behavior Consortium, 2020, (Accepted/In press) In: Molecular Psychiatry.Research output: Contribution to journal › Article › peer-review
24 Scopus citations -
Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR)
Pastor, S., Tran, O., Jin, A., Carrado, D., Silva, B. A., Uppuluri, L., Abid, H. Z., Young, E., Crowley, T. B., Bailey, A. G., McGinn, D. E., McDonald-McGinn, D. M., Zackai, E. H., Xie, M., Taylor, D., Morrow, B. E., Xiao, M. & Emanuel, B. S., Dec 1 2020, In: Scientific reports. 10, 1, 12235.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations