Projects per year
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- 3 Similar Profiles
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Grants
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Support for the Rose F. Kennedy IDDRC
Schwartz, G. J., Morrow, B. E., Walkley, S. U., Molholm, S., Greally, J. M. & Dobrenis, K.
Eunice Kennedy Shriver National Institute of Child Health and Human Development
9/22/16 → 5/31/21
Project: Research project
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Molecular aspects of CRKL in heart development and human disease
National Heart, Lung, and Blood Institute
7/15/16 → 6/30/21
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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Tbx1 and canonical Wnt signaling in the second heart field
Morrow, B. E. & Chenleng, C.
9/15/15 → 8/31/16
Project: Research project
Publications
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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
7 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
14 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 Access2 Scopus citations -
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins
Vervoort, L., Demaerel, W., Rengifo, L. Y., Odrzywolski, A., Vergaelen, E., Hestand, M. S., Breckpot, J., Devriendt, K., Swillen, A., Mcdonald-Mcginn, D. M., Fiksinski, A. M., Zinkstok, J. R., Morrow, B. E., Heung, T., Vorstman, J. A. S., Bassett, A. S., Chow, E. W. C., Shashi, V. & Vermeesch, J. R., Nov 15 2019, In: Human molecular genetics. 28, 22, p. 3724-3733 10 p.Research output: Contribution to journal › Article › peer-review