Projects per year
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Collaborations and top research areas from the last five years
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Cell fate choices by Tbx1 in forming the mammalian heart
Morrow, B. E. (PI) & Zheng, D. (CoPI)
National Heart, Lung, and Blood Institute
8/20/20 → 4/30/27
Project: Research project
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Cancer Center Support Grant
Almo, S. C. (CoPI), Hogue-Angeletti, R. (CoPI), Augenlicht, L. H. (CoPI), Condeelis, J. S. (CoPI), Desai, K. (CoPI), Edelmann, W. (CoPI), Goldman, I. D. (CoPI), Greally, J. M. (CoPI), Herbst, L. H. (CoPI), Keller, S. M. (CoPI), Kim, M. Y. (CoPI), Mahmood, R. (CoPI), Montagna, C. (CoPI), Morrow, B. E. (CoPI), Pollard, J. W. (CoPI), Porcelli, S. A. (CoPI), Rohan, T. E. (CoPI), Scharff, M. D. (CoPI), Seither, R. (CoPI), Skoultchi, A. I. (CoPI), Sparano, J. A. (CoPI), Stanley, P. M. (CoPI), Steidl, U. U. (PI), Bresnick, A. R. (CoPI), Skoultchi, A. I. (CoPI), Adedimeji, A. A. (CoPI), Beck, A. A. P. (CoPI), Morrow, B. E. (CoPI), Blanchard, J. S. (CoPI), Halmos, B. B. (CoPI), Morrow, B. B. (CoPI), Diamond, B. B. (CoPI), Will, B. B. (CoPI), Rapkin, B. D. (CoPI), Chu, E. (CoPI), Montagna, C. C. (CoPI), Stein, D. T. (CoPI), Gaertner, D. D. J. (CoPI), Ho, G. Y. (CoPI), Goel, S. (CoPI), Hosgood, H. D. H. (CoPI), Strickler, H. H. D. (CoPI), Pollard, J. J. W. (CoPI), Dutcher, J. J. P. (CoPI), Backer, J. M. (CoPI), Sparano, J. J. A. (CoPI), Maianti, J. P. (CoPI), Aguirre-ghiso, J. J. A. (CoPI), Gritsman, K. K. (CoPI), Cannizzaro, L. A. (CoPI), Hackett, L. L. E. (CoPI), Scharff, M. M. D. (CoPI), Brenowitz, M. D. (CoPI), Ohri, N. N. (CoPI), Stanley, P. (CoPI), Gupta, R. R. K. (CoPI), Depinho, R. R. A. (CoPI), Kucherlapati, R. (CoPI), Schramm, V. L. (CoPI), Steidl, U. G. (CoPI), Almo, S. C. (CoPI), Xue, X. X. N. (CoPI), Alderman, M. H. (CoPI), Atkinson, P. H. (CoPI), Bases, R. E. (CoPI), Birshstein, B. K. (CoPI), Bloom, B. R. (CoPI), Blumenfeld, O. O. (CoPI), Brenowitz, M. D. (CoPI), Brewer, F. C. (CoPI), Buhl, S. (CoPI), Chance, M. R. (CoPI), Chase, J. W. (CoPI), Childs, G. J. (CoPI), Depinho, R. (CoPI), Depinho, R. A. (CoPI), Duran-reynals, M. L. (CoPI), Dutcher, J. P. (CoPI), Eagle, H. (CoPI), Fant, J. (CoPI), Gaertner, D. J. (CoPI), Grills, G. (CoPI), Gupta, R. K. (CoPI), Horwitz, S. B. (CoPI), Horwitz, M. S. (CoPI), Hurwitz, J. (CoPI), Kadish, A. S. (CoPI), Klinger, H. P. (CoPI), Krauter, K. S. (CoPI), Kucherlapati, R. S. (CoPI), Levine, W. G. (CoPI), Lilly, F. (CoPI), Maio, J. J. (CoPI), Maitra, U. (CoPI), Makman, M. H. (CoPI), Marians, K. J. (CoPI), Nathenson, S. G. (CoPI), Orr, G. A. (CoPI), Peisach, J. (CoPI), Pickering, K. (CoPI), Rajan, T. V. (CoPI), Reid, L. M. (CoPI), Rubin, C. S. (CoPI), Russel, R. (CoPI), Satir, B. H. (CoPI), Schildkraut, C. L. (CoPI), Schulman, L. H. (CoPI), Serrano, L. J. (CoPI), Shapiro, L. (CoPI), Shin, S.-I. (CoPI), Wadler, S. H. (CoPI), Warner, J. R. (CoPI), West, M. (CoPI), Wiernik, P. H. (CoPI) & Diamond, B. (CoPI)
6/1/85 → 6/30/27
Project: Research project
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NEUROGENOMICS CORE
Morrow, B. E. (PI)
Eunice Kennedy Shriver National Institute of Child Health and Human Development
6/1/23 → 5/31/26
Project: Research project
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Molecular pathogenesis of congenital heart disease mediated by neural crest and second heart field cells
Zheng, D. (CoPI) & Morrow, B. E. (PI)
5/12/22 → 4/30/23
Project: Research project
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Genetic modifiers of congenital heart disease in 22q11.2 deletion syndrome
Morrow, B. E. (PI)
National Heart, Lung, and Blood Institute
2/1/22 → 1/31/26
Project: Research project
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Genome-wide tandem repeat expansions modify schizophrenia risk in the presence of a 22q11.2 deletion
International 22q11.2 Brain Behavior Consortium (IBBC), Sep 2026, In: Molecular Psychiatry. 31, 9, p. 4934-4946 13 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Optical mapping in Black genomes: Distinct LCR22 structures and 22q11.2 deletion syndrome mechanisms
Pastor, S., Tran, O., Lapointe, R., Olali, A. Z., Wallace, D. C., Morrow, B., Zackai, E. H., McDonald-McGinn, D. M. & Emanuel, B. S., Jan 2026, In: Genetics in Medicine. 28, 1, 101614.Research output: Contribution to journal › Article › peer-review
Open Access2 Link opens in a new tab Scopus citations -
Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions
Nelson, T. J., McGinn, D. E., Crowley, T. B., Rockart, L., Green, A., Giunta, V., Tran, O., Miller, D., Breckpot, J., Swillen, A., Digilio, M. C., Unolt, M., Putotto, C., Pulvirenti, F., Marino, B., Emanuel, B. S., Zackai, E. H., Zhang, Z. D., Goldmuntz, E. & Boot, E. & 3 others, , May 2026, In: Clinical Genetics. 109, 5, p. 859-868 10 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Reduced dosage of Kmt2d modifies Tbx1 haploinsufficiency toward phenotypes of 22q11.2DS
Miller, D., Jackson, K., Cox, T. C. & Morrow, B. E., Aug 24 2026, In: JCI Insight. 11, 16, e206763.Research output: Contribution to journal › Article › peer-review
Open Access -
Response to Wojcik and Fraiman
Pastor, S., Tran, O., Lapointe, R., Olali, A. Z., Wallace, D. C., Morrow, B., Zackai, E. H., McDonald-McGinn, D. M. & Emanuel, B. S., Jun 2026, In: Genetics in Medicine. 28, 6, 102576.Research output: Contribution to journal › Letter › peer-review