• 9753 Citations
  • 45 h-Index
1977 …2022

Research output per year

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Fingerprint 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

  • CANCER RESEARCH CENTER

    Brewer, C. F., Bases, R., Kadish, A., Wiernik, P., Orr, G., Bloom, B., Shapiro, L., Lilly, F., Chase, J., Atkinson, P., Maio, J., Reid, L., Levine, W., Nathenson, S., Fant, J., Warner, J., Peisach, J., Horwitz, M., Krauter, K., Makman, M., Blumenfeld, O., Schulman, L., Klinger, H., Rajan, T., Wadler, S., Chance, M., Buhl, S., Desai, K., Pollard, J. W., Brenowitz, M. D., Stanley, P., Skoultchi, A. I., Sparano, J. A., Hurwitz, J., Duran-Reynals, M., Serrano, L., Alderman, M., Shin, S., West, M., Birshstein, B., Marians, K., Eagle, H., Russel, R., Grills, G., Pickering, K., Mahmood, R., Keller, S. M., Herbst, L., Seither, R., Satir, B. H., Rubin, C. S., Scharff, M. D., Maitra, U., Band Horwitz, S., Schildkraut, C. L., Ho, G. Y. F., Cannizzaro, L. A., Childs, G. J., Augenlicht, L. H., Almo, S. C., Greally, J. M., Angeletti, R. H., Porcelli, S. A., Morrow, B. E., Condeelis, J. S., Montagna, C., Edelmann, W., Kim, M., Rohan, T. E., Goldman, I. D., Kucherlapati, R., Gupta, R., Depinho, R., Dutcher, J., Diamond, B., Gaertner, D. J., Keller, S. M., Pollard, J. W., Kucherlapati, R., Gupta, R., Depinho, R., Dutcher, J., Diamond, B., Gaertner, D. J., Keller, S. M., Xue, X. (., Blanchard, J. S., Beck, A. P., Rapkin, B. D., Strickler, H., Goel, S., Bresnick, A. R., Steidl, U. G., Schramm, V. L. & Condeelis, J. S.

    National Institutes of Health

    6/1/776/30/22

    Project: Research project

  • Publications

    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 journalArticle

  • Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

    International 22q11.2DS Brain and Behavior Consortium, Jan 1 2020, (Accepted/In press) In : Molecular Psychiatry.

    Research output: Contribution to journalArticle

  • 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 journalArticle

  • Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion status

    Xie, H. M., Taylor, D. M., Zhang, Z., McDonald-McGinn, D. M., Zackai, E. H., Stambolian, D., Hakonarson, H., Morrow, B. E., Emanuel, B. S. & Goldmuntz, E., Jan 1 2019, In : Birth Defects Research. 111, 13, p. 888-905 18 p.

    Research output: Contribution to journalArticle

  • Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects

    on behalf of the Pediatric Cardiac Genomics Consortium¶, Jan 1 2019, In : PloS one. 14, 7, e0219926.

    Research output: Contribution to journalArticle

    Open Access
  • 1 Scopus citations