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Bernice E. Morrow, Ph.D.

  • 10008 Citations
  • 46 h-Index
1980 …2020

Research output per year

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Grants

Tbx1 and canonical Wnt signaling in the second heart field

Morrow, B. E. & Chenleng, C.

National Institutes of Health

9/15/15 → 8/31/16

Project: Research project

    • Genetic Basis of Syndromic and Non-Syndromic Congential Heart Defects

    Morrow, B. E., Emanuel, B. & Goldmuntz, E.

    National Institutes of Health

    9/24/11 → 6/30/16

    Project: Research project

    • Developmental Genetics of the Pharyngeal Apparatus

    Morrow, B. E.

    7/1/09 → 6/30/12

    Project: Research project

    Genetic Basis of Birth Defects in 22q11 Deletion Syndrome

    Morrow, B. E.

    5/1/09 → 4/30/12

    Project: Research project

    Sequence Variations in Low Copy Repeats on 22q11.2

    Morrow, B. E.

    5/1/09 → 4/30/11

    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 journal › Article

    • 3 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

    Open Access

    • 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 journal › Article

    • 8 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

    Open Access
    • 1 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