• 10008 Citations
  • 46 h-Index
1980 …2020

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

  • Developmental Genetics of the Pharyngeal Apparatus

    Morrow, B. E.

    7/1/096/30/12

    Project: Research project

    Sequence Variations in Low Copy Repeats on 22q11.2

    Morrow, B. E.

    5/1/094/30/11

    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 journalArticle

  • 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 journalArticle

    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 journalArticle

  • 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 journalArticle

    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 journalArticle