• 9664 Citations
  • 45 h-Index
1977 …2021
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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.

  • 1 Similar Profiles
DiGeorge Syndrome Medicine & Life Sciences
Genes Medicine & Life Sciences
Genomic Segmental Duplications Medicine & Life Sciences
Chromosomes Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Genome Medicine & Life Sciences
Homologous Recombination Medicine & Life Sciences
Chromosome Deletion Medicine & Life Sciences

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Grants 1977 2021

Human Development
Heart Diseases
DiGeorge Syndrome
Exome
Neural Crest
DiGeorge Syndrome
Heart Diseases
Genes
Thoracic Aorta
National Institute of Child Health and Human Development (U.S.)
DiGeorge Syndrome
Catenins
Persistent Truncus Arteriosus
Alleles
Genes
Genes
DiGeorge Syndrome
Embryonic Structures
Neural Crest
Mesoderm
Genomic Segmental Duplications
DiGeorge Syndrome
Chromosomes, Human, Pair 22
Gene Conversion
Chromosomes

Publications 1980 2019

  • 9664 Citations
  • 45 h-Index
  • 138 Article
  • 2 Chapter
  • 2 Review article
  • 1 Comment/debate

Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins

International 22q11.2 Brain & Behavior Consortium, Nov 15 2019, In : Human molecular genetics. 28, 22, p. 3724-3733 10 p.

Research output: Contribution to journalArticle

Chromosome Deletion
Homologous Recombination
DiGeorge Syndrome
Alleles
Chromosome Breakpoints

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.

Research output: Contribution to journalArticle

Defects
Gene Regulatory Networks
Genes
Embryonic Structures
DiGeorge Syndrome
1 Citation (Scopus)

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
Genome-Wide Association Study
Meta-Analysis
Genes
heart
Association reactions

Spatiotemporal Gene Coexpression and Regulation in Mouse Cardiomyocytes of Early Cardiac Morphogenesis

Liu, Y., Lu, P., Wang, Y., Morrow, B. E., Zhou, B. & Zheng, D., Aug 6 2019, In : Journal of the American Heart Association. 8, 15, p. e012941

Research output: Contribution to journalArticle

Open Access
Morphogenesis
Cardiac Myocytes
Transcription Factors
Genes
Congenital Heart Defects
1 Citation (Scopus)

Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11.2 deletion syndrome

Hasten, E. & Morrow, B. E., Aug 1 2019, In : PLoS genetics. 15, 8, p. e1008301

Research output: Contribution to journalArticle

Open Access
DiGeorge Syndrome
Endoderm
pouches
embryo
embryo (animal)