• 9535 Citations
  • 45 h-Index
1977 …2021
If you made any changes in Pure, your changes will be visible here soon.

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
Genetic Recombination Medicine & Life Sciences
Morphogenesis Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

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
22q11 Deletion Syndrome
DiGeorge Syndrome
Base Pairing
Genes
Haploinsufficiency

Publications 1980 2019

  • 9535 Citations
  • 45 h-Index
  • 137 Article
  • 2 Chapter
  • 2 Review article
  • 1 Comment/debate

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

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

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)

The 22q11 low copy repeats are characterized by unprecedented size and structural variability

Demaerel, W., Mostovoy, Y., Yilmaz, F., Vervoort, L., Pastor, S., Hestand, M. S., Swillen, A., Vergaelen, E., Geiger, E. A., Coughlin, C. R., Chow, S. K., McDonald-McGinn, D., Morrow, B. E., Kwok, P. Y., Xiao, M., Emanuel, B. S., Shaikh, T. H. & Vermeesch, J. R., Sep 1 2019, In : Genome research. 29, 9, p. 1389-1401 13 p.

Research output: Contribution to journalArticle

Open Access
22q11 Deletion Syndrome
Genomic Segmental Duplications
Homologous Recombination
Alleles
Genome