Projects per year
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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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
Molecular aspects of CRKL in heart development and human disease
7/15/16 → 6/30/20
Project: Research project
Human Development
Heart Diseases
DiGeorge Syndrome
Exome
Neural Crest
Genetic Basis of Syndromic and Non-Syndromic Congential Heart Defects
Morrow, B. E., Emanuel, B. & Goldmuntz, E.
9/24/11 → 6/30/21
Project: Research project
DiGeorge Syndrome
Heart Diseases
Genes
Thoracic Aorta
National Institute of Child Health and Human Development (U.S.)
Tbx1 and canonical Wnt signaling in the second heart field
Morrow, B. E. & Chenleng, C.
9/15/15 → 8/31/17
Project: Research project
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
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 journal › Article
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 journal › Article
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. e012941Research output: Contribution to journal › Article
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. e1008301Research output: Contribution to journal › Article
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 journal › Article
Open Access
22q11 Deletion Syndrome
Genomic Segmental Duplications
Homologous Recombination
Alleles
Genome