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
Genomic Segmental Duplications
DiGeorge Syndrome
Chromosomes, Human, Pair 22
Gene Conversion
Chromosomes
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
1
Citation
(Scopus)
Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2
on behalf of the International Chromosome 22q11.2, International 22q11.2 Brain and Behavior Consortia, Apr 1 2018, In : Human Molecular Genetics. 27, 7, p. 1150-1163 14 p.Research output: Contribution to journal › Article
DiGeorge Syndrome
Genetic Recombination
Chromosomes
Base Pairing
Genomic Segmental Duplications
2
Citations
(Scopus)
Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome
Hasten, E., McDonald-McGinn, D. M., Crowley, T. B., Zackai, E., Emanuel, B. S., Morrow, B. E. & Racedo, S., Jun 1 2018, In : Human Molecular Genetics. 27, 11, p. 1847-1857 11 p.Research output: Contribution to journal › Article
Heart Diseases
DiGeorge Syndrome
Embryonic Structures
Persistent Truncus Arteriosus
Synteny