Brenda J. Barry - Concepedia

Author

Brenda J. Barry

Also Known As

B BARRY, B J Barry, B. Barry, B.J. Barry, Brenda Barry, Brenda J Barry, Brenda J. Barry, Brenda J. Barry, K Dies, Manzini, M. Chiara

Publications

5.1K

Citations

H-Index

Concepts

All Affiliations

Howard Hughes Medical Institute Boston Children's Hospital Harvard University Broad Institute University of California, San Francisco

About

Brenda J. Barry is an author at Howard Hughes Medical Institute specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	21	3K
2	Health Sciences	2	2	301
3	Natural Sciences	2	2	95
4	Engineering	1	1	183
5	Public Health	1	1	741

Brenda J. Barry

Publications

Citations

H-Index

Page 1

	Year	Citations
Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry Eric M. Morrow, Seung-Yun Yoo, Steven W. Flavell, Science GeneticsGenetic EpidemiologyGenomicsAutism LociGenome-wide Association Study	2008	741
Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations Annapurna Poduri, Gilad D. Evrony, Xuyu Cai, Neuron Developmental BiologyNeurophysiologyNeuroanatomyDevelopmental Cognitive NeuroscienceSomatic Activation	2012	471
Somatic Mutations in Cerebral Cortical Malformations Saumya Shekhar Jamuar, Anh-Thu N. Lam, Martin Kircher, New England Journal of Medicine	2014	386
Mutations in PNKP cause microcephaly, seizures and defects in DNA repair Jun Shen, Edward C. Gilmore, Christine A Marshall, Nature Genetics Genome InstabilityGenetic DisorderGeneticsMolecular GeneticsDisease Gene Identification	2010	289
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture Timothy W. Yu, Ganeshwaran H. Mochida, David J. Tischfield, Nature Genetics Centrosome-associated ProteinDevelopmental BiologyBrain StructureBrain DevelopmentNeuroanatomy	2010	282
Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia Alissa M. D’Gama, Ying Geng, Javier Couto, Annals of Neurology	2015	280
Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly Fowzan S. Alkuraya, Xuyu Cai, Carina Emery, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsDisease Gene Identification	2011	219
CXC Chemokine Receptor-2 Ligands Are Required for Neutrophil-Mediated Host Defense in Experimental Brain Abscesses Tammy Kielian, Brenda J. Barry, William F. Hickey The Journal of Immunology	2001	218
Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations as a Cause of Walker-Warburg Syndrome M. Chiara Manzini, Dimira Tambunan, R. Sean Hill, The American Journal of Human Genetics EngineeringMendelian DisorderGenetic DisorderExome SequencingGenetics	2012	183
Microcephaly Gene Links Trithorax and REST/NRSF to Control Neural Stem Cell Proliferation and Differentiation Yawei J. Yang, Andrew E. Baltus, Rebecca S. Mathew, Cell Induced Pluripotent Stem CellDevelopmental BiologyMedicineAdult Stem CellStem Cell Research	2012	178

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