Hitisha P. Zaveri - Concepedia

Author

Hitisha P. Zaveri

Baylor College of Medicine

Also Known As

H.P. Zaveri, Hitisha P Zaveri, Hitisha P. Zaveri, Hitisha P. Zaveri (381760)

Publications

410

Citations

H-Index

Concepts

All Affiliations

Baylor College of Medicine University of Iowa Wayne State University Howard Hughes Medical Institute Erasmus MC - Sophia Children’s Hospital

About

Hitisha P. Zaveri is an author at Baylor College of Medicine specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	215
2	Cell Biology	2	2	92
3	Health Sciences	1	1	33
4	Cellular Physiology	1	1	75
5	Emergency Medicine	1	1	31

Hitisha P. Zaveri

Publications

401

Citations

H-Index

Page 1

	Year	Citations
Stromal <i>Fat4</i> acts non-autonomously with <i>Dachsous1/2</i> to restrict the nephron progenitor pool Mazdak Bagherie-Lachidan, Antoine Reginensi, Hitisha P. Zaveri, Development Nephron Progenitor PoolReciprocal SignallingCellular PhysiologyTissue DevelopmentCell Regulation	2015	75
An Allelic Series of Mice Reveals a Role for RERE in the Development of Multiple Organs Affected in Chromosome 1p36 Deletions Bum‐Joon Kim, Hitisha P. Zaveri, Oleg A. Shchelochkov, PLoS ONE	2013	70
Identification of Critical Regions and Candidate Genes for Cardiovascular Malformations and Cardiomyopathy Associated with Deletions of Chromosome 1p36 Hitisha P. Zaveri, T. Beck, Andrés Hernández, PLoS ONE GeneticsCardiac Critical RegionsMolecular GeneticsDisease Gene IdentificationGenomics	2014	59
Delineation of a less than 200 kb minimal deleted region for cardiac malformations on chromosome 7p22 Elliott G. Richards, Hitisha P. Zaveri, Varina L. Wolf, American Journal of Medical Genetics Part A	2011	52
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice T. Beck, Danielle Veenma, Oleg A. Shchelochkov, Human Molecular Genetics	2012	44
VACTERL Association Etiology: The Impact of de novo and Rare Copy Number Variations Erwin Brosens, H. J. Eussen, Yolande van Bever, Molecular Syndromology Recurrent Rare CnvsMolecular EpidemiologyGeneticsPathologyDisease Gene Identification	2012	33
Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula Erwin Brosens, Florian Marsch, Elisabeth M. de Jong, European Journal of Human Genetics EsophagusCopy Number VariationsGastroenterologyThoracic SurgerySurgery	2016	31
Novel Frem1-Related Mouse Phenotypes and Evidence of Genetic Interactions with Gata4 and Slit3 T. Beck, Oleg A. Shchelochkov, Zhiyin Yu, PLoS ONE GeneticsGene CharacterizationMolecular GeneticsExtracellular Matrix ProteinRectal Prolapse	2013	17
Contribution of <i>LPP</i> copy number and sequence changes to esophageal atresia, tracheoesophageal fistula, and VACTERL association Andrés Hernández, Erwin Brosens, Hitisha P. Zaveri, American Journal of Medical Genetics Part A	2012	10
RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects Bum‐Joon Kim, Hitisha P. Zaveri, Valerie K. Jordan, Disease Models & Mechanisms	2018	10

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