Geping Zhao - Concepedia

Author

Geping Zhao

Center for Human Genetics

Also Known As

G Zhao, Geping Zhao

Publications

757

Citations

H-Index

Concepts

All Affiliations

Center for Human Genetics Boston University Icahn School of Medicine at Mount Sinai University of Florida Boston Children's Hospital

About

Geping Zhao is an author at Center for Human Genetics specializing in genetics, molecular genetics, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	310
2	Molecular Genetics	4	4	310
3	Pathology	4	4	425
4	Public Health	2	2	90
5	Pharmacology	1	1	23

Geping Zhao

Publications

749

Citations

H-Index

Page 1

	Year	Citations
TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome Jeff M. Milunsky, Tom A. Maher, Geping Zhao, The American Journal of Human Genetics Developmental AnomalyMendelian DisorderGenetic DisorderTfap2a Mutations ResultPathology	2008	207
A Neuroligin-4 Missense Mutation Associated with Autism Impairs Neuroligin-4 Folding and Endoplasmic Reticulum Export Chen Zhang, Jeff M. Milunsky, Stephanie Newton, Journal of Neuroscience	2009	186
LADD syndrome is caused by<i>FGF10</i>mutations JM Milunsky, Geping Zhao, Randall S. Colby, Clinical Genetics GeneticsPathologyMolecular GeneticsDisease Gene IdentificationClinical Genetics	2006	138
An Ashkenazi Jewish SMN1 haplotype specific to duplication alleles improves pan-ethnic carrier screening for spinal muscular atrophy Minjie Luo, Liu Liu, Inga Peter, Genetics in Medicine Duplication AllelesAllelic VariantPan-ethnic CarrierGenetic DisorderGenetics	2013	82
Genotype–phenotype analysis of the branchio‐oculo‐facial syndrome Jeff M. Milunsky, Tom M. Maher, Geping Zhao, American Journal of Medical Genetics Part A GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification	2010	67
Structural variation at the <i>CYP2C</i> locus: Characterization of deletion and duplication alleles Mariana Rodrigues Botton, Xingwu Lu, Geping Zhao, Human Mutation Structural VariationHuman Cyp2c LocusGeneticsGenetic EpidemiologyHuman Polymorphism	2019	23
Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi‐Ethnic Allele and Copy Number Variant Detection Stuart A. Scott, Erick R. Scott, Yoshinori Seki, Clinical and Translational Science	2020	19
Analytical Validation of a Personalized Medicine APOL1 Genotyping Assay for Nondiabetic Chronic Kidney Disease Risk Assessment Jinglan Zhang, Anastasia Fedick, Stephanie Wasserman, Journal of Molecular Diagnostics	2016	14
TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome Jeff M. Milunsky, Tom A. Maher, Geping Zhao, The American Journal of Human Genetics Developmental AnomalyMendelian DisorderGenetic DisorderTfap2a Mutations ResultPathology	2009	13

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