Khanh-Nhat Tran-Viet

Author

Center for Human Genetics

Also Known As

K N Tran-Viet, KN TRAN‐VIET, Khan-Nhat Tran-Viet, Khanh-Nhat Tran-Viet

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Center for Human Genetics Duke University Duke Medical Center Duke University Hospital National University of Singapore

About

Khanh-Nhat Tran-Viet is an author at Center for Human Genetics specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	466
2	Molecular Genetics	3	3	383
3	Biology	1	1	27
4	Molecular Biology	1	1	241
5	Molecular Medicine	1	1	83

Khanh-Nhat Tran-Viet

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity Tomokazu Souma, Stuart W. Tompson, Benjamin R. Thomson, Journal of Clinical Investigation	2016	286
Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31 Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, The American Journal of Human Genetics Mitochondrial MyopathyMendelian DisorderMitochondrial FunctionGenetic DisorderGenetics	2006	241
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31 Christian Beetz, Rebecca Schüle, Tine Deconinck, Brain	2008	180
Mutations in SCO2 Are Associated with Autosomal-Dominant High-Grade Myopia Khanh-Nhat Tran-Viet, Caldwell Powell, Veluchamy A. Barathi, The American Journal of Human Genetics OphthalmologyGenetic DisorderGeneticsMolecular GeneticsMedical Genetics	2013	115
CYP1B1, MYOC, and LTBP2 Mutations in Primary Congenital Glaucoma Patients in the United States Sing-Hui Lim, Khanh-Nhat Tran-Viet, Tammy L. Yanovitch, American Journal of Ophthalmology Developmental BiologyLtbp2 MutationsGeneticsMedicineUnited States	2012	83
Functional evidence implicating a novel <i>TOR1A</i> mutation in idiopathic, late-onset focal dystonia Nicole Calakos, Melissa A Gottron, G. Wang, Journal of Medical Genetics	2009	71
Genetic Association of Insulin-like Growth Factor-1 Polymorphisms with High-Grade Myopia in an International Family Cohort Ravikanth Metlapally, Chang‐Seok Ki, Yi‐Ju Li, Investigative Ophthalmology & Visual Science	2010	69
<i>COL1A1</i>and<i>COL2A1</i>Genes and Myopia Susceptibility: Evidence of Association and Suggestive Linkage to the<i>COL2A1</i>Locus Ravikanth Metlapally, Yi‐Ju Li, Khanh-Nhat Tran-Viet, Investigative Ophthalmology & Visual Science	2009	60
Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis Vincent Soler, Khanh-Nhat Tran-Viet, Stéphane Galiacy, Journal of Medical Genetics	2013	55
Association Mapping of the High-Grade Myopia<i>MYP3</i>Locus Reveals Novel Candidates<i>UHRF1BP1L</i>,<i>PTPRR</i>, and<i>PPFIA2</i> Felicia Hawthorne, Sheng Feng, Ravikanth Metlapally, Investigative Ophthalmology & Visual Science	2013	36

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