Kari Branham - Concepedia

Author

Kari Branham

Also Known As

Branham, Kari, Emily Y Chew, K Branham, K. E. Branham, K.E. Branham, Kang, Hyun Min, Kari Branham, Kari E Branham, Kari E H Branham, Kari E. Branham

208

Publications

12K

Citations

H-Index

Concepts

All Affiliations

University of Michigan National Eye Institute National Institutes of Health Oregon Health & Science University University of Pennsylvania

About

Kari Branham is an author at University of Michigan specializing in medicine, ophthalmology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	30	5K
2	Public Health	6	6	2.7K
3	Natural Sciences	4	4	279
4	Engineering	1	1	10
5	Anatomy	1	1	13

Kari Branham

Publications

7.7K

Citations

H-Index

Page 1

	Year	Citations
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey, Nature Genetics Genome-wide Association StudyOcular DiseaseOphthalmologyGeneticsAge-related Diseases	2015	1.6K
Seven new loci associated with age-related macular degeneration Lars G. Fritsche, Wei Chen, Matthew Schu, Nature Genetics Ocular DiseaseOphthalmologyAge-related DiseasesPathologyNew Loci	2013	790
Genetic variants near <i>TIMP3</i> and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration Wei Chen, Dwight Stambolian, Albert O. Edwards, Proceedings of the National Academy of Sciences	2010	511
A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration Atsuhiro Kanda, Wei Chen, Mohammad Othman, Proceedings of the National Academy of Sciences Ocular DiseaseAgingGeneticsTag SnpsGenetic Epidemiology	2007	437
Strong Association of the Y402H Variant in Complement Factor H at 1q32 with Susceptibility to Age-Related Macular Degeneration Sepideh Zareparsi, Kari Branham, Mingyao Li, The American Journal of Human Genetics Ocular DiseaseOphthalmologyGeneticsImmunologyGenetic Epidemiology	2005	364
CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration Mingyao Li, Pelin Atmaca-Sönmez, Mohammad Othman, Nature Genetics Ocular DiseaseMendelian DisorderOphthalmologyGenetic DisorderGenetics	2006	347
Next‐generation genetic testing for retinitis pigmentosa Kornelia Neveling, Rob W.J. Collin, Christian Gilissen, Human Mutation	2012	284
E2-2 Protein and Fuchs's Corneal Dystrophy Keith H. Baratz, Nirubol Tosakulwong, Euijung Ryu, New England Journal of Medicine	2010	282
High-Resolution Imaging with Adaptive Optics in Patients with Inherited Retinal Degeneration Jacque L. Duncan, Yuhua Zhang, Jarel K. Gandhi, Investigative Ophthalmology & Visual Science	2007	258
Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements Feng Wang, Hui Wang, Han-Fang Tuan, Human Genetics Molecular Diagnostic TechniquesRetinitis PigmentosaGeneticsMedicineNext-generation Sequencing	2013	235

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