John R. Heckenlively

Author

Also Known As

David C. Musch, Hampson Sisler, J Heckenlively, J R Heckenlively, J. R. Heckenlively, J.R. HECKENLIVELY, J.R. Heckenlively, JOHN R. HECKENLIVELY, John Heckenlively, John R Heckenlively

420

Publications

23.8K

Citations

H-Index

142

Concepts

All Affiliations

University of Michigan University of California, Los Angeles Doheny Eye Institute Jackson Laboratory W.K. Kellogg Foundation

About

John R. Heckenlively is an author at University of Michigan specializing in medicine, ophthalmology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	54	96	12.8K
2	Natural Sciences	4	4	275
3	Education	1	1	30
4	Engineering	1	1	103
5	Health Sciences	1	1	353

John R. Heckenlively

175

Publications

21K

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
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice. Simon W. M. John, Richard S. Smith, Olga V. Savinova, PubMed	1998	558
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
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12) Anneke I. den Hollander, Jacoline B. ten Brink, Yvette J.M. de Kok, Nature Genetics BiologyDevelopmental BiologyGeneticsGenomic MechanismGenetic Mechanism	1999	470
Rhodopsin mutations in autosomal dominant retinitis pigmentosa. Ching‐Hwa Sung, Carol Davenport, Jill C. Hennessey, Proceedings of the National Academy of Sciences Ocular DiseasePhotoreceptor CellRhodopsin MutationsOphthalmologyPoint Mutations	1991	466
Effective gene therapy with nonintegrating lentiviral vectors Rafael J. Yáñez‐Muñoz, Kamaljit S. Balaggan, Angus MacNeil, Nature Medicine Gene TherapiesAntiviral TherapyGenetic EngineeringVirologyGene Vector	2006	455
Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene Bo Chang, Norman L. Hawes, Machelle T. Pardue, Vision Research Missense MutationsOcular DiseaseRetinaPhotoreceptor CellOphthalmology	2007	406
In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse Bo Chang, Hemant Khanna, Norman L. Hawes, Human Molecular Genetics	2006	379
Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene Anneke I. den Hollander, John R. Heckenlively, L. Ingeborgh van den Born, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderRetinitis PigmentosaGenetics	2001	361

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