Michael B. Gorin

Also affiliated with Duke University, Doheny Eye Institute, Institute of Human Genetics, VA Northeast Ohio Healthcare System

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 17 papers. Top paper: “Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy”.

Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.005

N/A

1.3DataRank · unranked

55 citations

Xénia Latypova, Lokuliyanage Dona Samudita Senaratne, Ludovic Martin, Daniel C. Koboldt, Georgios Kellaris +72 more

Systems genomics in age-related macular degeneration

Experimental Eye Research(2022)10.1016/j.exer.2022.109248

N/A

1.1DataRank · unranked

40 citations

Robert F. Mullins, Luz D. Orozco, Andrew P. Voigt, Hsu-Hsin Chen, Tobias Strunz +16 more

Seven new loci associated with age-related macular degeneration

Nature Genetics(2013)10.1038/ng.2578

N/A

1.0DataRank · unranked

798 citations

Lars G. Fritsche, Wei Chen, Brian L. Yaspan, Yi Yu, Guðmar Þorleifsson +141 more

Assessing the Clinical Utility of Expanded Macular OCTs Using Machine Learning

Translational Vision Science & Technology(2021)10.1167/tvst.10.6.32

N/A

0.416DataRank · unranked

15 citations

Cecilia S. Lee, Marian Blazes, Aaron Lee, Michael B. Gorin, Andrew Lin

Systematic assessment of the contribution of structural variants to inherited retinal diseases

Human Molecular Genetics(2023)10.1093/hmg/ddad032

N/A

0.373DataRank · unranked

11 citations

Meng C. Wang, Xinye Qian, Yumei Li, Keqing Wang, Jongsu Choi +13 more

Consensus Guidelines for Ocular Surveillance of von Hippel-Lindau Disease

Ophthalmology(2023)10.1016/j.ophtha.2023.12.014

N/A

0DataRank · unranked

23 citations

Emmanuel Chang, Emily Y. Chew, Dan S. Gombos, Michael B. Gorin, Carol L. Shields +2 more

Systematic assessment of the contribution of structural variants to inherited retinal diseases

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.02.522522

N/A

0DataRank · unranked

5 citations

Meng C. Wang, Xinye Qian, Yumei Li, Keqing Wang, Jongsu Choi +13 more

Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseases

Human Molecular Genetics(2024)10.1093/hmg/ddae028

N/A

0DataRank · unranked

11 citations

Meng Wang, Hafiz Muhammad Jafar Hussain, David E Rauch, Molly Marra, Mark E. Pennesi +14 more

Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma

Nature Communications(2025)10.1038/s41467-025-58686-6

N/A

0DataRank · unranked

11 citations

Bryan R. Gorman, Lu‐Chen Weng, Sean J. Jurgens, Panisa Singhanetr, Marisa G. Tieger +28 more

Dissecting the biological complexity of age-related macular degeneration: Is it one disease, multiple separate diseases, or a spectrum?

Experimental Eye Research(2025)10.1016/j.exer.2025.110304

N/A

0DataRank · unranked

9 citations

Benjamin R. Thompson, James T. Handa, Philip J. Luthert, Usha Chakravarthy, Karl G. Csaky +13 more

Biallelic loss-of-function variants in C19orf44 lead to retinal degeneration

Journal of Medical Genetics(2025)10.1136/jmg-2025-110681

N/A

0DataRank · unranked

1 citations

Meng Wang, Yumei Li, Sabika Firasat, Mark E. Pennesi, Michael B. Gorin +10 more

Prevalence of Myocilin Mutations in a Cohort of Patients with Juvenile Open-Angle Glaucoma from sub-Saharan Africa

Ophthalmology Glaucoma(2025)10.1016/j.ogla.2025.04.010

N/A

0DataRank · unranked

1 citations

Brian P. Young, Angela W Nyunt, O F Fafowora, Magdalene Ajani, Tarela Sarimiye +9 more

Variants in CFAP410 cause a range of retinal and skeletal phenotypes

npj Genomic Medicine(2025)10.1038/s41525-025-00489-1

N/A

0DataRank · unranked

0 citations

Amy E. Pohodich, David G. Birch, Kaylie Webb-Jones, Byron L. Lam, Emily H. Jung +44 more

Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration

Journal of the American Statistical Association(2020)10.1080/01621459.2020.1799809

N/A

0DataRank · unranked

9 citations

Chi‐Yang Chiu, Qi Yan, Wei Chen, Michael B. Gorin, Yvette P. Conley +13 more

Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome

Ophthalmic Genetics(2021)10.1080/13816810.2021.1946704

N/A

0DataRank · unranked

34 citations

Cristy A. Ku, Mariana Matioli da Palma, Michalis Georgiou, Elena Schiff, Byron L. Lam +16 more

Assessing Variant Causality and Severity Using Retinal Pigment Epithelial Cells Derived from Stargardt Disease Patients

Translational Vision Science & Technology(2022)10.1167/tvst.11.3.33

N/A

0DataRank · unranked

10 citations

Jun Wang, Sangbae Kim, Yumei Li, Anupama Dimashkie, Zhichun Jiang +6 more

Measurement of the Inner Macular Layers for Monitoring of Glaucoma

Ophthalmology Glaucoma(2022)10.1016/j.ogla.2022.06.006

N/A

0DataRank · unranked

1 citations

Vahid Mohammadzadeh, Massood Mohammadi, Veronica Toriz, Nancy Rosa, Michael B. Gorin +3 more