Molly Marra

Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicine

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 10 papers. Top paper: “Systematic assessment of the contribution of structural variants to inherited retinal diseases”.

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

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

0.269DataRank · unranked

5 citations

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

Expanding the phenotypic and genotypic spectrum of patients with HGSNAT -related retinopathy

Ophthalmic Genetics(2023)10.1080/13816810.2023.2245035

N/A

0DataRank · unranked

6 citations

Molly Marra, Austin D. Igelman, Cristy A. Ku, Amanda Burr, Katherine Andersen +6 more

Vitelliform maculopathy in MELAS syndrome

American Journal of Ophthalmology Case Reports(2023)10.1016/j.ajoc.2023.101842

N/A

0DataRank · unranked

3 citations

Cristy A. Ku, Molly Marra, Mark E. Pennesi, Paul Yang, Cody Jahrig

Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration

Genetics in Medicine(2024)10.1016/j.gim.2024.101106

N/A

0DataRank · unranked

14 citations

Kim Rodenburg, Tamar Hayman, Giacomo Calzetti, Karolina Kamińska, Mathieu Quinodoz +20 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

Targeted long-read sequencing enriches disease-relevant genomic regions of interest to provide complete Mendelian disease diagnostics

JCI Insight(2024)10.1172/jci.insight.183902

N/A

0DataRank · unranked

10 citations

Jennifer Huey, Riccardo Sangermano, Emily Place, Kinga M. Bujakowska, Molly Marra +6 more

Signal Peptide Variants in Inherited Retinal Diseases: A Multi-Institutional Case Series

International Journal of Molecular Sciences(2022)10.3390/ijms232113361

N/A

0DataRank · unranked

6 citations

Rebecca Procopio, Tobin B. T. Thuma, Molly Marra, Natalio Izquierdo, Michael A. Klufas +4 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

Novel Pathogenic Mutations Identified from Whole-Genome Sequencing in Unsolved Cases of Patients Affected with Inherited Retinal Diseases

Genes(2023)10.3390/genes14020447

N/A

0DataRank · unranked

10 citations

Meng Wang, Austin Huang, Ryan Schmidt, Xinye Qian, Paul Yang +5 more