🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Hafiz Muhammad Jafar Hussain

ORCID: 0000-0001-5269-8971

Also affiliated with Baylor College of Medicine

Biochemistry, 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 4 papers. Top paper: “Novel Pathogenic Mutations Identified from Whole-Genome Sequencing in Unsolved Cases of Patients Affected with Inherited Retinal Diseases”.

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

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

Phenotypic and Genetic Heterogeneity of a Pakistani Cohort of 15 Consanguineous Families Segregating Variants in Leber Congenital Amaurosis-Associated Genes

Genes(2024)10.3390/genes15121646

N/A

0DataRank · unranked

1 citations

Sumaira Altaf, Yumei Li, Sana Bibi, Jamal Shah, Kiran Afshan +6 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