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

Saghar Ghasemi Firouzabadi

Genetic Analysis (Norway)

ORCID: 0000-0001-8989-5741

Also affiliated with University of Social Welfare and Rehabilitation Sciences, Gorgan University of Agricultural Sciences and Natural Resources

Biochemistry, Genetics and Molecular BiologyNeuroscience

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 3 papers. Top paper: “Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia”.

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.015

N/A

0.604DataRank · unranked

55 citations

Mona Grimmel, Matias Wagner, J. Christopher Hennings, Christian Marx, René G. Feichtinger +41 more

Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly

Brain(2022)10.1093/brain/awac074

N/A

0DataRank · unranked

15 citations

J. Pedro Fernández-Murray, Mahtab Tavasoli, Heinrich Sticht, Gisela Stoltenburg‐Didinger, Leila Motlagh Scholle +24 more

Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy

medRxiv(2025)10.1101/2025.11.04.25339178

N/A

0DataRank · unranked

0 citations

Yung-Chun Wang, Peter T. Skidmore, Carolina I. Galaz-Montoya, Sara A. Lewis, Bader Alhaddad +52 more