Nadirah Damseh

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: “Heterozygous nonsense variants in the ferritin heavy-chain gene FTH1 cause a neuroferritinopathy”.

Heterozygous nonsense variants in the ferritin heavy-chain gene FTH1 cause a neuroferritinopathy

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100236

N/A

0DataRank · unranked

17 citations

Jesus A Tintos-Hernández, Chaya N. Murali, Monica Penon‐Portmann, Marco Flores‐Méndez, Adrian Santana +12 more

Pontocerebellar hypoplasia associated with p.Arg183Trp homozygous variant in EXOSC1 gene: A case report

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63198

N/A

0DataRank · unranked

11 citations

Ali N. Obeidat, Khondakar Sayef Ahammed, Motee Al‐Ashhab, Motee Abu Awad, Ambro van Hoof +1 more

Heterozygous Nonsense Variants in the Ferritin Heavy Chain Gene FTH1 Cause a Novel Pediatric Neuroferritinopathy

medRxiv(2023)10.1101/2023.01.30.23285099

N/A

0DataRank · unranked

1 citations

Jesus A Tintos-Hernández, Chaya N. Murali, Monica Penon‐Portmann, Marco Flores‐Méndez, Adrian Santana +12 more

ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy

Genetics in Medicine(2025)10.1016/j.gim.2025.101506

N/A

0DataRank · unranked

3 citations

Chu-Ting Chang, A. Declève, Gloria Brunori, W.H. Ludlam, Alden Huang +93 more