Aliaa H. Abdelhakim

Columbia University Irving Medical Center

Also affiliated with Columbia University

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 4 papers. Top paper: “Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency”.

Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency

Orphanet Journal of Rare Diseases(2020)10.1186/s13023-020-01600-8

N/A

0DataRank · unranked

14 citations

Avinash V. Dharmadhikari, Sara D. Ragi, José Ronaldo Lima de Carvalho, Christine L. Xu, Amanda Thomas‐Wilson +8 more

Heterogeneity of comprehensive clinical phenotype and longitudinal adaptive function and correlation with computational predictions of severity of missense genotypes in KIF1A-associated neurological disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101169

N/A

0DataRank · unranked

14 citations

Wenxing Li, Sean Calamia, Cara H. Kanner, Jennifer M Bain, Aliaa H. Abdelhakim +9 more

Ophthalmic Findings in the KIF1A-Associated Neurologic Disorder (KAND)

American Journal of Ophthalmology(2024)10.1016/j.ajo.2024.06.025

N/A

0DataRank · unranked

5 citations

Scott E. Brodie, Wendy K. Chung, Aliaa H. Abdelhakim

Biallelic potential disease-causing missense variants in TAF1A in two siblings with infantile restrictive cardiomyopathy

European Journal of Medical Genetics(2024)10.1016/j.ejmg.2024.104968

N/A

0DataRank · unranked

1 citations

Wenyuan Xu, Aliaa H. Abdelhakim, Anastasiya Matveyenko, Matthias Szabolcs, William C. Copeland +6 more