Ali Naini

Biochemistry, Genetics and Molecular BiologyEngineering

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

Whole-Exome Sequencing Identifies a Novel POLG Frameshift Variant in an Adult Patient Presenting with Progressive External Ophthalmoplegia and Mitochondrial DNA Depletion

Case Reports in Genetics(2021)10.1155/2021/9969071

N/A

0DataRank · unranked

2 citations

Joseph Americo Fernandes, Mahesh Mansukhani, William C. Copeland, Ali Naini, Justin Kurtz

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

Relationships of mitochondrial DNA mutations and select clinical diagnoses in perinatally HIV- and ART-exposed uninfected children

Mitochondrion(2024)10.1016/j.mito.2024.101949

N/A

0DataRank · unranked

0 citations

Carmen J. Marsit, Deborah Kacanek, Jonathan S. Russell, Gavin Hudson, Russell B. Van Dyke +3 more