Umut Altunoğlu

Also affiliated with Istanbul University

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 3 papers. Top paper: “Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder”.

Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder

Brain(2024)10.1093/brain/awae363

N/A

0.104DataRank · unranked

1 citations

Elisa Calì, Reza Maroofian, Maha S. Zaki, Alistair T. Pagnamenta, Zafar Ali +51 more

Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.009

N/A

0DataRank · unranked

16 citations

Ana Rivera‐Barahona, Carmen‐Lisset Flores, Ghada A. Otaify, Rasha M. Elhossini, Marina Leonor Pérez-Sanz +14 more

Trichothiodystrophy‐associated MPLKIP maintains DBR1 levels for proper lariat debranching and ectodermal differentiation

EMBO Molecular Medicine(2023)10.15252/emmm.202317973

N/A

0DataRank · unranked

12 citations

Alex Pines, Tuğba Kalaycı, José María Heredia‐Genestar, Anja Raams, Marion Rietveld +15 more