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

Wan Hee Yoon

Oklahoma Medical Research Foundation

ORCID: 0000-0002-9459-3139
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 11 papers. Top paper: “A biallelic pathogenic variant in the OGDH gene results in a neurological disorder with features of a mitochondrial disease”.

A biallelic pathogenic variant in the OGDH gene results in a neurological disorder with features of a mitochondrial disease

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12248
N/A
0DataRank · unranked
59 citations

Klaudia Strucinska, Satoshi Matsuzaki, Sukyeong Lee, Yue Si, Kenneth M. Humphries +3 more

Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.01.007
N/A
0DataRank · unranked
52 citations

Klaudia Strucinska, Mikel Muñoz Oreja, Andrew Parrish, Richard Caswell, Karen Stals +24 more

Functional interpretation of ATAD3A variants in neuro-mitochondrial phenotypes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.05.318519
N/A
0DataRank · unranked
2 citations

Yohan Park, Saskia B. Wortmann, Adam C. Gunning, Suk‐young Lee, Lita Duraine +13 more

Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.003
N/A
0DataRank · unranked
34 citations

Stéphanie Efthymiou, Simone Seiffert, Karen Vargas Parra, Sukyeong Lee, Alessia Nasca +35 more

Functional interpretation of ATAD3A variants in neuro-mitochondrial phenotypes

Genome Medicine(2021)10.1186/s13073-021-00873-3
N/A
0DataRank · unranked
32 citations

Yohan Park, Saskia B. Wortmann, Adam C. Gunning, Shlomit Ezer, Sukyeong Lee +15 more

Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalities

Genetics in Medicine(2022)10.1016/j.gim.2022.11.001
N/A
0DataRank · unranked
30 citations

Madison Chilian, Ehsan Ghayoor Karimiani, Helga Progri, Daniela Buhaş, Melis Köse +17 more

CRISPR/Cas9-mediated tissue-specific knockout and cDNA rescue using sgRNAs that target exon-intron junctions in Drosophila melanogaster

STAR Protocols(2022)10.1016/j.xpro.2022.101465
N/A
0DataRank · unranked
8 citations

Karen Vargas Parra, Abigail Sandoval, Juan David Ramírez, Wan Hee Yoon, Madison Chilian

Clonally Selected Lines After CRISPR-Cas Editing Are Not Isogenic

The CRISPR Journal(2023)10.1089/crispr.2022.0050
N/A
0DataRank · unranked
14 citations

Milovan Šuvakov, Jessica Mariani, Kristen Drucker, Yohan Park, Yeongjun Jang +9 more

Recent progress in using Drosophila as a platform for human genetic disease research

Journal of genetic medicine(2023)10.5734/jgm.2023.20.2.39
N/A
0DataRank · unranked
3 citations

Wan Hee Yoon

Elevated cholesterol in ATAD3 mutants is a compensatory mechanism that leads to membrane cholesterol aggregation

Brain(2024)10.1093/brain/awae018
N/A
0DataRank · unranked
10 citations

Abigail Sandoval, Ove Bruland, Diego Pérez‐Rodríguez, Uxoa Fernández‐Pelayo, Amaia López de Arbina +21 more

Allele-specific correction of ATAD3A pathogenic variants via template-free CRISPR-Cas9 editing and gene conversion

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.10.23.684255
N/A
0DataRank · unranked
0 citations

Yohan Park, Anel LaGrone, Milovan Šuvakov, Ping Zhang, Hyekyung Park +7 more