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

Go Hun Seo

Seoul Medical Center

ORCID: 0000-0003-1518-1791

Also affiliated with Syneos Health (South Korea), SNP Genetics (South Korea)

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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 6 papers. Top paper: “A homozygous in-frame duplication within the LRRCT consensus sequence of CFAP410 causes cone-rod dystrophy, macular staphyloma and short stature”.

A homozygous in-frame duplication within the LRRCT consensus sequence of CFAP410 causes cone-rod dystrophy, macular staphyloma and short stature

Ophthalmic Genetics(2021)10.1080/13816810.2021.2010773

N/A

0.292DataRank · unranked

6 citations

Winston Lee, Pei‐Kang Liu, Sarah R. Levi, Hung-Hsi Wang, Nelson Chen +8 more

Pilot study of EVIDENCE: High diagnostic yield and clinical utility of whole exome sequencing using an automated interpretation system for patients with suspected genetic disorders

N/A

0.269DataRank · unranked

5 citations

Taeho Kim, Jung-young Park, Jungsul Lee, Sehwan Kim, Dhong-gun Won +15 more

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

PKHD1L1 , A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss

medRxiv(2023)10.1101/2023.10.08.23296081

N/A

0DataRank · unranked

3 citations

Pedro De‐la‐Torre, Mina Zamani, Hanjun Wang, Hina Khan, T. Morris +12 more

Inherited CARD9 Deficiency Due to a Founder Effect in East Asia

Journal of Clinical Immunology(2024)10.1007/s10875-024-01724-7

N/A

0DataRank · unranked

7 citations

Beom Hee Lee, Yuki Hirata, Yuzaburo Inoue, Hidetaka Majima, Yusuke Imanaka +18 more

In vivo consequences of varying degrees of OTOA alteration elucidated using knock-in mouse models and pseudogene contamination-free long-read sequencing

Genes & Diseases(2025)10.1016/j.gendis.2025.101533

N/A

0DataRank · unranked

1 citations

Bong Jik Kim, Chung Lee, Go Hun Seo, Hane Lee, Jin Hee Han +5 more