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

Lung‐Kun Yeh

Chang Gung University

ORCID: 0000-0003-1925-2059

Also affiliated with Chang Gung Memorial Hospital, Linkou Chang Gung Memorial Hospital

Medicine

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 5 papers. Top paper: “A novel KCNV2 mutation in a patient taking hydroxychloroquine associated with cone dystrophy with supernormal rod response”.

A novel KCNV2 mutation in a patient taking hydroxychloroquine associated with cone dystrophy with supernormal rod response

Ophthalmic Genetics(2021)10.1080/13816810.2021.1920039
N/A
0DataRank · unranked
2 citations

Joseph Ryu, Lung‐Kun Yeh, Kuan‐Jen Chen, Stephen H. Tsang, Laura Liu +2 more

Conditional Deletion of Activating Rearranged During Transfection Receptor Tyrosine Kinase Leads to Impairment of Photoreceptor Ribbon Synapses and Disrupted Visual Function in Mice

Frontiers in Neuroscience(2021)10.3389/fnins.2021.728905
N/A
0DataRank · unranked
1 citations

Meng‐Lin Liao, Wan‐Chun Huang, Pei‐Kang Liu, Sarah R. Levi, Yun-Ju Tseng +6 more

Clinical Characteristics and Genetic Variants in Taiwanese Patients With PROM1-Related Inherited Retinal Disorders

Investigative Ophthalmology & Visual Science(2023)10.1167/iovs.64.14.25
N/A
0DataRank · unranked
8 citations

Peiliang Wu, Eugene Yu‐Chuan Kang, Yi‐Chun Chi, Laura A. Jenny, Pei‐Hsuan Lin +12 more

Transforming growth factor beta receptor 2 (Tgfbr2) deficiency in keratocytes results in corneal ectasia

The Ocular Surface(2023)10.1016/j.jtos.2023.06.014
N/A
0DataRank · unranked
8 citations

Olivia Betty Zolnik, Shingo Yasuda, Lung‐Kun Yeh, Yong Yuan, Winston W.‐Y. Kao +3 more

Genetic underpinnings explored: OPA1 deletion and complex phenotypes on chromosome 3q29

BMC Medical Genomics(2024)10.1186/s12920-024-01850-6
N/A
0DataRank · unranked
2 citations

Pei‐Hsuan Lin, Peiliang Wu, Eugene Yu‐Chuan Kang, Laura Liu, Lung‐Kun Yeh +4 more