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

Siying Lin

University of Manchester

ORCID: 0000-0003-1122-8396

Also affiliated with Manchester University NHS Foundation Trust, Moorfields Eye Hospital, Genomics (United Kingdom), University College London

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 4%percentile
0.653Author DataRank

Indexed papers

2in 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 2 indexed papers 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 →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom

medRxiv(2024)10.1101/2024.03.24.24304809
Top 45%
0.405DataRank
Top 45%9 citations

Thales A. C. de Guimarães, Saoud Al‐Khuzaei, Malena Daich Varela, Sagnik Sen, Pallavi Bagga +32 more

Papers

Driven by 15 papers — median percentile 47. Top paper: “Rare disease gene association discovery in the 100,000 GenomesProject”.

Rare disease gene association discovery in the 100,000 GenomesProject

Nature(2025)10.1038/s41586-025-08623-w
N/A
0.515DataRank · unranked
18 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom

medRxiv(2024)10.1101/2024.03.24.24304809
Top 45%
0.405DataRank
Top 45%9 citations

Thales A. C. de Guimarães, Saoud Al‐Khuzaei, Malena Daich Varela, Sagnik Sen, Pallavi Bagga +32 more

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

Nature Genetics(2026)10.1038/s41588-025-02451-4
N/A
0.370DataRank · unranked
8 citations

Kim Rodenburg, Zuzana Cvackova, Karolina Kaminska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +212 more

Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations

medRxiv(2025)10.1101/2025.07.03.25330767
Top 60%
0.248DataRank
Top 60%4 citations

Thales A. C. de Guimarães, Saoud Al‐Khuzaei, Malena Daich Varela, Mital Shah, Gunjan Naik +32 more

Substitution of a single non-coding nucleotide upstream of TMEM216 causes non-syndromic retinitis pigmentosa and is associated with reduced TMEM216 expression

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.020
N/A
0DataRank · unranked
7 citations

Pooja Biswas, Anne-Marie Berry, Riccardo Sangermano, Mukhtar Ullah, Siying Lin +40 more

Variants in NR6A1 cause a novel oculo-vertebral-renal (OVR) syndrome

medRxiv(2024)10.1101/2024.11.09.24316578
N/A
0DataRank · unranked
2 citations

Ehsan Ullah, Aman George, Mara I Maftei, Elangovan Elangovan, Daniel Sanchez-Mendoza +18 more

Variants in NR6A1 cause a novel oculo-vertebral-renal (OVR) syndrome

Research Square(2024)10.21203/rs.3.rs-5375105/v1
N/A
0DataRank · unranked
0 citations

Uma M Neelathi, Ehsan Ullah, Aman George, Mara I Maftei, Elangovan Boobalan +18 more

Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene

Nature Machine Intelligence(2025)10.1038/s42256-025-01040-8
N/A
0DataRank · unranked
23 citations

William Woof, Siying Lin, Biraja Ghoshal, Bernardo Mendes, Yoga Advaith Veturi +42 more

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data

medRxiv(2023)10.1101/2023.12.20.23300294
N/A
0DataRank · unranked
3 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

Variants in NR6A1 cause a novel oculo vertebral renal syndrome

Nature Communications(2025)10.1038/s41467-025-60574-y
N/A
0DataRank · unranked
8 citations

Ehsan Ullah, Aman George, Mara I Maftei, Elangovan Boobalan, Daniel Sanchez-Mendoza +18 more

Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy

Genetics in Medicine(2025)10.1016/j.gim.2025.101401
N/A
0DataRank · unranked
4 citations

Maayan Avraham, Sandeep Sarma Asodu, Abigail R. Moye, Riccardo Sangermano, Leah Rizel +19 more

Bi-allelic loss-of-function variants in POC5 cause a syndromic retinal, endocrine, and neuromuscular ciliopathy

Genetics in Medicine(2025)10.1016/j.gim.2025.101513
N/A
0DataRank · unranked
1 citations

Ingrid M. Jazet, Suzanne Yzer, Jeroen Pas, Serwet Demirdas, Elisabeth F. C. van Rossum +39 more

Clinical and Biochemical Characterization of Specific GUCY2D Alleles Associated With a Rare Form of Night Blindness

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.6.22
N/A
0DataRank · unranked
1 citations

Igor V. Peshenko, Malena Daich Varela, Siying Lin, Gavin Arno, Omar A. Mahroo +6 more

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa

medRxiv(2025)10.1101/2025.01.06.24317169
N/A
0DataRank · unranked
15 citations

Kim Rodenburg, Zuzana Cvačková, Karolina Kamińska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +95 more

Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency

Genetics in Medicine(2021)10.1016/j.gim.2021.10.014
N/A
0DataRank · unranked
4 citations

Siying Lin, Promita Ghosh, Francesca Clementina Radio, Emily Farrow, Isabelle Thiffault +35 more