Delphine Blain

Also affiliated with National Eye Institute

Biochemistry, Genetics and Molecular BiologyMedicine

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 3%percentile

1.7Author 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 →

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

Genotype–phenotype associations in a large PRPH2‐related retinopathy cohort

Human Mutation(2020)10.1002/humu.24065

Top 13%

1.7DataRank

Top 13%41 citations

Kerry Goetz, Bin Guan, Ehsan Ullah, Delphine Blain, Wadih M. Zein +3 more

Papers

Driven by 17 papers — median percentile 87. Top paper: “Genotype–phenotype associations in a large PRPH2‐related retinopathy cohort”.

Genotype–phenotype associations in a large PRPH2‐related retinopathy cohort

Human Mutation(2020)10.1002/humu.24065

Top 13%

1.7DataRank

Top 13%41 citations

Kerry Goetz, Bin Guan, Ehsan Ullah, Delphine Blain, Wadih M. Zein +3 more

The qMini assay identifies an overlooked class of splice variants

medRxiv(2023)10.1101/2023.11.02.23297963

N/A

0.104DataRank · unranked

1 citations

Chelsea Bender, Madhulatha Pantrangi, Nia Moore, Melissa Reeves, Amelia Naik +10 more

Response to Finsterer’s “Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome”

Ophthalmic Genetics(2020)10.1080/13816810.2020.1832295

N/A

0DataRank · unranked

0 citations

Robert B. Hufnagel, Delphine Blain, Andrea Gropman, Brian P. Brooks, Julia Chertkof

Clinical diagnosis of presumed SOX2 gonadosomatic mosaicism

Ophthalmic Genetics(2021)10.1080/13816810.2021.1888127

N/A

0DataRank · unranked

4 citations

Robert B. Hufnagel, Bin Guan, Delphine Blain, Julie C. Sapp, Andrea Gropman +5 more

Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia

Human Mutation(2022)10.1002/humu.24371

N/A

0DataRank · unranked

20 citations

Britta Baumann, Peggy Reuter, Sten Andréasson, Isabelle Audo, Carmen Ayuso +46 more

De novo frameshift mutation in YAP1 associated with bilateral uveal coloboma and microphthalmia

Ophthalmic Genetics(2022)10.1080/13816810.2022.2028299

N/A

0DataRank · unranked

5 citations

Bin Guan, Ehsan Ullah, Delphine Blain, Robert B. Hufnagel, Brian P. Brooks +1 more

Zfp503/Nlz2 is Required for RPE Differentiation and Optic Fissure Closure

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.28.486078

N/A

0DataRank · unranked

0 citations

A. Thompson, Ramakrishna P. Alur, David McGaughey, Lijin Dong, Grace Shih +22 more

A novel variant affecting the cytoplasmic tail of the FAT1 protocadherin causing coloboma and renal failure: A case report

Ophthalmic Genetics(2023)10.1080/13816810.2022.2089360

N/A

0DataRank · unranked

0 citations

Ehsan Ullah, Delphine Blain, Julie Christensen, Carmen C. Brewer, James E. Balow +5 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

OUTER RETINAL MICROCAVITATIONS IN RETINITIS PIGMENTOSA

Retina(2024)10.1097/iae.0000000000004091

N/A

0DataRank · unranked

0 citations

Laryssa A. Huryn, Robert B. Hufnagel, Ehsan Ullah, Aime Agather, Delphine Blain +4 more

Seeing in Color: Inclusion and Characterization of Hereditary Eye Disease in African Americans

Translational Vision Science & Technology(2024)10.1167/tvst.13.9.4

N/A

0DataRank · unranked

0 citations

Raisa Ionin, Laryssa A. Huryn, Catherine A. Cukras, Delphine Blain, Aime Agather +5 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

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

Case Report: Association of Ocular Colobomas With a Novel Missense Variant in CDC42, a Member of the Rho Family of Small GTPases

Clinical Genetics(2025)10.1111/cge.14768

N/A

0DataRank · unranked

0 citations

Nawaal Shinwari, Aleksey Porollo, Eniolami O. Dosunmu, Ehsan Ullah, Bin Guan +7 more

Ocular and Systemic Findings in Adults with Uveal Coloboma

Ophthalmology(2020)10.1016/j.ophtha.2020.05.028

N/A

0DataRank · unranked

14 citations

Laryssa A. Huryn, Robert B. Hufnagel, Wadih M. Zein, Delphine Blain, Brian P. Brooks +1 more

The Developmental Landscape of Children With Uveal Coloboma and Its Relationship With Clinical Phenotype and Genetics

American Journal of Ophthalmology(2025)10.1016/j.ajo.2025.11.011

N/A

0DataRank · unranked

0 citations

Alexandra T. Hehn, Delphine Blain, Cristan Farmer, Lisa Joseph, Edythe Wiggs +5 more

Retinoschisis associated with Kearns-Sayre syndrome

Ophthalmic Genetics(2020)10.1080/13816810.2020.1799416

N/A

0DataRank · unranked

8 citations

Robert B. Hufnagel, Delphine Blain, Andrea Gropman, Brian P. Brooks, Julia Chertkof

Delphine Blain

Indexed papers

Top data-sharing exemplar

Papers