Daniel P. Gale

Also affiliated with The Royal Free Hospital, Kidney Care UK, University College London

MedicineBiochemistry, Genetics and Molecular BiologyImmunology and Microbiology

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 9 papers. Top paper: “Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1”.

Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1

Kidney International(2020)10.1016/j.kint.2020.04.038

N/A

0DataRank · unranked

147 citations

Patrick Hofmann, Kendrah Kidd, Inès Dufour, Hendrica Belge, Céline Schaeffer +28 more

Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations

Kidney International Reports(2020)10.1016/j.ekir.2020.06.029

N/A

0DataRank · unranked

54 citations

Petr Vyleťal, Céline Schaeffer, Eric Olinger, Martina Živná, Kateřina Hodaňová +37 more

Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

Kidney International(2022)10.1016/j.kint.2022.03.019

N/A

0DataRank · unranked

193 citations

Émilie Cornec-Le Gall, Jan Halbritter, Krzysztof Kiryluk, Andrew Mallett, Rulan S. Parekh +57 more

The 2019 and 2021 International Workshops on Alport Syndrome

European Journal of Human Genetics(2022)10.1038/s41431-022-01075-0

N/A

0DataRank · unranked

37 citations

Jie Ding, Constantinos Deltas, Judy Savige, Beata S. Lipska‐Ziętkiewicz, Julia Hoefele +21 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

Rare disease gene association discovery in the 100,000 GenomesProject

Nature(2025)10.1038/s41586-025-08623-w

N/A

0DataRank · unranked

18 citations

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

Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries

Kidney International(2025)10.1016/j.kint.2025.02.026

N/A

0DataRank · unranked

7 citations

Steffen Fieuws, Jonas Hofstetter, David Pitcher, Lotte Vanmeerbeek, Stefanie Haeberle +95 more

The impact of a secondary, rare, non-pathogenic PKD1 variant on disease progression in autosomal dominant polycystic kidney disease

Journal of Nephrology(2025)10.1007/s40620-025-02211-x

N/A

0DataRank · unranked

0 citations

Kane E. Collins, Sophia Heneghan, Edmund Gilbert, Hana Yang, Sarah R. Senum +82 more

Biallelic TMEM72 Variants in Patients with a Nephronophthisis-Like Phenotype

The Nephron journals/Nephron journals(2025)10.1159/000549598

N/A

0DataRank · unranked

0 citations

Rozemarijn Snoek, Siebren Faber, Aurelius J.C. Roskothen-Shevchuk, Elena Sendino Garví, Edith Peters +30 more