Constantinos Deltas

Also affiliated with University of Nicosia, University of Cyprus

MedicineBiochemistry, 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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 8 papers. Top paper: “Germline MBD4 deficiency causes a multi-tumor predisposition syndrome”.

Germline MBD4 deficiency causes a multi-tumor predisposition syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.018

N/A

1.9DataRank · unranked

79 citations

Hannah D. West, Edward Chew, Sara Galavotti, Christoffer Flensburg, Judith E. Grolleman +64 more

The 2019 and 2021 International Workshops on Alport Syndrome

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

N/A

0.546DataRank · unranked

37 citations

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

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to mutations identifies distinct clinical subtypes

Kidney International(2020)10.1016/j.kint.2020.06.041

N/A

0DataRank · unranked

43 citations

Kendrah Kidd, Mohamad Zaidan, Petr Vyleťal, Veronika Barešová, Kateřina Hodaňová +51 more

Genomic Classifiers in Personalized Prostate Cancer Radiation Therapy Approaches: A Systematic Review and Future Perspectives Based on International Consensus

International Journal of Radiation Oncology*Biology*Physics(2022)10.1016/j.ijrobp.2022.12.038

N/A

0DataRank · unranked

25 citations

Cédric Draulans, Amar U. Kishan, Daniel E. Spratt, Ashley E. Ross, Tobias Maurer +35 more

Eight-Fold Increased COVID-19 Mortality in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 Mutations: An Observational Study

medRxiv(2024)10.1101/2024.07.03.24309887

N/A

0DataRank · unranked

0 citations

Adrienne H. Williams, Abbigail Taylor, Lauren Martin, Victoria Robins, John A. Sayer +21 more

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

Long-Read Sequencing of the MUC1 VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and Progression

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.09.06.673538

N/A

0DataRank · unranked

3 citations

Anna Přistoupilová, Kendrah Kidd, Václav Janoušek, Martin Radina, Petr Vyleťal +38 more

A glycine substitution in the collagenous domain of Col4a3 in mice recapitulates late onset Alport syndrome

Matrix Biology Plus(2020)10.1016/j.mbplus.2020.100053

N/A

0DataRank · unranked

12 citations

Isavella Savva, Myrtani Pieri, Pavlos Ioannou, Petros Petrou, Gregory Papagregoriou +10 more