Valentina Cipriani

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

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.

The genomic landscape of syndromic and non-syndromic hearing loss within the 100,000 Genomes Project cohort

medRxiv(2025)10.1101/2025.02.06.25321804

Top 100%

0DataRank

Top 100%0 citations

Damian Smedley, Valentina Cipriani, Gudrun E. Moore, Philip Stanier, Michael R. Bowl +4 more

Papers

Driven by 14 papers — median percentile 0. Top paper: “Defining the role of common variation in the genomic and biological architecture of adult human height”.

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics(2014)10.1038/ng.3097

N/A

1.1DataRank · unranked

2093 citations

Emilio Rodríguez-Ruiz, The PAGE Consortium, Diana O. Perkins, Tonu Esko, Jian Yang +479 more

The genetic architecture of type 2 diabetes

Nature(2016)10.1038/nature18642

N/A

1.1DataRank · unranked

1106 citations

Menachem Fromer, Tanya M. Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J. Gaulton +334 more

Seven new loci associated with age-related macular degeneration

Nature Genetics(2013)10.1038/ng.2578

N/A

1.0DataRank · unranked

798 citations

Lars G. Fritsche, Wei Chen, Brian L. Yaspan, Yi Yu, Guðmar Þorleifsson +141 more

Phenotype‐driven approaches to enhance variant prioritization and diagnosis of rare disease

Human Mutation(2022)10.1002/humu.24380

N/A

0DataRank · unranked

75 citations

Catherine Kelly, Valentina Cipriani, Christopher J. Mungall, Justin T Reese, Daniel Daniš +3 more

Phenotype-aware prioritisation of rare Mendelian disease variants

Trends in Genetics(2022)10.1016/j.tig.2022.07.002

N/A

0DataRank · unranked

33 citations

Anita Szabó, Nikolas Pontikos, Gavin Arno, Peter N. Robinson, Julius O.B. Jacobsen +3 more

Evaluation of phenotype-driven gene prioritization methods for Mendelian diseases

Briefings in Bioinformatics(2022)10.1093/bib/bbac188

N/A

0DataRank · unranked

15 citations

Catherine Kelly, Valentina Cipriani, Peter N. Robinson, Damian Smedley, Julius O.B. Jacobsen

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development

BMC Biology(2023)10.1186/s12915-022-01475-0

N/A

0DataRank · unranked

23 citations

Louise Lanoue, Dave Clary, Kendall Higgins, Lynette Bower, Ann M. Flenniken +95 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

Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries

Nature Genetics(2024)10.1038/s41588-024-01764-0

N/A

0DataRank · unranked

40 citations

Georgios Voloudakis, Robert P. Igo, Tyler G. Kinzy, Christopher Halladay, Tim B. Bigdeli +94 more

Efficient reinterpretation of rare disease cases using Exomiser

npj Genomic Medicine(2024)10.1038/s41525-024-00456-2

N/A

0DataRank · unranked

20 citations

Julius O.B. Jacobsen, Susan Walker, Valentina Cipriani, Nomi L. Harris, Melissa A Haendel +4 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

The genomic landscape of syndromic and non-syndromic hearing loss within the 100,000 Genomes Project cohort

medRxiv(2025)10.1101/2025.02.06.25321804

Top 100%

0DataRank

Top 100%0 citations

Damian Smedley, Valentina Cipriani, Gudrun E. Moore, Philip Stanier, Michael R. Bowl +4 more

A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Scientific Reports(2020)10.1038/s41598-020-58510-9

N/A

0DataRank · unranked

63 citations

Susette Lauwen, Christina Kiel, Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey +95 more

Beyond factor H: The impact of genetic-risk variants for age-related macular degeneration on circulating factor-H-like 1 and factor-H-related protein concentrations

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.05.015

N/A

0DataRank · unranked

52 citations

Anna Tierney, John R. Griffiths, Verena Zuber, Panagiotis I. Sergouniotis, John R.W. Yates +5 more

Valentina Cipriani

Indexed papers

Top data-sharing exemplar

Papers