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

Siranoush Manoukian

Tumori Foundation

ORCID: 0000-0002-6034-7562
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 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 →

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.

Supplementary Table 3 from Triple-Negative versus Non–Triple-Negative Breast Cancers in High-Risk Women: Phenotype Features and Survival from the HIBCRIT-1 MRI-Including Screening Study

10.1158/1078-0432.22460277
Top 100%
0DataRank
Top 100%0 citations

Filippo Santoro, Giovanni Di Leo, Siranoush Manoukian, Clelia de Giacomi, Stefano Corcione +12 more

Papers

Driven by 20 papers — median percentile 0. Top paper: “Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers”.

Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

Communications Biology(2022)10.1038/s42003-022-03978-6
N/A
0.607DataRank · unranked
15 citations

John F. Pearson, Louise Marquart, Joe Dennis, George A. R. Wiggins, Daniel R. Barnes +95 more

Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

UNC Libraries(2020)10.17615/bg56-kz70
N/A
0.449DataRank · unranked
19 citations

Trinidad Caldés, Maria A. Caligo, Alessandra Viel, Susan J. Ramus, Kathleen Claes +95 more

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

Nature Communications(2020)10.1038/s41467-019-14100-6
N/A
0DataRank · unranked
49 citations

Jean Abraham, Irene L. Andrulis, Hoda Anton‐Culver, Volker Arndt, Alan Ashworth +95 more

Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

UNC Libraries(2020)10.17615/ff36-yj54
N/A
0DataRank · unranked
0 citations

Pascal Guénel, Nichola Johnson, Mitul Shah, Douglas F. Easton, Diana Torres +95 more

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

UNC Libraries(2020)10.17615/yq45-7g05
N/A
0DataRank · unranked
0 citations

Mads Thomassen, Maria A. Caligo, Lesley McGuffog, Liliana Varesco, Daniela Zaffaroni +27 more

Breast and Prostate Cancer Risks for MaleBRCA1andBRCA2Pathogenic Variant Carriers Using Polygenic Risk Scores

JNCI Journal of the National Cancer Institute(2021)10.1093/jnci/djab147
N/A
0DataRank · unranked
44 citations

Valentina Silvestri, Goska Leslie, Lesley McGuffog, Joe Dennis, Xin Yang +95 more

Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants

Genetics in Medicine(2021)10.1016/j.gim.2021.08.016
N/A
0DataRank · unranked
30 citations

Christoph Engel, Miguel de la Hoya, Paolo Peterlongo, Drakoulis Yannoukakos, Luca Livraghi +56 more

CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

British Journal of Cancer(2021)10.1038/s41416-020-01185-w
N/A
0DataRank · unranked
9 citations

Nichola Johnson, AOCS Group, ABCTB Investigators, KConFab Investigators, Sarah Maguire +95 more

Rare Copy Number Variants (CNVs) and Breast Cancer Risk

Research Square(2021)10.21203/rs.3.rs-602209/v1
N/A
0DataRank · unranked
0 citations

Jonathan P. Tyrer, Logan C. Walker, Kyriaki Michailidou, Leila Dorling, Manjeet Bola +95 more

Rare copy number variants (CNVs) and breast cancer risk

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.20.444828
N/A
0DataRank · unranked
0 citations

Jonathan P. Tyrer, Logan C. Walker, Kyriaki Michailidou, Leila Dorling, Manjeet K. Bolla +95 more

A Likelihood Ratio Approach for Utilizing Case-Control Data in the Clinical Classification of Rare Sequence Variants: Application to BRCA1 and BRCA2

Human Mutation(2023)10.1155/2023/9961341
N/A
0DataRank · unranked
7 citations

Denise G O'Mahony, Michael T. Parsons, Hongyan Li, Joe Dennis, Kristiina Aittomäkkiki +95 more

Atypical cancer risk profile in carriers of Italian founder BRCA1 variant p.His1673del: Implications for classification and clinical management

Cancer Medicine(2024)10.1002/cam4.70114
N/A
0DataRank · unranked
3 citations

Cristina Fortuño, Laura Caleca, Bing Feng, Courtney Carroll, Michael T. Parsons +27 more

Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk

medRxiv(2024)10.1101/2024.02.29.24303243
N/A
0DataRank · unranked
3 citations

Jonathan P. Tyrer, Joe Dennis, Goska Leslie, Manjeet K. Bolla, Michael Lush +95 more

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

Research Explorer (The University of Manchester)(2024)10.17615/dprd-7a14
N/A
0DataRank · unranked
0 citations

Dhanya Ramachandran, John Abraham, Mythily Sachchithananthan, Nadège Presneau, Robert Winqvist +95 more

Large-scale meta-analysis and precision functional assays identify FANCM regions in which PTVs confer different risks for ER-negative and triple-negative breast cancer

The Breast(2025)10.1016/j.breast.2025.104619
N/A
0DataRank · unranked
1 citations

Gisella Figlioli, Clémence Mooser, Irene Casamassima, Violette Azzoni, Jahnavi Srivatsa +95 more

Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 Women

Cancers(2025)10.3390/cancers17213561
N/A
0DataRank · unranked
0 citations

Christine Kim Yan Loo, Ryan Jak Yang Lim, Mui Heng Goh, Mustapha Abubakar, Thomas U. Ahearn +95 more

Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer

npj Genomic Medicine(2025)10.1038/s41525-025-00529-w
N/A
0DataRank · unranked
0 citations

Jonathan P. Tyrer, Joe Dennis, Goska Leslie, Manjeet K. Bolla, Michael Lush +95 more

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

Nature Genetics(2020)10.1038/s41588-020-0611-8
N/A
0DataRank · unranked
243 citations

D. Timothy Bishop, Stuart MacGregor, Mitchell J. Machiela, Alexander Stratigos, Paola Ghiorzo +95 more

Supplementary Table 3 from Triple-Negative versus Non–Triple-Negative Breast Cancers in High-Risk Women: Phenotype Features and Survival from the HIBCRIT-1 MRI-Including Screening Study

10.1158/1078-0432.22460277
Top 100%
0DataRank
Top 100%0 citations

Filippo Santoro, Giovanni Di Leo, Siranoush Manoukian, Clelia de Giacomi, Stefano Corcione +12 more

Characterization of the Cancer Spectrum in Men With GermlineBRCA1andBRCA2Pathogenic Variants

JAMA Oncology(2020)10.1001/jamaoncol.2020.2134
N/A
0DataRank · unranked
67 citations

Goska Leslie, Daniel R. Barnes, and the CIMBA Group, Bjarni A. Agnarsson, Kristiina Aittomäki +95 more