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

Sara R. Rashkin

St. Jude Children's Research Hospital

ORCID: 0000-0001-5542-6891
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 1%percentile
4.9Author DataRank

Indexed papers

2in 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 2 indexed papers 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.

Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts

Nature Communications(2020)10.1038/s41467-020-18246-6
Top 4%
4.9DataRank
Top 4%313 citations

Rebecca E. Graff, Linda Kachuri, Khanh K. Thai, Stacey Alexeeff, Maruta A. Blatchins +14 more

Papers

Driven by 16 papers — median percentile 48. Top paper: “Pan-cancer analysis demonstrates that integrating polygenic risk scores with modifiable risk factors improves risk prediction”.

Pan-cancer analysis demonstrates that integrating polygenic risk scores with modifiable risk factors improves risk prediction

Nature Communications(2020)10.1038/s41467-020-19600-4
N/A
6.1DataRank · unranked
202 citations

Rebecca E. Graff, Karl Smith-Byrne, Travis J. Meyers, Sara R. Rashkin, Elad Ziv +3 more

Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts

Nature Communications(2020)10.1038/s41467-020-18246-6
Top 4%
4.9DataRank
Top 4%313 citations

Rebecca E. Graff, Linda Kachuri, Khanh K. Thai, Stacey Alexeeff, Maruta A. Blatchins +14 more

A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility

Cancer Research(2020)10.1158/0008-5472.can-20-2635
N/A
0.989DataRank · unranked
25 citations

Taylor B. Cavazos, Sara R. Rashkin, Clinton L. Cario, Rebecca E. Graff, Caroline G. Tai +21 more

Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts

Nature Communications(2021)10.1038/s41467-021-21288-z
N/A
0.731DataRank · unranked
130 citations

Taylor B. Cavazos, Khanh K. Thai, Linda Kachuri, Sara R. Rashkin, Joshua Hoffman +16 more

Genomewide Meta‐Analysis Validates a Role for S1PR1 in Microtubule Targeting Agent‐Induced Sensory Peripheral Neuropathy

Clinical Pharmacology & Therapeutics(2020)10.1002/cpt.1958
N/A
0.581DataRank · unranked
47 citations

Chenling Xiong, Carol Ho, Taisei Mushiroda, J Chen, Flora Mulkey +13 more

Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden

JNCI Journal of the National Cancer Institute(2022)10.1093/jnci/djac087
N/A
0.494DataRank · unranked
26 citations

Joshua Atkins, Ricardo Cortez Cardoso Penha, Karl Smith-Byrne, Valérie Gaborieau, Catherine Voegele +28 more

Cross-Cancer Evaluation of Polygenic Risk Scores for 17 Cancer Types in Two Large Cohorts

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.18.911578
N/A
0.425DataRank · unranked
16 citations

Taylor B. Cavazos, Khanh K. Thai, Linda Kachuri, Sara R. Rashkin, Joshua Hoffman +16 more

A genome‐wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62759
N/A
0.417DataRank · unranked
9 citations

Mario A. Cleves, Gary M. Shaw, Wendy N. Nembhard, Eirini Nestoridi, Mary M. Jenkins +11 more

Genetic analysis of lung cancer reveals novel susceptibility loci and germline impact on somatic mutation burden

medRxiv(2021)10.1101/2021.04.26.21254132
N/A
0.194DataRank · unranked
2 citations

Joshua Atkins, Ricardo Cortez Cardoso Penha, Karl Smith-Byrne, Valérie Gaborieau, Catherine Voegele +28 more

Genome-Wide Meta-Analysis Validates a Role for S1PR1 in Microtubule Targeting Agent-Induced Sensory Peripheral Neuropathy

medRxiv(2020)10.1101/2020.04.23.20076208
N/A
0.165DataRank · unranked
2 citations

Chenling Xiong, Carol Ho, Taisei Mushiroda, J Chen, Flora Mulkey +13 more

Pan-cancer analysis demonstrates that integrating polygenic risk scores with modifiable risk factors improves risk prediction

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.28.922088
N/A
0DataRank · unranked
28 citations

Rebecca E. Graff, Karl Smith‐Byrne, Travis J. Meyers, Sara R. Rashkin, Elad Ziv +3 more

Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility

Nature Communications(2020)10.1038/s41467-019-13855-2
N/A
0DataRank · unranked
45 citations

Mattias Johansson, Sara R. Rashkin, Rebecca E. Graff, Yohan Bossé, Venkata Manem +46 more

The landscape of host genetic factors involved in immune response to common viral infections

Genome Medicine(2020)10.1186/s13073-020-00790-x
N/A
0DataRank · unranked
126 citations

Stephen Francis, Maike L. Morrison, George A. Wendt, Yohan Bossé, Taylor B. Cavazos +4 more

Data from A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility

(2023)10.1158/0008-5472.c.6513064
Top 100%
0DataRank
Top 100%0 citations

Taylor B. Cavazos, Sara R. Rashkin, Clinton L. Cario, Rebecca E. Graff, Caroline G. Tai +21 more

The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria

Human Molecular Genetics(2024)10.1093/hmg/ddae014
N/A
0DataRank · unranked
12 citations

Titilope A. Adeyemo, Ajoke Idayat Oyetunji, Bassey Inyang, Afolashade Akinrindoye, Baraka Stewart Mkumbe +30 more

A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study

UNC Libraries(2024)10.17615/ph8v-yc50
N/A
0DataRank · unranked
0 citations

Mary M. Jenkins, Sara R. Rashkin, Paul A. Romitti, Andrew F. Olshan, Marilyn L. Browne +11 more