Elisabeth A. Rosenthal

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 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.

Penetrance of breast cancer genes from the eMERGE III Network

10.1101/2021.04.24.21255936

Top 100%

0DataRank

Top 100%0 citations

Julia Wynn, Ning Shang, Cong Liu, Alexander Fedotov, Miranda L.G. Hallquist +24 more

Papers

Driven by 22 papers — median percentile 0. Top paper: “The power of genetic diversity in genome-wide association studies of lipids”.

The power of genetic diversity in genome-wide association studies of lipids

Nature(2021)10.1038/s41586-021-04064-3

N/A

9.9DataRank · unranked

1069 citations

Shoa L. Clarke, Kuan-Han H. Wu, Stavroula Kanoni, Greg J. M. Zajac, Shweta Ramdas +95 more

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

Nature Medicine(2024)10.1038/s41591-024-02796-z

N/A

4.8DataRank · unranked

196 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin +73 more

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Genetics in Medicine(2023)10.1016/j.gim.2023.100006

N/A

2.6DataRank · unranked

121 citations

Aimee Allworth, Harris T. Bland, Pedro J. Caraballo, Rex L. Chisholm, Ellen Wright Clayton +95 more

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.06.012

N/A

0.626DataRank · unranked

64 citations

Jonathan Judd, Sarah E. Graham, Stavroula Kanoni, Yuxuan Wang, Ida Surakka +95 more

Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

Genome biology(2022)10.1186/s13059-022-02837-1

N/A

0.626DataRank · unranked

64 citations

Sarah E. Graham, Yuxuan Wang, Ida Surakka, Shweta Ramdas, Xiang Zhu +95 more

Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network

Scientific Reports(2023)10.1038/s41598-023-27481-y

N/A

0.489DataRank · unranked

25 citations

Luke V. Rasmussen, Ken Wiley, Thomas N. Person, David Cronkite, Sunghwan Sohn +34 more

Author Correction: The power of genetic diversity in genome-wide association studies of lipids

Nature(2023)10.1038/s41586-023-06194-2

N/A

0.416DataRank · unranked

15 citations

Shoa L. Clarke, Kuan-Han H. Wu, Stavroula Kanoni, Greg J. M. Zajac, Shweta Ramdas +95 more

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

medRxiv(2023)10.1101/2023.05.25.23290535

N/A

0.330DataRank · unranked

8 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Josh Arias, Gillian M. Belbin +71 more

Clinical associations with a polygenic predisposition to benign lower white blood cell counts

Nature Communications(2024)10.1038/s41467-024-47804-5

N/A

0.312DataRank · unranked

7 citations

John P. Shelley, Alyson L. Dickson, Jacy Zanussi, Laura L. Daniel, Neil S. Zheng +23 more

Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.26.559521

N/A

0.312DataRank · unranked

7 citations

Jonas Korlach, Kiara C. Eldred, Elliott Swanson, Jason G. Underwood, Yong-Han Hank Cheng +31 more

Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis

Human Genetics and Genomics Advances(2020)10.1016/j.xhgg.2020.100010

N/A

0.269DataRank · unranked

5 citations

Xiaoliang Wang, Pierre Fontanillas, Esther Kim, Sirisak Chanprasert, Allan Gordon +55 more

Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51786

N/A

0.241DataRank · unranked

4 citations

Ghayda Mirzaa, Elizabeth Blue, Giuseppe Albano, Danny E. Miller, Aimee Allworth +28 more

Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts

Rare(2024)10.1016/j.rare.2024.100040

N/A

0.208DataRank · unranked

3 citations

Samuel J. Huang, Alyna Khan, Katie Golden‐Grant, Brenna Boyd, Elisabeth A. Rosenthal +37 more

Multiple polygenic score approach in colorectal cancer risk prediction

Scientific Reports(2025)10.1038/s41598-025-21956-w

N/A

0.104DataRank · unranked

1 citations

Minta Thomas, Elisabeth A. Rosenthal, Amanda I. Phipps, Lori C. Sakoda, Franzel J. B. van Duijnhoven +39 more

Penetrance of breast cancer genes from the eMERGE III Network

10.1101/2021.04.24.21255936

Top 100%

0DataRank

Top 100%0 citations

Julia Wynn, Ning Shang, Cong Liu, Alexander Fedotov, Miranda L.G. Hallquist +24 more

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

UNC Libraries(2020)10.17615/02rz-mz46

N/A

0DataRank · unranked

0 citations

Jane Ranchalis, Mitzi L. Murray, Ann Katherine M. Foreman, Seema M. Jamal, Andrew D. Johnson +27 more

Clinical consequences of a polygenic predisposition to benign lower white blood cell counts

medRxiv(2023)10.1101/2023.08.20.23294331

N/A

0DataRank · unranked

0 citations

John P. Shelley, Alyson L. Dickson, Jacy Zanussi, Laura L. Daniel, Neil S. Zheng +23 more

Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.008

N/A

0DataRank · unranked

3 citations

Eunjin Ryu, Benjamin Steger, Abhijit Dixit, Yoshihiko Saito, Juyeong Yoo +36 more

Comparing Ancestry Standardization Approaches for a Transancestry Colorectal Cancer Polygenic Risk Score

Genetic Epidemiology(2024)10.1002/gepi.22590

N/A

0DataRank · unranked

2 citations

Li Hsu, Minta Thomas, Ulrike Peters, Christopher Kachulis, Karynne Patterson +2 more

Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition

Nature Genetics(2025)10.1038/s41588-024-02067-0

N/A

0DataRank · unranked

34 citations

Jonas Korlach, Kiara C. Eldred, Elliott Swanson, Jason G. Underwood, Stephanie C. Bohaczuk +33 more

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser

Genome Medicine(2025)10.1186/s13073-025-01546-1

N/A

0DataRank · unranked

8 citations

Shruti Marwaha, Alistair Ward, Shilpa N. Kobren, Jennefer N. Carter, Undiagnosed Diseases Network +94 more

Loci identified by a genome‐wide association study of carotid artery stenosis in the eMERGE network

Genetic Epidemiology(2020)10.1002/gepi.22360

N/A

0DataRank · unranked

10 citations

Daniel Seung Kim, David R. Crosslin, Ian B. Stanaway, Elisabeth A. Rosenthal, David Carrell +19 more

Elisabeth A. Rosenthal

Indexed papers

Top data-sharing exemplar

Papers