Marcy E. Richardson

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.

Data Supplement 1 from Pathogenic Variants in Cancer Susceptibility Genes Predispose to Ductal Carcinoma In Situ of the Breast

Figshare(2025)10.1158/1078-0432.28141741

Top 100%

0DataRank

Top 100%0 citations

Ronan E. Couch, Rachid Karam, Chunling Hu, Nicholas Boddicker, Eric C. Polley +37 more

Papers

Driven by 28 papers — median percentile 0. Top paper: “Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants”.

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.08.022

N/A

0.434DataRank · unranked

17 citations

Megan Holdren, Terra Brannan, Miguel de la Hoya, Amanda B. Spurdle, Sean V. Tavtigian +16 more

Saturation genome editing-based functional evaluation and clinical classification of BRCA2 single nucleotide variants

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.12.14.571597

N/A

0.269DataRank · unranked

5 citations

Chunling Hu, Jie Na, Steven N. Hart, Rohan Gnanaolivu, Mohamed Abozaid +18 more

Curated multiple sequence alignment for the Adenomatous Polyposis Coli (APC) gene and accuracy of in silico pathogenicity predictions

PLoS ONE(2020)10.1371/journal.pone.0233673

N/A

0DataRank · unranked

3 citations

Dylan J. Martini, David J. Hermel, Dana Solcz, Marcy E. Richardson, Tina Pesaran +3 more

Prevalence of pathogenic variants in DNA damage response genes in patients undergoing cancer risk assessment and reporting a personal history of early-onset renal cancer

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.21.958256

N/A

0DataRank · unranked

0 citations

Elena V. Demidova, Randy W. Lesh, Lily Hoang, Marcy E. Richardson, Andrea Forman +7 more

Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTEN

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.001

N/A

0DataRank · unranked

128 citations

Carolyn Horton, Jennifer N. Dines, Alan F. Rubin, Marcy E. Richardson, Kelly McGoldrick +7 more

Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.02.005

N/A

0DataRank · unranked

63 citations

Chunling Hu, Kun Y. Lee, Holly LaDuca, Kelly Fulk, Kate Durda +10 more

Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group

Genetics in Medicine(2023)10.1016/j.gim.2023.101036

N/A

0DataRank · unranked

70 citations

Marcie Steeves, Pınar Bayrak‐Toydemir, Katherine A. Benson, Bradley P. Coe, Laura K. Conlin +42 more

Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel

Genetics in Medicine(2023)10.1016/j.gim.2023.100992

N/A

0DataRank · unranked

33 citations

Xiaoyu Yin, Marcy E. Richardson, Marta Pineda, Andreas Laner, Deborah Ritter +27 more

BRCA1 frameshift variants leading to extended incorrect protein C termini

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100240

N/A

0DataRank · unranked

3 citations

Tzeh Keong Foo, Marcy E. Richardson, John Michael O. Rañola, Jamie Weyandt, Matthew J. Varga +13 more

A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations

medRxiv(2023)10.1101/2023.08.08.23293676

N/A

0DataRank · unranked

4 citations

Tomoki Nomakuchi, Elizabeth Chao, Carolyn Horton, Jill S. Dolinsky, Amal Yussuf +12 more

Breast cancer risk associated with missense variants in BRCA2.

Journal of Clinical Oncology(2023)10.1200/jco.2023.41.16_suppl.10501

N/A

0DataRank · unranked

0 citations

Marcy E. Richardson, Rachid Karam, Nicholas Boddicker, Chunling Hu, Yohannes A. Tecleab +6 more

Saturation genome editing-based functional evaluation and clinical classification of BRCA2 single nucleotide variants

Research Square(2023)10.21203/rs.3.rs-3736200/v1

N/A

0DataRank · unranked

0 citations

Huaizhi Huang, Chunling Hu, Jie Na, Steven N. Hart, Rohan Gnanaolivu +18 more

Functional analysis and clinical classification of 462 germline BRCA2 missense variants affecting the DNA binding domain

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.002

N/A

0DataRank · unranked

17 citations

Huaizhi Huang, Jie Na, Carolyn A. Lumby, Mohamed Abozaid, Megan Holdren +21 more

Large-scale application of ClinGen-InSiGHT APC-specific ACMG/AMP variant classification criteria leads to substantial reduction in VUS

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.09.002

N/A

0DataRank · unranked

15 citations

Marcy E. Richardson, Andreas Laner, Xuemei Shi, Elisabet Ognedal, Valeria Vasta +27 more

Pathogenic Variants in Cancer Susceptibility Genes Predispose to Ductal Carcinoma In Situ of the Breast

Clinical Cancer Research(2024)10.1158/1078-0432.ccr-24-1884

N/A

0DataRank · unranked

11 citations

Ronan E. Couch, Rachid Karam, Chunling Hu, Nicholas Boddicker, Eric C. Polley +37 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

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline ATM sequence variants

medRxiv(2024)10.1101/2024.05.28.24307502

N/A

0DataRank · unranked

2 citations

Megan Holdren, Terra Brannan, Miguel de la Hoya, Amanda B. Spurdle, Sean V. Tavtigian +16 more

Saturation genome editing-based functional evaluation and clinical classification of BRCA2 single nucleotide variants.

Journal of Clinical Oncology(2024)10.1200/jco.2024.42.16_suppl.10511

N/A

0DataRank · unranked

0 citations

Huaizhi Huang, Tina Pesaran, Rachid Karam, Siddhartha Yadav, Susan M. Domchek +6 more

Functional evaluation and clinical classification of BRCA2 variants

Nature(2025)10.1038/s41586-024-08388-8

N/A

0DataRank · unranked

55 citations

Chunling Hu, Jie Na, Steven N. Hart, Rohan Gnanaolivu, Mohamed Abozaid +39 more

A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations

Nature Communications(2025)10.1038/s41467-025-57077-1

N/A

0DataRank · unranked

14 citations

Tomoki Nomakuchi, Elizabeth Chao, Carolyn Horton, Jill S. Dolinsky, Amal Yussuf +23 more

ACMG/AMP interpretation of BRCA1 missense variants: Structure-informed scores add evidence strength granularity to the PP3/BP4 computational evidence

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.011

N/A

0DataRank · unranked

11 citations

Nitsan Rotenberg, Ada Esteban‐Sánchez, Cristina Fortuño, Alicia Gómez-Sanz, Matthew J. Varga +7 more

Integration of protein stability and AlphaMissense scores improves bioinformatic impact prediction for p53 missense and in-frame amino acid deletion variants

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.012

N/A

0DataRank · unranked

8 citations

Cristina Fortuño, Matthew J. Varga, Adam Chamberlin, Lobna Ramadane‐Morchadi, Bing Feng +4 more

Association of gene variant type and location with breast cancer risk in the general population

Annals of Oncology(2025)10.1016/j.annonc.2025.04.010

N/A

0DataRank · unranked

8 citations

Nicholas Boddicker, Siddhartha Yadav, Cai-Xia Hu, Steven N. Hart, Christine B. Ambrosone +40 more

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline PALB2 sequence variants

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.020

N/A

0DataRank · unranked

4 citations

Megan F.H. Bishop, Megan Holdren, Miguel de la Hoya, Amanda B. Spurdle, Sean V. Tavtigian +15 more

Data Supplement 1 from Pathogenic Variants in Cancer Susceptibility Genes Predispose to Ductal Carcinoma In Situ of the Breast

Figshare(2025)10.1158/1078-0432.28141741

Top 100%

0DataRank

Top 100%0 citations

Ronan E. Couch, Rachid Karam, Chunling Hu, Nicholas Boddicker, Eric C. Polley +37 more

Site-saturation functional screens identify PALB2 missense variants associated with increased breast cancer risk

Nature Communications(2026)10.1038/s41467-025-67252-z

N/A

0DataRank · unranked

0 citations

Sabine C. Knaup, Roberta Menafra, Merel E. Braspenning, Magdalena B. Rother, Petra Kleiblova +78 more

Comprehensively Testing the Function of Missense Variation in the STK11 Tumour Suppressor

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.07.14.664734

N/A

0DataRank · unranked

0 citations

Atina G. Coté, Warren van Loggerenberg, Marinella Gebbia, Nishka Kishore, Jochen Weile +19 more

Prevalence of pathogenic variants in DNA damage response and repair genes in patients undergoing cancer risk assessment and reporting a personal history of early-onset renal cancer

Scientific Reports(2020)10.1038/s41598-020-70449-5

N/A

0DataRank · unranked

32 citations

Elena V. Demidova, Randy W. Lesh, Lily Hoang, Marcy E. Richardson, Andrea Forman +7 more

Marcy E. Richardson

Indexed papers

Top data-sharing exemplar

Papers