Rachid Karam

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

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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Germline pathogenic variants in cancer predisposition genes among women with invasive lobular cancer of breast.

Journal of Clinical Oncology(2021)10.1200/jco.2021.39.15_suppl.10581

Top 100%

0DataRank

Top 100%0 citations

Chunling Hu, Susan M. Domchek, Jeffrey N. Weitzel, David E. Goldgar, Peter Kraft +11 more

Papers

Driven by 21 papers — median percentile 0. Top paper: “High-Density Blood Transcriptomics Reveals Precision Immune Signatures of SARS-CoV-2 Infection in Hospitalized Individuals”.

High-Density Blood Transcriptomics Reveals Precision Immune Signatures of SARS-CoV-2 Infection in Hospitalized Individuals

Frontiers in Immunology(2021)10.3389/fimmu.2021.694243

N/A

1.1DataRank · unranked

43 citations

Nicholas Hartog, Dave Chesla, William E. Faber, Chanise P. Love, Rachid Karam +25 more

Optimising clinical care through CDH1-specific germline variant curation: improvement of clinical assertions and updated curation guidelines

Journal of Medical Genetics(2022)10.1136/jmg-2022-108807

N/A

0.745DataRank · unranked

24 citations

Jamie L. Maciaszek, Bryony A. Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa +19 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

Germline pathogenic variants in cancer predisposition genes among women with invasive lobular cancer of breast.

Journal of Clinical Oncology(2021)10.1200/jco.2021.39.15_suppl.10581

Top 100%

0DataRank

Top 100%0 citations

Chunling Hu, Susan M. Domchek, Jeffrey N. Weitzel, David E. Goldgar, Peter Kraft +11 more

Simplified and more sensitive criteria for identifying individuals with pathogenic CDH1 variants

Journal of Medical Genetics(2022)10.1136/jmedgenet-2021-108169

N/A

0DataRank · unranked

9 citations

Rosa M. Xicola, Nicolette J. Rodriguez, Rachid Karam, Xavier Llor, Benjamin A. Lerner

An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance

npj Genomic Medicine(2022)10.1038/s41525-022-00302-3

N/A

0DataRank · unranked

5 citations

Gary Lipton, Steven N. Hart, Kun Y. Lee, Chunling Hu, Eric C. Polley +9 more

Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.002

N/A

0DataRank · unranked

315 citations

Miguel de la Hoya, George A. R. Wiggins, Amanda Lindy, Lisa M. Vincent, Michael T. Parsons +28 more

APPLICATION OF THE ACMG/AMP FRAMEWORK TO CAPTURE EVIDENCE RELEVANT TO PREDICTED AND OBSERVED IMPACT ON SPLICING: RECOMMENDATIONS FROM THE CLINGEN SVI SPLICING SUBGROUP

medRxiv(2023)10.1101/2023.02.24.23286431

N/A

0DataRank · unranked

17 citations

Miguel de la Hoya, George A. R. Wiggins, Amanda Lindy, Lisa M. Vincent, Michael T. Parsons +11 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

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

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

Hereditary diffuse gastric cancer spectrum associated with germline CTNNA1 loss of function revealed by clinical and molecular data from 351 carrier families and over 37 000 non-carrier controls

Gut(2025)10.1136/gutjnl-2024-334601

N/A

0DataRank · unranked

7 citations

Alexandre Dias, Ana Maria Pedro, Marta Ferreira, André Pinto-Oliveira, Celina São José +51 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

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

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

Identification of de novo variants from parent-proband duos via long-read sequencing

medRxiv(2025)10.1101/2025.02.24.25322424

N/A

0DataRank · unranked

0 citations

Emmanuèle C. Délot, Georgia Pitsava, Christine Lambert, Cairbre Fanslow, Primo Baybayan +12 more

Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast

Journal of Clinical Oncology(2021)10.1200/jco.21.00640

N/A

0DataRank · unranked

51 citations

Chunling Hu, Katherine L. Nathanson, Jeffrey N. Weitzel, David E. Goldgar, Peter Kraft +37 more

ClinGen CDH1 specifications for the ACMG/AMP guidelines: improvement of germline variant clinical assertions and updated curation guidelines

medRxiv(2021)10.1101/2021.11.01.21265332

N/A

0DataRank · unranked

0 citations

Jamie L. Maciaszek, Bryony A. Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa +19 more

Rachid Karam

Indexed papers

Top data-sharing exemplar

Papers