Steven M. Harrison

Also affiliated with Ambry Genetics (United States)

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

10.6Author DataRank

Indexed papers

3in 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 3 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.

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x

Top 2%

8.6DataRank

Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

Papers

Driven by 30 papers — median percentile 83. Top paper: “ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)”.

ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2021)10.1038/s41436-021-01172-3

N/A

13.5DataRank · unranked

563 citations

Kristy Lee, Wendy K. Chung, Allan Gordon, Gail E. Herman, Teri E. Klein +13 more

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2021)10.1038/s41436-021-01171-4

N/A

9.7DataRank · unranked

266 citations

Kristy Lee, Allan Gordon, Laura M. Amendola, Kathy Adelman, Sherri J. Bale +13 more

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x

Top 2%

8.6DataRank

Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines

Genome Medicine(2022)10.1186/s13073-021-01004-8

N/A

2.6DataRank · unranked

85 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 more

Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2021)10.1038/s41436-021-01278-8

N/A

1.6DataRank · unranked

29 citations

Kristy Lee, Wendy K. Chung, Allan Gordon, Gail E. Herman, Teri E. Klein +13 more

The Clinical Genome Resource (ClinGen): Advancing genomic knowledge through global curation

Genetics in Medicine(2024)10.1016/j.gim.2024.101228

Top 17%

1.2DataRank

Top 17%59 citations

Danielle R. Azzariti, Larry Babb, Jonathan S. Berg, Leslie G. Biesecker, Zo Bly +28 more

Harmonizing variant classification for return of results in the All of Us Research Program

Human Mutation(2021)10.1002/humu.24317

Top 27%

0.738DataRank

Top 27%17 citations

Christina Austin‐Tse, Serra Kim, Matthew S. Lebo, Annette Leon, David R. Murdock +8 more

A calibrated functional patch clamp assay to enhance clinical variant interpretation in KCNH2 -related long QT syndrome

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.13.472492

N/A

0DataRank · unranked

0 citations

Ebony Richardson, Jessica Farr, Adam P. Hill, Rizwan Ullah, Brett M. Kroncke +6 more

Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.10.013

N/A

0DataRank · unranked

548 citations

Alicia B. Byrne, Bing Feng, Kymberleigh A. Pagel, Sean D. Mooney, Rachel Karchin +20 more

Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program

Genome Medicine(2022)10.1186/s13073-022-01031-z

N/A

0DataRank · unranked

63 citations

Donna M. Muzny, Joshua D. Smith, Kimberly Walker, Cynthia L. Neben, Christina M. Lockwood +16 more

A calibrated functional patch-clamp assay to enhance clinical variant interpretation in KCNH2-related long QT syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.05.002

N/A

0DataRank · unranked

41 citations

Ebony Richardson, Jessica Farr, Adam P. Hill, Rizwan Ullah, Brett M. Kroncke +6 more

Evidence-based calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for clinical use of PP3/BP4 criteria

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.17.484479

N/A

0DataRank · unranked

34 citations

Alicia B. Byrne, Bing Feng, Kymberleigh A. Pagel, Sean D. Mooney, Rachel Karchin +9 more

ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2023)10.1016/j.gim.2023.100866

N/A

0DataRank · unranked

425 citations

Kristy Lee, Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung +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

Advanced variant classification framework reduces the false positive rate of predicted loss-of-function variants in population sequencing data

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.08.005

N/A

0DataRank · unranked

30 citations

Sanna Gudmundsson, Samantha Baxter, Eleanor G. Seaby, Eleina England, Jordan C. Wood +8 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

Advanced variant classification framework reduces the false positive rate of predicted loss of function (pLoF) variants in population sequencing data

medRxiv(2023)10.1101/2023.03.08.23286955

N/A

0DataRank · unranked

4 citations

Sanna Gudmundsson, Samantha Baxter, Eleanor G. Seaby, Eleina England, Jordan C. Wood +8 more

Assessment of the evidence yield for the calibrated PP3/BP4 computational recommendations

Genetics in Medicine(2024)10.1016/j.gim.2024.101213

N/A

0DataRank · unranked

16 citations

Vikas Pejaver, Timothy Bergquist, Leslie G. Biesecker, Alicia B. Byrne, Emily A.W. Nadeau +21 more

Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2024)10.1016/j.gim.2024.101142

N/A

0DataRank · unranked

13 citations

Kristy Lee, Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung +8 more

Calibration of additional computational tools expands ClinGen recommendation options for variant classification with PP3/BP4 criteria

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.17.611902

N/A

0DataRank · unranked

13 citations

Sarah L. Stenton, Emily A.W. Nadeau, Alicia B. Byrne, Marc S. Greenblatt, Steven M. Harrison +8 more

ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2025)10.1016/j.gim.2025.101454

N/A

0DataRank · unranked

56 citations

Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung, Michael H. Gollob +11 more

Calibration of additional computational tools expands ClinGen recommendation options for variant classification with PP3/BP4 criteria

Genetics in Medicine(2025)10.1016/j.gim.2025.101402

N/A

0DataRank · unranked

45 citations

Sarah L. Stenton, Emily A.W. Nadeau, Alicia B. Byrne, Marc S. Greenblatt, Steven M. Harrison +20 more

Fitting a naturally scaled point system to the ACMG/AMP variant classification guidelines

Human Mutation(2020)10.1002/humu.24088

N/A

0DataRank · unranked

343 citations

Steven M. Harrison, Kenneth M. Boucher, Leslie G. Biesecker, Sean V. Tavtigian

Extracting and calibrating evidence of variant pathogenicity from population biobank data

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.012

N/A

0DataRank · unranked

9 citations

Tian Yu, Lara Brown, Vikas Pejaver, Matthew S. Lebo, Steven M. Harrison +2 more

Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene

BMC Medical Genetics(2020)10.1186/s12881-020-0973-x

N/A

0DataRank · unranked

31 citations

Thomas Jascur, Steven M. Harrison, Angelena Edwards, Luke Smith, Erin S. Choi +9 more

Correspondence on “The role of clinical response to treatment in determining pathogenicity of genomic variants” by Shen et al.

Genetics in Medicine(2020)10.1038/s41436-020-01032-6

N/A

0DataRank · unranked

1 citations

Steven M. Harrison, Heidi L. Rehm, Leslie G. Biesecker

ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants

UNC Libraries(2020)10.17615/0r6z-dk65

N/A

0DataRank · unranked

0 citations

Kevin Riehle, Heidi L. Rehm, Rajarshi Ghosh, Tristan H Nelson, Aaron B. Baker +16 more

Low frequency of treatable pediatric disease alleles in gnomAD: An opportunity for future genomic screening of newborns

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100059

N/A

0DataRank · unranked

12 citations

Steven M. Harrison, Jared H. Rowe, Jessica I. Gold, Elissa Furutani, Alessandra Biffi +5 more

ClinGen Variant Curation Interface: A Variant Classification Platform for the Application of Evidence Criteria from ACMG/AMP Guidelines

medRxiv(2021)10.1101/2021.02.12.21251663

N/A

0DataRank · unranked

5 citations

Matt W. Wright, Rao Madhavrao, Steven M. Harrison, Jennifer L Goldstein, Xi Luo +30 more

Creation of an Expert Curated Variant List for Clinical Genomic Test Development and Validation: A ClinGen and GeT-RM Collaborative Project

medRxiv(2021)10.1101/2021.06.09.21258594

N/A

0DataRank · unranked

1 citations

Steven M. Harrison, Edward R. Lockhart, Karl V. Voelkerding, Ira M. Lubin, ClinGen Expert Panels +4 more

Steven M. Harrison

Indexed papers

Top data-sharing exemplar

Papers