Publications by authors named "Steven Harrison"

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Navigating in Zero-Visibility: A Haptic Guidance System for Improving Egress and Situation Awareness of Professional Firefighters.
Andrew Emlyn Slater, Spencer Ferris, James A Dixon, Christopher Renshaw, Timothy E Moore, Steven J Harrison

Hum Factors· November 2025

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Understanding the effects of real-time head position feedback on postural sway in terms of changes in underlying deterministic and stochastic dynamical processes.
Steven J Harrison, Benjamin De Bari, Ryan Poutre, Jeffrey M Kinsella-Shaw

PLoS One· October 2025

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Specification of frequency criteria for secondary findings genes to improve variant classification concordance.
Jennifer J Johnston, Kristy Lee, Deborah I Ritter, Steven M Harrison, Leslie G Biesecker

bioRxiv· September 2025

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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).
Kristy Lee, Noura S Abul-Husn, Laura M Amendola, Kyle B Brothers, Wendy K Chung, Steven M Harrison

Genet Med· August 2025

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Extracting and calibrating evidence of variant pathogenicity from population biobank data.
Vineel Bhat, Tian Yu, Lara Brown, Vikas Pejaver, Matthew Lebo, Steven Harrison

Am J Hum Genet· August 2025

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Understanding how gene-disease relationships can impact clinical utility: adaptations and challenges in hereditary cancer testing.
Jennifer Herrera-Mullar, Carolyn Horton, Amybeth Weaver, Meghan Towne, Jennifer M Huang, Steven M Harrison

Genome Med· July 2025

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Distinct rates of VUS reclassification are observed when subclassifying VUS by evidence level.
Gwendolyn Bennett, Izabela Karbassi, Wenjie Chen, Steven M Harrison, Matthew S Lebo

Genet Med· June 2025

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Calibration of additional computational tools expands ClinGen recommendation options for variant classification with PP3/BP4 criteria.
Timothy Bergquist, Sarah L Stenton, Emily A W Nadeau, Alicia B Byrne, Marc S Greenblatt, Steven M Harrison

Genet Med· June 2025

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Extracting and calibrating evidence of variant pathogenicity from population biobank data.
Vineel Bhat, Tian Yu, Lara Brown, Vikas Pejaver, Matthew Lebo, Steven Harrison

medRxiv· May 2025

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An Ecological-Dynamical Perspective on Latash's Misnomers in Motor Control.
Raoul M Bongers, Vitor L S Profeta, Steven J Harrison

Motor Control· January 2025

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Assessment of the evidence yield for the calibrated PP3/BP4 computational recommendations.
Sarah L Stenton, Vikas Pejaver, Timothy Bergquist, Leslie G Biesecker, Alicia B Byrne, Steven M Harrison

Genet Med· November 2024

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Distinct rates of VUS reclassification are observed when subclassifying VUS by evidence level.
Gwendolyn Bennett, Izabela Karbassi, Wenjie Chen, Steven M Harrison, Matthew S Lebo

medRxiv· November 2024

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Calibration of additional computational tools expands ClinGen recommendation options for variant classification with PP3/BP4 criteria.
Timothy Bergquist, Sarah L Stenton, Emily A W Nadeau, Alicia B Byrne, Marc S Greenblatt, Steven M Harrison

bioRxiv· September 2024

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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).
Adam S Gordon, Kristy Lee, Noura S Abul-Husn, Laura M Amendola, Kyle Brothers, Steven M Harrison

Genet Med· July 2024

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Clinical interpretation of KCNH2 variants using a robust PS3/BS3 functional patch-clamp assay.
Kate L Thomson, Connie Jiang, Ebony Richardson, Dominik S Westphal, Tobias Burkard, Steven M Harrison

HGG Adv· April 2024

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Genetic sex validation for sample tracking in next-generation sequencing clinical testing.
Jianhong Hu, Viktoriya Korchina, Hana Zouk, Maegan V Harden, David Murdock, Steven M Harrison

BMC Res Notes· March 2024

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Assessment of the evidence yield for the calibrated PP3/BP4 computational recommendations.
Sarah L Stenton, Vikas Pejaver, Timothy Bergquist, Leslie G Biesecker, Alicia B Byrne, Steven Harrison

medRxiv· March 2024

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Diagnostic Outcomes of Concurrent DNA and RNA Sequencing in Individuals Undergoing Hereditary Cancer Testing.
Carolyn Horton, Lily Hoang, Heather Zimmermann, Colin Young, Jessica Grzybowski, Steven Harrison

JAMA Oncol· February 2024

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ClinGen guidance for use of the PP1/BS4 co-segregation and PP4 phenotype specificity criteria for sequence variant pathogenicity classification.
Leslie G Biesecker, Alicia B Byrne, Steven M Harrison, Tina Pesaran, Alejandro A Schäffer

Am J Hum Genet· January 2024

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The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change.
Heidi L Rehm, Joseph T Alaimo, Swaroop Aradhya, Pinar Bayrak-Toydemir, Hunter Best, Steven M Harrison

Genet Med· December 2023

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Advanced variant classification framework reduces the false positive rate of predicted loss-of-function variants in population sequencing data.
Moriel Singer-Berk, Sanna Gudmundsson, Samantha Baxter, Eleanor G Seaby, Eleina England, Steven M Harrison

Am J Hum Genet· September 2023

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Genetic Sex Validation for Sample Tracking in Clinical Testing.
Jianhong Hu, Viktoriya Korchina, Hana Zouk, Maegan V Harden, David Murdock, Steven M Harrison

Res Sq· September 2023

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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).
David T Miller, Kristy Lee, Noura S Abul-Husn, Laura M Amendola, Kyle Brothers, Steven M Harrison

Genet Med· August 2023

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Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup.
Logan C Walker, Miguel de la Hoya, George A R Wiggins, Amanda Lindy, Lisa M Vincent, Steven M Harrison

Am J Hum Genet· July 2023

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Advanced variant classification framework reduces the false positive rate of predicted loss of function (pLoF) variants in population sequencing data.
Moriel Singer-Berk, Sanna Gudmundsson, Samantha Baxter, Eleanor G Seaby, Eleina England, Steven M Harrison

medRxiv· March 2023

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