Publications by authors named "Thomas Person"

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Enabling the clinical application of artificial intelligence in genomics: a perspective of the AMIA Genomics and Translational Bioinformatics Workgroup.
Nephi A Walton, Radha Nagarajan, Chen Wang, Murat Sincan, Robert R Freimuth, Thomas Nate Person

J Am Med Inform Assoc· January 2024

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Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.
Jennifer A Pacheco, Luke V Rasmussen, Ken Wiley, Thomas Nate Person, David J Cronkite

Sci Rep· February 2023

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The Development of an Infrastructure to Facilitate the Use of Whole Genome Sequencing for Population Health.
Nephi A Walton, Brent Hafen, Sara Graceffo, Nykole Sutherland, Melanie Emmerson, Thomas N Person

J Pers Med· November 2022

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Creating a Home for Genomic Data in the Electronic Health Record.
Nephi Walton, Darren Johnson, Bret Heale, Thomas Person, Marc Williams

AMIA Annu Symp Proc· April 2022

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Erratum to "Sex-specific association of RAGE and HMGB1 genotype variations with susceptibility to ischemic stroke in Caucasians" [J. Clin. Neurosci. 94C (2021) 328-331].
Philipp Hendrix, Andrea Berger, Thomas N Person, Mudit Gupta, Ramin Zand

J Clin Neurosci· March 2022

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Sex-specific association of RAGE and HMGB1 genotype variations with susceptibility to ischemic stroke in Caucasians.
Philipp Hendrix, Andrea Berger, Thomas N Person, Mudit Gupta, Ramin Zand

J Clin Neurosci· December 2021

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User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis.
Alanna Kulchak Rahm, Nephi A Walton, Lynn K Feldman, Conner Jenkins, Troy Jenkins, Thomas N Person

BMJ Health Care Inform· May 2021

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Cysteine-Altering Variants Are a Risk Factor for Stroke in the Elderly Population.
Remco J Hack, Julie W Rutten, Thomas N Person, Jiang Li, Ayesha Khan

Stroke· December 2020

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Matrix Gla protein polymorphism rs1800801 associates with recurrence of ischemic stroke.
Philipp Hendrix, Nelson Sofoluke, Matthew Adams, Saran Kunaprayoon, Ramin Zand, Thomas N Person

PLoS One· August 2020

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Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Valérie Turcot, Yingchang Lu, Heather M Highland, Claudia Schurmann, Anne E Justice, Thomas N Person

Nat Genet· July 2019

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Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants.
Christopher M Haggerty, Scott M Damrauer, Michael G Levin, David Birtwell, David J Carey, Thomas N Person

Circulation· July 2019

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Risk Factors for Acute Ischemic Stroke Caused by Anterior Large Vessel Occlusion.
Philipp Hendrix, Nelson Sofoluke, Matthew D Adams, Saran Kunaprayoon, Ramin Zand, Thomas N Person

Stroke· May 2019

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Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population.
Jason E Miller, Raghu P Metpally, Thomas N Person, Sarathbabu Krishnamurthy, Venkata Ramesh Dasari

BMC Med Genomics· May 2019

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Correction to: Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population.
Jason E Miller, Raghu P Metpally, Thomas N Person, Sarathbabu Krishnamurthy, Venkata Ramesh Dasari

BMC Med Genomics· May 2019

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Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Valérie Turcot, Yingchang Lu, Heather M Highland, Claudia Schurmann, Anne E Justice, Thomas N Person

Nat Genet· May 2018

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Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Valérie Turcot, Yingchang Lu, Heather M Highland, Claudia Schurmann, Anne E Justice, Thomas N Person

Nat Genet· May 2018

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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Valérie Turcot, Yingchang Lu, Heather M Highland, Claudia Schurmann, Anne E Justice, Thomas N Person

Nat Genet· January 2018

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Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing.
Christopher M Haggerty, Cynthia A James, Hugh Calkins, Crystal Tichnell, Joseph B Leader, Thomas N Person

Genet Med· November 2017

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Rare and low-frequency coding variants alter human adult height.
Eirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, Ken Sin Lo, Andrew R Wood, Thomas N Person

Nature· February 2017

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SeqHBase: a big data toolset for family based sequencing data analysis.
Min He, Thomas N Person, Scott J Hebbring, Ethan Heinzen, Zhan Ye

J Med Genet· April 2015

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Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.
Joshua C Randall, Thomas W Winkler, Zoltán Kutalik, Sonja I Berndt, Anne U Jackson, Thomas Person

PLoS Genet· June 2013

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Interrupted aortic arch in the adult.
Elizabeth A Gordon, Thomas Person, Minoo Kavarana, John S Ikonomidis

J Card Surg· July 2011

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Management of acute esophageal necrosis syndrome.
Conor W McLaughlin, Thomas D Person, Chadrick E Denlinger

J Thorac Cardiovasc Surg· March 2011

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