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Thomas Nate Person
Thomas Nate Person
Penn State University, Intermountain Healthcare
Verified email at psu.edu - Homepage
Title
Cited by
Cited by
Year
Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
6302017
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
FE Dewey, MF Murray, JD Overton, L Habegger, JB Leader, SN Fetterolf, ...
Science 354 (6319), aaf6814, 2016
5462016
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits
JC Randall, TW Winkler, Z Kutalik, SI Berndt, AU Jackson, KL Monda, ...
PLoS genetics 9 (6), e1003500, 2013
4652013
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
3182018
Exome sequencing–based screening for BRCA1/2 expected pathogenic variants among adult biobank participants
K Manickam, AH Buchanan, MLB Schwartz, MLG Hallquist, JL Williams, ...
JAMA Network Open 1 (5), e182140-e182140, 2018
1952018
Genomics-first evaluation of heart disease associated with titin-truncating variants
CM Haggerty, SM Damrauer, MG Levin, D Birtwell, DJ Carey, AM Golden, ...
Circulation 140 (1), 42-54, 2019
1172019
Harmonizing clinical sequencing and interpretation for the eMERGE III network
H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ...
The American Journal of Human Genetics 105 (3), 588-605, 2019
922019
Convergent horizontal gene transfer and cross-talk of mobile nucleic acids in parasitic plants
Z Yang, EK Wafula, G Kim, S Shahid, JR McNeal, PE Ralph, PR Timilsena, ...
Nature Plants 5 (9), 991-1001, 2019
752019
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome …
CM Haggerty, CA James, H Calkins, C Tichnell, JB Leader, DN Hartzel, ...
Genetics in Medicine 19 (11), 1245-1252, 2017
522017
Risk factors for acute ischemic stroke caused by anterior large vessel occlusion
P Hendrix, N Sofoluke, MD Adams, S Kunaprayoon, R Zand, ...
Stroke 50 (5), 1074-1080, 2019
362019
Cysteine-Altering NOTCH3 Variants Are a Risk Factor for Stroke in the Elderly Population
RJ Hack, JW Rutten, TN Person, J Li, A Khan, CJ Griessenauer, ...
Stroke 51 (12), 3562-3569, 2020
322020
GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms
LD Ward, HC Tu, CB Quenneville, S Tsour, AO Flynn-Carroll, MM Parker, ...
Nature Communications 12 (1), 4571, 2021
242021
SeqHBase: a big data toolset for family based sequencing data analysis
M He, TN Person, SJ Hebbring, E Heinzen, Z Ye, SJ Schrodi, ...
Journal of medical genetics 52 (4), 282-288, 2015
212015
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (5), 766-767, 2018
162018
ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma
K Praveen, GC Patel, L Gurski, AH Ayer, T Persaud, MD Still, L Miloscio, ...
Communications biology 5 (1), 1051, 2022
92022
Pilot implementation of clinical genomic data into the native electronic health record: challenges of scalability
NA Walton, DK Johnson, TN Person, JC Reynolds, MS Williams
ACI open 4 (02), e162-e166, 2020
92020
Genomic data in the electronic health record
NA Walton, DK Johnson, TN Person, S Chamala
Advances in Molecular Pathology 2 (1), 21-33, 2019
82019
Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network
JA Pacheco, LV Rasmussen, K Wiley Jr, TN Person, DJ Cronkite, S Sohn, ...
Scientific reports 13 (1), 1971, 2023
62023
The development of an infrastructure to facilitate the use of whole genome sequencing for population health
NA Walton, B Hafen, S Graceffo, N Sutherland, M Emmerson, R Palmquist, ...
Journal of Personalized Medicine 12 (11), 1867, 2022
52022
User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis
AK Rahm, NA Walton, LK Feldman, C Jenkins, T Jenkins, TN Person, ...
BMJ Health & Care Informatics 28 (1), 2021
52021
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