Matrix Gla protein polymorphism rs1800801 associates with recurrence of ischemic stroke
Hendrix, Philipp, Sofoluke, Nelson, Adams, Matthew, Kunaprayoon, Saran, Zand, Ramin, Kolinovsky, Amy N, Person, Thomas N, Gupta, Mudit, Goren, Oded, Kirchner, H Lester, Schirmer, Clemens M, Rost, Natalia S, Faber, James E, Griessenauer, Christoph J
Published in PloS one (25.06.2020)
Published in PloS one (25.06.2020)
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User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis
Kulchak Rahm, Alanna, Walton, Nephi A, Feldman, Lynn K, Jenkins, Conner, Jenkins, Troy, Person, Thomas N, Peterson, Joeseph, Reynolds, Jonathon C, Robinson, Peter N, Woltz, Makenzie A, Williams, Marc S, Segal, Michael M
Published in BMJ health & care informatics (07.05.2021)
Published in BMJ health & care informatics (07.05.2021)
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Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population
Miller, Jason E, Metpally, Raghu P, Person, Thomas N, Krishnamurthy, Sarathbabu, Dasari, Venkata Ramesh, Shivakumar, Manu, Lavage, Daniel R, Cook, Adam M, Carey, David J, Ritchie, Marylyn D, Kim, Dokyoon, Gogoi, Radhika
Published in BMC medical genomics (03.05.2019)
Published in BMC medical genomics (03.05.2019)
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Correction to: Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population
Miller, Jason E, Metpally, Raghu P, Person, Thomas N, Krishnamurthy, Sarathbabu, Dasari, Venkata Ramesh, Shivakumar, Manu, Lavage, Daniel R, Cook, Adam M, Carey, David J, Ritchie, Marylyn D, Kim, Dokyoon, Gogoi, Radhika
Published in BMC medical genomics (22.05.2019)
Published in BMC medical genomics (22.05.2019)
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Genomic Data in the Electronic Health Record
Walton, Nephi A., MD, MS, Johnson, Darren K., MS, Person, Thomas N., MS, Chamala, Srikar, PhD
Published in Advances in Molecular Pathology (01.11.2019)
Published in Advances in Molecular Pathology (01.11.2019)
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Journal Article
Cysteine-Altering NOTCH3 Variants Are a Risk Factor for Stroke in the Elderly Population
Hack, Remco J, Rutten, Julie W, Person, Thomas N, Li, Jiang, Khan, Ayesha, Griessenauer, Christoph J, Abedi, Vida, Lesnik Oberstein, Saskia A.J, Zand, Ramin
Published in Stroke (1970) (01.12.2020)
Published in Stroke (1970) (01.12.2020)
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Risk Factors for Acute Ischemic Stroke Caused by Anterior Large Vessel Occlusion
Hendrix, Philipp, Sofoluke, Nelson, Adams, Matthew D, Kunaprayoon, Saran, Zand, Ramin, Kolinovsky, Amy N, Person, Thomas N, Gupta, Mudit, Goren, Oded, Schirmer, Clemens M, Rost, Natalia S, Faber, James E, Griessenauer, Christoph J
Published in Stroke (1970) (01.05.2019)
Published in Stroke (1970) (01.05.2019)
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Journal Article
Sex-specific association of RAGE and HMGB1 genotype variations with susceptibility to ischemic stroke in Caucasians
Hendrix, Philipp, Berger, Andrea, Person, Thomas N., Gupta, Mudit, Zand, Ramin, Li, Jiang, Abedi, Vida, Goren, Oded, Schirmer, Clemens M., Griessenauer, Christoph J.
Published in Journal of clinical neuroscience (01.12.2021)
Published in Journal of clinical neuroscience (01.12.2021)
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Journal Article
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]
Hendrix, Philipp, Berger, Andrea, Person, Thomas N., Gupta, Mudit, Zand, Ramin, Li, Jiang, Abedi, Vida, Goren, Oded, Schirmer, Clemens M., Griessenauer, Christoph J.
Published in Journal of clinical neuroscience (01.03.2022)
Published in Journal of clinical neuroscience (01.03.2022)
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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
Haggerty, Christopher M, James, Cynthia A, Calkins, Hugh, Tichnell, Crystal, Leader, Joseph B, Hartzel, Dustin N, Nevius, Christopher D, Pendergrass, Sarah A, Person, Thomas N, Schwartz, Marci, Ritchie, Marylyn D, Carey, David J, Ledbetter, David H, Williams, Marc S, Dewey, Frederick E, Lopez, Alexander, Penn, John, Overton, John D, Reid, Jeffrey G, Lebo, Matthew, Mason-Suares, Heather, Austin-Tse, Christina, Rehm, Heidi L, Delisle, Brian P, Makowski, Daniel J, Mehra, Vishal C, Murray, Michael F, Fornwalt, Brandon K
Published in Genetics in medicine (01.11.2017)
Published in Genetics in medicine (01.11.2017)
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SeqHBase: a big data toolset for family based sequencing data analysis
He, Min, Person, Thomas N, Hebbring, Scott J, Heinzen, Ethan, Ye, Zhan, Schrodi, Steven J, McPherson, Elizabeth W, Lin, Simon M, Peissig, Peggy L, Brilliant, Murray H, O'Rawe, Jason, Robison, Reid J, Lyon, Gholson J, Wang, Kai
Published in Journal of medical genetics (01.04.2015)
Published in Journal of medical genetics (01.04.2015)
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Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants
Haggerty, Christopher M, Damrauer, Scott M, Levin, Michael G, Birtwell, David, Carey, David J, Golden, Alicia M, Hartzel, Dustin N, Hu, Yirui, Judy, Renae, Kelly, Melissa A, Kember, Rachel L, Lester Kirchner, H, Leader, Joseph B, Liang, Lusha, McDermott-Roe, Chris, Babu, Apoorva, Morley, Michael, Nealy, Zachariah, Person, Thomas N, Pulenthiran, Arichanah, Small, Aeron, Smelser, Diane T, Stahl, Richard C, Sturm, Amy C, Williams, Heather, Baras, Aris, Margulies, Kenneth B, Cappola, Thomas P, Dewey, Frederick E, Verma, Anurag, Zhang, Xinyuang, Correa, Adolfo, Hall, Michael E, Wilson, James G, Ritchie, Marylyn D, Rader, Daniel J, Murray, Michael F, Fornwalt, Brandon K, Arany, Zoltan
Published in Circulation (New York, N.Y.) (02.07.2019)
Published in Circulation (New York, N.Y.) (02.07.2019)
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The Development of an Infrastructure to Facilitate the Use of Whole Genome Sequencing for Population Health
Walton, Nephi A, Hafen, Brent, Graceffo, Sara, Sutherland, Nykole, Emmerson, Melanie, Palmquist, Rachel, Formea, Christine M, Purcell, Maricel, Heale, Bret, Brown, Matthew A, Danford, Christopher J, Rachamadugu, Sumathi I, Person, Thomas N, Shortt, Katherine A, Christensen, G Bryce, Evans, Jared M, Raghunath, Sharanya, Johnson, Christopher P, Knight, Stacey, Le, Viet T, Anderson, Jeffrey L, Van Meter, Margaret, Reading, Teresa, Haslem, Derrick S, Hansen, Ivy C, Batcher, Betsey, Barker, Tyler, Sheffield, Travis J, Yandava, Bhaskara, Taylor, David P, Ranade-Kharkar, Pallavi, Giauque, Christopher C, Eyring, Kenneth R, Breinholt, Jesse W, Miller, Mickey R, Carter, Payton R, Gillman, Jason L, Gunn, Andrew W, Knowlton, Kirk U, Bonkowsky, Joshua L, Stefansson, Kari, Nadauld, Lincoln D, McLeod, Howard L
Published in Journal of personalized medicine (08.11.2022)
Published in Journal of personalized medicine (08.11.2022)
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Journal Article
Electronic Health Record Phenotype in Subjects with Genetic Variants Associated with Arrhythmogenic Right Ventricular Cardiomyopathy: A Study in 30,716 Subjects with Exome Sequencing: Genotype-Phenotype Association in Incidental ARVC Genetic Findings
Haggerty, Christopher M., James, Cynthia A., Calkins, Hugh, Tichnell, Crystal, Leader, Joseph B., Hartzel, Dustin N., Nevius, Christopher D., Pendergrass, Sarah A., Person, Thomas N., Schwartz, Marci, Ritchie, Marylyn D., Carey, David J., Ledbetter, David H., Williams, Marc S., Dewey, Frederick E., Lopez, Alexander, Penn, John, Overton, John D., Reid, Jeffrey G., Lebo, Matthew, Mason-Suares, Heather, Austin-Tse, Christina, Rehm, Heidi L., Delisle, Brian P., Makowski, Daniel J., Mehra, Vishal C., Murray, Michael F., Fornwalt, Brandon K.
Published in Genetics in medicine (04.05.2017)
Published in Genetics in medicine (04.05.2017)
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