Hasil Pencarian - Matthew T. Oetjens

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  1. 1
    Analysis of the canid Y-chromosome phylogeny using short-read sequencing data reveals the presence of distinct haplogroups among Neolithic European dogs

    Analysis of the canid Y-chromosome phylogeny using short-read sequencing data reveals the presence of distinct haplogroups among Neolithic European dogs oleh Matthew T. Oetjens, Axel Martin, Krishna R. Veeramah, Jeffrey M. Kidd

    Diterbitkan 2018-05-01
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  2. 2
    Population stratification in the context of diverse epidemiologic surveys sans genome-wide data

    Population stratification in the context of diverse epidemiologic surveys sans genome-wide data oleh Matthew T. Oetjens, Kristin eBrown-Gentry, Robert eGoodloe, Holli H. Dilks, Dana C. Crawford

    Diterbitkan 2016-05-01
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  3. 3
    A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk

    A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk oleh Alexander S. F. Berry, Brenda M. Finucane, Scott M. Myers, Lauren K. Walsh, John M. Seibert, Christa Lese Martin, David H. Ledbetter, Matthew T. Oetjens

    Diterbitkan 2024-10-01
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  4. 4
    Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients.

    Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients. oleh Matthew T Oetjens, Jonathan Z Luo, Alexander Chang, Joseph B Leader, Dustin N Hartzel, Bryn S Moore, Natasha T Strande, H Lester Kirchner, David H Ledbetter, Anne E Justice, David J Carey, Tooraj Mirshahi

    Diterbitkan 2020-01-01
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  5. 5
    Yield of Familial Hypercholesterolemia Genetic and Phenotypic Diagnoses After Electronic Health Record and Genomic Data Screening

    Yield of Familial Hypercholesterolemia Genetic and Phenotypic Diagnoses After Electronic Health Record and Genomic Data Screening oleh Samuel S. Gidding, H. Lester Kirchner, Andrew Brangan, William Howard, Melissa A. Kelly, Kelly D. Myers, Kelly M. Morgan, Matthew T. Oetjens, Timothy C. Shuey, David Staszak, Natasha T. Strande, Nicole L. Walters, Kristen D. Yu, Katherine A. Wilemon, Marc S. Williams, Amy C. Sturm, Laney K. Jones

    Diterbitkan 2023-07-01
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  6. 6
    An evolutionary genomic approach to identify genes involved in human birth timing.

    An evolutionary genomic approach to identify genes involved in human birth timing. oleh Jevon Plunkett, Scott Doniger, Guilherme Orabona, Thomas Morgan, Ritva Haataja, Mikko Hallman, Hilkka Puttonen, Ramkumar Menon, Edward Kuczynski, Errol Norwitz, Victoria Snegovskikh, Aarno Palotie, Leena Peltonen, Vineta Fellman, Emily A DeFranco, Bimal P Chaudhari, Tracy L McGregor, Jude J McElroy, Matthew T Oetjens, Kari Teramo, Ingrid Borecki, Justin Fay, Louis Muglia

    Diterbitkan 2011-04-01
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  7. 7
    Comprehensive identification of somatic nucleotide variants in human brain tissue

    Comprehensive identification of somatic nucleotide variants in human brain tissue oleh Yifan Wang, Taejeong Bae, Jeremy Thorpe, Maxwell A. Sherman, Attila G. Jones, Sean Cho, Kenneth Daily, Yanmei Dou, Javier Ganz, Alon Galor, Irene Lobon, Reenal Pattni, Chaggai Rosenbluh, Simone Tomasi, Livia Tomasini, Xiaoxu Yang, Bo Zhou, Schahram Akbarian, Laurel L. Ball, Sara Bizzotto, Sarah B. Emery, Ryan Doan, Liana Fasching, Yeongjun Jang, David Juan, Esther Lizano, Lovelace J. Luquette, John B. Moldovan, Rujuta Narurkar, Matthew T. Oetjens, Rachel E. Rodin, Shobana Sekar, Joo Heon Shin, Eduardo Soriano, Richard E. Straub, Weichen Zhou, Andrew Chess, Joseph G. Gleeson, Tomas Marquès-Bonet, Peter J. Park, Mette A. Peters, Jonathan Pevsner, Christopher A. Walsh, Daniel R. Weinberger, Brain Somatic Mosaicism Network, Flora M. Vaccarino, John V. Moran, Alexander E. Urban, Jeffrey M. Kidd, Ryan E. Mills, Alexej Abyzov

    Diterbitkan 2021-03-01
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