Výsledky vyhledávání - Matthew T. Oetjens

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  1. 1
    Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders

    Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders Autor Matthew T. Oetjens, Melissa Kelly, Amy C. Sturm, C. L. Martin, David H. Ledbetter

    Vydáno 2019
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  2. 2
    X and Y gene dosage effects are primary contributors to human sexual dimorphism: The case of height

    X and Y gene dosage effects are primary contributors to human sexual dimorphism: The case of height Autor Alexander S. F. Berry, Brenda Finucane, Scott M. Myers, Alastair J. Martin, David H. Ledbetter, Huntington F. Willard, Matthew T. Oetjens

    Vydáno 2025
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  3. 3
    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 Autor Matthew T. Oetjens, Jonathan Z. Luo, Alex R. 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

    Vydáno 2020
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  4. 4
    Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population

    Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population Autor Alastair J. Martin, Karen E. Wain, Matthew T. Oetjens, Kasia Tolwinski, Emily Palen, Abby E. Hare-Harris, Lukas Habegger, Evan K. Maxwell, Jeffrey G. Reid, Lauren K. Walsh, Scott M. Myers, David H. Ledbetter

    Vydáno 2020
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  5. 5
    Ancient European dog genomes reveal continuity since the Early Neolithic

    Ancient European dog genomes reveal continuity since the Early Neolithic Autor Laura R. Botigué, Shiya Song, Amelie Scheu, Shyamalika Gopalan, Amanda L. Pendleton, Matthew T. Oetjens, Angela M. Taravella Oill, Timo Seregély, Andrea Zeeb‐Lanz, Rose-Marie Arbogast, Dean Bobo, Kevin G. Daly, Martina Unterländer, Joachim Bürger, Jeffrey M. Kidd, Krishna R. Veeramah

    Vydáno 2017
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  6. 6
    Predicting Clopidogrel Response Using DNA Samples Linked to an Electronic Health Record

    Predicting Clopidogrel Response Using DNA Samples Linked to an Electronic Health Record Autor Jessica Delaney, Andrea H. Ramirez, Erica Bowton, Jill M. Pulley, Melissa Basford, Jonathan S. Schildcrout, Y. Shi, Raquel Zink, Matthew T. Oetjens, Hai-liang Xu, John H. Cleator, Eiman Jahangir, Marylyn D. Ritchie, Daniel R. Masys, Dan M. Roden, Dana C. Crawford, Joshua C. Denny

    Vydáno 2011
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  7. 7
    Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases

    Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases Autor Rebecca I. Torene, María J. Guillen Sacoto, Francisca Millan, Zhancheng Zhang, Stephen McGee, Matthew T. Oetjens, Elizabeth M. Heise, Karen Chong, Richard Sidlow, Lauren O’Grady, Inderneel Sahai, Christa Lese Martin, David H. Ledbetter, Scott M. Myers, Kevin J. Mitchell, Kyle Retterer

    Vydáno 2023
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  8. 8
    Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy

    Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy Autor Andrés Moreno-De-Luca, Francisca Millan, Denis R. Pesacreta, Houda Zghal Elloumi, Matthew T. Oetjens, Claire Teigen, Karen E. Wain, Julie Scuffins, Scott M. Myers, Rebecca I. Torene, Vladimir G. Gainullin, Kevin J. Arvai, H. Lester Kirchner, David H. Ledbetter, Kyle Retterer, Christa Lese Martin

    Vydáno 2021
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  9. 9
    Predicting warfarin dosage in European–Americans and African–Americans using DNA samples linked to an electronic health record

    Predicting warfarin dosage in European–Americans and African–Americans using DNA samples linked to an electronic health record Autor Andrea H. Ramirez, Yaping Shi, Jonathan S. Schildcrout, Jessica Delaney, Hua Xu, Matthew T. Oetjens, Rebecca L. Zuvich, Melissa Basford, Erica Bowton, Min Jiang, Peter Speltz, Raquel Zink, James D. Cowan, Jill M. Pulley, Marylyn D. Ritchie, Daniel R. Masys, Dan M. Roden, Dana C. Crawford, Joshua C. Denny

    Vydáno 2012
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  10. 10
    An Evolutionary Genomic Approach to Identify Genes Involved in Human Birth Timing

    An Evolutionary Genomic Approach to Identify Genes Involved in Human Birth Timing Autor Jevon Plunkett, Scott W Doniger, Guilherme Müller Orabona, Thomas Morgan, Ritva Haataja, Mikko Hallman, Hilkka Puttonen, Ramkumar Menon, Edward Kuczynski, Errol R. Norwitz, Victoria Snegovskikh, Aarno Palotie, Leena Peltonen, Vineta Fellman, Emily DeFranco, Bimal P. Chaudhari, Tracy L. McGregor, Jude J. McElroy, Matthew T. Oetjens, Kari Teramo, Ingrid B. Borecki, Justin C. Fay, Louis J. Muglia

    Vydáno 2011
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  11. 11
    Association of the FTO Obesity Risk Variant rs8050136 With Percentage of Energy Intake From Fat in Multiple Racial/Ethnic Populations

    Association of the FTO Obesity Risk Variant rs8050136 With Percentage of Energy Intake From Fat in Multiple Racial/Ethnic Populations Autor Sungshim Lani Park, Iona Cheng, Sarah A. Pendergrass, Anna Kucharska‐Newton, Unhee Lim, José Luis Ambite, Christian Caberto, Kristine R. Monroe, Fredrick R. Schumacher, Lucia A. Hindorff, Matthew T. Oetjens, Sarah Wilson, Robert Goodloe, Shelly-Ann Love, Brian E. Henderson, Laurence N. Kolonel, Christopher A. Haiman, Dana C. Crawford, Kari E. North, Gerardo Heiss, Marylyn D. Ritchie, Lynne R. Wilkens, Loı̈c Le Marchand

    Vydáno 2013
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  12. 12
    Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis

    Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis Autor Gemme Campbell‐Salome, Laney K. Jones, Max Masnick, Nephi Walton, Catherine D. Ahmed, Adam H. Buchanan, Andrew Brangan, Edward D. Esplin, David Kann, Ilene Ladd, Melissa Kelly, Iris Kindt, H. Lester Kirchner, Mary P. McGowan, Megan McMinn, Ana Morales, Kelly D. Myers, Matthew T. Oetjens, Alanna Kulchak Rahm, Tara Schmidlen, Amanda Sheldon, Emilie Simmons, Moran Snir, Natasha T. Strande, Nicole L. Walters, Katherine Wilemon, Marc S. Williams, Samuel S. Gidding, Amy C. Sturm

    Vydáno 2021
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  13. 13
    Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study

    Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study Autor Minoli A. Perera, Larisa H. Cavallari, Nita A. Limdi, Eric R. Gamazon, Anuar Konkashbaev, Roxana Daneshjou, Anna Pluzhnikov, Dana C. Crawford, Jelai Wang, Nianjun Liu, Nicholas P. Tatonetti, Stéphane Bourgeois, Harumi Takahashi, Yukiko Bradford, Benjamin Burkley, Robert J. Desnick, Jonathan L. Halperin, Sherief Khalifa, Taimour Langaee, Steven A. Lubitz, Edith A. Nutescu, Matthew T. Oetjens, Mohamed H. Shahin, Shitalben Patel, Hersh Sagreiya, Matthew Tector, Karen E. Weck, Mark J. Rieder, Stuart A. Scott, Alan H.B. Wu, James K. Burmester, Mia Wadelius, Panos Deloukas, Michael J. Wagner, Taisei Mushiroda, Michiaki Kubo, Dan M. Roden, Nancy J. Cox, Russ B. Altman, Teri E. Klein, Yusuke Nakamura, Julie A. Johnson

    Vydáno 2013
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  14. 14
    Comprehensive identification of somatic nucleotide variants in human brain tissue

    Comprehensive identification of somatic nucleotide variants in human brain tissue Autor Yifan Wang, Taejeong Bae, Jeremy Thorpe, Maxwell A. Sherman, Attila Jones, Sean Cho, Kenneth Daily, Yanmei Dou, Javier Ganz, Alon Galor, Irene Lobón, Reenal Pattni, Chaggai Rosenbluh, Simone Tomasi, Livia Tomasini, Xiaoxu Yang, Bo Zhou, Schahram Akbarian, Laurel Ball, Sara Bizzotto, Sarah B. Emery, Ryan N. 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, Tomàs Marquès‐Bonet, Peter J. Park, Mette A. Peters, Jonathan Pevsner, Christopher A. Walsh, Daniel R. Weinberger, Flora M. Vaccarino, John V. Moran, Alexander E. Urban, Jeffrey M. Kidd, Ryan E. Mills, Alexej Abyzov

    Vydáno 2021
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  15. 15
    Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

    Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank Autor Sean J. Jurgens, Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, James P. Pirruccello, Jennifer L. Halford, Lu‐Chen Weng, Victor Nauffal, Carolina Roselli, Amelia Weber Hall, Matthew T. Oetjens, Braxton Lagerman, David P. vanMaanen, Gonçalo R. Abecasis, Xiaodong Bai, Suganthi Balasubramanian, Aris Baras, Christina Beechert, Boris Boutkov, Michael Cantor, Giovanni Coppola, Tanima De, Andrew Deubler, Aris N. Economides, Gisu Eom, Manuel A. R. Ferreira, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Lukas Habegger, Alicia Hawes, Marcus B. Jones, Katia Karalis, Shareef Khalid, Olga Krasheninina, Rouel Lanche, Michael Lattari, Dadong Li, Alexander Lopez, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Lyndon J. Mitnaul, Mona Nafde, Jonas B. Nielsen, Sean O’Keeffe, Max Orelus, John D. Overton, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Jeffrey G. Reid, William Salerno, Thomas D. Schleicher, Alan R. Shuldiner, Katherine Siminovitch, Jeffrey Staples, Ricardo H. Ulloa, Niek Verweij, Louis Widom, Sarah E. Wolf, Krishna G. Aragam, Kathryn L. Lunetta, Christopher M. Haggerty, Steven A. Lubitz, Patrick T. Ellinor

    Vydáno 2022
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  16. 16
    Family-GWAS reveals effects of environment and mating on genetic associations

    Family-GWAS reveals effects of environment and mating on genetic associations Autor Tammy Tan, Hariharan Jayashankar, Junming Guan, Seyed Moeen Nehzati, Mahdi Mir, Michael Bennett, Esben Agerbo, Rafael Ahlskog, Ville Anapaz, Bjørn Olav Åsvold, Stefania Benónísdóttir, Laxmi Bhatta, Dorret I. Boomsma, Ben Brumpton, Archie Campbell, Christopher F. Chabris, Rosa Cheesman, Zhengming Chen, Eco J. C. de Geus, Erik A. Ehli, Abdelrahman G. Elnahas, Andrea Ganna, Alexandros Giannelis, Liisa Hakaste, Ailin Falkmo Hansen, Alexandra Havdahl, Caroline Hayward, Jouke‐Jan Hottenga, Mikkel Aagaard Houmark, Kristian Hveem, Jaakko Kaprio, Arnulf Langhammer, Antti Latvala, James J. Lee, Mikko Lehtovirta, Liming Li, Kuang Lin, Richard Karlsson Linnér, Stefano Lombardi, Nicholas G. Martin, Matt McGue, Sarah E. Medland, Andres Metspalu, Brittany L. Mitchell, Guiyan Ni, Ilja M. Nolte, Matthew T. Oetjens, Sven Oskarsson, Teemu Palviainen, Rashmi B. Prasad, Anu Reigo, Kadri Reis, Julia Sidorenko, Karri Silventoinen, Harold Snieder, Jaakko Tuomilehto, Bjarni J. Vilhjálmsson, Robin Walters, Emily A. Willoughby, Bendik S. Winsvold, Eivind Ystrøm, Jonathan Flint, Loic Yengo, Peter M. Visscher, Augustine Kong, Elliot M. Tucker‐Drob, Richard Border, David Cesarini, Patrick Turley, Aysu Okbay, Daniel J. Benjamin, Alexander I. Young

    Vydáno 2024
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  17. 17
    Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network

    Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network Autor Michael J. McConnell, John V. Moran, Alexej Abyzov, Schahram Akbarian, Taejeong Bae, Isidro Cortés‐Ciriano, Jennifer A. Erwin, Liana Fasching, Diane A. Flasch, Donald Freed, Javier Ganz, Andrew E. Jaffe, Kenneth Y. Kwan, Min‐Seok Kwon, Michael A. Lodato, Ryan E. Mills, Apuã C.M. Paquola, Rachel E. Rodin, Chaggai Rosenbluh, Nenad Šestan, Maxwell A. Sherman, Joo Heon Shin, Saera Song, Richard E. Straub, Jeremy Thorpe, Daniel R. Weinberger, Alexander E. Urban, Bo Zhou, Fred H. Gage, Thomas Lehner, Geetha Senthil, Christopher A. Walsh, Andrew Chess, Eric Courchesne, Joseph G. Gleeson, Jeffrey M. Kidd, Peter J. Park, Jonathan Pevsner, Flora M. Vaccarino, Alison R. Barton, Stefan Bekiranov, Craig L. Bohrson, Ian Burbulis, William D. Chronister, Gianfilippo Coppola, Kenneth Daily, Alissa M. D’Gama, Sarah B. Emery, Trenton J. Frisbie, Tianliuyun Gao, Attila Gulyás-Kovács, Mark F. Haakenson, Jason M. Keil, Huira C. Kopera, Mandy M. Lam, Eunjung Alice Lee, Tomàs Marquès‐Bonet, Gary W. Mathern, John B. Moldovan, Matthew T. Oetjens, Larsson Omberg, Mette A. Peters, Sirisha Pochareddy, Tiziano Pramparo, Aakrosh Ratan, Tiziana Sanavia, Lei Shi, Mario Škarica, Jia Wang, Meiyan Wang, Yifan Wang, Margaret E. Wierman, Matthew J. Wolpert, Mollie B. Woodworth, Xuefang Zhao, Weichen Zhou

    Vydáno 2017
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  18. 18
    GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms

    GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms Autor Lucas D. Ward, Ho-Chou Tu, Chelsea B. Quenneville, Shira Tsour, Alexander O. Flynn-Carroll, Margaret M. Parker, Aimée M. Deaton, Patrick Haslett, Luca A. Lotta, Niek Verweij, Manuel A. R. Ferreira, Gonçalo R. Abecasis, Michael Cantor, Giovanni Coppola, Jeffrey G. Reid, Alan R. Shuldiner, Katia Karalis, Katherine Siminovitch, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Xiaodong Bai, Suganthi Balasubramanian, Andrew Blumenfeld, Boris Boutkov, Gisu Eom, Lukas Habegger, Alicia Hawes, Shareef Khalid, Olga Krasheninina, Rouel Lanche, Adam J. Mansfield, Evan K. Maxwell, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Razvan Panea, Tommy Polanco, Ayesha Rasool, William Salerno, Jeffrey Staples, Dadong Li, Deepika Sharma, Fabrício S. P. Kury, Jonas B. Nielsen, Tanima De, Marcus B. Jones, Jason Mighty, Michelle G. LeBlanc, Lyndon J. Mitnaul, Aris Baras, Michael Cantor, Aris N. Economides, Jeffrey G. Reid, Andrew Deubler, Katherine Siminovitch, Lance J. Adams, Jackie Blank, Dale L. Bodian, Derek Boris, Adam H. Buchanan, David J. Carey, Ryan Colonie, F. Daniel Davis, Dustin N. Hartzel, Melissa Kelly, H. Lester Kirchner, Joseph B. Leader, David H. Ledbetter, J. Neil Manus, Christa Lese Martin, Raghu Metpally, Michelle N. Meyer, Tooraj Mirshahi, Matthew T. Oetjens, Thomas N. Person, Christopher D. Still, Natasha T. Strande, Amy C. Sturm, Jen Wagner, Marc S. Williams, Aris Baras, Gregory Hinkle, Paul Nioi

    Vydáno 2021
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  19. 19
    Whole-genome sequencing reveals host factors underlying critical COVID-19

    Whole-genome sequencing reveals host factors underlying critical COVID-19 Autor Athanasios Kousathanas, Erola Pairo‐Castineira, Konrad Rawlik, A. Stuckey, Christopher A. Odhams, Susan Walker, Clark D Russell, Tomas Malinauskas, Yang Wu, Jonathan Millar, Xia Shen, Katherine S. Elliott, Fiona Griffiths, Wilna Oosthuyzen, Kirstie Morrice, Seán Keating, Bo Wang, Daniel R. Rhodes, Lucija Klarić, Marie Zechner, Nick Parkinson, Afshan Siddiq, Peter Goddard, Sally Donovan, David M. Maslove, Alistair Nichol, Malcolm G. Semple, Tala Zainy, F. Maleady-Crowe, Linda Todd, Shahla Salehi, Julian C. Knight, Greg Elgar, G. C. Chan, Prabhu Arumugam, Christine Patch, Augusto Rendon, David Bentley, Clare Kingsley, Jack A. Kosmicki, Julie Horowitz, Aris Baras, Gonçalo R. Abecasis, Manuel A. R. Ferreira, Anne E. Justice, Tooraj Mirshahi, Matthew T. Oetjens, Daniel J. Rader, Marylyn D. Ritchie, Anurag Verma, Tom Fowler, Manu Shankar‐Hari, Charlotte Summers, Charles Hinds, Peter Horby, Lowell Ling, Daniel F. McAuley, Hugh Montgomery, Peter Openshaw, Paul Elliott, Timothy Walsh, Albert Tenesa, J. Kenneth Baillie, Colin B. Begg, Sara Clohisey, Charles Hinds, Peter Horby, Julian C. Knight, Lowell Ling, David M. Maslove, Daniel F. McAuley, Johnny Millar, Hugh Montgomery, Alistair Nichol, Peter Openshaw, Alexandre C. Pereira, Chris P. Ponting, Kathy Rowan, Malcolm G. Semple, Manu Shankar‐Hari, Charlotte Summers, Timothy Walsh, Latha Aravindan, Ruth Armstrong, Heather Biggs, Ceilia Boz, Adam Brown, Richard E. Clark, Audrey Coutts, J. Terrence Coyle, Louise Cullum, Sukamal Das, Nicky Day, Lorna Donnelly, Esther Duncan, Angie Fawkes, Paul Finernan, Max Head Fourman, Anita Furlong, James Furniss

    Vydáno 2022
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  20. 20
    The impact of common and rare genetic variants on bradyarrhythmia development

    The impact of common and rare genetic variants on bradyarrhythmia development Autor Lu‐Chen Weng, Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall, Valerie N. Morrill, Xin Wang, Victor Nauffal, Yan V. Sun, Dominik Beer, Simon S. K. Lee, Girish N. Nadkarni, ThuyVy Duong, Biqi Wang, Tomasz Czuba, Thomas R. Austin, Zachary T. Yoneda, Daniel J. Friedman, Anne Clayton, Matthew C. Hyman, Renae Judy, Allan C. Skanes, Kate M. Orland, Timothy Treu, Matthew T. Oetjens, Álvaro Alonso, Elsayed Z. Soliman, Honghuang Lin, Kathryn L. Lunetta, Jesper van der Pals, Tariq Z. Issa, Navid A. Nafissi, Heidi T May, Peter Leong‐Sit, Carolina Roselli, Seung Hoan Choi, Goncalo Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Xiaodong Bai, Suganthi Balasubramanian, Andrew Blumenfeld, Boris Boutkov, Gisu Eom, Lukas Habegger, Alicia Hawes, Shareef Khalid, Olga Krasheninina, Rouel Lanche, Adam J. Mansfield, Evan K. Maxwell, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Razvan Panea, Tommy Polanco, Ayesha Rasool, William Salerno, Jeffrey Staples, Marcus B. Jones, Lyndon J. Mitnaul, Habib Khan, Stacey Knight, Richard Karlsson Linnér, Connie R. Bezzina, Samuli Ripatti, Susan R. Heckbert, J. Michael Gaziano, Ruth J. F. Loos, Bruce M. Psaty, J. Gustav Smith, Emelia J. Benjamin, Dan E. Arking, Daniel J. Rader, Svati H. Shah, Dan M. Roden, Scott M. Damrauer, Lee L. Eckhardt, Jason D. Roberts, Michael J. Cutler

    Vydáno 2025
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