Результаты поиска - Thomas M. Morgan

Отмена результатов
  1. 1
    African Genetic Diversity: Implications for Cytochrome P450-mediated Drug Metabolism and Drug Development

    African Genetic Diversity: Implications for Cytochrome P450-mediated Drug Metabolism and Drug Development по Iris Rajman, Laura Knapp, Thomas M. Morgan, Collen Masimirembwa

    Опубликовано 2017
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    Revisão
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  2. 2
    Family History in Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis (PFAPA) Syndrome

    Family History in Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis (PFAPA) Syndrome по Kalpana Manthiram, Emily Nesbitt, Thomas M. Morgan, Kathryn M. Edwards

    Опубликовано 2016
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    Artigo
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  3. 3
    Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome

    Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome по Thomas Fernandez, Thomas M. Morgan, Nicole R. Davis, Ami Klin, Ashley Morris, Anita Farhi, Richard P. Lifton, Matthew W. State

    Опубликовано 2004
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    Carta
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  4. 4
    A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y

    A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y по Leigh D. Plant, Peter N. Bowers, Qianyong Liu, Thomas M. Morgan, Tingting Zhang, Matthew W. State, Weidong Chen, Rick A. Kittles, Steven A. Goldstein

    Опубликовано 2006
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    Artigo
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  5. 5
    Brief Report: Risk of Adverse Fetal Outcomes Associated With Immunosuppressive Medications for Chronic Immune‐Mediated Diseases in Pregnancy

    Brief Report: Risk of Adverse Fetal Outcomes Associated With Immunosuppressive Medications for Chronic Immune‐Mediated Diseases in Pregnancy по William O. Cooper, T. Craig Cheetham, De‐Kun Li, C. Michael Stein, S. Todd Callahan, Thomas M. Morgan, Ayumi Shintani, Ning Chen, Marie R. Griffin, Wayne A. Ray

    Опубликовано 2013
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    Artigo
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  6. 6
    Variation in Recovery

    Variation in Recovery по Judith H. Lichtman, Nancy P. Lorenze, Gail D’Onofrio, John A. Spertus, Stacy Tessler Lindau, Thomas M. Morgan, Jeph Herrin, Héctor Bueno, Jennifer A. Mattera, Paul M. Ridker, Harlan M. Krumholz

    Опубликовано 2010
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    Artigo
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  7. 7
    Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3

    Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3 по Nicola M. Solomon, Shelley Ross, S. M. Forrest, Paul Q. Thomas, Thomas M. Morgan, Joseph L. Belsky, Frans A. Hol, Pamela S. Karnes, N J Hopwood, Sean Myers, Alva Tan, Garry L. Warne

    Опубликовано 2007
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    Carta
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  8. 8
    Additional support for the association of SLITRK1 var321 and Tourette syndrome

    Additional support for the association of SLITRK1 var321 and Tourette syndrome по Brian J. O’Roak, Thomas M. Morgan, Daniel O. Fishman, Ester Saus, Pino Alonso, Mónica Gratacòs, Xavier Estivill, Omri Teltsh, Yoav Kohn, Kenneth K. Kídd, J Cho, Richard P. Lifton, Matthew W. State

    Опубликовано 2010
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    Carta
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  9. 9
    Limitations of exome sequencing in detecting rare and undiagnosed diseases

    Limitations of exome sequencing in detecting rare and undiagnosed diseases по Kendall J. Burdick, Joy D. Cogan, Lynette Rives, Amy K. Robertson, Mary Koziura, Elly Brokamp, Laura Duncan, Vickie Hannig, Jean P. Pfotenhauer, Rena Vanzo, Michael S. Paul, Anna Bican, Thomas M. Morgan, Jessica Duis, John H. Newman, Rizwan Hamid, John A. Phillips

    Опубликовано 2020
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    Artigo
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  10. 10
    Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype

    Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype по Matthew W. State, John M. Greally, Adam Cuker, Peter N. Bowers, Octavian Henegariu, Thomas M. Morgan, Murat Günel, Michael L. DiLuna, Robert A. King, Carol Nelson, Abigail L. Donovan, George M. Anderson, James F. Leckman, Trevor Hawkins, David L. Pauls, Richard P. Lifton, David C. Ward

    Опубликовано 2003
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    Artigo
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  11. 11
    Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans

    Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans по A. Gulhan Ercan‐Sencicek, Samira Jambi, Daniel Franjic, S. Nishimura, Mingfeng Li, Paul El-Fishawy, Thomas M. Morgan, Stephan Sanders, Kaya Bilgüvar, Mohnish Suri, Michele H. Johnson, Abha R. Gupta, Zafer Yüksel, Shrikant Mane, Elena L. Grigorenko, Marina R. Picciotto, Arthur S. Alberts, Murat Günel, Nenad Šestan, Matthew W. State

    Опубликовано 2014
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    Artigo
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  12. 12
    USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder

    USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder по Yi-Heng Hao, Michael D. Fountain, Klementina Fon Tacer, Fan Xia, Weimin Bi, Sung‐Hae Kang, Ankita Patel, Jill A. Rosenfeld, Cédric Le Caignec, Bertrand Isidor, Ian D. Krantz, Sarah E. Noon, Jean P. Pfotenhauer, Thomas M. Morgan, Rocio Moran, Robert C. Pedersen, Margarita Sáenz, Christian P. Schaaf, Patrick Ryan Potts

    Опубликовано 2015
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    Artigo
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  13. 13
    Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders

    Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders по Betul Bakkaloglu, Brian J. O’Roak, Angeliki Louvi, Abha R. Gupta, Jesse F. Abelson, Thomas M. Morgan, Katarzyna Chawarska, Ami Klin, A. Gulhan Ercan‐Sencicek, Althea Stillman, Gamze Tanrįöver, Brett S. Abrahams, Jackie A. Duvall, Elissa M. Robbins, Daniel H. Geschwind, Thomas Biederer, Murat Günel, Richard P. Lifton, Matthew W. State

    Опубликовано 2008
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    Artigo
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  14. 14
    L-Histidine Decarboxylase and Tourette's Syndrome

    L-Histidine Decarboxylase and Tourette's Syndrome по A. Gulhan Ercan‐Sencicek, Althea Stillman, Ananda K. Ghosh, Kaya Bilgüvar, Brian J. O’Roak, Christopher E. Mason, Thomas Abbott, Abha R. Gupta, Robert A. King, David L. Pauls, Jay A. Tischfield, Gary A. Heiman, Harvey S. Singer, Donald L. Gilbert, Pieter J. Hoekstra, Thomas M. Morgan, Erin Loring, Katsuhito Yasuno, Thomas Fernandez, Stephan Sanders, Angeliki Louvi, Judy H. Cho, Shrikant Mane, Christopher M. Colangelo, Thomas Biederer, Richard P. Lifton, Murat Günel, Matthew W. State

    Опубликовано 2010
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  15. 15
    Neuropathy target esterase impairments cause Oliver–McFarlane and Laurence–Moon syndromes

    Neuropathy target esterase impairments cause Oliver–McFarlane and Laurence–Moon syndromes по Robert B. Hufnagel, Gavin Arno, Nichole D. Hein, Joshua Hersheson, Megana Prasad, Yvonne C. Anderson, Laura A. Krueger, Louise Gregory, Corinne Stoetzel, Thomas Jaworek, Sarah Hull, Abi Li, Vincent Plagnol, Christi M. Willen, Thomas M. Morgan, Cynthia A. Prows, Rashmi S. Hegde, Saima Riazuddin, Gregory A. Grabowski, Rudy J. Richardson, Klaus Dieterich, Taosheng Huang, Tamás Révész, Juan Pedro Martı́nez-Barberá, Robert A. Sisk, Craig Jefferies, Henry Houlden, Mehul Dattani, John K. Fink, Hélène Dollfus, Anthony T. Moore, Zubair M. Ahmed

    Опубликовано 2014
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    Artigo
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  16. 16
    Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian Families

    Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian Families по Thandiswa Ngcungcu, Martin Oti, Jan Cezary Sitek, Bjørn Ivar Haukanes, Bolan Linghu, Robert E. Bruccoleri, Tomasz Stokowy, Edward J. Oakeley, Fengtang Yang, Jiang Zhu, Marc Sultan, Joost Schalkwijk, Ivonne M.J.J. van Vlijmen‐Willems, Charlotte von der Lippe, Han G. Brunner, Kari M. Ersland, Wayne Grayson, Stine Buechmann-Moller, Olav Sundnes, Nanguneri Nirmala, Thomas M. Morgan, Hans van Bokhoven, Vidar M. Steen, Peter Hull, Joseph D. Szustakowski, Frank Staedtler, Huiqing Zhou, Torunn Fiskerstrand, Michèle Ramsay

    Опубликовано 2017
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    Artigo
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  17. 17
    Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies

    Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies по Michael D. Fountain, David S. Oleson, Megan Rech, Lara Segebrecht, Jill V. Hunter, John McCarthy, Philip J. Lupo, Manuel Holtgrewe, Rocio Moran, Jill A. Rosenfeld, Bertrand Isidor, Cédric Le Caignec, Margarita Sáenz, Robert C. Pedersen, Thomas M. Morgan, Jean P. Pfotenhauer, Fan Xia, Weimin Bi, Sung-Hae L. Kang, Ankita Patel, Ian D. Krantz, Sarah E. Raible, Wendy E. Smith, Ingrid Cristian, Erin Torti, Jane Juusola, Francisca Millan, Ingrid M. Wentzensen, Richard Person, Sébastien Küry, Stéphane Bézieau, Kévin Uguen, Claude Férec, Arnold Münnich, Mieke M. van Haelst, Klaske D. Lichtenbelt, Koen L.I. van Gassen, Tanner Hagelstrom, Aditi Chawla, Denise Perry, Ryan J. Taft, Marilyn C. Jones, Diane Masser‐Frye, David A. Dyment, Sunita Venkateswaran, Chumei Li, Luis Escobar, Denise Horn, Rebecca C. Spillmann, Loren D.M. Peña, Jolanta Wierzba, Tim M. Strom, Ilaria Parenti, Frank J. Kaiser, Nadja Ehmke, Christian P. Schaaf

    Опубликовано 2019
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  18. 18
    TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities

    TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities по Wojciech Wiszniewski, Jill V. Hunter, Neil A. Hanchard, Jason R. Willer, Chad A. Shaw, Qi Tian, Anna Illner, Xueqing Wang, Sau Wai Cheung, Ankita Patel, Ian M. Campbell, Violet Gelowani, Patricia Hixson, Audrey R. Ester, Mahshid S. Azamian, Lorraine Potocki, Gladys Zapata, Patricia Hernandez, Melissa B. Ramocki, Regie Lyn P. Santos‐Cortez, Gao Wang, Michele K. York, Monica J. Justice, Zili D. Chu, Patricia I. Bader, Lisa Omo-Griffith, Nirupama S. Madduri, Gunter Scharer, Heather P. Crawford, Pattamawadee Yanatatsaneejit, Anna Eifert, Jeffery Kerr, Carlos A. Bacino, Adiaha I.A. Franklin, Robin P. Goin‐Kochel, Gayle Simpson, LaDonna Immken, Muhammad Ehteshamul Haque, Marija Stosic, Misti Williams, Thomas M. Morgan, Sumit Pruthi, Reed A. Omary, Simeon A. Boyadjiev, Kay K. Win, Aye Thida, Matthew E. Hurles, Martin L. Hibberd, Chiea Chuen Khor, Nguyễn Văn Vĩnh Châu, Thomas E. Gallagher, Apiwat Mutirangura, Paweł Stankiewicz, Arthur L. Beaudet, Mirjana Maletić‐Savatić, Jill A. Rosenfeld, Lisa G. Shaffer, Erica E. Davis, John W. Belmont, Sarah J. Dunstan, Cameron P. Simmons, Penelope E. Bonnen, Suzanne M. Leal, Nicholas Katsanis, James R. Lupski, Seema R. Lalani

    Опубликовано 2013
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    Artigo
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  19. 19
    Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies

    Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies по Themistocles L. Assimes, Hilma Hólm, Sekar Kathiresan, Muredach P. Reilly, Guðmar Þorleifsson, Benjamin F. Voight, Jeanette Erdmann, Christina Willenborg, Dhananjay Vaidya, Changchun Xie, C. C. Patterson, Thomas M. Morgan, Mary Susan Burnett, Mingyao Li, Mark A. Hlatky, Joshua W. Knowles, John R. Thompson, Devin Absher, Carlos Iribarren, Alan S. Go, Stephen P. Fortmann, Stephen Sidney, Neil Risch, Hua Tang, Richard M. Myers, Kenneth I. Berger, Monika Stoll, Svati H. Shah, Guðmundur Þorgeirsson, Karl Andersen, Aki S. Havulinna, J. Enrique Herrera, Nauder Faraday, Yoonhee Kim, Brian G. Kral, Rasika A. Mathias, Ingo Ruczinski, Bhoom Suktitipat, Alexander F. Wilson, Lisa R. Yanek, Lewis C. Becker, Patrick Linsel‐Nitschke, Wolfgang Lieb, Inke R. König, Christian Hengstenberg, Marcus Fischer, Klaus Stark, Wibke Reinhard, Janina Winogradow, Martina Grassl, Anika Großhennig, Michael Preuß, Stefan Schreiber, H-Erich Wichmann, Christa Meisinger, Jean Yee, Yechiel Friedlander, Ron Do, James B. Meigs, Gordon H. Williams, David M. Nathan, Calum A. MacRae, Liming Qu, Robert L. Wilensky, William Matthai, Atif Qasim, Hákon Hákonarson, Augusto D. Pichard, Kenneth M. Kent, Lowell F. Satler, Joseph Lindsay, Ron Waksman, Christopher W. Knouff, Dawn Waterworth, Max Walker, Vincent Mooser, Jaume Marrugat, Gavin Lucas, Isaac Subirana, Joan Sala, Rafel Ramos, Nicola Martinelli, Oliviero Olivieri, Elisabetta Trabetti, Giovanni Malerba, Pier Franco Pignatti, Candace Guiducci, Daniel B. Mirel, Melissa Parkin, Joel N. Hirschhorn, Rosanna Asselta, Stefano Duga, Yan V. Sun, Mark J. Daly, Shaun Purcell, Sandra Eifert, Peter S. Braund, Benjamin J. Wright, Anthony J. Balmforth, Stephen G. Ball

    Опубликовано 2010
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  20. 20
    Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

    Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease по Heribert Schunkert, Inke R. König, Sekar Kathiresan, Muredach P. Reilly, Themistocles L. Assimes, Hilma Hólm, Michael Preuß, Alexandre F.R. Stewart, Maja Barbalić, Christian Gieger, Devin Absher, Zouhair Aherrahrou, Hooman Allayee, David Altshuler, Sonia S. Anand, Karl Andersen, Jeffrey L. Anderson, Diego Ardissino, Stephen G. Ball, Anthony J. Balmforth, Timothy Barnes, Diane M. Becker, Lewis C. Becker, Kenneth I. Berger, Joshua C. Bis, S. Matthijs Boekholdt, Eric Boerwinkle, Peter S. Braund, Matthew A. Brown, Mary Susan Burnett, Ian Buysschaert, John F. Carlquist, Li Chen, Sven Cichon, Veryan Codd, R. W. Davies, George Dedoussis, Abbas Dehghan, Serkalem Demissie, Joseph M. Devaney, Patrick Diemert, Ron Do, Angela Doering, Sandra Eifert, Nour Eddine El Mokhtari, Stephen G. Ellis, Roberto Elosúa, James C. Engert, Stephen E. Epstein, Ulf dé Fairé, Marcus Fischer, Aaron R. Folsom, Jennifer Freyer, Bruna Gigante, Domenico Girelli, Sólveig Grétarsdóttir, Vilmundur Guðnason, Jeffrey R. Gulcher, Eran Halperin, Naomi Hammond, Stanley L. Hazen, Albert Hofman, Benjamin D. Horne, Thomas Illig, Carlos Iribarren, Gregory T. Jones, J. Wouter Jukema, Michael Kaiser, Lee M. Kaplan, John J.P. Kastelein, Kay‐Tee Khaw, Joshua W. Knowles, Genovefa Kolovou, Augustine Kong, Reijo Laaksonen, Diether Lambrechts, Karin Leander, Guillaume Lettre, Mingyao Li, Wolfgang Lieb, Christina Loley, Andrew Lotery, Pier Mannuccio Mannucci, Seraya Maouche, Nicola Martinelli, Pascal McKeown, Christa Meisinger, Thomas Meitinger, Olle Melander, Pier Angelica Merlini, Vincent Mooser, Thomas M. Morgan, Hae‐Won Uh, Joseph B. Muhlestein, Thomas Münzel, Yan V. Sun, Janja Nahrstaedt, Christopher P. Nelson, Markus M. Nöthen, Oliviero Olivieri

    Опубликовано 2011
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