Rezultati pretrage - William M. McMahon

Detaljiziraj rezultate
  1. 1
    Psychiatric Comorbidity and Medication Use in Adults with Autism Spectrum Disorder

    Psychiatric Comorbidity and Medication Use in Adults with Autism Spectrum Disorder od Tara R. Buck, Joseph Viskochil, Megan Farley, Hilary Coon, William M. McMahon, Jubel Morgan, Deborah A. Bilder

    Izdano 2014
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  2. 2
    Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees

    Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees od Hilary Coon, Michele Villalobos, Reid Robison, Nicola J. Camp, Dale S. Cannon, Kristina Allen‐Brady, Judith S. Miller, William M. McMahon

    Izdano 2010
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  3. 3
    Maternal Prenatal Weight Gain and Autism Spectrum Disorders

    Maternal Prenatal Weight Gain and Autism Spectrum Disorders od Deborah A. Bilder, Amanda V. Bakian, Joseph Viskochil, Erin Clark, Elizabeth L. Botts, Ken R. Smith, Richard Pimentel, William M. McMahon, Hilary Coon

    Izdano 2013
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  4. 4
    Comparative Analysis of Suicide, Accidental, and Undetermined Cause of Death Classification

    Comparative Analysis of Suicide, Accidental, and Undetermined Cause of Death Classification od Douglas Gray, Hilary Coon, Erin McGlade, W. Brandon Callor, Josh Byrd, Joseph Viskochil, Amanda V. Bakian, Deborah Yurgelun‐Todd, Todd C. Grey, William M. McMahon

    Izdano 2014
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  5. 5
    Excess Mortality and Causes of Death in Autism Spectrum Disorders: A Follow up of the 1980s Utah/UCLA Autism Epidemiologic Study

    Excess Mortality and Causes of Death in Autism Spectrum Disorders: A Follow up of the 1980s Utah/UCLA Autism Epidemiologic Study od Deborah A. Bilder, Elizabeth L. Botts, Ken R. Smith, Richard Pimentel, Megan Farley, Joseph Viskochil, William M. McMahon, Heidi Block, Edward Ritvo, Riva-Ariella Ritvo, Hilary Coon

    Izdano 2012
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  6. 6
    Sensory features in autism: Findings from a large <scp>population‐based</scp> surveillance system

    Sensory features in autism: Findings from a large <scp>population‐based</scp> surveillance system od Anne V. Kirby, Deborah A. Bilder, Lisa D. Wiggins, Michelle M. Hughes, John L. Davis, Jennifer Hall‐Lande, Li‐Ching Lee, William M. McMahon, Amanda V. Bakian

    Izdano 2022
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  7. 7
    Familial Autoimmune Thyroid Disease as a Risk Factor for Regression in Children with Autism Spectrum Disorder: A CPEA Study

    Familial Autoimmune Thyroid Disease as a Risk Factor for Regression in Children with Autism Spectrum Disorder: A CPEA Study od Cynthia A. Molloy, Ardythe L. Morrow, Jareen Meinzen‐Derr, Géraldine Dawson, Raphael Bernier, Michelle Dunn, Susan Hyman, William M. McMahon, Julie Goudie-Nice, Susan Hepburn, Nancy J. Minshew, Sally J. Rogers, Marian Sigman, M. Anne Spence, Helen Tager‐Flusberg, Fred R. Volkmar, Catherine Lord

    Izdano 2006
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  8. 8
    Lifetime Prevalence, Age of Risk, and Genetic Relationships of Comorbid Psychiatric Disorders in Tourette Syndrome

    Lifetime Prevalence, Age of Risk, and Genetic Relationships of Comorbid Psychiatric Disorders in Tourette Syndrome od Matthew E. Hirschtritt, Paul C. Lee, David L. Pauls, Yves Dion, Marco A. Grados, Cornelia Illmann, Robert A. King, Paul Sandor, William M. McMahon, Gholson J. Lyon, Daniëlle C. Cath, Roger Kurlan, Mary M. Robertson, Lisa Osiecki, Jeremiah M. Scharf, Carol A. Mathews

    Izdano 2015
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  9. 9
    Obsessive‐compulsive symptom dimensions in affected sibling pairs diagnosed with Gilles de la Tourette syndrome

    Obsessive‐compulsive symptom dimensions in affected sibling pairs diagnosed with Gilles de la Tourette syndrome od James F. Leckman, David L. Pauls, Heping Zhang, Maria Conceição do Rosário, Liliya Katsovich, Kenneth K. Kídd, A.J. Pakstis, John P. Alsobrook, Mary M. Robertson, William M. McMahon, John T. Walkup, B.J.M. van de Wetering, Robert A. King, Donald J. Cohen

    Izdano 2002
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  10. 10
    Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypes

    Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypes od Timothy B. Baker, Robert B. Weiss, Daniel M. Bolt, Andrew von Niederhausern, Michael C. Fiore, Diane M. Dunn, Megan E. Piper, Nori Matsunami, Stevens S. Smith, Hilary Coon, William M. McMahon, Mary Beth Scholand, Nanda Singh, John R. Hoidal, Su‐Young Kim, Mark Leppert, Dale S. Cannon

    Izdano 2009
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  11. 11
    Autism Spectrum Symptoms in a Tourette’s Disorder Sample

    Autism Spectrum Symptoms in a Tourette’s Disorder Sample od Sabrina M. Darrow, Marco A. Grados, Paul Sandor, Matthew E. Hirschtritt, Cornelia Illmann, Lisa Osiecki, Yves Dion, Robert A. King, David L. Pauls, Cathy L. Budman, Daniëlle C. Cath, Erica Greenberg, Gholson J. Lyon, William M. McMahon, Paul C. Lee, Kevin Delucchi, Jeremiah M. Scharf, Carol A. Mathews

    Izdano 2017
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  12. 12
    Genetic risk factors in two Utah pedigrees at high risk for suicide

    Genetic risk factors in two Utah pedigrees at high risk for suicide od Hilary Coon, Todd M. Darlington, Richard Pimentel, Ken R. Smith, Chad Huff, Hao Hu, Leslie Jerominski, Joanna Hansen, M. Klein, W. Brandon Callor, Josh Byrd, Amanda V. Bakian, Sheila E. Crowell, William M. McMahon, Venkatesh Rajamanickam, Nicola J. Camp, Erin McGlade, Deborah Yurgelun‐Todd, Todd C. Grey, Douglas Gray

    Izdano 2013
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  13. 13
    A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region as a Risk Factor for Age-Dependent Nicotine Addiction

    A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region as a Risk Factor for Age-Dependent Nicotine Addiction od Robert B. Weiss, Timothy B. Baker, Dale S. Cannon, Andrew von Niederhausern, Diane M. Dunn, Nori Matsunami, Nanda A. Singh, Lisa Baird, Hilary Coon, William M. McMahon, Megan E. Piper, Michael C. Fiore, Mary Beth Scholand, John E. Connett, Richard E. Kanner, Lorise C. Gahring, Scott W. Rogers, John R. Hoidal, Mark Leppert

    Izdano 2008
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  14. 14
    Genetic and phenotypic overlap of specific obsessive-compulsive and attention-deficit/hyperactive subtypes with Tourette syndrome

    Genetic and phenotypic overlap of specific obsessive-compulsive and attention-deficit/hyperactive subtypes with Tourette syndrome od Matthew E. Hirschtritt, Sabrina M. Darrow, Cornelia Illmann, Lisa Osiecki, Marco A. Grados, Paul Sandor, Yves Dion, Robert A. King, David L. Pauls, Cathy L. Budman, Daniëlle C. Cath, Erica Greenberg, Gholson J. Lyon, Dongmei Yu, Lauren M. McGrath, William M. McMahon, P. C. Lee, Kevin Delucchi, Jeremiah M. Scharf, Carol A. Mathews

    Izdano 2017
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  15. 15
    Identification of Two Heritable Cross-Disorder Endophenotypes for Tourette Syndrome

    Identification of Two Heritable Cross-Disorder Endophenotypes for Tourette Syndrome od Sabrina M. Darrow, Matthew E. Hirschtritt, Lea K. Davis, Cornelia Illmann, Lisa Osiecki, Marco A. Grados, Paul Sandor, Yves Dion, Robert A. King, David L. Pauls, Cathy L. Budman, Daniëlle C. Cath, Erica Greenberg, Gholson J. Lyon, Dongmei Yu, Lauren M. McGrath, William M. McMahon, Paul C. Lee, Kevin Delucchi, Jeremiah M. Scharf, Carol A. Mathews

    Izdano 2016
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  16. 16
    Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

    Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes od Maja Bućan, Brett S. Abrahams, Kai Wang, Joseph Glessner, Edward I. Herman, Lisa I. Sonnenblick, Ana I. Alvarez Retuerto, Marcin Imieliński, Dexter Hadley, Jonathan P. Bradfield, Cecilia Kim, Nicole B. Gidaya, Ingrid Lindquist, Ted Hutman, Marian Sigman, Vlad Kustanovich, Clara Lajonchere, Andrew Singleton, Junhyong Kim, Thomas H. Wassink, William M. McMahon, Thomas Owley, John A. Sweeney, Hilary Coon, John I. Nürnberger, Mingyao Li, Rita M. Cantor, Nancy J. Minshew, James S. Sutcliffe, Edwin H. Cook, Géraldine Dawson, Joseph D. Buxbaum, Struan F.A. Grant, Gerard D. Schellenberg, Daniel H. Geschwind, Hákon Hákonarson

    Izdano 2009
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  17. 17
    Synaptic processes and immune-related pathways implicated in Tourette syndrome

    Synaptic processes and immune-related pathways implicated in Tourette syndrome od Fotis Tsetsos, Dongmei Yu, Jae Hoon Sul, Alden Y. Huang, Cornelia Illmann, Lisa Osiecki, Sabrina M. Darrow, Matthew E. Hirschtritt, Erica Greenberg, Kirsten Müller‐Vahl, Manfred Stuhrmann, Yves Dion, Guy A. Rouleau, H.N. Aschauer, M. Stamenković, Monika Schlögelhofer, Paul Sandor, Cathy L. Barr, Marco A. Grados, Harvey S. Singer, Markus M. Nöthen, Johannes Hebebrand, Anke Hinney, Robert A. King, Thomas Fernandez, Csaba Barta, Zsanett Tárnok, Péter Nagy, Christel Depienne, Yulia Worbe, Andreas Hartmann, Cathy L. Budman, Renata Rizzo, Gholson J. Lyon, William M. McMahon, James R. Batterson, Daniëlle C. Cath, Irene A. Malaty, Michael S. Okun, Cheston M. Berlin, Douglas W. Woods, Paul C. Lee, Joseph Jankovic, Mary M. Robertson, Donald L. Gilbert, Lawrence W. Brown, Barbara J. Coffey, Andrea Dietrich, Pieter J. Hoekstra, Samuel Kuperman, Samuel H. Zinner, Michael Wagner, James A. Knowles, A. Jeremy Willsey, Jay A. Tischfield, Gary A. Heiman, Nancy J. Cox, Nelson B. Freimer, Benjamin M. Neale, Lea K. Davis, Giovanni Coppola, Carol A. Mathews, Jeremiah M. Scharf, Peristera Paschou, Cathy L. Barr, James R. Batterson, Cheston M. Berlin, Cathy L. Budman, Daniëlle C. Cath, Giovanni Coppola, Nancy J. Cox, Sabrina M. Darrow, Lea K. Davis, Yves Dion, Nelson B. Freimer, Marco A. Grados, Erica Greenberg, Matthew E. Hirschtritt, Alden Y. Huang, Cornelia Illmann, Robert A. King, Roger Kurlan, James F. Leckman, Gholson J. Lyon, Irene A. Malaty, Carol A. Mathews, William M. McMahon, Benjamin M. Neale, Michael S. Okun, Lisa Osiecki, Mary M. Robertson, Guy A. Rouleau, Paul Sandor, Jeremiah M. Scharf, Harvey S. Singer, Jan Smit, Jae Hoon Sul, Dongmei Yu, Harald Aschauer Harald Aschauer, Csaba Barta

    Izdano 2021
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  18. 18
    Common genetic variants on 5p14.1 associate with autism spectrum disorders

    Common genetic variants on 5p14.1 associate with autism spectrum disorders od Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bućan, Joseph Glessner, Brett S. Abrahams, Daria Salyakina, Marcin Imieliński, Jonathan P. Bradfield, Patrick Sleiman, Chong Ae Kim, Cuiping Hou, Edward C. Frackelton, Rosetta Chiavacci, Nagahide Takahashi, Takeshi Sakurai, Eric Rappaport, Clara Lajonchere, Jeffrey Munson, Annette Estes, Olena Korvatska, Joseph Piven, Lisa I. Sonnenblick, Ana I. Alvarez Retuerto, Edward I. Herman, Hongmei Dong, Ted Hutman, Marian Sigman, Sally Ozonoff, Ami Klin, Thomas Owley, John A. Sweeney, Camille W. Brune, Rita M. Cantor, Raphael Bernier, John R. Gilbert, Michael L. Cuccaro, William M. McMahon, Judith Miller, Matthew W. State, Thomas H. Wassink, Hilary Coon, Susan E. Levy, Robert T. Schultz, John I. Nürnberger, Jonathan L. Haines, James S. Sutcliffe, Edwin H. Cook, Nancy J. Minshew, Joseph D. Buxbaum, Géraldine Dawson, Struan F.A. Grant, Daniel H. Geschwind, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Hákon Hákonarson

    Izdano 2009
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  19. 19
    Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

    Autism genome-wide copy number variation reveals ubiquitin and neuronal genes od Joseph Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E. Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W. Brune, Jonathan P. Bradfield, Marcin Imieliński, Edward C. Frackelton, Jennifer Reichert, Emily L. Crawford, Jeffrey Munson, Patrick Sleiman, Rosetta Chiavacci, Kiran Annaiah, Kelly Thomas, Cuiping Hou, Wendy Glaberson, James H. Flory, F. George Otieno, Maria Garris, Latha Soorya, Lambertus Klei, Joseph Piven, Kacie J. Meyer, Evdokia Anagnostou, Takeshi Sakurai, Rachel M. Game, Danielle S. Rudd, Danielle Zurawiecki, Christopher J. McDougle, Lea K. Davis, Judith Miller, David J. Posey, Shana M. Michaels, Alexander Kolevzon, Jeremy M. Silverman, Raphael Bernier, Susan E. Levy, Robert T. Schultz, Géraldine Dawson, Thomas Owley, William M. McMahon, Thomas H. Wassink, John A. Sweeney, John I. Nürnberger, Hilary Coon, James S. Sutcliffe, Nancy J. Minshew, Struan F.A. Grant, Maja Bućan, Edwin H. Cook, Joseph D. Buxbaum, Bernie Devlin, Gerard D. Schellenberg, Hákon Hákonarson

    Izdano 2009
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  20. 20
    Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

    Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome od Alden Y. Huang, Dongmei Yu, Lea K. Davis, Jae Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason Chen, Lauren M. McGrath, Cornelia Illmann, Paul Sandor, Cathy L. Barr, Marco A. Grados, Harvey S. Singer, Markus M. Nöthen, Johannes Hebebrand, Robert A. King, Yves Dion, Guy A. Rouleau, Cathy L. Budman, Christel Depienne, Yulia Worbe, Andreas Hartmann, Kirsten Müller‐Vahl, Manfred Stuhrmann, H.N. Aschauer, M. Stamenković, Monika Schloegelhofer, Anastasios Konstantinidis, Gholson J. Lyon, William M. McMahon, Csaba Barta, Zsanett Tárnok, Péter Nagy, James R. Batterson, Renata Rizzo, Daniëlle C. Cath, Tomasz Wolańczyk, Cheston M. Berlin, Irene A. Malaty, Michael S. Okun, Douglas W. Woods, Elliott Rees, Carlos N. Pato, Michele T. Pato, James A. Knowles, Daniëlle Posthuma, David L. Pauls, Nancy J. Cox, Benjamin M. Neale, Nelson B. Freimer, Peristera Paschou, Carol A. Mathews, Jeremiah M. Scharf, Giovanni Coppola, Ruth D. Bruun, Sylvain Chouinard, Sabrina M. Darrow, Erica Greenberg, Matthew E. Hirschtritt, Roger Kurlan, James F. Leckman, Mary M. Robertson, Johannes H. Smit

    Izdano 2017
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