المؤلفون: Huang, Alden Y, Yu, Dongmei, Davis, Lea K, Sul, Jae Hoon, Tsetsos, Fotis, Ramensky, Vasily, Zelaya, Ivette, Ramos, Eliana Marisa, Osiecki, Lisa, Chen, Jason A, McGrath, Lauren M, Illmann, Cornelia, Sandor, Paul, Barr, Cathy L, Grados, Marco, Singer, Harvey S, Nöthen, Markus M, Hebebrand, Johannes, King, Robert A, Dion, Yves, Rouleau, Guy, Budman, Cathy L, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Müller-Vahl, Kirsten R, Stuhrmann, Manfred, Aschauer, Harald, Stamenkovic, Mara, Schloegelhofer, Monika, Konstantinidis, Anastasios, Lyon, Gholson J, McMahon, William M, Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Batterson, James R, Rizzo, Renata, Cath, Danielle C, Wolanczyk, Tomasz, Berlin, Cheston, Malaty, Irene A, Okun, Michael S, Woods, Douglas W, Rees, Elliott, Pato, Carlos N, Pato, Michele T, Knowles, James A, Posthuma, Danielle, Pauls, David L, Cox, Nancy J, Neale, Benjamin M, Freimer, Nelson B, Paschou, Peristera, Mathews, Carol A, Scharf, Jeremiah M, Coppola, Giovanni, Tourette Syndrome Association International Consortium for Genetics (TSAICG), Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI)

المصدر: Neuron. 94(6)

مصطلحات موضوعية: Tourette Syndrome Association International Consortium for Genetics, Gilles de la Tourette Syndrome GWAS Replication Initiative, Humans, Tourette Syndrome, Genetic Predisposition to Disease, Calcium-Binding Proteins, Cell Adhesion Molecules, Neuronal, Neural Cell Adhesion Molecules, Nerve Tissue Proteins, Odds Ratio, Case-Control Studies, Genotype, Adolescent, Adult, Child, Female, Male, Genome-Wide Association Study, Young Adult, DNA Copy Number Variations, Contactins, White People, CNTN6, NRXN1, copy number variation, genetics, neurodevelopmental disorders, structural variation, tic disorders, Prevention, Human Genome, Genetics, Brain Disorders, Neurodegenerative, Neurosciences, Mental Health, 2.1 Biological and endogenous factors, Aetiology, Psychology, Cognitive Sciences, Neurology & Neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5fg5q9h1Test

المؤلفون: Willsey, A Jeremy, Fernandez, Thomas V, Yu, Dongmei, King, Robert A, Dietrich, Andrea, Xing, Jinchuan, Sanders, Stephan J, Mandell, Jeffrey D, Huang, Alden Y, Richer, Petra, Smith, Louw, Dong, Shan, Samocha, Kaitlin E, Tourette International Collaborative Genetics (TIC Genetics), Tourette Syndrome Association International Consortium for Genetics (TSAICG), Neale, Benjamin M, Coppola, Giovanni, Mathews, Carol A, Tischfield, Jay A, Scharf, Jeremiah M, State, Matthew W, Heiman, Gary A

المصدر: Neuron. 94(3)

مصطلحات موضوعية: Tourette International Collaborative Genetics, Tourette Syndrome Association International Consortium for Genetics, Humans, Tourette Syndrome, Genetic Predisposition to Disease, Intracellular Signaling Peptides and Proteins, Proteins, Cell Cycle Proteins, Fibronectins, Cadherins, Receptors, Cell Surface, Phosphoproteins, Odds Ratio, Cohort Studies, Sequence Analysis, DNA, Parents, Mutation, Adult, Child, Female, Male, Genetic Variation, TIC Genetics, TSAICG, Tourette disorder, Tourette syndrome, de novo variants, gene discovery, whole-exome sequencing, Biotechnology, Brain Disorders, Human Genome, Neurosciences, Clinical Research, Genetics, 2.1 Biological and endogenous factors, Aetiology, Psychology, Cognitive Sciences, Neurology & Neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/7br7z7z3Test

المؤلفون: Darrow, Sabrina M, Hirschtritt, Matthew E, Davis, Lea K, Illmann, Cornelia, Osiecki, Lisa, Grados, Marco, Sandor, Paul, Dion, Yves, King, Robert, Pauls, David, Budman, Cathy L, Cath, Danielle C, Greenberg, Erica, Lyon, Gholson J, Yu, Dongmei, McGrath, Lauren M, McMahon, William M, Lee, Paul C, Delucchi, Kevin L, Scharf, Jeremiah M, Mathews, Carol A, Tourette Syndrome Association International Consortium for Genetics

المصدر: The American journal of psychiatry. 174(4)

مصطلحات موضوعية: Tourette Syndrome Association International Consortium for Genetics, Humans, Tourette Syndrome, Genetic Predisposition to Disease, Risk Assessment, Mothers, Obsessive-Compulsive Disorder, Attention Deficit Disorder with Hyperactivity, Comorbidity, Multifactorial Inheritance, Phenotype, Adolescent, Adult, Middle Aged, Child, Child, Preschool, Child of Impaired Parents, Female, Male, Genome-Wide Association Study, Young Adult, Endophenotypes, Attention Deficit Hyperactivity Disorder, Genetics, Latent Variable Modeling, Tourette’s Disorder, Genetic Testing, Pediatric, Brain Disorders, Serious Mental Illness, Mental Health, Clinical Research, Anxiety Disorders, Human Genome, Attention Deficit Hyperactivity Disorder (ADHD), Neurodegenerative, Aetiology, 2.1 Biological and endogenous factors, Mental health, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/8045q280Test

المؤلفون: Hirschtritt, Matthew E, Darrow, Sabrina M, Illmann, Cornelia, Osiecki, Lisa, Grados, Marco, Sandor, Paul, Dion, Yves, King, Robert A, Pauls, David L, Budman, Cathy L, Cath, Danielle C, Greenberg, Erica, Lyon, Gholson J, Yu, Dongmei, McGrath, Lauren M, McMahon, William M, Lee, Paul C, Delucchi, Kevin L, Scharf, Jeremiah M, Mathews, Carol A, Tourette Syndrome Association International Consortium for Genetics (TSAICG)

المصدر: Neurology. 87(5)

مصطلحات موضوعية: Tourette Syndrome Association International Consortium for Genetics, Humans, Tourette Syndrome, Tics, Factor Analysis, Statistical, Social Behavior, Obsessive-Compulsive Disorder, Attention Deficit Disorder with Hyperactivity, Age of Onset, Comorbidity, Phenotype, Adolescent, Adult, Canada, United States, Netherlands, Female, Male, Young Adult, United Kingdom, Inhibition, Psychological, Brain Disorders, Neurodegenerative, Neurosciences, Genetics, Serious Mental Illness, Mental Health, Mental health, Clinical Sciences, Cognitive Sciences, Neurology & Neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/6v01n60zTest

المؤلفون: de Leeuw, Christiaan, Goudriaan, Andrea, Smit, August B, Yu, Dongmei, Mathews, Carol A, Scharf, Jeremiah M, Tourette Syndrome Association International Consortium for Genetics, Verheijen, Mark HG, Posthuma, Danielle

المصدر: European journal of human genetics : EJHG. 23(11)

مصطلحات موضوعية: Tourette Syndrome Association International Consortium for Genetics, Astrocytes, Microglia, Oligodendroglia, Neurons, Humans, Tourette Syndrome, Genetic Predisposition to Disease, Glutamic Acid, Genotype, Genome-Wide Association Study, Human Genome, Brain Disorders, Genetics, Neurosciences, Mental Health, Neurodegenerative, 2.1 Biological and endogenous factors, Aetiology, Neurological, Clinical Sciences, Genetics & Heredity

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3q2413w0Test

المؤلفون: Hirschtritt, Matthew E, Lee, Paul C, Pauls, David L, Dion, Yves, Grados, Marco A, Illmann, Cornelia, King, Robert A, Sandor, Paul, McMahon, William M, Lyon, Gholson J, Cath, Danielle C, Kurlan, Roger, Robertson, Mary M, Osiecki, Lisa, Scharf, Jeremiah M, Mathews, Carol A, Tourette Syndrome Association International Consortium for Genetics

المصدر: JAMA psychiatry. 72(4)

مصطلحات موضوعية: Tourette Syndrome Association International Consortium for Genetics, Humans, Tourette Syndrome, Prevalence, Risk Factors, Mental Disorders, Age Factors, Age of Onset, Comorbidity, Age Distribution, Adolescent, Child, Child, Preschool, Canada, United States, Netherlands, Female, Male, Young Adult, United Kingdom, Brain Disorders, Neurodegenerative, Clinical Research, Anxiety Disorders, Behavioral and Social Science, Serious Mental Illness, Genetics, Attention Deficit Hyperactivity Disorder (ADHD), Pediatric, Neurosciences, Prevention, Mental Health, Aetiology, 2.3 Psychological, social and economic factors, Mental health, Other Medical and Health Sciences, Psychology, Cognitive Sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/1nn846ssTest

المؤلفون: Nag, Abhishek, Bochukova, Elena G, Kremeyer, Barbara, Campbell, Desmond D, Muller, Heike, Valencia-Duarte, Ana V, Cardona, Julio, Rivas, Isabel C, Mesa, Sandra C, Cuartas, Mauricio, Garcia, Jharley, Bedoya, Gabriel, Cornejo, William, Herrera, Luis D, Romero, Roxana, Fournier, Eduardo, Reus, Victor I, Lowe, Thomas L, Farooqi, I Sadaf, Tourette Syndrome Association International Consortium for Genetics, Mathews, Carol A, McGrath, Lauren M, Yu, Dongmei, Cook, Ed, Wang, Kai, Scharf, Jeremiah M, Pauls, David L, Freimer, Nelson B, Plagnol, Vincent, Ruiz-Linares, Andrés

المصدر: PloS one. 8(3)

مصطلحات موضوعية: Tourette Syndrome Association International Consortium for Genetics, Humans, Tourette Syndrome, Genetic Predisposition to Disease, Calcium-Binding Proteins, Cell Adhesion Molecules, Neuronal, Neural Cell Adhesion Molecules, Nerve Tissue Proteins, Collagen Type IX, Genotype, Polymorphism, Single Nucleotide, Adolescent, Child, Female, Male, DNA Copy Number Variations, Neurodegenerative, Mental Health, Human Genome, Genetics, Brain Disorders, Intellectual and Developmental Disabilities (IDD), Schizophrenia, Neurosciences, Aetiology, 2.1 Biological and endogenous factors, Mental health, General Science & Technology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/1z76j84nTest

المؤلفون: Hirschtritt, ME, Lee, PC, Pauls, DL, Dion, Y, Grados, MA, Illmann, C, King, RA, Sandor, P, McMahon, WM, Lyon, GJ, Cath, DC, Kurlan, R, Robertson, MM, Osiecki, L, Scharf, JM, Mathews, CA, Posthuma, D, Singer, HS, Yu, D, Cox, NJ, Freimer, NB, Budman, CL, Chouinard, S, Rouleau, GA, Barr, CL

المساهمون: Complex Trait Genetics, Neuroscience Campus Amsterdam - Neurobiology of Mental Health

المصدر: JAMA Psychiatry, 72(4), 325-333. American Medical Association
Hirschtritt, M E, Lee, P C, Pauls, D L, Dion, Y, Grados, M A, Illmann, C, King, R A, Sandor, P, McMahon, W M, Lyon, G J, Cath, D C, Kurlan, R, Robertson, M M, Osiecki, L, Scharf, J M, Mathews, C A, Posthuma, D, Singer, H S, Yu, D, Cox, N J, Freimer, N B, Budman, C L, Chouinard, S, Rouleau, G & Barr, C L 2015, ' Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome ', JAMA Psychiatry, vol. 72, no. 4, pp. 325-333 . https://doi.org/10.1001/jamapsychiatry.2014.2650Test
JAMA Psychiatry, 72(4), 325. American Medical Association
Hirschtritt, ME; Lee, PC; Pauls, DL; Dion, Y; Grados, MA; Illmann, C; et al.(2015). Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in tourette syndrome. JAMA Psychiatry, 72(4), 325-333. doi: 10.1001/jamapsychiatry.2014.2650. UCSF: Retrieved from: http://www.escholarship.org/uc/item/1nn846ssTest

مصطلحات موضوعية: Male, medicine.medical_specialty, Tic disorder, Canada, Adolescent, for the Tourette Syndrome Association International Consortium for Genetics, Comorbidity, Tourette syndrome, behavioral disciplines and activities, Young Adult, Age Distribution, SDG 3 - Good Health and Well-being, Risk Factors, mental disorders, medicine, Prevalence, Attention deficit hyperactivity disorder, Humans, Age of Onset, Psychiatry, Preschool, Child, Netherlands, Mental Disorders, Age Factors, Great Britain, medicine.disease, United States, 3. Good health, Psychiatry and Mental health, Mood disorders, Child, Preschool, Anxiety, Female, Mental disorders diagnosed in childhood, medicine.symptom, Psychology, Anxiety disorder, Clinical psychology, Tourette Syndrome

وصف الملف: image/pdf; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de90c202d1cb8b1ba2dae0a1867b4df2Test
https://research.vu.nl/en/publications/7310da1b-6871-4cea-95d2-01d98428069eTest

المؤلفون: Barbara Kremeyer, Roxana Romero, Nelson B. Freimer, H. Müller, Thomas L. Lowe, Ana Victoria Valencia-Duarte, Lauren M. McGrath, Abhishek Nag, Kai Wang, David L. Pauls, Gabriel Bedoya, J. García, Carol A. Mathews, Desmond Campbell, Jeremiah M. Scharf, M. Cuartas, Luis Diego Herrera, Vincent Plagnol, Dongmei Yu, I. Sadaf Farooqi, Julio César Cardona, Sandra Catalina Mesa, Eduardo Fournier, Elena G. Bochukova, Victor I. Reus, Isabel C. Rivas, Ed Cook, William Cornejo, Andres Ruiz-Linares

المساهمون: Zhang, Ge

المصدر: PLoS ONE, Vol 8, Iss 3, p e59061 (2013)
Repositorio UdeA
Universidad de Antioquia
instacron:Universidad de Antioquia
PLoS ONE
PloS one, vol 8, iss 3
Nag, A; Bochukova, EG; Kremeyer, B; Campbell, DD; Muller, H; Valencia-Duarte, AV; et al.(2013). CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1. PLoS ONE, 8(3). doi: 10.1371/journal.pone.0059061. UCSF: Retrieved from: http://www.escholarship.org/uc/item/1z76j84nTest

مصطلحات موضوعية: Male, Heredity, Neuronal, Genome-wide association study, Neurodegenerative, Bioinformatics, Tourette syndrome, 0302 clinical medicine, Adolescent Psychiatry, Genotype, 2.1 Biological and endogenous factors, Trastornos del Neurodesarrollo, Copy-number variation, Aetiology, Child, Neural Cell Adhesion Molecules, Genetics, Psychiatry, Child Psychiatry, 0303 health sciences, Multidisciplinary, Single Nucleotide, Genomics, Genome Scans, SNP genotyping, Mental Health, Schizophrenia, Medicine, Female, Research Article, Adolescent, DNA Copy Number Variations, General Science & Technology, Intellectual and Developmental Disabilities (IDD), Cell Adhesion Molecules, Neuronal, Science, Nerve Tissue Proteins, Biology, Polymorphism, Single Nucleotide, Collagen Type IX, 03 medical and health sciences, Tourette Syndrome Association International Consortium for Genetics, Genome Analysis Tools, medicine, Genome-Wide Association Studies, Humans, Genetic Predisposition to Disease, Polymorphism, Genetic Association Studies, 030304 developmental biology, Quantitative Traits, Complex Traits, Human Genome, Calcium-Binding Proteins, Neurosciences, Computational Biology, Human Genetics, medicine.disease, Genetic architecture, Brain Disorders, Neurodevelopmental Disorders, Autism, Structural Genomics, Cell Adhesion Molecules, Síndrome de Tourette, 030217 neurology & neurosurgery, Tourette Syndrome

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dcc87add691eab2583d72048407a49aTest
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23533600/pdf/?tool=EBITest