المؤلفون: Yu, Dongmei, Mathews, Carol A, Scharf, Jeremiah M, Neale, Benjamin M, Davis, Lea K, Gamazon, Eric R, Derks, Eske M, Evans, Patrick, Edlund, Christopher K, Crane, Jacquelyn, Fagerness, Jesen A, Osiecki, Lisa, Gallagher, Patience, Gerber, Gloria, Haddad, Stephen, Illmann, Cornelia, McGrath, Lauren M, Mayerfeld, Catherine, Arepalli, Sampath, Barlassina, Cristina, Barr, Cathy L, Bellodi, Laura, Benarroch, Fortu, Berrió, Gabriel Bedoya, Bienvenu, O Joseph, Black, Donald W, Bloch, Michael H, Brentani, Helena, Bruun, Ruth D, Budman, Cathy L, Camarena, Beatriz, Campbell, Desmond D, Cappi, Carolina, Silgado, Julio C Cardona, Cavallini, Maria C, Chavira, Denise A, Chouinard, Sylvain, Cook, Edwin H, Cookson, MR, Coric, Vladimir, Cullen, Bernadette, Cusi, Daniele, Delorme, Richard, Denys, Damiaan, Dion, Yves, Eapen, Valsama, Egberts, Karin, Falkai, Peter, Fernandez, Thomas, Fournier, Eduardo, Garrido, Helena, Geller, Daniel, Gilbert, Donald L, Girard, Simon L, Grabe, Hans J, Grados, Marco A, Greenberg, Benjamin D, Gross-Tsur, Varda, Grünblatt, Edna, Hardy, John, Heiman, Gary A, Hemmings, Sian MJ, Herrera, Luis D, Hezel, Dianne M, Hoekstra, Pieter J, Jankovic, Joseph, Kennedy, James L, King, Robert A, Konkashbaev, Anuar I, Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F, Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Lowe, Thomas L, Lupoli, Sara, Macciardi, Fabio, Maier, Wolfgang, Manunta, Paolo, Marconi, Maurizio, McCracken, James T, Mesa Restrepo, Sandra C, Moessner, Rainald, Moorjani, Priya, Morgan, Jubel, Muller, Heike, Murphy, Dennis L, Naarden, Allan L, Nurmi, Erika, Ochoa, William Cornejo, Ophoff, Roel A, Pakstis, Andrew J, Pato, Michele T, Pato, Carlos N, Piacentini, John, Pittenger, Christopher, Pollak, Yehuda

المصدر: The American journal of psychiatry. 172(1)

مصطلحات موضوعية: Humans, Tourette Syndrome, Severity of Illness Index, Obsessive-Compulsive Disorder, Psychiatric Status Rating Scales, Comorbidity, Polymorphism, Single Nucleotide, Adult, Female, Male, Genome-Wide Association Study, Human Genome, Genetics, Brain Disorders, Serious Mental Illness, Neurodegenerative, Prevention, Anxiety Disorders, Mental Health, Neurosciences, 2.1 Biological and endogenous factors, Aetiology, Mental health, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3zn1b380Test

المؤلفون: McGrath, Lauren M, Yu, Dongmei, Marshall, Christian, Davis, Lea K, Thiruvahindrapuram, Bhooma, Li, Bingbin, Cappi, Carolina, Gerber, Gloria, Wolf, Aaron, Schroeder, Frederick A, Osiecki, Lisa, O'Dushlaine, Colm, Kirby, Andrew, Illmann, Cornelia, Haddad, Stephen, Gallagher, Patience, Fagerness, Jesen A, Barr, Cathy L, Bellodi, Laura, Benarroch, Fortu, Bienvenu, O Joseph, Black, Donald W, Bloch, Michael H, Bruun, Ruth D, Budman, Cathy L, Camarena, Beatriz, Cath, Danielle C, Cavallini, Maria C, Chouinard, Sylvain, Coric, Vladimir, Cullen, Bernadette, Delorme, Richard, Denys, Damiaan, Derks, Eske M, Dion, Yves, Rosário, Maria C, Eapen, Valsama, Evans, Patrick, Falkai, Peter, Fernandez, Thomas V, Garrido, Helena, Geller, Daniel, Grabe, Hans J, Grados, Marco A, Greenberg, Benjamin D, Gross-Tsur, Varda, Grünblatt, Edna, Heiman, Gary A, Hemmings, Sian MJ, Herrera, Luis D, Hounie, Ana G, Jankovic, Joseph, Kennedy, James L, King, Robert A, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F, Lennertz, Leonhard, Lochner, Christine, Lowe, Thomas L, Lyon, Gholson J, Macciardi, Fabio, Maier, Wolfgang, McCracken, James T, McMahon, William, Murphy, Dennis L, Naarden, Allan L, Neale, Benjamin M, Nurmi, Erika, Pakstis, Andrew J, Pato, Michele T, Pato, Carlos N, Piacentini, John, Pittenger, Christopher, Pollak, Yehuda, Reus, Victor I, Richter, Margaret A, Riddle, Mark, Robertson, Mary M, Rosenberg, David, Rouleau, Guy A, Ruhrmann, Stephan, Sampaio, Aline S, Samuels, Jack, Sandor, Paul, Sheppard, Brooke, Singer, Harvey S, Smit, Jan H, Stein, Dan J, Tischfield, Jay A, Vallada, Homero, Veenstra-VanderWeele, Jeremy, Walitza, Susanne, Wang, Ying, Wendland, Jens R, Shugart, Yin Yao, Miguel, Euripedes C, Nicolini, Humberto, Oostra, Ben A

المصدر: Journal of the American Academy of Child & Adolescent Psychiatry. 53(8)

مصطلحات موضوعية: Human Genome, Genetics, Brain Disorders, Serious Mental Illness, Neurodegenerative, Mental Health, Tourette Syndrome, Neurosciences, Intellectual and Developmental Disabilities (IDD), Aetiology, 2.1 Biological and endogenous factors, Mental health, Adolescent, DNA Copy Number Variations, Diagnostic and Statistical Manual of Mental Disorders, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Obsessive-Compulsive Disorder, Polymorphism, Single Nucleotide, Tourette syndrome, obsessive-compulsive disorder, copy number variation, genetics, 16p13.11, Medical and Health Sciences, Psychology and Cognitive Sciences, Developmental & Child Psychology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/221498r1Test

المؤلفون: Davis, Lea K, Yu, Dongmei, Keenan, Clare L, Gamazon, Eric R, Konkashbaev, Anuar I, Derks, Eske M, Neale, Benjamin M, Yang, Jian, Lee, S. Hong, Evans, Patrick, Barr, Cathy L, Bellodi, Laura, Benarroch, Fortu, Berrio, Gabriel Bedoya, Bienvenu, Oscar J, Bloch, Michael H, Blom, Rianne M, Bruun, Ruth D, Budman, Cathy L, Camarena, Beatriz, Campbell, Desmond, Cappi, Carolina, Cardona Silgado, Julio C, Cath, Danielle C, Cavallini, Maria C, Chavira, Denise A, Chouinard, Sylvain, Conti, David V, Cook, Edwin H, Coric, Vladimir, Cullen, Bernadette A, Deforce, Dieter, Delorme, Richard, Dion, Yves, Edlund, Christopher K, Egberts, Karin, Falkai, Peter, Fernandez, Thomas V, Gallagher, Patience J, Garrido, Helena, Geller, Daniel, Girard, Simon L, Grabe, Hans J, Grados, Marco A, Greenberg, Benjamin D, Gross-Tsur, Varda, Haddad, Stephen, Heiman, Gary A, Hemmings, Sian M. J, Hounie, Ana G, Illmann, Cornelia, Jankovic, Joseph, Jenike, Michael A, Kennedy, James L, King, Robert A, Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F, Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Lowe, Thomas L, Macciardi, Fabio, McCracken, James T, McGrath, Lauren M, Mesa Restrepo, Sandra C, Moessner, Rainald, Morgan, Jubel, Muller, Heike, Murphy, Dennis L, Naarden, Allan L, Ochoa, William Cornejo, Ophoff, Roel A, Osiecki, Lisa, Pakstis, Andrew J, Pato, Michele T, Pato, Carlos N, Piacentini, John, Pittenger, Christopher, Pollak, Yehuda, Rauch, Scott L, Renner, Tobias J, Reus, Victor I, Richter, Margaret A, Riddle, Mark A, Robertson, Mary M, Romero, Roxana, Rosàrio, Maria C, Rosenberg, David, Rouleau, Guy A, Ruhrmann, Stephan, Ruiz-Linares, Andres, Sampaio, Aline S, Samuels, Jack, Sandor, Paul, Sheppard, Brooke, Singer, Harvey S, Smit, Jan H

المصدر: PLoS Genetics. 9(10)

مصطلحات موضوعية: Missing Heritability, Tic Disorders, Neuropsychiatric Disorders, Complex Diseases, Common Snps, Gilles, Family, Brain, Expression, Autism

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/21h67097Test

المؤلفون: Department of Psychiatry, UCSF Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA 94143, USA ( host institution ), Willsey, A. Jeremy ( author ), Fernandez, Thomas V. ( author ), Yu, Dongmei ( author ), King, Robert A. ( author ), Dietrich, Andrea ( author ), Xing, Jinchuan ( author ), Sanders, Stephan J. ( author ), Mandell, Jeffrey D. ( author ), Huang, Alden Y. ( author ), Richer, Petra ( author ), Smith, Louw ( author ), Dong, Shan ( author ), Samocha, Kaitlin E. ( author ), Neale, Benjamin M. ( author ), Coppola, Giovanni ( author ), Mathews, Carol A. ( UF author ), Tischfield, Jay A. ( author ), Scharf, Jeremiah M. ( author ), State, Matthew W. ( author ), Heiman, Gary A. ( author ), Abdulkadir, Mohamed ( author ), Bohnenpoll, Julia ( author ), Bromberg, Yana ( author ), Brown, Lawrence W. ( author ), Cheon, Keun-Ah ( author ), Coffey, Barbara J. ( author ), Deng, Li ( author ), Elzerman, Lonneke ( author ), Fründt, Odette ( author ), Garcia-Delgar, Blanca ( author ), Gedvilaite, Erika ( author ), Gilbert, Donald L. ( author ), Grice, Dorothy E. ( author ), Hagstrøm, Julie ( author ), Hedderly, Tammy ( author ), Heyman, Isobel ( author ), Hoekstra, Pieter J. ( author ), Hong, Hyun Ju ( author ), Huyser, Chaim ( author ), Ibanez-Gomez, Laura ( author ), Kim, Young Key ( author ), Kim, Young-Shin ( author ), Koh, Yun-Joo ( author ), Kook, Sodahm ( author ), Kuperman, Samuel ( author ), Lamerz, Andreas ( author ), Leventhal, Bennett ( author ), Ludolph, Andrea G. ( author ), Lühr da Silva, Claudia ( author ), Madruga-Garrido, Marcos ( author ), Maras, Athanasios ( author ), Mir, Pablo ( author ), Morer, Astrid ( author ), Münchau, Alexander ( author ), Murphy, Tara L. ( author ), Nasello, Cara ( author ), Openneer, Thaïra J.C. ( author ), Plessen, Kerstin J. ( author ), Roessner, Veit ( author ), Sanders, Stephan ( author ), Shin, Eun-Young ( author ), Sival, Deborah A. ( author ), Song, Dong-Ho ( author ), Song, Jungeun ( author ), Stolte, Anne Marie ( author ), Sun, Nawei ( author ), Tübing, Jennifer ( author ), Visscher, Frank ( author ), Walker, Michael F. ( author ), Wanderer, Sina ( author ), Wang, Shuoguo ( author ), Woods, Martin ( author ), Zhang, Yeting ( author ), Zhou, Anbo ( author ), Zinner, Samuel H. ( author ), Barr, Cathy L. ( author ), Batterson, James R. ( author ), Berlin, Cheston ( author ), Bruun, Ruth D. ( author ), Budman, Cathy L. ( author ), Cath, Danielle C. ( author ), Chouinard, Sylvain ( author ), Cox, Nancy J. ( author ), Darrow, Sabrina ( author ), Davis, Lea K. ( author ), Dion, Yves ( author ), Freimer, Nelson B. ( author ), Grados, Marco A. ( author ), Hirschtritt, Matthew E. ( author ), Illmann, Cornelia ( author ), Kurlan, Roger ( author ), Leckman, James F. ( author ), Lyon, Gholson J. ( author ), Malaty, Irene A. ( author ), Mathews, Carol A. ( author ), MaMahon, William M. ( author ), Okun, Michael S. ( author ), Osiecki, Lisa ( author ), Pauls, David L. ( author ), Posthuma, Danielle ( author ), Ramensky, Vasily ( author ), Robertson, Mary M. ( author ), Rouleau, Guy A. ( author ), Sandor, Paul ( author ), Singer, Harvey S. ( author ), Smit, Jan ( author ), Sul, Jae-Hoon ( author )

مصطلحات موضوعية: Tourette disorder, Tourette syndrome, de novo variants, whole-exome sequencing, gene discovery, TIC Genetics, TSAICG

وصف الملف: Pages 486-499.e9

العلاقة: Neuron; S0896627317303501; http://ufdc.ufl.edu/LS00591325/00001Test

الإتاحة: https://doi.org/10.1016/j.neuron.2017.04.024Test
http://ufdc.ufl.edu/LS00591325/00001Test

المؤلفون: Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA ( host institution ), Huang, Alden Y. ( author ), Yu, Dongmei ( author ), Davis, Lea K. ( author ), Sul, Jae Hoon ( author ), Tsetsos, Fotis ( author ), Ramensky, Vasily ( author ), Zelaya, Ivette ( author ), Ramos, Eliana Marisa ( author ), Osiecki, Lisa ( author ), Chen, Jason A. ( author ), McGrath, Lauren M. ( author ), Illmann, Cornelia ( author ), Sandor, Paul ( author ), Barr, Cathy L. ( author ), Grados, Marco ( author ), Singer, Harvey S. ( author ), Nöthen, Markus M. ( author ), Hebebrand, Johannes ( author ), King, Robert A. ( author ), Dion, Yves ( author ), Rouleau, Guy ( author ), Budman, Cathy L. ( author ), Depienne, Christel ( author ), Worbe, Yulia ( author ), Hartmann, Andreas ( author ), Müller-Vahl, Kirsten R. ( author ), Stuhrmann, Manfred ( author ), Aschauer, Harald ( author ), Stamenkovic, Mara ( author ), Schloegelhofer, Monika ( author ), Konstantinidis, Anastasios ( author ), Lyon, Gholson J. ( author ), McMahon, William M. ( author ), Barta, Csaba ( author ), Tarnok, Zsanett ( author ), Nagy, Peter ( author ), Batterson, James R. ( author ), Rizzo, Renata ( author ), Cath, Danielle C. ( author ), Wolanczyk, Tomasz ( author ), Berlin, Cheston ( author ), Malaty, Irene A. ( UF author ), Okun, Michael S. ( UF author ), Woods, Douglas W. ( author ), Rees, Elliott ( author ), Pato, Carlos N. ( author ), Pato, Michele T. ( author ), Knowles, James A. ( author ), Posthuma, Danielle ( author ), Pauls, David L. ( author ), Cox, Nancy J. ( author ), Neale, Benjamin M. ( author ), Freimer, Nelson B. ( author ), Paschou, Peristera ( author ), Mathews, Carol A. ( UF author ), Scharf, Jeremiah M. ( author ), Coppola, Giovanni ( author ), Bruun, Ruth D. ( author ), Chouinard, Sylvain ( author ), Darrow, Sabrina ( author ), Greenberg, Erica ( author ), Hirschtritt, Matthew E. ( author ), Kurlan, Roger ( author ), Leckman, James F. ( author ), Robertson, Mary M. ( author ), Smit, Jan ( author )

مصطلحات موضوعية: Tourette Syndrome, tic disorders, neurodevelopmental disorders, genetics, structural variation, copy number variation, NRXN1, CNTN6

وصف الملف: Pages 1101-1111.e7

العلاقة: Neuron; S0896627317305081; http://ufdc.ufl.edu/LS00591631/00001Test

الإتاحة: https://doi.org/10.1016/j.neuron.2017.06.010Test
http://ufdc.ufl.edu/LS00591631/00001Test

المؤلفون: Yu, DongMei, Keenan, Clare L., Gamazon, Eric R., Konkashbaev, Anuar I., Derks, Eske M., Neale, Benjamin M., Yang, Jian, Lee, S. Hong, Evans, Patrick, Barr, Cathy L., Bellodi, Laura, Benarroch, Fortu, Berrio, Gabriel Bedoya, Bienvenu, Oscar J., Bloch, Michael H., Blom, Rianne M., Bruun, Ruth D., Budman, Cathy L., Camarena, Beatriz, Campbell, Desmond, Cappi, Carolina, Cardona Silgado, Julio C., Cath, Danielle C., Cavallini, Maria C., Chavira, Denise A., Chouinard, Sylvian, Conti, David V., Cook, Edwin H., Coric, Vladimir, Cullen, Bernadette A., Deforce, Dieter, Delorme, Richard, Dion, Yves, Edlund, Christopher K., Egberts, Karin, Falkai, Peter, Fernandez, Thomas V., Gallagher, Patience J., Garrido, Helena, Geller, Daniel, Girard, Simon L., Grabe, Hans J., Grados, Marco A., Greenberg, Benjamin D., Gross-Tsur, Varda, Haddad, Stephen, Heiman, Gary A., Hemmings, Sian M. J., Hounie, Ana G., Illmann, Cornelia, Jankovic, Joseph, Jenike, Micheal A., Kennedy, James L., King, Robert A., Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F., Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Lowe, Thomas L., Macciardi, Fabio, McCracken, James T., McGrath, Lauren M., Restrepo, Sandra C. Mesa, Moessner, Rainald, Morgan, Jubel, Muller, Heike, Murphy, Dennis L., Naarden, Allan L., Ochoa, William Cornejo, Ophoff, Roel A., Osiecki, Lisa, Pakstis, Andrew J., Pato, Michele T., Pato, Carlos N., Piacentini, John, Pittenger, Christopher, Pollak, Yehunda, Rauch, Scott L., Renner, Tobias J., Reus, Victor I., Richter, Margaret A., Riddle, Mark A., Robertson, Mary M., Romero, Roxana, Rosàrio, Maria C., Rosenberg, David, Rouleau, Guy A., Ruhrmann, Stephan, Ruiz-Linares, Andreas, Sampaio, Aline S., Samuels, Jack, Sandor, Paul, Sheppard, Broke, Singer, Harvey S., Smit, Jan H., Stein, Dan J., Strengman, E., Tischfield, Jay A., Valencia Duarte, Ana V., Vallada, Homero, Van Nieuwerburgh, Flip, Veenstra-VanderWeele, Jeremy, Walitza, Susanne, Wang, Ying, Wendland, Jens R., Westenberg, Herman G. M., Shugart, Yin Yao, Miguel, Euripedes C., McMahon, William, Wagner, Michael, Nicolini, Humberto, Posthuma, Danielle, Hanna, Gregory L., Heutink, Peter, Denys, Damiaan, Arnold, Paul D., Oostra, Ben A., Nestadt, Gerald, Freimer, Nelson B., Pauls, David L., Wray, Naomi R., Stewart, S. Evelyn, Mathews, Carol A., Knowles, James A., Cox, Nancy J., Scharf, Jeremiah M., http://data.europeana.eu/agent/base/139083Test, http://data.europeana.eu/agent/base/113589Test, Davis, Lea K.

الوصول الحر: https://www.europeana.eu/item/2048441/item_DKCYXUCIPSRZQMEOTZNOJTTQQGFXR4SH?utm_source=api&utm_medium=api&utm_campaign=YuvuWBeCaTest

المؤلفون: Davis, Lea K., Yu, Dongmei, Keenan, Clare L., Gamazon, Eric R., Konkashbaev, Anuar I., Derks, Eske M., Neale, Benjamin M., Yang, Jian, Lee, S. Hong, Evans, Patrick, Barr, Cathy L., Bellodi, Laura, Benarroch, Fortu, Berrio, Gabriel Bedoya, Bienvenu, Oscar J., Bloch, Michael H., Blom, Rianne M., Bruun, Ruth D., Budman, Cathy L., Camarena, Beatriz, Campbell, Desmond, Cappi, Carolina, Cardona Silgado, Julio C., Cath, Danielle C., Cavallini, Maria C., Chavira, Denise A., Chouinard, Sylvian, Conti, David V., Cook, Edwin H., Coric, Vladimir, Cullen, Bernadette A., Deforce, Dieter, Delorme, Richard, Dion, Yves, Edlund, Christopher K., Egberts, Karin, Falkai, Peter, Fernandez, Thomas V., Gallagher, Patience J., Garrido, Helena, Geller, Daniel, Girard, Simon L., Grabe, Hans J., Grados, Marco A., Greenberg, Benjamin D., Gross-Tsur, Varda, Haddad, Stephen, Heiman, Gary A., Hemmings, Sian M. J., Hounie, Ana G., Illmann, Cornelia, Jankovic, Joseph, Jenike, Micheal A., Kennedy, James L., King, Robert A., Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F., Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Lowe, Thomas L., Macciardi, Fabio, McCracken, James T., McGrath, Lauren M., Restrepo, Sandra C. Mesa, Moessner, Rainald, Morgan, Jubel, Muller, Heike, Murphy, Dennis L., Naarden, Allan L., Ochoa, William Cornejo, Ophoff, Roel A., Osiecki, Lisa, Pakstis, Andrew J., Pato, Michele T., Pato, Carlos N., Piacentini, John, Pittenger, Christopher, Pollak, Yehunda, Rauch, Scott L., Renner, Tobias J., Reus, Victor I., Richter, Margaret A., Riddle, Mark A., Robertson, Mary M., Romero, Roxana, Rosàrio, Maria C., Rosenberg, David, Rouleau, Guy A., Ruhrmann, Stephan, Ruiz-Linares, Andreas, Sampaio, Aline S., Samuels, Jack, Sandor, Paul, Sheppard, Broke, Singer, Harvey S., Smit, Jan H., Stein, Dan J., Strengman, E., Tischfield, Jay A., Valencia Duarte, Ana V., Vallada, Homero, Van Nieuwerburgh, Flip, Veenstra-VanderWeele, Jeremy, Walitza, Susanne, Wang, Ying, Wendland, Jens R., Westenberg, Herman G. M., Shugart, Yin Yao, Miguel, Euripedes C., McMahon, William, Wagner, Michael, Nicolini, Humberto, Posthuma, Danielle, Hanna, Gregory L., Heutink, Peter, Denys, Damiaan, Arnold, Paul D., Oostra, Ben A., Nestadt, Gerald, Freimer, Nelson B., Pauls, David L., Wray, Naomi R., Stewart, S. Evelyn, Mathews, Carol A., Knowles, James A., Cox, Nancy J., Scharf, Jeremiah M.

مصطلحات موضوعية: ddc:616

وصف الملف: application/pdf

العلاقة: https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/12737Test; urn:nbn:de:bvb:20-opus-127377; https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-127377Test; https://doi.org/10.1371/journal.pgen.1003864Test; https://opus.bibliothek.uni-wuerzburg.de/files/12737/058_Davis_Plos_Genetics.pdfTest

الإتاحة: https://doi.org/10.1371/journal.pgen.1003864Test
https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/12737Test
https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-127377Test
https://opus.bibliothek.uni-wuerzburg.de/files/12737/058_Davis_Plos_Genetics.pdfTest

المؤلفون: Keller, Matthew C., Davis, Lea K., Yu, Dongmei, Keenan, Clare L., Gamazon, Eric R., Konkashbaev, Anuar I., Derks, Eske M., Neale, Benjamin M., Yang, Jian, Lee, S. Hong, Evans, Patrick, Barr, Cathy L., Bellodi, Laura, Benarroch, Fortu, Berrio, Gabriel Bedoya, Bienvenu, Oscar J., Bloch, Michael H., Blom, Rianne M., Bruun, Ruth D., Budman, Cathy L., Camarena, Beatriz, Campbell, Desmond, Cappi, Carolina, Cardona Silgado, Julio C., Cath, Danielle C., Cavallini, Maria C., Chavira, Denise A., Chouinard, Sylvain, Conti, David V., Cook, Edwin H., Coric, Vladimir, Cullen, Bernadette A., Deforce, Dieter, Delorme, Richard, Dion, Yves, Edlund, Christopher K., Egberts, Karin, Falkai, Peter, Fernandez, Thomas V., Gallagher, Patience J., Garrido, Helena, Geller, Daniel, Girard, Simon L., Grabe, Hans J., Grados, Marco A., Greenberg, Benjamin D., Gross-Tsur, Varda, Haddad, Stephen, Heiman, Gary A., Hemmings, Sian M. J., Hounie, Ana G., Illmann, Cornelia, Jankovic, Joseph, Jenike, Michael A., Kennedy, James L., King, Robert A., Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F., Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Lowe, Thomas L., Macciardi, Fabio, McCracken, James T., McGrath, Lauren M., Mesa Restrepo, Sandra C., Moessner, Rainald, Morgan, Jubel, Muller, Heike, Murphy, Dennis L., Naarden, Allan L., Ochoa, William Cornejo, Ophoff, Roel A., Osiecki, Lisa, Pakstis, Andrew J., Pato, Michele T., Pato, Carlos N., Piacentini, John, Pittenger, Christopher, Pollak, Yehuda, Rauch, Scott L., Renner, Tobias J., Reus, Victor I., Richter, Margaret A., Riddle, Mark A., Robertson, Mary M., Romero, Roxana, Rosàrio, Maria C., Rosenberg, David, Rouleau, Guy A., Ruhrmann, Stephan, Ruiz-Linares, Andres, Sampaio, Aline S., Samuels, Jack, Sandor, Paul, Sheppard, Brooke, Singer, Harvey S., Smit, Jan H., Stein, Dan J., Strengman, E., Tischfield, Jay A., Valencia Duarte, Ana V., Vallada, Homero, Van Nieuwerburgh, Filip, Veenstra-VanderWeele, Jeremy, Walitza, Susanne, Wang, Ying, Wendland, Jens R., Westenberg, Herman G. M., Shugart, Yin Yao, Miguel, Euripedes C., McMahon, William, Wagner, Michael, Nicolini, Humberto, Posthuma, Danielle, Hanna, Gregory L., Heutink, Peter, Denys, Damiaan, Arnold, Paul D., Oostra, Ben A., Nestadt, Gerald, Freimer, Nelson B., Pauls, David L., Wray, Naomi R., Stewart, S. Evelyn, Mathews, Carol A., Knowles, James A., Cox, Nancy J., Scharf, Jeremiah M.

وصف الملف: text

العلاقة: http://eprints.gla.ac.uk/136784/1/136784.PDFTest; Keller, M. C. et al. (2013) Partitioning the heritability of Tourette Syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS Genetics , 9(10), e1003864. (doi:10.1371/journal.pgen.1003864 ) (PMID:24204291) (PMCID:PMC3812053)

الإتاحة: https://doi.org/10.1371/journal.pgen.1003864Test
http://eprints.gla.ac.uk/136784Test/
http://eprints.gla.ac.uk/136784/1/136784.PDFTest

المؤلفون: Keen-Kim, Dianne, Mathews, Carol A., Reus, Victor I., Lowe, Thomas L., Herrera, Luis Diego, Budman, Cathy L., Gross-Tsur, Varda, Pulver, Ann E., Bruun, Ruth D., Erenberg, Gerald, Naarden, Allan, Sabatti, Chiara, Freimer, Nelson B.

مصطلحات موضوعية: ARTICLES

وصف الملف: text/html

العلاقة: http://hmg.oxfordjournals.org/cgi/content/short/15/22/3324Test; http://dx.doi.org/10.1093/hmg/ddl408Test

الإتاحة: https://doi.org/10.1093/hmg/ddl408Test
http://hmg.oxfordjournals.org/cgi/content/short/15/22/3324Test

المؤلفون: Yu, Dongmei, Sul, Jae Hoon, Tsetsos, Fotis, Nawaz, Muhammad S., Huang, Alden Y., Zelaya, Ivette, Illmann, Cornelia, Osiecki, Lisa, Darrow, Sabrina M., Hirschtritt, Matthew E., Greenberg, Erica, Muller-Vahl, Kirsten R., Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy, Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Sandor, Paul, Barr, Cathy L., Grados, Marco, Singer, Harvey S., Nöthen, Markus M., Hebebrand, Johannes, Hinney, Anke, King, Robert A., Fernandez, Thomas V., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L., Rizzo, Renata, Lyon, Gholson J., McMahon, William M., Batterson, James R., Cath, Danielle C., Malaty, Irene A., Okun, Michael S., Berlin, Cheston, Woods, Douglas W., Lee, Paul C., Jankovic, Joseph, Robertson, Mary M., Gilbert, Donald L., Brown, Lawrence W., Coffey, Barbara J., Dietrich, Andrea, Hoekstra, Pieter J., Kuperman, Samuel, Zinner, Samuel H., Luðvigsson, Pétur, Sæmundsen, Evald, Thorarensen, Ólafur, Atzmon, Gil, Barzilai, Nir, Wagner, Michael, Moessner, Rainald, Ophoff, Roel, Pato, Carlos N., Pato, Michele T., Knowles, James A., Roffman, Joshua L., Smoller, Jordan W., Buckner, Randy L., Jeremy Willsey, A., Tischfield, Jay A., Heiman, Gary A., Stefansson, Hreinn, Stefansson, Kári, Posthuma, Danielle, Cox, Nancy J., Pauls, David L., Freimer, Nelson B., Neale, Benjamin M., Davis, Lea K., Paschou, Peristera, Coppola, Giovanni, Mathews, Carol A., Scharf, Jeremiah M., Bruun, Ruth D., Chouinard, Sylvain, Grados, Marco A., Kurlan, Roger, Leckman, James F., Rouleau, Guy A., Smit, Jan, Wolanczyk, Tomasz

المساهمون: Complex Trait Genetics, Amsterdam Neuroscience - Cellular & Molecular Mechanisms, Clinical Cognitive Neuropsychiatry Research Program (CCNP), Amsterdam Reproduction & Development (AR&D), Amsterdam Neuroscience - Complex Trait Genetics, Plastic, Reconstructive and Hand Surgery, ANS - Cellular & Molecular Mechanisms, Child Psychiatry

المصدر: American Journal of Psychiatry, 176(3), 217-227. American Psychiatric Association
American Journal of Psychiatry, 176(3), 217-227. AMER PSYCHIATRIC PUBLISHING, INC
Tourette Association of America International Consortium for Genetics, Gilles de la Tourette GWAS Replication Initiative, Tourette International Collaborative Genetics Study & Psychiatric Genomics Consortium Tourette Syndrome Working Group 2019, ' Interrogating the genetic determinants of Tourette's syndrome and other tiC disorders through genome-wide association studies ', American Journal of Psychiatry, vol. 176, no. 3, pp. 217-227 . https://doi.org/10.1176/appi.ajp.2018.18070857Test
Yu, D, Sul, J H, Tsetsos, F, Nawaz, M S, Huang, A Y, Zelaya, I, Illmann, C, Osiecki, L, Darrow, S M, Hirschtritt, M E, Greenberg, E, Muller-Vahl, K R, Stuhrmann, M, Dion, Y, Rouleau, G, Aschauer, H, Stamenkovic, M, Psychiatric Genomics Consortium Tourette Syndrome Working Group, Schlögelhofer, M, Sandor, P, Barr, C L, Grados, M, Singer, H S, Nöthen, M M, Hebebrand, J, Hinney, A, King, R A, Fernandez, T V, Barta, C, Tarnok, Z, Nagy, P, Depienne, C, Worbe, Y, Hartmann, A, Budman, C L, Rizzo, R, Lyon, G J, McMahon, W M, Batterson, J R, Cath, D C, Malaty, I A, Okun, M S, Berlin, C, Woods, D W, Lee, P C, Jankovic, J, Robertson, M M, Gilbert, D L, Brown, L W, Smit, J, Tourette Association of America International Consortium for Genetics, Gilles de la Tourette GWAS Replication Initiative & Tourette International Collaborative Genetics Study 2019, ' Interrogating the genetic determinants of Tourette's syndrome and other tiC disorders through genome-wide association studies ', American Journal of Psychiatry, vol. 176, no. 3, pp. 217-227 . https://doi.org/10.1176/appi.ajp.2018.18070857Test
American journal of psychiatry, 176(3), 217-227. American Psychiatric Association

مصطلحات موضوعية: medicine.medical_specialty, Multifactorial Inheritance, congenital, hereditary, and neonatal diseases and abnormalities, Tourette's syndrome, Medizin, Genome-wide association study, Biology, Tourette syndrome, Polymorphism, Single Nucleotide, Severity of Illness Index, Article, 03 medical and health sciences, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Risk Factors, mental disorders, Child and adolescent psychiatry, medicine, Humans, Genetic Predisposition to Disease, Copy-number variation, Genetics, COPY NUMBER VARIANTS, RISK, medicine.disease, Genetic architecture, 030227 psychiatry, Psychiatry and Mental health, fms-Like Tyrosine Kinase 3, Case-Control Studies, Tic Disorders, 030217 neurology & neurosurgery, Genome-Wide Association Study, Tourette Syndrome

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09b5c523aeaced47b2e0bb30dadc23e2Test
https://research.vu.nl/en/publications/1bf0c4dd-5573-40e1-a14a-b6093461f054Test