نتائج البحث - "Hounie A. G."

المساهمون: Psychiatry, APH - Methodology, APH - Mental Health, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, Amsterdam Neuroscience - Complex Trait Genetics, Adult Psychiatry, ANS - Compulsivity, Impulsivity & Attention, Complex Trait Genetics

المصدر: Translational Psychiatry, 11
Burton, C L, Lemire, M, Xiao, B, Corfield, E C, Erdman, L, Bralten, J, Poelmans, G, Yu, D, Shaheen, S M, Goodale, T, Sinopoli, V M, Soreni, N, Hanna, G L, Fitzgerald, K, Rosenberg, D, Nestadt, G, Paterson, A D, Strug, L J, Schachar, R, Crosbie, J, Arnold, P D & OCD Working Group of the Psychiatric Genomics Consortium 2021, ' Genome-wide association study of pediatric obsessive-compulsive traits : shared genetic risk between traits and disorder ', Translational Psychiatry, vol. 11, no. 1, 91 . https://doi.org/10.1038/s41398-020-01121-9Test
Translational Psychiatry, 11, 1
Translational Psychiatry
Translational Psychiatry, Vol 11, Iss 1, Pp 1-10 (2021)
OCD Working Group of the Psychiatric Genomics Consortium 2021, ' Genome-wide association study of pediatric obsessive-compulsive traits : shared genetic risk between traits and disorder ', Translational Psychiatry, vol. 11, no. 1, 91 . https://doi.org/10.1038/s41398-020-01121-9Test
Translational Psychiatry, 11(1):91. Nature Publishing Group
Translational psychiatry, 11(1):91. Nature Publishing Group

مصطلحات موضوعية: Obsessive-Compulsive Disorder, Adolescent, Locus (genetics), Genome-wide association study, Biology, Genetic correlation, Article, lcsh:RC321-571, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, All institutes and research themes of the Radboud University Medical Center, Risk Factors, Statistical significance, Human behaviour, mental disorders, Humans, Genetic risk, Child, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, Biological Psychiatry, 030304 developmental biology, Genetic association, Genetics, 0303 health sciences, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Obsessive-compulsive trait, Genomics, 3. Good health, Psychiatry and Mental health, Phenotype, Trait, Compulsive Behavior, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f13cc3bf390ecedd059ab198db424373Test
http://hdl.handle.net/2066/231401Test

8

دورية أكاديمية

Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture

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

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9

دورية أكاديمية

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

المؤلفون: Davis, L. K., Yu, D., Keenan, C. L., Gamazon, E. R., Konkashbaev, A. I., Derks, E. M., Neale, B. M., Yang, J., Lee, S. H., Evans, P., Barr, C. L., Bellodi, L., Benarroch, F., Berrio, G. B., Bienvenu, O. J., Bloch, M. H., Blom, R. M., Bruun, R. D., Budman, C. L., Camarena, B., Campbell, D., Cappi, C., Cardona Silgado, J. C., Cath, D. C., Cavallini, M. C., Chavira, D. A., Chouinard, S., Conti, D. V., Cook, E. H., Coric, V., Cullen, B. A., Deforce, D., Delorme, R., Dion, Y., Edlund, C. K., Egberts, K., Falkai, P., Fernandez, T. V., Gallagher, P. J., Garrido, H., Geller, D., Girard, Simon, Grabe, H. J., Grados, M. A., Greenberg, B. D., Gross-Tsur, V., Haddad, S., Heiman, G. A., Hemmings, S. M.J., Hounie, A. G., Illmann, C., Jankovic, J., Jenike, M. A., Kennedy, J. L., King, R. A., Kremeyer, B., Kurlan, R., Lanzagorta, N., Leboyer, M., Leckman, J. F., Lennertz, L., Liu, C., Lochner, C., Lowe, T. L., Macciardi, F., McCracken, J. T., McGrath, L. M., Mesa Restrepo, S. C., Moessner, R., Morgan, J., Muller, H., Murphy, D. L., Naarden, A. L., Ochoa, W. C., Ophoff, R. A., Osiecki, L., Pakstis, A. J., Pato, M. T., Pato, C. N., Piacentini, J., Pittenger, C., Pollak, Y., Rauch, S. L., Renner, T. J., Reus, V. I., Richter, M. A., Riddle, M. A., Robertson, M. M., Romero, R., Rosario, M. C., Rosenberg, D., Rouleau, G. A., Ruhrmann, S., Ruiz-Linares, A., Sampaio, A. S., Samuels, J., Sandor, P., Sheppard, B., Singer, H. S., Smit, J. H., Stein, D. J., Strengman, E., Tischfield, J. A., Valencia Duarte, A. V., Vallada, H., Van Nieuwerburgh, F., Veenstra-Vanderweele, J., Walitza, S., Wang, Y., Wendland, J. R., Westenberg, H. G.M., Shugart, Y. Y., Miguel, E. C., McMahon, W., Wagner, M., Nicolini, H., Posthuma, D., Hanna, G. L., Heutink, P., Denys, D., Arnold, P. D., Oostra, B. A., Nestadt, G., Freimer, N. B., Pauls, D. L., Wray, N. R., Stewart, S. E., Mathews, C. A., Knowles, J. A., Cox, N. J., Scharf, J. M.

مصطلحات موضوعية: Génétique

وصف الملف: application/pdf

العلاقة: https://constellation.uqac.ca/5144Test/; http://dx.doi.org/doi:10.1371/journal.pgen.1003864Test; https://constellation.uqac.ca/5144/1/Davis2013_Partitioning_the_heritability.pdfTest; Davis L. K., Yu D., Keenan C. L., Gamazon E. R., Konkashbaev A. I., Derks E. M., Neale B. M., Yang J., Lee S. H., Evans P., Barr C. L., Bellodi L., Benarroch F., Berrio G. B., Bienvenu O. J., Bloch M. H., Blom R. M., Bruun R. D., Budman C. L., Camarena B., Campbell D., Cappi C., Cardona Silgado J. C., Cath D. C., Cavallini M. C., Chavira D. A., Chouinard S., Conti D. V., Cook E. H., Coric V., Cullen B. A., Deforce D., Delorme R., Dion Y., Edlund C. K., Egberts K., Falkai P., Fernandez T. V., Gallagher P. J., Garrido H., Geller D., Girard Simon, Grabe H. J., Grados M. A., Greenberg B. D., Gross-Tsur V., Haddad S., Heiman G. A., Hemmings S. M.J., Hounie A. G., Illmann C., Jankovic J., Jenike M. A., Kennedy J. L., King R. A., Kremeyer B., Kurlan R., Lanzagorta N., Leboyer M., Leckman J. F., Lennertz L., Liu C., Lochner C., Lowe T. L., Macciardi F., McCracken J. T., McGrath L. M., Mesa Restrepo S. C., Moessner R., Morgan J., Muller H., Murphy D. L., Naarden A. L., Ochoa W. C., Ophoff R. A., Osiecki L., Pakstis A. J., Pato M. T., Pato C. N., Piacentini J., Pittenger C., Pollak Y., Rauch S. L., Renner T. J., Reus V. I., Richter M. A., Riddle M. A., Robertson M. M., Romero R., Rosario M. C., Rosenberg D., Rouleau G. A., Ruhrmann S., Ruiz-Linares A., Sampaio A. S., Samuels J., Sandor P., Sheppard B., Singer H. S., Smit J. H., Stein D. J., Strengman E., Tischfield J. A., Valencia Duarte A. V., Vallada H., Van Nieuwerburgh F., Veenstra-Vanderweele J., Walitza S., Wang Y., Wendland J. R., Westenberg H. G.M., Shugart Y. Y., Miguel E. C., McMahon W., Wagner M., Nicolini H., Posthuma D., Hanna G. L., Heutink P., Denys D., Arnold P. D., Oostra B. A., Nestadt G., Freimer N. B., Pauls D. L., Wray N. R., Stewart S. E., Mathews C. A., Knowles J. A., Cox N. J. et Scharf J. M. (2013). Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PloS Genetics, 9, (10), e1003864.

الإتاحة: https://doi.org/10.1371/journal.pgen.1003864Test
https://constellation.uqac.ca/5144/1/Davis2013_Partitioning_the_heritability.pdfTest

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10

دورية أكاديمية

Partitioning the heritability of Tourette Syndrome and obsessive compulsive disorder reveals differences in genetic architecture

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

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