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1دورية أكاديمية
المؤلفون: Tsetsos, F., Yu, D., Sul, J.H., Huang, A.Y., Illmann, C., Osiecki, L., Darrow, S.M., Hirschtritt, M.E., Greenberg, E., Muller-Vahl, K.R., Stuhrmann, M., Dion, Y., Rouleau, G.A., Aschauer, H., Stamenkovic, M., Schlögelhofer, M., Sandor, P., Barr, C.L., Grados, M.A., 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., Coffey, B.J., Dietrich, A., Hoekstra, P.J., Kuperman, S., Zinner, S.H., Wagner, M., Knowles, J.A., Jeremy Willsey, A., Tischfield, J.A., Heiman, G.A., Cox, N.J., Freimer, N.B., Neale, B.M., Davis, L.K., Coppola, G., Mathews, C.A., Scharf, J.M., Paschou, P., Darrow, S., Kurlan, R., Leckman, J.F., Smit, J.H., Aschauer, HAH, Konstantinidis, A., Müller-Vahl, K., Wolanczyk, T., Brown, L., Cheon, K.A., Garcia-Delgar, B., Gilbert, D., Grice, D.E., Hagstrøm, J., Hedderly, T., Heyman, I., Huyser, C., Kim, Y.K., Kim, Y.S., Koh, Y.J., Kook, S., Leventhal, B.L., Madruga-Garrido, M., Mir, P., Morer, A., Münchau, A., Plessen, K.J., Roessner, V., Shin, E.Y., Song, D.H., Song, J., Willsey, A.J., Zinner, S., Fernandez, T., Heiman, G., Hoekstra, P., Tischfield, J., Woods, D.
المساهمون: 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
المصدر: Translational psychiatry, vol. 11, no. 1, pp. 56
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33462189; info:eu-repo/semantics/altIdentifier/eissn/2158-3188; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_F4282F0490A38; https://serval.unil.ch/notice/serval:BIB_F4282F0490A3Test; urn:issn:2158-3188; https://serval.unil.ch/resource/serval:BIB_F4282F0490A3.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_F4282F0490A38Test
الإتاحة: https://doi.org/10.1038/s41398-020-01082-zTest
https://serval.unil.ch/notice/serval:BIB_F4282F0490A3Test
https://serval.unil.ch/resource/serval:BIB_F4282F0490A3.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_F4282F0490A38Test -
2دورية أكاديمية
المؤلفون: Findling, R.L., Blumer, J.L., Kauffman, R., Batterson, J.R., Gilbert, D.L., Bramer, S., Marcus, R.
المصدر: European Neuropsychopharmacology ; volume 13, page S335 ; ISSN 0924-977X
مصطلحات موضوعية: Pharmacology (medical), Biological Psychiatry, Psychiatry and Mental health, Neurology (clinical), Neurology, Pharmacology
الإتاحة: https://doi.org/10.1016/s0924-977xTest(03)92080-3
https://api.elsevier.com/content/article/PII:S0924977X03920803?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0924977X03920803?httpAccept=text/plainTest -
3دورية أكاديمية
المؤلفون: Jain, P., Miller-Fleming, T., Topaloudi, A., Yu, D., Drineas, P., Georgitsi, M., Yang, Z., Rizzo, R., Müller-Vahl, K.R., Tumer, Z., Mol Debes, N., Hartmann, A., Depienne, C., Worbe, Y., Mir, P., Cath, D.C., Boomsma, D.I., Roessner, V., Wolanczyk, T., Janik, P., Szejko, N., Zekanowski, C., Barta, C., Nemoda, Z., Tarnok, Z., Buxbaum, J.D., Grice, D., Glennon, J., Stefansson, H., Hengerer, B., Benaroya-Milshtein, N., Cardona, F., Hedderly, T., Heyman, I., Huyser, C., Morer, A., Mueller, N., Munchau, A., Plessen, K.J., Porcelli, C., Walitza, S., Schrag, A., Martino, D., Dietrich, A., Mathews, C.A., Scharf, J.M., Hoekstra, P.J., Davis, L.K., Paschou, P.
المساهمون: Psychiatric Genomics Consortium Tourette Syndrome Working Group (PGC-TS), EMTICS collaborative group, TS-EUROTRAIN Network, Als, T.D., Aschauer, H., Atzmon, G., Bækvad-Hansen, M., Barta, C., Barr, C.L., Barzilai, N., Batterson, J.R., Batterson, R., Benarroch, F., Berlin, C., Boberg, J., Bodmer, B., Bohnenpoll, J., Børglum, A.D., Brown, L.W., Bruun, R., Budman, C.L., Buckner, R.L., Buxbaum, J.D., Bybjerg-Grauholm, J., Cath, D.C., Cheon, K.A., Chouinard, S., Coffey, B.J., Coppola, G., Crowley, J.J., Dahl, N., Davis, L.K., Darrow, S.M., Daly, M.J., Depienne, C., De Rubeis, S., Dietrich, A., Dion, Y., Djurfeldt, D.R., Domenech-Salgado, L., Eapen, V., Elzerman, L., Fernandez, T.V., Freimer Carolin Fremer, N.B., Garcia-Delgar, B., Garrido, M., Gilbert, D.L., Giusti-Rodriguez, P., Grados, M., Greenberg, E., Grove, J., Grice, D.E., Hagstrom, J., Halvorsen, M., Hartmann, A., Hansen, B., Haavik, J., Hebebrand, J., Heiman, G.A., Herrera, L., Heyman, I., Hinney, A., Hirschtritt, M.E., Hoekstra, P.J., Sul, J.H., Hong, H.J., Hougaard, D.M., Huang, A.Y., Ibanez-Gomez, L., Ivankovic, F., Jankovic, J., Karlsson, E.K., Kaprio, J.A., Kim, Y.K., Kim, Y.S., King, R.A., Knowles, J.A., Koh, Y.J., Kook, S., Khalifa, N., Konstantinidis, A., Kuperman, S., Kurlan, R., Kvale, G., Leckman, J., Lee, P.C., Leventhal, B., Lichtenstein, P., Lindbald-Toh, K., Lowe, T., Ludolph, A., da Silva, C.L., Luðvigsson, P., Luykx, J., Lyon, G.J., Mahjani, B., Maras, A., Mataix-Cols, D., Mattheisen, M., Mathews, C.A.
المصدر: Translational psychiatry, vol. 13, no. 1, pp. 69
مصطلحات موضوعية: Male, Female, Humans, Tourette Syndrome/genetics, Diabetes Mellitus, Type 2, Autism Spectrum Disorder/genetics, Attention Deficit Disorder with Hyperactivity/genetics, Risk Factors
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36823209; info:eu-repo/semantics/altIdentifier/eissn/2158-3188; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_D89B5DC77CB53; https://serval.unil.ch/notice/serval:BIB_D89B5DC77CB5Test; urn:issn:2158-3188; https://serval.unil.ch/resource/serval:BIB_D89B5DC77CB5.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_D89B5DC77CB53Test
الإتاحة: https://doi.org/10.1038/s41398-023-02341-5Test
https://serval.unil.ch/notice/serval:BIB_D89B5DC77CB5Test
https://serval.unil.ch/resource/serval:BIB_D89B5DC77CB5.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_D89B5DC77CB53Test -
4دورية أكاديمية
المؤلفون: Wang, S., Mandell, J.D., Kumar, Y., Sun, N., Morris, M.T., Arbelaez, J., Nasello, C., Dong, S., Duhn, C., Zhao, X., Yang, Z., Padmanabhuni, S.S., Yu, D., King, R.A., Dietrich, A., Khalifa, N., Dahl, N., Huang, A.Y., Neale, B.M., Coppola, G., Mathews, C.A., Scharf, J.M., Fernandez, T.V., Buxbaum, J.D., De Rubeis, S., Grice, D.E., Xing, J., Heiman, G.A., Tischfield, J.A., Paschou, P., Willsey, A.J., State, M.W.
المساهمون: Tourette International Collaborative Genetics Study (TIC Genetics), Tourette Syndrome Genetics Southern and Eastern Europe Initiative (TSGENESEE), Tourette Association of America International Consortium for Genetics (TAAICG), Abdulkadir, M., Arbelaez, J., Bodmer, B., Bromberg, Y., Brown, L.W., Cheon, K.A., Coffey, B.J., Deng, L., Dietrich, A., Dong, S., Duhn, C., Elzerman, L., Fernandez, T.V., Fremer, C., Garcia-Delgar, B., Gilbert, D.L., Grice, D.E., Hagstrøm, J., Hedderly, T., Heiman, G.A., Heyman, I., Hoekstra, P.J., Hong, H.J., Huyser, C., Kim, E.J., Kim, Y.K., Kim, Y.S., King, R.A., Koh, Y.J., Kook, S., Kuperman, S., Leventhal, B.L., Ludolph, A.G., Madruga-Garrido, M., Mandell, J.D., Maras, A., Mir, P., Morer, A., Morris, M.T., Müller-Vahl, K., Münchau, A., Murphy, T.L., Nasello, C., Plessen, K.J., Poisner, H., Roessner, V., Sanders, S.J., Shin, E.Y., Song, D.H., Song, J., State, M.W., Sun, N., Thackray, J.K., Tischfield, J.A., Tübing, J., Visscher, F., Wanderer, S., Wang, S., Willsey, A.J., Woods, M., Xing, J., Zhang, Y., Zhao, X., Zinner, S.H., Androutsos, C., Barta, C., Farkas, L., Fichna, J., Georgitsi, M., Janik, P., Karagiannidis, I., Koumoula, A., Nagy, P., Paschou, P., Puchala, J., Rizzo, R., Szejko, N., Szymanska, U., Tarnok, Z., Tsironi, V., Wolanczyk, T., Zekanowski, C., Barr, C.L., Batterson, J.R., Berlin, C., Bruun, R.D., Budman, C.L., Cath, D.C., Chouinard, S., Coppola, G., Cox, N.J., Darrow, S., Davis, L.K., Dion, Y., Freimer, N.B., Grados, M.A., Hirschtritt, M.E.
المصدر: Cell reports, vol. 24, no. 13, pp. 3441-3454.e12
مصطلحات موضوعية: Adult, Cadherins/genetics, Cell Polarity, Child, DNA Copy Number Variations, Female, Humans, Male, Pedigree, Receptors, Cell Surface/genetics, Tourette Syndrome/genetics, Tourette Syndrome/pathology, TIC Genetics, Tourette disorder, copy number variants, de novo variants, gene discovery, microarray genotyping, multiplex, simplex, whole exome sequencing
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30257206; info:eu-repo/semantics/altIdentifier/eissn/2211-1247; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_916205B4C8EC2; https://serval.unil.ch/notice/serval:BIB_916205B4C8ECTest; https://serval.unil.ch/resource/serval:BIB_916205B4C8EC.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_916205B4C8EC2Test
الإتاحة: https://doi.org/10.1016/j.celrep.2018.08.082Test
https://serval.unil.ch/notice/serval:BIB_916205B4C8ECTest
https://serval.unil.ch/resource/serval:BIB_916205B4C8EC.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_916205B4C8EC2Test -
5
المؤلفون: Sheng Wang, Jeffrey D. Mandell, Yogesh Kumar, Nawei Sun, Montana T. Morris, Juan Arbelaez, Cara Nasello, Shan Dong, Clif Duhn, Xin Zhao, Zhiyu Yang, Shanmukha S. Padmanabhuni, Dongmei Yu, Robert A. King, Andrea Dietrich, Najah Khalifa, Niklas Dahl, Alden Y. Huang, Benjamin M. Neale, Giovanni Coppola, Carol A. Mathews, Jeremiah M. Scharf, Thomas V. Fernandez, Joseph D. Buxbaum, Silvia De Rubeis, Dorothy E. Grice, Jinchuan Xing, Gary A. Heiman, Jay A. Tischfield, Peristera Paschou, A. Jeremy Willsey, Matthew W. State, Mohamed Abdulkadir, Benjamin Bodmer, Yana Bromberg, Lawrence W. Brown, Keun-Ah Cheon, Barbara J. Coffey, Li Deng, Lonneke Elzerman, Carolin Fremer, Blanca Garcia-Delgar, Donald L. Gilbert, Julie Hagstrøm, Tammy Hedderly, Isobel Heyman, Pieter J. Hoekstra, Hyun Ju Hong, Chaim Huyser, Eun-Joo Kim, Young Key Kim, Young-Shin Kim, Yun-Joo Koh, Sodahm Kook, Samuel Kuperman, Bennett L Leventhal, Andrea G. Ludolph, Marcos Madruga-Garrido, Athanasios Maras, Pablo Mir, Astrid Morer, Montana T Morris, Kirsten Müller-Vahl, Alexander Münchau, Tara L. Murphy, Kerstin J. Plessen, Hannah Poisner, Veit Roessner, Stephan J. Sanders, Eun-Young Shin, Dong-Ho Song, Jungeun Song, Joshua K. Thackray, Jennifer Tübing, Frank Visscher, Sina Wanderer, A Jeremy Willsey, Martin Woods, Yeting Zhang, Samuel H. Zinner, Christos Androutsos, Csaba Barta, Luca Farkas, Jakub Fichna, Marianthi Georgitsi, Piotr Janik, Iordanis Karagiannidis, Anastasia Koumoula, Peter Nagy, Joanna Puchala, Renata Rizzo, Natalia Szejko, Urszula Szymanska, Zsanett Tarnok, Vaia Tsironi, Tomasz Wolanczyk, Cezary Zekanowski, Cathy L. Barr, James R. Batterson, Cheston Berlin, Ruth D. Bruun, Cathy L. Budman, Danielle C. Cath, Sylvain Chouinard, Nancy J. Cox, Sabrina Darrow, Lea K. Davis, Yves Dion, Nelson B. Freimer, Marco A. Grados, Matthew E. Hirschtritt, Cornelia Illmann, Roger Kurlan, James F. Leckman, Gholson J. Lyon, Irene A. Malaty, William M. MacMahon, Michael S. Okun, Lisa Osiecki, David L. Pauls, Danielle Posthuma, Vasily Ramensky, Mary M. Robertson, Guy A. Rouleau, Paul Sandor, Harvey S. Singer, Jan Smit, Jae-Hoon Sul
المساهمون: Tourette International Collaborative Genetics Study (TIC Genetics), Tourette Syndrome Genetics Southern and Eastern Europe Initiative (TSGENESEE), Tourette Association of America International Consortium for Genetics (TAAICG), Abdulkadir, M., Arbelaez, J., Bodmer, B., Bromberg, Y., Brown, L.W., Cheon, K.A., Coffey, B.J., Deng, L., Dietrich, A., Dong, S., Duhn, C., Elzerman, L., Fernandez, T.V., Fremer, C., Garcia-Delgar, B., Gilbert, D.L., Grice, D.E., Hagstrøm, J., Hedderly, T., Heiman, G.A., Heyman, I., Hoekstra, P.J., Hong, H.J., Huyser, C., Kim, E.J., Kim, Y.K., Kim, Y.S., King, R.A., Koh, Y.J., Kook, S., Kuperman, S., Leventhal, B.L., Ludolph, A.G., Madruga-Garrido, M., Mandell, J.D., Maras, A., Mir, P., Morer, A., Morris, M.T., Müller-Vahl, K., Münchau, A., Murphy, T.L., Nasello, C., Plessen, K.J., Poisner, H., Roessner, V., Sanders, S.J., Shin, E.Y., Song, D.H., Song, J., State, M.W., Sun, N., Thackray, J.K., Tischfield, J.A., Tübing, J., Visscher, F., Wanderer, S., Wang, S., Willsey, A.J., Woods, M., Xing, J., Zhang, Y., Zhao, X., Zinner, S.H., Androutsos, C., Barta, C., Farkas, L., Fichna, J., Georgitsi, M., Janik, P., Karagiannidis, I., Koumoula, A., Nagy, P., Paschou, P., Puchala, J., Rizzo, R., Szejko, N., Szymanska, U., Tarnok, Z., Tsironi, V., Wolanczyk, T., Zekanowski, C., Barr, C.L., Batterson, J.R., Berlin, C., Bruun, R.D., Budman, C.L., Cath, D.C., Chouinard, S., Coppola, G., Cox, N.J., Darrow, S., Davis, L.K., Dion, Y., Freimer, N.B., Grados, M.A., Hirschtritt, M.E., Huang, A.Y., Illmann, C., Kurlan, R., Leckman, J.F., Lyon, G.J., Malaty, I.A., Mathews, C.A., MacMahon, W.M., Neale, B.M., Okun, M.S., Osiecki, L., Pauls, D.L., Posthuma, D., Ramensky, V., Robertson, M.M., Rouleau, G.A., Sandor, P., Scharf, J.M., Singer, H.S., Smit, J., Sul, J.H., Yu, D.
المصدر: Cell Reports, Vol 24, Iss 13, Pp 3441-3454.e12 (2018)
Cell reports, vol. 24, no. 13, pp. 3441-3454.e12
Cell reports
Cell reports, 24(13), 3441-3454.e12. CELL PRESSمصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, DNA Copy Number Variations, Receptors, Cell Surface, Biology, Genome, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 0302 clinical medicine, RARE, SCHIZOPHRENIA, medicine, Humans, Copy-number variation, Child, NEURODEVELOPMENTAL DISORDERS, Gene, lcsh:QH301-705.5, Exome sequencing, 030304 developmental biology, Medicinsk genetik, Sequence (medicine), Genetics, 0303 health sciences, SEVERE INTELLECTUAL DISABILITY, Cadherin, MUTATIONS, AUTISM SPECTRUM DISORDER, Cell Polarity, OBSESSIVE-COMPULSIVE DISORDER, Cadherins, medicine.disease, Pedigree, PREVALENCE, CONGENITAL HEART-DISEASE, GENOME, 030104 developmental biology, lcsh:Biology (General), Schizophrenia, Medical genetics, Female, Cadherins/genetics, Receptors, Cell Surface/genetics, Tourette Syndrome/genetics, Tourette Syndrome/pathology, TIC Genetics, Tourette disorder, cell polarity, copy number variants, de novo variants, gene discovery, microarray genotyping, multiplex, simplex, whole exome sequencing, Medical Genetics, 030217 neurology & neurosurgery, Tourette Syndrome
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e531960f737482f236b0bf416aab09c3Test
http://www.sciencedirect.com/science/article/pii/S221112471831386XTest