المؤلفون: Lee, I. O., Wolstencroft, J., Housby, H., van den Bree, M. B. M., Chawner, S. J. R. A., Hall, J., IMAGINE ID Consortium, Skuse, D. H.

وصف الملف: application/pdf

العلاقة: https://orca.cardiff.ac.uk/id/eprint/169128/1/jir.13139.pdfTest; Lee, I. O., Wolstencroft, J., Housby, H., van den Bree, M. B. M. https://orca.cardiff.ac.uk/view/cardiffauthors/A000189T.htmlTest orcid:0000-0002-4426-3254 orcid:0000-0002-4426-3254, Chawner, S. J. R. A. https://orca.cardiff.ac.uk/view/cardiffauthors/A2989204.htmlTest, Hall, J. https://orca.cardiff.ac.uk/view/cardiffauthors/A680258Q.htmlTest orcid:0000-0003-2737-9009 orcid:0000-0003-2737-9009, IMAGINE ID Consortium and Skuse, D. H. 2024. The inequity of education, health and care plan provision for children and young people with intellectual and developmental disabilities. Journal of Intellectual Disability Research 10.1111/jir.13139 https://doi.org/10.1111/jir.13139Test file https://orca.cardiff.ac.uk/id/eprint/169128/1/jir.13139.pdfTest

الإتاحة: https://doi.org/10.1111/jir.13139Test
https://orca.cardiff.ac.uk/id/eprint/169128Test/
https://orca.cardiff.ac.uk/id/eprint/169128/1/jir.13139.pdfTest

المؤلفون: Drakulic D., Djurovic S., Syed Y. A., Trattaro S., Caporale N., Falk A., Ofir R., Heine V. M., Chawner S. J. R. A., Rodriguez-Moreno A., Van Den Bree M. B. M., Testa G., Petrakis S., Harwood A. J.

المساهمون: D. Drakulic, S. Djurovic, Y.A. Syed, S. Trattaro, N. Caporale, A. Falk, R. Ofir, V.M. Heine, S.J.R.A. Chawner, A. Rodriguez-Moreno, M.B.M. Van Den Bree, G. Testa, S. Petraki, A.J. Harwood

مصطلحات موضوعية: Autism spectrum disorders (ASD), Copy number variants (CNVs), human iPSC, Neurodevelopmental disorders (NDD), animal, autism spectrum disorder, gene expression regulation, genetic predisposition to disease, genomic, human, induced pluripotent stem cell, neurodevelopmental disorder, neuron, synapse, DNA copy number variation, disease susceptibility, Settore BIO/11 - Biologia Molecolare, Settore BIO/13 - Biologia Applicata, Settore BIO/18 - Genetica, Settore MED/03 - Genetica Medica, Settore MED/39 - Neuropsichiatria Infantile, Settore MED/26 - Neurologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32487215; info:eu-repo/semantics/altIdentifier/wos/WOS:000540785500002; volume:11; issue:1; firstpage:1; lastpage:18; numberofpages:18; journal:MOLECULAR AUTISM; https://hdl.handle.net/2434/919418Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85085908802

الإتاحة: https://doi.org/10.1186/s13229-020-00343-4Test
https://hdl.handle.net/2434/919418Test

المؤلفون: Maillard, A. M., Hippolyte, L., Rodríguez Herreros, Borja, Chawner, S. J. R. A, Dremmel, D., Agüera, Zaida, Fagundo, Ana Beatriz, Pain, Arnab, Martin-Brevet, S., Hilbert, A., Kurz, S., Etienne, R., Draganski, B., Jiménez-Murcia, Susana, Männik, K., Metspalu, Andres, Reigo, A., Isidor, B., Le Caignec, C., Albert, D., Mignot, C., Keren, B., van den Bree, M. B. M, Munsch, S., Fernández Aranda, Fernando, Beckmann, J., Reymond, Alexandre, Jacquemont, S., 16p11.2 European Consortium

المصدر: Articles publicats en revistes (Ciències Clíniques)

مصطلحات موضوعية: Obesitat, Malalties mentals, Obesity, Mental illness

وصف الملف: 7 p.; application/pdf

العلاقة: Versió postprint del document publicat a: https://doi.org/10.1038/ijo.2015.247Test; International Journal of Obesity, 2016, vol. 40, num. 5, p. 870-876; https://doi.org/10.1038/ijo.2015.247Test; info:eu-repo/grantAgreement/EC/H2020/692145/EU//ePerMed; http://hdl.handle.net/2445/128023Test; 656303

الإتاحة: https://doi.org/10.1038/ijo.2015.247Test
http://hdl.handle.net/2445/128023Test

المؤلفون: Maillard, A M, Hippolyte, L, Rodriguez-Herreros, B, Chawner, S J R A, Dremmel, D, Agüera, Z, Fagundo, A B, Pain, A, Martin-Brevet, S, Hilbert, A, Kurz, S, Etienne, R, Draganski, B, Jimenez-Murcia, S, Männik, K, Metspalu, A, Reigo, A, Isidor, B, Le Caignec, C, David, A, Mignot, C, Keren, B, van den Bree, M B M, Munsch, S, Fernandez-Aranda, F, Beckmann, J S, Reymond, A, Jacquemont, S

المصدر: International Journal of Obesity ; volume 40, issue 5, page 870-876 ; ISSN 0307-0565 1476-5497

مصطلحات موضوعية: Nutrition and Dietetics, Endocrinology, Diabetes and Metabolism, Medicine (miscellaneous)

الإتاحة: https://doi.org/10.1038/ijo.2015.247Test
https://www.nature.com/articles/ijo2015247.pdfTest
https://www.nature.com/articles/ijo2015247Test

المؤلفون: D'Angelo, D., Lebon, S., Chen, Q., Martin-Brevet, S., Snyder, L. G., Hippolyte, L., Hanson, E., Maillard, A. M., Faucett, W. A., Mace, A., Pain, A., Bernier, R., Chawner, S. J. R. A., David, A., Andrieux, J., Aylward, E., Baujat, G., Caldeira, I., Conus, P., Ferrari, C., Forzano, F., Gerard, M., Goin-Kochel, R. P., Grant, E., Hunter, J. V., Isidor, B., Jacquette, A., Jonch, A. E., Keren, B., Lacombe, D., Le Caignec, C., Martin, C. L., Mannik, K., Metspalu, A., Mignot, C., Mukherjee, P., Owen, M. J., Passeggeri, M., Rooryck-Thambo, C., Rosenfeld, J. A., Spence, S. J., Steinman, K. J., Tjernagel, J., Van Haelst, M., Shen, Y., Draganski, B., Sherr, E. H., Ledbetter, D. H., van den Bree, M. B. M., Beckmann, J. S., Spiro, J. E., Reymond, A., Jacquemont, S., Chung, W. K., Knoers, N. V. A. M., Martinet, D., Belfiore, M., Cuvellier, J. -C., Devries, B., Delrue, M. -A., Doco-Fenzy, M., Lebel, R., Leheup, B., Lewis, S., Mencarelli, M. A., Minet, J. -C., Vincent-Delorme, C., Moerman, A., Mucciolo, M., Ounap, K., Rajcan-Separovic, E., Renieri, A., Sanlaville, D., Faas, B. H., Koolen, D. A., Vulto-Van Silfhout, A., de Leeuw, N., Rosanfeld, J. A., Filges, I., Achatz, E., Roetzer, K. M., Bonneau, D., Guichet, A., Lazaro, L., Plessis, G., Kroisel, P. M., Reis, A., Jonveaux, P., Chantot-Bastaraud, S., Rauch, A., Demeer, B., Nordgren, A., Labalme, A., Ferrarini, A., Ramelli, G. P., Guilmatre, A., Joly-Helas, G., Haize, S., Layet, V., Le Gallic, S., de Freminville, B., Touraine, R., Van Binsbergen, E., Mathieu-Dramard, M., Barth, M., Blaumeiser, B., Masurel, A., Cailler, P., Olivier-Faivre, L., Malacarne, M., Coutton, C., Dieterich, K., Satre, V., Wallgren-Pettersson, C., Tensgrom, C., Kaksonen, S., Duban-Bedu, B., Holder, M., Rossi, M., Gaillard, D., Bock, D., Bednarek, N., Guillin, O., Bizzarri, V., Flori, E., Silengo, M., Kooy, R. F., Aboura, A., Beri, M., Delobel, B., Drunat, S., Jaros, Z., Kolk, A., Reigo, A., Zufferey, F., Beckmann, N., Faravelli, F., Alupay, H., Aaronson, B., Ackerman, S., Ankenman, K., Anwar, A., Atwell, C., Bowe, A., Beaudet, A. L., Benedetti, M., Berg, J., Berman, J., Berry, L. N., Bibb, A. L., Blaskey, L., Brennan, J., Brewton, C. M., Buckner, R., Bukshpun, P., Burko, J., Cali, P., Cerban, B., Chang, Y., Cheong, M., Chow, V., Chu, Z., Chudnovskaya, D., Cornew, L., Dale, C., Dell, J., Dempsey, A. G., Deschamps, T., Earl, R., Edgar, J., Elgin, J., Endre, J., Evans, Y. L., Findlay, A., Fischbach, G. D., Fisk, C., Fregeau, B., Gaetz, B., Gaetz, L., Garza, S., Gerdts, J., Glenn, O., Gobuty, S. E., Golembski, R., Greenup, M., Heiken, K., Hines, K., Hinkley, L., Jackson, F. I., Jenkins, J., Jeremy, R. J., Johnson, K., Kanne, S. M., Kessler, S., Khan, S. Y., Ku, M., Kuschner, E., Laakman, A. L., Lam, P., Lasala, M. W., Lee, H., La, K., Levy, S., Lian, A., Llorens, A. V., Loftus, K., Luks, T. L., Marco, E. J., Martin, S., Martin, A. J., Marzano, G., Masson, C., Mcgovern, K. E., Keehn, R. M., Miller, D. T., Miller, F. K., Moss, T. J., Murray, R., Nagarajan, S. S., Nowell, K. P., Owen, J., Paal, A. M., Packer, A., Page, P. Z., Paul, B. M., Peters, A., Peterson, D., Poduri, A., Pojman, N. J., Porche, K., Proud, M. B., Qasmieh, S., Ramocki, M. B., Reilly, B., Roberts, T. P. L., Shaw, D., Sinha, T., Smith, B., Snow, A., Swarnakar, V., Thieu, T., Triantafallou, C., Vaughan, R., Wakahiro, M., Wallace, A., Ward, T., Wenegrat, J., Wolken, A.

المساهمون: Blaumeiser, Bettina, Kooy, Frank, Other departments, Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study, 16p11.2 European Consortium, Simons Variation in Individuals Project (VIP) Consortium, Knoers, VA., Martinet, D., Belfiore, M., Cuvellier, JC., de Vries, B., Delrue, MA., Doco-Fenzy, M., Lebel, R., Leheup, B., Lewis, S., Mencarelli, MA., Minet, JC., Vincent-Delorme, C., Moerman, A., Mucciolo, M., Ounap, K., Rajcan-Separovic, E., Renieri, A., Sanlaville, D., Faas, BH., Koolen, DA., Vulto-van Silfhout, A., de Leeuw, N., Rosenfeld, JA., Filges, I., Achatz, E., Roetzer, KM., Bonneau, D., Guichet, A., Lazaro, L., Plessis, G., Kroisel, PM., Reis, A., Jonveaux, P., Chantot-Bastaraud, S., Rauch, A., Demeer, B., Nordgren, A., Labalme, A., Ferrarini, A., Ramelli, GP., Guilmatre, A., Joly-Helas, G., Haize, S., Layet, V., Le Gallic, S., de Fréminville, B., Touraine, R., Van Binsbergen, E., Mathieu-Dramard, M., Barth, M., Blaumeiser, B., Masurel, A., Cailler, P., Olivier-Faivre, L., Malacarne, M., Coutton, C., Dieterich, K., Satre, V., Wallgren-Pettersson, C., Tensgrom, C., Kaksonen, S., Duban-Bedu, B., Holder, M., Rossi, M., Gaillard, D., Bock, D., Bednarek, N., Guillin, O., Bizzarri, V., Flori, E., Silengo, M., Kooy, RF., Aboura, A., Beri, M., Delobel, B., Drunat, S., Jaros, Z., Kolk, A., Reigo, A., Zufferey, F., Beckmann, N., Faravelli, F., Alupay, H., Aaronson, B., Ackerman, S., Ankenman, K., Anwar, A., Atwell, C., Bowe, A., Beaudet, AL., Benedetti, M., Berg, J., Berman, J., Berry, LN., Bibb, AL., Blaskey, L., Brennan, J., Brewton, CM., Buckner, R., Bukshpun, P., Burko, J., Cali, P., Cerban, B., Chang, Y., Cheong, M., Chow, V., Chu, Z., Chudnovskaya, D., Cornew, L., Dale, C., Dell, J., Dempsey, AG., Deschamps, T., Earl, R., Edgar, J., Elgin, J., Olson, JE., Evans, YL., Findlay, A., Fischbach, GD., Fisk, C., Fregeau, B., Gaetz, B., Gaetz, L., Garza, S., Gerdts, J., Glenn, O., Gobuty, SE., Golembski, R., Greenup, M., Heiken, K., Hines, K., Hinkley, L., Jackson, FI., Jenkins J.3rd, Jeremy, RJ., Johnson, K., Kanne, SM., Kessler, S., Khan, SY., Ku, M., Kuschner, E., Laakman, AL., Lam, P., Lasala, MW., Lee, H., LaGuerre, K., Levy, S., Lian Cavanagh, A., Llorens, AV., Loftus Campe, K., Luks, TL., Marco, EJ., Martin, S., Martin, AJ., Marzano, G., Masson, C., McGovern, KE., McNally Keehn, R., Miller, DT., Miller, FK., Moss, TJ., Murray, R., Nagarajan, SS., Nowell, KP., Owen, J., Paal, AM., Packer, A., Page, PZ., Paul, BM., Peters, A., Peterson, D., Poduri, A., Pojman, NJ., Porche, K., Proud, MB., Qasmieh, S., Ramocki, MB., Reilly, B., Roberts, TP., Shaw, D., Sinha, T., Smith-Packard, B., Snow Gallagher, A., Swarnakar, V., Thieu, T., Triantafallou, C., Vaughan, R., Wakahiro, M., Wallace, A., Ward, T., Wenegrat, J., Wolken, A., Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D)

المصدر: JAMA psychiatry
Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study 2016, ' Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities ', JAMA Psychiatry, vol. 73, no. 1, pp. 20-30 . https://doi.org/10.1001/jamapsychiatry.2015.2123Test
JAMA PSYCHIATRY
JAMA psychiatry, 73(1), 20-30. American Medical Association
JAMA Psychiatry, 73, 1, pp. 20-30
JAMA Psychiatry
Jama Psychiatry, vol. 73, no. 1, pp. 20-30
JAMA Psychiatry, 73(1), 20. American Medical Association
JAMA Psychiatry, 73(1), 20-30. American Medical Association
JAMA Psychiatry, 73, 20-30

مصطلحات موضوعية: Male, 0301 basic medicine, Proband, Pediatrics, Autism Spectrum Disorder, Developmental Disabilities, Chromosome Disorders, Comorbidity, Nonverbal learning disorder, Cohort Studies, Cognition, 0302 clinical medicine, Cerebellum, Chromosome Duplication, Gene duplication, Copy-number variation, Non-U.S. Gov't, Child, 2. Zero hunger, Intelligence quotient, Research Support, Non-U.S. Gov't, Middle Aged, Psychiatry and Mental health, Microcephaly, Female, Schizophrenic Psychology, Chromosome Deletion, Psychology, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9], Human, Adult, medicine.medical_specialty, Adolescent, DNA Copy Number Variations, Research Support, Nervous System Malformations, Article, Chromosomes, Young Adult, 03 medical and health sciences, Intellectual Disability, Journal Article, medicine, Humans, Autistic Disorder, Preschool, Psychiatry, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Epilepsy, Pair 16, Other Research Radboud Institute for Health Sciences [Radboudumc 0], Case-control study, Autism Spectrum Disorder/epidemiology, Autism Spectrum Disorder/genetics, Autistic Disorder/epidemiology, Autistic Disorder/genetics, Case-Control Studies, Cerebellum/abnormalities, Child, Preschool, Chromosome Disorders/epidemiology, Chromosome Disorders/genetics, Chromosomes, Human, Pair 16/genetics, Developmental Disabilities/epidemiology, Developmental Disabilities/genetics, Epilepsy/epidemiology, Epilepsy/genetics, Intellectual Disability/epidemiology, Intellectual Disability/genetics, Microcephaly/epidemiology, Microcephaly/genetics, Nervous System Malformations/epidemiology, Nervous System Malformations/genetics, Schizophrenia/epidemiology, Schizophrenia/genetics, medicine.disease, 030104 developmental biology, Chromosomes, Human, Pair 16, Schizophrenia, Autism, Human medicine, 030217 neurology & neurosurgery

وصف الملف: image/pdf; pdf; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::221714038bda1846e56d6e2e8e45f87aTest
http://archpsyc.jamanetwork.com/article.aspx?articleid=2471269Test

المؤلفون: D'Angelo D., Lebon S., Chen Q., Martin-Brevet S., Snyder L. G., Hippolyte L., Hanson E., Maillard A. M., Faucett W. A., Mace A., Pain A., Bernier R., Chawner S. J. R. A., David A., Andrieux J., Aylward E., Baujat G., Caldeira I., Conus P., Ferrari C., Forzano F., Gerard M., Goin-Kochel R. P., Grant E., Hunter J. V., Isidor B., Jacquette A., Jonch A. E., Keren B., Lacombe D., Le Caignec C., Martin C. L., Mannik K., Metspalu A., Mignot C., Mukherjee P., Owen M. J., Passeggeri M., Rooryck-Thambo C., Rosenfeld J. A., Spence S. J., Steinman K. J., Tjernagel J., Van Haelst M., Shen Y., Draganski B., Sherr E. H., Ledbetter D. H., van den Bree M. B. M., Beckmann J. S., Spiro J. E., Reymond A., Jacquemont S., Chung W. K., Knoers N. V. A. M., Martinet D., Belfiore M., Cuvellier J. -C., deVries B., Delrue M. -A., Doco-Fenzy M., Lebel R., Leheup B., Lewis S., Mencarelli M. A., Minet J. -C., Vincent-Delorme C., Moerman A., Mucciolo M., Ounap K., Rajcan-Separovic E., Renieri A., Sanlaville D., Faas B. H., Koolen D. A., Vulto-Van Silfhout A., de Leeuw N., Rosanfeld J. A., Filges I., Achatz E., Roetzer K. M., Bonneau D., Guichet A., Lazaro L., Plessis G., Kroisel P. M., Reis A., Jonveaux P., Chantot-Bastaraud S., Rauch A., Demeer B., Nordgren A., Labalme A., Ferrarini A., Ramelli G. P., Guilmatre A., Joly-Helas G., Haize S., Layet V., Le Gallic S., de Freminville B., Touraine R., Van Binsbergen E., Mathieu-Dramard M., Barth M., Blaumeiser B., Masurel A., Cailler P., Olivier-Faivre L., Malacarne M., Coutton C., Dieterich K., Satre V., Wallgren-Pettersson C., Tensgrom C., Kaksonen S., Duban-Bedu B., Holder M., Rossi M., Gaillard D., Bock D., Bednarek N., Guillin O., Bizzarri V., Flori E., Silengo M., Kooy R. F., Aboura A., Beri M., Delobel B., Drunat S., Jaros Z., Kolk A., Reigo A., Zufferey F., Beckmann N., Faravelli F., Alupay H., Aaronson B., Ackerman S., Ankenman K., Anwar A., Atwell C., Bowe A., Beaudet A. L., Benedetti M., Berg J., Berman J., Berry L. N., Bibb A. L., Blaskey L., Brennan J., Brewton C. M., Buckner R., Bukshpun P., Burko J., Cali P., Cerban B., Chang Y., Cheong M., Chow V., Chu Z., Chudnovskaya D., Cornew L., Dale C., Dell J., Dempsey A. G., Deschamps T., Earl R., Edgar J., Elgin J., Endre J., Evans Y. L., Findlay A., Fischbach G. D., Fisk C., Fregeau B., Gaetz B., Gaetz L., Garza S., Gerdts J., Glenn O., Gobuty S. E., Golembski R., Greenup M., Heiken K., Hines K., Hinkley L., Jackson F. I., Jenkins J., Jeremy R. J., Johnson K., Kanne S. M., Kessler S., Khan S. Y., Ku M., Kuschner E., Laakman A. L., Lam P., Lasala M. W., Lee H., La K., Levy S., Lian A., Llorens A. V., Loftus K., Luks T. L., Marco E. J., Martin S., Martin A. J., Marzano G., Masson C., McGovern K. E., Keehn R. M., Miller D. T., Miller F. K., Moss T. J., Murray R., Nagarajan S. S., Nowell K. P., Owen J., Paal A. M., Packer A., Page P. Z., Paul B. M., Peters A., Peterson D., Poduri A., Pojman N. J., Porche K., Proud M. B., Qasmieh S., Ramocki M. B., Reilly B., Roberts T. P. L., Shaw D., Sinha T., Smith B., Snow A., Swarnakar V., Thieu T., Triantafallou C., Vaughan R., Wakahiro M., Wallace A., Ward T., Wenegrat J., Wolken A.

المساهمون: D'Angelo, D., Lebon, S., Chen, Q., Martin-Brevet, S., Snyder, L. G., Hippolyte, L., Hanson, E., Maillard, A. M., Faucett, W. A., Mace, A., Pain, A., Bernier, R., Chawner, S. J. R. A., David, A., Andrieux, J., Aylward, E., Baujat, G., Caldeira, I., Conus, P., Ferrari, C., Forzano, F., Gerard, M., Goin-Kochel, R. P., Grant, E., Hunter, J. V., Isidor, B., Jacquette, A., Jonch, A. E., Keren, B., Lacombe, D., Le Caignec, C., Martin, C. L., Mannik, K., Metspalu, A., Mignot, C., Mukherjee, P., Owen, M. J., Passeggeri, M., Rooryck-Thambo, C., Rosenfeld, J. A., Spence, S. J., Steinman, K. J., Tjernagel, J., Van Haelst, M., Shen, Y., Draganski, B., Sherr, E. H., Ledbetter, D. H., van den Bree, M. B. M., Beckmann, J. S., Spiro, J. E., Reymond, A., Jacquemont, S., Chung, W. K., Knoers, N. V. A. M., Martinet, D., Belfiore, M., Cuvellier, J. -C., Devries, B., Delrue, M. -A., Doco-Fenzy, M., Lebel, R., Leheup, B., Lewis, S., Mencarelli, M. A., Minet, J. -C., Vincent-Delorme, C., Moerman, A., Mucciolo, M., Ounap, K., Rajcan-Separovic, E., Renieri, A., Sanlaville, D., Faas, B. H., Koolen, D. A., Vulto-Van Silfhout, A., de Leeuw, N., Rosanfeld, J. A., Filges, I., Achatz, E., Roetzer, K. M., Bonneau, D., Guichet, A., Lazaro, L., Plessis, G., Kroisel, P. M., Reis, A., Jonveaux, P., Chantot-Bastaraud, S., Rauch, A., Demeer, B., Nordgren, A., Labalme, A., Ferrarini, A., Ramelli, G. P., Guilmatre, A., Joly-Helas, G., Haize, S., Layet, V., Le Gallic, S.

مصطلحات موضوعية: Adolescent, Adult, Autism Spectrum Disorder, Autistic Disorder, Case-Control Studie, Cerebellum, Child, Preschool, Chromosome Deletion, Chromosome Disorder, Chromosomes, Human, Pair 16, Cohort Studie, Comorbidity, DNA Copy Number Variation, Developmental Disabilitie, Epilepsy, Female, Intellectual Disability, Male, Microcephaly, Middle Aged, Nervous System Malformation, Schizophrenia, Schizophrenic Psychology, Young Adult, Chromosome Duplication, Cognition

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26629640; info:eu-repo/semantics/altIdentifier/wos/WOS:000367820000006; volume:73; issue:1; firstpage:20; lastpage:30; numberofpages:11; journal:JAMA PSYCHIATRY; http://hdl.handle.net/11365/1126841Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84954141702; https://jamanetwork.com/journals/jamapsychiatry/fullarticle/2471269Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5894477Test/

الإتاحة: https://doi.org/10.1001/jamapsychiatry.2015.2123Test
http://hdl.handle.net/11365/1126841Test
https://jamanetwork.com/journals/jamapsychiatry/fullarticle/2471269Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5894477Test/

المؤلفون: Aas M., Blokland G. A. M., Chawner S. J. R. A., Choi S. -W., Estrada J., Forsingdal A., Friedrich M., Ganesham S., Hall L., Haslinger D., Huckins L., Loken E., Malan-Muller S., Martin J., Misiewicz Z., Pagliaroli L., Pardinas A. F., Pisanu C., Quadri G., Santoro M. L., Shaw A. D., Ranlund S., Song J., Tesli M., Tropeano M., Van Der Voet M., Wolfe K., Cormack F. K., DeLisi L.

المساهمون: Aas, M., Blokland, G. A. M., Chawner, S. J. R. A., Choi, S. -W., Estrada, J., Forsingdal, A., Friedrich, M., Ganesham, S., Hall, L., Haslinger, D., Huckins, L., Loken, E., Malan-Muller, S., Martin, J., Misiewicz, Z., Pagliaroli, L., Pardinas, A. F., Pisanu, C., Quadri, G., Santoro, M. L., Shaw, A. D., Ranlund, S., Song, J., Tesli, M., Tropeano, M., Van Der Voet, M., Wolfe, K., Cormack, F. K., Delisi, L.

مصطلحات موضوعية: Attention-deficit hyperactivity disorder, Bipolar disorder, Genetic, Genomic, International society of psychiatric genetic, Mood disorder, Schizophrenia, World congress of psychiatric genetics

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26565519; info:eu-repo/semantics/altIdentifier/wos/WOS:000373506600001; volume:26; issue:1; firstpage:1; lastpage:47; numberofpages:47; journal:PSYCHIATRIC GENETICS; http://hdl.handle.net/11584/286672Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84952360872

الإتاحة: https://doi.org/10.1097/YPG.0000000000000112Test
http://hdl.handle.net/11584/286672Test