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

المساهمون: Medical Research Council

المصدر: Journal of Intellectual Disability Research ; volume 68, issue 10, page 1167-1183 ; ISSN 0964-2633 1365-2788

الاتاحة: http://dx.doi.org/10.1111/jir.13139
https://onlinelibrary.wiley.com/doi/pdf/10.1111/jir.13139

المؤلفون: Modenato C., Kumar K., Moreau C., Martin-Brevet S., Huguet G., Schramm C., Jean-Louis M., Martin C. -O., Younis N., Tamer P., Douard E., Thebault-Dagher F., Cote V., Charlebois A. -R., Deguire F., Maillard A. M., Rodriguez-Herreros B., Pain A., Richetin S., Addor M. -C., Andrieux J., Arveiler B., Baujat G., Sloan-Bena F., Belfiore M., Bonneau D., Bouquillon S., Boute O., Brusco A., Busa T., Caberg J. -H., Campion D., Colombert V., Cordier M. -P., David A., Debray F. -G., Delrue M. -A., Doco-Fenzy M., Dunkhase-Heinl U., Edery P., Fagerberg C., Faivre L., Forzano F., Genevieve D., Gerard M., Giachino D., Guichet A., Guillin O., Heron D., Isidor B., Jacquette A., Jaillard S., Journel H., Keren B., Lacombe D., Lebon S., Le Caignec C., Lemaitre M. -P., Lespinasse J., Mathieu-Dramart M., Mercier S., Mignot C., Missirian C., Petit F., Pilekaer Sorensen K., Pinson L., Plessis G., Prieur F., Raymond A., Rooryck-Thambo C., Rossi M., Sanlaville D., Schlott Kristiansen B., Schluth-Bolard C., Till M., Van Haelst M., Van Maldergem L., 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., Olson J. E., 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., LaGuerre K., Levy S., Cavanagh A. L., Llorens A. V., Campe K. L., Luks T. L., Marco E. J., Martin S., Martin A. J., Marzano G., Masson C., McGovern K. E., Keehn R. M. N., 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-Packard B., Gallagher A. S., Swarnakar V., Thieu T., Triantafallou C., Vaughan R., Wakahiro M., Wallace A., Ward T., Wenegrat J., Wolken A., Melie-Garcia L., Kushan L., Silva A. I., van den Bree M. B. M., Linden D. E. J., Owen M. J., Hall J., Lippe S., Chakravarty M., Bzdok D., Bearden C. E., Draganski B., Jacquemont S.

المساهمون: Modenato C., Kumar K., Moreau C., Martin-Brevet S., Huguet G., Schramm C., Jean-Louis M., Martin C.-O., Younis N., Tamer P., Douard E., Thebault-Dagher F., Cote V., Charlebois A.-R., Deguire F., Maillard A.M., Rodriguez-Herreros B., Pain A., Richetin S., Addor M.-C., Andrieux J., Arveiler B., Baujat G., Sloan-Bena F., Belfiore M., Bonneau D., Bouquillon S., Boute O., Brusco A., Busa T., Caberg J.-H., Campion D., Colombert V., Cordier M.-P., David A., Debray F.-G., Delrue M.-A., Doco-Fenzy M., Dunkhase-Heinl U., Edery P., Fagerberg C., Faivre L., Forzano F., Genevieve D., Gerard M., Giachino D., Guichet A., Guillin O., Heron D., Isidor B., Jacquette A., Jaillard S., Journel H., Keren B., Lacombe D., Lebon S., Le Caignec C., Lemaitre M.-P., Lespinasse J., Mathieu-Dramart M., Mercier S., Mignot C., Missirian C., Petit F., Pilekaer Sorensen K., Pinson L., Plessis G., Prieur F., Raymond A., Rooryck-Thambo C., Rossi M., Sanlaville D., Schlott Kristiansen B., Schluth-Bolard C., Till M., Van Haelst M., Van Maldergem L., 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.

مصطلحات موضوعية: Brain, Human, Magnetic Resonance Imaging, Neuroimaging, DNA Copy Number Variation, Schizophrenia

Relation: info:eu-repo/semantics/altIdentifier/pmid/34285187; info:eu-repo/semantics/altIdentifier/wos/WOS:000674910100001; volume:11; issue:1; firstpage:399; lastpage:408; numberofpages:10; journal:TRANSLATIONAL PSYCHIATRY; http://hdl.handle.net/2318/1808624; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85111690086; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292542/pdf/41398_2021_Article_1490.pdf

الاتاحة: http://hdl.handle.net/2318/1808624
https://doi.org/10.1038/s41398-021-01490-9
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292542/pdf/41398_2021_Article_1490.pdf

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

Relation: 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/2434/919418; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85085908802

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

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

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

الاتاحة: http://hdl.handle.net/2445/128023

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

الاتاحة: http://dx.doi.org/10.1038/ijo.2015.247
https://www.nature.com/articles/ijo2015247.pdf
https://www.nature.com/articles/ijo2015247

المؤلفون: Eaton, C. B., Thomas, R. H., Hamandi, K. H., Payne, G. C., Kerr, M. P., Linden, D. E. J., Owen, M. J., Cunningham, A. C., Bartsch, U. B., Struik, S. S., van den Bree, M. B. M.

Relation: Eaton, C. B. https://orca.cardiff.ac.uk/view/cardiffauthors/A21710265.html orcid:0000-0001-6739-1999 orcid:0000-0001-6739-1999, Thomas, R. H. https://orca.cardiff.ac.uk/view/cardiffauthors/A124167S.html orcid:0000-0003-2062-8623 orcid:0000-0003-2062-8623, Hamandi, K. H. https://orca.cardiff.ac.uk/view/cardiffauthors/A105670D.html, Payne, G. C., Kerr, M. P. https://orca.cardiff.ac.uk/view/cardiffauthors/A054378J.html, Linden, D. E. J. https://orca.cardiff.ac.uk/view/cardiffauthors/A235504V.html orcid:0000-0002-5638-9292 orcid:0000-0002-5638-9292, Owen, M. J. https://orca.cardiff.ac.uk/view/cardiffauthors/A069868J.html orcid:0000-0003-4798-0862 orcid:0000-0003-4798-0862, Cunningham, A. C. https://orca.cardiff.ac.uk/view/cardiffauthors/A1369220G.html, Bartsch, U. B., Struik, S. S. and van den Bree, M. B. M. https://orca.cardiff.ac.uk/view/cardiffauthors/A000189T.html orcid:0000-0002-4426-3254 orcid:0000-0002-4426-3254 2019. Prevalence and aetiology of epileptic seizures in young people with 22Q11.2 Deletion syndrome and relationships with other neurodevelopmental disorders. Presented at: SSBP 22nd Educational Day and Research Symposium 2019, Birmingham, England, 4-6 September 2019. Journal of Intellectual Disability Research. , vol. 9. Wiley, p. 1080. 10.1111/jir.12676 https://doi.org/10.1111/jir.12676

الاتاحة: https://orca.cardiff.ac.uk/id/eprint/136480/
https://doi.org/10.1111/jir.12676

المؤلفون: Moulding, H. A., Bartsch, U., Hall, J., Jones, M. W., Linden, D. E., Owen, M. J., van den Bree, M. B. M.

المصدر: Psychological Medicine ; volume 50, issue 7, page 1191-1202 ; ISSN 0033-2917 1469-8978

الاتاحة: http://dx.doi.org/10.1017/s0033291719001119
https://www.cambridge.org/core/services/aop-cambridge-core/content/view/S0033291719001119

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.2015.2123
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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::221714038bda1846e56d6e2e8e45f87a
http://archpsyc.jamanetwork.com/article.aspx?articleid=2471269

المؤلفون: Moulding, H. A., Bartsch, U., Hall, J., Jones, M. W., Linden, D. E., Owen, M. J., van den Bree, M. B. M.

المصدر: Psychological Medicine; May2020, Vol. 50 Issue 7, p1191-1202, 12p

مصطلحات موضوعية: DIAGNOSIS of autism, ATTENTION-deficit hyperactivity disorder, BEHAVIOR disorders in children, COGNITIVE testing, INSOMNIA, MOVEMENT disorders, PATHOLOGICAL psychology, QUESTIONNAIRES, RISK assessment, SLEEP disorders, RESTLESS legs syndrome, ANXIETY disorders, EXECUTIVE function, DIGEORGE syndrome, DISEASE complications, DISEASE risk factors

المؤلفون: Bergen, A W, van den Bree, M B M, Yeager, M, Welch, R, Ganjei, J K, Haque, K, Bacanu, S, Berrettin, W H, Grice, D E, Goldman, D, Bulik, C M, Klump, K, Fichter, M, Halmi, K, Kaplan, A, Strober, M, Treasure, J, Woodside, B, Kaye, W H

المصدر: Bergen , A W , van den Bree , M B M , Yeager , M , Welch , R , Ganjei , J K , Haque , K , Bacanu , S , Berrettin , W H , Grice , D E , Goldman , D , Bulik , C M , Klump , K , Fichter , M , Halmi , K , Kaplan , A , Strober , M , Treasure , J , Woodside , B & Kaye , W H 2003 , ' Candidate genes for anorexia nervosa in the 1 p33-36 linkage region: ....

Relation: https://kclpure.kcl.ac.uk/portal/en/publications/ea8b9621-863a-4c7a-9f1d-bf7f0eaf6ddd

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/ea8b9621-863a-4c7a-9f1d-bf7f0eaf6ddd
https://doi.org/10.1038/sj.mp.4001318
http://www.scopus.com/inward/record.url?scp=12444258372&partnerID=8YFLogxK

المؤلفون: Bergen, A W, van den Bree, M B M, Yeager, M, Welch, R, Ganjei, J K, Haque, K, Bacanu, S, Berrettini, W H, Grice, D E, Bulik, C M, Klump, K, Fichter, M, Halmi, K, Kaplan, A, Strober, M, Treasure, J, Woodside, D B, Kaye, W H

المصدر: Bergen , A W , van den Bree , M B M , Yeager , M , Welch , R , Ganjei , J K , Haque , K , Bacanu , S , Berrettini , W H , Grice , D E , Bulik , C M , Klump , K , Fichter , M , Halmi , K , Kaplan , A , Strober , M , Treasure , J , Woodside , D B & Kaye , W H 2003 , ' Candidate genes for anorexia nervosa in the 1p33-36 linkage region: Serotonin 1D and delta ....

Relation: https://kclpure.kcl.ac.uk/portal/en/publications/7adb13ac-03e7-45aa-80e5-b1825d604632

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/7adb13ac-03e7-45aa-80e5-b1825d604632

المؤلفون: Schneider, M., Debbane, M., Bassett, A. S., Chow, E. W. C., Fung, W. L. A., Van Den Bree, M. B. M., Owen, M., Murphy, K. C., Niarchou, M., Kates, W. R., Antshel, K. M., Fremont, W., McDonald-McGinn, D. M., Gur, R. E., Zackai, E. H., Vorstman, J., Duijff, S. N., Klaassen, P. W. J., Swillen, A., Gothelf, D., Green, T., Weizman, A., Van Amelsvoort, T., Evers, L., Boot, E., Shashi, V., Hooper, S. R., Bearden, C. E., Jalbrzikowski, M., Armando, M., Vicari, Stefano, Murphy, D. G., Ousley, O., Campbell, L. E., Simon, T. J., Eliez, S., Vicari S. (ORCID:0000-0002-5395-2262)

مصطلحات الفهرس: neurogenetic disorder, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, info:eu-repo/semantics/article

URL: http://hdl.handle.net/10807/167157
info:eu-repo/semantics/altIdentifier/pmid/24577245
info:eu-repo/semantics/altIdentifier/wos/WOS:000336638600010
volume:171
issue:6
firstpage:627
lastpage:639
numberofpages:13
issueyear:2014
journal:THE AMERICAN JOURNAL OF PSYCHIATRY

المؤلفون: Johnson, Eric O., van den Bree, M. B. M., Pickens, Roy W.

المصدر: Alcoholism: Clinical and Experimental Research ; volume 20, issue 8, page 1472-1480 ; ISSN 0145-6008 1530-0277

الاتاحة: http://dx.doi.org/10.1111/j.1530-0277.1996.tb01151.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1530-0277.1996.tb01151.x
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1530-0277.1996.tb01151.x

المؤلفون: Johnson, Eric O., van den Bree, M. B. M., Pickens, Roy W.

المصدر: Alcoholism: Clinical and Experimental Research ; volume 20, issue 1, page 67-74 ; ISSN 0145-6008 1530-0277

الاتاحة: http://dx.doi.org/10.1111/j.1530-0277.1996.tb01046.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1530-0277.1996.tb01046.x
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1530-0277.1996.tb01046.x

المؤلفون: Bergen, A W, van den Bree, M B M, Yeager, M, Welch, R, Ganjei, J K, Haque, K, Bacanu, S, Berrettini, W H, Grice, D E, Goldman, D, Bulik, C M, Klump, K, Fichter, M, Halmi, K, Kaplan, A, Strober, M, Treasure, J, Woodside, B, Kaye, W H

المصدر: Molecular Psychiatry; 2003, Vol. 8 Issue 4, p397, 10p

مصطلحات موضوعية: ANOREXIA nervosa, SEROTONIN, GENES, OPIOIDS

المؤلفون: Spady, D. W., Schopflocher, D. P., Svenson, L. W., Coleman, K. J., Tiller, C. L., Sanchez, J., Menon, G. J., Kassam-Adams, N., Garcia-España, J. F., Fein, J. A., Van den Bree, M. B. M., Pickworth, W. B., Naidech, A. M., Janjua, N., Kreiter, K. T., Sacco, R. L., Silvenius, J., Diener, H., Mulligan, K., Zackin, R.

المصدر: JAMA: Journal of the American Medical Association; 5/25/2005, Vol. 293 Issue 20, p2449-2451, 3p

مصطلحات موضوعية: MEDICAL research, URINARY incontinence, COMORBIDITY, MARIJUANA abuse, POST-traumatic stress disorder

المؤلفون: Boomsma, D. I., van den Bree, M. B. M., Orlebeke, J. F., Molenaar, P. C. M.

المصدر: Behavior Genetics; January 1989, Vol. 19 Issue: 1 p123-141, 19p

المؤلفون: Eaton, C. B., Thomas, R. H., Hamandi, K. H., Payne, G. C., Kerr, M. P., Linden, D. E. J., Owen, M. J., Cunningham, A. C., Bartsch, U. B., Struik, S. S., van den Bree, M. B. M.

مصطلحات الفهرس: Conference or Workshop Item, PeerReviewed

URL: https://orca.cardiff.ac.uk/id/eprint/136480/
https://doi.org/10.1111/jir.12676
https://orca.cardiff.ac.uk/id/eprint/136480
https://doi.org/10.1111/jir.12676
10.1111/jir.12676

المؤلفون: Vicari S.

المساهمون: Schneider, M., Debbane, M., Bassett, A. S., Chow, E. W. C., Fung, W. L. A., Van Den Bree, M. B. M., Owen, M., Murphy, K. C., Niarchou, M., Kates, W. R., Antshel, K. M., Fremont, W., McDonald-McGinn, D. M., Gur, R. E., Zackai, E. H., Vorstman, J., Duijff, S. N., Klaassen, P. W. J., Swillen, A., Gothelf, D., Green, T., Weizman, A., Van Amelsvoort, T., Evers, L., Boot, E., Shashi, V., Hooper, S. R., Bearden, C. E., Jalbrzikowski, M., Armando, M., Vicari, Stefano, Murphy, D. G., Ousley, O., Campbell, L. E., Simon, T. J., Eliez, S.

مصطلحات موضوعية: neurogenetic disorder, Settore MED/39 - NEUROPSICHIATRIA INFANTILE

Relation: info:eu-repo/semantics/altIdentifier/pmid/24577245; info:eu-repo/semantics/altIdentifier/wos/WOS:000336638600010; volume:171; issue:6; firstpage:627; lastpage:639; numberofpages:13; issueyear:2014; journal:THE AMERICAN JOURNAL OF PSYCHIATRY; http://hdl.handle.net/10807/167157; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84901937317

الاتاحة: http://hdl.handle.net/10807/167157
https://doi.org/10.1176/appi.ajp.2013.13070864