المؤلفون: Hunt, KA, Smyth, DJ, Balschun, T, Ban, M, Mistry, V, Ahmad, T, Anand, V, Barrett, JC, Bhaw-Rosun, L, Bockett, NA, Brand, OJ, Brouwer, E, Concannon, P, Cooper, JD, Dias, KRM, van Diemen, CC, Dubois, PC, Edkins, S, Folster-Holst, R, Fransen, K, Glass, DN, Heap, GAR, Hofmann, S, Huizinga, TWJ, Hunt, S, Langford, C, Lee, J, Mansfield, J, Marrosu, MG, Mathew, CG, Mein, CA, Muller-Quernheim, J, Nutland, S, Onengut-Gumuscu, S, Ouwehand, W, Pearce, K, Prescott, NJ, Posthumus, MD, Potter, S, Rosati, G, Sambrook, J, Satsangi, J, Schreiber, S, Shtir, C, Simmonds, MJ, Sudman, M, Thompson, SD, Toes, R, Trynka, G, Vyse, TJ, Walker, NM, Weidinger, S, Zhernakova, A, Zoledziewska, M, Weersma, RK, Gough, SCL, Sawcer, S, Wijmenga, C, Parkes, M, Cucca, F, Franke, A, Deloukas, P, Rich, SS, Todd, JA, van Heel, DA

المصدر: Nature genetics. 44(1):3-5

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:123857374

المؤلفون: Hunt, K.A., Smyth, D.J., Balschun, T., Ban, M., Mistry, V., Ahmad, T., Anand, V., Barrett, J.C., Bhaw-Rosun, L., Bockett, N.A., Brand, O.J., Brouwer, E., Concannon, P., Cooper, J.D., Dias, K.R.M., Diemen, C.C. van, Dubois, P.C., Edkins, S., Folster-Holst, R., Fransen, K., Glass, D.N., Heap, G.A.R., Hofmann, S., Huizinga, T.W.J., Hunt, S., Langford, C., Lee, J., Mansfield, J., Marrosu, M.G., Mathew, C.G., Mein, C.A., Muller-Quernheim, J., Nutland, S., Onengut-Gumuscu, S., Ouwehand, W., Pearce, K., Prescott, N.J., Posthumus, M.D., Potter, S., Rosati, G., Sambrook, J., Satsangi, J., Schreiber, S., Shtir, C., Simmonds, M.J., Sudman, M., Thompson, S.D., Toes, R., Trynka, G., Vyse, T.J., Walker, N.M., Weidinger, S., Zhernakova, A., Zoledziewska, M., Weersma, R.K., Gough, S.C.L., Sawcer, S., Wijmenga, C., Parkes, M., Cucca, F., Franke, A., Deloukas, P., Rich, S.S., Todd, J.A., Heel, D.A. van, Type 1 Diabet Genetics, UK Inflammatory Bowel Dis IBD, Wellcome Trust Case

المصدر: Nature Genetics, 44(1), 3-5

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4ba8eee19bf77847ccf9259124e6bd6f
https://hdl.handle.net/1887/117960

المؤلفون: Williams, NM, Franke, B, Mick, E, Anney, RJL, Freitag, CM, Gill, M, Thapar, A, O'Donovan, MC, Owen, MJ, Holmans, P, Kent, L, Middleton, F, Zhang-James, Y, Liu, L, Meyer, J, Nguyen, TT, Romanos, J, Romanos, M, Seitz, C, Renner, TJ, Walitza, S, Warnke, A, Palmason, H, Buitelaar, J, Rommelse, N, Vasquez, AA, Hawi, Z, Langley, K, Sergeant, J, Steinhausen, HC, Roeyers, Herbert, Biederman, J, Zaharieva, I, Hakonarson, H, Elia, J, Lionel, AC, Crosbie, J, Marshall, CR, Schachar, R, Scherer, SW, Todorov, A, Smalley, SL, Loo, S, Nelson, S, Shtir, C, Asherson, P, Reif, A, Lesch, KP, Faraone, SV

المساهمون: Psychiatrie & Neuropsychologie, Farmacologie en Toxicologie, RS: CARIM School for Cardiovascular Diseases

المصدر: American Journal of Psychiatry, 169, 195-204
American Journal of Psychiatry, 169, 2, pp. 195-204
Williams, N M, Franke, B, Mick, E, Anney, R J L, Freitag, C M, Gill, M, Thapar, A, O'Donovan, M C, Owen, M J, Holmans, P, Kent, L, Middleton, F, Zhang-James, Y, Liu, L, Meyer, J, Nguyen, T T, Romanos, J, Romanos, M, Seitz, C, Renner, T J, Walitza, S, Warnke, A, Palmason, H, Buitelaar, J, Rommelse, N, Vasquez, A A, Hawi, Z, Langley, K, Sergeant, J, Steinhausen, H-C, Roeyers, H, Biederman, J, Zaharieva, I, Hakonarson, H, Elia, J, Lionel, A C, Crosbie, J, Marshall, C R, Schachar, R, Scherer, S W, Todorov, A, Smalley, S L, Loo, S, Nelson, S, Shtir, C, Asherson, P, Reif, A, Lesch, K-P & Faraone, S V 2012, ' Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3 ', American Journal of Psychiatry, vol. 169, no. 2, pp. 195-204 . https://doi.org/10.1176/appi.ajp.2011.11060822
American Journal of Psychiatry, 169(2), 195-204. American Psychiatric Publishing, Inc.
The American journal of psychiatry, vol 169, iss 2
AMERICAN JOURNAL OF PSYCHIATRY

مصطلحات موضوعية: CANDIDATE GENE, Canada, Adolescent, alpha7 Nicotinic Acetylcholine Receptor, Genetics and epigenetic pathways of disease [NCMLS 6], DCN MP - Plasticity and memory, Gene Dosage, Inheritance Patterns, Social Sciences, ASSOCIATION SCAN, DCN PAC - Perception action and control, Nicotinic, MICRODUPLICATIONS, Medical and Health Sciences, Mental health [NCEBP 9], Fluorescence, Genomic disorders and inherited multi-system disorders DCN MP - Plasticity and memory [IGMD 3], MOLECULAR-GENETICS, SCHIZOPHRENIA, Receptors, mental disorders, ADHD, Humans, Genetic Predisposition to Disease, DCN PAC - Perception action and control NCEBP 9 - Mental health, Polymorphism, Child, Preschool, QH426, CHROMOSOMAL DELETIONS, In Situ Hybridization, Psychiatry, AUTISM SPECTRUM DISORDER, Psychology and Cognitive Sciences, Single Nucleotide, Genomic disorders and inherited multi-system disorders [DCN PAC - Perception action and control IGMD 3], R1, United States, United Kingdom, NICOTINIC RECEPTOR, Causality, Segmental Duplications, Attention Deficit Disorder with Hyperactivity, Genomic, RC0321, Female, DEFICIT/HYPERACTIVITY DISORDER, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::67db53c4f8b1d8b8b8b1797cd4103e8f
http://hdl.handle.net/2066/108017

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