المؤلفون: Børglum, Anders¹ (AUTHOR), Robinson, Elise² (AUTHOR), Vorstman, Jacob³ (AUTHOR)

المصدر: European Neuropsychopharmacology. Oct2022, Vol. 63, pe18-e19. 2p.

مصطلحات موضوعية: *AUTISM

المؤلفون: Børglum, Anders¹ (AUTHOR), Robinson, Elise² (AUTHOR), Sebat, Jonathan³ (AUTHOR)

المصدر: European Neuropsychopharmacology. Oct2021, Vol. 51, pe12-e12. 1p.

مصطلحات موضوعية: *AUTISM, *HETEROGENEITY, *GENES, *AUTISTIC children

المؤلفون: Jefsen, Oskar Hougaard^1,2 (AUTHOR) oskar.jefsen@clin.au.dk, Holde, Katrine³ (AUTHOR), McGrath, John J.^3,4,5 (AUTHOR), Rajagopal, Veera Manikandan^6,7,8,9 (AUTHOR), Albiñana, Clara^3,6 (AUTHOR), Vilhjálmsson, Bjarni Jóhann^3,10 (AUTHOR), Grove, Jakob^6,7,8,9,10 (AUTHOR), Agerbo, Esben^3,6,9,11 (AUTHOR), Yilmaz, Zeynep^3,12,13 (AUTHOR), Plana-Ripoll, Oleguer¹⁴ (AUTHOR), Munk-Olsen, Trine^3,6,11 (AUTHOR), Demontis, Ditte^6,7,8 (AUTHOR), Børglum, Anders^6,7,8,9 (AUTHOR), Mors, Ole¹ (AUTHOR), Bulik, Cynthia M.^12,15,16 (AUTHOR), Mortensen, Preben Bo^3,6 (AUTHOR), Petersen, Liselotte Vogdrup^3,6 (AUTHOR)

المصدر: Biological Psychiatry. Aug2024, Vol. 96 Issue 3, p222-229. 8p.

مصطلحات موضوعية: *MONOGENIC & polygenic inheritance (Genetics), *MENTAL illness, *ELEMENTARY schools, *AUTISM spectrum disorders, *GENETIC correlations, *NOMOGRAPHY (Mathematics)

المؤلفون: Agrawal, Arpana¹ (AUTHOR), Børglum, Anders² (AUTHOR), Sebat, Jonathan³ (AUTHOR)

المصدر: European Neuropsychopharmacology. 2019 Supplement4, Vol. 29, pS1022-S1022. 1p.

مصطلحات موضوعية: *22Q11 deletion syndrome, *CONSORTIA, *SUBSTANCE-induced disorders, *SINGLE nucleotide polymorphisms

المؤلفون: Børglum, Anders¹ (AUTHOR), Neale, Benjamin² (AUTHOR), Franke, Barbara³ (AUTHOR)

المصدر: European Neuropsychopharmacology. 2019 Supplement 3, Vol. 29, pS722-S722. 1p.

مصطلحات موضوعية: *HERITABILITY, *EXOMES, *ATTENTION-deficit hyperactivity disorder, *AUTISM spectrum disorders, *GENETIC correlations, *ETIOLOGY of diseases, *MENTAL illness

المؤلفون: Børglum, Anders¹

المصدر: European Neuropsychopharmacology. Sep2017 Supplement 3, Vol. 27, pS359-S360. 1p.

مصطلحات موضوعية: *ATTENTION-deficit hyperactivity disorder, *AUTISM spectrum disorders, *HERITABILITY, *GENETICS

المؤلفون: Demontis, Ditte^1,2,3,4,5,6 ditte@biomed.au.dk, Lescai, Francesco^1,2,3,4,5,6, Børglum, Anders^1,2,3,4,5,6, Glerup, Simon^1,2,3,4,5,6, Østergaard, Søren Dinesen^1,2,3,4,5,6, Mors, Ole^1,2,3,4,5,6, Li, Qibin^1,2,3,4,5,6, Liang, Jieqin^1,2,3,4,5,6, Jiang, Hui^1,2,3,4,5,6, Li, Yingrui^1,2,3,4,5,6, Wang, Jun^1,2,3,4,5,6, Lesch, Klaus-Peter^1,2,3,4,5,6, Reif, Andreas^1,2,3,4,5,6, Buitelaar, Jan K.^1,2,3,4,5,6, Franke, Barbara^1,2,3,4,5,6

المصدر: Journal of the American Academy of Child & Adolescent Psychiatry. Jun2016, Vol. 55 Issue 6, p521-523. 3p.

مصطلحات موضوعية: *ATTENTION-deficit hyperactivity disorder, *HUMAN behavior, *EXOMES, *GENETICS

المؤلفون: Yang, Zhiyu¹ (AUTHOR), Wu, Hanrui¹ (AUTHOR), Lee, Phil H.^2,3,4 (AUTHOR), Tsetsos, Fotis⁵ (AUTHOR), Davis, Lea K.⁶ (AUTHOR), Yu, Dongmei^2,3,4 (AUTHOR), Lee, Sang Hong^7,8 (AUTHOR), Dalsgaard, Søren^9,10,11 (AUTHOR), Haavik, Jan^12,13 (AUTHOR), Barta, Csaba¹⁴ (AUTHOR), Zayats, Tetyana^12,15 (AUTHOR), Eapen, Valsamma¹⁶ (AUTHOR), Wray, Naomi R.^7,17 (AUTHOR), Devlin, Bernie¹⁸ (AUTHOR), Daly, Mark^15,19 (AUTHOR), Neale, Benjamin^15,19,20 (AUTHOR), Børglum, Anders D.^9,21,22,23 (AUTHOR), Crowley, James J.^24,25 (AUTHOR), Scharf, Jeremiah^2,3,4 (AUTHOR), Mathews, Carol A.^26,27 (AUTHOR)

المصدر: Biological Psychiatry. Sep2021, Vol. 90 Issue 5, p317-327. 11p.

مصطلحات موضوعية: *TOURETTE syndrome, *GENOME-wide association studies, *AUTISM spectrum disorders, *HYPOTHALAMUS, *GENETIC correlations, *COMORBIDITY

المؤلفون: Cordero, Juan¹ (AUTHOR), Grove, Jakob¹ (AUTHOR), Demontis, Ditte¹ (AUTHOR), Staunstrup, Nicklas¹ (AUTHOR), Mors, Ole¹ (AUTHOR), Børglum, Anders¹ (AUTHOR), Starnawska, Anna¹ (AUTHOR)

المصدر: European Neuropsychopharmacology. 2023 Supplement 1, Vol. 75, pS95-S96. 2p.

مصطلحات موضوعية: *GENETIC variation, *MENTAL illness, *EPIGENETICS, *LOCUS (Genetics), *AMINO acid sequence, *KNOWLEDGE gap theory, *CORD blood, *SYNAPSES

المؤلفون: Martin, Joanna¹ (AUTHOR) martinjm1@cardiff.ac.uk, Khramtsova, Ekaterina A.^1,2,3 (AUTHOR), Goleva, Slavina B.⁴ (AUTHOR), Blokland, Gabriëlla A.M.^5,6,7 (AUTHOR), Traglia, Michela^8,9,10 (AUTHOR), Walters, Raymond K.^11,12 (AUTHOR), Hübel, Christopher^13,14 (AUTHOR), Coleman, Jonathan R.I.^13,15 (AUTHOR), Breen, Gerome^13,15 (AUTHOR), Børglum, Anders D.^16,17,18 (AUTHOR), Demontis, Ditte^16,17,18 (AUTHOR), Grove, Jakob^16,17,18 (AUTHOR), Werge, Thomas^19,20,21,22 (AUTHOR), Bralten, Janita²³ (AUTHOR), Bulik, Cynthia M.^14,24,25 (AUTHOR), Lee, Phil H.²⁶ (AUTHOR), Mathews, Carol A.^27,28 (AUTHOR), Peterson, Roseann E.^29,30 (AUTHOR), Winham, Stacey J.³¹ (AUTHOR), Wray, Naomi³² (AUTHOR)

المصدر: Biological Psychiatry. Jun2021, Vol. 89 Issue 12, p1127-1137. 11p.

مصطلحات موضوعية: *GENOME-wide association studies, *PHENOTYPES, *SINGLE nucleotide polymorphisms, *RISK-taking behavior, *STATISTICAL association, *GENETIC sex determination, *GENETIC correlations, *HERITABILITY