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Page 1
A burden of rare copy number variants in obsessive-compulsive disorder.
Halvorsen MW, de Schipper E, Bäckman J, Strom NI, Hagen K; Nordic OCD and Related Disorders Consortium (NORDiC); Lindblad-Toh K, Karlsson EK, Pedersen NL, Wallert J, Bulik CM, Fundín B, Landén M, Kvale G, Hansen B, Haavik J, Mattheisen M, Rück C, Mataix-Cols D, Crowley JJ. Halvorsen MW, et al. Mol Psychiatry. 2024 Oct 27. doi: 10.1038/s41380-024-02763-7. Online ahead of print. Mol Psychiatry. 2024. PMID: 39463448
Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder.
Yilmaz Z, Halvorsen M, Bryois J, Yu D, Thornton LM, Zerwas S, Micali N, Moessner R, Burton CL, Zai G, Erdman L, Kas MJ, Arnold PD, Davis LK, Knowles JA, Breen G, Scharf JM, Nestadt G, Mathews CA, Bulik CM, Mattheisen M, Crowley JJ; Eating Disorders Working Group of the Psychiatric Genomics Consortium, Tourette Syndrome/Obsessive–Compulsive Disorder Working Group of the Psychiatric Genomics Consortium. Yilmaz Z, et al. Mol Psychiatry. 2020 Sep;25(9):2036-2046. doi: 10.1038/s41380-018-0115-4. Epub 2018 Aug 7. Mol Psychiatry. 2020. PMID: 30087453 Free PMC article.
Nordic OCD & Related Disorders Consortium: Rationale, design, and methods.
Mataix-Cols D, Hansen B, Mattheisen M, Karlsson EK, Addington AM, Boberg J, Djurfeldt DR, Halvorsen M, Lichtenstein P, Solem S, Lindblad-Toh K; Nordic OCD and Related Disorders Consortium (NORDiC); Haavik J, Kvale G, Rück C, Crowley JJ. Mataix-Cols D, et al. Am J Med Genet B Neuropsychiatr Genet. 2020 Jan;183(1):38-50. doi: 10.1002/ajmg.b.32756. Epub 2019 Aug 19. Am J Med Genet B Neuropsychiatr Genet. 2020. PMID: 31424634 Free PMC article.
Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis.
Strom NI, Grove J, Meier SM, Bækvad-Hansen M, Becker Nissen J, Damm Als T, Halvorsen M, Nordentoft M, Mortensen PB, Hougaard DM, Werge T, Mors O, Børglum AD, Crowley JJ, Bybjerg-Grauholm J, Mattheisen M. Strom NI, et al. Front Genet. 2021 Aug 31;12:711624. doi: 10.3389/fgene.2021.711624. eCollection 2021. Front Genet. 2021. PMID: 34531895 Free PMC article.
Predicting eating disorder and anxiety symptoms using disorder-specific and transdiagnostic polygenic scores for anorexia nervosa and obsessive-compulsive disorder.
Yilmaz Z, Schaumberg K, Halvorsen M, Goodman EL, Brosof LC, Crowley JJ; Anorexia Nervosa Genetics Initiative; Eating Disorders Working Group of the Psychiatric Genomics Consortium; Tourette Syndrome/Obsessive-Compulsive Disorder Working Group of the Psychiatric Genomics Consortium; Mathews CA, Mattheisen M, Breen G, Bulik CM, Micali N, Zerwas SC. Yilmaz Z, et al. Psychol Med. 2023 May;53(7):3021-3035. doi: 10.1017/S0033291721005079. Epub 2022 Mar 4. Psychol Med. 2023. PMID: 35243971 Free PMC article.
Genome-wide association study identifies 30 obsessive-compulsive disorder associated loci.
Strom NI, Gerring ZF, Galimberti M, Yu D, Halvorsen MW, Abdellaoui A, Rodriguez-Fontenla C, Sealock JM, Bigdeli T, Coleman JR, Mahjani B, Thorp JG, Bey K, Burton CL, Luykx JJ, Zai G, Alemany S, Andre C, Askland KD, Banaj N, Barlassina C, Nissen JB, Bienvenu OJ, Black D, Bloch MH, Boberg J, Børte S, Bosch R, Breen M, Brennan BP, Brentani H, Buxbaum JD, Bybjerg-Grauholm J, Byrne EM, Cabana-Dominguez J, Camarena B, Camarena A, Cappi C, Carracedo A, Casas M, Cavallini MC, Ciullo V, Cook EH, Crosby J, Cullen BA, De Schipper EJ, Delorme R, Djurovic S, Elias JA, Estivill X, Falkenstein MJ, Fundin BT, Garner L, German C, Gironda C, Goes FS, Grados MA, Grove J, Guo W, Haavik J, Hagen K, Harrington K, Havdahl A, Höffler KD, Hounie AG, Hucks D, Hultman C, Janecka M, Jenike E, Karlsson EK, Kelley K, Klawohn J, Krasnow JE, Krebs K, Lange C, Lanzagorta N, Levey D, Lindblad-Toh K, Macciardi F, Maher B, Mathes B, McArthur E, McGregor N, McLaughlin NC, Meier S, Miguel EC, Mulhern M, Nestadt PS, Nurmi EL, O'Connell KS, Osiecki L, Ousdal OT, Palviainen T, Pedersen NL, Piras F, Piras F, Potluri S, Rabionet R, Ramirez A, Rauch S, Reichenberg A, Riddle MA, Ripke S, Rosário MC, Sampaio AS, Schiel… See abstract for full author list ➔ Strom NI, et al. Among authors: halvorsen mw. medRxiv [Preprint]. 2024 Mar 13:2024.03.13.24304161. doi: 10.1101/2024.03.13.24304161. medRxiv. 2024. PMID: 38712091 Free PMC article. Preprint.
Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.
Halvorsen M, Huh R, Oskolkov N, Wen J, Netotea S, Giusti-Rodriguez P, Karlsson R, Bryois J, Nystedt B, Ameur A, Kähler AK, Ancalade N, Farrell M, Crowley JJ, Li Y, Magnusson PKE, Gyllensten U, Hultman CM, Sullivan PF, Szatkiewicz JP. Halvorsen M, et al. Nat Commun. 2020 Apr 15;11(1):1842. doi: 10.1038/s41467-020-15707-w. Nat Commun. 2020. PMID: 32296054 Free PMC article.
Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree.
Halvorsen M, Szatkiewicz J, Mudgal P, Yu D; Psychiatric Genomics Consortium TS/OCD Working Group; Nordsletten AE, Mataix-Cols D, Mathews CA, Scharf JM, Mattheisen M, Robertson MM, McQuillin A, Crowley JJ. Halvorsen M, et al. Mol Psychiatry. 2021 Dec;26(12):7522-7529. doi: 10.1038/s41380-021-01277-w. Epub 2021 Sep 15. Mol Psychiatry. 2021. PMID: 34526668 Free PMC article.
Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.
Halvorsen M, Huh R, Oskolkov N, Wen J, Netotea S, Giusti-Rodriguez P, Karlsson R, Bryois J, Nystedt B, Ameur A, Kähler AK, Ancalade N, Farrell M, Crowley JJ, Li Y, Magnusson PKE, Gyllensten U, Hultman CM, Sullivan PF, Szatkiewicz JP. Halvorsen M, et al. Nat Commun. 2022 Jan 5;13(1):191. doi: 10.1038/s41467-021-27826-z. Nat Commun. 2022. PMID: 34987162 Free PMC article. No abstract available.
28 results