Matthew Halvorsen

Publikationer
Populärvetenskap och samverkan

Artiklar

Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 2024;:e32983

Genomics of severe and treatment-resistant obsessive-compulsive disorder treated with deep brain stimulation: A preliminary investigation.

Chen LL; Naesström M; Halvorsen M; Fytagoridis A; Crowley SB; Mataix-Cols D; Rück C; Crowley JJ; Pascal D
Article: BMC PSYCHIATRY. 2023;23(1):863

ARFID Genes and Environment (ARFID-GEN): study protocol.

Bulik CM; Micali N; MacDermod CM; Qi B; Munn-Chernoff MA; Thornton LM; White J; Dinkler L; Pisetsky EM; Johnson J; Devine KR; Ortiz SN; Silverman AE; Berthold N; Dumain A; Guintivano J; Halvorsen M; Crowley JJ
Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 2023;195(4):e32962

Latin American Trans-ancestry INitiative for OCD genomics (LATINO): Study protocol.

Crowley JJ; Cappi C; Ochoa-Panaifo ME; Frederick RM; Kook M; Wiese AD; Rancourt D; Atkinson EG; Giusti-Rodriguez P; Anderberg JL; Latin American Trans‐ancestry INitiative for OCD g; Brazilian Obsessive‐Compulsive Spectrum Disorder W; Abramowitz JS; Adorno VR; Aguirre C; Alves GS; Alves GS; Ancalade N; Arellano Espinosa AA; Arnold PD; Ayton DM; Barbosa IG; Castano LMB; Barrera CN; Berardo MC; Berrones D; Best JR; Bigdeli TB; Burton CL; Buxbaum JD; Callahan JL; Carneiro MCB; Cepeda SL; Chazelle E; Chire JM; Munoz MC; Quiroz PC; Cobite J; Comer JS; Costa DL; Crosbie J; Cruz VO; Dager G; Daza LF; de la Rosa-Gómez A; Del Río D; Delage FZ; Dreher CB; Fay L; Fazio T; Ferrão YA; Ferreira GM; Figueroa EG; Fontenelle LF; Forero DA; Fragoso DTH; Gadad BS; Garrison SR; González A; Gonzalez LD; González MA; Gonzalez-Barrios P; Goodman WK; Grice DE; Guintivano J; Guttfreund DG; Guzick AG; Halvorsen MW; Hovey JD; Huang H; Irreño-Sotomonte J; Janssen-Aguilar R; Jensen M; Jimenez Reynolds AZ; Lujambio JAJ; Khalfe N; Knutsen MA; Lack C; Lanzagorta N; Lima MO; Longhurst MO; Lozada Martinez DA; Luna ES; Marques AH; Martinez MS; de Los Angeles Matos M; Maye CE; McGuire JF; Menezes G; Minaya C; Miño T; Mithani SM; de Oca CM; Morales-Rivero A; Moreira-de-Oliveira ME; Morris OJ; Muñoz SI; Naqqash Z; Núñez Bracho AA; Núñez Bracho BE; Rojas MCO; Olavarria Castaman LA; Balmaceda TO; Ortega I; Patel DI; Patrick AK; Paz Y Mino M; Perales Orellana JL; Stumpf BP; Peregrina T; Duarte TP; Piacsek KL; Placencia M; Prieto MB; Quarantini LC; Quarantini-Alvim Y; Ramos RT; Ramos IC; Ramos VR; Ramsey KA; Ray EV; Richter MA; Riemann BC; Rivas JC; Rosario MC; Ruggero CJ; Ruiz-Chow AA; Ruiz-Velasco A; Sagarnaga MN; Sampaio AS; Saraiva LC; Schachar RJ; Schneider SC; Schweissing EJ; Seligman LD; Shavitt RG; Soileau KJ; Stewart SE; Storch SB; Strouphauer ER; Cuevas VT; Timpano KR; la Garza BT-D; Vallejo-Silva A; Vargas-Medrano J; Vásquez MI; Martinez GV; Weinzimmer SA; Yanez MA; Zai G; Zapata-Restrepo LM; Zappa LM; Zepeda-Burgos RM; Zoghbi AW; Miguel EC; Rodriguez CI; Martinez Mallen MC; Moya PR; Borda T; Moyano MB; Mattheisen M; Pereira S; Lázaro-Muñoz G; Martinez-Gonzalez KG; Pato MT; Nicolini H; Storch EA
Article: BMJ OPEN. 2023;13(10):e069427

Swedish multimodal cohort of patients with anxiety or depression treated with internet-delivered psychotherapy (MULTI-PSYCH).

Boberg J; Kaldo V; Mataix-Cols D; Crowley JJ; Roelstraete B; Halvorsen M; Forsell E; Isacsson NH; Sullivan PF; Svanborg C; Andersson EH; Lindefors N; Kravchenko O; Mattheisen M; Danielsdottir HB; Ivanova E; Boman M; Fernández de la Cruz L; Wallert J; Rück C
Article: PSYCHOLOGICAL MEDICINE. 2023;53(7):3021-3035

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 ; Tourette Syndrome/Obsessive-Compulsive Disorder Wo; Mathews CA; Mattheisen M; Breen G; Bulik CM; Micali N; Zerwas SC
Article: MOLECULAR PSYCHIATRY. 2023;28(1):475-482

Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia.

Wen J; Trost B; Engchuan W; Halvorsen M; Pallotto LM; Mitina A; Ancalade N; Farrell M; Backstrom I; Guo K; Pellecchia G; Thiruvahindrapuram B; Giusti-Rodriguez P; Rosen JD; Li Y; Won H; Magnusson PKE; Gyllensten U; Bassett AS; Hultman CM; Sullivan PF; Yuen RKC; Szatkiewicz JP
Article: TRANSLATIONAL PSYCHIATRY. 2022;12(1):357

Predicting remission after internet-delivered psychotherapy in patients with depression using machine learning and multi-modal data.

Wallert J; Boberg J; Kaldo V; Mataix-Cols D; Flygare O; Crowley JJ; Halvorsen M; Ben Abdesslem F; Boman M; Andersson E; Hentati Isacsson N; Ivanova E; Rück C
Article: AMERICAN JOURNAL OF PSYCHIATRY. 2022;179(3):216-225

The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum.

Mahjani B; Klei L; Mattheisen M; Halvorsen MW; Reichenberg A; Roeder K; Pedersen NL; Boberg J; de Schipper E; Bulik CM; Landén M; Fundín B; Mataix-Cols D; Sandin S; Hultman CM; Crowley JJ; Buxbaum JD; Rück C; Devlin B; Grice DE
Article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 2021;118(52):e2115140118

De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca2+ regulation.

Halvorsen M; Gould L; Wang X; Grant G; Moya R; Rabin R; Ackerman MJ; Tester DJ; Lin PT; Pappas JG; Maurano MT; Goldstein DB; Tsien RW; Devinsky O
Article: MOLECULAR PSYCHIATRY. 2021;26(12):7522-7529

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 Gro; Nordsletten AE; Mataix-Cols D; Mathews CA; Scharf JM; Mattheisen M; Robertson MM; McQuillin A; Crowley JJ
Article: NATURE NEUROSCIENCE. 2021;24(8):1071-1076

Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variants.

Halvorsen M; Samuels J; Wang Y; Greenberg BD; Fyer AJ; McCracken JT; Geller DA; Knowles JA; Zoghbi AW; Pottinger TD; Grados MA; Riddle MA; Bienvenu OJ; Nestadt PS; Krasnow J; Goes FS; Maher B; Nestadt G; Goldstein DB
Article: FRONTIERS IN GENETICS. 2021;12:711624

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
Article: MOLECULAR PSYCHIATRY. 2020;25(9):2036-2046

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
Article: BLOOD. 2020;136(5):533-541

Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease.

Desch KC; Ozel AB; Halvorsen M; Jacobi PM; Golden K; Underwood M; Germain M; Tregouet D-A; Reitsma PH; Kearon C; Mokry L; Richards JB; Williams F; Li JZ; Goldstein D; Ginsburg D
Article: NATURE COMMUNICATIONS. 2020;11(1):1842

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
Article: CEREBRAL CORTEX. 2020;30(2):587-596

Altered Brain Structure in Infants with Turner Syndrome.

Davenport ML; Cornea E; Xia K; Crowley JJ; Halvorsen MW; Goldman BD; Reinhartsen D; DeRamus M; Pretzel R; Styner M; Gilmore JH; Hooper SR; Knickmeyer RC
Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 2020;183(1):38-50

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 (NORDi; Haavik J; Kvale G; Rück C; Crowley JJ
Article: MOLECULAR GENETICS & GENOMIC MEDICINE. 2020;8(1):e1008

Sudden unexpected death in asymptomatic infants due to PPA2 variants.

Phoon CKL; Halvorsen M; Goldstein DB; Rabin R; Cecchin F; Crandall L; Devinsky O
Article: PLOS COMPUTATIONAL BIOLOGY. 2018;14(10):e1006506

meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays.

Gelfman S; Wang Q; Lu Y-F; Hall D; Bostick CD; Dhindsa R; Halvorsen M; McSweeney KM; Cotterill E; Edinburgh T; Beaumont MA; Frankel WN; Petrovski S; Allen AS; Boland MJ; Goldstein DB; Eglen SJ
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2017;25(12):1377-1387

Next-generation sequencing of patients with congenital anosmia.

Alkelai A; Olender T; Dode C; Shushan S; Tatarskyy P; Furman-Haran E; Boyko V; Gross-Isseroff R; Halvorsen M; Greenbaum L; Milgrom R; Yamada K; Haneishi A; Blau I; Lancet D
Article: NATURE COMMUNICATIONS. 2017;8(1):236

Annotating pathogenic non-coding variants in genic regions.

Gelfman S; Wang Q; McSweeney KM; Ren Z; La Carpia F; Halvorsen M; Schoch K; Ratzon F; Heinzen EL; Boland MJ; Petrovski S; Goldstein DB
Article: EBIOMEDICINE. 2017;17:95-100

Whole Exome Sequencing Reveals Severe Thrombophilia in Acute Unprovoked Idiopathic Fatal Pulmonary Embolism.

Halvorsen M; Lin Y; Sampson BA; Wang D; Zhou B; Eng LS; Um SY; Devinsky O; Goldstein DB; Tang Y
Article: GENETICS IN MEDICINE. 2016;18(7):746-749

Mosaic mutations in early-onset genetic diseases.

Halvorsen M; Petrovski S; Shellhaas R; Tang Y; Crandall L; Goldstein D; Devinsky O
Article: BMC MEDICAL GENOMICS. 2016;9:19

A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer.

Mucaki EJ; Caminsky NG; Perri AM; Lu R; Laederach A; Halvorsen M; Knoll JHM; Rogan PK
Article: EPILEPSIA. 2016;57(3):376-385

Differential gene expression in dentate granule cells in mesial temporal lobe epilepsy with and without hippocampal sclerosis.

Griffin NG; Wang Y; Hulette CM; Halvorsen M; Cronin KD; Walley NM; Haglund MM; Radtke RA; Skene JHP; Sinha SR; Heinzen EL
Article: PLOS GENETICS. 2015;11(9):e1005492

The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity.

Petrovski S; Gussow AB; Wang Q; Halvorsen M; Han Y; Weir WH; Allen AS; Goldstein DB
Article: RNA. 2015;21(7):1274-1285

Multiple conformations are a conserved and regulatory feature of the RB1 5' UTR.

Kutchko KM; Sanders W; Ziehr B; Phillips G; Solem A; Halvorsen M; Weeks KM; Moorman N; Laederach A
Article: RNA. 2012;18(1):77-87

Structural effects of linkage disequilibrium on the transcriptome.

Martin JS; Halvorsen M; Davis-Neulander L; Ritz J; Gopinath C; Beauregard A; Laederach A
Article: MOLECULAR GENETICS AND METABOLISM. 2011;104(4):457-469

A novel application of pattern recognition for accurate SNP and indel discovery from high-throughput data: targeted resequencing of the glucocorticoid receptor co-chaperone FKBP5 in a Caucasian population.

Pelleymounter LL; Moon I; Johnson JA; Laederach A; Halvorsen M; Eckloff B; Abo R; Rossetti S
Article: RNA. 2011;17(7):1204-1212

Sharing and archiving nucleic acid structure mapping data.

Rocca-Serra P; Bellaousov S; Birmingham A; Chen C; Cordero P; Das R; Davis-Neulander L; Duncan CDS; Halvorsen M; Knight R; Leontis NB; Mathews DH; Ritz J; Stombaugh J; Weeks KM; Zirbel CL; Laederach A
Article: PLOS GENETICS. 2010;6(8):e1001074

Disease-associated mutations that alter the RNA structural ensemble.

Halvorsen M; Martin JS; Broadaway S; Laederach A
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Alla övriga publikationer

Preprint: RES SQ. 2024;RES SQ

A Burden of Rare Copy Number Variants in Obsessive-Compulsive Disorder.

Halvorsen M; de Schipper E; Boberg J; Strom N; Hagen K; Lindblad-Toh K; Karlsson E; Pedersen N; Bulik C; Fundín B; Landén M; Kvale G; Hansen B; Haavik J; Mattheisen M; Rück C; Mataix-Cols D; Crowley J
Preprint: RES SQ. 2023;RES SQ

Arfid Genes and Environment (ARFID-GEN): Study Protocol.

Bulik CM; Micali N; MacDermod CM; Qi B; Munn-Chernoff MA; Thornton LM; White J; Dinkler L; Pisetsky EM; Johnson J; Devine KR; Ortiz SN; Silverman AE; Berthold N; Dumain A; Guintivano J; Halvorsen M; James J
Preprint: MEDRXIV. 2023;MEDRXIV

Genomics of severe and treatment-resistant obsessive-compulsive disorder treated with deep brain stimulation: a preliminary investigation.

Chen LL; Naesström M; Halvorsen M; Fytagoridis A; Mataix-Cols D; Rück C; Crowley JJ; Pascal D
Corrigendum: NATURE COMMUNICATIONS. 2022;13(1):191

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
Review: PSYCHOLOGICAL MEDICINE. 2021;51(13):2201-2209

Genetic architecture of Tourette syndrome: our current understanding.

Domènech L; Cappi C; Halvorsen M
Review: WILEY INTERDISCIPLINARY REVIEWS-RNA. 2015;6(5):517-532

The potential of the riboSNitch in personalized medicine.

Solem AC; Halvorsen M; Ramos SBV; Laederach A

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