Publications by Ida Elken Sønderby

57 publications found

  1. Barak EN, Kolskår KK, Dahl C, Alnæs D, Andreassen OA, Nærland T, Sønderby IE, Tamnes CK, Westlye LT (2026)
    Birth Weight and Neurodevelopmental Disorders Across Diagnostic Categories: A Registry-Based Case-Control Study in Clinically Ascertained Samples
    Child Psychiatry Hum Dev (in press)
    DOI 10.1007/s10578-026-02090-8, PubMed 42645711
  2. Ystaas LAR, Parekh P, Parker N, Akkouh I, Birkenæs V, Sønderby IE, Koch E, Hagen E, Frei O, Shadrin A, Andreassen OA, O'Connell KS (2026)
    Genetic liability to addiction underlies comorbid bipolar and substance use disorders
    Biol Psychiatry (in press)
    DOI 10.1016/j.biopsych.2026.08.008, PubMed 42636965
  3. Parekh P, Parker N, Pecheva D, Frei E, Vaudel M, Smith DM, Rigby A, Jahołkowski P, Sønderby IE, Birkenæs V, Bakken NR, Fan CC, Makowski C, Kopal J, Loughnan R, Hagler DJ, van der Meer D, Johansson S, Njølstad PR, Jernigan TL, Thompson WK, Frei O, Shadrin AA, Nichols TE, Andreassen OA, Dale AM (2026)
    FEMA-Long: Modeling unstructured covariances for discovery of time-dependent effects in large-scale longitudinal datasets
    PLoS Genet, 22 (6), e1012184
    DOI 10.1371/journal.pgen.1012184, PubMed 42275417
  4. Korbmacher M, Boen R, Andreassen OA, Westlye LT, Sønderby IE, Maximov II (2026)
    White matter microstructure differences between 15q11.2 copy number variation carriers and non-carriers in mid-to-late life
    Transl Psychiatry, 16 (1)
    DOI 10.1038/s41398-026-03962-2, PubMed 41856989
  5. Boen R, Villalón-Reina JE, Kushan L, O'Hora KP, Fung H, Parker N, Akkouh IA, Alnæs D, O'Hara R, Marzelli MJ, Foland-Ross L, Chick CF, Cotto I, Reiss AL, Hallmayer J, Thompson PM, Andreassen OA, Sønderby IE, Bearden CE (2026)
    Gene dosage effects of 22q11.2 copy number variants on in-vivo measures of white matter axonal density and dispersion
    Mol Psychiatry, 31 (7), 3687-3698
    DOI 10.1038/s41380-026-03489-4, PubMed 41720882
  6. Gurholt TP, Beck D, Voldsbekk I, Parker N, Askeland-Gjerde DE, de Lange AG, van der Meer D, Tamnes CK, Thompson PM, Sønderby IE, Maximov II, Westlye LT, Andreassen OA (2026)
    Linking obesity with white matter microstructure highlights the importance of brainstem tracts and sex differences
    Brain Commun, 8 (1), fcag026
    DOI 10.1093/braincomms/fcag026, PubMed 41717138
  7. van der Meer D, Shadrin AA, Stinson SE, Koch E, Rokicki J, Rahman Z, Bergstedt J, Ottas A, Sønderby IE, Rødevand L, Fuhrer J, Quintana DS, Dale AM, O'Connell KS, Djurovic S, Lehto K, Milani L, Alver M, Andreassen OA (2026)
    Divergent Patterns of Genetic Overlap Between Severe Mental Disorders and Metabolic Markers
    Am J Psychiatry, 183 (7), 482-493
    DOI 10.1176/appi.ajp.20250259, PubMed 41703690
  8. Hope S, Lin A, Rodevand L, Hübenette SJ, Quintana DS, Sønderby IE, Cheng W, Frei O, Bahrami S, Hindley GFL, Kaale A, Shadrin AA, O'Connell KS, Parker N, Djurovic S, Nærland T, Andreassen OA (2025)
    Shared genetic architecture between autism spectrum disorder, loneliness, and social isolation reveals novel genetic loci
    Psychiatr Genet, 36 (1), 13-25
    DOI 10.1097/YPG.0000000000000406, PubMed 41263488
  9. Birkenæs V, Parekh P, Hegemann L, Bakken NR, Frei E, Jaholkowski P, Smeland OB, Susser E, Rodriguez KM, Tesfaye M, Andreassen OA, Havdahl A, Sønderby IE (2025)
    Youth psychotic experiences: psychometric evaluation and diagnostic associations of the CAPE-16 in adolescents from the Norwegian Mother, Father and Child Cohort
    J Child Psychol Psychiatry, 67 (1), 27-40
    DOI 10.1111/jcpp.70007, PubMed 40759589
  10. van der Meer D, Rahman Z, Ottas A, Parekh P, Kutrolli G, Stinson SE, Koromina M, Rokicki J, Sønderby IE, Parker N, Tesfaye M, Hindley G, Rødevand LN, Koch E, Estonian Biobank Research Team, Steen NE, Berg JP, O'Connell KS, Smeland OB, Frei O, Dale AM, Djurovic S, Lehto K, Alver M, Milani L, Shadrin AA, Andreassen OA (2025)
    Pleiotropic and sex-specific genetic mechanisms of circulating metabolic markers
    Nat Commun, 16 (1), 4961
    DOI 10.1038/s41467-025-60058-z, PubMed 40436851
  11. Silva AI, Sønderby IE, Kirov G, Abdellaoui A, Agartz I, Ames D, Armstrong NJ, Artiges E, Banaschewski T, Bassett AS, Bearden CE, Blangero J, Boen R, Boomsma DI, Bülow R, Butcher NJ, Calhoun V, Campbell LE, Chow EWC, Ciufolini S, Craig MC, Crespo-Farroco B, Cunningham AC, Dalvie S, Daly E, Dazzan P, de Geus EJC, de Zubicaray GI, Doherty JL, Donohoe G et al. (2025)
    Penetrance of Neurodevelopmental Copy Number Variants Is Associated With Variations in Cortical Morphology
    Biol Psychiatry Cogn Neurosci Neuroimaging, 10 (10), 1093-1106
    DOI 10.1016/j.bpsc.2025.05.010, PubMed 40414598
  12. Koch E, Smart S, Einarsson G, Kämpe A, Jonsson L, Alver M, Iveson M, Göteson A, Pardiñas AF, Sønderby IE, O'Connell KS, Li Q, Lu Y, Stefánsson H, Stefánsson K, Whalley H, Landén M, O'Donovan MC, Smerud K, Dawson GR, Werge T, Buil A, Reif A, Milani L, Molden E, Fabbri C, Serretti A, Walters J, Lewis CM, Andreassen OA (2025)
    Recommendations for defining treatment outcomes in major psychiatric disorders using real-world data
    Lancet Psychiatry, 12 (6), 457-468
    DOI 10.1016/S2215-0366(25)00061-6, PubMed 40222385
  13. Gurholt TP, Elvsåshagen T, Bahrami S, Rahman Z, Shadrin A, Askeland-Gjerde DE, van der Meer D, Frei O, Kaufmann T, Sønderby IE, Halvorsen S, Westlye LT, Andreassen OA (2024)
    Large-scale brainstem neuroimaging and genetic analyses provide new insights into the neuronal mechanisms of hypertension
    HGG Adv, 6 (1), 100392
    DOI 10.1016/j.xhgg.2024.100392, PubMed 39663699
  14. Szabo A, O'Connell KS, Akkouh IA, Ueland T, Sønderby IE, Hope S, Røe AB, Dønnum MS, Sjaastad I, Steen NE, Ueland T, Sæther LS, Osete JR, Andreassen OA, Nærland T, Djurovic S (2024)
    Elevated levels of peripheral and central nervous system immune markers reflect innate immune dysregulation in autism spectrum disorder
    Psychiatry Res, 342, 116245
    DOI 10.1016/j.psychres.2024.116245, PubMed 39481220
  15. Ivarsdottir EV, Gudmundsson J, Tragante V, Sveinbjornsson G, Kristmundsdottir S, Stacey SN, Halldorsson GH, Magnusson MI, Oddsson A, Walters GB, Sigurdsson A, Saevarsdottir S, Beyter D, Thorleifsson G, Halldorsson BV, Melsted P, Stefansson H, Jonsdottir I, Sørensen E, Pedersen OB, Erikstrup C, Bøgsted M, Pøhl M, Røder A, Stroomberg HV, Gögenur I, Hillingsø J, Bojesen SE, Lassen U, Høgdall E et al. (2024)
    Gene-based burden tests of rare germline variants identify six cancer susceptibility genes
    Nat Genet, 56 (11), 2422-2433
    DOI 10.1038/s41588-024-01966-6, PubMed 39472694
  16. Andersson P, Linge J, Gurholt TP, Sønderby IE, Hindley G, Andreassen OA, Dahlqvist Leinhard O (2024)
    Poor muscle health and cardiometabolic risks associated with antidepressant treatment
    Obesity (Silver Spring), 32 (10), 1857-1869
    DOI 10.1002/oby.24085, PubMed 39315407
  17. Akdeniz BC, Frei O, Hagen E, Filiz TT, Karthikeyan S, Pasman J, Jangmo A, Bergstedt J, Shorter JR, Zetterberg R, Meijsen J, Sønderby IE, Buil A, Tesli M, Lu Y, Sullivan P, Andreassen OA, Hovig E (2024)
    COSGAP: COntainerized Statistical Genetics Analysis Pipelines
    Bioinform Adv, 4 (1), vbae067
    DOI 10.1093/bioadv/vbae067, PubMed 38808072
  18. Kopal J, Kumar K, Shafighi K, Saltoun K, Modenato C, Moreau CA, Huguet G, Jean-Louis M, Martin CO, Saci Z, Younis N, Douard E, Jizi K, Beauchamp-Chatel A, Kushan L, Silva AI, van den Bree MBM, Linden DEJ, Owen MJ, Hall J, Lippé S, Draganski B, Sønderby IE, Andreassen OA, Glahn DC, Thompson PM, Bearden CE, Zatorre R, Jacquemont S, Bzdok D (2024)
    Author Correction: Using rare genetic mutations to revisit structural brain asymmetry
    Nat Commun, 15 (1), 3098
    DOI 10.1038/s41467-024-47545-5, PubMed 38600109
  19. Kopal J, Kumar K, Shafighi K, Saltoun K, Modenato C, Moreau CA, Huguet G, Jean-Louis M, Martin CO, Saci Z, Younis N, Douard E, Jizi K, Beauchamp-Chatel A, Kushan L, Silva AI, van den Bree MBM, Linden DEJ, Owen MJ, Hall J, Lippé S, Draganski B, Sønderby IE, Andreassen OA, Glahn DC, Thompson PM, Bearden CE, Zatorre R, Jacquemont S, Bzdok D (2024)
    Using rare genetic mutations to revisit structural brain asymmetry
    Nat Commun, 15 (1), 2639
    DOI 10.1038/s41467-024-46784-w, PubMed 38531844
  20. Gurholt TP, Borda MG, Parker N, Fominykh V, Kjelkenes R, Linge J, van der Meer D, Sønderby IE, Duque G, Westlye LT, Aarsland D, Andreassen OA (2024)
    Linking sarcopenia, brain structure and cognitive performance: a large-scale UK Biobank study
    Brain Commun, 6 (2), fcae083
    DOI 10.1093/braincomms/fcae083, PubMed 38510210
  21. Boen R, Kaufmann T, van der Meer D, Frei O, Agartz I, Ames D, Andersson M, Armstrong NJ, Artiges E, Atkins JR, Bauer J, Benedetti F, Boomsma DI, Brodaty H, Brosch K, Buckner RL, Cairns MJ, Calhoun V, Caspers S, Cichon S, Corvin AP, Crespo-Facorro B, Dannlowski U, David FS, de Geus EJC, de Zubicaray GI, Desrivières S, Doherty JL, Donohoe G, Ehrlich S et al. (2023)
    Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers
    Biol Psychiatry, 95 (2), 147-160
    DOI 10.1016/j.biopsych.2023.08.018, PubMed 37661008
  22. Kumar K, Modenato C, Moreau C, Ching CRK, Harvey A, Martin-Brevet S, Huguet G, Jean-Louis M, Douard E, Martin CO, Younis N, Tamer P, Maillard AM, Rodriguez-Herreros B, Pain A, 16p11.2 European Consortium, Simons Searchlight Consortium, Kushan L, Isaev D, Alpert K, Ragothaman A, Turner JA, Wang L, Ho TC, Schmaal L, Silva AI, van den Bree MBM, Linden DEJ, Owen MJ, Hall J, Lippé S et al. (2023)
    Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants
    Am J Psychiatry, 180 (9), 685-698
    DOI 10.1176/appi.ajp.20220304, PubMed 37434504
  23. Oddsson A, Sulem P, Sveinbjornsson G, Arnadottir GA, Steinthorsdottir V, Halldorsson GH, Atlason BA, Oskarsson GR, Helgason H, Nielsen HS, Westergaard D, Karjalainen JM, Katrinardottir H, Fridriksdottir R, Jensson BO, Tragante V, Ferkingstad E, Jonsson H, Gudjonsson SA, Beyter D, Moore KHS, Thordardottir HB, Kristmundsdottir S, Stefansson OA, Rantapää-Dahlqvist S, Sonderby IE, Didriksen M, Stridh P, Haavik J, Tryggvadottir L et al. (2023)
    Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
    Nat Commun, 14 (1), 3923
    DOI 10.1038/s41467-023-39492-4, PubMed 37400429
  24. Oddsson A, Sulem P, Sveinbjornsson G, Arnadottir GA, Steinthorsdottir V, Halldorsson GH, Atlason BA, Oskarsson GR, Helgason H, Nielsen HS, Westergaard D, Karjalainen JM, Katrinardottir H, Fridriksdottir R, Jensson BO, Tragante V, Ferkingstad E, Jonsson H, Gudjonsson SA, Beyter D, Moore KHS, Thordardottir HB, Kristmundsdottir S, Stefansson OA, Rantapää-Dahlqvist S, Sonderby IE, Didriksen M, Stridh P, Haavik J, Tryggvadottir L et al. (2023)
    Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
    Nat Commun, 14 (1), 3453
    DOI 10.1038/s41467-023-38951-2, PubMed 37301908
  25. Kopal J, Kumar K, Saltoun K, Modenato C, Moreau CA, Martin-Brevet S, Huguet G, Jean-Louis M, Martin CO, Saci Z, Younis N, Tamer P, Douard E, Maillard AM, Rodriguez-Herreros B, Pain A, Richetin S, Kushan L, Silva AI, van den Bree MBM, Linden DEJ, Owen MJ, Hall J, Lippé S, Draganski B, Sønderby IE, Andreassen OA, Glahn DC, Thompson PM, Bearden CE et al. (2023)
    Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence
    Nat Hum Behav, 7 (6), 1001-1017
    DOI 10.1038/s41562-023-01541-9, PubMed 36864136
  26. Boen R, Kaufmann T, Frei O, van der Meer D, Djurovic S, Andreassen OA, Selmer KK, Alnæs D, Sønderby IE (2023)
    No signs of neurodegenerative effects in 15q11.2 BP1-BP2 copy number variant carriers in the UK Biobank
    Transl Psychiatry, 13 (1), 61
    DOI 10.1038/s41398-023-02358-w, PubMed 36807331
  27. Granerud G, Elvsåshagen T, Arntzen E, Juhasz K, Emilsen NM, Sønderby IE, Nærland T, Malt EA (2022)
    A family study of symbolic learning and synaptic plasticity in autism spectrum disorder
    Front Hum Neurosci, 16, 950922
    DOI 10.3389/fnhum.2022.950922, PubMed 36504626
  28. van der Meer D, Gurholt TP, Sønderby IE, Shadrin AA, Hindley G, Rahman Z, de Lange AG, Frei O, Leinhard OD, Linge J, Simon R, Beck D, Westlye LT, Halvorsen S, Dale AM, Karlsen TH, Kaufmann T, Andreassen OA (2022)
    The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition
    Commun Biol, 5 (1), 1271
    DOI 10.1038/s42003-022-04237-4, PubMed 36402844
  29. Modenato C, Martin-Brevet S, Moreau CA, Rodriguez-Herreros B, Kumar K, Draganski B, Sønderby IE, Jacquemont S (2021)
    Lessons Learned From Neuroimaging Studies of Copy Number Variants: A Systematic Review
    Biol Psychiatry, 90 (9), 596-610
    DOI 10.1016/j.biopsych.2021.05.028, PubMed 34509290
  30. Gurholt TP, Kaufmann T, Frei O, Alnæs D, Haukvik UK, van der Meer D, Moberget T, O'Connell KS, Leinhard OD, Linge J, Simon R, Smeland OB, Sønderby IE, Winterton A, Steen NE, Westlye LT, Andreassen OA (2021)
    Population-based body-brain mapping links brain morphology with anthropometrics and body composition
    Transl Psychiatry, 11 (1), 295
    DOI 10.1038/s41398-021-01414-7, PubMed 34006848
  31. Sønderby IE, van der Meer D, Moreau C, Kaufmann T, Walters GB, Ellegaard M, Abdellaoui A, Ames D, Amunts K, Andersson M, Armstrong NJ, Bernard M, Blackburn NB, Blangero J, Boomsma DI, Brodaty H, Brouwer RM, Bülow R, Bøen R, Cahn W, Calhoun VD, Caspers S, Ching CRK, Cichon S, Ciufolini S, Crespo-Facorro B, Curran JE, Dale AM, Dalvie S, Dazzan P et al. (2021)
    1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans
    Transl Psychiatry, 11 (1), 182
    DOI 10.1038/s41398-021-01213-0, PubMed 33753722
  32. O'Connell KS, Sønderby IE, Frei O, van der Meer D, Athanasiu L, Smeland OB, Alnæs D, Kaufmann T, Westlye LT, Steen VM, Andreassen OA, Hughes T, Djurovic S (2021)
    Association between complement component 4A expression, cognitive performance and brain imaging measures in UK Biobank
    Psychol Med, 52 (15), 3497-3507
    DOI 10.1017/S0033291721000179, PubMed 33653435
  33. Sønderby IE, Ching CRK, Thomopoulos SI, van der Meer D, Sun D, Villalon-Reina JE, Agartz I, Amunts K, Arango C, Armstrong NJ, Ayesa-Arriola R, Bakker G, Bassett AS, Boomsma DI, Bülow R, Butcher NJ, Calhoun VD, Caspers S, Chow EWC, Cichon S, Ciufolini S, Craig MC, Crespo-Facorro B, Cunningham AC, Dale AM, Dazzan P, de Zubicaray GI, Djurovic S, Doherty JL, Donohoe G et al. (2021)
    Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs
    Hum Brain Mapp, 43 (1), 300-328
    DOI 10.1002/hbm.25354, PubMed 33615640
  34. Thompson PM, Jahanshad N, Ching CRK, Salminen LE, Thomopoulos SI, Bright J, Baune BT, Bertolín S, Bralten J, Bruin WB, Bülow R, Chen J, Chye Y, Dannlowski U, de Kovel CGF, Donohoe G, Eyler LT, Faraone SV, Favre P, Filippi CA, Frodl T, Garijo D, Gil Y, Grabe HJ, Grasby KL, Hajek T, Han LKM, Hatton SN, Hilbert K, Ho TC et al. (2020)
    ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries
    Transl Psychiatry, 10 (1), 100
    DOI 10.1038/s41398-020-0705-1, PubMed 32198361
  35. Grasby KL, Jahanshad N, Painter JN, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Pizzagalli F, Ching CRK, McMahon MAB, Shatokhina N, Zsembik LCP, Thomopoulos SI, Zhu AH, Strike LT, Agartz I, Alhusaini S, Almeida MAA, Alnæs D, Amlien IK, Andersson M, Ard T, Armstrong NJ, Ashley-Koch A, Atkins JR, Bernard M, Brouwer RM, Buimer EEL, Bülow R, Bürger C et al. (2020)
    The genetic architecture of the human cerebral cortex
    Science, 367 (6484)
    DOI 10.1126/science.aay6690, PubMed 32193296
  36. Córdova-Palomera A, van der Meer D, Kaufmann T, Bettella F, Wang Y, Alnæs D, Doan NT, Agartz I, Bertolino A, Buitelaar JK, Coynel D, Djurovic S, Dørum ES, Espeseth T, Fazio L, Franke B, Frei O, Håberg A, Le Hellard S, Jönsson EG, Kolskår KK, Lund MJ, Moberget T, Nordvik JE, Nyberg L, Papassotiropoulos A, Pergola G, de Quervain D, Rampino A, Richard G et al. (2020)
    Genetic control of variability in subcortical and intracranial volumes
    Mol Psychiatry, 26 (8), 3876-3883
    DOI 10.1038/s41380-020-0664-1, PubMed 32047264
  37. Writing Committee for the ENIGMA-CNV Working Group, van der Meer D, Sønderby IE, Kaufmann T, Walters GB, Abdellaoui A, Ames D, Amunts K, Andersson M, Armstrong NJ, Bernard M, Blackburn NB, Blangero J, Boomsma DI, Brodaty H, Brouwer RM, Bülow R, Cahn W, Calhoun VD, Caspers S, Cavalleri GL, Ching CRK, Cichon S, Ciufolini S, Corvin A, Crespo-Facorro B, Curran JE, Dalvie S, Dazzan P, de Geus EJC et al. (2020)
    Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition
    JAMA Psychiatry, 77 (4), 420-430
    DOI 10.1001/jamapsychiatry.2019.3779, PubMed 31665216
  38. Gudmundsson OO, Walters GB, Ingason A, Johansson S, Zayats T, Athanasiu L, Sonderby IE, Gustafsson O, Nawaz MS, Jonsson GF, Jonsson L, Knappskog PM, Ingvarsdottir E, Davidsdottir K, Djurovic S, Knudsen GPS, Askeland RB, Haraldsdottir GS, Baldursson G, Magnusson P, Sigurdsson E, Gudbjartsson DF, Stefansson H, Andreassen OA, Haavik J, Reichborn-Kjennerud T, Stefansson K (2019)
    Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder
    Transl Psychiatry, 9 (1), 258
    DOI 10.1038/s41398-019-0599-y, PubMed 31624239
  39. Sønderby IE, Gústafsson Ó, Doan NT, Hibar DP, Martin-Brevet S, Abdellaoui A, Ames D, Amunts K, Andersson M, Armstrong NJ, Bernard M, Blackburn N, Blangero J, Boomsma DI, Bralten J, Brattbak HR, Brodaty H, Brouwer RM, Bülow R, Calhoun V, Caspers S, Cavalleri G, Chen CH, Cichon S, Ciufolini S, Corvin A, Crespo-Facorro B, Curran JE, Dale AM, Dalvie S et al. (2020)
    Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
    Mol Psychiatry, 25 (3), 692-695
    DOI 10.1038/s41380-019-0358-8, PubMed 30705424
  40. Hughes T, Sønderby IE, Polushina T, Hansson L, Holmgren A, Athanasiu L, Melbø-Jørgensen C, Hassani S, Hoeffding LK, Herms S, Bergen SE, Karlsson R, Song J, Rietschel M, Nöthen MM, Forstner AJ, Hoffmann P, Hultman CM, Landén M, Cichon S, Werge T, Andreassen OA, Le Hellard S, Djurovic S (2018)
    Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder
    Transl Psychiatry, 8 (1), 210
    DOI 10.1038/s41398-018-0175-x, PubMed 30297702
  41. Sønderby IE, Gústafsson Ó, Doan NT, Hibar DP, Martin-Brevet S, Abdellaoui A, Ames D, Amunts K, Andersson M, Armstrong NJ, Bernard M, Blackburn N, Blangero J, Boomsma DI, Bralten J, Brattbak HR, Brodaty H, Brouwer RM, Bülow R, Calhoun V, Caspers S, Cavalleri G, Chen CH, Cichon S, Ciufolini S, Corvin A, Crespo-Facorro B, Curran JE, Dale AM, Dalvie S et al. (2018)
    Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
    Mol Psychiatry, 25 (3), 584-602
    DOI 10.1038/s41380-018-0118-1, PubMed 30283035
  42. van der Meer D, Rokicki J, Kaufmann T, Córdova-Palomera A, Moberget T, Alnæs D, Bettella F, Frei O, Doan NT, Sønderby IE, Smeland OB, Agartz I, Bertolino A, Bralten J, Brandt CL, Buitelaar JK, Djurovic S, van Donkelaar M, Dørum ES, Espeseth T, Faraone SV, Fernández G, Fisher SE, Franke B, Haatveit B, Hartman CA, Hoekstra PJ, Håberg AK, Jönsson EG, Kolskår KK et al. (2018)
    Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes
    Mol Psychiatry, 25 (11), 3053-3065
    DOI 10.1038/s41380-018-0262-7, PubMed 30279459
  43. Stokowy T, Polushina T, Sønderby IE, Karlsson R, Giddaluru S, Le Hellard S, Bergen SE, Sullivan PF, Andreassen OA, Djurovic S, Hultman CM, Steen VM (2018)
    Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes
    Sci Rep, 8 (1), 6915
    DOI 10.1038/s41598-018-25280-4, PubMed 29720671
  44. Córdova-Palomera A, Kaufmann T, Bettella F, Wang Y, Doan NT, van der Meer D, Alnæs D, Rokicki J, Moberget T, Sønderby IE, Andreassen OA, Westlye LT (2018)
    Effects of autozygosity and schizophrenia polygenic risk on cognitive and brain developmental trajectories
    Eur J Hum Genet, 26 (7), 1049-1059
    DOI 10.1038/s41431-018-0134-2, PubMed 29700391
  45. Hughes T, Hansson L, Sønderby IE, Athanasiu L, Zuber V, Tesli M, Song J, Hultman CM, Bergen SE, Landén M, Melle I, Andreassen OA, Djurovic S (2015)
    A Loss-of-Function Variant in a Minor Isoform of ANK3 Protects Against Bipolar Disorder and Schizophrenia
    Biol Psychiatry, 80 (4), 323-330
    DOI 10.1016/j.biopsych.2015.09.021, PubMed 26682468
  46. Athanasiu L, Smorr LL, Tesli M, Røssberg JI, Sønderby IE, Spigset O, Djurovic S, Andreassen OA (2015)
    Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs
    J Psychopharmacol, 29 (8), 884-91
    DOI 10.1177/0269881115584469, PubMed 25944848
  47. Goulart LF, Bettella F, Sønderby IE, Schork AJ, Thompson WK, Mattingsdal M, Steen VM, Zuber V, Wang Y, Dale AM, PRACTICAL/ELLIPSE consortium, Andreassen OA, Djurovic S (2015)
    MicroRNAs enrichment in GWAS of complex human phenotypes
    BMC Genomics, 16 (1), 304
    DOI 10.1186/s12864-015-1513-5, PubMed 25884492
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