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
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
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(2024) Youth Psychotic Experiences: Diagnostic Associations and Evaluation of the CAPE-16 medRxiv DOI 10.1101/2024.04.18.24306017, PubMed 38699352
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 DCet al.(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
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 DCet al.(2024) Using rare genetic mutations to revisit structural brain asymmetry Nat Commun, 15(1), 2639 DOI 10.1038/s41467-024-46784-w, PubMed 38531844
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
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 EJCet 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
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 AIet 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
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 Set 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
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 Set 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
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 DCet al.(2023) Using rare genetic mutations to revisit structural brain asymmetry bioRxiv DOI 10.1101/2023.04.17.537199, PubMed 37131672
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, Richetin S, 16p11.2 European Consortium, Simons Searchlight Consortium, Kushan L, Isaev D, Alpert K, Ragothaman A, Turner JA, Wang L, Ho TC, Schmaal Let al.(2023) Subcortical brain alterations in carriers of genomic copy number variants medRxiv DOI 10.1101/2023.02.14.23285913, PubMed 36865328
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 Bet 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
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
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
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
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
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
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 Set 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
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), 1-11(in press) DOI 10.1017/S0033291721000179, PubMed 33653435
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 AMet 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
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 KLet 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
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 JRet al.(2020) The genetic architecture of the human cerebral cortex Science, 367(6484) DOI 10.1126/science.aay6690, PubMed 32193296
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 Let 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
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 Aet 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
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 Jet al.(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
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 Set 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
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
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 Set 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
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 Bet 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
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
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
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
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
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
Zai CC, Manchia M, Sønderby IE, Yilmaz Z, De Luca V, Tiwari AK, Squassina A, Zai GC, Shaikh SA, Strauss J, King N, Le Foll B, Kaplan AS, Finseth PI, Vaaler AE, Djurovic S, Andreassen OA, Vincent JB, Kennedy JL(2014) Investigation of the genetic interaction between BDNF and DRD3 genes in suicidical behaviour in psychiatric disorders World J Biol Psychiatry, 16(3), 171-9 DOI 10.3109/15622975.2014.953011, PubMed 25264289
Finseth PI, Sønderby IE, Djurovic S, Agartz I, Malt UF, Melle I, Morken G, Andreassen OA, Vaaler AE, Tesli M(2013) Association analysis between suicidal behaviour and candidate genes of bipolar disorder and schizophrenia J Affect Disord, 163, 110-4 DOI 10.1016/j.jad.2013.12.018, PubMed 24461634
Tesli M, Egeland R, Sønderby IE, Haukvik UK, Bettella F, Hibar DP, Thompson PM, Rimol LM, Melle I, Agartz I, Djurovic S, Andreassen OA(2013) No evidence for association between bipolar disorder risk gene variants and brain structural phenotypes J Affect Disord, 151(1), 291-7 DOI 10.1016/j.jad.2013.06.008, PubMed 23820096
Mattingsdal M, Brown AA, Djurovic S, Sønderby IE, Server A, Melle I, Agartz I, Hovig E, Jensen J, Andreassen OA(2012) Pathway analysis of genetic markers associated with a functional MRI faces paradigm implicates polymorphisms in calcium responsive pathways Neuroimage, 70, 143-9 DOI 10.1016/j.neuroimage.2012.12.035, PubMed 23274185
Whiteman NK, Gloss AD, Sackton TB, Groen SC, Humphrey PT, Lapoint RT, Sønderby IE, Halkier BA, Kocks C, Ausubel FM, Pierce NE(2012) Genes involved in the evolution of herbivory by a leaf-mining, Drosophilid fly Genome Biol Evol, 4(9), 900-16 DOI 10.1093/gbe/evs063, PubMed 22813779
Müller R, de Vos M, Sun JY, Sønderby IE, Halkier BA, Wittstock U, Jander G(2010) Differential effects of indole and aliphatic glucosinolates on lepidopteran herbivores J Chem Ecol, 36(8), 905-13 DOI 10.1007/s10886-010-9825-z, PubMed 20617455
Sønderby IE, Burow M, Rowe HC, Kliebenstein DJ, Halkier BA(2010) A complex interplay of three R2R3 MYB transcription factors determines the profile of aliphatic glucosinolates in Arabidopsis Plant Physiol, 153(1), 348-63 DOI 10.1104/pp.109.149286, PubMed 20348214
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Sun JY, Sønderby IE, Halkier BA, Jander G, de Vos M(2009) Non-volatile intact indole glucosinolates are host recognition cues for ovipositing Plutella xylostella J Chem Ecol, 35(12), 1427-36 DOI 10.1007/s10886-009-9723-4, PubMed 20054620
Sønderby IE, Hansen BG, Bjarnholt N, Ticconi C, Halkier BA, Kliebenstein DJ(2007) A systems biology approach identifies a R2R3 MYB gene subfamily with distinct and overlapping functions in regulation of aliphatic glucosinolates PLoS One, 2(12), e1322 DOI 10.1371/journal.pone.0001322, PubMed 18094747
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
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
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(2024) Youth Psychotic Experiences: Diagnostic Associations and Evaluation of the CAPE-16 medRxiv DOI 10.1101/2024.04.18.24306017, PubMed 38699352