Publications by Ida Elken Sønderby

48 publications found

1. 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 et al. (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
2. 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 et al. (2025)
   Penetrance of neurodevelopmental copy number variants is associated with variations in cortical morphology
   Biol Psychiatry Cogn Neurosci Neuroimaging (in press)
   DOI 10.1016/j.bpsc.2025.05.010, PubMed 40414598
3. 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 et al. (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
4. 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
5. 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
6. 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 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
7. 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
8. 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
9. 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 et 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
10. 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 et 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
11. 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
12. 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 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
13. 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 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
14. 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 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
15. 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 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
16. 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 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
17. 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
18. 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
19. 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
20. 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
21. 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
22. 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 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
23. 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
24. 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 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
25. 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 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
26. 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 et al. (2020)
    The genetic architecture of the human cerebral cortex
    Science, 367 (6484)
    DOI 10.1126/science.aay6690, PubMed 32193296
27. 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 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
28. 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 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
29. 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 et 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
30. 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 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
31. 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
32. 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 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
33. 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 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
34. 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
35. 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
36. 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
37. 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
38. 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
39. 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
40. 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
41. 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
42. 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
43. 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
44. 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
45. 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
46. Sønderby IE, Geu-Flores F, Halkier BA (2010)
    Biosynthesis of glucosinolates--gene discovery and beyond
    Trends Plant Sci, 15 (5), 283-90
    DOI 10.1016/j.tplants.2010.02.005, PubMed 20303821
47. 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
48. 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