Publications published since 2015 from OUS - Department of Medical Genetics

968 publications found

Publications 2024

1. Akman T, Arendt LM, Geisler J, Kristensen VN, Frigessi A, Köhn-Luque A (2024)
   Modeling of Mouse Experiments Suggests that Optimal Anti-Hormonal Treatment for Breast Cancer is Diet-Dependent
   Bull Math Biol, 86 (4), 42
   DOI 10.1007/s11538-023-01253-1, PubMed 38498130
2. Andreou D, Steen NE, Mørch-Johnsen L, Jørgensen KN, Wortinger LA, Barth C, Szabo A, O'Connell KS, Lekva T, Hjell G, Johansen IT, Ormerod MBEG, Haukvik UK, Aukrust P, Djurovic S, Yolken RH, Andreassen OA, Ueland T, Agartz I (2024)
   Toxoplasma gondii infection associated with inflammasome activation and neuronal injury
   Sci Rep, 14 (1), 5327
   DOI 10.1038/s41598-024-55887-9, PubMed 38438515
3. Anjum M, Ariansen I, Hjellvik V, Selmer R, Kjerpeseth LJ, Skovlund E, Myrstad M, Ellekjær H, Christophersen IE, Tveit A, Berge T (2024)
   Stroke and bleeding risk in atrial fibrillation with CHA2DS2-VASC risk score of one: the Norwegian AFNOR study
   Eur Heart J, 45 (1), 57-66
   DOI 10.1093/eurheartj/ehad659, PubMed 37995254
4. Artaza H, Eriksson D, Lavrichenko K, Aranda-Guillén M, Bratland E, Vaudel M, Knappskog P, Husebye ES, Bensing S, Wolff ASB, Kämpe O, Røyrvik EC, Johansson S (2024)
   Rare copy number variation in autoimmune Addison's disease
   Front Immunol, 15, 1374499
   DOI 10.3389/fimmu.2024.1374499, PubMed 38562931
5. Balakittnen J, Ekanayake Weeramange C, Wallace DF, Duijf PHG, Cristino AS, Hartel G, Barrero RA, Taheri T, Kenny L, Vasani S, Batstone M, Breik O, Punyadeera C (2024)
   A novel saliva-based miRNA profile to diagnose and predict oral cancer
   Int J Oral Sci, 16 (1), 14
   DOI 10.1038/s41368-023-00273-w, PubMed 38368395
6. Bhatia S, Khanna KK, Duijf PHG (2024)
   Targeting chromosomal instability and aneuploidy in cancer
   Trends Pharmacol Sci, 45 (3), 210-224
   DOI 10.1016/j.tips.2024.01.009, PubMed 38355324
7. Bjune K, Halvorsen PS, Wangensteen H, Leren TP, Bogsrud MP, Strøm TB (2024)
   Flavonoids regulate LDLR through different mechanisms tied to their specific structures
   J Lipid Res, 100539 (in press)
   DOI 10.1016/j.jlr.2024.100539, PubMed 38556050
8. Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD (2024)
   Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing
   Eur J Hum Genet (in press)
   DOI 10.1038/s41431-023-01519-1, PubMed 38172175
9. Carrizosa C, Undlien DE, Vigeland MD (2024)
   shinyseg: a web application for flexible cosegregation and sensitivity analysis
   Bioinformatics (in press)
   DOI 10.1093/bioinformatics/btae201, PubMed 38598476
10. Cobb L, de Muinck E, Kollias S, Skage M, Gilfillan GD, Sydenham MAK, Qiao SW, Star B (2024)
    High-throughput sequencing of insect specimens with sub-optimal DNA preservation using a practical, plate-based Illumina-compatible Tn5 transposase library preparation method
    PLoS One, 19 (3), e0300865
    DOI 10.1371/journal.pone.0300865, PubMed 38517905
11. de la Peña Avalos B, Paquet N, Tropée R, Coulombe Y, Palacios H, Leung JW, Masson JY, Duijf PHG, Dray E (2024)
    The protein phosphatase EYA4 promotes homologous recombination (HR) through dephosphorylation of tyrosine 315 on RAD51
    Nucleic Acids Res, 52 (3), 1173-1187
    DOI 10.1093/nar/gkad1177, PubMed 38084915
12. Efthymiou S, Scala M, Nagaraj V, Ochenkowska K, Komdeur FL, Liang RA, Abdel-Hamid MS, Sultan T, Barøy T, Van Ghelue M, Vona B, Maroofian R, Zafar F, Alkuraya FS, Zaki MS, Severino M, Duru KC, Tryon RC, Brauteset LV, Ansari M, Hamilton M, van Haelst MM, van Haaften G, Zara F, Houlden H et al. (2024)
    Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome
    Brain (in press)
    DOI 10.1093/brain/awae010, PubMed 38217872
13. Grindedal EM, Zucknick M, Stormorken A, Rønne E, Tandstad NM, Isaacs WB, Axcrona K, Mæhle L (2024)
    Outcomes of 10 years of PSA screening for prostate cancer in Norwegian men with Lynch syndrome
    Prostate (in press)
    DOI 10.1002/pros.24711, PubMed 38629217
14. 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
15. Hendricks LAJ, Verbeek KCJ, Schuurs-Hoeijmakers JHM, Mensenkamp AR, Brems H, de Putter R, Anastasiadou VC, Villy MC, Jahn A, Steinke-Lange V, Baldassarri M, Irmejs A, de Jong MM, Links TP, Leter EM, Bosch DGM, Høberg-Vetti H, Tveit Haavind M, Jørgensen K, Mæhle L, Blatnik A, Brunet J, Darder E, Tham E, Hoogerbrugge N et al. (2024)
    Lifestyle Factors and Breast Cancer in Females with PTEN Hamartoma Tumor Syndrome (PHTS)
    Cancers (Basel), 16 (5)
    DOI 10.3390/cancers16050953, PubMed 38473316
16. Hindley G, Drange OK, Lin A, Kutrolli G, Shadrin AA, Parker N, O'Connell KS, Rødevand L, Cheng W, Bahrami S, Karadag N, Holen B, Jaholkowski P, Woldeyohannes MT, Djurovic S, Dale AM, Frei O, Ueland T, Smeland OB, Andreassen OA (2024)
    Corrigendum to "Cross-trait genome-wide association analysis of C-reactive protein level and psychiatric disorders" [Psychoneuroendocrinology 157 (2023) 106368]
    Psychoneuroendocrinology, 162, 106980
    DOI 10.1016/j.psyneuen.2024.106980, PubMed 38336601
17. Holmgren A, Akkouh I, O'Connell KS, Osete JR, Bjørnstad PM, Djurovic S, Hughes T (2024)
    Bipolar patients display stoichiometric imbalance of gene expression in post-mortem brain samples
    Mol Psychiatry (in press)
    DOI 10.1038/s41380-023-02398-0, PubMed 38351171
18. Husain RA, Jiao X, Hennings JC, Giesecke J, Palsule G, Beck-Wödl S, Osmanović D, Bjørgo K, Mir A, Ilyas M, Abbasi SM, Efthymiou S, Dominik N, Maroofian R, Houlden H, Rankin J, Pagnamenta AT, Nashabat M, Altwaijri W, Alfadhel M, Umair M, Khouj E, Reardon W, El-Hattab AW, Mekki M et al. (2024)
    Biallelic NUDT2 variants defective in mRNA decapping cause a neurodevelopmental disease
    Brain, 147 (4), 1197-1205
    DOI 10.1093/brain/awad434, PubMed 38141063
19. Karadag N, Hagen E, Shadrin AA, van der Meer D, O'Connell KS, Rahman Z, Kutrolli G, Parker N, Bahrami S, Fominykh V, Heuser K, Taubøll E, Ueland T, Steen NE, Djurovic S, Dale AM, Frei O, Andreassen OA, Smeland OB (2024)
    Unraveling the shared genetics of common epilepsies and general cognitive ability
    medRxiv
    DOI 10.1101/2024.03.25.24304773, PubMed 38585944
20. King ES, Tadele DS, Pierce B, Hinczewski M, Scott JG (2024)
    Diverse mutant selection windows shape spatial heterogeneity in evolving populations
    PLoS Comput Biol, 20 (2), e1011878
    DOI 10.1371/journal.pcbi.1011878, PubMed 38386690
21. Koch E, Kämpe A, Alver M, Sigurðarson S, Einarsson G, Partanen J, Smith RL, Jaholkowski P, Taipale H, Lähteenvuo M, Steen NE, Smeland OB, Djurovic S, Molden E, FinnGen, Estonian Biobank Research Team, Sigurdsson E, Stefánsson H, Stefánsson K, Palotie A, Milani L, O'Connell KS, Andreassen OA (2024)
    Polygenic liability for antipsychotic dosage and polypharmacy - a real-world registry and biobank study
    Neuropsychopharmacology (in press)
    DOI 10.1038/s41386-023-01792-0, PubMed 38184734
22. Koch E, Pardiñas AF, O'Connell KS, Selvaggi P, Camacho Collados J, Babic A, Marshall SE, Van der Eycken E, Angulo C, Lu Y, Sullivan PF, Dale AM, Molden E, Posthuma D, White N, Schubert A, Djurovic S, Heimer H, Stefánsson H, Stefánsson K, Werge T, Sønderby I, O'Donovan MC, Walters JTR, Milani L et al. (2024)
    How Real-World Data Can Facilitate the Development of Precision Medicine Treatment in Psychiatry
    Biol Psychiatry (in press)
    DOI 10.1016/j.biopsych.2024.01.001, PubMed 38185234
23. 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
24. 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
25. Kulseth MA (2024)
    Correspondence on "Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants" by Vogel et al
    Genet Med, 26 (3), 101038
    DOI 10.1016/j.gim.2023.101038, PubMed 38226981
26. Lehtonen J, Sulonen AM, Almusa H, Lehtokari VL, Johari M, Palva A, Hakonen AH, Wartiovaara K, Lehesjoki AE, Udd B, Wallgren-Pettersson C, Pelin K, Savarese M, Saarela J (2024)
    Haplotype information of large neuromuscular disease genes provided by linked-read sequencing has a potential to increase diagnostic yield
    Sci Rep, 14 (1), 4306
    DOI 10.1038/s41598-024-54866-4, PubMed 38383731
27. Lind SM, Sletten M, Hellenes M, Mathelier A, Tekpli X, Tinholt M, Iversen N (2024)
    Coagulation factor V in breast cancer: a p53-regulated tumor suppressor and predictive marker for treatment response to chemotherapy
    J Thromb Haemost (in press)
    DOI 10.1016/j.jtha.2024.02.008, PubMed 38382738
28. Maltas J, Tadele DS, Durmaz A, McFarland CD, Hinczewski M, Scott JG (2024)
    Frequency-dependent ecological interactions increase the prevalence, and shape the distribution, of pre-existing drug resistance
    bioRxiv
    DOI 10.1101/2023.03.16.533001, PubMed 36993678
29. Nurmi K, Silventoinen K, Keskitalo S, Rajamäki K, Kouri VP, Kinnunen M, Jalil S, Maldonado R, Wartiovaara K, Nievas EI, Denita-Juárez SP, Duncan CJA, Kuismin O, Saarela J, Romo I, Martelius T, Parantainen J, Beklen A, Bilicka M, Matikainen S, Nordström DC, Kaustio M, Wartiovaara-Kautto U, Kilpivaara O, Klein C et al. (2024)
    Truncating NFKB1 variants cause combined NLRP3 inflammasome activation and type I interferon signaling and predispose to necrotizing fasciitis
    Cell Rep Med, 101503 (in press)
    DOI 10.1016/j.xcrm.2024.101503, PubMed 38593810
30. Rauluseviciute I, Riudavets-Puig R, Blanc-Mathieu R, Castro-Mondragon JA, Ferenc K, Kumar V, Lemma RB, Lucas J, Chèneby J, Baranasic D, Khan A, Fornes O, Gundersen S, Johansen M, Hovig E, Lenhard B, Sandelin A, Wasserman WW, Parcy F, Mathelier A (2024)
    JASPAR 2024: 20th anniversary of the open-access database of transcription factor binding profiles
    Nucleic Acids Res, 52 (D1), D174-D182
    DOI 10.1093/nar/gkad1059, PubMed 37962376
31. Seton KA, Espejo-Oltra JA, Giménez-Orenga K, Haagmans R, Ramadan DJ, Mehlsen J, European ME Research Group for Early Career Researchers (Young EMERG) (2024)
    Advancing Research and Treatment: An Overview of Clinical Trials in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Future Perspectives
    J Clin Med, 13 (2)
    DOI 10.3390/jcm13020325, PubMed 38256459
32. Shadrin AA, Hindley G, Hagen E, Parker N, Tesfaye M, Jaholkowski P, Rahman Z, Kutrolli G, Fominykh V, Djurovic S, Smeland OB, O'Connell KS, van der Meer D, Frei O, Andreassen OA, Dale AM (2024)
    Dissecting the genetic overlap between three complex phenotypes with trivariate MiXeR
    medRxiv
    DOI 10.1101/2024.02.23.24303236, PubMed 38464132
33. Sæther LS, Szabo A, Akkouh IA, Haatveit B, Mohn C, Vaskinn A, Aukrust P, Ormerod MBEG, Eiel Steen N, Melle I, Djurovic S, Andreassen OA, Ueland T, Ueland T (2024)
    Cognitive and inflammatory heterogeneity in severe mental illness: Translating findings from blood to brain
    Brain Behav Immun, 118, 287-299
    DOI 10.1016/j.bbi.2024.03.014, PubMed 38461955
34. Tesfaye M, Jaholkowski P, Shadrin AA, van der Meer D, Hindley GFL, Holen B, Parker N, Parekh P, Birkenæs V, Rahman Z, Bahrami S, Kutrolli G, Frei O, Djurovic S, Dale AM, Smeland OB, O'Connell KS, Andreassen OA (2024)
    Identification of Novel Genomic Loci for Anxiety and Extensive Genetic Overlap with Psychiatric Disorders
    medRxiv
    DOI 10.1101/2023.09.01.23294920, PubMed 37693403
35. Tinholt M, Tekpli X, Torland LA, Tahiri A, Geisler J, Kristensen V, Sandset PM, Iversen N (2024)
    The breast cancer coagulome in the tumor microenvironment and its role in prognosis and treatment response to chemotherapy
    J Thromb Haemost (in press)
    DOI 10.1016/j.jtha.2024.01.003, PubMed 38237862
36. Tissink EP, Shadrin AA, van der Meer D, Parker N, Hindley G, Roelfs D, Frei O, Fan CC, Nagel M, Nærland T, Budisteanu M, Djurovic S, Westlye LT, van den Heuvel MP, Posthuma D, Kaufmann T, Dale AM, Andreassen OA (2024)
    Abundant pleiotropy across neuroimaging modalities identified through a multivariate genome-wide association study
    Nat Commun, 15 (1), 2655
    DOI 10.1038/s41467-024-46817-4, PubMed 38531894
37. Tsoulia T, Sundaram AYM, Braaen S, Jørgensen JB, Rimstad E, Wessel Ø, Dahle MK (2024)
    Transcriptomics of early responses to purified Piscine orthoreovirus-1 in Atlantic salmon (Salmo salar L.) red blood cells compared to non-susceptible cell lines
    Front Immunol, 15, 1359552
    DOI 10.3389/fimmu.2024.1359552, PubMed 38420125
38. van der Meer D, Cheng W, Rokicki J, Fernandez-Cabello S, Shadrin A, Smeland OB, Ehrhart F, Gülöksüz S, Pries LK, Lin B, Rutten BPF, van Os J, O'Donovan M, Richards AL, Steen NE, Djurovic S, Westlye LT, Andreassen OA, Kaufmann T, , (2024)
    Clustering Schizophrenia Genes by Their Temporal Expression Patterns Aids Functional Interpretation
    Schizophr Bull, 50 (2), 327-338
    DOI 10.1093/schbul/sbad140, PubMed 37824720
39. Wortinger LA, Stavrum AK, Shadrin AA, Szabo A, Rukke SH, Nerland S, Smelror RE, Jørgensen KN, Barth C, Andreou D, Weibell MA, Djurovic S, Andreassen OA, Thoresen M, Ursini G, Agartz I, Le Hellard S (2024)
    Divergent epigenetic responses to perinatal asphyxia in severe mental disorders
    Transl Psychiatry, 14 (1), 16
    DOI 10.1038/s41398-023-02709-7, PubMed 38191519
40. Wu C, Gunnarsson EB, Myklebust EM, Köhn-Luque A, Tadele DS, Enserink JM, Frigessi A, Foo J, Leder K (2024)
    Using birth-death processes to infer tumor subpopulation structure from live-cell imaging drug screening data
    PLoS Comput Biol, 20 (3), e1011888
    DOI 10.1371/journal.pcbi.1011888, PubMed 38446830
41. Yiangou K, Mavaddat N, Dennis J, Zanti M, Wang Q, Bolla MK, Abubakar M, Ahearn TU, Andrulis IL, Anton-Culver H, Antonenkova NN, Arndt V, Aronson KJ, Augustinsson A, Baten A, Behrens S, Bermisheva M, de Gonzalez AB, Białkowska K, Boddicker N, Bodelon C, Bogdanova NV, Bojesen SE, Brantley KD, Brauch H et al. (2024)
    Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction
    medRxiv
    DOI 10.1101/2024.02.12.24302043, PubMed 38410445

Publications 2023

1. Adams MN, Croft LV, Urquhart A, Saleem MAM, Rockstroh A, Duijf PHG, Thomas PB, Ferguson GP, Najib IM, Shah ET, Bolderson E, Nagaraj S, Williams ED, Nelson CC, O'Byrne KJ, Richard DJ (2023)
   hSSB1 (NABP2/OBFC2B) modulates the DNA damage and androgen-induced transcriptional response in prostate cancer
   Prostate, 83 (7), 628-640
   DOI 10.1002/pros.24496, PubMed 36811381
2. Akkouh IA, Ueland T, Szabo A, Hughes T, Smeland OB, Andreassen OA, Osete JR, Djurovic S (2023)
   Longitudinal Transcriptomic Analysis of Human Cortical Spheroids Identifies Axonal Dysregulation in the Prenatal Brain as a Mediator of Genetic Risk for Schizophrenia
   Biol Psychiatry, 95 (7), 687-698
   DOI 10.1016/j.biopsych.2023.08.017, PubMed 37661009
3. Almaas R, Atneosen-Åsegg M, Ytre-Arne ME, Melheim M, Sorte HS, Cízková D, Reims HM, Bezrouk A, Harrison SP, Strand J, Hermansen JU, Andersen SS, Eiklid KL, Mokrý J, Sullivan GJ, Stray-Pedersen A (2023)
   Aagenaes syndrome/lymphedema cholestasis syndrome 1 is caused by a founder variant in the 5'-untranslated region of UNC45A
   J Hepatol, 79 (4), 945-954
   DOI 10.1016/j.jhep.2023.05.037, PubMed 37328071
4. Álvarez I, Tirado-Herranz A, Alvarez-Palomo B, Osete JR, Edel MJ (2023)
   Proteomic Analysis of Human iPSC-Derived Neural Stem Cells and Motor Neurons Identifies Proteasome Structural Alterations
   Cells, 12 (24)
   DOI 10.3390/cells12242800, PubMed 38132120
5. Andersen EL, Solberg MG, Walle-Hansen MM, Enger S, Onarheim S, Olufsen M, Berge T, Christophersen IE, Ulimoen SR, Tveit A (2023)
   Feasibility of Patient-Managed ECG Recordings to Detect the Time of Atrial Fibrillation Recurrence after Electrical Cardioversion: Results from the PRE-ELECTRIC Study
   Cardiology, 148 (4), 347-352
   DOI 10.1159/000530304, PubMed 37040720
6. Asl ER, Rostamzadeh D, Duijf PHG, Mafi S, Mansoori B, Barati S, Cho WC, Mansoori B (2023)
   Mutant P53 in the formation and progression of the tumor microenvironment: Friend or foe
   Life Sci, 315, 121361
   DOI 10.1016/j.lfs.2022.121361, PubMed 36608871
7. Bang L, Bahrami S, Hindley G, Smeland OB, Rødevand L, Jaholkowski PP, Shadrin A, Connell KSO, Frei O, Lin A, Rahman Z, Cheng W, Parker N, Fan CC, Dale AM, Djurovic S, Bulik CM, Andreassen OA (2023)
   Genome-wide analysis of anorexia nervosa and major psychiatric disorders and related traits reveals genetic overlap and identifies novel risk loci for anorexia nervosa
   Transl Psychiatry, 13 (1), 291
   DOI 10.1038/s41398-023-02585-1, PubMed 37658054
8. Barker-Clarke R, Gray JM, Tadele DS, Hinczewski M, Scott JG (2023)
   Maintaining, masking, and mimicking selection: the interplay of cell-intrinsic and cell-extrinsic effects upon eco-evolutionary dynamics
   bioRxiv
   DOI 10.1101/2023.03.15.532871, PubMed 36993598
9. Bassi N, Hovland HN, Rasheed K, Jarhelle E, Pedersen N, Mchaina EK, Bakkan SME, Iversen N, Høberg-Vetti H, Haukanes BI, Knappskog PM, Aukrust I, Ognedal E, Van Ghelue M (2023)
   Functional analyses of rare germline BRCA1 variants by transcriptional activation and homologous recombination repair assays
   BMC Cancer, 23 (1), 368
   DOI 10.1186/s12885-023-10790-w, PubMed 37085799
10. Bhatia S, Gunter JH, Burgess JT, Adams MN, O'Byrne K, Thompson EW, Duijf PH (2023)
    Stochastic epithelial-mesenchymal transitions diversify non-cancerous lung cell behaviours
    Transl Oncol, 37, 101760
    DOI 10.1016/j.tranon.2023.101760, PubMed 37611490
11. Birkenæs V, Refsum Bakken N, Frei E, Jaholkowski P, Smeland OB, Tesfaye M, Agartz I, Susser E, Bresnahan M, Røysamb E, Nordbø Jørgensen K, Nesvåg R, Havdahl A, Andreassen OA, Elken Sønderby I (2023)
    Psychometric Properties and Diagnostic Associations of the Short-Form Community Assessment of Psychic Experiences in a Population-Based Sample of 29 021 Adult Men
    Schizophr Bull, 49 (5), 1229-1238
    DOI 10.1093/schbul/sbad074, PubMed 37262330
12. Bitarafan F, Khodaeian M, Garrousi F, Khalesi R, Ghazi Nader D, Karimi B, Alibakhshi R, Garshasbi M (2023)
    Reporting a novel growth hormone receptor gene variant in an Iranian consanguineous pedigree with Laron syndrome: a case report
    BMC Endocr Disord, 23 (1), 155
    DOI 10.1186/s12902-023-01388-1, PubMed 37474955
13. Bitter H, Midtvedt Ø, Gunnarsson R, Lande A (2023)
    [A woman in her thirties with frequent mucosal ulcers]
    Tidsskr Nor Laegeforen, 143 (8)
    DOI 10.4045/tidsskr.22.0650, PubMed 37254975
14. Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD (2023)
    A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing
    Eur J Hum Genet (in press)
    DOI 10.1038/s41431-023-01494-7, PubMed 38030917
15. 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
16. 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
17. Brun MK, Bjørlykke KH, Viken MK, Stenvik GE, Klaasen RA, Gehin JE, Warren DJ, Sexton J, Sandanger Ø, Kvien TK, Mørk C, Haavardsholm EA, Jahnsen J, Goll GL, Lie BA, Bolstad N, Jørgensen KK, Syversen SW (2023)
    HLA-DQ2 is associated with anti-drug antibody formation to infliximab in patients with immune-mediated inflammatory diseases
    J Intern Med, 293 (5), 648-655
    DOI 10.1111/joim.13616, PubMed 36843323
18. Chaudhry FA, Sajjad TA, Heiberg A (2023)
    [Not Available]
    Tidsskr Nor Laegeforen, 143 (18)
    DOI 10.4045/tidsskr.23.0733, PubMed 38088291
19. Cheng W, Parker N, Karadag N, Koch E, Hindley G, Icick R, Shadrin A, O'Connell KS, Bjella T, Bahrami S, Rahman Z, Tesfaye M, Jaholkowski P, Rødevand L, Holen B, Lagerberg TV, Steen NE, Djurovic S, Dale AM, Frei O, Smeland OB, Andreassen OA (2023)
    The relationship between cannabis use, schizophrenia, and bipolar disorder: a genetically informed study
    Lancet Psychiatry, 10 (6), 441-451
    DOI 10.1016/S2215-0366(23)00143-8, PubMed 37208114
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Publications 2022

1. Absalom NL, Liao VWY, Johannesen KMH, Gardella E, Jacobs J, Lesca G, Gokce-Samar Z, Arzimanoglou A, Zeidler S, Striano P, Meyer P, Benkel-Herrenbrueck I, Mero IL, Rummel J, Chebib M, Møller RS, Ahring PK (2022)
   Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies
   Nat Commun, 13 (1), 1822
   DOI 10.1038/s41467-022-29280-x, PubMed 35383156
2. Ahearn TU, Zhang H, Michailidou K, Milne RL, Bolla MK, Dennis J, Dunning AM, Lush M, Wang Q, Andrulis IL, Anton-Culver H, Arndt V, Aronson KJ, Auer PL, Augustinsson A, Baten A, Becher H, Behrens S, Benitez J, Bermisheva M, Blomqvist C, Bojesen SE, Bonanni B, Børresen-Dale AL, Brauch H et al. (2022)
   Common variants in breast cancer risk loci predispose to distinct tumor subtypes
   Breast Cancer Res, 24 (1), 2
   DOI 10.1186/s13058-021-01484-x, PubMed 34983606
3. Ahring PK, Liao VWY, Gardella E, Johannesen KM, Krey I, Selmer KK, Stadheim BF, Davis H, Peinhardt C, Koko M, Coorg RK, Syrbe S, Bertsche A, Santiago-Sim T, Diemer T, Fenger CD, Platzer K, Eichler EE, Lerche H, Lemke JR, Chebib M, Møller RS (2022)
   Gain-of-function variants in GABRD reveal a novel pathway for neurodevelopmental disorders and epilepsy
   Brain, 145 (4), 1299-1309
   DOI 10.1093/brain/awab391, PubMed 34633442
4. Akkouh IA, Hribkova H, Grabiec M, Budinska E, Szabo A, Kasparek T, Andreassen OA, Sun YM, Djurovic S (2022)
   Derivation and Molecular Characterization of a Morphological Subpopulation of Human iPSC Astrocytes Reveal a Potential Role in Schizophrenia and Clozapine Response
   Schizophr Bull, 48 (1), 190-198
   DOI 10.1093/schbul/sbab092, PubMed 34357384
5. Bahrami S, Hindley G, Winsvold BS, O'Connell KS, Frei O, Shadrin A, Cheng W, Bettella F, Rødevand L, Odegaard KJ, Fan CC, Pirinen MJ, Hautakangas HM, HUNT All-In Headache, Dale AM, Djurovic S, Smeland OB, Andreassen OA (2022)
   Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools
   Brain, 145 (1), 142-153
   DOI 10.1093/brain/awab267, PubMed 34273149
6. Balakittnen J, Weeramange CE, Wallace DF, Duijf PHG, Cristino AS, Kenny L, Vasani S, Punyadeera C (2022)
   Noncoding RNAs in oral cancer
   Wiley Interdiscip Rev RNA, 14 (3), e1754
   DOI 10.1002/wrna.1754, PubMed 35959932
7. Bjørklund SS, Aure MR, Häkkinen J, Vallon-Christersson J, Kumar S, Evensen KB, Fleischer T, Tost J, OSBREAC, Sahlberg KK, Mathelier A, Bhanot G, Ganesan S, Tekpli X, Kristensen VN (2022)
   Subtype and cell type specific expression of lncRNAs provide insight into breast cancer
   Commun Biol, 5 (1), 834
   DOI 10.1038/s42003-022-03559-7, PubMed 35982125
8. Boen R, Raud L, Huster RJ (2022)
   Inhibitory Control and the Structural Parcelation of the Right Inferior Frontal Gyrus
   Front Hum Neurosci, 16, 787079
   DOI 10.3389/fnhum.2022.787079, PubMed 35280211
9. Breast Cancer Association Consortium, Mavaddat N, Dorling L, Carvalho S, Allen J, González-Neira A, Keeman R, Bolla MK, Dennis J, Wang Q, Ahearn TU, Andrulis IL, Beckmann MW, Behrens S, Benitez J, Bermisheva M, Blomqvist C, Bogdanova NV, Bojesen SE, Briceno I, Brüning T, Camp NJ, Campbell A, Castelao JE, Chang-Claude J et al. (2022)
   Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes
   JAMA Oncol, 8 (3), e216744
   DOI 10.1001/jamaoncol.2021.6744, PubMed 35084436
10. Castro-Mondragon JA, Aure MR, Lingjærde OC, Langerød A, Martens JWM, Børresen-Dale AL, Kristensen VN, Mathelier A (2022)
    Cis-regulatory mutations associate with transcriptional and post-transcriptional deregulation of gene regulatory programs in cancers
    Nucleic Acids Res, 50 (21), 12131-12148
    DOI 10.1093/nar/gkac1143, PubMed 36477895
11. Castro-Mondragon JA, Riudavets-Puig R, Rauluseviciute I, Lemma RB, Turchi L, Blanc-Mathieu R, Lucas J, Boddie P, Khan A, Manosalva Pérez N, Fornes O, Leung TY, Aguirre A, Hammal F, Schmelter D, Baranasic D, Ballester B, Sandelin A, Lenhard B, Vandepoele K, Wasserman WW, Parcy F, Mathelier A (2022)
    JASPAR 2022: the 9th release of the open-access database of transcription factor binding profiles
    Nucleic Acids Res, 50 (D1), D165-D173
    DOI 10.1093/nar/gkab1113, PubMed 34850907
12. Celse T, Tingaud-Sequeira A, Dieterich K, Siegfried G, Lecaignec C, Bouneau L, Fannemel M, Salaun G, Laffargue F, Martinez G, Satre V, Vieville G, Bidart M, Soussi Zander C, Turesson AC, Splitt M, Reboul D, Chiesa J, Khau Van Kien P, Godin M, Gruchy N, Goel H, Palmer E, Demetriou K, Shalhoub C et al. (2022)
    OTX2 duplications: a recurrent cause of oculo-auriculo-vertebral spectrum
    J Med Genet, 60 (6), 620-626
    DOI 10.1136/jmg-2022-108678, PubMed 36368868
13. Chen H, Fan S, Stone J, Thompson DJ, Douglas J, Li S, Scott C, Bolla MK, Wang Q, Dennis J, Michailidou K, Li C, Peters U, Hopper JL, Southey MC, Nguyen-Dumont T, Nguyen TL, Fasching PA, Behrens A, Cadby G, Murphy RA, Aronson K, Howell A, Astley S, Couch F et al. (2022)
    Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci
    Breast Cancer Res, 24 (1), 27
    DOI 10.1186/s13058-022-01524-0, PubMed 35414113
14. Cheng W, van der Meer D, Parker N, Hindley G, O'Connell KS, Wang Y, Shadrin AA, Alnæs D, Bahrami S, Lin A, Karadag N, Holen B, Fernandez-Cabello S, Fan CC, Dale AM, Djurovic S, Westlye LT, Frei O, Smeland OB, Andreassen OA (2022)
    Shared genetic architecture between schizophrenia and subcortical brain volumes implicates early neurodevelopmental processes and brain development in childhood
    Mol Psychiatry, 27 (12), 5167-5176
    DOI 10.1038/s41380-022-01751-z, PubMed 36100668
15. Cherik F, Reilly J, Kerkhof J, Levy M, McConkey H, Barat-Houari M, Butler KM, Coubes C, Lee JA, Le Guyader G, Louie RJ, Patterson WG, Tedder ML, Bak M, Hammer TB, Craigen W, Démurger F, Dubourg C, Fradin M, Franciskovich R, Frengen E, Friedman J, Palares NR, Iascone M, Misceo D et al. (2022)
    DNA methylation episignature in Gabriele-de Vries syndrome
    Genet Med, 24 (4), 905-914
    DOI 10.1016/j.gim.2021.12.003, PubMed 35027293
16. Dalen ML, Vigerust NF, Hammarström C, Holmstrøm H, Andresen JH (2022)
    Neonatal interstitial lung disease in a girl with Jacobsen syndrome: a case report
    J Med Case Rep, 16 (1), 117
    DOI 10.1186/s13256-022-03351-5, PubMed 35321730
17. de la Morena-Barrio ME, Suchon P, Jacobsen EM, Iversen N, Miñano A, de la Morena-Barrio B, Bravo-Pérez C, Padilla J, Cifuentes R, Asenjo S, Deleuze JF, Trégouët DA, Lozano ML, Vicente V, Sandset PM, Morange PE, Corral J (2022)
    Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays
    Blood, 140 (2), 140-151
    DOI 10.1182/blood.2021014708, PubMed 35486842
18. Dennis J, Tyrer JP, Walker LC, Michailidou K, Dorling L, Bolla MK, Wang Q, Ahearn TU, Andrulis IL, Anton-Culver H, Antonenkova NN, Arndt V, Aronson KJ, Freeman LEB, Beckmann MW, Behrens S, Benitez J, Bermisheva M, Bogdanova NV, Bojesen SE, Brenner H, Castelao JE, Chang-Claude J, Chenevix-Trench G, Clarke CL et al. (2022)
    Rare germline copy number variants (CNVs) and breast cancer risk
    Commun Biol, 5 (1), 65
    DOI 10.1038/s42003-021-02990-6, PubMed 35042965
19. Diaz-Lundahl S, Sundaram AYM, Gillund P, Gilfillan GD, Olsaker I, Krogenæs A (2022)
    Gene Expression in Embryos From Norwegian Red Bulls With High or Low Non Return Rate: An RNA-Seq Study of in vivo-Produced Single Embryos
    Front Genet, 12, 780113
    DOI 10.3389/fgene.2021.780113, PubMed 35096004
20. Dixon-Suen SC, Lewis SJ, Martin RM, English DR, Boyle T, Giles GG, Michailidou K, Bolla MK, Wang Q, Dennis J, Lush M, Investigators A, Ahearn TU, Ambrosone CB, Andrulis IL, Anton-Culver H, Arndt V, Aronson KJ, Augustinsson A, Auvinen P, Beane Freeman LE, Becher H, Beckmann MW, Behrens S, Bermisheva M et al. (2022)
    Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study
    Br J Sports Med, 56 (20), 1157-1170
    DOI 10.1136/bjsports-2021-105132, PubMed 36328784
21. Dorling L, Carvalho S, Allen J, Parsons MT, Fortuno C, González-Neira A, Heijl SM, Adank MA, Ahearn TU, Andrulis IL, Auvinen P, Becher H, Beckmann MW, Behrens S, Bermisheva M, Bogdanova NV, Bojesen SE, Bolla MK, Bremer M, Briceno I, Camp NJ, Campbell A, Castelao JE, Chang-Claude J, Chanock SJ et al. (2022)
    Breast cancer risks associated with missense variants in breast cancer susceptibility genes
    Genome Med, 14 (1), 51
    DOI 10.1186/s13073-022-01052-8, PubMed 35585550
22. Elkjaer Greenwood Ormerod MB, Ueland T, Frogner Werner MC, Hjell G, Rødevand L, Sæther LS, Lunding SH, Johansen IT, Ueland T, Lagerberg TV, Melle I, Djurovic S, Andreassen OA, Steen NE (2022)
    Composite immune marker scores associated with severe mental disorders and illness course
    Brain Behav Immun Health, 24, 100483
    DOI 10.1016/j.bbih.2022.100483, PubMed 35856063
23. Engh JA, Ueland T, Agartz I, Andreou D, Aukrust P, Boye B, Bøen E, Drange OK, Elvsåshagen T, Hope S, Høegh MC, Joa I, Johnsen E, Kroken RA, Lagerberg TV, Lekva T, Malt UF, Melle I, Morken G, Nærland T, Steen VM, Wedervang-Resell K, Weibell MA, Westlye LT, Djurovic S et al. (2022)
    Plasma Levels of the Cytokines B Cell-Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL) in Schizophrenia, Bipolar, and Major Depressive Disorder: A Cross Sectional, Multisite Study
    Schizophr Bull, 48 (1), 37-46
    DOI 10.1093/schbul/sbab106, PubMed 34499169
24. Eriksen KO, Wigers AR, Wedding IM, Erichsen AK, Barøy T, Søberg K, Jørstad ØK (2022)
    A novel homozygous variant in the SPG7 gene presenting with childhood optic nerve atrophy
    Am J Ophthalmol Case Rep, 26, 101400
    DOI 10.1016/j.ajoc.2022.101400, PubMed 35243150
25. Goris A, Vandebergh M, McCauley JL, Saarela J, Cotsapas C (2022)
    Genetics of multiple sclerosis: lessons from polygenicity
    Lancet Neurol, 21 (9), 830-842
    DOI 10.1016/S1474-4422(22)00255-1, PubMed 35963264
26. 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
27. Grimholt U, Sundaram AYM, Bøe CA, Dahle MK, Lukacs M (2022)
    Tetraploid Ancestry Provided Atlantic Salmon With Two Paralogue Functional T Cell Receptor Beta Regions Whereof One Is Completely Novel
    Front Immunol, 13, 930312
    DOI 10.3389/fimmu.2022.930312, PubMed 35784332
28. Grootes I, Keeman R, Blows FM, Milne RL, Giles GG, Swerdlow AJ, Fasching PA, Abubakar M, Andrulis IL, Anton-Culver H, Beckmann MW, Blomqvist C, Bojesen SE, Bolla MK, Bonanni B, Briceno I, Burwinkel B, Camp NJ, Castelao JE, Choi JY, Clarke CL, Couch FJ, Cox A, Cross SS, Czene K et al. (2022)
    Incorporating progesterone receptor expression into the PREDICT breast prognostic model
    Eur J Cancer, 173, 178-193
    DOI 10.1016/j.ejca.2022.06.011, PubMed 35933885
29. Hajdarevic R, Lande A, Mehlsen J, Rydland A, Sosa DD, Strand EB, Mella O, Pociot F, Fluge Ø, Lie BA, Viken MK (2022)
    Genetic association study in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) identifies several potential risk loci
    Brain Behav Immun, 102, 362-369
    DOI 10.1016/j.bbi.2022.03.010, PubMed 35318112
30. Hardcastle A, Berry AM, Campbell IM, Zhao X, Liu P, Gerard AE, Rosenfeld JA, Sisoudiya SD, Hernandez-Garcia A, Loddo S, Di Tommaso S, Novelli A, Dentici ML, Capolino R, Digilio MC, Graziani L, Rustad CF, Neas K, Ferrero GB, Brusco A, Di Gregorio E, Wellesley D, Beneteau C, Joubert M, Van Den Bogaert K et al. (2022)
    Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data
    Am J Med Genet A, 188 (10), 2958-2968
    DOI 10.1002/ajmg.a.62919, PubMed 35904974
31. Harrison GF, Leaton LA, Harrison EA, Kichula KM, Viken MK, Shortt J, Gignoux CR, Lie BA, Vukcevic D, Leslie S, Norman PJ (2022)
    Allele imputation for the killer cell immunoglobulin-like receptor KIR3DL1/S1
    PLoS Comput Biol, 18 (2), e1009059
    DOI 10.1371/journal.pcbi.1009059, PubMed 35192601
32. Hellstrøm T, Andelic N, Holthe ØØ, Helseth E, Server A, Eiklid K, Sigurdardottir S (2022)
    APOE-ε4 Is Associated With Reduced Verbal Memory Performance and Higher Emotional, Cognitive, and Everyday Executive Function Symptoms Two Months After Mild Traumatic Brain Injury
    Front Neurol, 13, 735206
    DOI 10.3389/fneur.2022.735206, PubMed 35250800
33. Hindley G, Frei O, Shadrin AA, Cheng W, O'Connell KS, Icick R, Parker N, Bahrami S, Karadag N, Roelfs D, Holen B, Lin A, Fan CC, Djurovic S, Dale AM, Smeland OB, Andreassen OA (2022)
    Charting the Landscape of Genetic Overlap Between Mental Disorders and Related Traits Beyond Genetic Correlation
    Am J Psychiatry, 179 (11), 833-843
    DOI 10.1176/appi.ajp.21101051, PubMed 36069018
34. Hindley G, O'Connell KS, Rahman Z, Frei O, Bahrami S, Shadrin A, Høegh MC, Cheng W, Karadag N, Lin A, Rødevand L, Fan CC, Djurovic S, Lagerberg TV, Dale AM, Smeland OB, Andreassen OA (2022)
    The shared genetic basis of mood instability and psychiatric disorders: A cross-trait genome-wide association analysis
    Am J Med Genet B Neuropsychiatr Genet, 189 (6), 207-218
    DOI 10.1002/ajmg.b.32907, PubMed 35841185
35. Hjell G, Szabo A, Mørch-Johnsen L, Holst R, Tesli N, Bell C, Fischer-Vieler T, Werner MCF, Lunding SH, Ormerod MBEG, Johansen IT, Dieset I, Djurovic S, Melle I, Ueland T, Andreassen OA, Steen NE, Haukvik UK (2022)
    Interleukin-18 signaling system links to agitation in severe mental disorders
    Psychoneuroendocrinology, 140, 105721
    DOI 10.1016/j.psyneuen.2022.105721, PubMed 35301151
36. Holmgren A, Hansson L, Bjerkaas-Kjeldal K, Impellizzeri AAR, Gilfillan GD, Djurovic S, Hughes T (2022)
    Mapping the expression of an ANK3 isoform associated with bipolar disorder in the human brain
    Transl Psychiatry, 12 (1), 45
    DOI 10.1038/s41398-022-01784-6, PubMed 35091539
37. Hovland A, Mundal LJ, Veierød MB, Holven KB, Bogsrud MP, Tell GS, Leren TP, Retterstøl K (2022)
    The risk of various types of cardiovascular diseases in mutation positive familial hypercholesterolemia; a review
    Front Genet, 13, 1072108
    DOI 10.3389/fgene.2022.1072108, PubMed 36561318
38. Hovland HN, Al-Adhami R, Ariansen SL, Van Ghelue M, Sjursen W, Lima S, Bolstad M, Berger AH, Høberg-Vetti H, Knappskog P, Haukanes BI, Aukrust I, Ognedal E (2022)
    BRCA1 Norway: comparison of classification for BRCA1 germline variants detected in families with suspected hereditary breast and ovarian cancer between different laboratories
    Fam Cancer, 21 (4), 389-398
    DOI 10.1007/s10689-021-00286-6, PubMed 34981296
39. Huynh-Le MP, Karunamuni R, Fan CC, Asona L, Thompson WK, Martinez ME, Eeles RA, Kote-Jarai Z, Muir KR, Lophatananon A, Schleutker J, Pashayan N, Batra J, Grönberg H, Neal DE, Nordestgaard BG, Tangen CM, MacInnis RJ, Wolk A, Albanes D, Haiman CA, Travis RC, Blot WJ, Stanford JL, Mucci LA et al. (2022)
    Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score
    Prostate Cancer Prostatic Dis, 25 (4), 755-761
    DOI 10.1038/s41391-022-00497-7, PubMed 35152271
40. Høyer H, Busk ØL, Esbensen QY, Røsby O, Hilmarsen HT, Russell MB, Nyman TA, Braathen GJ, Nilsen HL (2022)
    Clinical characteristics and proteome modifications in two Charcot-Marie-Tooth families with the AARS1 Arg326Trp mutation
    BMC Neurol, 22 (1), 299
    DOI 10.1186/s12883-022-02828-6, PubMed 35971119
41. Håberg SE, Page CM, Lee Y, Nustad HE, Magnus MC, Haftorn KL, Carlsen EØ, Denault WRP, Bohlin J, Jugessur A, Magnus P, Gjessing HK, Lyle R (2022)
    DNA methylation in newborns conceived by assisted reproductive technology
    Nat Commun, 13 (1), 1896
    DOI 10.1038/s41467-022-29540-w, PubMed 35393427
42. Icick R, Shadrin A, Holen B, Karadag N, Lin A, Hindley G, O'Connell K, Frei O, Bahrami S, Høegh MC, Cheng W, Fan CC, Djurovic S, Dale AM, Lagerberg TV, Smeland OB, Andreassen OA (2022)
    Genetic overlap between mood instability and alcohol-related phenotypes suggests shared biological underpinnings
    Neuropsychopharmacology, 47 (11), 1883-1891
    DOI 10.1038/s41386-022-01401-6, PubMed 35953530
43. Jansen IE, van der Lee SJ, Gomez-Fonseca D, de Rojas I, Dalmasso MC, Grenier-Boley B, Zettergren A, Mishra A, Ali M, Andrade V, Bellenguez C, Kleineidam L, Küçükali F, Sung YJ, Tesí N, Vromen EM, Wightman DP, Alcolea D, Alegret M, Alvarez I, Amouyel P, Athanasiu L, Bahrami S, Bailly H, Belbin O et al. (2022)
    Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers
    Acta Neuropathol, 144 (5), 821-842
    DOI 10.1007/s00401-022-02454-z, PubMed 36066633
44. Johannessen J, Nærland T, Hope S, Torske T, Kaale A, Wirgenes KV, Malt E, Djurovic S, Rietschel M, Andreassen OA (2022)
    Correction to: Attitudes among parents of persons with autism spectrum disorder towards information about genetic risk and future health
    Eur J Hum Genet, 30 (10), 1198
    DOI 10.1038/s41431-021-01021-6, PubMed 34903869
45. Kallak TK, Fransson E, Bränn E, Berglund H, Lager S, Comasco E, Lyle R, Skalkidou A (2022)
    Maternal prenatal depressive symptoms and toddler behavior: an umbilical cord blood epigenome-wide association study
    Transl Psychiatry, 12 (1), 186
    DOI 10.1038/s41398-022-01954-6, PubMed 35513368
46. Langton DJ, Bhalekar RM, Joyce TJ, Rushton SP, Wainwright BJ, Nargol ME, Shyam N, Lie BA, Pabbruwe MB, Stewart AJ, Waller S, Natu S, Ren R, Hornick R, Darlay R, Su EP, Nargol AVF (2022)
    The influence of HLA genotype on the development of metal hypersensitivity following joint replacement
    Commun Med (Lond), 2, 73
    DOI 10.1038/s43856-022-00137-0, PubMed 35761834
47. Langton DJ, Bhalekar RM, Joyce TJ, Rushton SP, Wainwright BJ, Nargol ME, Shyam N, Lie BA, Pabbruwe MB, Stewart AJ, Waller S, Natu S, Ren R, Hornick R, Darlay R, Su EP, Nargol AVF (2022)
    Erratum: Author Correction: The influence of HLA genotype on the development of metal hypersensitivity following joint replacement
    Commun Med (Lond), 2, 91
    DOI 10.1038/s43856-022-00158-9, PubMed 35856082
48. Lemma RB, Fleischer T, Martinsen E, Ledsaak M, Kristensen V, Eskeland R, Gabrielsen OS, Mathelier A (2022)
    Pioneer transcription factors are associated with the modulation of DNA methylation patterns across cancers
    Epigenetics Chromatin, 15 (1), 13
    DOI 10.1186/s13072-022-00444-9, PubMed 35440061
49. Leren TP, Bogsrud MP (2022)
    Cascade screening for familial hypercholesterolemia should be organized at a national level
    Curr Opin Lipidol, 33 (4), 231-236
    DOI 10.1097/MOL.0000000000000832, PubMed 35942821
50. Li J, Li YR, Glessner JT, Yang J, March ME, Kao C, Vaccaro CN, Bradfield JP, Li J, Mentch FD, Qu HQ, Qi X, Chang X, Hou C, Abrams DJ, Qiu H, Wei Z, Connolly JJ, Wang F, Snyder J, Flatø B, Thompson SD, Langefeld CD, Lie BA, Munro JE et al. (2022)
    Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis
    Arthritis Rheumatol, 74 (8), 1420-1429
    DOI 10.1002/art.42129, PubMed 35347896
51. Lirussi L, Ayyildiz D, Liu Y, Montaldo NP, Carracedo S, Aure MR, Jobert L, Tekpli X, Touma J, Sauer T, Dalla E, Kristensen VN, Geisler J, Piazza S, Tell G, Nilsen H (2022)
    A regulatory network comprising let-7 miRNA and SMUG1 is associated with good prognosis in ER+ breast tumours
    Nucleic Acids Res, 50 (18), 10449-10468
    DOI 10.1093/nar/gkac807, PubMed 36156150
52. Maggadóttir SM, Kvalheim G, Wernhoff P, Sæbøe-Larssen S, Revheim ME, Josefsen D, Wälchli S, Helland Å, Inderberg EM (2022)
    A phase I/II escalation trial design T-RAD: Treatment of metastatic lung cancer with mRNA-engineered T cells expressing a T cell receptor targeting human telomerase reverse transcriptase (hTERT)
    Front Oncol, 12, 1031232
    DOI 10.3389/fonc.2022.1031232, PubMed 36439452
53. Melnes T, Bogsrud MP, Thorsen I, Fossum J, Christensen JJ, Narverud I, Retterstøl K, Ulven SM, Holven KB (2022)
    What characterizes event-free elderly FH patients? A comprehensive lipoprotein profiling
    Nutr Metab Cardiovasc Dis, 32 (7), 1651-1660
    DOI 10.1016/j.numecd.2022.03.028, PubMed 35527125
54. Metcalfe KA, Gronwald J, Tung NM, McCuaig JM, Eisen A, Elser C, Foulkes WD, Neuhausen SL, Senter L, Moller P, Bordeleau L, Fruscio R, Velsher L, Zakalik D, Olopade OI, Eng C, Pal T, Cullinane CA, Couch FJ, Kotsopoulos J, Sun P, Lubinski J, Narod SA (2022)
    The risks of cancer in older women with BRCA pathogenic variants: How far have we come?
    Cancer, 129 (6), 901-907
    DOI 10.1002/cncr.34615, PubMed 36571512
55. Mo T, Brandal SHB, Köhn-Luque A, Engebraaten O, Kristensen VN, Fleischer T, Hompland T, Seierstad T (2022)
    Quantification of Tumor Hypoxia through Unsupervised Modelling of Consumption and Supply Hypoxia MR Imaging in Breast Cancer
    Cancers (Basel), 14 (5)
    DOI 10.3390/cancers14051326, PubMed 35267636
56. Motazedi E, Cheng W, Thomassen JQ, Frei O, Rongve A, Athanasiu L, Bahrami S, Shadrin A, Ulstein I, Stordal E, Brækhus A, Saltvedt I, Sando SB, O'Connell KS, Hindley G, van der Meer D, Bergh S, Nordestgaard BG, Tybjærg-Hansen A, Bråthen G, Pihlstrøm L, Djurovic S, Frikke-Schmidt R, Fladby T, Aarsland D et al. (2022)
    Using Polygenic Hazard Scores to Predict Age at Onset of Alzheimer's Disease in Nordic Populations
    J Alzheimers Dis, 88 (4), 1533-1544
    DOI 10.3233/JAD-220174, PubMed 35848024
57. Mundal LJ, Hovland A, Igland J, Vetrhus M, Veierød MB, Holven KB, Bogsrud MP, Tell GS, Leren TP, Retterstøl K (2022)
    Increased risk of peripheral artery disease in persons with familial hypercholesterolaemia: a prospective registry study
    Eur J Prev Cardiol, 28 (18), e11-e13
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