Publications 2017

We have listed only items that contain BBMRI-NL or the grant number in the affiliation, funding and/or acknowledgement section of the article. Items are listed per year in alphabetical order.

  • Alharbi FF, Souverein PC, de Groot MCH, Blom MT, de Boer A, Klungel OH, Tan HL: The impact of serum potassium-influencing antihypertensive drugs on the risk of out-of-hospital cardiac arrest: A case-control study. British Journal of Clinical Pharmacology 83(11): 2541-2548.
  • Amin N, Belonogova NM, Jovanova O, Brouwer RWW, van Rooij JGJ, van den Hout MC, Svishcheva GR, Kraaij R, Zorkoltseva IV, Kirichenko AV, et al.: Nonsynonymous variation in NKPD1 increases depressive symptoms in European populations. Biological Psychiatry 81(8): 702-707.
  • Amin N, Jovanova O, Adams HHH, Dehghan A, Kavousi M, Vernooij MW, Peeters RP, de Vrij FMS, van der Lee SJ, van Rooij JGJ, et al.: Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms. Molecular Psychiatry 22(4): 537-543.
  • Atanasovska B, Rensen SS, van der Sijde MR, Marsman G, Kumar V, Jonkers I, Withoff S, Shiri-Sverdlov R, Greve JWM, Faber KN, et al.: A liver-specific long noncoding RNA with a role in cell viability is elevated in human nonalcoholic steatohepatitis. Hepatology 66(3): 794-808.
  • Barrdahl M, Rudolph A, Hopper JL, Southey MC, Broeks A, Fasching PA, Beckmann MW, Gago-Dominguez M, Castelao JE, Guenel P, et al.: Gene-environment interactions involving functional variants: Results from the breast cancer association consortium. International Journal of Cancer 141(9): 1830-1840.
  • Ben-Avraham D, Karasik D, Verghese J, Lunetta KL, Smith JA, Eicher JD, Vered R, Deelen J, Arnold AM, Buchman AS, et al.: The complex genetics of gait speed: Genome-wide meta-analysis approach. Aging 9(1): 209-246.
  • Berg van den ME, Warren HR, Cabrera CP, Verweij N, Mifsud B, Haessler J, Bihlmeyer NA, Fu YP, Weiss S, Lin HJ, et al.: Discovery of novel heart rate-associated loci using the exome chip. Human Molecular Genetics 26(12): 2346-2363.
  • Bigdeli TB, Ripke S, Peterson RE, Trzaskowski M, Bacanu SA, Abdellaoui A, Andlauer TFM, Beekman ATF, Berger K, Blackwood DHR, et al.: Genetic effects influencing risk for major depressive disorder in China and Europe. Translational Psychiatry 7(3): e1074.
  • Bonder MJ, Luijk R, Zhernakova DV, Moed M, Deelen P, Vermaat M, van Iterson M, van Dijk F, van Galen M, Bot J, et al.: Disease variants alter transcription factor levels and methylation of their binding sites. Nature Genetics 49(1): 133-138.
  • Bonvanie IJ, Janssens KA, Rosmalen JG, Oldehinkel AJ: Life events and functional somatic symptoms: A population study in older adolescents. Br J Psychol 108(2): 318-333.
  • Bot M, Middeldorp CM, de Geus EJC, Lau HM, Sinke M, van Nieuwenhuizen B, Smit JH, Boomsma DI, Penninx BWJH: Validity of LIDAS (lifetime depression assessment self-report): A self-report online assessment of lifetime major depressive disorder. Psychological Medicine 47(2): 279-289.
  • Braun KVE, Dhana K, de Vries PS, Voortman T, van Meurs JBJ, Uitterlinden AG, Hofman A, Hu FB, Franco OH, Dehghan A, et al.: Epigenome-wide association study (EWAS) on lipids: The Rotterdam study. Clinical Epigenetics 9: 15.
  • Bredenoord AL, Boeckhout M: Ancillary care obligations for social media platforms. Am J Bioeth 17(3): 29-31.
  • Brinksma DM, Hoekstra PJ, van den Hoofdakker B, de Bildt A, Buitelaar JK, Hartman CA, Dietrich A: Age-dependent role of pre- and perinatal factors in interaction with genes on ADHD symptoms across adolescence. Journal of Psychiatric Research 90: 110-117.
  • Brouckaert O, Rudolph A, Laenen A, Keeman R, Bolla MK, Wang Q, Soubry A, Wildiers H, Andrulis IL, Arndt V, et al.: Reproductive profiles and risk of breast cancer subtypes: A multi-center case-only study. Breast Cancer Research 19(1): 119.
  • Brouwer E: Novel therapeutic approaches to large vessel vasculitis. Rheumatology 56(S2): 19: I88
  • Brouwer-Brolsma EM, Streppel MT, van Lee L, Geelen A, Sluik D, van de Wiel AM, de Vries JHM, van 't Veer P, Feskens EJM: A national dietary assessment reference database (NDARD) for the Dutch population: Rationale behind the design. Nutrients 9(10): 13.
  • Buljubasic N, Akkerhuis KM, Cheng JM, Oemrawsingh RM, GarciaGarcia HM, de Boer SPM, Regar E, van Geuns RJM, Serruys P, Boersma E, et al.: Fibrinogen in relation to degree and composition of coronary plaque on intravascular ultrasound in patients undergoing coronary angiography. Coronary Artery Disease 28(1): 23-32.
  • Deckert J, Weber H, Villmann C, Lonsdorf TB, Richter J, Andreatta M, Arias-Vasquez A, Hommers L, Kent L, Schartner C, et al.: GLRB allelic variation associated with agoraphobic cognitions, increased startle response and fear network activation: A potential neurogenetic pathway to panic disorder. Molecular Psychiatry 22(10): 1431-1439.
  • Dijk van FE, Mostert J, Glennon J, Onnink M, Dammers J, Vasquez AA, Kan C, Verkes RJ, Hoogman M, Franke B, et al.: Five factor model personality traits relate to adult attention-deficit/hyperactivity disorder but not to their distinct neurocognitive profiles. Psychiatry Research 258: 255-261.
  • Direk N, Williams S, Smith JA, Ripke S, Air T, Amare AT, Amin N, Baune BT, Bennett DA, Blackwood DHR, et al.: An analysis of two genomewide association meta-analyses identifies a new locus for broad depression phenotype. Biological Psychiatry 82(5): 322-329.
  • Ehli EA, Abdellaoui A, Fedko IO, Grieser C, Nohzadeh-Malakshah S, Willemsen G, de Geus EJ, Boomsma DI, Davies GE, Hottenga JJ: A method to customize population-specific arrays for genome-wide association testing. European Journal of Human Genetics 25(2): 267-270.
  • Ellis BJ, Oldehinkel AJ, Nederhof E: The adaptive calibration model of stress responsivity: An empirical test in the tracking adolescents' individual lives survey study. Development and Psychopathology 29(3): 1001-1021.
  • Elsenburg LK, Smidt N, Liefbroer AC: The longitudinal relation between accumulation of adverse life events and body mass index from early adolescence to young adulthood. Psychosomatic Medicine 79(3): 365-373.
  • Elsenburg LK, Smidt N, Hoek HW, Liefbroer AC: Body mass index trajectories from adolescence to early young adulthood: Do adverse life events play a role? Obesity 25(12): 2142-2148.
  • Eppinga RN, Kofink D, Dullaart RPF, Dalmeijer GW, Lipsic E, van Veldhuisen DJ, van der Horst ICC, Asselbergs FW, van der Harst P: Effect of metformin on metabolites and relation with myocardial infarct size and left ventricular ejection fraction after myocardial infarction. Circulation – Cardiovascular Genetics 10(1): 59.
  • Ferreira MA, Vonk JM, Baurecht H, Marenholz I, Tian C, Hoffman JD, Helmer Q, Tillander A, Ullemar V, van Dongen J, et al.: Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Nature Genetics 49(12): 1752-1757.
  • Franken A, Laceulle OM, Van Aken MAG, Ormel J: Using response surface analysis to interpret the impact of parent-offspring personality similarity on adolescent externalizing problems. European Journal of Personality 31(1): 104-117.
  • Gallo V, Dijk FN, Holloway JW, Ring SM, Koppelman GH, Postma DS, Strachan DP, Granell R, de Jongste JC, Jaddoe VWV, et al.: TRPA1 gene polymorphisms and childhood asthma. Pediatric Allergy and Immunology 28(2): 191-198.
  • Gerritsen L, Milaneschi Y, Vinkers CH, van Hemert AM, van Velzen L, Schmaal L, Penninx B: Hpa axis genes, and their interaction with childhood maltreatment, are related to cortisol levels and stressrelated phenotypes. Neuropsychopharmacology 42(12): 2446-2455.
  • Gialluisi A, Guadalupe T, Francks C, Fisher SE: Neuroimaging genetic analyses of novel candidate genes associated with reading and language. Brain and Language 172: 9-15.
  • Graff M, Scott RA, Justice AE, Young KL, Feitosa MF, Barata L, Winkler TW, Chu AY, Mahajan A, Hadley D, et al.: Genome-wide physical activity interactions in adiposity. A meta-analysis of 200,452 adults. PLoS Genetics 13(4): e1006528.
  • Gudmundsson J, Thorleifsson G, Sigurdsson JK, Stefansdottir L, Jonasson JG, Gudjonsson SA, Gudbjartsson DF, Masson G, Johannsdottir H, Halldorsson GH, et al.: A genome-wide association study yields five novel thyroid cancer risk loci. Nature Communications 8: 14517.
  • Hamdi Y, Soucy P, Kuchenbaeker KB, Pastinen T, Droit A, Lemacon A, Adlard J, Aittomaki K, Andrulis IL, Arason A, et al.: Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: Identification of a modifier of breast cancer risk at locus 11q22.3. Breast Cancer Research and Treatment 161(1): 117-134.
  • Hart 't LM, Vogelzangs N, van Greevenbroek MM, van der Kallen CJ, Slieker RC, Mook-Kanamori DO, van Dijk KW, Dekker JM, Nijpels G: Blood metabolites associate with glycaemic control in type 2 diabetes independent of glucose lowering medication. Diabetologia 60: S99.
  • Hillger JM, le Roy B, Wang Z, Mulder-Krieger T, Boomsma DI, Slagboom PE, Danen EHJ, Ijzerman AP, Heitman LH: Phenotypic screening of cannabinoid receptor 2 ligands shows different sensitivity to genotype. Biochemical Pharmacology 130: 60-70.
  • Holstege H, van der Lee SJ, Hulsman M, Wong TH, van Rooij JGJ, Weiss M, Louwersheimer E, Wolters FJ, Amin N, Uitterlinden AG, et al.: Characterization of pathogenic SORL1 genetic variants for association with Alzheimer’s disease: A clinical interpretation strategy. European Journal of Human Genetics 25(8): 973-981.
  • Hulsegge G, Spijkerman AMW, van der Schouw YT, Bakker SJL, Gansevoort RT, Smit HA, Verschuren WMM: Trajectories of metabolic risk factors and biochemical markers prior to the onset of type 2 diabetes: The population-based longitudinal doetinchem study. Nutrition & Diabetes 7(8): UNSP e270.
  • Hulzen van KJE, Scholz CJ, Franke B, Ripke S, Klein M, McQuillin A, Sonuga-Barke EJ, Kelsoe JR, Landen M, Andreassen OA, et al.: Genetic overlap between attention-deficit/hyperactivity disorder and bipolar disorder: Evidence from genome-wide association study meta-analysis. Biological Psychiatry 82(9): 634-641.
  • Iterson van M, van Zwet EW, Heijmans BT, Consortium B: Controlling bias and inflation in epigenome- and transcriptome-wide association studies using the empirical null distribution. Genome Biology 18(1): 19.
  • Jagt-Jelsma van der W, de Vries-Schot M, Scheepers P, van Deurzen PAM, Klip H, Buitelaar JK: Longitudinal study of religiosity and mental health of adolescents with psychiatric problems. The TRAILS study. European Psychiatry 45: 65-71.
  • Jansen R, Hottenga JJ, Nivard MG, Abdellaoui A, Laport B, de Geus EJ, Wright FA, Penninx B, Boomsma DI: Conditional eQTL analysis reveals allelic heterogeneity of gene expression. Human Molecular Genetics 26(8): 1444-1451.
  • Jansen R, Lamers F, Milaneschi Y, Hottenga JJ, Willemsen G, van Grootheest G, Mei H, Boomsma DI, Penninx BWJH, Consortium B: LPS stimulated whole blood RNA sequencing of MDD subtypes. European Neuropsychopharmacology 27: S214-S215.
  • Jansen IE, Gibbs JR, Nalls MA, Price TR, Lubbe S, van Rooij J, Uitterlinden AG, Kraaij R, Williams NM, Brice A, et al.: Establishing the role of rare coding variants in known Parkinson’s disease risk loci. Neurobiology of Aging 59: 220 e211-220 e218.
  • Jeronimus BF, Riese H, Oldehinkel AJ, Ormel J: Why does frustration predict psychopathology? Multiple prospective pathways over adolescence: A TRAILS study. European Journal of Personality 31(1): 85-103.
  • ustice AE, Winkler TW, Feitosa MF, Graff M, Fisher VA, Young K, Barata L, Deng X, Czajkowski J, Hadley D, et al.: Genome-wide metaanalysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nature Communications 8: 14977.
  • Kaakinen M, Magi R, Lagou V, Claringbould A, Gaulton K, Fischer K, Morris A, Prokopenko I, Consortium B, Consortium E: Multiphenotype genome-wide meta-analysis of lipid levels and BMI in 64,736 Europeans suggests shared genetic architecture. Genetic Epidemiology 41(7): 652-653.
  • Karlsson Linnér R, Marioni RE, Rietveld CA, Simpkin AJ, Davies NM, Watanabe K, Armstrong NJ, Auro K, Baumbach C, Bonder MJ, et al.: An epigenome-wide association study meta-analysis of educational attainment. Molecular Psychiatry 22(12): 1680-1690.
  • Kavaklioglu T, Guadalupe T, Zwiers M, Marquand AF, Onnink M, Shumskaya E, Brunner H, Fernandez G, Fisher SE, Francks C: Structural asymmetries of the human cerebellum in relation to cerebral cortical asymmetries and handedness. Brain Structure & Function 222(4): 1611-1623.
  • Klein M, Stein JL, Thompson P, Faraone S, Borglum A, Faraone SV, Thompson PM, Medland SE, Arias-Vasquez A, Franke B, et al.: Investigating the overlap between common genetic factors for ADHD risk and brain volume measures. Biological Psychiatry 81(10): S42-S42.
  • Kluiver de H, Buizer-Voskamp JE, Dolan CV, Boomsma DI: Paternal age and psychiatric disorders: A review. Am J Med Genet B Neuropsychiatr Genet 174(3): 202-213.
  • Kretschmer T, Vollebergh W, Oldehinkel AJ: Parent–child positivity and romantic relationships in emerging adulthood congruence, compensation, and the role of social skills. International Journal of Behavioral Development 41(2): 198–210.
  • Lecarpentier J, Silvestri V, Kuchenbaecker KB, Barrowdale D, Dennis J, McGuffog L, Soucy P, Leslie G, Rizzolo P, Navazio AS, et al.: Prediction of breast and prostate cancer risks in male BRCA1 and BRCA2 mutation carriers using polygenic risk scores. Journal of Clinical Oncology 35(20): 2240-2250.
  • Lin BD, Willemsen G, Fedko IO, Jansen R, Penninx BWJH, de Geus E, Kluft C, Hottenga J, Boomsma DI: Heritability and GWAS studies for monocyte-lymphocyte ratio. Twin Research and Human Genetics 20(2): 97-107.
  • Lin BD, Carnero-Montoro E, Bell JT, Boomsma DI, de Geus EJ, Jansen R, Kluft C, Mangino M, Penninx B, Spector TD, et al.: 2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio. Journal of Human Genetics 62(11): 979-988.
  • Liu J, van Klinken JB, Semiz S, van Dijk KW, Verhoeven A, Hankemeier T, Harms AC, Sijbrands E, Sheehan NA, van Duijn CM, et al.: A Mendelian randomization study of metabolite profiles, fasting glucose, and type 2 diabetes. Diabetes 66(11): 2915-2926.
  • Liu J, Semiz S, van der Lee SJ, van der Spek A, Verhoeven A, van Klinken JB, Sijbrands E, Harms AC, Hankemeier T, van Dijk KW, et al.: Metabolomics based markers predict type 2 diabetes in a 14-year follow-up study. Metabolomics 13(9): 104.
  • Makama M, Drukker CA, Rutgers EJT, Slaets L, Cardoso F, Rookus MA, Tryfonidis K, Van't Veer LJ, Schmidt MK: An association study of established breast cancer reproductive and lifestyle risk factors with tumour subtype defined by the prognostic 70-gene expression signature (mammaprint (R)). European Journal of Cancer 75: 5-13.
  • Mandaviya PR, Aissi D, Dekkers KF, Joehanes R, Kasela S, Truong V, Stolk L, van Heemst D, Ikram MA, Lindemans J, et al.: Homocysteine levels associate with subtle changes in leukocyte DNA methylation: An epigenome-wide analysis. Epigenomics 9(11): 1403-1422.
  • Mandaviya PR, Joehanes R, Aissi D, Kuhnel B, Marioni RE, Truong V, Stolk L, Beekman M, Bonder MJ, Franke L, et al.: Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes. PLoS One 12(10): 19.
  • Marouli E, Graff M, Medina-Gomez C, Lo KS, Wood AR, Kjaer TR, Fine RS, Lu Y, Schurmann C, Highland HM, et al.: Rare and low-frequency coding variants alter human adult height. Nature 542(7640): 186- 190.
  • McArtort DB, Bochao D, Hottenga LJJ, Boonnsma DI, Willemsen G, Lubke GH: Using a multivariate model to assess the interactive effects of demographics and lifestyle on the hematological profile. Biomarkers in Medicine 11(6): 427-438.
  • Meessen J, Saberi Hosnijeh F, Wesseling J, Slagboom E, Uitterlinden A, Nelissen R, van Meurs J, Meulenbelt I: Metabolomics in osteoarthritis: A fatty acids link. Bone & Joint Journal 99- B(Orthopaedic Proceedings Suppl.1): 13.
  • Merker S, Reif A, Ziegler GC, Weber H, Mayer U, Ehlis AC, Conzelmann A, Johansson S, Muller-Reible C, Nanda I, et al.: SLC2A3 singlenucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attentiondeficit/hyperactivity disorder. Journal of Child Psychology and Psychiatry 58(7): 798-809.
  • Mertens B, Datta S, Hankemeier T, Beekman M, Uh H-W: Statistical analysis of lipidomics data in a case-control study. In “Part of the Frontiers in Probability and the Statistical Sciences book series (FROPROSTAS) - Statistical Analysis of Proteomics, Metabolomics, and Lipidomics Data Using Mass Spectrometry” 2017: 277-295, Springer.
  • Milaneschi Y, Lamers F, Peyrot WJ, Baune BT, Breen G, Dehghan A, Forstner AJ, Grabe HJ, Homuth G, Kan C, et al.: Genetic association of major depression with atypical features and obesity-related immunometabolic dysregulations. JAMA Psychiatry 74(12): 1214- 1225.
  • Most van der PJ, Kupers LK, Snieder H, Nolte I: QCEWAS: Automated quality control of results of epigenome-wide association studies. Bioinformatics 33(8): 1243-1245.
  • Nano J, Ghanbari M, Wang WS, de Vries PS, Dhana K, Muka T, Uitterlinden AG, van Meurs JBJ, Hofman A, Franco OH, et al.: Epigenome-wide association study identifies methylation sites associated with liver enzymes and hepatic steatosis. Gastroenterology 153(4): 1096-1106.e2.
  • Nedeljkovic I, Lahousse L, Carnero Montoro E, Faiz A, Vonk JM, de Jong K, van der Plaat DA, van Diemen CC, van den Berge M, Obeidat Me, et al.: COPD GWAS variant at 19q13.2 in relation with DNA methylation and gene expression. Human Molecular Genetics.
  • Nivard MG, Gage SH, Hottenga JJ, van Beijsterveldt C, Abdellaoui A, Baselmans BML, Ligthart L, St Pourcain B, Boomsma DI, Munafò MR, et al.: Genetic overlap between schizophrenia and developmental psychopathology: Longitudinal and multivariate polygenic risk prediction of common psychiatric traits during development. Schizophrenia Bulletin 43(6): 1197-1207.
  • Ormel J, Oerlemans AM, Raven D, Laceulle OM, Hartman CA, Veenstra R, Verhulst FC, Vollebergh W, Rosmalen JGM, Reijneveld SA, et al.: Functional outcomes of child and adolescent mental disorders. Current disorder most important but psychiatric history matters as well. Psychological Medicine 47(7): 1271-1282.
  • Pang C, Kelpin F, van Enckevort D, Eklund N, Silander K, Hendriksen D, de Haan M, Jetten J, de Boer T, Charbon B, et al.: BiobankUniverse: Automatic matchmaking between datasets for biobank data discovery and integration. Bioinformatics 33(22): 3627-3634.
  • Papachristou E, Oldehinkel AJ, Ormel J, Raven D, Hartman CA, Frangou S, Reichenberg A: The predictive value of childhood subthreshold manic symptoms for adolescent and adult psychiatric outcomes. Journal of Affective Disorders 212: 86-92.
  • Peeters M, Oldehinkel T, Vollebergh W: Behavioral control and reward sensitivity in adolescents' risk taking behavior: A longitudinal TRAILS study. Frontiers in Psychology 8: 11.
  • Plaat van der DA, de Jong K, Lahousse L, Faiz A, Vonk JM, van Diemen CC, Nedeljkovic I, Amin N, Brusselle GG, Hofman A, et al.: Genomewide association study on the FEV1/FVC ratio in never-smokers identifies HHIP and FAM13A. Journal of Allergy and Clinical Immunology 139(2): 533-540.
  • Plomp R, Ruhaak LR, Uh HW, Reiding KR, Selman M, HouwingDuistermaat JJ, Slagboom PE, Beekman M, Wuhrer M: Subclassspecific IgG glycosylation is associated with markers of inflammation and metabolic health. Scientific Reports 7(1): 12325.
  • Power RA, Tansey KE, Buttenschon HN, Cohen-Woods S, Bigdeli T, Hall LS, Kutalik Z, Lee SH, Ripke S, Steinberg S, et al.: Genome-wide association for major depression through age at onset stratification: Major depressive disorder working group of the psychiatric genomics consortium. Biological Psychiatry 81(4): 325-335.
  • Proynova R, Alexandre D, Lablans M, van Enckevort D, Mate S, Eklund N, Silander K, Hummel M, Holub P, Uckert F: A decentralized it architecture for locating and negotiating access to biobank samples. Stud Health Technol Inform 243: 75-79.
  • Raven D, Jorg F, Visser E, Oldehinkel AJ, Schoevers RA: Time-totreatment of mental disorders in a community sample of Dutch adolescents. A TRAILS study. Epidemiology and Psychiatric Sciences 26(2): 177-188.
  • Reiding KR, Ruhaak LR, Uh HW, El Bouhaddani S, van den Akker EB, Plomp R, McDonnell LA, Houwing-Duistermaat JJ, Slagboom PE, Beekman M, et al.: Human plasma n-glycosylation as analyzed by matrix-assisted laser desorption/ionization-fourier transform ion cyclotron resonance-MS associates with markers of inflammation and metabolic health. Molecular & Cellular Proteomics 16(2): 228- 242.
  • Richard MA, Huan TX, Ligthart S, Gondalia R, Jhun MA, Brody JA, Irvin MR, Marioni R, Shen JC, Tsai PC, et al.: DNA methylation analysis identifies loci for blood pressure regulation. American Journal of Human Genetics 101(6): 888-902.
  • Rivera M, Locke AE, Corre T, Czamara D, Wolf C, Ching-Lopez A, Milaneschi Y, Kloiber S, Cohen-Woods S, Rucker J, et al.: Interaction between the FTO gene, body mass index and depression: Metaanalysis of 13,701 individuals. British Journal of Psychiatry 211(2): 70-76.
  • Robak LA, Jansen IE, van Rooij J, Uitterlinden AG, Kraaij R, Jankovic J, Heutink P, Shulman JM, International Parkinson's Disease Genomics Consortium: Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease. Brain 140(12): 3191-3203.
  • Robinson-Cohen C, Lutsey PL, Kleber ME, Nielson CM, Mitchell BD, Bis JC, Eny KM, Portas L, Eriksson J, Lorentzon M, et al.: Genetic variants associated with circulating parathyroid hormone. Journal of the American Society of Nephrology 28(5): 1553-1565.
  • Roeling MP, Willemsen G, Boomsma DI: Heritability of working in a creative profession. Behavior Genetics 47(3): 298-304.
  • Rooij van JGJ, Jhamai M, Arp PP, Nouwens SCA, Verkerk M, Hofman A, Ikram MA, Verkerk AJ, van Meurs JBJ, Rivadeneira F, et al.: Population-specific genetic variation in large sequencing data sets: Why more data is still better. European Journal of Human Genetics 25(10): 1173-1175.
  • Roy A, Oldehinkel AJ, Hartman CA: Cognitive functioning in adolescents with self-reported ADHD and depression: Results from a population-based study. J Abnorm Child Psychol 45(1): 69-81.
  • Simons C, Schouten LJ, Godschalk RW, van Engeland M, van den Brandt PA, van Schooten FJ, Weijenberg MP: Energy restriction at young age, genetic variants in the insulin-like growth factor pathway and colorectal cancer risk in the Netherlands cohort study. International Journal of Cancer 140(2): 272-284.
  • Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, et al.: Rarecoding variants in PLCG2, ABI3, and TREM2 implicate microglialmediated innate immunity in Alzheimer’s disease. Nature Genetics 49(9): 1373-1384.
  • Slieker RC, van der Heijden AAW, van Leeuwen N, Nijpels G, Beulens JWJ, t Hart LM: Poor glycaemic control is associated with altered blood gene expression levels of cell cycle and immune related genes. The Hoorn diabetes care system cohort. Diabetologia 60: S9- S9.
  • Smith D, Helgason H, Sulem P, Bjornsdottir US, Lim AC, Sveinbjornsson G, Hasegawa H, Brown M, Ketchem RR, Gavala M, et al.: A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma. PLoS Genetics 13(3): 24.
  • Sohail M, Vakhrusheva OA, Sul JH, Pulit SL, Francioli LC, van den Berg LH, Veldink JH, de Bakker PIW, Bazykin GA, Kondrashov AS, et al.: Negative selection in humans and fruit flies involves synergistic epistasis. Science 356(6337): 539-542.
  • Spek van der A, Luik AI, Kocevska D, Liu CY, Brouwer RWW, van Rooij JGJ, van den Hout MCGN, Kraaij R, Hofman A, Uitterlinden AG, et al.: Exome-wide meta-analysis identifies rare 3 '-UTR variantin ERCC1/CD3EAP associated with symptoms of sleep apnea. Frontiers in Genetics 8: 151.
  • Tollenaar MS, Molendijk ML, Penninx B, Milaneschi Y, Antypa N: The association of childhood maltreatment with depression and anxiety is not moderated by the oxytocin receptor gene. European Archives of Psychiatry and Clinical Neuroscience 267(6): 517-526.
  • Treur JL, Verweij KJH, Abdellaoui A, Fedko IO, de Zeeuw EL, Ehli EA, Davies GE, Hottenga JJ, Willemsen G, Boomsma DI, et al.: Testing familial transmission of smoking with two different research designs. Nicotine & Tobacco Research: ntx121.
  • Velde van der KJ, de Boer EN, van Diemen CC, Sikkema-Raddatz B, Abbott KM, Knopperts A, Franke L, Sijmons RH, de Koning TJ, Wijmenga C, et al.: GAVIN: Gene-aware variant interpretation for medical sequencing. Genome Biology 18(1): 6.
  • Veldman K, Reijneveld SA, Verhulst FC, Ortiz JA, Bultmann U: A life course perspective on mental health problems, employment, and work outcomes. Scandinavian Journal of Work Environment & Health 43(4): 316-325.
  • Verweij KJH, Treur JL, Vreeker A, Brunt TM, Willemsen G, Boomsma DI, Vink JM: Heritability of lifetime ecstasy use. Drug and Alcohol Dependence 178: 66-69.
  • Verduijn J, Milaneschi Y, Peyrot WJ, Hottenga JJ, Abdellaoui A, de Geus EJ, Smit JH, Breen G, Lewis CM, Boomsma DI, et al.: Using clinical characteristics to identify which patients with major depressive disorder have a higher genetic load for three psychiatric disorders. Biological Psychiatry 81(4): 316-324.
  • Vink JM, Jansen R, Brooks A, Willemsen G, van Grootheest G, de Geus E, Smit JH, Penninx BWJH, Boomsma DI: Differential gene expression patterns between smokers and non-smokers: Cause or consequence? Addict Biol 22(2): 550-560.
  • Vries de PS, Sabater-Lleal M, Chasman DI, Trompet S, Ahluwalia TS, Teumer A, Kleber ME, Chen MH, Wang JJ, Attia JR, et al.: Comparison of HapMap and 1000 genomes reference panels in a large-scale genome-wide association study. PLoS One 12(1): e0167742.
  • Waateringe van RP, Kobold ACM, van Vliet-Ostaptchouk JV, van der Klauw MM, Koerts J, Anton G, Peters A, Trischler G, Kvaloy K, Naess M, et al.: Influence of storage and inter- and intra-assay variability on the measurement of inflammatory biomarkers in populationbased biobanking. Biopreservation and Biobanking 15(6): 512-518.
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