If you made any changes in Pure these will be visible here soon.

Research Output 2004 2019

Filter
Article

2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio

Lin, B. D., Carnero-Montoro, E., Bell, J. T., Boomsma, D. I., de Geus, E. J., Jansen, R., Kluft, C., Mangino, M., Penninx, B., Spector, T. D., Willemsen, G. & Hottenga, J-J., Nov 2017, In : Journal of human genetics. 62, 11, p. 979-988 10 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Neutrophils
Blood Platelets
Lymphocytes
Single Nucleotide Polymorphism
Genome-Wide Association Study

A characterization of cis- and trans-heritability of RNA-Seq-based gene expression

BIOS Consortium, 26 Sep 2019, In : European Journal of Human Genetics.

Research output: Contribution to JournalArticleAcademicpeer-review

RNA
Gene Expression
Genes
Genome-Wide Association Study
Cytokines

ADHD in Dutch adults: heritability and linkage study

Savyuk, V., Hottenga, J. J., Slagboom, P. E., Distel, M. A., de Geus, E. J. C., Willemsen, G. & Boomsma, D. I., 2011, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 156, 3, p. 352-362

Research output: Contribution to JournalArticleAcademicpeer-review

Attention Deficit Disorder with Hyperactivity
Phenotype
Netherlands
Self Report
Siblings

A framework for the detection of de novo mutations in family-based sequencing data

Francioli, L. C., Cretu-Stancu, M., Garimella, K. V., Fromer, M., Kloosterman, W. P., Boomsma, D. I., Abdellaoui, A., Hottenga, J. J., Willemsen, G., Samocha, K. E., Neale, B. M., Daly, M. J., Banks, E., DePristo, M. A. & Bakker, P. I. W., Jan 2017, In : European Journal of Human Genetics. 25, 2, p. 227-233

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access

A Genetic Investigation of the Well-Being Spectrum

Baselmans, B. M. L., van de Weijer, M. P., Abdellaoui, A., Vink, J. M., Hottenga, J. J., Willemsen, G., Nivard, M. G., de Geus, E. J. C., Boomsma, D. I. & Bartels, M., 15 May 2019, In : Behavior Genetics. 49, 3, p. 286-297 12 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Phenotype
phenotype
Loneliness
Health
genetic correlation

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

Manning, A. K., Hivert, M. F., Scott, R. A., Grimsby, J. L., Bouatia-Naji, N., Chen, H., Rybin, D., Liu, C. T., Bielak, L. F., Prokopenko, I., Amin, N., Barnes, D., Cadby, G., Hottenga, J. J., Ingelsson, E., Boomsma, D. I., de Geus, E. J. C., Penninx, B. W. J. H., Willemsen, G., Wilson, J. F. & 14 othersWitteman, J. C. M., Wright, A. F., Yaghootkar, H., Zelenika, D., Zemunik, T., Zgaga, L., Wareham, N. J., McCarthy, M. I., Barroso, I., Watanabe, R. M., Florez, J. C., Dupuis, J., Meigs, J. B. & Langenberg, C., 2012, In : Nature Genetics. 44, 6, p. 659-669

Research output: Contribution to JournalArticleAcademicpeer-review

Insulin Resistance
Fasting
Body Mass Index
Genome
Insulin

A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts

Middeldorp, C. M., Hammerschlag, A. R., Ouwens, K. G., Blokhuis, M. M., St. Pourcain, B., Greven, C. U., Pappa, I., Tiesler, C. M. T., Ang, W., Nolte, I. M., Vilor-Tejedor, N., Bacelis, J., Ebejer, J. L., Zhao, H., Davies, G. E., Ehli, E. A., Evans, D. M., Fedko, I. O., Guxens, M., Hottenga, J. J. & 31 othersHudziak, J. J., Jugessur, A., Kemp, J. P., Krapohl, E., Martin, N. G., Murcia, M., Myhre, R., Ormel, J., Ring, S. M., Standl, M., Stergiakouli, E., Stoltenberg, C., Thiering, E., Timpson, N. J., Trzaskowski, M., van der Most, P. J., Wang, C., Nyholt, DR., Medland, S. E., Neale, B. M., Jacobsson, B., Sunyer, J., Hartman, C. A., Whitehouse, A. J. O., Pennell, C. E., Heinrich, J., Plomin, R., Davey Smith, G., Tiemeier, H., Posthuma, D. & Boomsma, D. I., 2016, In : Journal of the American Academy of Child and Adolescent Psychiatry. 55, 10, p. 896-905 10.

Research output: Contribution to JournalArticleAcademicpeer-review

Genome-Wide Association Study
Attention Deficit Disorder with Hyperactivity
Single Nucleotide Polymorphism
Meta-Analysis
Pediatrics

A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans

Palmer, N. D., McDonough, C. W., Hicks, P. J., Roh, B. H., Wing, M. R., Sandy An, S., Hester, J. M., Cooke, J. N., Bostrom, M. A., Rudock, M. E., Talbert, M. E., Lewis, J. P., Hottenga, J. J., de Geus, E. J. C., Willemsen, G., Boomsma, D. I., Ferrara, A., Lu, L., Ziegler, J. T., Sale, M. M. & 11 othersDivers, J., Shriner, D., Adeyemo, A., Rotimi, C. N., Ng, M. C. Y., Langefeld, C. D., Freedman, B. I., Bowden, D. W., Posthuma, D., Penninx, B. W. J. H. & Sladek, R., 2012, In : PLoS ONE. 7, 1, p. e29202 e29202.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
File
African Americans
Medical problems
noninsulin-dependent diabetes mellitus
Type 2 Diabetes Mellitus
Single Nucleotide Polymorphism

A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations

Lind, P. A., Macgregor, S., Vink, J. M., Pergadia, M. L., Hansell, N., de Moor, M. H. M., Smit, A. B., Hottenga, J. J., Richter, M., Heath, A. C., Martin, N. G., Willemsen, G., de Geus, E. J. C., Vogelzangs, N., Penninx, B. W. J. H., Whitfield, J. B., Montgomery, GW., Boomsma, D. I. & Madden, P. A. F., 2010, In : Twin Research and Human Genetics. 13, 1, p. 10-29

Research output: Contribution to JournalArticleAcademicpeer-review

Tobacco Use Disorder
Alcoholism
Single Nucleotide Polymorphism
Tobacco Use
Gene Frequency

A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation

Estrada, K., Krawczak, M., Schreiber, S., van Duijn, K., Stolk, L., van Meurs, J. B. J., Liu, F., Penninx, B. W. J. H., Smit, J. H., Vogelzangs, N., Hottenga, J. J., Willemsen, G., de Geus, E. J. C., Lorentzon, M., von Eller-Eberstein, H., Lips, P. T. A. M., van Schoor, N. M., Pop, V., de Keijzer, J., Hofman, A. & 8 othersAulchenko, Y. S., Oostra, B. A., Ohlsson, C., Boomsma, D. I., Uitterlinden, A. G., van Duijn, C. M., Rivadeneira, F. F. & Kayser, M., 2009, In : Human Molecular Genetics. 18, 18, p. 3516-3524

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
File
C-Type Natriuretic Peptide
Body Height
Genome-Wide Association Study
Population
Single Nucleotide Polymorphism
Open Access
File
Migraine without Aura
Migraine Disorders
Genome
Population

A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol

Surakka, I., Isaacs, A., Karssen, L. C., Laurila, P. P. P., Middelberg, R. P. S., Tikkanen, E., Ried, J. S., Lamina, C., Mangino, M., Igl, W., Hottenga, J. J., Lagou, V., van der Harst, P., Mateo Leach, I., Esko, T., Kutalik, Z., Wainwright, N. W., Struchalin, M. V., Sarin, A. P., Kangas, A. J. & 57 othersViikari, J. S., Perola, M., Rantanen, T., Petersen, A. K., Soininen, P., Johansson, Å., Soranzo, N., Heath, A. C., Papamarkou, T., Prokopenko, I., Tönjes, A., Kronenberg, F., Döring, A., Rivadeneira, F., Montgomery, GW., Whitfield, J. B., Kähönen, M., Lehtimäki, T., Freimer, N. B., Willemsen, G., de Geus, E. J. C., Palotie, A., Sandhu, M. S., Waterworth, D., Metspalu, A., Stumvoll, M., Uitterlinden, A. G., Navis, G., Wijmenga, C., Wolffenbuttel, B. H. R., Taskinen, M. R., Ala-Korpela, M., Kaprio, J., Kyvik, K. O., Boomsma, D. I., Pedersen, N. L., Gyllensten, U., Wilson, J. F., Rudan, I., Campbell, H., Pramstaller, P. P., Spector, T. D., Witteman, J. C. M., Eriksson, J. G., Salomaa, V., Oostra, B. A., Raitakari, O. T., Wichmann, H. E., Gieger, C., Järvelin, M. J., Martin, N. G., Hofman, A., McCarthy, M. I., Peltonen, L., van Duijn, C. M., Aulchenko, Y. S. & Ripatti, S., 2011, In : PLoS Genetics. 7, 10, e1002333.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
File
waist-to-hip ratio
Waist-Hip Ratio
genome
lipid
Cholesterol

A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site

Nürnberg, S. T., Rendon, A., Smethurst, P. A., Paul, D. S., Voss, K., Thon, J. N., Lloyd-Jones, H., Sambrook, J. G., Tijssen, M. R., Hottenga, J. J., de Geus, E. J. C., Willemsen, G., Boomsma, D. I., Italiano Jr, J. E., Deloukas, P., Gottgens, B., Soranzo, N. & Ouwehand, W. H., 2012, In : Blood. 120, 24, p. 4859-4868

Research output: Contribution to JournalArticleAcademicpeer-review

Megakaryocytes
Genome-Wide Association Study
Platelets
Blood Platelets
Binding Sites

A linear mixed-model approach to study multivariate gene-environment interactions

't Hoen, P. A., van Meurs, J. B. J., Isaacs, A., Jansen, R., Franke, L., Boomsma, D. I., Pool, R., van Dongen, J., Hottenga, J. J., Van Greevenbroek, M. J., Stehouwer, C. D. A., van der Kallen, C. J. H., Schalkwijk, C. G., Wijmenga, C., Zhernakova, A., Tigchelaar, E. F., Slagboom, P. E., Beekman, M., Deelen, J., van Heemst, D. & 30 othersVeldink, J. H., van den Berg, L. H., van Duijn, C. M., Hofman, B. A., Uitterlinden, A. G., Jhamai, P. M., Verbiest, M., Suchiman, H. E. D., Verkerk, M., van der Breggen, R., van Rooij, J., Lakenberg, N., Mei, H., van Iterson, M., van Galen, M., Bot, J., van’t Hof, P., Deelen, P., Nooren, I., Moed, M., Vermaat, M., Zhernakova, D. V., Luijk, R., Jan Bonder, M., van Dijk, F., Arindrarto, W., Kielbasa, P. S. M., Swertz, M. A., van Zwet, E. W. & BIOS Consortium, Jan 2019, In : Nature Genetics. 51, 1, p. 180-186 7 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Gene-Environment Interaction
Linear Models
Genotype
Body Mass Index
Diet

A mega-analysis of genome-wide association studies for major depressive disorder

Ripke, S., Wray, N. R., Lewis, C. M., Hamilton, S. P., Weissman, M. M., Breen, G., Byrne, E. M., Blackwood, D. H., Boomsma, D. I., Cichon, S., Heath, A. C., Holsboer, F., Lucae, S., Madden, P. A., Martin, N. G., McGuffin, P., Muglia, P., Noethen, M. M., Penninx, B. W. J. H., Pergadia, M. L. & 96 othersPotash, J. B., Rietschel, M., Lin, D., Müller-Myhsok, B., Shi, J., Steinberg, S., Grabe, H. J., Lichtenstein, P., Magnusson, P., Perlis, R. H., Preisig, M., Smoller, J. W., Stefansson, K., Uher, R., Kutalik, Z., Tansey, K. E., Teumer, A., Viktorin, A., Barnes, M. R., Bettecken, T., Binder, E. B., Breuer, R., Castro, V. M., Churchill, S. E., Coryell, W. H., Craddock, N., Craig, I. W., Czamara, D., de Geus, E. J. C., Degenhardt, F., Farmer, A. E., Fava, M., Frank, J., Gainer, V. S., Gallagher, P. J., Gordon, S. D., Goryachev, S., Gross, M., Guipponi, M., Henders, A. K., Herms, S., Hickie, I. B., Hoefels, S., Hoogendijk, W. J. G., Hottenga, J. J., Iosifescu, D. V., Ising, M., Jones, I., Jones, L., Jung-Ying, T., Knowles, J. A., Kohane, I. S., Kohli, M. A., Korszun, A., Landen, M., Lawson, W. B., Lewis, G., MacIntyre, D. J., Maier, W., Mattheisen, M., McGrath, P. J., McIntosh, A., McLean, A., Middeldorp, C. M., Middleton, L., Montgomery, G. M., Murphy, S. N., Nauck, M., Nolen, W. A., Nyholt, DR., O'Donovan, M., Oskarsson, H., Pedersen, N., Scheftner, W. A., Schulz, A., Schulze, T. G., Shyn, S. I., Sigurdsson, E., Slager, S. L., Smit, J. H., Stefansson, H., Steffens, M., Thorgeirsson, T. E., Tozzi, F., Treutlein, J., Uhr, M., van den Oord, E. J., Grootheest, G., Völzke, H., Weilburg, J. B., Willemsen, G., Zitman, F. G., Neale, B., Daly, M., Levinson, D. F. & Sullivan, P. F., 2013, In : Molecular Psychiatry. 18, 4, p. 497-511

Research output: Contribution to JournalArticleAcademicpeer-review

Genome-Wide Association Study
Major Depressive Disorder
Single Nucleotide Polymorphism
Bipolar Disorder
Genome

A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration

de Vries, P. S., Chasman, D. I., Sabater-Lleal, M., Chen, M. H., Huffman, J. E., Steri, M., Tang, W., Teumer, A., Marioni, R. E., Grossmann, V., Hottenga, J. J., Willemsen, G., de Geus, E. J. C., Boomsma, D. I., Cucca, F., Tracy, R., Watkins, H., Reiner, A. P., Folsom, A. R., Ridker, P. M. & 4 othersO'Donnell, C. J., Smith, N. L., Strachan, D. P. & Dehghan, A., 2016, In : Human Molecular Genetics. 25, 2, p. 358-370

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Fibrinogen
Meta-Analysis
X Chromosome
Genome
Genome-Wide Association Study

A method to customize population-specific arrays for genome-wide association testing

Ehli, E. A., Abdellaoui, A., Fedko, I. O., Grieser, C., Nohzadeh-Malakshah, S., Willemsen, G., de Geus, E. J. C., Boomsma, D. I., Davies, G. E. & Hottenga, J. J., 1 Feb 2017, In : European Journal of Human Genetics. 25, 2, p. 267-270

Research output: Contribution to JournalArticleAcademicpeer-review

Single Nucleotide Polymorphism
Genome
Netherlands
KIR Receptors
Population

Analysis of shared heritability in common disorders of the brain

The Brainstorm Consortium, 22 Jun 2018, In : Science. 360, 6395, p. 1-15 15 p., 8757.

Research output: Contribution to JournalArticleAcademicpeer-review

Brain Diseases
Psychiatry
Phenotype
Genetic Heterogeneity
Genome-Wide Association Study

An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

Direk, N., Williams, S., Smith, J. A., Ripke, S., Air, T., Amare, A. T., Amin, N., Baune, B. T., Bennett, D. A., Blackwood, D. H. R., Boomsma, D., Breen, G., Buttenschøn, H. N., Byrne, E. M., Børglum, A. D., Castelao, E., Cichon, S., Clarke, T-K., Cornelis, M. C., Dannlowski, U. & 82 othersDe Jager, P. L., Demirkan, A., Domenici, E., van Duijn, C. M., Dunn, E. C., Eriksson, J. G., Esko, T., Faul, J. D., Ferrucci, L., Fornage, M., de Geus, E., Gill, M., Gordon, S. D., Grabe, H-J., van Grootheest, G., Hamilton, S. P., Hartman, C. A., Heath, A. C., Hek, K., Hofman, A., Homuth, G., Horn, C., Jan Hottenga, J., Kardia, S. L. R., Kloiber, S., Koenen, K., Kutalik, Z., Ladwig, K-H., Lahti, J., Levinson, D. F., Lewis, C. M., Lewis, G., Li, Q. S., Llewellyn, D. J., Lucae, S., Lunetta, K. L., MacIntyre, D. J., Madden, P. A. F., Martin, N. G., McIntosh, A. M., Metspalu, A., Milaneschi, Y., Montgomery, G. W., Mors, O., Mosley, T. H., Murabito, J. M., Müller-Myhsok, B., Nöthen, M. M., Nyholt, D. R., O'Donovan, M. C., Penninx, B. W., Pergadia, M. L., Perlis, R., Potash, J. B., Preisig, M., Purcell, S. M., Quiroz, J. A., Räikkönen, K., Rice, J. P., Rietschel, M., Rivera, M., Schulze, T. G., Shi, J., Shyn, S. I., Sinnamon, G. C., Smit, J. H., Smoller, J. W., Snieder, H., Tanaka, T., Tansey, K. E., Teumer, A., Uher, R., Umbricht, D., Van der Auwera, S., Ware, E. B., Weir, D. R., Weissman, M. M., Willemsen, G., Yang, J., Zhao, W., Tiemeier, H. & Sullivan, P. F., 1 Aug 2017, In : Biological Psychiatry. 82, 5, p. 322-329

Research output: Contribution to JournalArticleAcademicpeer-review

Genome-Wide Association Study
Meta-Analysis
Depression
Phenotype
Major Depressive Disorder

An Extended Twin-Pedigree Study of Neuroticism in the Netherlands Twin Register

Boomsma, D. I., Helmer, Q., Nieuwboer, H. A., Hottenga, J. J., de Moor, M. H., van den Berg, S. M., Davies, G. E., Vink, J. M., Schouten, M. J., Dolan, C. V., Willemsen, G., Bartels, M., van Beijsterveldt, C. E. M., Ligthart, L. & de Geus, E. J., 1 Jan 2018, In : Behavior Genetics. 48, 1, p. 1-11

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Twin Studies
Pedigree
pedigree
Netherlands
households

Anxiety and depression in children and adults: influence of serotonergic and neurotrophic genes?

Middeldorp, C. M., Slof-Op 't Landt, M. C. T., Medland, S. E., van Beijsterveldt, C. E. M., Bartels, M., Willemsen, G., Hottenga, J. J., de Geus, E. J. C., Suchiman, H. E. D., Dolan, C. V., Neale, M. C., Slagboom, P. E. & Boomsma, D. I., 2010, In : Genes, Brain and Behavior. 9, 6, p. 808-816

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Anxiety
Depression
Single Nucleotide Polymorphism
Neurogenesis
Genes

A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms

The EAGLE-ADHD Consortium, 18 Jan 2019, In : Behavior Genetics. p. 1-16 16 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
File
Impulsive Behavior
Single Nucleotide Polymorphism
Meta-Analysis
signs and symptoms (animals and humans)
meta-analysis

Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

de Jong, S., Diniz, M. J. A., Saloma, A., Gadelha, A., Santoro, M. L., Ota, V. K., Noto, C., Curtis, C., Newhouse, S. J., Patel, H., Hall, L. S., O`Reilly, P. F., Belangero, S. I., Bressan, R. A., Breen, G. & Major Depressive Disorder and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium, 8 Oct 2018, In : Communications biology. 1, p. 1-10 10 p., 163.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
behavior disorders
Major Depressive Disorder
Bipolar Disorder
Psychiatry
Pedigree

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

Ried, J. S., Jeff, J. M., Chu, A. Y., Bragg-Gresham, J. L., van Dongen, J., Huffman, J. E., Ahluwalia, T. S., Cadby, G., Eklund, N., Eriksson, J., de Geus, E. J. C., Hottenga, J. J., Penninx, B. W. J. H., Willemsen, G., Boomsma, D. I., McCarthy, M. I., North, K. E., O'Connell, J. R., Schlessinger, D., Thorsteinsdottir, U. & 5 othersStrachan, D. P., Frayling, T. M., Hirschhorn, J. N., Müller-Nurasyid, M. & Loos, R. J. F., 2016, In : Nature Communications. 7, 13357.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
loci
Principal Component Analysis
phenotype
Meta-Analysis
Phenotype

A recessive genetic model and runs of homozygosity in major depressive disorder

Power, R. A., Keller, M. C., Ripke, S., Abdellaoui, A., Wray, N. R., Sullivan, P. F., Boomsma, D. I., de Geus, E. J. C., Hottenga, J. J., Middeldorp, C. M., Penninx, B. W. J. H., Willemsen, G. & Breen, G., 2014, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 165, 2, p. 157-166 10 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Genome-Wide Association Study
Genetic Models
Major Depressive Disorder
Genome
Schizophrenia

A SNP panel for identification of DNA and RNA specimens

Yousefi, S., Abbassi-Daloii, T., Kraaijenbrink, T., Vermaat, M., Mei, H., van 't Hof, P., van Iterson, M., Zhernakova, D. V., Claringbould, A., Franke, L., 't Hart, L. M., Slieker, R. C., van der Heijden, A., de Knijff, P., 't Hoen, P. A. C., BIOS consortium, Boomsma, D. I., van Dongen, J., Hottenga, J. J. & Pool, R., 25 Jan 2018, In : BMC Genomics. 19, 1, p. 90

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Single Nucleotide Polymorphism
RNA
DNA
Genotype
RNA Sequence Analysis

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Speliotes, E. K., Willer, C. J., Berndt, S. I., Monda, K. L., Thorleifson, G., Jackson, A. U., Lango Allen, H., Lindgren, C. M., Luan, J., Mägi, R., Hottenga, J. J., de Geus, E. J. C., Martin, N. G., Willemsen, G., Boomsma, D. I., Penninx, B. W. J. H., Uitterlinden, A. G., Zillikens, M. C., Visscher, P. M., Peltonen, L. & 11 othersvan Duijn, C. M., Thorsteinsdottir, U., Abecasis, G. R., Barroso, I., Boehnke, M., Stefansson, K., North, K. E., McCarthy, M. I., Hirschhorn, J. N., Ingelsson, E. & Loos, R. J. F., 2010, In : Nature Genetics. 42, 11, p. 937-948

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Body Mass Index
Obesity
Single Nucleotide Polymorphism
Genetic Loci
methanohexohydroisoindoline ethylguanidine hemisulfate

Association Between Autozygosity and Major Depression: Stratification Due to Religious Assortment

Abdellaoui, A., Hottenga, J. J., Xiao, X., Scheet, P., Ehli, E. A., Davies, G. E., Hudziak, J. J., Smit, D. J. A., Bartels, M., Willemsen, G., Brooks, A., Sullivan, P. F., Smit, J. H., de Geus, E. J. C., Penninx, B. W. J. H. & Boomsma, D. I., 2013, In : Behavior Genetics. 43, 6, p. 455-467

Research output: Contribution to JournalArticleAcademicpeer-review

stratification
genome
Genome
Inbreeding
inbreeding

Association between rs1051730 and smoking during pregnancy in Dutch women

Mbarek, H., van Beijsterveldt, C. E. M., Hottenga, J. J., Dolan, C. V., Boomsma, D. I., Willemsen, G. & Vink, J. M., Jun 2019, In : Nicotine and Tobacco Research. 21, 6, p. 835-840 6 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Smoking
Pregnancy
Pregnant Women
Parturition
Smoking Cessation

Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent

Fernández-Rhodes, L., Demerath, E. W., Cousminer, D. L., Tao, R., Dreyfus, J. G., Esko, T., Smith, A. V., Gudnason, V., Harris, T. B., Launer, L., McArdle, P. F., Yerges-Armstrong, L. M., Elks, C. E., Strachan, D. P., Kutalik, Z., Vollenweider, P., Feenstra, B., Boyd, H. A., Metspalu, A., Mihailov, E. & 55 othersBroer, L., Zillikens, M. C., Oostra, B. A., van Duijn, C. M., Lunetta, K. L., Perry, J. R., Murray, A., Koller, D. L., Lai, D., Corre, T., Toniolo, D., Albrecht, E., Stöckl, D., Grallert, H., Gieger, C., Hayward, C., Polasek, O., Rudan, I., Wilson, J. F., He, C., Kraft, P., Hu, F. B., Hunter, D. J., Hottenga, J. J., Willemsen, G., Boomsma, D. I., Byrne, E. M., Martin, N. G., Montgomery, G. W., Warrington, N. M., Pennell, C. E., Stolk, L., Visser, J. A., Hofman, A., Uitterlinden, A. G., Rivadeneira, F., Lin, P., Fisher, S. L., Bierut, L. J., Crisponi, L., Porcu, E., Mangino, M., Zhai, G., Spector, T. D., Buring, J. E., Rose, L. M., Ridker, P. M., Poole, C., Hirschhorn, J. N., Murabito, J. M., Chasman, D. I., Widén, E., North, K. E., Ong, K. K. & Franceschini, N., 2013, In : American Journal of Epidemiology. 178, 3, p. 451-460

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Menarche
Adiposity
Obesity
Genome-Wide Association Study
Body Mass Index

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

Writing Committee for the ENIGMA-CNV Working Group , 30 Oct 2019, In : JAMA Psychiatry. p. 1-11 11 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Cognition
Aptitude
Brain
Iceland
Parietal Lobe

Association of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

Abdellaoui, A., Dolan, C. V., Hottenga, J. J., Mbarek, H., Middeldorp, C. M., Nivard, M. G., Posthuma, D., Willemsen, G., Boomsma, D. I., de Geus, E. JC., W J H Penninx, B., Jansen, R. & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Jan 2019, In : Biological Psychiatry: Cognitive Neuroscience and Neuroimaging. 4, 1, p. 91-100 10 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Major Depressive Disorder
Anisotropy
Genome
Radiation
Diffusion Tensor Imaging

Associations between ADH glene variants and alcohol phenotypes in Dutch adults

van Beek, J. H. D. A., Willemsen, G., de Moor, M. H. M., Hottenga, J. J. & Boomsma, D. I., 2010, In : Twin Research and Human Genetics. 13, 1, p. 30-42

Research output: Contribution to JournalArticleAcademicpeer-review

File
Single Nucleotide Polymorphism
Alcohols
Phenotype
Alcohol Drinking
Multigene Family

Associations between smoking and caffeine consumption in two European cohorts

Treur, J. L., Taylor, A. E., Ware, J. J., McMahon, G., Hottenga, J. J., Baselmans, B. M. L., Willemsen, G., Boomsma, D. I., Munafò, M. & Vink, J. M., 2016, In : Addiction. 111, 6, p. 1059-1068

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Caffeine
Smoking
Confidence Intervals
Netherlands
Energy Drinks

Attention-Deficit/Hyperactivity Disorder Polygenic Risk Scores Predict Attention Problems in a Population-Based Sample of Children

Blokhuis, M. M., Middeldorp, C. M., Kan, K. J., Abdellaoui, A., van Beijsterveldt, C. E. M., Ehli, E. A., Davies, G. E., Scheet, P., Xiao, X., Hudziak, J. J., Hottenga, J. J., Neale, B. M. & Boomsma, D. I., 2014, In : Journal of the American Academy of Child and Adolescent Psychiatry. 53, 10, p. 1123-1129 7 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Attention Deficit Disorder with Hyperactivity
Population
Impulsive Behavior

Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation

Luijk, R., Wu, H., Ward-Caviness, C. K., Hannon, E., Carnero-Montoro, E., Min, J. L., Mandaviya, P., Müller-Nurasyid, M., Mei, H., van der Maarel, S. M., Beekman, M., der Breggen, R. V., Deelen, J., Lakenberg, N., Moed, M., Suchiman, H. E. D., Arindrarto, W., van’t Hof, P., Jan Bonder, M., Deelen, P. & 32 othersTigchelaar, E. F., Zhernakova, A., Zhernakova, D. V., van Dongen, J., Hottenga, J. J., Pool, R., Isaacs, A., Hofman, B. A., Jhamai, M., van der Kallen, C. J. H., Schalkwijk, C. G., Stehouwer, C. D. A., van den Berg, L. H., van Galen, M., Vermaat, M., van Rooij, J., Uitterlinden, A. G., Verbiest, M., Verkerk, M., Kielbasa, P. S. M., Bot, J., Nooren, I., van Dijk, F., Swertz, M. A., van Heemst, D., Relton, C., Mill, J., Waldenberger, M., Bell, J. T., Jansen, R., Boomsma, D. I. & BIOS Consortium, 14 Sep 2018, In : Nature Communications. 9, 1, p. 1-9 9 p., 3738.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
X Chromosome Inactivation
methylation
chromosomes
DNA Methylation
Chromosomes

A whole genome association study of neuroticism using DNA pooling.

Shifman, S., Bhomra, A., Smiley, S., Wray, N. R., James, M. R., Martin, N. G., Hettema, J. M., An, S. S., Neale, M. C., van den Oord, E. J. C. G., Kendler, K., Chen, X., Boomsma, D. I., Middeldorp, C. M., Hottenga, J. J., Slagboom, P. E. & Flint, J., 2008, In : Molecular Psychiatry. 13, 3, p. 302-312

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
File
Genome-Wide Association Study
Single Nucleotide Polymorphism
DNA
Odds Ratio
Genome

Biological, clinical and population relevance of 95 loci for blood lipids

Teslovich, T. M., Musunuru, K., Smith, A. V., Edmondson, A. C., Stylianou, I. M., Willemsen, G., Uitterlinden, A. G., Penninx, B. W. J. H., Montgomery, GW., Martin, N. G., Hottenga, J. J., de Geus, E. J. C., Boomsma, D. I., van Duijn, C. M., Peltonen, L., Abecasis, G. R., Boehnke, M. & Kathiresan, S., 2010, In : Nature. 466, 7307, p. 707-713

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Lipids
Population
Coronary Artery Disease
Lipoproteins
Genome

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Abdellaoui, A., Derks, E. M., Dolan, C. V., Hottenga, J. J., Mbarek, H., Middeldorp, C. M., Milaneschi, Y., Nivard, M., Peyrot, W. J., Posthuma, D., Willemsen, G., Boomsma, D. I., de Geus, E. J. C., W J H Penninx, B. & Sullivan, P., 11 Nov 2019, In : Molecular Psychiatry.

Research output: Contribution to JournalArticleAcademicpeer-review

Bipolar Disorder
Psychiatry
Schizophrenia
Depression
Major Depressive Disorder

Blood lipids influence DNA methylation in circulating cells

Dekkers, K. F., van Iterson, M., Slieker, R. C., Moed, M. H., Bonder, M. J., van Galen, M., Mei, H., Zhernakova, D. V., Van den Berg, L. H., Deelen, J., van Dongen, J., van Heemst, D., Hofman, A., Hottenga, J. J., van der Kallen, C. J. H., Schalkwijk, C. G., Stehouwer, C. D. A., Tigchelaar, E. F., Uitterlinden, A. G., Willemsen, G. & 14 othersZhernakova, A., Franke, L., 't Hoen, P. A. C., Jansen, R., van Meurs, J., Boomsma, D. I., van Duijn, C. M., van Greevenbroek, M. M. J., Veldink, J. H., Wijmenga, C., van Zwet, E. W., Slagboom, P. E., Jukema, J. W. & Heijmans, B. T., 2016, In : Genome Biology. 17, 138, p. 1-12

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
methylation
DNA methylation
DNA Methylation
blood lipids
blood

Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohorts

Vimaleswaran, K. S., Berry, D. J., Lu, C., Tikkanen, E., Pilz, S., Hiraki, L. T., Cooper, J. D., Dastani, Z., Li, R., Houston, D. K., Wood, A. R., Michaëlsson, K., Vandenput, L., Zgaga, L., Yerges-Armstrong, L. M., McCarthy, M. I., Dupuis, J., Kaakinen, M., Kleber, M. E., Jameson, K. & 46 othersArden, N., Raitakari, O., Viikari, J., Lohman, K. K., Ferrucci, L., Melhus, H., Ingelsson, E., Byberg, L., Lind, L., Lorentzon, M., Salomaa, V., Campbell, H., Dunlop, M., Mitchell, B. D., Herzig, K. H., Pouta, A., Hartikainen, A. L., Hottenga, J. J., de Geus, E. J. C., Willemsen, G., Boomsma, D. I., Penninx, B. W. J. H., Uitterlinden, A. G., Visscher, P. M., van Duijn, C. M., Streeten, E. A., Theodoratou, E., Jula, A., Wareham, N. J., Ohlsson, C., Frayling, T. M., Kritchevsky, S. B., Spector, T. D., Richards, J. B., Lehtimäki, T., Ouwehand, W. H., Kraft, P., Cooper, C., März, W., Power, C., Loos, R. J., Wang, T. J., Järvelin, M. R., Whittaker, J. C., Hingorani, A. D. & Hyppönen, E., 2013, In : PLoS Medicine. 10, 2, e1001383.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Mendelian Randomization Analysis
Vitamin D
Body Mass Index
Obesity
Single Nucleotide Polymorphism

Causes of variation in the neutrophil-lymphocyte and platelet-lymphocyte ratios: a twin-family study

Lin, B., Hottenga, J. J., Abdellaoui, A., Dolan, C. V., de Geus, E. J. C., Kluft, C., Boomsma, D. I. & Willemsen, G., 2016, In : Biomarkers in medicine. 10, 10, p. 1061-1072

Research output: Contribution to JournalArticleAcademicpeer-review

Twin Studies
Lymphocytes
Platelets
Neutrophils
Blood Platelets

Chromosome 9: linkage for borderline personality disorder features.

Distel, M. A., Hottenga, J. J., Trull, T. J. & Boomsma, D. I., 2008, In : Psychiatric Genetics. 18, 6, p. 302-307

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
File
Chromosomes, Human, Pair 9
Borderline Personality Disorder
Neurofibromin 2
Genotype
Chromosomes, Human, Pair 4

Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Abdellaoui, A., Dolan, C. V., Hottenga, J. J., Jansen, R., Mbarek, H., Middeldorp, C. M., Milaneschi, Y., Nivard, M., Peyrot, W. J., Posthuma, D. & Willemsen, G., 5 Aug 2019, In : Biological Psychiatry. p. 1-12 12 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
HLA Antigens
Haplotypes
Alleles
Depression
Major Histocompatibility Complex

CNV Concordance in 1,097 MZ Twin Pairs

Abdellaoui, A., Ehli, E. A., Hottenga, J. J., Weber, Z., Mbarek, H., Willemsen, G., van Beijsterveldt, C. E. M., Brooks, A., Hudziak, J. J., Sullivan, P. F., de Geus, E. J. C., Davies, G. E. & Boomsma, D. I., 2015, In : Twin Research and Human Genetics. 18, 1, p. 1-12 12 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Monozygotic Twins
Cheek
DNA
Epithelium
Overlapping Genes

Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression

Culverhouse, R. C., Saccone, N. L., Horton, A. C., Ma, Y., Anstey, K. J., Banaschewski, T., Burmeister, M., Cohen-Woods, S., Etain, B., Fisher, H. L., Goldman, N., Guillaume, S., Horwood, J., Juhasz, G., Lester, K. J., Mandelli, L., Middeldorp, C. M., Olié, E., Villafuerte, S., Air, T. M. & 73 othersAraya, R., Bowes, L., Burns, M. R., Byrne, E. M., Coffey, J. C., Coventry, W. L., Gawronski, K. A. B., Glei, D., Hatzimanolis, A., Hottenga, J-J., Jaussent, I., Jawahar, C., Jennen-Steinmetz, C., Kramer, J. R., Lajnef, M., Little, K., Meyer zu Schwabedissen, H., Nauck, M., Nederhof, E., Petschner, P., Peyrot, W. J., Schwahn, C., Sinnamon, G., Stacey, D., Tian, Y., Toben, C., Van der Auwera, S., Wainwright, N. W., Wang, J-C., Willemsen, G., Anderson, I. M., Arolt, V., Åslund, C., Bagdy, G., Baune, B. T., Bellivier, F., Boomsma, D. I., Courtet, P., Dannlowski, U., de Geus, E. J. C., Deakin, J. F. W., Easteal, S., Eley, T. C., Fergusson, D. M., Goate, A. M., Gonda, X., Grabe, H. J., Holzman, C., Johnson, E. O., Kennedy, D. M., Laucht, M., Martin, N. G., Munafò, M. R., Nilsson, K. W., Oldehinkel, A. J., Olsson, C. A., Ormel, J., Otte, C., Patton, G. C., Penninx, B. W. J. H., Ritchie, K., Sarchiapone, M., Scheid, J. M., Serretti, A., Smit, J. H., Stefanis, N. C., Surtees, P. G., Völzke, H., Weinstein, M., Whooley, M. A., Nurnberger, J. I., Breslau, N. & Bierut, L. J., 2 Jan 2018, In : Molecular Psychiatry. 23, 1, p. 133-142

Research output: Contribution to JournalArticleAcademicpeer-review

Meta-Analysis
Genotype
Depression
Alleles
Serotonin Plasma Membrane Transport Proteins

Combined genome scans for body stature in 6,602 European twins: Evidence for common Caucasian loci.

Perola, M., Sammalisto, S., Hiekkalinna, T., Martin, N. G., Visscher, P. M., Montgomery, GW., Benyamin, B., Harris, J. R., Boomsma, D. I., Willemsen, G., Hottenga, J. J., Christensen, K., Kyvik, K., Sorensen, T. I. A., Pedersen, N. L., Magnusson, P. K. E., Spector, T. D., Widen, E., Silventoinen, K., Kaprio, J. & 2 othersPalotie, A. & Peltonen, L., 2007, In : PLoS Genetics. 3, 6, 10 p., e97.

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
File
Quantitative Trait Loci
Software
genome
Genome
Chromosomes, Human, Pair 20

Combined Linkage and Association Analyses of the 124-bp Allele of Marker D2S2944 with Anxiety, Depression, Neuroticism and Major Depression

Beem, A. L., de Geus, E. J. C., Hottenga, J. J., Sullivan, P. F., Willemsen, G., Slagboom, P. E. & Boomsma, D. I., 2006, In : Behavior Genetics. 36, 1, p. 127-136

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
File
anxiety
linkage (genetics)
allele
Anxiety
Alleles

Common genetic variants influence human subcortical brain structures

Hibar, D. P., Stein, J. L., Renteria, M. E., Arias-Vasquez, A., Desrivières, S., Jahanshad, N., Toro, R., Wittfeld, K., Abramovic, L., Andersson, M., Aribisala, B. S., Armstrong, N. J., Bernard, M., Bohlken, M. M., Biks, M. P., Bralten, J., Brown, A. A., Chakravarty, M. M., Chen, Q., Ching, C. R. K. & 267 othersCuellar-Partida, G., den Braber, A., Giddaluru, S., Goldman, A. L., Grimm, O., Guadalupe, T., Hass, J., Woldehawariat, G., Holmes, A. J., Hoogman, M., Janowitz, D., Jia, T., Kim, S., Klein, M., Kraemer, B., Lee, P. H., Olde Loohuis, L. M., Luciano, M., Macare, C., Mather, K. A., Mattheisen, M., Milaneschi, Y., Nho, K., Papmeyer, M., Ramasamy, A., Risacher, S. L., Roiz-Santiañez, R., Rose, E. J., Salami, A., Sämann, P. G., Schmaal, L., Schork, A. J., Shin, J., Strike, L. T., Teumer, A., Donkelaar, M. M. J., van Eijk, K. R., Walters, R. K., Westlye, L. T., Welan, C. D., Winkler, A. M., Zwiers, M. P., Alhusaini, S., Athanasiu, L., Ehrlich, S., Hakobjan, M. M. H., Hartberg, C. B., Haukvik, U. K., Heister, A. J. G. A. M., Hoehn, D., Kasperaviciute, D., Liewald, D. C. M., Lopez, L. M., Makkinje, R. R., Matarin, M., Naber, M. A. M., Reese McKay, D., Needham, M., Nugent, A. C., Pütz, B., Royle, N. A., Shen, L., Sprooten, E., Trabzuni, D., van der Marel, S. S. L., van Hulzen, K. J. E., Walton, E., Wolf, C., Almasy, L., Ames, D., Arepalli, S., Assareh, A. A., Bastin, M. E., Brodaty, H., Bulayeva, K. B., Carless, M. A., Cichon, S., Corvin, A., Curran, J. E., Czisch, M., de Zubicaray, G. I., Dillman, A., Duggirala, R., Dyer, T. D., Erk, S., Fedko, I. O., Ferrucci, L., Foroud, T. M., Fox, P. T., Fukunaga, M., Gibbs, J. R., Göring, H. H. H., Green, R. C., Guelfi, S., Hansell, N. K., Hartman, C. A., Hegenscheid, K., Heinz, A., Hernandez, D. G., Heslenfeld, D. J., Hoekstra, P. J., Holsboer, F., Homuth, G., Hottenga, J. J., Ikeda, M., Jack, C. R. . J., Jenkinson, M., Johnson, R., Kanai, R., Keil, M., Kent, J. W. J., Kochunov, P., Kwok, J. B., Lawrie, S. M., Liu, X., Longo, D. L., McMahon, K. L., Meisenzahl, E., Melle, I., Mohnke, S., Montgomery, G. W., Mostert, J. C., Mühleisen, T. W., Nalls, M. A., Nichols, T. E., Nilsson, L. G., Nöthen, M. M., Ohi, K., Olvera, R. L., Perez-Iglesias, R., Pike, G. B., Potkin, S. G., Reinvang, I., Reppermund, S., Rietschel, M., Romanczuk-Seiferth, N., Rosen, G. D., Rujescu, D., Schnell, K., Schofield, P. R., Smith, C., Steen, V. M., Sussmann, J. E., Thalamuthu, A., Toga, A. W., Traynor, B. J., Troncoso, J., Turner, J. A., Valdés Hernández, M. C., van t Ent, D., van der Brug, M., van der Wee, N. J. A., van Tol, M. J., Veltman, D. J., Wassink, T. H., Westmann, E., Zielke, R. H., Zonderman, A. B., Ashbrook, D. G., Hager, R., Lu, L., McMahon, F. J., Morris, D. W., Williams, R. W., Brunner, H. G., Buckner, R. L., Buitelaar, J. K., Cahn, W., Calhoun, V. D., Cavalleri, G. L., Crespo-Facorro, B., Dale, A. M., Davies, G. E., Delanty, N., Depondt, C., Djurovic, S., Drevets, W. C., Espeseth, T., Gollub, R. L., Ho, B. C., Hoffmann, W., Hosten, N., Kahn, R. S., Le Hellard, S., Meyer-Lindenberg, A., Müller-Myhsok, B., Nauck, M., Nyberg, L., Pandolfo, M., Penninx, B. W. J. H., Roffman, J. L., Sisodiya, SM., Smoller, J. W., van Bokhoven, H., van Haren, N. E. M., Völzke, H., Walter, H., Weiner, M. W., Wen, W., White, T., Agartz, I., Andreassen, O. A., Blangero, J., Boomsma, D. I., Brouwer, R. M., Cannon, D. M., Cookson, M. R., de Geus, E. J. C., Deary, I. J., Donohoe, G., Fernandez, G., Fisher, S. E., Francks, C., Glahn, D. C., Grabe, H. J., Gruber, O., Hardy, J., Hashimoto, R., Hulshoff Pol, H. E., Jönsson, E. G., Kloszewska, I., Lovestone, S., Mattay, V. S., Mecocci, P., McDonald, C., McIntosh, A. M., Ophoff, R. A., Paus, T., Pausova, Z., Ryten, M., Sachdev, P. S., Saykin, A. J., Simmons, A., Singleton, A., Soininen, H., Wardlaw, J. M., Weale, M. E., Weinberger, D. R., Adams, H. H. H., Launer, L. J., Seiler, S., Schmidt, R., Chauhan, G., Satizabal, C. L., Becker, J. T., Yanek, L., van der Lee, S. J., Ebling, M., Fischl, B., Longstreth, J. W. T., Greve, D., Schmidt, H., Nyquist, P., Vinke, L. N., van Duijn, C. M., Xue, L., Mazoyer, B., Bis, J. C., Gudnason, V., Seshadri, S., Arfan Ikram, M., Martin, N. G., Wright, M. J., Schumann, G., Franke, B., Thompson, P. M. & Medland, S. E., 2015, In : Nature. 520, 7546, p. 224-229 6 p.

Research output: Contribution to JournalArticleAcademicpeer-review

Putamen
Brain
Developmental Genes
Transport Vesicles
Caudate Nucleus

Common variants at 12q14 and 12q24 are associated with hippocampal volume

Bis, J. C., DeCarli, C. S., Vernon Smith, A., van der Lijn, F., Crivello, F., Fornage, M., Debette, S., Shulman, J. M., Schmidt, H., Srikanth, V., Schuur, M., Yu, L., Choi, S., Sigurdsson, S., Verhaaren, B. F. J., DeStefano, A. L., Lambert, J. C., Jack, C. R. . J., Struchalin, M., Stankovich, J. & 64 othersIbrahim-Verbaas, C. A., Fleischman, D., Zijdenbos, A., den Heijer, T., Mazoyer, B., Coker, L. H., Enzinger, C., Danoy, P., Amin, N., Arfanakis, K., van Buchem, M. A., de Bruijn, R. F. A. G., Beiser, A., Dufouil, C., Huang, J., Cavalieri, M., Thomson, R., Niessen, W. J., Chibnik, L. B., Gislason, G. K., Hofman, A., Pikula, A., Amouyel, P., Freeman, K. B., Phan, T. G., Oostra, B. A., Stein, J. L., Medland, S. E., Vasquez, A. A., Hibar, D. P., Wright, M. J., Franke, B., Martin, N. G., Thompson, P. M., Hottenga, J. J., Boomsma, D. I., Nalls, M. A., Uitterlinden, A. G., Au, R., Elbaz, A., Beare, R. J., van Swieten, J. C., Lopez, O. L., Harris, T. B., Chouraki, V., Breteler, M. M. B., de Jager, P. L., Becker, J. T., Vernooij, M. W., Knopman, D., Fazekas, F., Wolf, P. A., van der Lugt, A., Gudnason, V., Longstreth, J. W. T., Brown, M. A., Bennett, D. A., van Duijn, C. M., Mosley, T. H., Schmidt, R., Tzourio, C., Launer, L. J., Arfan Ikram, M. & Seshadri, S., 2012, In : Nature Genetics. 44, 5, p. 545-551

Research output: Contribution to JournalArticleAcademicpeer-review

Open Access
Genome-Wide Association Study
Single Nucleotide Polymorphism
Dementia
Alzheimer Disease
vascular factor