J. Hottenga

发表

Multivariate Genome-Wide and Integrated Transcriptome and Epigenome-Wide Analyses of the Well-being Spectrum

G. Willemsen, D. Boomsma, E. D. de Geus, 2017, bioRxiv.

Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility

J. Vonk, H. Boezen, P. Lanting, 2020, medRxiv.

Genetic comorbidity between major depression and cardio-metabolic disease, stratified by age at onset of major depression

N. Wray, I. Deary, M. Owen, 2019, bioRxiv.

Edinburgh Research Explorer Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

I. Giegling, S. Djurovic, R. Ophoff, 2017 .

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

J. J. Wang, J. Danesh, Toshiko Tanaka, 2014, Molecular Psychiatry.

The effect of FTO rs9939609 on major depression differs across MDD subtypes

Y. Milaneschi, B. Penninx, H. Mbarek, 2014, Molecular Psychiatry.

Skewed X-inactivation is common in the general female population

A. Uitterlinden, F. Hormozdiari, D. Cox, 2018, European Journal of Human Genetics.

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

Thomas W. Mühleisen, N. Wray, D. Rujescu, 2017, Translational Psychiatry.

Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium

T. Spector, R. Mägi, E. Mihailov, 2016, Translational Psychiatry.

Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM

N. Wray, A. Hofman, T. Spector, 2011, Molecular Psychiatry.

Genome-wide association analysis of coffee drinking suggests association with CYP1A1CYP1A2 and NRCAM

K. Stefánsson, M. Mangino, A. Chakravarti, 2012 .

Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking

L. Ferrucci, G. Abecasis, D. Rujescu, 2011, Translational Psychiatry.

Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking Terracciano, A

L. Ferrucci, D. Rujescu, I. Giegling, 2022 .

Genome-wide analyses of borderline personality features

C. Duijn, G. Willemsen, J. Hottenga, 2013, Molecular Psychiatry.

Short telomere length is associated with impaired cognitive performance in European ancestry cohorts

R. Marioni, I. Deary, N. Samani, 2017, Translational Psychiatry.

Gene expression in major depressive disorder

F. Wright, G. Willemsen, D. Posthuma, 2016, Molecular Psychiatry.

Polygenic dissection of major depression clinical heterogeneity

A. Dehghan, G. Willemsen, J. Hottenga, 2016, Molecular Psychiatry.

Gene expression in major depressive disorder.

F. Wright, G. Willemsen, D. Posthuma, 2016, Molecular psychiatry.

CHAPTER 4 The 3 p 21 . 1p 21 . 3 hereditary vascular retinopathy locus increases the risk for Raynaud phenomenon and migraine

M. Ferrari, J. Haan, R. Frants, 2006 .

[Roaming through methodology. XXXVII. Unintentional population stratification in genetic case-control studies].

J. Houwing-Duistermaat, C. M. van Duijn, J. Hottenga, 2002, Nederlandsch tijdschrift voor geneeskunde.

CHAPTER 8 Familial partial epilepsy with variable foci in a Dutch family : clinical characteristics and confirmation of linkage to chromosome 22 q

D. Lindhout, R. Frants, J. Hottenga, 2006 .

The 3p21.1-p21.3 Hereditary Vascular Retinopathy Locus Increases the Risk for Raynaud's Phenomenon and Migraine

J. Haan, R. Frants, J. Hottenga, 2005, Cephalalgia : an international journal of headache.