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Showing 201–228 of 228 results

Advanced filters: Author: Peter M Visscher Clear advanced filters

Unravelling the complex causal effects of substance use behaviours on common diseases

Xue et al. use 11 Mendelian Randomization methods to investigate the causal relationship between seven substance use behavioural traits and health outcomes. They identify risk effects of alcohol consumption as well as dosage dependent effects of coffee and tea on cardiovascular disease and osteoarthritis respectively.

Angli Xue
Zhihong Zhu
Jian Yang
ResearchOpen Access12 Mar 2024
Communications Medicine

Volume: 4, P: 1-13
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

Audrey E. Hendricks
Elena G. Bochukova
Hou-Feng Zheng
ResearchOpen Access29 Jun 2017
Scientific Reports

Volume: 7, P: 1-14
Extra c-myc oncogene copies in high risk cutaneous malignant melanoma and melanoma metastases

G M Kraehn
J Utikal
R U Peter
ResearchOpen Access03 Jan 2001
British Journal of Cancer

Volume: 84, P: 72-79
Multi-omic and multi-species meta-analyses of nicotine consumption

Rohan H. C. Palmer
Chelsie E. Benca-Bachman
Elissa J. Chesler
ResearchOpen Access04 Feb 2021
Translational Psychiatry

Volume: 11, P: 1-10
Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium

Artitaya Lophatananon
Sarah Stewart-Brown
Kenneth Muir
ResearchOpen Access01 Aug 2017
British Journal of Cancer

Volume: 117, P: 734-743
Testing replication of a 5-SNP set for general cognitive ability in six population samples

Michelle Luciano
Penelope A Lind
Robert Plomin
Research21 May 2008
European Journal of Human Genetics

Volume: 16, P: 1388-1395
Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders

Enda M. Byrne
Zhihong Zhu
Naomi R. Wray
Research12 May 2020
Molecular Psychiatry

Volume: 26, P: 2070-2081
Fast set-based association analysis using summary data from GWAS identifies novel gene loci for human complex traits

Andrew Bakshi
Zhihong Zhu
Jian Yang
ResearchOpen Access08 Sept 2016
Scientific Reports

Volume: 6, P: 1-9
GWAS on family history of Alzheimer’s disease

Riccardo E. Marioni
Sarah E. Harris
Peter M. Visscher
ResearchOpen Access18 May 2018
Translational Psychiatry

Volume: 8, P: 1-7
Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

Simone de Jong et al. examine the balance of common and rare risk for psychiatric disorders in a large family with high incidence of Bipolar Disorder and Major Depressive Disorder. They find that increased polygenic risk over generations could be partially due to assortative mating, which may explain the observation of anticipation in mood disorders.

Simone de Jong
Mateus Jose Abdalla Diniz
Gerome Breen
ResearchOpen Access08 Oct 2018
Communications Biology

Volume: 1, P: 1-10
The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects

W J Peyrot
S H Lee
B W J H Penninx
Research28 Apr 2015
Molecular Psychiatry

Volume: 20, P: 735-743
Erratum: Testing replication of a 5-SNP set for general cognitive ability in six population samples

Michelle Luciano
Penelope A Lind
Robert Plomin
Amendments and Corrections24 Jul 2008
European Journal of Human Genetics

Volume: 16, P: 1025
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

B Benyamin
BSt Pourcain
P M Visscher
Research29 Jan 2013
Molecular Psychiatry

Volume: 19, P: 253-258
Erratum: Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

Manuel A R Ferreira
Allan F McRae
Nicholas G Martin
Amendments and Corrections22 Sept 2011
European Journal of Human Genetics

Volume: 19, P: 1109
Correction: Corrigendum to: Sporadic cases are the norm for complex disease

Jian Yang
Peter M Visscher
Naomi R Wray
Amendments and Corrections19 Aug 2010
European Journal of Human Genetics

Volume: 18, P: 1044
Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

Manuel A R Ferreira
Allan F McRae
Nicholas G Martin
Research08 Dec 2010
European Journal of Human Genetics

Volume: 19, P: 458-464
Genetics of cognitive performance, education and learning: from research to policy?

Peter M. Visscher
Comments & OpinionOpen Access04 May 2022
npj Science of Learning

Volume: 7, P: 1-2
Age at first birth in women is genetically associated with increased risk of schizophrenia

Guiyan Ni
Jacob Gratten
Michael C. O’Donovan
ResearchOpen Access05 Jul 2018
Scientific Reports

Volume: 8, P: 1-14
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

A Hinney
M Kesselmeier
J Hebebrand
Research17 May 2016
Molecular Psychiatry

Volume: 22, P: 192-201
Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome

Pritesh Jain
Tyne Miller-Fleming
Peristera Paschou
ResearchOpen Access23 Feb 2023
Translational Psychiatry

Volume: 13, P: 1-10
Genetics and educational attainment

David Cesarini
Peter M. Visscher
ReviewsOpen Access01 Feb 2017
npj Science of Learning

Volume: 2, P: 1-7
Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree

Matthew Halvorsen
Jin Szatkiewicz
James J. Crowley
Research15 Sept 2021
Molecular Psychiatry

Volume: 26, P: 7522-7529
Correction: GWAS on family history of Alzheimer’s disease

Riccardo E. Marioni
Sarah E. Harris
Peter M. Visscher
Amendments and CorrectionsOpen Access06 Jun 2019
Translational Psychiatry

Volume: 9, P: 1-2
On Jim Watson's APOE status: genetic information is hard to hide

Dale R Nyholt
Chang-En Yu
Peter M Visscher
Correspondence22 Oct 2008
European Journal of Human Genetics

Volume: 17, P: 147-149
A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk

J A Revez
L Bain
M A R Ferreira
Research15 Aug 2013
Genes & Immunity

Volume: 14, P: 441-446
Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses

P M Visscher
M E Goddard
N R Wray
Reviews14 Jun 2011
Molecular Psychiatry

Volume: 17, P: 474-485
Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM

N Amin
E Byrne
C M van Duijn
ResearchOpen Access30 Aug 2011
Molecular Psychiatry

Volume: 17, P: 1116-1129
Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

Jonathan R. I. Coleman
Wouter J. Peyrot
Gerome Breen
Amendments and Corrections18 May 2020
Molecular Psychiatry

Volume: 26, P: 5465

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