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Showing 1–17 of 17 results

Advanced filters: Author: S Willis-Owen Clear advanced filters

The molecular genetic architecture of human personality: beyond self-report questionnaires

R P Ebstein
Reviews14 Mar 2006
Molecular Psychiatry

Volume: 11, P: 427-445
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

Variations in expression of the gene ORMDL3 were found to be associated with development of childhood asthma, suggesting this gene should be examined in more patient groups.

Miriam F. Moffatt
Michael Kabesch
William O. C. Cookson
Research04 Jul 2007
Nature

Volume: 448, P: 470-473
DCNP1: a novel candidate gene for major depression

S A G Willis-Owen
S Shifman
J Flint
Correspondence27 Sept 2005
Molecular Psychiatry

Volume: 11, P: 121-122
Comprehensive multi-cohort transcriptional meta-analysis of muscle diseases identifies a signature of disease severity

C. J. Walsh
J. Batt
C. C. dos Santos
ResearchOpen Access04 Jul 2022
Scientific Reports

Volume: 12, P: 1-14
COPD is accompanied by co-ordinated transcriptional perturbation in the quadriceps affecting the mitochondria and extracellular matrix

Saffron A. G. Willis-Owen
Anna Thompson
Samantha A. Natanek
ResearchOpen Access15 Aug 2018
Scientific Reports

Volume: 8, P: 1-9
Association of the serotonin transporter gene, neuroticism and smoking behaviours

Colin O’Gara
Jo Knight
Ian Craig
Research01 Mar 2008
Journal of Human Genetics

Volume: 53, P: 239-246
Global gene regulation during activation of immunoglobulin class switching in human B cells

Youming Zhang
David J. Fear
Miriam F. Moffatt
ResearchOpen Access29 Nov 2016
Scientific Reports

Volume: 6, P: 1-12
A whole genome association study of neuroticism using DNA pooling

S Shifman
A Bhomra
J Flint
Research31 Jul 2007
Molecular Psychiatry

Volume: 13, P: 302-312
Genomic attributes of airway commensal bacteria and mucosa

Systematic culture and genome sequencing of thoracic airway commensal bacteria finds many potential influences on lung health and disease. Polyomics of differentiated airway epithelium also suggest pathways that may sustain host-microbial interactions.

Leah Cuthbertson
Ulrike Löber
William. O. C. Cookson
ResearchOpen Access12 Feb 2024
Communications Biology

Volume: 7, P: 1-14
Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations

Michael Field
Ingrid E Scheffer
Jozef Gecz
Research22 Feb 2012
European Journal of Human Genetics

Volume: 20, P: 806-809
Y disruption, autosomal hypomethylation and poor male lung cancer survival

Saffron A. G. Willis-Owen
Clara Domingo-Sabugo
Miriam F. Moffatt
ResearchOpen Access14 Jun 2021
Scientific Reports

Volume: 11, P: 1-12
EGF receptor (EGFR) inhibition promotes a slow-twitch oxidative, over a fast-twitch, muscle phenotype

Margherita Ciano
Giada Mantellato
S. Amanda Natanek
ResearchOpen Access25 Jun 2019
Scientific Reports

Volume: 9, P: 1-9
Erratum: Mapping regulatory variants for the serotonin transporter gene based on allelic expression imbalance

J Martin
J Cleak
S Shifman
Amendments and Corrections27 Aug 2007
Molecular Psychiatry

Volume: 12, P: 881
Erratum: A functional AT/G polymorphism in the 5′-untranslated region of SETDB2 in the IgE locus on human chromosome 13q14

R J Holt
C Vandiedonck
Y Zhang
Amendments and CorrectionsOpen Access12 May 2016
Genes & Immunity

Volume: 18, P: 57
Mapping regulatory variants for the serotonin transporter gene based on allelic expression imbalance

J Martin
J Cleak
S Shifman
Correspondence24 Apr 2007
Molecular Psychiatry

Volume: 12, P: 421-422
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

H Hu
S A Haas
V M Kalscheuer
ResearchOpen Access03 Feb 2015
Molecular Psychiatry

Volume: 21, P: 133-148
A functional AT/G polymorphism in the 5′-untranslated region of SETDB2 in the IgE locus on human chromosome 13q14

R J Holt
C Vandiedonck
Y Zhang
ResearchOpen Access17 Sept 2015
Genes & Immunity

Volume: 16, P: 488-494

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Search

The molecular genetic architecture of human personality: beyond self-report questionnaires

Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

DCNP1: a novel candidate gene for major depression

Comprehensive multi-cohort transcriptional meta-analysis of muscle diseases identifies a signature of disease severity

COPD is accompanied by co-ordinated transcriptional perturbation in the quadriceps affecting the mitochondria and extracellular matrix

Association of the serotonin transporter gene, neuroticism and smoking behaviours

Global gene regulation during activation of immunoglobulin class switching in human B cells

A whole genome association study of neuroticism using DNA pooling

Genomic attributes of airway commensal bacteria and mucosa

Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations

Y disruption, autosomal hypomethylation and poor male lung cancer survival

EGF receptor (EGFR) inhibition promotes a slow-twitch oxidative, over a fast-twitch, muscle phenotype

Erratum: Mapping regulatory variants for the serotonin transporter gene based on allelic expression imbalance

Erratum: A functional AT/G polymorphism in the 5′-untranslated region of SETDB2 in the IgE locus on human chromosome 13q14

Mapping regulatory variants for the serotonin transporter gene based on allelic expression imbalance

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

A functional AT/G polymorphism in the 5′-untranslated region of SETDB2 in the IgE locus on human chromosome 13q14

Search

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