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Showing 1–29 of 29 results

Advanced filters: Author: Francesco Bettella Clear advanced filters

Genetic loci shared between major depression and intelligence with mixed directions of effect

Bahrami et al. identify substantial polygenic overlap between major depressive disorder and general intelligence. Despite low genetic correlation, the authors singled out 92 genomic loci shared by the two phenotypes, with a mixture of allelic effect directions.

Shahram Bahrami
Alexey Shadrin
Ole A. Andreassen
Research18 Jan 2021
Nature Human Behaviour

Volume: 5, P: 795-801
GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study

Arvid Rongve
Aree Witoelar
Ole A. Andreassen
ResearchOpen Access07 May 2019
Scientific Reports

Volume: 9, P: 1-8
Large-scale genomics unveil polygenic architecture of human cortical surface area

How genetic variation contributes to brain morphology is still poorly understood. Here Chenet al. combine brain imaging with single-nucleotide polymorphism data to discover that a substantial degree of cortical variation is derived from underlying genetic differences.

Chi-Hua Chen
Qian Peng
Anders M. Dale
ResearchOpen Access20 Jul 2015
Nature Communications

Volume: 6, P: 1-7
Identification of common genetic risk variants for autism spectrum disorder

A genome-wide-association meta-analysis of 18,381 austim spectrum disorder (ASD) cases and 27,969 controls identifies five risk loci. The authors find quantitative and qualitative polygenic heterogeneity across ASD subtypes.

Jakob Grove
Stephan Ripke
Anders D. Børglum
Research25 Feb 2019
Nature Genetics

Volume: 51, P: 431-444
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk

Genome-wide meta-analysis of clinically diagnosed Alzheimer’s disease (AD) and AD-by-proxy (71,880 AD cases, 383,378 controls) identifies new loci and functional pathways that contribute to AD risk.

Iris E. Jansen
Jeanne E. Savage
Danielle Posthuma
Research07 Jan 2019
Nature Genetics

Volume: 51, P: 404-413
Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Patrick Sullivan and colleagues report a multi-stage genome-wide association study for schizophrenia in a Swedish population. They identify 13 loci newly associated with schizophrenia.

Stephan Ripke
Colm O'Dushlaine
Patrick F Sullivan
Research25 Aug 2013
Nature Genetics

Volume: 45, P: 1150-1159
Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk

Iris E. Jansen
Jeanne E. Savage
Danielle Posthuma
Amendments and Corrections06 Feb 2020
Nature Genetics

Volume: 52, P: 354
Publisher Correction: Common brain disorders are associated with heritable patterns of apparent aging of the brain

Tobias Kaufmann
Dennis van der Meer
Lars T. Westlye
Amendments and Corrections17 Dec 2019
Nature Neuroscience

Volume: 23, P: 295
Common brain disorders are associated with heritable patterns of apparent aging of the brain

Using structural MRI data from 45,615 individuals aged 3–96 years, Kaufmann and colleagues reveal that common brain disorders are associated with heritable patterns of apparent aging of the brain.

Tobias Kaufmann
Dennis van der Meer
Lars T. Westlye
Research24 Sept 2019
Nature Neuroscience

Volume: 22, P: 1617-1623
Genome-wide meta-analysis identifies new susceptibility loci for migraine

Verneri Anttila and colleagues report meta-analysis of 29 genome-wide association studies for migraine. They identify five loci newly associated with migraine, three of which are associated with specific subtypes of migraine with or without aura.

Verneri Anttila
Bendik S Winsvold
Aarno Palotie
Research23 Jun 2013
Nature Genetics

Volume: 45, P: 912-917
Correction: Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence

Olav B Smeland
Shahram Bahrami
Ole A Andreassen
Amendments and Corrections15 Jul 2019
Molecular Psychiatry

Volume: 25, P: 914
An evolutionary timeline of the oxytocin signaling pathway

A study on the evolution of the oxytocin system illustrates the varied role of this neuropeptide in physiology and behavior

Alina M. Sartorius
Jaroslav Rokicki
Daniel S. Quintana
ResearchOpen Access17 Apr 2024
Communications Biology

Volume: 7, P: 1-13
Characterising the shared genetic determinants of bipolar disorder, schizophrenia and risk-taking

Guy Hindley
Shahram Bahrami
Ole A. Andreassen
ResearchOpen Access08 Sept 2021
Translational Psychiatry

Volume: 11, P: 1-10
Oxytocin-pathway polygenic scores for severe mental disorders and metabolic phenotypes in the UK Biobank

Adriano Winterton
Francesco Bettella
Daniel S. Quintana
ResearchOpen Access25 Nov 2021
Translational Psychiatry

Volume: 11, P: 1-9
Identification of pleiotropy at the gene level between psychiatric disorders and related traits

Tatiana Polushina
Niladri Banerjee
Stéphanie Le Hellard
ResearchOpen Access29 Jul 2021
Translational Psychiatry

Volume: 11, P: 1-9
Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study

Katrine K. Fjukstad
Lavinia Athanasiu
Ole A. Andreassen
Research06 Apr 2021
The Pharmacogenomics Journal

Volume: 21, P: 574-585
Polygenic scores for schizophrenia and general cognitive ability: associations with six cognitive domains, premorbid intelligence, and cognitive composite score in individuals with a psychotic disorder and in healthy controls

Magnus Johan Engen
Siv Hege Lyngstad
Ingrid Melle
ResearchOpen Access30 Nov 2020
Translational Psychiatry

Volume: 10, P: 1-9
Identification of genetic overlap and novel risk loci for attention-deficit/hyperactivity disorder and bipolar disorder

Kevin S. O’Connell
Alexey Shadrin
Ole A. Andreassen
Research02 Dec 2019
Molecular Psychiatry

Volume: 26, P: 4055-4065
Examining the association between genetic liability for schizophrenia and psychotic symptoms in Alzheimer’s disease

Byron Creese
Evangelos Vassos
Geir Selbaek
ResearchOpen Access22 Oct 2019
Translational Psychiatry

Volume: 9, P: 1-10
Meta-analysis of Alzheimer’s disease on 9,751 samples from Norway and IGAP study identifies four risk loci

Aree Witoelar
Arvid Rongve
Ole A. Andreassen
ResearchOpen Access27 Dec 2018
Scientific Reports

Volume: 8, P: 1-8
Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotype

Federica Cesca
Elisa Bettella
Alessandra Murgia
Research28 May 2020
Journal of Human Genetics

Volume: 65, P: 855-864
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes

Dennis van der Meer
Jaroslav Rokicki
Lars T. Westlye
ResearchOpen Access02 Oct 2018
Molecular Psychiatry

Volume: 25, P: 3053-3065
Effects of autozygosity and schizophrenia polygenic risk on cognitive and brain developmental trajectories

Aldo Córdova-Palomera
Tobias Kaufmann
Lars T. Westlye
Research27 Apr 2018
European Journal of Human Genetics

Volume: 26, P: 1049-1059
Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence

Olav B Smeland
Shahram Bahrami
Ole A Andreassen
Research04 Jan 2019
Molecular Psychiatry

Volume: 25, P: 844-853
Enrichment of genetic markers of recent human evolution in educational and cognitive traits

Saurabh Srinivasan
Francesco Bettella
Ole A. Andreassen
ResearchOpen Access22 Aug 2018
Scientific Reports

Volume: 8, P: 1-9
Genetic control of variability in subcortical and intracranial volumes

Aldo Córdova-Palomera
Dennis van der Meer
Lars T. Westlye
Research11 Feb 2020
Molecular Psychiatry

Volume: 26, P: 3876-3883
Identification of shared genetic variants between schizophrenia and lung cancer

Verena Zuber
Erik G. Jönsson
Ole A. Andreassen
ResearchOpen Access12 Jan 2018
Scientific Reports

Volume: 8, P: 1-8
Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data

Tatiana Polushina
Sudheer Giddaluru
Stéphanie Le Hellard
ResearchOpen Access18 Dec 2017
Translational Psychiatry

Volume: 7, P: 1-9
Author Correction: GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study

Arvid Rongve
Aree Witoelar
Ole A. Andreassen
Amendments and CorrectionsOpen Access17 Oct 2019
Scientific Reports

Volume: 9, P: 1-2

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Genetic loci shared between major depression and intelligence with mixed directions of effect

GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study

Large-scale genomics unveil polygenic architecture of human cortical surface area

Identification of common genetic risk variants for autism spectrum disorder

Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Author Correction: Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk

Publisher Correction: Common brain disorders are associated with heritable patterns of apparent aging of the brain

Common brain disorders are associated with heritable patterns of apparent aging of the brain

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Correction: Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence

An evolutionary timeline of the oxytocin signaling pathway

Characterising the shared genetic determinants of bipolar disorder, schizophrenia and risk-taking

Oxytocin-pathway polygenic scores for severe mental disorders and metabolic phenotypes in the UK Biobank

Identification of pleiotropy at the gene level between psychiatric disorders and related traits

Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study

Polygenic scores for schizophrenia and general cognitive ability: associations with six cognitive domains, premorbid intelligence, and cognitive composite score in individuals with a psychotic disorder and in healthy controls

Identification of genetic overlap and novel risk loci for attention-deficit/hyperactivity disorder and bipolar disorder

Examining the association between genetic liability for schizophrenia and psychotic symptoms in Alzheimer’s disease

Meta-analysis of Alzheimer’s disease on 9,751 samples from Norway and IGAP study identifies four risk loci

Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotype

Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes

Effects of autozygosity and schizophrenia polygenic risk on cognitive and brain developmental trajectories

Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence

Enrichment of genetic markers of recent human evolution in educational and cognitive traits

Genetic control of variability in subcortical and intracranial volumes

Identification of shared genetic variants between schizophrenia and lung cancer

Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data

Author Correction: GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study

Search

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