Lista de obras - Thorgeir E. Thorgeirsson

A common inversion under selection in Europeans

artículo científico publicado en 2005

A genetic risk factor for periodic limb movements in sleep

artículo científico publicado en 2007

A large-scale genome-wide association study meta-analysis of cannabis use disorder

artículo científico publicado en 2020

A limiting law for the electrostatics of the binding of polypeptides to phospholipid bilayers.

artículo científico publicado en 1995

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

artículo científico publicado en 2012

A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences

artículo científico publicado en 2016

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer

artículo científico publicado en 2010

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

artículo científico publicado en 2008

Addictions and their familiality in Iceland

artículo científico publicado en 2010

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

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

artículo científico publicado en 2019

Brain age prediction using deep learning uncovers associated sequence variants

scientific article published on 27 November 2019

Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly

artículo científico publicado en 2017

Commentary: Gene-environment interactions and smoking-related cancers

article

Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood

scientific article published on 30 October 2019

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

De novo design of a peptide which partitions between water and phospholipid bilayers as a monomeric alpha-helix ⬇️

artículo científico publicado el 1 de julio de 1998

Direct determination of the membrane affinities of individual amino acids.

artículo científico publicado en 1996

Direct measurement of small ligand-induced conformational changes in the aspartate chemoreceptor using EPR.

artículo científico publicado en 1998

Effects of temperature on rhodopsin photointermediates from lumirhodopsin to metarhodopsin II.

artículo científico publicado en 1993

Expanding the range of ZNF804A variants conferring risk of psychosis

artículo científico publicado en 2010

GPC5 rs2352028 variant and risk of lung cancer in never smokers

artículo científico publicado en 2010

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

artículo científico publicado en 2016

Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders

artículo científico publicado en 2016

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

artículo científico publicado en 2018

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

scientific journal article

Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence

artículo científico publicado en 2017

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study implicates CHRNA2 in cannabis use disorder

artículo científico publicado en 2019

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

scientific article published on 11 November 2019

Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence

artículo científico publicado en 2015

Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk

artículo científico publicado en 2011

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

artículo científico publicado en 2012

Integration of evidence across human and model organism studies: A meeting report

artículo científico publicado en 2021

Large recurrent microdeletions associated with schizophrenia

artículo científico publicado en 2008

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

artículo científico publicado en 2017

Nanosecond photolysis of rhodopsin: evidence for a new, blue-shifted intermediate.

artículo científico publicado en 1990

Neuregulin 1 and schizophrenia

artículo científico publicado en 2004

Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations ⬇️

artículo científico publicado en 2015

Photolysis intermediates of human rhodopsin.

artículo científico publicado en 1991

Photolysis of rhodopsin results in deprotonation of its retinal Schiff's base prior to formation of metarhodopsin II

artículo científico publicado el 1 de diciembre de 1992

Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction

artículo científico publicado en 2017

Polygenic risk scores for schizophrenia and bipolar disorder predict creativity

artículo científico publicado en 2015

Psychometric properties of the Icelandic NEO-FFI in a general population sample compared to a sample recruited for a study on the genetics of addiction

artículo científico publicado en 2014

Recombination rate and reproductive success in humans

artículo científico publicado en 2004

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

artículo científico publicado en 2017

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

artículo científico publicado en 2008

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

artículo científico publicado en 2010

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption

artículo científico publicado en 2011

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

artículo científico publicado en 2009

Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis

artículo científico publicado en 2017

The nature of nurture: Effects of parental genotypes

artículo científico publicado en 2018

Topology of an amphiphilic mitochondrial signal sequence in the membrane-inserted state: a spin labeling study.

artículo científico publicado en 1994

Transient channel-opening in bacteriorhodopsin: an EPR study.

artículo científico publicado en 1997

Truncating mutations in RBM12 are associated with psychosis

artículo científico publicado en 2017

Lista de obras de Thorgeir E. Thorgeirsson

A common inversion under selection in Europeans

A genetic risk factor for periodic limb movements in sleep

A large-scale genome-wide association study meta-analysis of cannabis use disorder

A limiting law for the electrostatics of the binding of polypeptides to phospholipid bilayers.

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

A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

Addictions and their familiality in Iceland

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

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Brain age prediction using deep learning uncovers associated sequence variants

Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly

Commentary: Gene-environment interactions and smoking-related cancers

Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood

Common variants conferring risk of schizophrenia

De novo design of a peptide which partitions between water and phospholipid bilayers as a monomeric alpha-helix ⬇️

Direct determination of the membrane affinities of individual amino acids.

Direct measurement of small ligand-induced conformational changes in the aspartate chemoreceptor using EPR.

Effects of temperature on rhodopsin photointermediates from lumirhodopsin to metarhodopsin II.

Expanding the range of ZNF804A variants conferring risk of psychosis

GPC5 rs2352028 variant and risk of lung cancer in never smokers

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence

Genome-wide association study identifies 30 loci associated with bipolar disorder.

Genome-wide association study implicates CHRNA2 in cannabis use disorder

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence

Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

Integration of evidence across human and model organism studies: A meeting report

Large recurrent microdeletions associated with schizophrenia

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

Nanosecond photolysis of rhodopsin: evidence for a new, blue-shifted intermediate.

Neuregulin 1 and schizophrenia

Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations ⬇️

Photolysis intermediates of human rhodopsin.

Photolysis of rhodopsin results in deprotonation of its retinal Schiff's base prior to formation of metarhodopsin II

Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction

Polygenic risk scores for schizophrenia and bipolar disorder predict creativity

Psychometric properties of the Icelandic NEO-FFI in a general population sample compared to a sample recruited for a study on the genetics of addiction

Recombination rate and reproductive success in humans

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis

The nature of nurture: Effects of parental genotypes

Topology of an amphiphilic mitochondrial signal sequence in the membrane-inserted state: a spin labeling study.

Transient channel-opening in bacteriorhodopsin: an EPR study.

Truncating mutations in RBM12 are associated with psychosis