about
Common variants conferring risk of schizophreniaLarge recurrent microdeletions associated with schizophreniaNeuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendationsGenome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumptionA mega-analysis of genome-wide association studies for major depressive disorderA variant associated with nicotine dependence, lung cancer and peripheral arterial diseaseSequence variants at the TERT-CLPTM1L locus associate with many cancer typesAddictions and their familiality in Iceland.A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences.Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.Recombination rate and reproductive success in humans.Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.Nanosecond photolysis of rhodopsin: evidence for a new, blue-shifted intermediate.A genetic risk factor for periodic limb movements in sleep.Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk.Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumptionNeuregulin 1 and schizophrenia.Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers.Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependencePsychometric properties of the Icelandic NEO-FFI in a general population sample compared to a sample recruited for a study on the genetics of addiction.Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics ConsortiumGenome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders.Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation.Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction.Polygenic risk scores for schizophrenia and bipolar disorder predict creativity.GPC5 rs2352028 variant and risk of lung cancer in never smokers.Photolysis intermediates of human rhodopsin.Effects of temperature on rhodopsin photointermediates from lumirhodopsin to metarhodopsin II.Transient channel-opening in bacteriorhodopsin: an EPR study.Direct measurement of small ligand-induced conformational changes in the aspartate chemoreceptor using EPR.Topology of an amphiphilic mitochondrial signal sequence in the membrane-inserted state: a spin labeling study.A limiting law for the electrostatics of the binding of polypeptides to phospholipid bilayers.Direct determination of the membrane affinities of individual amino acids.The nature of nurture: Effects of parental genotypes.Truncating mutations in RBM12 are associated with psychosis.Commentary: Gene-environment interactions and smoking-related cancers
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P50
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Thorgeir E. Thorgeirsson
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Thorgeir E. Thorgeirsson
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Thorgeir E. Thorgeirsson
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Thorgeir E. Thorgeirsson
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P106
P108
P21
P214
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P31
P496
0000-0002-5149-7040