Addictions and their familiality in Iceland |
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Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank |
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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use |
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Brain age prediction using deep learning uncovers associated sequence variants |
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Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly |
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Commentary: Gene-environment interactions and smoking-related cancers |
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Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood |
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A common inversion under selection in Europeans |
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Direct determination of the membrane affinities of individual amino acids. |
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Direct measurement of small ligand-induced conformational changes in the aspartate chemoreceptor using EPR. |
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Expanding the range of ZNF804A variants conferring risk of psychosis |
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A genetic risk factor for periodic limb movements in sleep |
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Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders |
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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. |
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Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption |
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Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium |
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Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence |
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Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology |
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Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression |
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Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence |
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Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk |
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Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes |
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GPC5 rs2352028 variant and risk of lung cancer in never smokers |
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Hvarfljómun og flúrljómun |
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Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers |
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Integration of evidence across human and model organism studies: A meeting report |
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Large recurrent microdeletions associated with schizophrenia |
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Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes |
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A large-scale genome-wide association study meta-analysis of cannabis use disorder |
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Laser photolysis studies of retinal proteins. |
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A limiting law for the electrostatics of the binding of polypeptides to phospholipid bilayers. |
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Mechanism of vibrational relaxation and intersystem crossing within excited ion-pair states of I2 |
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The nature of nurture : effects of parental genotypes |
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Neuregulin 1 and schizophrenia |
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Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations |
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Nornin í Múfftargötu |
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Photolysis intermediates of human rhodopsin. |
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Photolysis of rhodopsin results in deprotonation of its retinal Schiff's base prior to formation of metarhodopsin II |
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Polygenic risk scores for schizophrenia and bipolar disorder predict creativity |
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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 |
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A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences |
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Recombination rate and reproductive success in humans |
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Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation |
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Sequence variant on 8q24 confers susceptibility to urinary bladder cancer |
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Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior |
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Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption |
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Sequence variants at the TERT-CLPTM1L locus associate with many cancer types |
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Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis |
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Topology of an amphiphilic mitochondrial signal sequence in the membrane-inserted state: a spin labeling study. |
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Transient channel-opening in bacteriorhodopsin: an EPR study. |
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Truncating mutations in RBM12 are associated with psychosis. |
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A variant associated with nicotine dependence, lung cancer and peripheral arterial disease |
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