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Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesThe FU gene and its possible protein isoformsGenome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorderMeta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's diseaseGenetics of dyslexia: the evolving landscapeMutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplexG protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growthInvolvement of the atrial natriuretic peptide transcription factor GATA4 in alcohol dependence, relapse risk and treatment response to acamprosateVariant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopeciaLocalization of a gene for syndactyly type 1 to chromosome 2q34-q36.Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos diseaseGenome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's diseaseCommon variants conferring risk of schizophreniaAdaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short statureThe neuronal transporter gene SLC6A15 confers risk to major depressionMicroduplications of 16p11.2 are associated with schizophreniaGenome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorderDisruption of the neurexin 1 gene is associated with schizophreniaLarge recurrent microdeletions associated with schizophreniaIncreased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type IIIMonoamine related functional gene variants and relationships to monoamine metabolite concentrations in CSF of healthy volunteersVATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysisNovel genetic loci underlying human intracranial volume identified through genome-wide associationA common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer.Association between a polymorphism in the pseudoautosomal X-linked gene SYBL1 and bipolar affective disorderMutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle diseaseHypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosinThe hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approachGenome-wide association study reveals two new risk loci for bipolar disorderLoss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizationsLarge-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesA locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexiaMultiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.Lack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservationIdentification of mutations in the human hairless gene in two new families with congenital atrichiaGenetic relationship between five psychiatric disorders estimated from genome-wide SNPsGenome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanismsThe 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2AThe CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
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