Isolated populations and complex disease gene identification - Wikidata - wikimedia - TriplyDB

Isolated populations and complex disease gene identification

Isolated populations and complex disease gene identification

http://www.wikidata.org/entity/Q21183904

about

GENLIB: an R package for the analysis of genealogical data Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study Melanesian blond hair is caused by an amino acid change in TYRP1 Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe Novel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular Malaysia IGSF10 mutations dysregulate gonadotropin-releasing hormone neuronal migration resulting in delayed puberty.Comprehensive genomic analyses associate UGT8 variants with musical ability in a Mongolian population.Population neuroscience: why and how.Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.Population-based study of genetic variation in individuals with autism spectrum disorders from Croatia Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder A population-specific reference panel empowers genetic studies of Anabaptist populations.Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays Genetic variation in the Sorbs of eastern Germany in the context of broader European genetic diversity Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity Comparing population structure as inferred from genealogical versus genetic information.Genome-wide SNP analysis reveals no gain in power for association studies of common variants in the Finnish Saami Genome-wide analysis in Brazilian Xavante Indians reveals low degree of admixture A general approach for haplotype phasing across the full spectrum of relatedness High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results.Traces of forgotten historical events in mountain communities in Central Italy: A genetic insight.Detecting genetic isolation in human populations: a study of European language minorities A genome-wide analysis of population structure in the Finnish Saami with implications for genetic association studies Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population.Prevalence of adiposity and associated cardiometabolic risk factors in the Samoan genome-wide association study A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene.Family-Based Association Study of Pulmonary Function in a Population in Northeast Asia.Genetic mapping of habitual substance use, obesity-related traits, responses to mental and physical stress, and heart rate and blood pressure measurements reveals shared genes that are overrepresented in the neural synapse.Extensive genome-wide autozygosity in the population isolates of Daghestan.Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease Overcoming the dichotomy between open and isolated populations using genomic data from a large European dataset.Small effective population size and genetic homogeneity in the Val Borbera isolate.The Effects of Both Recent and Long-Term Selection and Genetic Drift Are Readily Evident in North American Barley Breeding Populations.Fine-scale human genetic structure in Western France.THOC5: a novel gene involved in HDL-cholesterol metabolism.Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.A genome-wide scan study identifies a single nucleotide substitution in ASIP associated with white versus non-white coat-colour variation in sheep (Ovis aries)Using population isolates in genetic association studies.A Genetic Population Isolate in The Netherlands Showing Extensive Haplotype Sharing and Long Regions of Homozygosity.Assessment of cardiovascular disease risk factors in a genetically homogenous population of Parsi Zoroastrians in the United States: A pilot study.

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Isolated populations and complex disease gene identification

http://www.wikidata.org/entity/Q21183904

description

2008 nî lūn-bûn

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2008 թուականին հրատարակուած գիտական յօդուած

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2008 թվականին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Isolated populations and complex disease gene identification

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Jussi Naukkarinen

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Initial sequencing and analysis of the human genome

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

dbSNP: the NCBI database of genetic variation

IRAK-M is involved in the pathogenesis of early-onset persistent asthma

Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci

Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping

Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans

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8

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Kati Kristiansson

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23237712

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