Application of genome-wide single nucleotide polymorphism typing: simple association and beyond
about
Virtual karyotyping with SNP microarrays reduces uncertainty in the diagnosis of renal epithelial tumorsA nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial diseasePrivacy in the Genomic EraStructural genomic variation in ischemic stroke.Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics.Creation of an open-access, mutation-defined fibroblast resource for neurological disease research.SiDCoN: a tool to aid scoring of DNA copy number changes in SNP chip dataOnline genetic databases informing human genome epidemiology.Domestication, genomics and the future for banana.Enhancing genetic mapping of complex genomes through the design of highly-multiplexed SNP arrays: application to the large and unsequenced genomes of white spruce and black spruceReporting of human genome epidemiology (HuGE) association studies: an empirical assessment.Genome-wide autozygosity mapping in human populations.In vitro vs in silico detected SNPs for the development of a genotyping array: what can we learn from a non-model species?Population-based study of genetic variation in individuals with autism spectrum disorders from CroatiaHereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19.Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer's disease.DominantMapper: rule-based analysis of SNP data for rapid mapping of dominant diseases in related nuclear families.Towards a complete resolution of the genetic architecture of disease.Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.SNP array profiling of mouse cell lines identifies their strains of origin and reveals cross-contamination and widespread aneuploidy.Genome wide assessment of young onset Parkinson's disease from FinlandWhole genome SNP arrays as a potential diagnostic tool for the detection of characteristic chromosomal aberrations in renal epithelial tumors.A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome.Structural genomics: correlation blocks, population structure, and genome architecture.The association of CD46, SLAM and CD209 cellular receptor gene SNPs with variations in measles vaccine-induced immune responses: a replication study and examination of novel polymorphisms.A single-nucleotide polymorphism in the EAP1 gene is associated with amenorrhea/oligomenorrhea in nonhuman primates.Genomic patterns of homozygosity in worldwide human populationsExome sequencing reveals riboflavin transporter mutations as a cause of motor neuron diseaseKinSNP software for homozygosity mapping of disease genes using SNP microarraysMutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity.Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease.Molecular cytogenetics: making it safe for human embryonic stem cells to enter the clinic.Assessment of cumulative evidence on genetic associations: interim guidelines.Susceptibility genes in movement disorders.Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibilityInfantile parkinsonism-dystonia: a dopamine "transportopathy"DNA repair gene polymorphisms and risk of cutaneous melanoma: a systematic review and meta-analysis.Deciphering genetic disease in the genomic era: the model of GnRH deficiency.Gene hunting in the genomic era: approaches to diagnostic dilemmas in patients with primary immunodeficienciesEarly-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.
P2860
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P2860
Application of genome-wide single nucleotide polymorphism typing: simple association and beyond
description
2006 nî lūn-bûn
@nan
2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Application of genome-wide sin ...... simple association and beyond
@ast
Application of genome-wide sin ...... simple association and beyond
@en
Application of genome-wide sin ...... simple association and beyond.
@nl
type
label
Application of genome-wide sin ...... simple association and beyond
@ast
Application of genome-wide sin ...... simple association and beyond
@en
Application of genome-wide sin ...... simple association and beyond.
@nl
prefLabel
Application of genome-wide sin ...... simple association and beyond
@ast
Application of genome-wide sin ...... simple association and beyond
@en
Application of genome-wide sin ...... simple association and beyond.
@nl
P2860
P921
P1433
P1476
Application of genome-wide sin ...... simple association and beyond
@en
P2093
J Raphael Gibbs
P275
P2860
P356
10.1371/JOURNAL.PGEN.0020150
P577
2006-10-01T00:00:00Z
2006-10-06T00:00:00Z