Pages that link to "Q46468372"
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The following pages link to Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies (Q46468372):
Displaying 50 items.
- The impact of divergence time on the nature of population structure: an example from Iceland (Q21090210) (← links)
- Genetic structure of Europeans: a view from the North-East (Q21143785) (← links)
- Geographic patterns of genome admixture in Latin American Mestizos (Q21145052) (← links)
- Genetic variation and population structure in native Americans (Q21145222) (← links)
- Isolated populations and complex disease gene identification (Q21183904) (← links)
- High differentiation among eight villages in a secluded area of Sardinia revealed by genome-wide high density SNPs analysis (Q21562491) (← links)
- Toward a better understanding of ADHD: LPHN3 gene variants and the susceptibility to develop ADHD (Q22252571) (← links)
- Genome-wide association study of Tourette's syndrome (Q23936582) (← links)
- Genome-wide association studies for complex traits: consensus, uncertainty and challenges (Q24550632) (← links)
- Population structure and genome-wide patterns of variation in Ireland and Britain (Q24597285) (← links)
- Genetic markers and population history: Finland revisited (Q24600317) (← links)
- Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia (Q24606481) (← links)
- Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population (Q24606497) (← links)
- Genome-wide association scan for five major dimensions of personality (Q24608568) (← links)
- An association analysis of murine anxiety genes in humans implicates novel candidate genes for anxiety disorders (Q24643934) (← links)
- Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia (Q24643955) (← links)
- Genome-wide association analysis of metabolic traits in a birth cohort from a founder population (Q24654676) (← links)
- FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate (Q24655358) (← links)
- Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene (Q24656270) (← links)
- Comprehensive testing of positionally cloned asthma genes in two populations (Q24670496) (← links)
- Systems biology of the vervet monkey (Q26995525) (← links)
- Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe (Q27438161) (← links)
- Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families (Q28239852) (← links)
- A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication (Q28273217) (← links)
- Mitogenomic and microsatellite variation in descendants of the founder population of Newfoundland: high genetic diversity in an historically isolated population (Q28305528) (← links)
- Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort (Q28744011) (← links)
- The genome-wide patterns of variation expose significant substructure in a founder population (Q28754746) (← links)
- Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis (Q28943435) (← links)
- Genetics of Type 2 Diabetes: the Power of Isolated Populations (Q30250281) (← links)
- Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates (Q30490128) (← links)
- Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease (Q30493604) (← links)
- Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland (Q30809578) (← links)
- Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping (Q30840823) (← links)
- Evaluation of HapMap data in six populations of European descent (Q31152012) (← links)
- Volume measures for linkage disequilibrium (Q33263962) (← links)
- Combined effects of thrombosis pathway gene variants predict cardiovascular events (Q33293167) (← links)
- The value of some Corsican sub-populations for genetic association studies (Q33355654) (← links)
- Linkage disequilibrium compared between five populations of domestic sheep (Q33372975) (← links)
- A role of BRCA1 and BRCA2 germline mutations in breast cancer susceptibility within Sardinian population (Q33484437) (← links)
- Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD. (Q33488059) (← links)
- Association between protective and deleterious HLA alleles with multiple sclerosis in Central East Sardinia (Q33490625) (← links)
- Systematic analysis of circadian genes in a population-based sample reveals association of TIMELESS with depression and sleep disturbance (Q33533337) (← links)
- A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level (Q33540002) (← links)
- Of founder populations, long QT syndrome, and destiny (Q33575898) (← links)
- HLA Class I and II profiles in São Miguel Island (Azores): genetic diversity and linkage disequilibrium (Q33576275) (← links)
- Extent and distribution of linkage disequilibrium in the Old Order Amish (Q33611974) (← links)
- The impact of population demography and selection on the genetic architecture of complex traits (Q33686100) (← links)
- Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigrees. (Q33710047) (← links)
- Role of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorder (Q33753253) (← links)
- Association of ADIPOQ gene variants with body weight, type 2 diabetes and serum adiponectin concentrations: the Finnish Diabetes Prevention Study (Q33789542) (← links)