| scholarly article | Q13442814 |
| P50 | author | Uri Seligsohn | Q12403602 |
| David Reich | Q5238967 | ||
| Alicja Waliszewska | Q114403614 | ||
| Angelica A Saetta | Q53850095 | ||
| Cristian Capelli | Q54103166 | ||
| Joel Hirschhorn | Q56277942 | ||
| Leif Groop | Q27214742 | ||
| Nick Patterson | Q29014620 | ||
| Kristin Ardlie | Q32646968 | ||
| Alkes Price | Q32652800 | ||
| P2093 | author name string | David B Goldstein | |
| Penelope Korkolopoulou | |||
| Vincenzo L Pascali | |||
| Andres Ruiz-Linares | |||
| James Nemesh | |||
| Lori Arbeitman | |||
| Francesca Scarnicci | |||
| Alexis Ramos | |||
| Johannah Butler | |||
| Christine Schirmer | |||
| P2860 | cites work | Contribution of Factor VII Genotype to Activated FVII Levels | Q63953589 |
| Analysis of PRNP gene codon 129 polymorphism in the Greek population | Q82881572 | ||
| European population substructure: clustering of northern and southern populations | Q21092502 | ||
| Population structure and eigenanalysis | Q21145248 | ||
| A map of recent positive selection in the human genome | Q21563624 | ||
| Population genetic structure of variable drug response | Q22122041 | ||
| Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews | Q22242041 | ||
| Control of confounding of genetic associations in stratified populations | Q22337167 | ||
| The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes | Q24290189 | ||
| Geographic distribution of disease mutations in the Ashkenazi Jewish population supports genetic drift over selection | Q24532103 | ||
| A High-Density Admixture Map for Disease Gene Discovery in African Americans | Q24533390 | ||
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| A haplotype map of the human genome | Q24679827 | ||
| A simple and improved correction for population stratification in case-control studies | Q35752599 | ||
| Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals | Q40206193 | ||
| Do Ashkenazi Jews have a higher than expected cancer burden? Implications for cancer control prioritization efforts | Q40701901 | ||
| Synthetic Maps of Human Gene Frequencies in Europeans | Q40927811 | ||
| Shifts in angiotensin I converting enzyme insertion allele frequency across Europe: implications for Alzheimer's disease risk | Q42707507 | ||
| A genetic profile of contemporary Jewish populations | Q47596505 | ||
| Demonstrating stratification in a European American population | Q57418313 | ||
| Measuring European population stratification with microarray genotype data | Q24682611 | ||
| Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
| Population structure in the Mediterranean basin: a Y chromosome perspective | Q28235513 | ||
| A genome-wide association study identifies IL23R as an inflammatory bowel disease gene | Q28270603 | ||
| SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans | Q28287208 | ||
| Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data | Q28943545 | ||
| Genomic control for association studies | Q29547213 | ||
| Population structure, differential bias and genomic control in a large-scale, case-control association study | Q29614945 | ||
| Chip-based genotyping by mass spectrometry | Q30761976 | ||
| Association mapping in structured populations | Q33903172 | ||
| Lactase haplotype diversity in the Old World | Q34043700 | ||
| Sequences associated with human iris pigmentation. | Q34287539 | ||
| Large-scale SNP analysis reveals clustered and continuous patterns of human genetic variation | Q34432345 | ||
| Coronary heart disease incidence in northern and southern European populations: a reanalysis of the seven countries study for a European coronary risk chart | Q35567095 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | e236 | |
| P577 | publication date | 2007-11-19 | |
| P1433 | published in | PLOS Genetics | Q1893441 |
| P1476 | title | Discerning the ancestry of European Americans in genetic association studies | |
| P478 | volume | 4 |
| Q34075621 | A Map of Copy Number Variations in Chinese Populations |
| Q36528988 | A Method for Inferring an Individual's Genetic Ancestry and Degree of Admixture Associated with Six Major Continental Populations |
| Q42622030 | A common cortactin gene variation confers differential susceptibility to severe asthma |
| Q40145037 | A comparison of DMET Plus microarray and genome-wide technologies by assessing population substructure |
| Q36439842 | A comprehensive genetic approach for improving prediction of skin cancer risk in humans |
| Q48243404 | A functional variant in the 3'-UTR of angiopoietin-1 might reduce stroke risk by interfering with the binding efficiency of microRNA 211. |
| Q33894914 | A genetic risk score combining ten psoriasis risk loci improves disease prediction |
| Q35909380 | A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex |
| Q21183899 | A genome-wide genetic signature of Jewish ancestry perfectly separates individuals with and without full Jewish ancestry in a large random sample of European Americans |
| Q28943492 | A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci |
| Q35208836 | A geographic cline of skull and brain morphology among individuals of European Ancestry |
| Q27487536 | A globally occurring indel polymorphism in the promoter of the IFNA2 gene is not associated with severity of malaria but with the positivity rate of HCV |
| Q37058530 | A minimum set of ancestry informative markers for determining admixture proportions in a mixed American population: the Brazilian set |
| Q37493049 | A panel of ancestry informative markers to estimate and correct potential effects of population stratification in Han Chinese |
| Q37895389 | A review of software for microarray genotyping |
| Q36916494 | A small number of candidate gene SNPs reveal continental ancestry in African Americans. |
| Q24632742 | A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels |
| Q24632067 | Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry |
| Q30358860 | Absence of population structure across elevational gradients despite large phenotypic variation in mountain chickadees (Poecile gambeli). |
| Q34598361 | Accounting for ancestry: population substructure and genome-wide association studies |
| Q21283815 | Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies |
| Q35067645 | Alpha1‐antitrypsin deficiency–related alleles Z and S and the risk of Wegener's granulomatosis |
| Q33486736 | An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels |
| Q33484433 | An assessment of the portability of ancestry informative markers between human populations |
| Q33401217 | An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European population |
| Q44675584 | An integrated analysis of the association between Ts gene polymorphisms and clinical outcome in gastric and colorectal cancer patients treated with 5-FU-based regimens |
| Q38113566 | An overview of STRUCTURE: applications, parameter settings, and supporting software |
| Q30000838 | An overview of the genetic structure within the Italian population from genome-wide data |
| Q21562489 | Analysis of East Asia genetic substructure using genome-wide SNP arrays |
| Q30840823 | Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping |
| Q33747836 | Ancestral Informative Marker Selection and Population Structure Visualization Using Sparse Laplacian Eigenfunctions |
| Q42690314 | Ancestry inference using principal component analysis and spatial analysis: a distance-based analysis to account for population substructure |
| Q34804773 | Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America |
| Q33315565 | Application of ancestry informative markers to association studies in European Americans |
| Q43353521 | Application of highly differentiated SNPs between Japanese Black and Holstein to a breed assignment test between Japanese Black and F1 (Japanese Black x Holstein) and Holstein |
| Q34130326 | Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency |
| Q33911951 | Association of Y chromosome haplogroup I with HIV progression, and HAART outcome. |
| Q58213082 | Association study of IL10 and IL23R-IL12RB2 in Iranian patients with Behçet's disease |
| Q33614419 | Association study of serotonin pathway genes in attempted suicide |
| Q47113776 | Assortative Mating by Ethnicity in Longevous Families |
| Q33653632 | Asthma-susceptibility variants identified using probands in case-control and family-based analyses |
| Q47136309 | Between Lake Baikal and the Baltic Sea: genomic history of the gateway to Europe |
| Q36383677 | Biogeographic ancestry, self-identified race, and admixture-phenotype associations in the Heart SCORE Study |
| Q39701155 | Brazilian urban population genetic structure reveals a high degree of admixture. |
| Q33832877 | CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis |
| Q37591169 | Catechol-O-methyltransferase Val158met polymorphism interacts with early experience to predict executive functions in early childhood |
| Q26810487 | Characterizing Race/Ethnicity and Genetic Ancestry for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort |
| Q33965544 | Choice of population structure informative principal components for adjustment in a case-control study |
| Q33767014 | Clustering by genetic ancestry using genome-wide SNP data |
| Q38974312 | Clustering of 770,000 genomes reveals post-colonial population structure of North America |
| Q33728463 | CoAIMs: a cost-effective panel of ancestry informative markers for determining continental origins. |
| Q37641476 | Common variations within HACE1 gene and neuroblastoma susceptibility in a Southern Chinese population. |
| Q37352061 | Commonalities in the genetics of Alzheimer's disease and Parkinson's disease |
| Q33821390 | Comprehensive genetic assessment of a functional TLR9 promoter polymorphism: no replicable association with asthma or asthma-related phenotypes |
| Q33381588 | Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies |
| Q42163147 | Confirmation of a founder effect in a Northern European population of a new β-globin variant: HBB:c.23_26dup (codons 8/9 (+AGAA)). |
| Q35051003 | Control of Population Stratification by Correlation-Selected Principal Components |
| Q37455637 | Converging evidence for the Nogo-66 receptor gene in schizophrenia |
| Q40599766 | Detection of selective sweeps in structured populations: a comparison of recent methods |
| Q24604314 | Different differences: The use of ‘genetic ancestry’ versus race in biomedical human genetic research |
| Q56457854 | ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height |
| Q35477725 | Echoes from Sepharad: signatures on the maternal gene pool of crypto-Jewish descendants |
| Q37571405 | Empirical prediction of genomic susceptibilities for multiple cancer classes |
| Q36683768 | Environmental and genetic factors influence age at menarche in women with polycystic ovary syndrome |
| Q47427882 | Establishment of a standardized system to perform population structure analyses with limited sample size or with different sets of SNP genotypes |
| Q34270588 | European American stratification in ovarian cancer case control data: the utility of genome-wide data for inferring ancestry |
| Q30429712 | European ancestry as a risk factor for atrial fibrillation in African Americans |
| Q24648104 | European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups |
| Q37335908 | European population substructure is associated with mucocutaneous manifestations and autoantibody production in systemic lupus erythematosus |
| Q37043591 | Evaluating reported candidate gene associations with polycystic ovary syndrome |
| Q33519744 | Evaluation of self-reported ethnicity in a case-control population: the stroke prevention in young women study |
| Q30415504 | Evidence for chromosome 2p16.3 polycystic ovary syndrome susceptibility locus in affected women of European ancestry |
| Q36524374 | Explicit Modeling of Ancestry Improves Polygenic Risk Scores and BLUP Prediction |
| Q36785358 | Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia |
| Q29614705 | Fast model-based estimation of ancestry in unrelated individuals |
| Q37793706 | Fine-scale population structure and the era of next-generation sequencing. |
| Q34978887 | Fine-scaled human genetic structure revealed by SNP microarrays |
| Q24610574 | Five years of GWAS discovery |
| Q33816773 | Functional promoter variants in sphingosine 1-phosphate receptor 3 associate with susceptibility to sepsis-associated acute respiratory distress syndrome |
| Q36467059 | Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals |
| Q24644872 | Genes mirror geography within Europe |
| Q36721624 | Genes, environments, and developmental research: methods for a multi-site study of early substance abuse |
| Q35694393 | Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal. |
| Q36809691 | Genetic ancestry inference using support vector machines, and the active emergence of a unique American population |
| Q35208177 | Genetic architecture of prostate cancer in the Ashkenazi Jewish population |
| Q46913948 | Genetic association analysis of N-methyl-D-aspartate receptor subunit gene GRIN2B and clinical response to clozapine |
| Q28478042 | Genetic background of patients from a university medical center in Manhattan: implications for personalized medicine |
| Q34458840 | Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records |
| Q35714739 | Genetic contribution to multiple sclerosis risk among Ashkenazi Jews |
| Q36766616 | Genetic determinants of macular pigments in women of the Carotenoids in Age-Related Eye Disease Study |
| Q37537304 | Genetic evidence for role of carotenoids in age-related macular degeneration in the Carotenoids in Age-Related Eye Disease Study (CAREDS). |
| Q92705854 | Genetic history of the population of Crete |
| Q60935312 | Genetic legacy of state centralization in the Kuba Kingdom of the Democratic Republic of the Congo |
| Q37443227 | Genetic polymorphisms of peptidase inhibitor 3 (elafin) are associated with acute respiratory distress syndrome |
| Q28732735 | Genetic signatures of exceptional longevity in humans |
| Q21143785 | Genetic structure of Europeans: a view from the North-East |
| Q33586898 | Genetic structure of the Spanish population. |
| Q40205805 | Genetic variants associated with susceptibility of Ashkenazi Jews to West Nile virus infection. |
| Q34455341 | Genetic variation of DKK3 may modify renal disease severity in ADPKD. |
| Q28267312 | Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers |
| Q27438161 | Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe |
| Q33851563 | Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits |
| Q35138418 | Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin. |
| Q33838241 | Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE |
| Q24550632 | Genome-wide association studies for complex traits: consensus, uncertainty and challenges |
| Q21560748 | Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations |
| Q35030975 | Genome-wide association study confirms extant PD risk loci among the Dutch |
| Q28248384 | Genome-wide association study identifies five new schizophrenia loci |
| Q28943289 | Genome-wide association study implicates PARD3B-based AIDS restriction |
| Q21147078 | Genome-wide insights into the patterns and determinants of fine-scale population structure in humans |
| Q31158833 | Genome-wide methylation data mirror ancestry information |
| Q21283811 | Genomic microsatellites identify shared Jewish ancestry intermediate between Middle Eastern and European populations |
| Q28486019 | Genotype-based ancestral background consistently predicts efficacy and side effects across treatments in CATIE and STAR*D |
| Q38375215 | Geographic substructure in craniometric estimates of admixture for contemporary American populations |
| Q37176308 | Geographical structure and differential natural selection among North European populations |
| Q33739524 | High mammographic density in women of Ashkenazi Jewish descent. |
| Q34145740 | High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency. |
| Q92528008 | High-resolution inference of genetic relationships among Jewish populations |
| Q59336766 | Human ancestry indentification under resource constraints -- what can one chromosome tell us about human biogeographical ancestry? |
| Q33794200 | Human embryonic stem cells from aneuploid blastocysts identified by pre-implantation genetic screening |
| Q35255077 | IGF-1 gene polymorphisms in Polish families with high-grade myopia |
| Q33603693 | Identification of population substructure among Jews using STR markers and dependence on reference populations included |
| Q57249724 | Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans |
| Q28275237 | Identification of ten loci associated with height highlights new biological pathways in human growth |
| Q44469372 | Impact of population substructure on trend tests for genetic case-control association studies |
| Q21184013 | Implications for health and disease in the genetic signature of the Ashkenazi Jewish population |
| Q36865877 | Improved ancestry inference using weights from external reference panels |
| Q38375854 | Including additional controls from public databases improves the power of a genome-wide association study |
| Q36976071 | Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel |
| Q33678719 | Inferring geographic coordinates of origin for Europeans using small panels of ancestry informative markers |
| Q33569169 | Insulin Resistance and the Polycystic Ovary Syndrome Revisited: An Update on Mechanisms and Implications |
| Q37140897 | Insulin-like growth factor-1- and interleukin-6-related gene variation and risk of multiple myeloma |
| Q36260421 | Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies |
| Q34354618 | Integrative analysis of single nucleotide polymorphisms and gene expression efficiently distinguishes samples from closely related ethnic populations |
| Q37137046 | Interaction Between Two Cholesterol Metabolism Genes Influences Memory: Findings from the Wisconsin Registry for Alzheimer's Prevention |
| Q44199896 | Investigation of the fine structure of European populations with applications to disease association studies |
| Q37380101 | Is the observed association between dairy intake and fibroids in African Americans explained by genetic ancestry? |
| Q30419436 | Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci |
| Q30425020 | Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci |
| Q36376710 | Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array |
| Q24643421 | MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis |
| Q33525039 | Magnitude of stratification in human populations and impacts on genome wide association studies |
| Q36356924 | Mapping the genetic diversity of HLA haplotypes in the Japanese populations |
| Q34458862 | Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height |
| Q36183352 | Meta-analysis of genetic polymorphisms in granulomatosis with polyangiitis (Wegener's) reveals shared susceptibility loci with rheumatoid arthritis |
| Q24642565 | Mitochondrial DNA haplogroups influence AIDS progression |
| Q43405341 | Modeling geographic risk of complex congenital heart defects in Eastern Wisconsin |
| Q57129465 | Multiple correspondence discriminant analysis: An application to detect stratification in copy number variation |
| Q57697549 | No association between genetic ancestry and susceptibility to asthma or atopy in Canary Islanders |
| Q21091050 | North African influences and potential bias in case-control association studies in the Spanish population |
| Q33349442 | Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women |
| Q36615898 | Novel loci and pathways significantly associated with longevity |
| Q24630531 | Nurses transforming health care using genetics and genomics |
| Q34759018 | PNPLA3 variants specifically confer increased risk for histologic nonalcoholic fatty liver disease but not metabolic disease |
| Q47224421 | POPSTR: Inference of Admixed Population Structure Based on Single-Nucleotide Polymorphisms and Copy Number Variations |
| Q51604912 | PTPN22 C1858T and the risk of psoriasis: a meta-analysis |
| Q36716040 | Perspectives in Polycystic Ovary Syndrome: From Hair to Eternity |
| Q34204647 | Perspectives on Human Population Structure at the Cusp of the Sequencing Era |
| Q33896815 | Pitfalls of predicting complex traits from SNPs |
| Q55005493 | Planning the human variome project: the Spain report. |
| Q35177861 | Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients |
| Q36920069 | Polycystic ovary syndrome is not associated with genetic variants that mark risk of type 2 diabetes |
| Q39682956 | Population differentiation as a test for selective sweeps |
| Q35098240 | Population stratification and patterns of linkage disequilibrium |
| Q30424048 | Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset |
| Q33348644 | Population substructure and control selection in genome-wide association studies |
| Q33886401 | Predicting Diabetic Nephropathy Using a Multifactorial Genetic Model |
| Q34544496 | Principal-component analysis for assessment of population stratification in mitochondrial medical genetics |
| Q33519218 | Principal-component-based population structure adjustment in the North American Rheumatoid Arthritis Consortium data: impact of single-nucleotide polymorphism set and analysis method |
| Q36032642 | Protective effect of human endogenous retrovirus K dUTPase variants on psoriasis susceptibility |
| Q39219360 | Psoriasis risk SNPs and their association with HIV-1 control |
| Q33539723 | Rapid assessment of genetic ancestry in populations of unknown origin by genome-wide genotyping of pooled samples |
| Q28238782 | Recent advances in the genetics of autoimmune disease |
| Q39353137 | Relationship between polycystic ovary syndrome and ancestry in European Americans |
| Q37026820 | Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility |
| Q33519292 | Replication of recently identified associated single-nucleotide polymorphisms from six autoimmune diseases in Genetic Analysis Workshop 16 rheumatoid arthritis data |
| Q37315484 | Rheumatoid arthritis: a view of the current genetic landscape |
| Q37179785 | Searching for disease susceptibility variants in structured populations |
| Q30151263 | Secular change of sexually dimorphic cranial variables in Euro-Americans and Germans |
| Q34184913 | Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins |
| Q57192890 | Sex Differences in Genetic Associations With Longevity |
| Q42360748 | Shared polymorphisms and modifiable behavior factors for myocardial infarction and high cholesterol in a retrospective population study |
| Q50485708 | Simultaneous purifying selection on the ancestral MC1R allele and positive selection on the melanoma-risk allele V60L in south Europeans |
| Q37273694 | Single nucleotide polymorphism arrays: a decade of biological, computational and technological advances |
| Q36680666 | Sparse principal component analysis for identifying ancestry-informative markers in genome-wide association studies |
| Q36337875 | Structured mating: Patterns and implications |
| Q53950127 | Testing the null hypothesis: comments on 'Culture-gene coevolution of individualism-collectivism and the serotonin transporter gene'. |
| Q24615900 | The GenoChip: a new tool for genetic anthropology |
| Q37397644 | The KCNJ8-S422L variant previously associated with J-wave syndromes is found at an increased frequency in Ashkenazi Jews |
| Q34994823 | The MYH9/APOL1 region and chronic kidney disease in European-Americans |
| Q24606475 | The Missing Link of Jewish European Ancestry: Contrasting the Rhineland and the Khazarian Hypotheses |
| Q37072688 | The TRIB3 Q84R polymorphism and risk of early-onset type 2 diabetes |
| Q26722302 | The fine-scale genetic structure of the British population |
| Q28754746 | The genome-wide patterns of variation expose significant substructure in a founder population |
| Q28284600 | The genome-wide structure of the Jewish people |
| Q21090210 | The impact of divergence time on the nature of population structure: an example from Iceland |
| Q30407754 | The inflammatory gene pathway is not a major contributor to polycystic ovary snydrome |
| Q33700373 | Theoretical Formulation of Principal Components Analysis to Detect and Correct for Population Stratification |
| Q33471464 | Toll-like receptor polymorphisms and susceptibility to urinary tract infections in adult women |
| Q28749149 | Toward a more uniform sampling of human genetic diversity: a survey of worldwide populations by high-density genotyping |
| Q33370082 | Tracing sub-structure in the European American population with PCA-informative markers |
| Q92548390 | Transcriptome variation in human populations and its potential application in forensics |
| Q58797706 | Transcriptomic population markers for human population discrimination |
| Q37693206 | Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription |
| Q35684795 | Type 2 deiodinase and host responses of sepsis and acute lung injury |
| Q39960259 | Ulcerative Colitis Is Under Dual (Mitochondrial and Nuclear) Genetic Control. |
| Q33515702 | Variation in genetic admixture and population structure among Latinos: the Los Angeles Latino eye study (LALES). |
| Q33692217 | Variation in oxytocin receptor gene (OXTR) polymorphisms is associated with emotional and behavioral reactions to betrayal |
| Q35026214 | Venous thromboembolism and varicose veins share familial susceptibility: a nationwide family study in Sweden |
| Q36464400 | Vitamin D intake and season modify the effects of the GC and CYP2R1 genes on 25-hydroxyvitamin D concentrations |
| Q38890726 | What Ancestry Can Tell Us About the Genetic Origins of Inter-Ethnic Differences in Asthma Expression |
| Q42078668 | hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets |
Search more.