| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1025091010 |
| P356 | DOI | 10.1186/GB-2010-11-1-R10 |
| P932 | PMC publication ID | 2847713 |
| P698 | PubMed publication ID | 20109212 |
| P5875 | ResearchGate publication ID | 41172533 |
| P50 | author | Marcus W. Feldman | Q15989759 |
| Devin Absher | Q29840829 | ||
| P2093 | author name string | Jun Z Li | |
| Richard Myers | |||
| Sohini Ramachandran | |||
| Amanda M Casto | |||
| P2860 | cites work | Sex-biased evolutionary forces shape genomic patterns of human diversity | Q21090214 |
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| dbSNP: the NCBI database of genetic variation | Q24608672 | ||
| TRPC channel activation by extracellular thioredoxin | Q24650851 | ||
| Signals of recent positive selection in a worldwide sample of human populations | Q24651949 | ||
| Accelerated genetic drift on chromosome X during the human dispersal out of Africa | Q24655578 | ||
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| Natural selection has driven population differentiation in modern humans | Q28267194 | ||
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| Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse | Q28297185 | ||
| Evidence for positive selection on Protocadherin Y gene in Homo sapiens: implications for schizophrenia | Q28298071 | ||
| DNA synthesis and neuronal apoptosis caused by familial Alzheimer disease mutants of the amyloid precursor protein are mediated by the p21 activated kinase PAK3 | Q28573591 | ||
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| Extensive linkage disequilibrium, a common 16.7-kilobase deletion, and evidence of balancing selection in the human protocadherin alpha cluster | Q33904511 | ||
| The X chromosome in population genetics | Q34288109 | ||
| Estimation of individual admixture: analytical and study design considerations | Q34394604 | ||
| Ethnic-affiliation estimation by use of population-specific DNA markers | Q34421878 | ||
| Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia | Q34557770 | ||
| Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness | Q34976269 | ||
| Robustness of the inference of human population structure: a comparison of X-chromosomal and autosomal microsatellites | Q36474733 | ||
| Genetic risk factors in male infertility | Q36870998 | ||
| Extranigral neurodegeneration in Parkinson's disease | Q39920071 | ||
| Evaluating signatures of sex-specific processes in the human genome | Q42591451 | ||
| A comparative expression analysis of four MRX genes regulating intracellular signalling via small GTPases | Q48117476 | ||
| Searching for evidence of positive selection in the human genome using patterns of microsatellite variability | Q49017216 | ||
| EDA2R is associated with androgenetic alopecia. | Q51574039 | ||
| PAK3 related mental disability: further characterization of the phenotype | Q81245890 | ||
| ARHGEF9 disruption in a female patient is associated with X linked mental retardation and sensory hyperarousal | Q81347149 | ||
| P433 | issue | 1 | |
| P304 | page(s) | R10 | |
| P577 | publication date | 2010-01-28 | |
| P1433 | published in | Genome Biology | Q5533480 |
| P1476 | title | Characterization of X-linked SNP genotypic variation in globally distributed human populations | |
| P478 | volume | 11 |
| Q57083810 | A method for the analysis of 32 X chromosome insertion deletion polymorphisms in a single PCR |
| Q35132109 | Analyses of X-linked and autosomal genetic variation in population-scale whole genome sequencing |
| Q34471605 | Autosomal admixture levels are informative about sex bias in admixed populations |
| Q36050114 | Beyond 2/3 and 1/3: The Complex Signatures of Sex-Biased Admixture on the X Chromosome |
| Q54993990 | Contrasting Patterns of Genomic Diversity Reveal Accelerated Genetic Drift but Reduced Directional Selection on X-Chromosome in Wild and Domestic Sheep Species. |
| Q34000898 | Contrasting X-linked and autosomal diversity across 14 human populations |
| Q34381812 | Estimators of the human effective sex ratio detect sex biases on different timescales |
| Q30792009 | Exploring the occurrence of classic selective sweeps in humans using whole-genome sequencing data sets |
| Q28066294 | Explosive genetic evidence for explosive human population growth |
| Q55354280 | Genetic Differentiation of North-East Argentina Populations Based on 30 Binary X Chromosome Markers. |
| Q33799136 | Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations? |
| Q37945702 | Joint analysis of demography and selection in population genetics: where do we stand and where could we go? |
| Q33762290 | Looking for signatures of sex-specific demography and local adaptation on the X chromosome |
| Q51701612 | Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements. |
| Q49980704 | Paternal lineage early onset hereditary ovarian cancers: A Familial Ovarian Cancer Registry study |
| Q22951230 | READemption-a tool for the computational analysis of deep-sequencing-based transcriptome data |
| Q45140506 | Refining the genetic portrait of Portuguese Roma through X-chromosomal markers |
| Q37596588 | Sex-linked and autosomal microsatellites provide new insights into island populations of the tammar wallaby. |
| Q90190593 | The inference of sex-biased human demography from whole-genome data |
| Q28661452 | X-linked MTMR8 diversity and evolutionary history of sub-Saharan populations |
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