Pages that link to "Q24548130"
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The following pages link to Estimate of the mutation rate per nucleotide in humans (Q24548130):
Displaying 50 items.
- Sex-biased evolutionary forces shape genomic patterns of human diversity (Q21090214) (← links)
- High-Throughput Sequencing of Three Lemnoideae (Duckweeds) Chloroplast Genomes from Total DNA (Q21135218) (← links)
- Forces shaping the fastest evolving regions in the human genome (Q21145252) (← links)
- Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history (Q21145273) (← links)
- Continued colonization of the human genome by mitochondrial DNA (Q21146409) (← links)
- Duplication and relocation of the functional DPY19L2 gene within low copy repeats (Q21266579) (← links)
- Calculating expected DNA remnants from ancient founding events in human population genetics (Q21283776) (← links)
- Complex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humans (Q21283863) (← links)
- The ups and downs of mutation frequencies during aging can account for the Apert syndrome paternal age effect (Q21563340) (← links)
- Deterministic mutation rate variation in the human genome (Q22065757) (← links)
- Analysis of genetic inheritance in a family quartet by whole-genome sequencing (Q22065898) (← links)
- Variation in genome-wide mutation rates within and between human families (Q22122055) (← links)
- Are rare variants responsible for susceptibility to complex diseases? (Q22337172) (← links)
- Heterozygous mutations of OTX2 cause severe ocular malformations (Q24530768) (← links)
- Genomic divergences between humans and other hominoids and the effective population size of the common ancestor of humans and chimpanzees (Q24535718) (← links)
- Likelihood and Bayes estimation of ancestral population sizes in hominoids using data from multiple loci (Q24543216) (← links)
- Nucleotide variation at Msn and Alas2, two genes flanking the centromere of the X chromosome in humans (Q24545685) (← links)
- A revised root for the human Y chromosomal phylogenetic tree: the origin of patrilineal diversity in Africa (Q24616008) (← links)
- A map of human genome variation from population-scale sequencing (Q24617794) (← links)
- Direct measure of the de novo mutation rate in autism and schizophrenia cohorts (Q24618002) (← links)
- Estimating the human mutation rate using autozygosity in a founder population (Q24622247) (← links)
- Mobile elements reveal small population size in the ancient ancestors of Homo sapiens (Q24630088) (← links)
- Rate of de novo mutations and the importance of father's age to disease risk (Q24632353) (← links)
- Rates and fitness consequences of new mutations in humans (Q24633781) (← links)
- The amino-acid mutational spectrum of human genetic disease (Q24793270) (← links)
- Whole-genome screening indicates a possible burst of formation of processed pseudogenes and Alu repeats by particular L1 subfamilies in ancestral primates (Q24793332) (← links)
- Gene conversion homogenizes the CMT1A paralogous repeats (Q24797658) (← links)
- PAX6 mutations: genotype-phenotype correlations (Q24810863) (← links)
- Genomic rearrangements by LINE-1 insertion-mediated deletion in the human and chimpanzee lineages (Q24813998) (← links)
- Uncertainty principle of genetic information in a living cell (Q24815727) (← links)
- MAOA haplotypes associated with thrombocyte-MAO activity (Q24816706) (← links)
- Molecular Signatures of Natural Selection for Polymorphic Genes of the Human Dopaminergic and Serotonergic Systems: A Review (Q26745243) (← links)
- Influence of paternal preconception exposures on their offspring: through epigenetics to phenotype (Q26747589) (← links)
- Factors influencing the effect size distribution of adaptive substitutions (Q26751053) (← links)
- Fifteen years of genomewide scans for selection: trends, lessons and unaddressed genetic sources of complication (Q26801693) (← links)
- The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and function (Q26821785) (← links)
- Breaking bad: The mutagenic effect of DNA repair (Q26827700) (← links)
- Epigenetic inheritance: a contributor to species differentiation? (Q26830614) (← links)
- Child development and molecular genetics: 14 years later (Q26853446) (← links)
- Creating diseases to understand what prevents them: genetic analysis of inflammation in the gastrointestinal tract (Q26861393) (← links)
- Comparing algorithms that reconstruct cell lineage trees utilizing information on microsatellite mutations (Q27324018) (← links)
- Early Neolithic genomes from the eastern Fertile Crescent (Q27480266) (← links)
- Selection on Human Genes as Revealed by Comparisons to Chimpanzee cDNA (Q28202148) (← links)
- Paternal age effect mutations and selfish spermatogonial selection: causes and consequences for human disease (Q28259472) (← links)
- Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation (Q28263098) (← links)
- Y-chromosome evidence of southern origin of the East Asian-specific haplogroup O3-M122 (Q28265715) (← links)
- Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis (Q28270878) (← links)
- Transition-transversion bias is not universal: a counter example from grasshopper pseudogenes (Q28469124) (← links)
- Positive selection for new disease mutations in the human germline: evidence from the heritable cancer syndrome multiple endocrine neoplasia type 2B (Q28480870) (← links)
- Mitotic evolution of Plasmodium falciparum shows a stable core genome but recombination in antigen families (Q28486079) (← links)