Human genetic variation
No two humans are genetically identical. Even monozygotic twins (who develop from one zygote) have infrequent genetic differences due to mutations occurring during development and gene copy-number variation. Differences between individuals, even closely related individuals, are the key to techniques such as genetic fingerprinting. As of 2017, there are a total of 324 million known variants from sequenced human genomes. As of 2015, the typical difference between the genomes of two individuals was estimated at 20 million base pairs (or 0.6% of the total of 3.2 billion base pairs).
Alleles occur at different frequencies in different human populations. Populations that are more geographically and ancestrally remote tend to differ more. The differences between populations represent a small proportion of overall human genetic variation. Populations also differ in the quantity of variation among their members. The greatest divergence between populations is found in sub-Saharan Africa, consistent with the recent African origin of non-African populations. Populations also vary in the proportion and locus of introgressed genes they received by archaic admixture both inside and outside of Africa.
The study of human genetic variation has evolutionary significance and medical applications. It can help scientists understand ancient human population migrations as well as how human groups are biologically related to one another. For medicine, study of human genetic variation may be important because some disease-causing alleles occur more often in people from specific geographic regions. New findings show that each human has on average 60 new mutations compared to their parents.
Causes of variationEdit
Causes of differences between individuals include independent assortment, the exchange of genes (crossing over and recombination) during reproduction (through meiosis) and various mutational events.
There are at least three reasons why genetic variation exists between populations. Natural selection may confer an adaptive advantage to individuals in a specific environment if an allele provides a competitive advantage. Alleles under selection are likely to occur only in those geographic regions where they confer an advantage. A second important process is genetic drift, which is the effect of random changes in the gene pool, under conditions where most mutations are neutral (that is, they do not appear to have any positive or negative selective effect on the organism). Finally, small migrant populations have statistical differences - called the founder effect - from the overall populations where they originated; when these migrants settle new areas, their descendant population typically differs from their population of origin: different genes predominate and it is less genetically diverse.
In humans, the main cause is genetic drift. Serial founder effects and past small population size (increasing the likelihood of genetic drift) may have had an important influence in neutral differences between populations. The second main cause of genetic variation is due to the high degree of neutrality of most mutations. A small, but significant number of genes appear to have undergone recent natural selection, and these selective pressures are sometimes specific to one region.
Measures of variationEdit
Genetic variation among humans occurs on many scales, from gross alterations in the human karyotype to single nucleotide changes. Chromosome abnormalities are detected in 1 of 160 live human births. Apart from sex chromosome disorders, most cases of aneuploidy result in death of the developing fetus (miscarriage); the most common extra autosomal chromosomes among live births are 21, 18 and 13.
Nucleotide diversity is the average proportion of nucleotides that differ between two individuals. As of 2004, the human nucleotide diversity was estimated to be 0.1% to 0.4% of base pairs. In 2015, the 1000 Genomes Project, which sequenced one thousand individuals from 26 human populations, found that "a typical [individual] genome differs from the reference human genome at 4.1 million to 5.0 million sites … affecting 20 million bases of sequence"; the latter figure corresponds to 0.6% of total number of base pairs. Nearly all (>99.9%) of these sites are small differences, either single nucleotide polymorphisms or brief insertions or deletions (indels) in the genetic sequence, but structural variations account for a greater number of base-pairs than the SNPs and indels.
Single nucleotide polymorphismsEdit
A single nucleotide polymorphism (SNP) is a difference in a single nucleotide between members of one species that occurs in at least 1% of the population. The 2,504 individuals characterized by the 1000 Genomes Project had 84.7 million SNPs among them. SNPs are the most common type of sequence variation, estimated in 1998 to account for 90% of all sequence variants. Other sequence variations are single base exchanges, deletions and insertions. SNPs occur on average about every 100 to 300 bases and so are the major source of heterogeneity.
A functional, or non-synonymous, SNP is one that affects some factor such as gene splicing or messenger RNA, and so causes a phenotypic difference between members of the species. About 3% to 5% of human SNPs are functional (see International HapMap Project). Neutral, or synonymous SNPs are still useful as genetic markers in genome-wide association studies, because of their sheer number and the stable inheritance over generations.
A coding SNP is one that occurs inside a gene. There are 105 Human Reference SNPs that result in premature stop codons in 103 genes. This corresponds to 0.5% of coding SNPs. They occur due to segmental duplication in the genome. These SNPs result in loss of protein, yet all these SNP alleles are common and are not purified in negative selection.
Structural variation is the variation in structure of an organism's chromosome. Structural variations, such as copy-number variation and deletions, inversions, insertions and duplications, account for much more human genetic variation than single nucleotide diversity. This was concluded in 2007 from analysis of the diploid full sequences of the genomes of two humans: Craig Venter and James D. Watson. This added to the two haploid sequences which were amalgamations of sequences from many individuals, published by the Human Genome Project and Celera Genomics respectively.
According to the 1000 Genomes Project, a typical human has 2,100 to 2,500 structural variations, which include approximately 1,000 large deletions, 160 copy-number variants, 915 Alu insertions, 128 L1 insertions, 51 SVA insertions, 4 NUMTs, and 10 inversions.
Copy number variationEdit
A copy-number variation (CNV) is a difference in the genome due to deleting or duplicating large regions of DNA on some chromosome. It is estimated that 0.4% of the genomes of unrelated humans differ with respect to copy number. When copy number variation is included, human-to-human genetic variation is estimated to be at least 0.5% (99.5% similarity). Copy number variations are inherited but can also arise during development.
Epigenetic variation is variation in the chemical tags that attach to DNA and affect how genes get read. The tags, "called epigenetic markings, act as switches that control how genes can be read." At some alleles, the epigenetic state of the DNA, and associated phenotype, can be inherited across generations of individuals.
Genetic variability is a measure of the tendency of individual genotypes in a population to vary (become different) from one another. Variability is different from genetic diversity, which is the amount of variation seen in a particular population. The variability of a trait is how much that trait tends to vary in response to environmental and genetic influences.
In biology, a cline is a continuum of species, populations, varieties, or forms of organisms that exhibit gradual phenotypic and/or genetic differences over a geographical area, typically as a result of environmental heterogeneity. In the scientific study of human genetic variation, a gene cline can be rigorously defined and subjected to quantitative metrics.
In the study of molecular evolution, a haplogroup is a group of similar haplotypes that share a common ancestor with a single nucleotide polymorphism (SNP) mutation. Haplogroups pertain to deep ancestral origins dating back thousands of years.
The most commonly studied human haplogroups are Y-chromosome (Y-DNA) haplogroups and mitochondrial DNA (mtDNA) haplogroups, both of which can be used to define genetic populations. Y-DNA is passed solely along the patrilineal line, from father to son, while mtDNA is passed down the matrilineal line, from mother to both daughter or son. The Y-DNA and mtDNA may change by chance mutation at each generation.
Variable number tandem repeatsEdit
A variable number tandem repeat (VNTR) is the variation of length of a tandem repeat. A tandem repeat is the adjacent repetition of a short nucleotide sequence. Tandem repeats exist on many chromosomes, and their length varies between individuals. Each variant acts as an inherited allele, so they are used for personal or parental identification. Their analysis is useful in genetics and biology research, forensics, and DNA fingerprinting.
History and geographic distributionEdit
Recent African origin of modern humansEdit
The recent African origin of modern humans paradigm assumes the dispersal of non-African populations of anatomically modern humans after 70,000 years ago. Dispersal within Africa occurred significantly earlier, at least 130,000 years ago. The "out of Africa" theory originates in the 19th century, as a tentative suggestion in Charles Darwin's Descent of Man, but remained speculative until the 1980s when it was supported by study of present-day mitochondrial DNA, combined with evidence from physical anthropology of archaic specimens.
According to a 2000 study of Y-chromosome sequence variation, human Y-chromosomes trace ancestry to Africa, and the descendants of the derived lineage left Africa and eventually were replaced by archaic human Y-chromosomes in Eurasia. The study also shows that a minority of contemporary populations in East Africa and the Khoisan are the descendants of the most ancestral patrilineages of anatomically modern humans that left Africa 35,000 to 89,000 years ago. Other evidence supporting the theory is that variations in skull measurements decrease with distance from Africa at the same rate as the decrease in genetic diversity. Human genetic diversity decreases in native populations with migratory distance from Africa, and this is thought to be due to bottlenecks during human migration, which are events that temporarily reduce population size.
A 2009 genetic clustering study, which genotyped 1327 polymorphic markers in various African populations, identified six ancestral clusters. The clustering corresponded closely with ethnicity, culture and language. A 2018 whole genome sequencing study of the world's populations observed similar clusters among the populations in Africa. At K=9, distinct ancestral components defined the Afroasiatic-speaking populations inhabiting North Africa and Northeast Africa; the Nilo-Saharan-speaking populations in Northeast Africa and East Africa; the Ari populations in Northeast Africa; the Niger-Congo-speaking populations in West-Central Africa, West Africa, East Africa and Southern Africa; the Pygmy populations in Central Africa; and the Khoisan populations in Southern Africa.
Because of the common ancestry of all humans, only a small number of variants have large differences in frequency between populations. However, some rare variants in the world's human population are much more frequent in at least one population (more than 5%).
It is commonly assumed that early humans left Africa, and thus must have passed through a population bottleneck before their African-Eurasian divergence around 100,000 years ago (ca. 3,000 generations). The rapid expansion of a previously small population has two important effects on the distribution of genetic variation. First, the so-called founder effect occurs when founder populations bring only a subset of the genetic variation from their ancestral population. Second, as founders become more geographically separated, the probability that two individuals from different founder populations will mate becomes smaller. The effect of this assortative mating is to reduce gene flow between geographical groups and to increase the genetic distance between groups.
The expansion of humans from Africa affected the distribution of genetic variation in two other ways. First, smaller (founder) populations experience greater genetic drift because of increased fluctuations in neutral polymorphisms. Second, new polymorphisms that arose in one group were less likely to be transmitted to other groups as gene flow was restricted.
Populations in Africa tend to have lower amounts of linkage disequilibrium than do populations outside Africa, partly because of the larger size of human populations in Africa over the course of human history and partly because the number of modern humans who left Africa to colonize the rest of the world appears to have been relatively low. In contrast, populations that have undergone dramatic size reductions or rapid expansions in the past and populations formed by the mixture of previously separate ancestral groups can have unusually high levels of linkage disequilibrium
Distribution of variationEdit
The distribution of genetic variants within and among human populations are impossible to describe succinctly because of the difficulty of defining a "population," the clinal nature of variation, and heterogeneity across the genome (Long and Kittles 2003). In general, however, an average of 85% of genetic variation exists within local populations, ~7% is between local populations within the same continent, and ~8% of variation occurs between large groups living on different continents. The recent African origin theory for humans would predict that in Africa there exists a great deal more diversity than elsewhere and that diversity should decrease the further from Africa a population is sampled.
Sub-Saharan Africa has the most human genetic diversity and the same has been shown to hold true for phenotypic variation in skull form. Phenotype is connected to genotype through gene expression. Genetic diversity decreases smoothly with migratory distance from that region, which many scientists believe to be the origin of modern humans, and that decrease is mirrored by a decrease in phenotypic variation. Skull measurements are an example of a physical attribute whose within-population variation decreases with distance from Africa.
The distribution of many physical traits resembles the distribution of genetic variation within and between human populations (American Association of Physical Anthropologists 1996; Keita and Kittles 1997). For example, ~90% of the variation in human head shapes occurs within continental groups, and ~10% separates groups, with a greater variability of head shape among individuals with recent African ancestors (Relethford 2002).
A prominent exception to the common distribution of physical characteristics within and among groups is skin color. Approximately 10% of the variance in skin color occurs within groups, and ~90% occurs between groups (Relethford 2002). This distribution of skin color and its geographic patterning — with people whose ancestors lived predominantly near the equator having darker skin than those with ancestors who lived predominantly in higher latitudes — indicate that this attribute has been under strong selective pressure. Darker skin appears to be strongly selected for in equatorial regions to prevent sunburn, skin cancer, the photolysis of folate, and damage to sweat glands.
Understanding how genetic diversity in the human population impacts various levels of gene expression is an active area of research. While earlier studies focused on the relationship between DNA variation and RNA expression, more recent efforts are characterizing the genetic control of various aspects of gene expression including chromatin states, translation, and protein levels. A study published in 2007 found that 25% of genes showed different levels of gene expression between populations of European and Asian descent. The primary cause of this difference in gene expression was thought to be SNPs in gene regulatory regions of DNA. Another study published in 2007 found that approximately 83% of genes were expressed at different levels among individuals and about 17% between populations of European and African descent.
Wright's Fixation index as measure of variationEdit
The population geneticist Sewall Wright developed the fixation index (often abbreviated to FST) as a way of measuring genetic differences between populations. This statistic is often used in taxonomy to compare differences between any two given populations by measuring the genetic differences among and between populations for individual genes, or for many genes simultaneously. It is often stated that the fixation index for humans is about 0.15. This translates to an estimated 85% of the variation measured in the overall human population is found within individuals of the same population, and about 15% of the variation occurs between populations. These estimates imply that any two individuals from different populations are almost as likely to be more similar to each other than either is to a member of their own group. "The shared evolutionary history of living humans has resulted in a high relatedness among all living people, as indicated for example by the very low fixation index (FST) among living human populations." Richard Lewontin, who affirmed these ratios, thus concluded neither "race" nor "subspecies" were appropriate or useful ways to describe human populations.
Wright himself believed that values >0.25 represent very great genetic variation and that an FST of 0.15–0.25 represented great variation. However, about 5% of human variation occurs between populations within continents, therefore FST values between continental groups of humans (or races) of as low as 0.1 (or possibly lower) have been found in some studies, suggesting more moderate levels of genetic variation. Graves (1996) has countered that FST should not be used as a marker of subspecies status, as the statistic is used to measure the degree of differentiation between populations, although see also Wright (1978).
Jeffrey Long and Rick Kittles give a long critique of the application of FST to human populations in their 2003 paper "Human Genetic Diversity and the Nonexistence of Biological Races". They find that the figure of 85% is misleading because it implies that all human populations contain on average 85% of all genetic diversity. They argue the underlying statistical model incorrectly assumes equal and independent histories of variation for each large human population. A more realistic approach is to understand that some human groups are parental to other groups and that these groups represent paraphyletic groups to their descent groups. For example, under the recent African origin theory the human population in Africa is paraphyletic to all other human groups because it represents the ancestral group from which all non-African populations derive, but more than that, non-African groups only derive from a small non-representative sample of this African population. This means that all non-African groups are more closely related to each other and to some African groups (probably east Africans) than they are to others, and further that the migration out of Africa represented a genetic bottleneck, with much of the diversity that existed in Africa not being carried out of Africa by the emigrating groups. Under this scenario, human populations do not have equal amounts of local variability, but rather diminished amounts of diversity the further from Africa any population lives. Long and Kittles find that rather than 85% of human genetic diversity existing in all human populations, about 100% of human diversity exists in a single African population, whereas only about 70% of human genetic diversity exists in a population derived from New Guinea. Long and Kittles argued that this still produces a global human population that is genetically homogeneous compared to other mammalian populations.
There is a hypothesis that anatomically modern humans interbred with Neanderthals during the Middle Paleolithic. In May 2010, the Neanderthal Genome Project presented genetic evidence that interbreeding did likely take place and that a small but significant[how?] portion of Neanderthal admixture is present in the DNA of modern Eurasians and Oceanians, and nearly absent in sub-Saharan African populations.
Between 4% and 6% of the genome of Melanesians (represented by the Papua New Guinean and Bougainville Islander) are thought to derive from Denisova hominins – a previously unknown species which shares a common origin with Neanderthals. It was possibly introduced during the early migration of the ancestors of Melanesians into Southeast Asia. This history of interaction suggests that Denisovans once ranged widely over eastern Asia.
Thus, Melanesians emerge as the most archaic-admixed population, having Denisovan/Neanderthal-related admixture of ~8%.
In a study published in 2013, Jeffrey Wall from University of California studied whole sequence-genome data and found higher rates of introgression in Asians compared to Europeans. Hammer et al. tested the hypothesis that contemporary African genomes have signatures of gene flow with archaic human ancestors and found evidence of archaic admixture in African genomes, suggesting that modest amounts of gene flow were widespread throughout time and space during the evolution of anatomically modern humans.
Categorization of the world populationEdit
New data on human genetic variation has reignited the debate about a possible biological basis for categorization of humans into races. Most of the controversy surrounds the question of how to interpret the genetic data and whether conclusions based on it are sound. Some researchers argue that self-identified race can be used as an indicator of geographic ancestry for certain health risks and medications.
Although the genetic differences among human groups are relatively small, these differences in certain genes such as duffy, ABCC11, SLC24A5, called ancestry-informative markers (AIMs) nevertheless can be used to reliably situate many individuals within broad, geographically based groupings. For example, computer analyses of hundreds of polymorphic loci sampled in globally distributed populations have revealed the existence of genetic clustering that roughly is associated with groups that historically have occupied large continental and subcontinental regions (Rosenberg et al. 2002; Bamshad et al. 2003).
Some commentators have argued that these patterns of variation provide a biological justification for the use of traditional racial categories. They argue that the continental clusterings correspond roughly with the division of human beings into sub-Saharan Africans; Europeans, Western Asians, Central Asians, Southern Asians and Northern Africans; Eastern Asians, Southeast Asians, Polynesians and Native Americans; and other inhabitants of Oceania (Melanesians, Micronesians & Australian Aborigines) (Risch et al. 2002). Other observers disagree, saying that the same data undercut traditional notions of racial groups (King and Motulsky 2002; Calafell 2003; Tishkoff and Kidd 2004). They point out, for example, that major populations considered races or subgroups within races do not necessarily form their own clusters.
Furthermore, because human genetic variation is clinal, many individuals affiliate with two or more continental groups. Thus, the genetically based "biogeographical ancestry" assigned to any given person generally will be broadly distributed and will be accompanied by sizable uncertainties (Pfaff et al. 2004).
In many parts of the world, groups have mixed in such a way that many individuals have relatively recent ancestors from widely separated regions. Although genetic analyses of large numbers of loci can produce estimates of the percentage of a person's ancestors coming from various continental populations (Shriver et al. 2003; Bamshad et al. 2004), these estimates may assume a false distinctiveness of the parental populations, since human groups have exchanged mates from local to continental scales throughout history (Cavalli-Sforza et al. 1994; Hoerder 2002). Even with large numbers of markers, information for estimating admixture proportions of individuals or groups is limited, and estimates typically will have wide confidence intervals (Pfaff et al. 2004).
Genetic data can be used to infer population structure and assign individuals to groups that often correspond with their self-identified geographical ancestry. Jorde and Wooding (2004) argued that "Analysis of many loci now yields reasonably accurate estimates of genetic similarity among individuals, rather than populations. Clustering of individuals is correlated with geographic origin or ancestry." However, identification by geographic origin may quickly break down when considering historical ancestry shared between individuals back in time.
An analysis of autosomal SNP data from the International HapMap Project (Phase II) and CEPH Human Genome Diversity Panel samples was published in 2009. The study of 53 populations taken from the HapMap and CEPH data (1138 unrelated individuals) suggested that natural selection may shape the human genome much more slowly than previously thought, with factors such as migration within and among continents more heavily influencing the distribution of genetic variations. A similar study published in 2010 found strong genome-wide evidence for selection due to changes in ecoregion, diet, and subsistence particularly in connection with polar ecoregions, with foraging, and with a diet rich in roots and tubers. In a 2016 study, principal component analysis of genome-wide data was capable of recovering previously-known targets for positive selection (without prior definition of populations) as well as a number of new candidate genes.
Forensic anthropologists can determine aspects of geographic ancestry (i.e. Asian, African, or European) from skeletal remains with a high degree of accuracy by analyzing skeletal measurements. According to some studies, individual test methods such as mid-facial measurements and femur traits can identify the geographic ancestry and by extension the racial category to which an individual would have been assigned during their lifetime, with over 80% accuracy, and in combination can be even more accurate. However, the skeletons of people who have recent ancestry in different geographical regions can exhibit characteristics of more than one ancestral group and, hence, cannot be identified as belonging to any single ancestral group.
Gene flow and admixtureEdit
Gene flow between two populations reduces the average genetic distance between the populations, only totally isolated human populations experience no gene flow and most populations have continuous gene flow with other neighboring populations which create the clinal distribution observed for moth genetic variation. When gene flow takes place between well-differentiated genetic populations the result is referred to as "genetic admixture".
Admixture mapping is a technique used to study how genetic variants cause differences in disease rates between population. Recent admixture populations that trace their ancestry to multiple continents are well suited for identifying genes for traits and diseases that differ in prevalence between parental populations. African-American populations have been the focus of numerous population genetic and admixture mapping studies, including studies of complex genetic traits such as white cell count, body-mass index, prostate cancer and renal disease.
An analysis of phenotypic and genetic variation including skin color and socio-economic status was carried out in the population of Cape Verde which has a well documented history of contact between Europeans and Africans. The studies showed that pattern of admixture in this population has been sex-biased and there is a significant interactions between socio economic status and skin color independent of the skin color and ancestry. Another study shows an increased risk of graft-versus-host disease complications after transplantation due to genetic variants in human leukocyte antigen (HLA) and non-HLA proteins.
Differences in allele frequencies contribute to group differences in the incidence of some monogenic diseases, and they may contribute to differences in the incidence of some common diseases. For the monogenic diseases, the frequency of causative alleles usually correlates best with ancestry, whether familial (for example, Ellis-van Creveld syndrome among the Pennsylvania Amish), ethnic (Tay–Sachs disease among Ashkenazi Jewish populations), or geographical (hemoglobinopathies among people with ancestors who lived in malarial regions). To the extent that ancestry corresponds with racial or ethnic groups or subgroups, the incidence of monogenic diseases can differ between groups categorized by race or ethnicity, and health-care professionals typically take these patterns into account in making diagnoses.
Even with common diseases involving numerous genetic variants and environmental factors, investigators point to evidence suggesting the involvement of differentially distributed alleles with small to moderate effects. Frequently cited examples include hypertension (Douglas et al. 1996), diabetes (Gower et al. 2003), obesity (Fernandez et al. 2003), and prostate cancer (Platz et al. 2000). However, in none of these cases has allelic variation in a susceptibility gene been shown to account for a significant fraction of the difference in disease prevalence among groups, and the role of genetic factors in generating these differences remains uncertain (Mountain and Risch 2004).
Some other variations on the other hand are beneficial to human, as they prevent certain diseases and increase the chance to adapt to the environment. For example, mutation in CCR5 gene that protects against AIDS. CCR5 gene is absent on the surface of cell due to mutation. Without CCR5 gene on the surface, there is nothing for HIV viruses to grab on and bind into. Therefore the mutation on CCR5 gene decreases the chance of an individual’s risk with AIDS. The mutation in CCR5 is also quite popular in certain areas, with more than 14% of the population carry the mutation in Europe and about 6–10% in Asia and North Africa.
Apart from mutations, many genes that may have aided humans in ancient times plague humans today. For example, it is suspected that genes that allow humans to more efficiently process food are those that make people susceptible to obesity and diabetes today.
Neil Risch of Stanford University has proposed that self-identified race/ethnic group could be a valid means of categorization in the USA for public health and policy considerations. A 2002 paper by Noah Rosenberg's group makes a similar claim: "The structure of human populations is relevant in various epidemiological contexts. As a result of variation in frequencies of both genetic and nongenetic risk factors, rates of disease and of such phenotypes as adverse drug response vary across populations. Further, information about a patient’s population of origin might provide health care practitioners with information about risk when direct causes of disease are unknown."
- Race and genetics
- Human evolutionary genetics
- Multiregional hypothesis
- Recent single origin hypothesis
- Isolation by distance
- Genealogical DNA test
- Y-chromosome haplogroups in populations of the world
- Human genetic clustering
- Genetic history of Europe
- Genetic history of South Asia
- African admixture in Europe
- Genetic history of indigenous peoples of the Americas
- Genetic history of the British Isles
- Bruder CE, Piotrowski A, Gijsbers AA, Andersson R, Erickson S, Diaz de Ståhl T, et al. (March 2008). "Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles". American Journal of Human Genetics. 82 (3): 763–71. doi:10.1016/j.ajhg.2007.12.011. PMC 2427204. PMID 18304490.
- NCBI (8 May 2017). "dbSNP's human build 150 has doubled the amount of RefSNP records!". NCBI Insights. Retrieved 16 May 2017.
- Auton A, Brooks LD, Durbin RM, Garrison EP, Kang HM, Korbel JO, et al. (October 2015). "A global reference for human genetic variation". Nature. 526 (7571): 68–74. Bibcode:2015Natur.526...68T. doi:10.1038/nature15393. PMC 4750478. PMID 26432245.
- "We are all mutants: First direct whole-genome measure of human mutation predicts 60 new mutations in each of us". Science Daily. 13 June 2011. Retrieved 5 September 2011.
- Conrad DF, Keebler JE, DePristo MA, Lindsay SJ, Zhang Y, Casals F, et al. (June 2011). "Variation in genome-wide mutation rates within and between human families". Nature Genetics. 43 (7): 712–4. doi:10.1038/ng.862. PMC 3322360. PMID 21666693.
- Guo J, Wu Y, Zhu Z, Zheng Z, Trzaskowski M, Zeng J, Robinson MR, Visscher PM, Yang J (May 2018). "Global genetic differentiation of complex traits shaped by natural selection in humans". Nature Communications. 9 (1): 1865. Bibcode:2018NatCo...9.1865G. doi:10.1038/s41467-018-04191-y. PMC 5951811. PMID 29760457.
- Wang ET, Kodama G, Baldi P, Moyzis RK (January 2006). "Global landscape of recent inferred Darwinian selection for Homo sapiens". Proceedings of the National Academy of Sciences of the United States of America. 103 (1): 135–40. Bibcode:2006PNAS..103..135W. doi:10.1073/pnas.0509691102. PMC 1317879. PMID 16371466.
By these criteria, 1.6% of Perlegen SNPs were found to exhibit the genetic architecture of selection.
- Kidd JM, Cooper GM, Donahue WF, Hayden HS, Sampas N, Graves T, et al. (May 2008). "Mapping and sequencing of structural variation from eight human genomes". Nature. 453 (7191): 56–64. Bibcode:2008Natur.453...56K. doi:10.1038/nature06862. PMC 2424287. PMID 18451855.
- Driscoll DA, Gross S (June 2009). "Clinical practice. Prenatal screening for aneuploidy". The New England Journal of Medicine. 360 (24): 2556–62. doi:10.1056/NEJMcp0900134. PMID 19516035.
- Jorde LB, Wooding SP (November 2004). "Genetic variation, classification and 'race'". Nature Genetics. 36 (11 Suppl): S28–33. doi:10.1038/ng1435. PMID 15508000.
- Tishkoff SA, Kidd KK (November 2004). "Implications of biogeography of human populations for 'race' and medicine". Nature Genetics. 36 (11 Suppl): S21–7. doi:10.1038/ng1438. PMID 15507999.
- Mullaney JM, Mills RE, Pittard WS, Devine SE (October 2010). "Small insertions and deletions (INDELs) in human genomes". Human Molecular Genetics. 19 (R2): R131–6. doi:10.1093/hmg/ddq400. PMC 2953750. PMID 20858594.
- Collins FS, Brooks LD, Chakravarti A (December 1998). "A DNA polymorphism discovery resource for research on human genetic variation". Genome Research. 8 (12): 1229–31. doi:10.1101/gr.8.12.1229. PMID 9872978.
- Thomas PE, Klinger R, Furlong LI, Hofmann-Apitius M, Friedrich CM (2011). "Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers". BMC Bioinformatics. 12 Suppl 4: S4. doi:10.1186/1471-2105-12-S4-S4. PMC 3194196. PMID 21992066.
- Ke X, Taylor MS, Cardon LR (April 2008). "Singleton SNPs in the human genome and implications for genome-wide association studies". European Journal of Human Genetics. 16 (4): 506–15. doi:10.1038/sj.ejhg.5201987. PMID 18197193.
- Ng PC, Levy S, Huang J, Stockwell TB, Walenz BP, Li K, et al. (August 2008). Schork NJ (ed.). "Genetic variation in an individual human exome". PLoS Genetics. 4 (8): e1000160. doi:10.1371/journal.pgen.1000160. PMC 2493042. PMID 18704161.
- Gross L (October 2007). "A new human genome sequence paves the way for individualized genomics". PLoS Biology. 5 (10): e266. doi:10.1371/journal.pbio.0050266. PMC 1964778. PMID 20076646.
- "First Individual Diploid Human Genome Published By Researchers at J. Craig Venter Institute". J. Craig Venter Institute. 3 September 2007. Archived from the original on 16 July 2011. Retrieved 5 September 2011.
- Levy S, Sutton G, Ng PC, Feuk L, Halpern AL, Walenz BP, et al. (September 2007). "The diploid genome sequence of an individual human". PLoS Biology. 5 (10): e254. doi:10.1371/journal.pbio.0050254. PMC 1964779. PMID 17803354.
- "Understanding Genetics: Human Health and the Genome". The Tech Museum of Innovation. 24 January 2008. Retrieved 5 September 2011.
- "First Diploid Human Genome Sequence Shows We're Surprisingly Different". Science Daily. 4 September 2007. Retrieved 5 September 2011.
- "Copy number variation may stem from replication misstep". EurekAlert!. 27 December 2007. Retrieved 5 September 2011.
- Lee JA, Carvalho CM, Lupski JR (December 2007). "A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders". Cell. 131 (7): 1235–47. doi:10.1016/j.cell.2007.11.037. PMID 18160035.
- Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, et al. (November 2006). "Global variation in copy number in the human genome". Nature. 444 (7118): 444–54. Bibcode:2006Natur.444..444R. doi:10.1038/nature05329. PMC 2669898. PMID 17122850.
- Dumas L, Kim YH, Karimpour-Fard A, Cox M, Hopkins J, Pollack JR, et al. (September 2007). "Gene copy number variation spanning 60 million years of human and primate evolution". Genome Research. 17 (9): 1266–77. doi:10.1101/gr.6557307. PMC 1950895. PMID 17666543.
- Prüfer K, Racimo F, Patterson N, Jay F, Sankararaman S, Sawyer S, et al. (January 2014). "The complete genome sequence of a Neanderthal from the Altai Mountains". Nature. 505 (7481): 43–9. Bibcode:2014Natur.505...43P. doi:10.1038/nature12886. PMC 4031459. PMID 24352235.
- Pratas D, Hosseini M, Silva R, Pinho A, Ferreira P (20–23 June 2017). Visualization of Distinct DNA Regions of the Modern Human Relatively to a Neanderthal Genome. Iberian Conference on Pattern Recognition and Image Analysis. Springer. Lecture Notes in Computer Science. 10255. pp. 235–242. doi:10.1007/978-3-319-58838-4_26. ISBN 978-3-319-58837-7.
- "Human Genetic Variation Fact Sheet". National Institute of General Medical Sciences. 19 August 2011. Retrieved 5 September 2011.
- Rakyan V, Whitelaw E (January 2003). "Transgenerational epigenetic inheritance". Current Biology. 13 (1): R6. doi:10.1016/S0960-9822(02)01377-5. PMID 12526754.
- "Cline". Microsoft Encarta Premium. 2009.
- King RC, Stansfield WD, Mulligan PK (2006). "Cline". A dictionary of genetics (7th ed.). Oxford University Press. ISBN 978-0195307610.
- Begon M, Townsend CR, Harper JL (2006). Ecology: From individuals to ecosystems (4th ed.). Wiley-Blackwell. p. 10. ISBN 978-1405111171.
- "Haplogroup". DNA-Newbie Glossary. International Society of Genetic Genealogy. Retrieved 5 September 2012.
- "The descent of man Chapter 6 – On the Affinities and Genealogy of Man". Darwin-online.org.uk. Retrieved 11 January 2011.
In each great region of the world the living mammals are closely related to the extinct species of the same region. It is, therefore, probable that Africa was formerly inhabited by extinct apes closely allied to the gorilla and chimpanzee; and as these two species are now man's nearest allies, it is somewhat more probable that our early progenitors lived on the African continent than elsewhere. But it is useless to speculate on this subject, for an ape nearly as large as a man, namely the Dryopithecus of Lartet, which was closely allied to the anthropomorphous Hylobates, existed in Europe during the Upper Miocene period; and since so remote a period the earth has certainly undergone many great revolutions, and there has been ample time for migration on the largest scale.
- Underhill PA, Shen P, Lin AA, Jin L, Passarino G, Yang WH, et al. (November 2000). "Y chromosome sequence variation and the history of human populations". Nature Genetics. 26 (3): 358–61. doi:10.1038/81685. PMID 11062480.
- "New Research Proves Single Origin Of Humans In Africa". Science Daily. 19 July 2007. Retrieved 5 September 2011.
- Manica A, Amos W, Balloux F, Hanihara T (July 2007). "The effect of ancient population bottlenecks on human phenotypic variation". Nature. 448 (7151): 346–8. Bibcode:2007Natur.448..346M. doi:10.1038/nature05951. PMC 1978547. PMID 17637668.
- Tishkoff SA, Reed FA, Friedlaender FR, Ehret C, Ranciaro A, Froment A, et al. (May 2009). "The genetic structure and history of Africans and African Americans" (PDF). Science. 324 (5930): 1035–44. Bibcode:2009Sci...324.1035T. doi:10.1126/science.1172257. PMC 2947357. PMID 19407144.
We incorporated geographic data into a Bayesian clustering analysis, assuming no admixture (TESS software) (25) and distinguished six clusters within continental Africa (Fig. 5A). The most geographically widespread cluster (orange) extends from far Western Africa (the Mandinka) through central Africa to the Bantu speakers of South Africa (the Venda and Xhosa) and corresponds to the distribution of the Niger-Kordofanian language family, possibly reflecting the spread of Bantu-speaking populations from near the Nigerian/Cameroon highlands across eastern and southern Africa within the past 5000 to 3000 years (26,27). Another inferred cluster includes the Pygmy and SAK populations (green), with a noncontiguous geographic distribution in central and southeastern Africa, consistent with the STRUCTURE (Fig. 3) and phylogenetic analyses (Fig. 1). Another geographically contiguous cluster extends across northern Africa (blue) into Mali (the Dogon), Ethiopia, and northern Kenya. With the exception of the Dogon, these populations speak an Afroasiatic language. Chadic-speaking and Nilo-Saharan–speaking populations from Nigeria, Cameroon, and central Chad, as well as several Nilo-Saharan–speaking populations from southern Sudan, constitute another cluster (red). Nilo-Saharan and Cushitic speakers from the Sudan, Kenya, and Tanzania, as well as some of the Bantu speakers from Kenya, Tanzania, and Rwanda (Hutu/Tutsi), constitute another cluster (purple), reflecting linguistic evidence for gene flow among these populations over the past ~5000 years (28,29). Finally, the Hadza are the sole constituents of a sixth cluster (yellow), consistent with their distinctive genetic structure identified by PCA and STRUCTURE.
- Schlebusch CM, Jakobsson M (August 2018). "Tales of Human Migration, Admixture, and Selection in Africa". Annual Review of Genomics and Human Genetics. 19: 405–428. doi:10.1146/annurev-genom-083117-021759. PMID 29727585. Retrieved 28 May 2018.
- Auton A, Brooks LD, Durbin RM, Garrison EP, Kang HM, Korbel JO, et al. (1000 Genomes Project Consortium) (October 2015). "A global reference for human genetic variation". Nature. 526 (7571): 68–74. Bibcode:2015Natur.526...68T. doi:10.1038/nature15393. PMC 4750478. PMID 26432245.
- Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, et al. (June 2002). "The structure of haplotype blocks in the human genome". Science. 296 (5576): 2225–9. Bibcode:2002Sci...296.2225G. doi:10.1126/science.1069424. PMID 12029063.
- Lewontin RC (1972). The Apportionment of Human Diversity. Evolutionary Biology. 6. pp. 381–97. doi:10.1007/978-1-4684-9063-3_14. ISBN 978-1-4684-9065-7.
- Bamshad MJ, Wooding S, Watkins WS, Ostler CT, Batzer MA, Jorde LB (March 2003). "Human population genetic structure and inference of group membership". American Journal of Human Genetics. 72 (3): 578–89. doi:10.1086/368061. PMC 1180234. PMID 12557124.
- Manica, Andrea, William Amos, François Balloux, and Tsunehiko Hanihara. “The Effect of Ancient Population Bottlenecks on Human Phenotypic Variation.” Nature 448, no. 7151 (July 2007): 346–48. https://doi.org/10.1038/nature05951.
- Jablonski NG (10 January 2014). "The Biological and Social Meaning of Skin Color". Living Color: The Biological and Social Meaning of Skin Color. University of California Press. ISBN 978-0-520-28386-2. JSTOR 10.1525/j.ctt1pn64b. Lay summary (12 July 2015).CS1 maint: ref=harv (link)
- Grubert F, Zaugg JB, Kasowski M, Ursu O, Spacek DV, Martin AR, et al. (August 2015). "Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions". Cell. 162 (5): 1051–65. doi:10.1016/j.cell.2015.07.048. PMC 4556133. PMID 26300125.
- Cenik C, Cenik ES, Byeon GW, Grubert F, Candille SI, Spacek D, et al. (November 2015). "Integrative analysis of RNA, translation, and protein levels reveals distinct regulatory variation across humans". Genome Research. 25 (11): 1610–21. doi:10.1101/gr.193342.115. PMC 4617958. PMID 26297486.
- Wu L, Candille SI, Choi Y, Xie D, Jiang L, Li-Pook-Than J, Tang H, Snyder M (July 2013). "Variation and genetic control of protein abundance in humans". Nature. 499 (7456): 79–82. Bibcode:2013Natur.499...79W. doi:10.1038/nature12223. PMC 3789121. PMID 23676674.
- Phillips ML (9 January 2007). "Ethnicity tied to gene expression". The Scientist. Retrieved 5 September 2011.
- Spielman RS, Bastone LA, Burdick JT, Morley M, Ewens WJ, Cheung VG (February 2007). "Common genetic variants account for differences in gene expression among ethnic groups". Nature Genetics. 39 (2): 226–31. doi:10.1038/ng1955. PMC 3005333. PMID 17206142.
- Swaminathan N (9 January 2007). "Ethnic Differences Traced to Variable Gene Expression". Scientific American. Retrieved 5 September 2011.
- Check E (2007). "Genetic expression speaks as loudly as gene type". Nature News. doi:10.1038/news070101-8.
- Bell L (15 January 2007). "Variable gene expression seen in different ethnic groups". BioNews.org. Retrieved 5 September 2011.
- Kamrani K (28 February 2008). "Differences of gene expression between human populations". Anthropology.net. Retrieved 5 September 2011.
- Storey JD, Madeoy J, Strout JL, Wurfel M, Ronald J, Akey JM (March 2007). "Gene-expression variation within and among human populations". American Journal of Human Genetics. 80 (3): 502–9. doi:10.1086/512017. PMC 1821107. PMID 17273971.
- Graves JL (2006). "What We Know and What We Don't Know: Human Genetic Variation and the Social Construction of Race". Is Race "Real"?. Social Science Research Council. Retrieved 22 January 2011.
- Keita SO, Kittles RA, Royal CD, Bonney GE, Furbert-Harris P, Dunston GM, Rotimi CN (November 2004). "Conceptualizing human variation". Nature Genetics. 36 (11 Suppl): S17–20. doi:10.1038/ng1455. PMID 15507998.
- Hawks J (2013). Significance of Neandertal and Denisovan Genomes in Human Evolution. Annual Review of Anthropology. 42. Annual Reviews. pp. 433–49. doi:10.1146/annurev-anthro-092412-155548. ISBN 978-0-8243-1942-7.
- * Wright S (1978). Evolution and the Genetics of Populations. 4, Variability Within and Among Natural Populations. Chicago, Illinois: Univ. Chicago Press. p. 438.CS1 maint: ref=harv (link)
- Long JC, Kittles RA (August 2003). "Human genetic diversity and the nonexistence of biological races". Human Biology. 75 (4): 449–71. doi:10.1353/hub.2003.0058. PMID 14655871.
- Reich D, Green RE, Kircher M, Krause J, Patterson N, Durand EY, et al. (December 2010). "Genetic history of an archaic hominin group from Denisova Cave in Siberia". Nature. 468 (7327): 1053–60. Bibcode:2010Natur.468.1053R. doi:10.1038/nature09710. PMC 4306417. PMID 21179161.
- Wall JD, Yang MA, Jay F, Kim SK, Durand EY, Stevison LS, et al. (May 2013). "Higher levels of neanderthal ancestry in East Asians than in Europeans". Genetics. 194 (1): 199–209. doi:10.1534/genetics.112.148213. PMC 3632468. PMID 23410836.
- Hammer MF, Woerner AE, Mendez FL, Watkins JC, Wall JD (September 2011). "Genetic evidence for archaic admixture in Africa". Proceedings of the National Academy of Sciences of the United States of America. 108 (37): 15123–8. Bibcode:2011PNAS..10815123H. doi:10.1073/pnas.1109300108. PMC 3174671. PMID 21896735.
- Rosenberg NA, Mahajan S, Gonzalez-Quevedo C, Blum MG, Nino-Rosales L, Ninis V, et al. (December 2006). "Low levels of genetic divergence across geographically and linguistically diverse populations from India". PLoS Genetics. 2 (12): e215. doi:10.1371/journal.pgen.0020215. PMC 1713257. PMID 17194221.
- Albers, Patrick K.; McVean, Gil (13 September 2018). "Dating genomic variants and shared ancestry in population-scale sequencing data". bioRxiv: 416610. doi:10.1101/416610.
- Coop G, Pickrell JK, Novembre J, Kudaravalli S, Li J, Absher D, et al. (June 2009). Schierup MH (ed.). "The role of geography in human adaptation". PLoS Genetics. 5 (6): e1000500. doi:10.1371/journal.pgen.1000500. PMC 2685456. PMID 19503611.CS1 maint: ref=harv (link) See also: Brown D (22 June 2009). "Among Many Peoples, Little Genomic Variety". The Washington Post. Retrieved 25 June 2009.. "Geography And History Shape Genetic Differences In Humans". Science Daily. 7 June 2009. Retrieved 25 June 2009..
- Hancock AM, Witonsky DB, Ehler E, Alkorta-Aranburu G, Beall C, Gebremedhin A, et al. (May 2010). "Colloquium paper: human adaptations to diet, subsistence, and ecoregion are due to subtle shifts in allele frequency". Proceedings of the National Academy of Sciences of the United States of America. 107 Suppl 2: 8924–30. Bibcode:2010PNAS..107.8924H. doi:10.1073/pnas.0914625107. PMC 3024024. PMID 20445095.
- Duforet-Frebourg N, Luu K, Laval G, Bazin E, Blum MG (April 2016). "Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data". Molecular Biology and Evolution. 33 (4): 1082–93. arXiv:1504.04543. doi:10.1093/molbev/msv334. PMC 4776707. PMID 26715629.
- "Does Race Exist?". NOVA. PBS. 15 February 2000. Retrieved 5 September 2011.
- Winkler CA, Nelson GW, Smith MW (2010). "Admixture mapping comes of age". Annual Review of Genomics and Human Genetics. 11: 65–89. doi:10.1146/annurev-genom-082509-141523. PMID 20594047.
- Bryc K, Auton A, Nelson MR, Oksenberg JR, Hauser SL, Williams S, et al. (January 2010). "Genome-wide patterns of population structure and admixture in West Africans and African Americans". Proceedings of the National Academy of Sciences of the United States of America. 107 (2): 786–91. Bibcode:2010PNAS..107..786B. doi:10.1073/pnas.0909559107. PMC 2818934. PMID 20080753.
- Beleza S, Campos J, Lopes J, Araújo II, Hoppfer Almada A, Correia e Silva A, et al. (2012). "The admixture structure and genetic variation of the archipelago of Cape Verde and its implications for admixture mapping studies". PLOS ONE. 7 (11): e51103. Bibcode:2012PLoSO...751103B. doi:10.1371/journal.pone.0051103. PMC 3511383. PMID 23226471.
- Arrieta-Bolaños E, Madrigal JA, Shaw BE (2012). "Human leukocyte antigen profiles of Latin American populations: differential admixture and its potential impact on hematopoietic stem cell transplantation". Bone Marrow Research. 2012: 1–13. doi:10.1155/2012/136087. PMC 3506882. PMID 23213535.
- Risch N, Burchard E, Ziv E, Tang H (July 2002). "Categorization of humans in biomedical research: genes, race and disease". Genome Biology. 3 (7): comment2007. doi:10.1186/gb-2002-3-7-comment2007. PMC 139378. PMID 12184798.
- Lu YF, Goldstein DB, Angrist M, Cavalleri G (July 2014). "Personalized medicine and human genetic diversity". Cold Spring Harbor Perspectives in Medicine. 4 (9): a008581. doi:10.1101/cshperspect.a008581. PMC 4143101. PMID 25059740.
- Limborska SA, Balanovsky OP, Balanovskaya EV, Slominsky PA, Schadrina MI, Livshits LA, et al. (2002). "Analysis of CCR5Delta32 geographic distribution and its correlation with some climatic and geographic factors". Human Heredity. 53 (1): 49–54. doi:10.1159/000048605. PMID 11901272.
- Tishkoff SA, Verrelli BC (2003). "Patterns of human genetic diversity: implications for human evolutionary history and disease". Annual Review of Genomics and Human Genetics. 4 (1): 293–340. doi:10.1146/annurev.genom.4.070802.110226. PMID 14527305.
- Tang H, Quertermous T, Rodriguez B, Kardia SL, Zhu X, Brown A, et al. (February 2005). "Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies". American Journal of Human Genetics. 76 (2): 268–75. doi:10.1086/427888. PMC 1196372. PMID 15625622.
- Risch N, Burchard E, Ziv E, Tang H (July 2002). "Categorization of humans in biomedical research: genes, race and disease". Genome Biology. 3 (7): comment2007. doi:10.1186/gb-2002-3-7-comment2007. PMC 139378. PMID 12184798.
- Rosenberg NA, Pritchard JK, Weber JL, Cann HM, Kidd KK, Zhivotovsky LA, Feldman MW (December 2002). "Genetic structure of human populations". Science. 298 (5602): 2381–5. Bibcode:2002Sci...298.2381R. doi:10.1126/science.1078311. PMID 12493913.
- Race, Ethnicity (October 2005). "The use of racial, ethnic, and ancestral categories in human genetics research". American Journal of Human Genetics. 77 (4): 519–32. doi:10.1086/491747. PMC 1275602. PMID 16175499.
- Altmüller J, Palmer LJ, Fischer G, Scherb H, Wjst M (November 2001). "Genomewide scans of complex human diseases: true linkage is hard to find". American Journal of Human Genetics. 69 (5): 936–50. doi:10.1086/324069. PMC 1274370. PMID 11565063.
- Aoki K (2002). "Sexual selection as a cause of human skin colour variation: Darwin's hypothesis revisited". Annals of Human Biology. 29 (6): 589–608. doi:10.1080/0301446021000019144. PMID 12573076.
- Bamshad M, Wooding S, Salisbury BA, Stephens JC (August 2004). "Deconstructing the relationship between genetics and race". Nature Reviews. Genetics. 5 (8): 598–609. doi:10.1038/nrg1401. PMID 15266342. reprint-zip
- Bamshad M, Wooding SP (February 2003). "Signatures of natural selection in the human genome". Nature Reviews. Genetics. 4 (2): 99–111. doi:10.1038/nrg999. PMID 12560807.
- Cann RL, Stoneking M, Wilson AC (1987). "Mitochondrial DNA and human evolution". Nature. 325 (6099): 31–36. Bibcode:1987Natur.325...31C. doi:10.1038/325031a0. PMID 3025745.
- Cardon LR, Abecasis GR (March 2003). "Using haplotype blocks to map human complex trait loci" (PDF). Trends in Genetics. 19 (3): 135–40. doi:10.1016/S0168-9525(03)00022-2. PMID 12615007.
- Cavalli-Sforza LL, Feldman MW (March 2003). "The application of molecular genetic approaches to the study of human evolution". Nature Genetics. 33 Suppl (3s): 266–75. doi:10.1038/ng1113. PMID 12610536.
- Collins FS (November 2004). "What we do and don't know about 'race', 'ethnicity', genetics and health at the dawn of the genome era". Nature Genetics. 36 (11 Suppl): S13–15. doi:10.1038/ng1436. PMID 15507997.
- Collins FS, Green ED, Guttmacher AE, Guyer MS (April 2003). "A vision for the future of genomics research". Nature. 422 (6934): 835–47. Bibcode:2003Natur.422..835C. doi:10.1038/nature01626. PMID 12695777.
- Ebersberger I, Metzler D, Schwarz C, Pääbo S (June 2002). "Genomewide comparison of DNA sequences between humans and chimpanzees". American Journal of Human Genetics. 70 (6): 1490–97. doi:10.1086/340787. PMC 379137. PMID 11992255.
- Edwards AW (August 2003). "Human genetic diversity: Lewontin's fallacy". BioEssays. 25 (8): 798–801. doi:10.1002/bies.10315. PMID 12879450.
- Foster MW, Sharp RR (October 2004). "Beyond race: towards a whole-genome perspective on human populations and genetic variation". Nature Reviews. Genetics. 5 (10): 790–96. doi:10.1038/nrg1452. PMID 15510170.
- Foster MW, Sharp RR, Freeman WL, Chino M, Bernsten D, Carter TH (June 1999). "The role of community review in evaluating the risks of human genetic variation research". American Journal of Human Genetics. 64 (6): 1719–27. doi:10.1086/302415. PMC 1377916. PMID 10330360.
- Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A, Cooper R, Ward R, Lander ES, Daly MJ, Altshuler D (June 2002). "The structure of haplotype blocks in the human genome". Science. 296 (5576): 2225–29. Bibcode:2002Sci...296.2225G. doi:10.1126/science.1069424. PMID 12029063.
- Harding RM, Healy E, Ray AJ, Ellis NS, Flanagan N, Todd C, Dixon C, Sajantila A, Jackson IJ, Birch-Machin MA, Rees JL (April 2000). "Evidence for variable selective pressures at MC1R". American Journal of Human Genetics. 66 (4): 1351–61. doi:10.1086/302863. PMC 1288200. PMID 10733465.
- Ingman M, Kaessmann H, Pääbo S, Gyllensten U (December 2000). "Mitochondrial genome variation and the origin of modern humans". Nature. 408 (6813): 708–13. Bibcode:2000Natur.408..708I. doi:10.1038/35047064. PMID 11130070.
- The International Hapmap Consortium (December 2003). "The International HapMap Project". Nature. 426 (6968): 789–96. Bibcode:2003Natur.426..789G. doi:10.1038/nature02168. hdl:2027.42/62838. PMID 14685227.
- The International Hapmap Consortium (June 2004). "Integrating ethics and science in the International HapMap Project". Nature Reviews. Genetics. 5 (6): 467–75. doi:10.1038/nrg1351. PMC 2271136. PMID 15153999.
- Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, et al. (February 2001). "Initial sequencing and analysis of the human genome". Nature. 409 (6822): 860–921. Bibcode:2001Natur.409..860L. doi:10.1038/35057062. PMID 11237011.
- Jorde LB, Bamshad M, Rogers AR (February 1998). "Using mitochondrial and nuclear DNA markers to reconstruct human evolution" (PDF). BioEssays. 20 (2): 126–36. doi:10.1002/(SICI)1521-1878(199802)20:2<126::AID-BIES5>3.0.CO;2-R. PMID 9631658. Archived from the original (PDF) on 28 November 2007. Retrieved 28 October 2007.
- Jorde LB, Watkins WS, Bamshad MJ, Dixon ME, Ricker CE, Seielstad MT, Batzer MA (March 2000). "The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data". American Journal of Human Genetics. 66 (3): 979–88. doi:10.1086/302825. PMC 1288178. PMID 10712212.
- Jorde LB, Watkins WS, Kere J, Nyman D, Eriksson AW (2000). "Gene mapping in isolated populations: new roles for old friends?". Human Heredity. 50 (1): 57–65. doi:10.1159/000022891. PMID 10545758.
- Kaessmann H, Heissig F, von Haeseler A, Pääbo S (May 1999). "DNA sequence variation in a non-coding region of low recombination on the human X chromosome". Nature Genetics. 22 (1): 78–81. doi:10.1038/8785. PMID 10319866.
- Kaessmann H, Wiebe V, Weiss G, Pääbo S (February 2001). "Great ape DNA sequences reveal a reduced diversity and an expansion in humans". Nature Genetics. 27 (2): 155–56. doi:10.1038/84773. PMID 11175781.
- Keita SO, Kittles RA (1997). "The Persistence of Racial Thinking and the Myth of Racial Divergence". American Anthropologist. 99 (3): 534–44. doi:10.1525/aa.1922.214.171.1244.
- Marks J (1995). Human Biodiversity: Genes, Race, and History. Aldine Transaction. ISBN 978-0-202-02033-4.
- Mountain JL, Risch N (November 2004). "Assessing genetic contributions to phenotypic differences among 'racial' and 'ethnic' groups". Nature Genetics. 36 (11 Suppl): S48–53. doi:10.1038/ng1456. PMID 15508003.
- Pääbo S (January 2003). "The mosaic that is our genome". Nature. 421 (6921): 409–12. Bibcode:2003Natur.421..409P. doi:10.1038/nature01400. PMID 12540910.
- Ramachandran S, Deshpande O, Roseman CC, Rosenberg NA, Feldman MW, Cavalli-Sforza LL (November 2005). "Support from the relationship of genetic and geographic distance in human populations for a serial founder effect originating in Africa". Proceedings of the National Academy of Sciences of the United States of America. 102 (44): 15942–47. Bibcode:2005PNAS..10215942R. doi:10.1073/pnas.0507611102. PMC 1276087. PMID 16243969.
- Relethford JH (August 2002). "Apportionment of global human genetic diversity based on craniometrics and skin color". American Journal of Physical Anthropology. 118 (4): 393–98. CiteSeerX 10.1.1.473.5972. doi:10.1002/ajpa.10079. PMID 12124919.
- Sankar P, Cho MK (November 2002). "Genetics. Toward a new vocabulary of human genetic variation". Science. 298 (5597): 1337–38. doi:10.1126/science.1074447. PMC 2271140. PMID 12434037.
- Sankar P, Cho MK, Condit CM, Hunt LM, Koenig B, Marshall P, Lee SS, Spicer P (June 2004). "Genetic research and health disparities". JAMA. 291 (24): 2985–89. doi:10.1001/jama.291.24.2985. PMC 2271142. PMID 15213210.
- Serre D, Pääbo S (September 2004). "Evidence for gradients of human genetic diversity within and among continents". Genome Research. 14 (9): 1679–85. doi:10.1101/gr.2529604. PMC 515312. PMID 15342553.
- Templeton AR (1998). "Human Races: A Genetic and Evolutionary Perspective". American Anthropologist. 100 (3): 632–50. doi:10.1525/aa.19126.96.36.1992.
- Weiss KM (1998). "Coming to Terms with Human Variation". Annual Review of Anthropology. 27: 273–300. doi:10.1146/annurev.anthro.27.1.273.
- Weiss KM, Terwilliger JD (October 2000). "How many diseases does it take to map a gene with SNPs?". Nature Genetics. 26 (2): 151–57. doi:10.1038/79866. PMID 11017069.
- Yu N, Jensen-Seaman MI, Chemnick L, Kidd JR, Deinard AS, Ryder O, Kidd KK, Li WH (August 2003). "Low nucleotide diversity in chimpanzees and bonobos". Genetics. 164 (4): 1511–18. PMC 1462640. PMID 12930756.
- Zietkiewicz E, Yotova V, Gehl D, Wambach T, Arrieta I, Batzer M, Cole DE, Hechtman P, Kaplan F, Modiano D, Moisan JP, Michalski R, Labuda D (November 2003). "Haplotypes in the dystrophin DNA segment point to a mosaic origin of modern human diversity". American Journal of Human Genetics. 73 (5): 994–1015. doi:10.1086/378777. PMC 1180505. PMID 14513410.
- Pennisi E (December 2007). "Breakthrough of the year. Human genetic variation". Science. 318 (5858): 1842–43. doi:10.1126/science.318.5858.1842. PMID 18096770.
- Ramachandran S, Tang H, Gutenkunst RN, Bustamante CD (2010). "Genetics and Genomics of Human Population Structure". In Speicher MR, Antonarakis SE, Motulsky AG (eds.). Vogel and Motulsky's Human Genetics: Problems and Approaches (4th ed.). Springer. ISBN 978-3-540-37653-8.
|Wikimedia Commons has media related to Human genetic diversity.|