| scholarly article | Q13442814 |
| P50 | author | Steven G. E. Marsh | Q7615026 |
| Frank Plummer | Q20006879 | ||
| Peter Parham | Q20980481 | ||
| Mary Carrington | Q29840699 | ||
| Martin Maiers | Q30524391 | ||
| Paul J Norman | Q33082884 | ||
| Lisbeth A Guethlein | Q48359703 | ||
| Meral Beksac | Q57078421 | ||
| Joshua Kimani | Q78623479 | ||
| Klara Dalva | Q96088012 | ||
| Alasdair McWhinnie | Q125258358 | ||
| P2093 | author name string | Subhash Kulkarni | |
| Loren Gragert | |||
| Farbod Babrzadeh | |||
| Richard E Green | |||
| Ma Luo | |||
| Derek Middleton | |||
| Baback Gharizadeh | |||
| Raja Rajalingam | |||
| Ann-Margaret Little | |||
| Laurent Abi-Rached | |||
| Sofia Tavoularis | |||
| Matthew J Jobin | |||
| P2860 | cites work | A Draft Sequence of the Neandertal Genome | Q22065895 |
| Genetic history of an archaic hominin group from Denisova Cave in Siberia | Q22122173 | ||
| A back migration from Asia to sub-Saharan Africa is supported by high-resolution analysis of human Y-chromosome haplotypes | Q24563871 | ||
| Allele frequency net: a database and online repository for immune gene frequencies in worldwide populations | Q24612449 | ||
| Ethiopians and Khoisan share the deepest clades of the human Y-chromosome phylogeny | Q24633152 | ||
| Out of Africa: modern human origins special feature: explaining worldwide patterns of human genetic variation using a coalescent-based serial founder model of migration outward from Africa | Q24646508 | ||
| The dawn of human matrilineal diversity | Q24656149 | ||
| A haplotype map of the human genome | Q24679827 | ||
| KIR2DS4 is a product of gene conversion with KIR3DL2 that introduced specificity for HLA-A * 11 while diminishing avidity for HLA-C | Q27657994 | ||
| The peopling of the Pacific from a bacterial perspective | Q28307498 | ||
| Synergistic polymorphism at two positions distal to the ligand-binding site makes KIR2DL2 a stronger receptor for HLA-C than KIR2DL3. | Q29568902 | ||
| Repeated adaptive introgression at a gene under multiallelic balancing selection | Q30397929 | ||
| REJECTOR: software for population history inference from genetic data via a rejection algorithm | Q33378018 | ||
| An X-linked haplotype of Neandertal origin is present among all non-African populations | Q34025486 | ||
| The IMGT/HLA database | Q34456881 | ||
| MHC class I molecules and KIRs in human history, health and survival | Q36047157 | ||
| MHC class I-specific inhibitory receptors and their ligands structure diverse human NK-cell repertoires toward a balance of missing self-response | Q36868743 | ||
| A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. | Q37161006 | ||
| The HLA-B73 antigen has a most unusual structure that defines a second lineage of HLA-B alleles | Q41472003 | ||
| HLA-A11 epitope loss isolates of Epstein-Barr virus from a highly A11+ population | Q41560713 | ||
| Unusual HLA-B alleles in two tribes of Brazilian Indians | Q41623569 | ||
| Unusual selection on the KIR3DL1/S1 natural killer cell receptor in africans | Q46103159 | ||
| Anthropology. A new view of the birth of Homo sapiens | Q46245934 | ||
| Recognition of HLA-A3 and HLA-A11 by KIR3DL2 is peptide-specific. | Q47431117 | ||
| Cw*1505: a novel HLA-C allele isolated from a B*7301 haplotype. | Q48086409 | ||
| HLA-B73: an atypical HLA-B molecule carrying a Bw6-epitope motif variant and a B pocket identical to HLA-B27. | Q48086953 | ||
| Balancing selection is the main force shaping the evolution of innate immunity genes | Q57755879 | ||
| The HLA polymorphsm of two distinctive South-American Indian tribes: The Kaingang and the Guarani | Q58488516 | ||
| New recombinant HLA-B alleles in a tribe of South American Amerindians indicate rapid evolution of MHC class I loci | Q59028899 | ||
| Analysis of the frequencies of HLA-A, B, and C alleles and haplotypes in the five major ethnic groups of the United States reveals high levels of diversity in these loci and contrasting distribution patterns in these populations | Q74480792 | ||
| P433 | issue | 6052 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 89-94 | |
| P577 | publication date | 2011-10-07 | |
| P1433 | published in | Science | Q192864 |
| P1476 | title | The shaping of modern human immune systems by multiregional admixture with archaic humans | |
| P478 | volume | 334 |
| Q59052995 | A Brief Overview of the Last 10 Years of Major Late Pleistocene Discoveries in the Old World: Homo floresiensis, Neanderthal, and Denisovan |
| Q35031374 | A KIR B centromeric region present in Africans but not Europeans protects pregnant women from pre-eclampsia |
| Q62381354 | A dispersal of Homo sapiens from southern to eastern Africa immediately preceded the out-of-Africa migration |
| Q38688783 | A genomic perspective on HLA evolution |
| Q109117027 | A genomic region associated with protection against severe COVID-19 is inherited from Neandertals |
| Q28728528 | A haplotype at STAT2 Introgressed from neanderthals and serves as a candidate of positive selection in Papua New Guinea |
| Q37320419 | A limit to the divergent allele advantage model supported by variable pathogen recognition across HLA-DRB1 allele lineages. |
| Q35593367 | A novel candidate region for genetic adaptation to high altitude in Andean populations |
| Q39064744 | A novel family of human leukocyte antigen class II receptors may have its origin in archaic human species |
| Q34399840 | A paleogenomic perspective on evolution and gene function: new insights from ancient DNA. |
| Q46208923 | A parsimonious neutral model suggests Neanderthal replacement was determined by migration and random species drift. |
| Q36334487 | AD-LIBS: inferring ancestry across hybrid genomes using low-coverage sequence data |
| Q35574773 | Adaptive Evolution as a Predictor of Species-Specific Innate Immune Response. |
| Q61803840 | Adaptive Introgression: An Untapped Evolutionary Mechanism for Crop Adaptation |
| Q34312048 | Adaptive evolution: evaluating empirical support for theoretical predictions |
| Q35589220 | Adaptive gene introgression after secondary contact |
| Q38125824 | Adaptive introgression in animals: examples and comparison to new mutation and standing variation as sources of adaptive variation |
| Q48131025 | Adaptive value of novel MHC immune gene variants |
| Q35254140 | Allele frequency net 2015 update: new features for HLA epitopes, KIR and disease and HLA adverse drug reaction associations |
| Q27687160 | Almost 20 years of Neanderthal palaeogenetics: adaptation, admixture, diversity, demography and extinction |
| Q28244310 | Altitude adaptation in Tibetans caused by introgression of Denisovan-like DNA |
| Q36516246 | Always on My Mind? Recognition of Attractive Faces May Not Depend on Attention |
| Q51146852 | Analysis of Human Sequence Data Reveals Two Pulses of Archaic Denisovan Admixture. |
| Q28597755 | Ancient DNA and human history |
| Q93101152 | Ancient Hybridization and Adaptive Introgression of an Invadolysin Gene in Schistosome Parasites |
| Q26996712 | Ancient genomics |
| Q46586148 | Ancient hybridization and genomic stabilization in a swordtail fish. |
| Q38931465 | Ancient selection for derived alleles at a GDF5 enhancer influencing human growth and osteoarthritis risk |
| Q33681777 | Archaic Adaptive Introgression in TBX15/WARS2. |
| Q38057640 | Archaic human genomics |
| Q28084535 | Archaic inheritance: supporting high-altitude life in Tibet |
| Q37416253 | Associations between human leukocyte antigen class I variants and the Mycobacterium tuberculosis subtypes causing disease |
| Q59489570 | Balancing selection and introgression of newt immune-response genes |
| Q34671949 | Balancing selection on a regulatory region exhibiting ancient variation that predates human-neandertal divergence |
| Q100307406 | Balancing selection versus allele and supertype turnover in MHC class II genes in guppies |
| Q113530490 | Black Feminist Theory in Prehistory |
| Q38888152 | Cancer tolerance, resistance, pathogenicity and virulence: deconstructing the disease state |
| Q50533781 | Characterization and clinical enrichment of HLA-C*07:02-restricted Cytomegalovirus-specific CD8+ T cells. |
| Q37415636 | Class I HLA haplotypes form two schools that educate NK cells in different ways |
| Q38568889 | Co-evolution of MHC class I and variable NK cell receptors in placental mammals |
| Q38568891 | Co-evolution of NK receptors and HLA ligands in humans is driven by reproduction |
| Q51559939 | Colonizing the world in spite of reduced MHC variation. |
| Q52687154 | Craniomandibular form and body size variation of first generation mouse hybrids: A model for hominin hybridization. |
| Q43165848 | Current perspectives on the intensity of natural selection of MHC loci. |
| Q39203922 | Cutting the Stone: Health Defined in the Era of Value-based Care |
| Q37153103 | Defining KIR and HLA Class I Genotypes at Highest Resolution via High-Throughput Sequencing. |
| Q57805334 | Deleterious variation shapes the genomic landscape of introgression |
| Q46502622 | Denisovans, Melanesians, Europeans, and Neandertals: The Confusion of DNA Assumptions and the Biological Species Concept |
| Q38460683 | Detecting balancing selection in genomes: limits and prospects. |
| Q38716685 | Detecting hybridization using ancient DNA. |
| Q34663979 | Detection of ancestry informative HLA alleles confirms the admixed origins of Japanese population. |
| Q91658389 | Differences in MHC-B diversity and KIR epitopes in two populations of wild chimpanzees |
| Q47185303 | Discovery of gorilla MHC-C expressing C1 ligand for KIR. |
| Q91062563 | Disease transmission and introgression can explain the long-lasting contact zone of modern humans and Neanderthals |
| Q46175384 | Disentangling Immediate Adaptive Introgression from Selection on Standing Introgressed Variation in Humans |
| Q40995549 | Distinguishing functional polymorphism from random variation in the sequences of >10,000 HLA-A, -B and -C alleles |
| Q38552461 | Distribution of HLA haplotypes across Japanese Archipelago: similarity, difference and admixture |
| Q89075998 | Divergent Allele Advantage at Human MHC Genes: Signatures of Past and Ongoing Selection |
| Q28732404 | Diverse approaches to analysing the history of human and pathogen evolution: how to tell the story of the past 70 000 years |
| Q41731150 | Diverse functionality among human NK cell receptors for the C1 epitope of HLA-C: KIR2DS2, KIR2DL2, and KIR2DL3. |
| Q57133422 | Don't throw out the sympatric speciation with the crater lake water: fine-scale investigation of introgression provides equivocal support for causal role of secondary gene flow in one of the clearest examples of sympatric speciation |
| Q38656174 | EPAS1 variants in high altitude Tibetan wolves were selectively introgressed into highland dogs |
| Q28607692 | Early modern human dispersal from Africa: genomic evidence for multiple waves of migration |
| Q31008103 | Eigenanalysis of SNP data with an identity by descent interpretation |
| Q37547474 | Elucidating the origin of HLA-B*73 allelic lineage: Did modern humans benefit by archaic introgression? |
| Q41380995 | Evidence for Adaptive Introgression of Disease Resistance Genes Among Closely Related Arabidopsis Species |
| Q26830001 | Evidence for archaic adaptive introgression in humans |
| Q57025279 | Evidence that RNA Viruses Drove Adaptive Introgression between Neanderthals and Modern Humans |
| Q22122318 | Evolution: What makes a modern human |
| Q56396355 | Evolutionary and Medical Consequences of Archaic Introgression into Modern Human Genomes |
| Q28715053 | Evolutionary medicine: its scope, interest and potential |
| Q64079960 | Fine-Scale Characterization of Genomic Structural Variation in the Human Genome Reveals Adaptive and Biomedically Relevant Hotspots |
| Q28601941 | First evidence of hybridization between golden jackal (Canis aureus) and domestic dog (Canis familiaris) as revealed by genetic markers |
| Q30000009 | Fixing Formalin: A Method to Recover Genomic-Scale DNA Sequence Data from Formalin-Fixed Museum Specimens Using High-Throughput Sequencing |
| Q38007345 | Functional primate genomics--leveraging the medical potential |
| Q34047556 | Genetic Adaptation and Neandertal Admixture Shaped the Immune System of Human Populations |
| Q42822566 | Genetic Time Travel |
| Q41842884 | Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acids |
| Q31151856 | Genetic origin of Behçet's disease population in Denizli, Turkey; population genetics data analysis; historical demography and geographical perspectives based on β-globin gene cluster haplotype variation |
| Q35168836 | Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci |
| Q28657760 | Genetic variation and adaptation in Africa: implications for human evolution and disease |
| Q36473385 | Genomic Signatures of Selective Pressures and Introgression from Archaic Hominins at Human Innate Immunity Genes |
| Q21144912 | Genomic data reveal a complex making of humans |
| Q40446900 | Geographic Population Structure in Epstein-Barr Virus Revealed by Comparative Genomics |
| Q30846768 | Gorilla MHC class I gene and sequence variation in a comparative context |
| Q41457540 | HLA class I variation in Iranian Lur and Kurd populations: high haplotype and allotype diversity with an abundance of KIR ligands. |
| Q94076941 | HLA-A、HLA-DRB1等位基因多态性与中国南方活动性肺结核患者遗传易感性的相关性 |
| Q52684468 | HLA-B*07, HLA-DRB1*07, HLA-DRB1*12, and HLA-C*03:02 Strongly Associate With BMI: Data From 1.3 Million Healthy Chinese Adults. |
| Q46309376 | Harnessing ancient genomes to study the history of human adaptation |
| Q36159552 | How microbiology helps define the rhizome of life |
| Q34197750 | Human evolution out of Africa: the role of refugia and climate change |
| Q36228947 | Human evolution: a tale from ancient genomes. |
| Q37126619 | Human phylogeography and diversity |
| Q21089902 | Human remains from the Pleistocene-Holocene transition of southwest China suggest a complex evolutionary history for East Asians |
| Q92925171 | Hybridization in human evolution: Insights from other organisms |
| Q90575788 | Inferred divergent gene regulation in archaic hominins reveals potential phenotypic differences |
| Q40387467 | Innate immunity and human diseases: from archaic introgression to natural selection |
| Q57049678 | Intragenus (Homo) variation in a chemokine receptor gene (CCR5) |
| Q33778843 | Introgression from domestic goat generated variation at the major histocompatibility complex of Alpine ibex |
| Q28602436 | Introgression of Neandertal- and Denisovan-like Haplotypes Contributes to Adaptive Variation in Human Toll-like Receptors |
| Q92001070 | KIR Variation in Iranians Combines High Haplotype and Allotype Diversity With an Abundance of Functional Inhibitory Receptors |
| Q34345310 | KIR diversity in Māori and Polynesians: populations in which HLA-B is not a significant KIR ligand. |
| Q38849746 | KIR2DS5 allotypes that recognize the C2 epitope of HLA-C are common among Africans and absent from Europeans |
| Q38870254 | Living in an adaptive world: Genomic dissection of the genus Homo and its immune response |
| Q35751442 | Loss and Gain of Natural Killer Cell Receptor Function in an African Hunter-Gatherer Population |
| Q34359146 | Major histocompatibility complex genomics and human disease |
| Q34342600 | Malaise, melancholia and madness: the evolutionary legacy of an inflammatory bias |
| Q55317822 | Meta-populational demes constitute a reservoir for large MHC allele diversity in wild house mice (Mus musculus). |
| Q56864608 | Modern human genomes reveal our inner Neanderthal |
| Q67223691 | Morphology of the Denisovan phalanx closer to modern humans than to Neanderthals |
| Q91610767 | Multiple selective sweeps of ancient polymorphisms in and around LTα located in the MHC class III region on chromosome 6 |
| Q34322389 | Neandertal origin of genetic variation at the cluster of OAS immunity genes |
| Q40720760 | Neanderthal genomics suggests a pleistocene time frame for the first epidemiologic transition |
| Q34391875 | Neanderthal introgression at chromosome 3p21.31 was under positive natural selection in East Asians |
| Q97905413 | Neanderthal introgression reintroduced functional ancestral alleles lost in Eurasian populations |
| Q47634422 | Neanderthal origin of the haplotypes carrying the functional variant Val92Met in the MC1R in modern humans |
| Q35676477 | Negligible nuclear introgression despite complete mitochondrial capture between two species of chipmunks |
| Q58085168 | Niche adaptation and viral transmission of human papillomaviruses from archaic hominins to modern humans |
| Q43443647 | No evidence for nuclear introgression despite complete mtDNA replacement in the Carpathian newt (Lissotriton montandoni). |
| Q21089837 | North African populations carry the signature of admixture with Neandertals |
| Q38005891 | Nothing in medicine makes sense, except in the light of evolution |
| Q28706270 | Nuclear genetic diversity in human lice (Pediculus humanus) reveals continental differences and high inbreeding among worldwide populations |
| Q28680670 | On the antiquity of language: the reinterpretation of Neandertal linguistic capacities and its consequences |
| Q37436665 | Outlier Loci and Selection Signatures of Simple Sequence Repeats (SSRs) in Flax (Linum usitatissimum L.). |
| Q34038578 | Paleontology. Did the Denisovans cross Wallace's Line? |
| Q24603841 | Polar and brown bear genomes reveal ancient admixture and demographic footprints of past climate change |
| Q38798040 | Population genomics reveals speciation and introgression between Brown Norway rats and their sibling species. |
| Q51410352 | Rebooting Human Immunology. |
| Q49222029 | Recent advances in understanding evolution of the placenta: insights from transcriptomics. |
| Q35849756 | Red Queen Processes Drive Positive Selection on Major Histocompatibility Complex (MHC) Genes |
| Q47377500 | Reintroduction of a Homocysteine Level-Associated Allele into East Asians by Neanderthal Introgression |
| Q34400818 | Resurrecting surviving Neandertal lineages from modern human genomes |
| Q36916982 | Review: Immunogenetics of human placentation |
| Q28728225 | Rhizome of life, catastrophes, sequence exchanges, gene creations, and giant viruses: how microbial genomics challenges Darwin |
| Q37547317 | Selective Landscapes in newt Immune Genes Inferred from Patterns of Nucleotide Variation |
| Q47980242 | Selective pressures on MHC class II genes in the guppy (Poecilia reticulata) as inferred by hierarchical analysis of population structure |
| Q38737497 | Sequences of 95 human MHC haplotypes reveal extreme coding variation in genes other than highly polymorphic HLA class I and II. |
| Q33639328 | Skewed Exposure to Environmental Antigens Complements Hygiene Hypothesis in Explaining the Rise of Allergy |
| Q52720612 | Strong Amerindian Mitonuclear Discordance in Puerto Rican Genomes Suggests Amerindian Mitochondrial Benefit. |
| Q36071869 | Strong reproductive isolation and narrow genomic tracts of differentiation among three woodpecker species in secondary contact. |
| Q34334824 | Study of cynomolgus monkey (Macaca fascicularis) Mhc DRB gene polymorphism in four populations |
| Q91740280 | THE EXPOSOME IN HUMAN EVOLUTION: FROM DUST TO DIESEL |
| Q36759843 | The Columbian Exchange as a source of adaptive introgression in human populations |
| Q35977651 | The Genetic Cost of Neanderthal Introgression |
| Q57307457 | The Hybrid Origin of “Modern” Humans |
| Q26744597 | The Impact of Evolutionary Driving Forces on Human Complex Diseases: A Population Genetics Approach |
| Q46479541 | The PNarec method for detection of ancient recombinations through phylogenetic network analysis |
| Q40690096 | The Polynesian gene pool: an early contribution by Amerindians to Easter Island |
| Q64095575 | The association analysis between HLA-A*26 and Behçet's disease |
| Q28304347 | The complete genome sequence of a Neanderthal from the Altai Mountains |
| Q114381991 | The contribution of ancient hominin genomes from Siberia to our understanding of human evolution |
| Q35130067 | The contribution of natural selection to present-day susceptibility to chronic inflammatory and autoimmune disease |
| Q36179949 | The evolution of human adiposity and obesity: where did it all go wrong? |
| Q33812612 | The genomic landscape of Neanderthal ancestry in present-day humans |
| Q27024634 | The human condition-a molecular approach |
| Q36935092 | The impact of natural selection on health and disease: uses of the population genetics approach in humans |
| Q27027962 | The impact of recent events on human genetic diversity |
| Q58577159 | The influence of Neanderthal alleles on cytotoxic response |
| Q36639417 | The major histocompatibility complex in Old World camelids and low polymorphism of its class II genes |
| Q97528107 | The origin of domestication genes in goats |
| Q28603615 | The phenotypic legacy of admixture between modern humans and Neandertals |
| Q26825108 | The telomeric sync model of speciation: species-wide telomere erosion triggers cycles of transposon-mediated genomic rearrangements, which underlie the saltatory appearance of nonadaptive characters |
| Q28516244 | Tracing the peopling of the world through genomics |
| Q35701135 | Tracking human migrations by the analysis of the distribution of HLA alleles, lineages and haplotypes in closed and open populations |
| Q39356598 | Transmission between Archaic and Modern Human Ancestors during the Evolution of the Oncogenic Human Papillomavirus 16. |
| Q64228645 | Two to Tango: Co-evolution of Hominid Natural Killer Cell Receptors and MHC |
| Q22065651 | UNEXPECTEDLY MANY EXTINCT HOMININS |
| Q28067740 | Understanding rare and common diseases in the context of human evolution |
| Q34477708 | Untangling the hybrid nature of modern pig genomes: a mosaic derived from biogeographically distinct and highly divergent Sus scrofa populations |
| Q37641722 | Variable NK cell receptors and their MHC class I ligands in immunity, reproduction and human evolution |
| Q28660599 | Worldwide patterns of ancestry, divergence, and admixture in domesticated cattle |
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