| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1085889871 |
| P356 | DOI | 10.1038/NATURE22336 |
| P698 | PubMed publication ID | 28593953 |
| P50 | author | Jean-Jacques Hublin | Q1684915 |
| Katerina Harvati | Q21264123 | ||
| Philipp Gunz | Q42306024 | ||
| Simon Neubauer | Q47502129 | ||
| Adeline Le Cabec | Q57077489 | ||
| P2093 | author name string | Stefano Benazzi | |
| Shara E. Bailey | |||
| Abdelouahed Ben-Ncer | |||
| Matthew M. Skinner | |||
| Inga Bergmann | |||
| Sarah E. Freidline | |||
| P2860 | cites work | The Later Stone Age calvaria from Iwo Eleru, Nigeria: morphology and chronology | Q21089939 |
| Possible interbreeding in late Italian Neanderthals? New data from the Mezzena jaw (Monti Lessini, Verona, Italy) | Q21559672 | ||
| Whole-mtDNA Genome Sequence Analysis of Ancient African Lineages | Q22066015 | ||
| Stratigraphic placement and age of modern humans from Kibish, Ethiopia | Q22122476 | ||
| Pleistocene Homo sapiens from Middle Awash, Ethiopia | Q22122501 | ||
| A high-coverage genome sequence from an archaic Denisovan individual | Q24595378 | ||
| An early modern human from the Peştera cu Oase, Romania | Q24673203 | ||
| Early modern humans from the Pestera Muierii, Baia de Fier, Romania | Q24676912 | ||
| Earliest evidence of modern human life history in North African early Homo sapiens | Q24678513 | ||
| The human chin revisited: what is it and who has it? | Q28145236 | ||
| Early dispersal of modern humans in Europe and implications for Neanderthal behaviour | Q28252076 | ||
| MIA - A free and open source software for gray scale medical image analysis | Q28657660 | ||
| The pattern of endocranial ontogenetic shape changes in humans | Q28751317 | ||
| Early modern human diversity suggests subdivided population structure and a complex out-of-Africa scenario | Q28754721 | ||
| Modern human origins: progress and prospects | Q28765062 | ||
| The age of the hominin fossils from Jebel Irhoud, Morocco, and the origins of the Middle Stone Age | Q30156628 | ||
| Principles for the virtual reconstruction of hominin crania | Q33347185 | ||
| The Late Upper Paleolithic skeleton Villabruna 1 (Italy): a source of data on biology and behavior of a 14,000 year-old hunter. | Q33516515 | ||
| Hominid molars from a Middle Stone Age level at the Mumba Rock Shelter, Tanzania | Q34166876 | ||
| A uniquely modern human pattern of endocranial development. Insights from a new cranial reconstruction of the Neandertal newborn from Mezmaiskaya | Q34244916 | ||
| Middle Pleistocene human facial morphology in an evolutionary and developmental context | Q34299828 | ||
| Reconstructed Homo habilis type OH 7 suggests deep-rooted species diversity in early Homo. | Q34465703 | ||
| Neandertal roots: Cranial and chronological evidence from Sima de los Huesos | Q35191943 | ||
| Preliminary observations on the BK 8518 mandible from Baringo, Kenya | Q38595942 | ||
| The fossil human remains from the Paleolithic site of Sidi Abderrahman (Morocco). | Q38878226 | ||
| Ohalo II H2: a 19,000-year-old skeleton from a water-logged site at the Sea of Galilee, Israel | Q39065741 | ||
| Recent human evolution in northwestern Africa | Q39085166 | ||
| Middle Pleistocene hominids from Olduvai Gorge, northern Tanzania | Q39398892 | ||
| Cervical and crown outline analysis of worn Neanderthal and modern human lower second deciduous molars | Q40069682 | ||
| Did a discrete event 200,000-100,000 years ago produce modern humans? | Q43860497 | ||
| Anterior tooth root morphology and size in Neanderthals: taxonomic and functional implications. | Q45979355 | ||
| Cioclovina (Romania): affinities of an early modern European | Q46297900 | ||
| Direct dating of Florisbad hominid. | Q46318706 | ||
| Allometry, merism, and tooth shape of the upper deciduous M2 and permanent M1. | Q46938369 | ||
| A Neandertal mandible from the Cova del Gegant (Sitges, Barcelona, Spain). | Q47273746 | ||
| Neandertal mandibles from the Sima de las Palomas del Cabezo Gordo, Murcia, southeastern Spain | Q47420777 | ||
| Discrimination of extant Pan species and subspecies using the enamel-dentine junction morphology of lower molars | Q47601663 | ||
| Enamel-dentine junction (EDJ) morphology distinguishes the lower molars of Australopithecus africanus and Paranthropus robustus | Q47653431 | ||
| Landmark methods for forms without landmarks: morphometrics of group differences in outline shape | Q48731684 | ||
| Extensions of the Procrustes Method for the Optimal Superimposition of Landmarks | Q56502573 | ||
| [Comparative morphologic characteristics of the Upper Paleolithic specimens from Oberkassel near Bonn] | Q57152763 | ||
| The rodents from the late middle Pleistocene hominid-bearing site of J'bel Irhoud, Morocco, and their chronological and paleoenvironmental implications | Q58181531 | ||
| Advances in Geometric Morphometrics | Q59160788 | ||
| Evolutionary interpretation of the modern human-like facial morphology of the Atapuerca Gran Dolina-TD6 hominins | Q59204292 | ||
| The origin of modern anatomy: By speciation or intraspecific evolution? | Q59345001 | ||
| Neurocranial evolution in modern humans: the case of Jebel Irhoud 1 | Q59443799 | ||
| P2507 | corrigendum / erratum | Author Correction: New fossils from Jebel Irhoud, Morocco and the pan-African origin of Homo sapiens | Q56380693 |
| P433 | issue | 7657 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Morocco | Q1028 |
| Homo sapiens | Q15978631 | ||
| P304 | page(s) | 289-292 | |
| P577 | publication date | 2017-06-07 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | New fossils from Jebel Irhoud, Morocco and the pan-African origin of Homo sapiens | |
| P478 | volume | 546 |
| Q48215893 | 150,000-year palaeoclimate record from northern Ethiopia supports early, multiple dispersals of modern humans from Africa. |
| Q96640504 | A 2,000-year-old specimen with intraerythrocytic Bartonella quintana |
| Q64972623 | A catalog of single nucleotide changes distinguishing modern humans from archaic hominins. |
| Q62381354 | A dispersal of Homo sapiens from southern to eastern Africa immediately preceded the out-of-Africa migration |
| Q46275374 | A multivariate assessment of the Dali hominin cranium from China: Morphological affinities and implications for Pleistocene evolution in East Asia |
| Q52594183 | A reassessment of the early archaeological record at Leang Burung 2, a Late Pleistocene rock-shelter site on the Indonesian island of Sulawesi. |
| Q53428694 | Advances in human behaviour came surprisingly early in Stone Age. |
| Q64085589 | African evolutionary history inferred from whole genome sequence data of 44 indigenous African populations |
| Q64082481 | Alleles associated with physical activity levels are estimated to be older than anatomically modern humans |
| Q45953900 | An Evolutionary Facelift: Varied Cranial Vaults of Early Homo sapiens. |
| Q92539574 | An Evolutionary Perspective on Vector-Borne Diseases |
| Q41510688 | An Upper Limit on the Functional Fraction of the Human Genome |
| Q60322493 | An early Aurignacian arrival in southwestern Europe |
| Q92134951 | An early dispersal of modern humans from Africa to Greece |
| Q92296503 | An upper bound for the background rate of human extinction |
| Q92860939 | Ancient West African foragers in the context of African population history |
| Q65514528 | Apidima Cave fossils provide earliest evidence of Homo sapiens in Eurasia |
| Q46299510 | Archaic Hominin Introgression in Africa Contributes to Functional Salivary MUC7 Genetic Variation. |
| Q91622844 | Archaic human remains from Hualongdong, China, and Middle Pleistocene human continuity and variation |
| Q128321130 | Behavioural modernity, investigative disintegration & Rubicon expectation |
| Q95533910 | Correction |
| Q60300830 | Covariation of the endocranium and splanchnocranium during great ape ontogeny |
| Q91971777 | Dating the skull from Broken Hill, Zambia, and its position in human evolution |
| Q90044614 | Deciphering African late middle Pleistocene hominin diversity and the origin of our species |
| Q55950877 | Defining the ‘generalist specialist’ niche for Pleistocene Homo sapiens |
| Q63866209 | Dental evolutionary rates and its implications for the Neanderthal-modern human divergence. |
| Q55882858 | Did Our Species Evolve in Subdivided Populations across Africa, and Why Does It Matter? |
| Q90372481 | Earliest African evidence of carcass processing and consumption in cave at 700 ka, Casablanca, Morocco |
| Q55223928 | Endocast morphology of Homo naledi from the Dinaledi Chamber, South Africa. |
| Q128321167 | Evolution and the Origins of Visual Art: An Archaeological Perspective |
| Q90009538 | Evolutionary Traits that Enable Scleractinian Corals to Survive Mass Extinction Events |
| Q56396355 | Evolutionary and Medical Consequences of Archaic Introgression into Modern Human Genomes |
| Q57532971 | Genetic Heterogeneity between Berbers and Arabs |
| Q91725008 | Genomic evidence for shared common ancestry of East African hunting-gathering populations and insights into local adaptation |
| Q122294583 | Geometric morphometric variability in the supraorbital and orbital region of Middle Pleistocene hominins: Implications for the taxonomy and evolution of later Homo |
| Q104471852 | Gravettian cranial morphology and human group affinities during the European Upper Palaeolithic |
| Q123952199 | Herbivore dental wear analysis since the end of the middle Pleistocene to the beginning of the Holocene in different archaeological contexts of Morocco |
| Q98513770 | High-throughput microCT scanning of small specimens: preparation, packing, parameters and post-processing |
| Q55882860 | Homo sapiens in Arabia by 85,000 years ago |
| Q91801331 | Human Genomic Diversity Where the Mediterranean Joins the Atlantic |
| Q91868824 | Human augmentation of ecosystems: objectives for food production and science by 2045 |
| Q93048923 | Human microbial ecology and the rising new medicine |
| Q91992695 | Human reproductive behavior, life history, and the Challenge Hypothesis: A 30-year review, retrospective and future directions |
| Q112983141 | Human teeth from securely stratified Middle Stone Age contexts at Sibudu, South Africa |
| Q93088100 | Hypotheses for the Evolution of Reduced Reactive Aggression in the Context of Human Self-Domestication |
| Q113528224 | Identifying biological affinities of Holocene northern Iberian populations through the inner structures of the upper first molars |
| Q128321145 | Investigating habitat heterogeneity of Late Pleistocene archaeological sites in eastern Africa from stable isotopes |
| Q57061721 | Is early silcrete heat treatment a new behavioural proxy in the Middle Stone Age? |
| Q49497809 | Israeli fossils are the oldest modern humans ever found outside of Africa |
| Q84497066 | Language evolution to revolution: the leap from rich-vocabulary non-recursive communication system to recursive language 70,000 years ago was associated with acquisition of a novel component of imagination, called Prefrontal Synthesis, enabled by a m |
| Q107356356 | Late Quaternary Biomass Burning in Northwest Africa and Interactions With Climate, Vegetation, and Humans |
| Q60670737 | Limits of long-term selection against Neandertal introgression |
| Q112804815 | Lithic Technology at Loiyangalani, a Late Middle Stone Age Site in the Serengeti, Tanzania |
| Q112982865 | Middle Palaeolithic occupations in central Saudi Arabia during MIS 5 and MIS 7: new insights on the origins of the peopling of Arabia |
| Q57094576 | Middle Stone Age human teeth from Magubike rockshelter, Iringa Region, Tanzania |
| Q92133758 | Molecular Mechanism of Functional Ingredients in Barley to Combat Human Chronic Diseases |
| Q51336151 | Mosquito-Borne Human Viral Diseases: Why Aedes aegypti? |
| Q91610767 | Multiple selective sweeps of ancient polymorphisms in and around LTα located in the MHC class III region on chromosome 6 |
| Q59702213 | Neandertal Introgression Sheds Light on Modern Human Endocranial Globularity |
| Q112805270 | New Light on the Silent Millennia: Mediterranean Africa, ca. 4000–900 BC |
| Q55867285 | Oldest Homo sapiens fossil claim rewrites our species' history |
| Q97516568 | On holes and strings: Earliest displays of human adornment in the Middle Palaeolithic |
| Q46530479 | On the origin of modern humans: Asian perspectives |
| Q64098134 | Out of Africa by spontaneous migration waves |
| Q57197794 | Out of Africa: demographic and colonization history of the Algerian mouse (Mus spretus Lataste) |
| Q55397791 | Outstanding questions in the study of archaic hominin admixture. |
| Q36395645 | Palaeoanthropology: On the origin of our species |
| Q93012669 | Population structure and the evolution of Homo sapiens in Africa |
| Q57258469 | Progressive aridification in East Africa over the last half million years and implications for human evolution |
| Q128152107 | Rapid increase in production of symbolic artifacts after 45,000 years ago is not a consequence of taphonomic bias |
| Q55168713 | Recently evolved human-specific methylated regions are enriched in schizophrenia signals. |
| Q100996201 | Reconstructing prehistoric demography: What role for extant hunter-gatherers? |
| Q99561662 | Regional patterns of diachronic technological change in the Howiesons Poort of southern Africa |
| Q93112633 | Reply to 'Dating on its own cannot resolve hominin occupation patterns' and 'No reliable evidence for a very early Aurignacian in Southern Iberia' |
| Q90050761 | Searching for Signatures of Cold Climate Adaptation in TRPM8 Gene in Populations of East Asian Ancestry |
| Q46296377 | Southern African ancient genomes estimate modern human divergence to 350,000 to 260,000 years ago. |
| Q61771741 | Specialized rainforest hunting by Homo sapiens ~45,000 years ago |
| Q56522844 | Supraorbital morphology and social dynamics in human evolution |
| Q125887443 | Symbolic expression in Pleistocene Sahul, Sunda, and Wallacea |
| Q49680023 | Teeth as pearls of wisdom |
| Q63664895 | Temporal evidence shows Australopithecus sediba is unlikely to be the ancestor of Homo |
| Q112777735 | The Fossil Human from Rabat-Kébibat (Morocco): Comparative Study of the Cranial and Mandibular Fragments |
| Q41994001 | The HLA-B landscape of Africa: signatures of pathogen-driven selection and molecular identification of candidate alleles to malaria protection |
| Q58106004 | The Lake CHAd Deep DRILLing project (CHADRILL) – targeting ∼ 10 million years of environmental and climate change in Africa |
| Q38669444 | The North African Middle Stone Age and its place in recent human evolution. |
| Q90678079 | The Prevotella copri Complex Comprises Four Distinct Clades Underrepresented in Westernized Populations |
| Q112803691 | The Role of North Africa in the Emergence and Development of Modern Behaviors: An Integrated Approach |
| Q56895491 | The Role of aDNA in Understanding the Coevolutionary Patterns of Human Sexually Transmitted Infections |
| Q30156628 | The age of the hominin fossils from Jebel Irhoud, Morocco, and the origins of the Middle Stone Age |
| Q92023552 | The ancestral and industrialized gut microbiota and implications for human health |
| Q47491209 | The evolution of modern human brain shape |
| Q63170520 | The evolutionary history of the human face |
| Q47192118 | The growth pattern of Neandertals, reconstructed from a juvenile skeleton from El Sidrón (Spain). |
| Q93083774 | The long walk to African genomics |
| Q49745486 | The peopling of the last Green Sahara revealed by high-coverage resequencing of trans-Saharan patrilineages |
| Q60019814 | The success of failed Homo sapiens dispersals out of Africa and into Asia |
| Q127531708 | Theoretical and Methodological Approaches to Ecological Changes, Social Behaviour and Human Intergroup Tolerance 300,000 to 30,000 BP |
| Q46319839 | Twentieth anniversary of Homo antecessor (1997-2017): a review |
| Q116152810 | Updating Neanderthals: Taking stock of more than 160 years of studies |
| Q47771376 | Variation in Akt protein kinases in human populations. |
| Q64236014 | Variation in the repulsive guidance molecule family in human populations |
| Q56001020 | When did Homo sapiens first reach Southeast Asia and Sahul? |
| Q89793880 | Which way to the dawn of speech?: Reanalyzing half a century of debates and data in light of speech science |
| Q61904250 | Which way to turn? Is the Haua Fteah a Levantine site? |
| Q63437286 | Whole-genome sequence analysis of a Pan African set of samples reveals archaic gene flow from an extinct basal population of modern humans into sub-Saharan populations |
| Q99578689 | ZMAT2 in Humans and Other Primates: A Highly Conserved and Understudied Gene |
Search more.