| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1098/RSTB.2015.0237 |
| P8608 | Fatcat ID | release_jyyvbufz4vd7toj33okiubiqwm |
| P932 | PMC publication ID | 4920294 |
| P698 | PubMed publication ID | 27298468 |
| P50 | author | Christopher B. Stringer | Q761415 |
| P2860 | cites work | Were rivers flowing across the Sahara during the last interglacial? Implications for human migration through Africa | Q21089750 |
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| A new hominid fossil skull (L.H. 18) from the Ngaloba Beds, Laetoli, northern Tanzania | Q34712766 | ||
| Why we are not all multiregionalists now. | Q35139705 | ||
| Neandertal roots: Cranial and chronological evidence from Sima de los Huesos | Q35191943 | ||
| The bony labyrinth of the middle Pleistocene Sima de los Huesos hominins (Sierra de Atapuerca, Spain). | Q35894420 | ||
| Earliest evidence of personal ornaments associated with burial: the Conus shells from Border Cave | Q35991851 | ||
| Iwo Eleru's place among Late Pleistocene and Early Holocene populations of North and East Africa | Q39491992 | ||
| Effects of brain and facial size on basicranial form in human and primate evolution | Q39884643 | ||
| Virtual ancestor reconstruction: Revealing the ancestor of modern humans and Neandertals | Q40017081 | ||
| Climatic variability, plasticity, and dispersal: A case study from Lake Tana, Ethiopia. | Q40426152 | ||
| Using genetic evidence to evaluate four palaeoanthropological hypotheses for the timing of Neanderthal and modern human origins | Q43405314 | ||
| Did a discrete event 200,000-100,000 years ago produce modern humans? | Q43860497 | ||
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| Direct dating of Florisbad hominid. | Q46318706 | ||
| A description of the Omo I postcranial skeleton, including newly discovered fossils | Q46472448 | ||
| Confirmation of a late middle Pleistocene age for the Omo Kibish 1 cranium by direct uranium-series dating | Q46804822 | ||
| A morphometric re-assessment of BOU-VP-16/1 from Herto, Ethiopia | Q46860987 | ||
| The status of Homo heidelbergensis (Schoetensack 1908). | Q47195372 | ||
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| Morphological description and comparison of the dental remains from Atapuerca-Sima de los Huesos site (Spain). | Q47247080 | ||
| U-series and ESR analyses of bones and teeth relating to the human burials from Skhul | Q47267806 | ||
| A critique of the chronometric evidence for hominid fossils: I. Africa and the Near East 500-50 ka. | Q47284202 | ||
| Excavating Neandertal and Denisovan DNA from the genomes of Melanesian individuals. | Q47325522 | ||
| Pathological alterations in the archaic Homo sapiens cranium from Eliye Springs, Kenya | Q47410906 | ||
| A new archaic Homo sapiens cranium from Eliye Springs, West Turkana, Kenya | Q47419401 | ||
| Evaluating developmental shape changes in Homo antecessor subadult facial morphology | Q47724318 | ||
| Omo human skeletal remains | Q47761084 | ||
| Modern human origins backdated | Q47797487 | ||
| P433 | issue | 1698 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Homo sapiens | Q15978631 |
| P577 | publication date | 2016-07-01 | |
| P1433 | published in | Philosophical Transactions of the Royal Society B | Q2153239 |
| P1476 | title | The origin and evolution of Homo sapiens | |
| P478 | volume | 371 |
| Q48215893 | 150,000-year palaeoclimate record from northern Ethiopia supports early, multiple dispersals of modern humans from Africa. |
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| Q62381354 | A dispersal of Homo sapiens from southern to eastern Africa immediately preceded the out-of-Africa migration |
| Q38368307 | Ancient Evolution and Dispersion of Human Papillomavirus Type 58 Variants |
| Q65514528 | Apidima Cave fossils provide earliest evidence of Homo sapiens in Eurasia |
| Q47218435 | Archaeology: Unexpectedly early signs of Americans |
| Q91622844 | Archaic human remains from Hualongdong, China, and Middle Pleistocene human continuity and variation |
| Q90242524 | Beyond multiregional and simple out-of-Africa models of human evolution |
| Q37598999 | Brain enlargement and dental reduction were not linked in hominin evolution |
| 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 |
| 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? |
| Q92536839 | From Physical Aggression to Verbal Behavior: Language Evolution and Self-Domestication Feedback Loop |
| Q122294583 | Geometric morphometric variability in the supraorbital and orbital region of Middle Pleistocene hominins: Implications for the taxonomy and evolution of later Homo |
| Q29886675 | Homo naledi and Pleistocene hominin evolution in subequatorial Africa |
| Q55882860 | Homo sapiens in Arabia by 85,000 years ago |
| Q91801331 | Human Genomic Diversity Where the Mediterranean Joins the Atlantic |
| Q112983141 | Human teeth from securely stratified Middle Stone Age contexts at Sibudu, South Africa |
| Q83227256 | Insights into the evolution of social systems and species from baboon studies |
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| Q91370287 | Knowing ourselves |
| Q28597310 | Major transitions in human evolution |
| Q112805401 | Middle Stone Age Bifacial Technology and Pressure Flaking at the MIS 3 Site of Toumboura III, Eastern Senegal |
| Q57094576 | Middle Stone Age human teeth from Magubike rockshelter, Iringa Region, Tanzania |
| Q36300598 | Neanderthal behaviour, diet, and disease inferred from ancient DNA in dental calculus |
| Q41958260 | New opportunities rising |
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| Q91638182 | No Country for Oldowan Men: Emerging Factors in Language Evolution |
| Q123314218 | Not by demography alone: Neanderthal extinction and null hypotheses in paleoanthropological explanation |
| Q116152806 | Nubian Levallois technology associated with southernmost Neanderthals |
| Q64098134 | Out of Africa by spontaneous migration waves |
| Q36395645 | Palaeoanthropology: On the origin of our species |
| Q91703268 | Playing with language, creating complexity: Has play contributed to the evolution of complex language? |
| Q93012669 | Population structure and the evolution of Homo sapiens in Africa |
| Q49222029 | Recent advances in understanding evolution of the placenta: insights from transcriptomics |
| Q42680482 | Self-domestication in Homo sapiens: Insights from comparative genomics. |
| Q46287254 | Shape analysis of spatial relationships between orbito-ocular and endocranial structures in modern humans and fossil hominids. |
| Q37304814 | Status effects on men's reproductive success |
| Q55317086 | The Emergence of Modern Languages: Has Human Self-Domestication Optimized Language Transmission? |
| Q42200163 | The Evolution of Lateralized Brain Circuits |
| Q112805134 | The Middle Stone Age (MSA) Technological Patterns, Innovations, and Behavioral Changes at Bed VIA of Mumba Rockshelter, Northern Tanzania |
| Q38669444 | The North African Middle Stone Age and its place in recent human evolution. |
| Q91739937 | The dental proteome of Homo antecessor |
| Q47491209 | The evolution of modern human brain shape |
| Q63170520 | The evolutionary history of the human face |
| Q46319839 | Twentieth anniversary of Homo antecessor (1997-2017): a review |
| Q64079906 | Williams Syndrome, Human Self-Domestication, and Language Evolution |
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