| scholarly article | Q13442814 |
| P2093 | author name string | Sarah A Tishkoff | |
| Richard R Hudson | |||
| Bruce T Lahn | |||
| Eric J Vallender | |||
| Jeffrey R Anderson | |||
| Sandra L Gilbert | |||
| P. D. Evans | |||
| Nitzan Mekel-Bobrov | |||
| Leila M Vaez-Azizi | |||
| P2860 | cites work | Stratigraphic placement and age of modern humans from Kibish, Ethiopia | Q22122476 |
| P433 | issue | 5741 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | microcephaly | Q431643 |
| brain size | Q1030681 | ||
| P304 | page(s) | 1717-1720 | |
| P577 | publication date | 2005-09-09 | |
| P1433 | published in | Science | Q192864 |
| P1476 | title | Microcephalin, a Gene Regulating Brain Size, Continues to Evolve Adaptively in Humans | |
| P478 | volume | 309 |
| Q37624088 | "Neuroarchaeology": exploring the links between neural and cultural plasticity. |
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| Q35822248 | A primary microcephaly protein complex forms a ring around parental centrioles. |
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| Q128152078 | Advances in the Study of the Origin of Humanness |
| Q35133190 | An evolutionary analysis of antigen processing and presentation across different timescales reveals pervasive selection |
| Q60907117 | Analysis validation has been neglected in the Age of Reproducibility |
| Q33556686 | Ancient and recent selective pressures shaped genetic diversity at AIM2-like nucleic acid sensors. |
| Q38057640 | Archaic human genomics |
| Q24570114 | Autosomal Recessive Primary Microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum |
| Q25257670 | Being positive about selection |
| Q55982506 | Brain Size Growth and Life History in Human Evolution |
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| Q24671786 | Brain shape in human microcephalics and Homo floresiensis |
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| Q36361047 | Clinical implications of human population differences in genome-wide rates of functional genotypes |
| Q22337065 | Comment on Papers by Evans et al. and Mekel-Bobrov et al. on Evidence for Positive Selection of MCPH1 and ASPM |
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| Q24657752 | Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutation |
| Q31066777 | Genetic, physiologic and ecogeographic factors contributing to variation in Homo sapiens: Homo floresiensis reconsidered |
| Q21560957 | Genome features of "Dark-fly", a Drosophila line reared long-term in a dark environment |
| Q33869396 | Genome-wide footprints of pig domestication and selection revealed through massive parallel sequencing of pooled DNA. |
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| Q36617412 | Human brain evolution |
| Q28303731 | Human brain evolution and the "Neuroevolutionary Time-depth Principle:" Implications for the Reclassification of fear-circuitry-related traits in DSM-V and for studying resilience to warzone-related posttraumatic stress disorder |
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| Q38212628 | Induced pluripotent stem cells for modeling of pediatric neurological disorders |
| Q83368965 | Intelligence and homosexuality |
| Q22337200 | Linguistic tone is related to the population frequency of the adaptive haplogroups of two brain size genes, ASPM and Microcephalin |
| Q21145227 | Localizing recent adaptive evolution in the human genome |
| Q48157928 | Long-standing balancing selection in the THBS4 gene: influence on sex-specific brain expression and gray matter volumes in Alzheimer disease. |
| Q42674018 | Long-term balancing selection maintains trans-specific polymorphisms in the human TRIM5 gene |
| Q128151837 | MATRIX THINKING: AN ADAPTATION AT THE FOUNDATION OF HUMAN SCIENCE, RELIGION, AND ART |
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| Q33284260 | Male and female brain evolution is subject to contrasting selection pressures in primates |
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| Q28658258 | Microcephaly genes evolved adaptively throughout the evolution of eutherian mammals |
| Q28750176 | Molecular evolution of genes in avian genomes |
| Q24684993 | Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas |
| Q34049975 | Molecular spandrels: tests of adaptation at the genetic level. |
| Q28757176 | Neanderthal brain size at birth provides insights into the evolution of human life history |
| Q34620100 | Neuroimaging endophenotypes: strategies for finding genes influencing brain structure and function |
| Q28730781 | Nicotinamide, NAD(P)(H), and Methyl-Group Homeostasis Evolved and Became a Determinant of Ageing Diseases: Hypotheses and Lessons from Pellagra |
| Q22337113 | No evidence that polymorphisms of brain regulator genes Microcephalin and ASPM are associated with general mental ability, head circumference or altruism |
| Q37810545 | Nonadaptive processes in primate and human evolution |
| Q22337142 | Normal variants of Microcephalin and ASPM do not account for brain size variability |
| Q28596060 | Paleopopulation genetics |
| Q47782527 | Pandora's growing box: Inferring the evolution and development of hominin brains from endocasts |
| Q36936750 | Patterns of molecular evolution associated with two selective sweeps in the Tb1-Dwarf8 region in maize |
| Q29616186 | Patterns of neural stem and progenitor cell division may underlie evolutionary cortical expansion |
| Q43433719 | Pervasive genetic integration directs the evolution of human skull shape |
| Q37102660 | Polymorphism due to multiple amino acid substitutions at a codon site within Ciona savignyi |
| Q28818628 | Population genetics of mouse lemur vomeronasal receptors: current versus past selection and demographic inference |
| Q34335449 | Population structure, migration, and diversifying selection in the Netherlands |
| Q33245589 | Positive selection on the nonhomologous end-joining factor Cernunnos-XLF in the human lineage |
| Q33285476 | Positive selection within the Schizophrenia-associated GABA(A) receptor beta(2) gene |
| Q33629131 | Primary microcephaly: do all roads lead to Rome? |
| Q30367885 | Proportionally more deleterious genetic variation in European than in African populations. |
| Q35189789 | Prospects for delaying the rising tide of worldwide, late-life dementias |
| Q28253753 | Recent and ongoing selection in the human genome |
| Q22337331 | Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language |
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| Q28756094 | Review. Genetic exchange and the origin of adaptations: prokaryotes to primates |
| Q30575526 | Role of BRCA1 in brain development. |
| Q36288960 | Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia. |
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| Q22337196 | Sex-dependent association of common variants of microcephaly genes with brain structure |
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| Q30577985 | The dynamic role of genetics on cortical patterning during childhood and adolescence |
| Q34026994 | The human brain: rewired and running hot. |
| Q21562200 | The microcephalin ancestral allele in a Neanderthal individual |
| Q36733705 | The mirror brain, concepts, and language: the price of anthropogenesis |
| Q22337141 | The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence |
| Q22065659 | To what extent did Neanderthals and modern humans interact? |
| Q34571921 | Understanding the recent evolution of the human genome: insights from human-chimpanzee genome comparisons |
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| Q33997612 | Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens" and "Microcephalin, a gene regulating brain size, continues to evolve adaptively in humans". |
| Q22337065 | Comment on Papers by Evans et al. and Mekel-Bobrov et al. on Evidence for Positive Selection of MCPH1 and ASPM |
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