Globularization and domestication.

The descent of man and selection in relation to sex

チャールス, ダ., & 茂穂, 田. (1907) · Tokyo Jinrui Gakkai zasshi · doi:10.1537/ase1887.22.495 · Cited by 10,909 · see citing works

The Cultural Origins of Human Cognition

Tomasello, M. (2009) · doi:10.2307/j.ctvjsf4jc · Cited by 6,368 · see citing works

A draft sequence of the Neandertal genome

Green, R. E., Krause, J., Briggs, A. W., Maricic, T., Stenzel, U., Kircher, M., Patterson, N., Li, H., Zhai, W., Fritz, M. H.-Y., et al. (2010) · Science · doi:10.1126/science.1188021 · Cited by 4,318 · see citing works

The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored

Szklarczyk, D., Franceschini, A., Kuhn, M., Simonovic, M., Roth, A. C., Mínguez, P., Doerks, T., Stark, M., Muller, J., Bork, P., et al. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq973 · Cited by 3,469 · see citing works

The descent of man, and selection in relation to sex

Darwin, C. R. (1871) · J. Murray eBooks · doi:10.5962/bhl.title.2092 · Cited by 3,249 · see citing works

The complete genome sequence of a Neanderthal from the Altai Mountains

Prüfer, K., Racimo, F., Patterson, N., Jay, F., Sankararaman, S., Sawyer, S., Heinze, A., Renaud, G., Sudmant, P. H., de Filippo, C., et al. (2014) · Nature · doi:10.1038/nature12886 · Cited by 2,254 · see citing works

A Natural History of Human Thinking

Tomasello, M. (2014) · doi:10.4159/9780674726369 · Cited by 1,923 · see citing works

The metabolic cost of neural information

Laughlin, S. B., van Steveninck, R. R. D. R., & Anderson, J. C. (1998) · Nature Neuroscience · doi:10.1038/236 · Cited by 1,175 · see citing works

Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats

Reiner, O., Carrozzo, R., Shen, Y. H., Wehnert, M., Faustinella, F., Dobyns, W. B., Caskey, C. T., & Ledbetter, D. H. (1993) · Nature · doi:10.1038/364717a0 · Cited by 1,057 · see citing works

Human-like social skills in dogs?

Hare, B., & Tomasello, M. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.07.003 · Cited by 967 · see citing works

The “Domestication Syndrome” in Mammals: A Unified Explanation Based on Neural Crest Cell Behavior and Genetics

Wilkins, A. S., Wrangham, R. W., & Fitch, W. T. (2014) · Genetics · doi:10.1534/genetics.114.165423 · Cited by 751 · see citing works

Neocortex Patterning by the Secreted Signaling Molecule FGF8

Fukuchi-Shimogori, T., & Grove, E. (2001) · Science · doi:10.1126/science.1064252 · Cited by 707 · see citing works

Human-specific loss of regulatory DNA and the evolution of human-specific traits

McLean, C. Y., Reno, P. L., Pollen, A. A., Bassan, A. I., Capellini, T. D., Guenther, C., Indjeian, V. B., Lim, X., Menke, D. B., Schaar, B. T., et al. (2011) · Nature · doi:10.1038/nature09774 · Cited by 535 · see citing works

Waardenburg Syndrome

Read, A., & Newton, V. E. (1997) · Humana Press eBooks · doi:10.1007/978-1-59259-726-0_112 · Cited by 484 · see citing works

Regulation of the GABA cell phenotype in hippocampus of schizophrenics and bipolars

Benes, F. M., Lim, B., Matzilevich, D., Walsh, J. P., Subburaju, S., & Minns, M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703806104 · Cited by 483 · see citing works

The evolution and development of cranial form in <i>Homo</i> <i>sapiens</i>

Lieberman, D. E., McBratney, B. M., & Krovitz, G. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.022440799 · Cited by 450 · see citing works

Documenting domestication: The intersection of genetics and archaeology

Zeder, M. A., Emshwiller, E., Smith, B. D., & Bradley, D. G. (2006) · Trends in Genetics · doi:10.1016/j.tig.2006.01.007 · Cited by 447 · see citing works

The Oxford Handbook of Language Evolution

Tallerman, M., & Gibson, K. (2011) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780199541119.001.0001 · Cited by 443 · see citing works

14-3-3ε is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller–Dieker syndrome

Toyo‐oka, K., Shionoya, A., Gambello, M. J., Cardoso, C., Leventer, R. J., Ward, H. L., Ayala, R., Tsai, L., Dobyns, W. B., Ledbetter, D. H., et al. (2003) · Nature Genetics · doi:10.1038/ng1169 · Cited by 403 · see citing works

Human-specific transcriptional regulation of CNS development genes by FOXP2

Konopka, G., Bomar, J. M., Winden, K., Coppola, G., Jonsson, Z. O., Gao, F., Peng, S., Preuss, T. M., Wohlschlegel, J. A., & Geschwind, D. H. (2009) · Nature · doi:10.1038/nature08549 · Cited by 390 · see citing works

Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1

Smith, D. S., Niethammer, M., Ayala, R., Zhou, Y., Gambello, M. J., Wynshaw-Boris, A. J., & Tsai, L. (2000) · Nature Cell Biology · doi:10.1038/35041000 · Cited by 380 · see citing works

Ndel1 Operates in a Common Pathway with LIS1 and Cytoplasmic Dynein to Regulate Cortical Neuronal Positioning

Shu, T., Ayala, R., Nguyen, M.-D., Xie, Z., Gleeson, J. G., & Tsai, L. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.030 · Cited by 361 · see citing works

Cell Migration from the Ganglionic Eminences Is Required for the Development of Hippocampal GABAergic Interneurons

Pleasure, S. J., Anderson, S. A., Hevner, R. F., Bagri, A., Marín, Ó., Lowenstein, D. H., & Rubenstein, J. L. R. (2000) · Neuron · doi:10.1016/s0896-6273(00)00149-5 · Cited by 356 · see citing works

Conservation of RET Regulatory Function from Human to Zebrafish Without Sequence Similarity

Fisher, S., Grice, E. A., Vinton, R. M., Bessling, S. L., & McCallion, A. S. (2006) · Science · doi:10.1126/science.1124070 · Cited by 354 · see citing works

Enhancer Divergence and cis-Regulatory Evolution in the Human and Chimp Neural Crest

Prescott, S. L., Srinivasan, R., Marchetto, M. C., Grishina, I., Narvaiza, I., Selleri, L., Gage, F. H., Swigut, T., & Wysocka, J. (2015) · Cell · doi:10.1016/j.cell.2015.08.036 · Cited by 352 · see citing works

Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator

Bamforth, S. D., Bragança, J., Eloranta, J. J., Murdoch, J. N., Marques, F. I. R., Kranc, K. R., Farza, H., Henderson, D. J., Hurst, H. C., & Bhattacharya, S. (2001) · Nature Genetics · doi:10.1038/ng768 · Cited by 346 · see citing works

Genome-wide association study reveals two new risk loci for bipolar disorder

Mühleisen, T. W., Leber, M., Schulze, T. G., Strohmaier, J., Degenhardt, F., Treutlein, J., Mattheisen, M., Forstner, A. J., Schumacher, J., Breuer, R., et al. (2014) · Nature Communications · doi:10.1038/ncomms4339 · Cited by 346 · see citing works

The Axon Guidance Receptor Gene ROBO1 Is a Candidate Gene for Developmental Dyslexia

Hannula‐Jouppi, K., Kaminen‐Ahola, N., Taipale, M., Eklund, R., Nopola‐Hemmi, J., Kääriäinen, H., & Kere, J. (2005) · PLoS Genetics · doi:10.1371/journal.pgen.0010050 · Cited by 329 · see citing works

Point Mutations and an Intragenic Deletion in LIS1, the Lissencephaly Causative Gene in Isolated Lissencephaly Sequence and Miller-Dieker Syndrome

Nigro, C. L., Chong, S. S., Smith, A. C. M., Dobyns, W. B., Carrozzo, R., & Ledbetter, D. H. (1997) · Human Molecular Genetics · doi:10.1093/hmg/6.2.157 · Cited by 321 · see citing works

A mutation in the Pax-6 gene in rat small eye is associated with impaired migration of midbrain crest cells

Matsuo, T., Osumi, N., Noji, S., Ohuchi, H., Koyama, E., Myokai, F., Matsuo, N., Taniguchi, S., Doi, H., Iseki, S., et al. (1993) · Nature Genetics · doi:10.1038/ng0493-299 · Cited by 315 · see citing works

Severe Expressive-Language Delay Related to Duplication of the Williams–Beuren Locus

Somerville, M. J., Mervis, C. Β., Young, E. J., Seo, E., Campo, M. D., Bamforth, S., Peregrine, E., Loo, W., Lilley, M., Jurado, L. A. P., et al. (2005) · New England Journal of Medicine · doi:10.1056/nejmoa051962 · Cited by 310 · see citing works

Mice Lacking Zfhx1b, the Gene That Codes for Smad-Interacting Protein-1, Reveal a Role for Multiple Neural Crest Cell Defects in the Etiology of Hirschsprung Disease–Mental Retardation Syndrome

de Putte, T. V., Maruhashi, M., Francis, A., Nelles, L., Kondoh, H., Huylebroeck, D., & Higashi, Y. (2003) · The American Journal of Human Genetics · doi:10.1086/346092 · Cited by 309 · see citing works

Brain development after birth differs between Neanderthals and modern humans

Gunz, P., Neubauer, S., Maureille, B., & Hublin, J.-J. (2010) · Current Biology · doi:10.1016/j.cub.2010.10.018 · Cited by 304 · see citing works

Geometric morphometrics and paleoneurology: brain shape evolution in the genus Homo

Bruner, E. (2004) · Journal of Human Evolution · doi:10.1016/j.jhevol.2004.03.009 · Cited by 301 · see citing works

Hedgehog signaling is required for cranial neural crest morphogenesis and chondrogenesis at the midline in the zebrafish skull

Wada, N., Javidan, Y., Nelson, S., Carney, T. J., Kelsh, R. N., & Schilling, T. F. (2005) · Development · doi:10.1242/dev.01943 · Cited by 297 · see citing works

Animal domestication and behavior

(2002) · doi:10.1079/9780851995977.0000 · Cited by 288 · see citing works

Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain

Spiteri, E., Konopka, G., Coppola, G., Bomar, J. M., Oldham, M. C., Ou, J., Vernes, S. C., Fisher, S. E., Ren, B., & Geschwind, D. H. (2007) · The American Journal of Human Genetics · doi:10.1086/522237 · Cited by 281 · see citing works

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain

Vernes, S. C., Oliver, P. L., Spiteri, E., Lockstone, H. E., Puliyadi, R., Taylor, J. M., Ho, J., Mombereau, C., Brewer, A., Lowy, E., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002145 · Cited by 276 · see citing works

Transcriptional Regulation of Cortical Neuron Migration by POU Domain Factors

McEvilly, R. J., de Diaz, M. O., Schonemann, M. D., Hooshmand, F., & Rosenfeld, M. G. (2002) · Science · doi:10.1126/science.1067132 · Cited by 271 · see citing works

RNA-Seq of Human Neurons Derived from iPS Cells Reveals Candidate Long Non-Coding RNAs Involved in Neurogenesis and Neuropsychiatric Disorders

Lin, M., Pedrosa, E., Shah, A., Hrabovsky, A., Maqbool, S., Zheng, D.-Y., & Lachman, H. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023356 · Cited by 262 · see citing works

A Recent Evolutionary Change Affects a Regulatory Element in the Human FOXP2 Gene

Maričić, T., Günther, V., Georgiev, O., Gehre, S., Ćurlin, M., Schreiweis, C., Naumann, R., Burbano, H. A., Meyer, M., Lalueza‐Fox, C., et al. (2012) · Molecular Biology and Evolution · doi:10.1093/molbev/mss271 · Cited by 261 · see citing works

Cultural evolution: implications for understanding the human language faculty and its evolution

Smith, K., & Kirby, S. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0145 · Cited by 254 · see citing works

Patterns of coding variation in the complete exomes of three Neandertals

Castellano, S., Parra, G., Sánchez-Quinto, F. A., Racimo, F., Kuhlwilm, M., Kircher, M., Sawyer, S., Fu, Q., Heinze, A., Nickel, B., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1405138111 · Cited by 247 · see citing works

DNA Methylation Status ofSOX10Correlates with Its Downregulation and Oligodendrocyte Dysfunction in Schizophrenia

Iwamoto, K., Bundo, M., Yamada, K., Takao, H., Iwayama‐Shigeno, Y., Yoshikawa, T., & Kato, T. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0766-05.2005 · Cited by 243 · see citing works

Current perspectives of the signaling pathways directing neural crest induction

Stuhlmiller, T. J., & García‐Castro, M. I. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-0991-8 · Cited by 225 · see citing works

Mitotic occupancy and lineage-specific transcriptional control of rRNA genes by Runx2

Young, D. W., Hassan, M. Q., Pratap, J., Galindo, M. A., Zaidi, S. K., Lee, S.-H., Yang, X., Xie, R., Javed, A., Underwood, J. M., et al. (2007) · Nature · doi:10.1038/nature05473 · Cited by 220 · see citing works

Reconstructing the DNA Methylation Maps of the Neandertal and the Denisovan

Gokhman, D., Lavi, E., Prüfer, K., Fraga, M. F., Riancho, J. A., Kelso, J. F., Pääbo, S., Meshorer, E., & Carmel, L. (2014) · Science · doi:10.1126/science.1250368 · Cited by 219 · see citing works

A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype

Potkin, S. G., Turner, J. A., Guffanti, G., Lakatos, A., Fallon, J. H., Nguyen, D. D., Mathalon, D. H., Ford, J. M., Lauriello, J., & Macciardi, F. M. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn155 · Cited by 219 · see citing works

Endocranial shape changes during growth in chimpanzees and humans: a morphometric analysis of unique and shared aspects

Neubauer, S., Gunz, P., & Hublin, J.-J. (2010) · Journal of Human Evolution · doi:10.1016/j.jhevol.2010.06.011 · Cited by 199 · see citing works

A new sequence motif linking lissencephaly, Treacher Collins and oral-facial-digital type 1 syndromes, microtubule dynamics and cell migration

Emes, R. D. (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.24.2813 · Cited by 198 · see citing works

The essential role of Cited2, a negative regulator for HIF-1α, in heart development and neurulation

Yin, Z., Haynie, J. M., Yang, X., Han, B., Kiatchoosakun, S., Restivo, J., Yuan, S., Prabhakar, N. R., Herrup, K., Conlon, R. A., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.162371799 · Cited by 197 · see citing works

The Human Condition—A Molecular Approach

Pääbo, S. (2014) · Cell · doi:10.1016/j.cell.2013.12.036 · Cited by 197 · see citing works

A uniquely modern human pattern of endocranial development. Insights from a new cranial reconstruction of the Neandertal newborn from Mezmaiskaya

Gunz, P., Neubauer, S., Golovanova, L., Doronichev, V., Maureille, B., & Hublin, J.-J. (2012) · Journal of Human Evolution · doi:10.1016/j.jhevol.2011.11.013 · Cited by 197 · see citing works

Craniofacial feminization, social tolerance, and the origins of behavioral modernity

Cieri, R. L., Churchill, S. E., Franciscus, R. G., Tan, J., & Hare, B. (2014) · Current Anthropology · doi:10.1086/677209 · Cited by 195 · see citing works

Evolution of the base of the brain in highly encephalized human species

Bastir, M., Rosas, A., Gunz, P., Peña-Melián, Á., Manzi, G., Harvati, K., Kruszynski, R., Stringer, C. B., & Hublin, J. (2011) · Nature Communications · doi:10.1038/ncomms1593 · Cited by 194 · see citing works

Vitamin A deficiency and relational memory deficit in adult mice: relationships with changes in brain retinoid signalling

Etchamendy, N., Enderlin, V., Marighetto, A., Pallet, V., Higueret, P., & Jaffard, R. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00099-8 · Cited by 185 · see citing works

The exon junction complex component Magoh controls brain size by regulating neural stem cell division

Silver, D. L., Watkins‐Chow, D. E., Schreck, K. C., Pierfelice, T. J., Larson, D. M., Burnetti, A., Liaw, H., Myung, K., Walsh, C. A., Gaiano, N., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2527 · Cited by 177 · see citing works

GDNF and GFRα1 promote formation of neuronal synapses by ligand-induced cell adhesion

Ledda, F., Paratcha, G., Sandoval‐Guzmán, T., & Ibáñez, C. F. (2007) · Nature Neuroscience · doi:10.1038/nn1855 · Cited by 176 · see citing works

Brain ontogeny and life history in Pleistocene hominins

Hublin, J.-J., Neubauer, S., & Gunz, P. (2015) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2014.0062 · Cited by 173 · see citing works

The Vitamin D Receptor, Runx2, and the Notch Signaling Pathway Cooperate in the Transcriptional Regulation of Osteopontin

Shen, Q., & Christakos, S. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m504166200 · Cited by 173 · see citing works

Neural-specific Sox2 input and differential Gli-binding affinity provide context and positional information in Shh-directed neural patterningPreprint

Peterson, K. A., Nishi, Y., Ma, W., Vedenko, A., Shokri, L., Zhang, X., McFarlane, M., Baizabal, J., Junker, J. P., van Oudenaarden, A., et al. (2012) · Genes & Development · doi:10.1101/gad.207142.112 · Cited by 166 · see citing works

Temporal control of neural crest lineage generation by Wnt/β-catenin signaling

Hari, L., Miescher, I., Shakhova, O., Suter, U., Chin, L., Taketo, M. M., Richardson, W. D., Kessaris, N., & Sommer, L. (2012) · Development · doi:10.1242/dev.073064 · Cited by 162 · see citing works

Neuronal GDNF Expression in the Adult Rat Nervous System Identified By In Situ Hybridization

Pochon, N. A.-M., Menoud, A., Tseng, J., Zurn, A. D., & Aebischer, P. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01623.x · Cited by 160 · see citing works

The shape of the human language-ready brain

Boeckx, C. A. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.00282 · Cited by 158 · see citing works

Origin matters: Differences in embryonic tissue origin and Wnt signaling determine the osteogenic potential and healing capacity of frontal and parietal calvarial bones

Quarto, N., Wan, D. C., Kwan, M. D., Panetta, N. J., Li, S., & Longaker, M. T. (2009) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.091116 · Cited by 157 · see citing works

DLX5 positions the neural crest and preplacode region at the border of the neural plate

McLarren, K. W., Litsiou, A., & Streit, A. (2003) · Developmental Biology · doi:10.1016/s0012-1606(03)00177-5 · Cited by 155 · see citing works

Dlx1&amp;2-Dependent Expression of Zfhx1b (Sip1, Zeb2) Regulates the Fate Switch between Cortical and Striatal Interneurons

McKinsey, G. L., Lindtner, S., Trzcinski, B., Visel, A., Pennacchio, L. A., Huylebroeck, D., Higashi, Y., & Rubenstein, J. L. R. (2013) · Neuron · doi:10.1016/j.neuron.2012.11.035 · Cited by 153 · see citing works

Dlx genes pattern mammalian jaw primordium by regulating both lower jaw-specific and upper jaw-specific genetic programs

Jeong, J., Li, X., McEvilly, R. J., Rosenfeld, M. G., Lufkin, T., & Rubenstein, J. L. R. (2008) · Development · doi:10.1242/dev.019778 · Cited by 151 · see citing works

Fgfr1 regulates patterning of the pharyngeal regionPreprint

Trokovic, N., Trokovic, R., Mai, P., & Partanen, J. M. (2003) · Genes & Development · doi:10.1101/gad.250703 · Cited by 151 · see citing works

Characterization of progenitor domains in the developing mouse thalamus

Vue, T. Y., Aaker, J., Taniguchi, A., Kazemzadeh, C., Skidmore, J. M., Martin, D. M., Martin, J. F., Treier, M., & Nakagawa, Y. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21467 · Cited by 144 · see citing works

Morphological Differences in the Parietal Lobes within the Human Genus

Bruner, E. (2010) · Current Anthropology · doi:10.1086/650729 · Cited by 144 · see citing works

Increased thalamic neurodegeneration following ischaemic cortical stroke in osteopontin-deficient mice.

Schroeter, M., Zickler, P., Denhardt, D., Hartung, H., & Jander, S. (2006) · Brain : a journal of neurology · doi:10.1093/brain/awl094 · Cited by 141 · see citing works

Culture shapes the evolution of cognition

Thompson, B., Kirby, S., & Smith, K. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1523631113 · Cited by 138 · see citing works

Elementary Syntactic Structures

Boeckx, C. A. (2014) · Cambridge University Press eBooks · doi:10.1017/cbo9781139524391 · Cited by 136 · see citing works

Bone-Specific Transcription Factor Runx2 Interacts with the 1α,25-Dihydroxyvitamin D3 Receptor To Up-Regulate Rat Osteocalcin Gene Expression in Osteoblastic Cells

Paredes, R., Arriagada, G., Cruzat, F., Villagra, A., Olate, J., Zaidi, K., van Wijnen, A. J., Lian, J. B., Stein, G. S., Stein, J. L., et al. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.20.8847-8861.2004 · Cited by 135 · see citing works

Mechanistic Differences in the Transcriptional Interpretation of Local and Long-Range Shh Morphogen Signaling

Oosterveen, T., Kurdija, S., Alekseenko, Z., Uhde, C. W., Bergsland, M., Sandberg, M., Andersson, E., Dias, J. M. M., Muhr, J., & Ericson, J. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.09.015 · Cited by 132 · see citing works

BMP-SHH Signaling Network Controls Epithelial Stem Cell Fate via Regulation of Its Niche in the Developing Tooth

Li, J., Feng, J., Liu, Y., Ho, T., Grimes, W., Ho, H. A., Park, S., Wang, S., & Chai, Y. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.02.021 · Cited by 132 · see citing works

Pax3 and Zic1 trigger the early neural crest gene regulatory network by the direct activation of multiple key neural crest specifiers

Plouhinec, J.-L., Roche, D. D., Pegoraro, C., Figueiredo, A. L., Maczkowiak, F., Brunet, L. J., Milet, C., Vert, J., Pollet, N., Harland, R. M., et al. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.12.010 · Cited by 129 · see citing works

NCAM1 association study of bipolar disorder and schizophrenia: polymorphisms and alternatively spliced isoforms lead to similarities and differences

Atz, M. E., Rollins, B. L., & Vawter, M. P. (2007) · Psychiatric Genetics · doi:10.1097/ypg.0b013e328012d850 · Cited by 125 · see citing works

A Stable Cranial Neural Crest Cell Line from Mouse

Ishii, M., Arias, A. C., Liu, L., Chen, Y., Bronner-Fraser, M. E., & Maxson, R. E. (2012) · Stem Cells and Development · doi:10.1089/scd.2012.0155 · Cited by 125 · see citing works

Formation of the Middle Ear: Recent Progress on the Developmental and Molecular Mechanisms

Mallo, M. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0154 · Cited by 120 · see citing works

PlexinA1 is a new Slit receptor and mediates axon guidance function of Slit C-terminal fragments

Delloye‐Bourgeois, C., Jacquier, A., Charoy, C., Reynaud, F., Nawabi, H., Thoinet, K., Kindbeiter, K., Yoshida, Y., Zagar, Y., Kong, Y., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3893 · Cited by 119 · see citing works

Clinical features and management issues in Mowat–Wilson syndrome

Adam, M. P., Schelley, S. L., Gallagher, R. C., Brady, A. N., Barr, K., Blumberg, B., Shieh, J. T. C., Graham, J. M., Slavotinek, A. M., Martin, M., et al. (2006) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.31530 · Cited by 112 · see citing works

Sonic Hedgehog promotes the development of multipotent neural crest progenitors endowed with both mesenchymal and neural potentials

Calloni, G. W., Pardanaud-Glavieux, C., Douarin, N. M. L., & Dupin, É. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708806104 · Cited by 111 · see citing works

Slit/Robo signaling is necessary to confine early neural crest cells to the ventral migratory pathway in the trunk

Li, J., Cheng, L., & Raper, J. A. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.03.021 · Cited by 110 · see citing works

Genetic background has a major effect on the penetrance and severity of craniofacial defects in mice heterozygous for the gene encoding the nucleolar protein treacle

Dixon, J., & Dixon, M. J. (2004) · Developmental Dynamics · doi:10.1002/dvdy.20004 · Cited by 106 · see citing works

Stage-Specific Control of Neural Crest Stem Cell Proliferation by the Small Rho GTPases Cdc42 and Rac1

Fuchs, S. P., Herzog, D., Sumara, G., Büchmann-Møller, S., Civenni, G., Wu, X., Chrostek‐Grashoff, A., Suter, U., Ricci, R., Relvas, J. B., et al. (2009) · Cell stem cell · doi:10.1016/j.stem.2009.01.017 · Cited by 104 · see citing works

Neural crest-specific removal of Zfhx1b in mouse leads to a wide range of neurocristopathies reminiscent of Mowat–Wilson syndrome

de Putte, T. V., Francis, A., Nelles, L., van Grunsven, L. A., & Huylebroeck, D. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddm093 · Cited by 100 · see citing works

The progression of calcific aortic valve disease through injury, cell dysfunction, and disruptive biologic and physical force feedback loops

Li, C., Xu, S., & Gotlieb, A. I. (2012) · Cardiovascular Pathology · doi:10.1016/j.carpath.2012.06.005 · Cited by 97 · see citing works

Phosphorylation of Sox9 is required for neural crest delamination and is regulated downstream of BMP and canonical Wnt signaling

Liu, J. A., Wu, M.-H., Yan, C. H., Chau, B. K. H., So, H., Ng, A., Chan, A., Cheah, K. S. E., Briscoe, J., & Cheung, M. C. H. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1211747110 · Cited by 96 · see citing works

GDNF Is Predominantly Expressed in the PV+ Neostriatal Interneuronal Ensemble in Normal Mouse and after Injury of the Nigrostriatal Pathway

Hidalgo‐Figueroa, M., Bonilla, S., Gutiérrez, F., Pascual, A., & López‐Barneo, J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2693-11.2012 · Cited by 95 · see citing works

mef2ca is required in cranial neural crest to effect Endothelin1 signaling in zebrafish

Miller, C. T., Swartz, M. E., Khuu, P. A., Walker, M. B., Eberhart, J. K., & Kimmel, C. B. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.05.018 · Cited by 94 · see citing works

Versican V0 and V1 Guide Migratory Neural Crest Cells

Dutt, S., Kléber, M., Matasci, M., Sommer, L., & Zimmermann, D. R. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m510834200 · Cited by 94 · see citing works

Decreased GABA levels in anterior cingulate cortex/medial prefrontal cortex in panic disorder

Long, Z., Medlock, C., Dzemidzic, M., Shin, Y.-W., Goddard, A. W., & Dydak, U. (2013) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2013.01.020 · Cited by 93 · see citing works

Oxford handbook of developmental behavioral neuroscience

(2010) · Choice Reviews Online · doi:10.5860/choice.47-6563 · Cited by 92 · see citing works

The Mind of Primitive Man.

Hallowell, A. I., & Boas, F. (1938) · American Sociological Review · doi:10.2307/2083909 · Cited by 89 · see citing works

Bmp7 Regulates the Survival, Proliferation, and Neurogenic Properties of Neural Progenitor Cells during Corticogenesis in the Mouse

Segklia, A., Seuntjens, E., Elkouris, M., Tsalavos, S., Stappers, E., Mitsiadis, T. A., Huylebroeck, D., Remboutsika, E., & Graf, D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034088 · Cited by 88 · see citing works

Expression of regulatory genes during differentiation of thalamic nuclei in mouse and monkey

Jones, E. G., & Rubenstein, J. L. R. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20234 · Cited by 88 · see citing works

Bone morphogenetic protein 7 (BMP7) mutations are associated with variable ocular, brain, ear, palate, and skeletal anomalies

Wyatt, A. W., Osborne, R. J., Stewart, H. S., & Ragge, N. (2010) · Human Mutation · doi:10.1002/humu.21280 · Cited by 86 · see citing works

Human-specific endogenous retroviral insert serves as an enhancer for the schizophrenia-linked gene PRODH

Suntsova, M., Gogvadze, E. V., Salozhin, S. V., Гайфуллин, Н., Eroshkin, F. M., Dmitriev, S. E., Martynova, N. Y., Kulikov, K., Malakhova, G., Тухбатова, Г. Р., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1318172110 · Cited by 85 · see citing works

The neural crest in vertebrate evolution

Douarin, N. M. L., & Dupin, É. (2012) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2012.06.001 · Cited by 85 · see citing works

A neural crest deficit in Down syndrome mice is associated with deficient mitotic response to Sonic hedgehog

Roper, R. J., VanHorn, J. F., Cargile, C. B., & Reeves, R. H. (2008) · Mechanisms of Development · doi:10.1016/j.mod.2008.11.002 · Cited by 84 · see citing works

Neuropathologic Research Strategies in Holoprosencephaly

Samat, H. B., & Flores-Samat, L. (2001) · Journal of Child Neurology · doi:10.1177/088307380101601211 · Cited by 83 · see citing works

Zebrafish dlx2a contributes to hindbrain neural crest survival, is necessary for differentiation of sensory ganglia and functions with dlx1a in maturation of the arch cartilage elements

Sperber, S. M., Saxena, V., Hatch, G., & Ekker, M. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.11.005 · Cited by 81 · see citing works

Noggin Enhances Dopamine Neuron Production from Human Embryonic Stem Cells and Improves Behavioral Outcome After Transplantation into Parkinsonian Rats

Chiba, S., Lee, Y. M., Zhou, W., & Freed, C. R. (2008) · Stem Cells · doi:10.1634/stemcells.2008-0085 · Cited by 80 · see citing works

The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos

Maczkowiak, F., Matéos, S., Wang, E., Roche, D. D., Harland, R. M., & Monsoro-Burq, A. H. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.01.022 · Cited by 78 · see citing works

Convergent differential regulation of SLIT-ROBO axon guidance genes in the brains of vocal learners

Wang, R., Chen, C., Hara, E., Rivas, M. V., Roulhac, P. L., Howard, J. T., Chakraborty, M., Audet, J., & Jarvis, E. D. (2015) · Journal of Comparative Neurology · doi:10.1002/cne.23719 · Cited by 74 · cited 2× · see citing works

Extracellular Matrix Protein Anosmin Promotes Neural Crest Formation and Regulates FGF, BMP, and WNT Activities

Endo, Y., Ishiwata-Endo, H., & Yamada, K. M. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.07.006 · Cited by 72 · see citing works

TheLhx2Transcription Factor Controls Thalamocortical Axonal Guidance by Specific Regulation of Robo1 and Robo2 Receptors

Marcos-Mondéjar, P., Peregrín, S., Li, J. Y. H., Carlsson, L., Tole, S., & López‐Bendito, G. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5851-11.2012 · Cited by 71 · see citing works

Vitamin A deficiency impairs postnatal cognitive function via inhibition of neuronal calcium excitability in hippocampus

Jiang, W., Yu, Q., Gong, M., Chen, L., Wen, E. Y., Bi, Y., Zhang, Y., Shi, Y., Qü, P., Liu, Y., et al. (2012) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2012.07697.x · Cited by 67 · see citing works

Relaxed Selection and the Role of Epigenesis in the Evolution of Language

BLUMBERG, M. S., Freeman, J. H., Robinson, S. R., & Deacon, T. W. (2009) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780195314731.013.0036 · Cited by 66 · see citing works

Globularity and language-readiness: generating new predictions by expanding the set of genes of interest

Boeckx, C. A., & Benítez‐Burraco, A. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.01324 · Cited by 65 · see citing works

Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease

Jiang, Q., Ho, Y.-Y., Hao, L., Nichols Berrios, C., & Chakravarti, A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021219 · Cited by 62 · see citing works

Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications

Lattanzi, W., Bukvić, N., Barba, M., Tamburrini, G., Bernardini, C., Michetti, F., & Rocco, C. D. (2012) · Child s Nervous System · doi:10.1007/s00381-012-1781-1 · Cited by 61 · see citing works

SoxB1-driven transcriptional network underlies neural-specific interpretation of morphogen signals

Oosterveen, T., Kurdija, S., Ensterö, M., Uhde, C. W., Bergsland, M., Sandberg, M., Sandberg, R., Muhr, J., & Ericson, J. (2013) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1220010110 · Cited by 61 · see citing works

The Oscillopathic Nature of Language Deficits in Autism: From Genes to Language Evolution

Benítez‐Burraco, A., & Murphy, E. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00120 · Cited by 61 · see citing works

Language Impairments in ASD Resulting from a Failed Domestication of the Human Brain

Benítez‐Burraco, A., Lattanzi, W., & Murphy, E. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00373 · Cited by 61 · see citing works

Dysfunctional gene splicing as a potential contributor to neuropsychiatric disorders

Glatt, S. J., Cohen, O. S., Faraone, S. V., & Tsuang, M. T. (2011) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.31181 · Cited by 59 · see citing works

Song Learning in Wild and Domesticated Strains of White‐Rumped Munia, Lonchura striata , Compared by Cross‐Fostering Procedures: Domestication Increases Song Variability by Decreasing Strain‐Specific Bias

Takahasi, M., & Okanoya, K. (2010) · Ethology · doi:10.1111/j.1439-0310.2010.01761.x · Cited by 57 · see citing works

Identification of Pax3 and Zic1 targets in the developing neural crest

Bae, C.-J., Park, B., Lee, Y., Tobias, J. W., Hong, C., & Saint‐Jeannet, J. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.12.011 · Cited by 57 · see citing works

Midbrain expression of Delta-like 1 homologue is regulated by GDNF and is associated with dopaminergic differentiation

Christophersen, N. S., Grønborg, M., Petersen, T. N., Fjord‐Larsen, L., Jørgensen, J. R., Juliusson, B., Blom, N., Rosenblad, C., & Brundin, P. (2007) · Experimental Neurology · doi:10.1016/j.expneurol.2007.01.014 · Cited by 56 · see citing works

The brain and the braincase: a spatial analysis on the midsagittal profile in adult humans

Bruner, E., Amano, H., de la Cuétara, J. M., & Ogihara, N. (2015) · Journal of Anatomy · doi:10.1111/joa.12355 · Cited by 55 · see citing works

Possible functional links among brain- and skull-related genes selected in modern humans

Benítez‐Burraco, A., & Boeckx, C. A. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.00794 · Cited by 54 · see citing works

LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQ

Leventer, R. J., Cardoso, C., Ledbetter, D. H., & Dobyns, W. B. (2001) · Neurology · doi:10.1212/wnl.57.3.416 · Cited by 54 · see citing works

Evolution of alternative splicing in primate brain transcriptomes

Lin, L., Shen, S., Jiang, P., Sato, S., Davidson, B. L., & Xing, Y. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq201 · Cited by 52 · see citing works

A Shared Pattern of Postnatal Endocranial Development in Extant Hominoids

Scott, N. A., Neubauer, S., Hublin, J., & Gunz, P. (2014) · Evolutionary Biology · doi:10.1007/s11692-014-9290-7 · Cited by 51 · see citing works

Domains of Brn‐2 that mediate homodimerization and interaction with general and melanocytic transcription factors

Smit, D. J., Smith, A. G., Parsons, P. G., Muscat, G. E. O., & Sturm, R. A. (2000) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2000.01737.x · Cited by 50 · see citing works

Biolinguistics: forays into human cognitive biology.

Boeckx, C. A. (2013) · PubMed · doi:10.4436/jass.91009 · Cited by 50 · see citing works

Region‐specific gene expression in early postnatal mouse thalamus

Yuge, K., Kataoka, A., Yoshida, A., Itoh, D., Aggarwal, M., Mori, S., Blackshaw, S., & Shimogori, T. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22532 · Cited by 49 · see citing works

Bmp2 is required for migration but not for induction of neural crest cells in the mouse

Correia, A. C., Costa, M., Moraes, F., Bom, J., Nóvoa, A., & Mallo, M. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21256 · Cited by 47 · see citing works

Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype–phenotype correlations

Yoshida, T., Kanegane, H., Osato, M., Yanagida, M., Miyawaki, T., Ito, Y., & Shigesada, K. (2003) · Blood Cells Molecules and Diseases · doi:10.1016/s1079-9796(03)00020-2 · Cited by 46 · see citing works

FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways

Devanna, P., Middelbeek, J., & Vernes, S. C. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00305 · Cited by 46 · see citing works

Autistic disorders in children with CHARGE association

Fernell, E., Olsson, V., Karlgren‐Leitner, C., Norlin, B., Hagberg, B. S., & Gillberg, C. (1999) · Developmental Medicine & Child Neurology · doi:10.1017/s0012162299000572 · Cited by 46 · see citing works

Response of caudate neurons to stimulation of intrinsic and peripheral afferents in normal, symptomatic, and recovered MPTP-treated cats

Rothblat, D. S., & Schneider, J. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-10-04372.1993 · Cited by 44 · see citing works

<scp>SLIT</scp>2/<scp>ROBO</scp>1‐miR‐218‐1‐<scp>RET</scp>/<scp>PLAG</scp>1: a new disease pathway involved in <scp>H</scp>irschsprung's disease

Tang, W., Tang, J., He, J., Zhou, Z., Qin, Y., Qin, J., Li, B., Xu, X., Geng, Q., Jiang, W., et al. (2015) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12454 · Cited by 43 · see citing works

SAMS, a Syndrome of Short Stature, Auditory-Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Is a Unique Neurocristopathy Caused by Mutations in Goosecoid

Parry, D. A., Logan, C. V., Stegmann, A. P. A., Abdelhamed, Z. A., Calder, A. D., Khan, S., Bonthron, D. T., Clowes, V. E., Sheridan, E. G., Ghali, N., et al. (2013) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2013.10.027 · Cited by 42 · see citing works

The Transcription Factor Runx2 Is under Circadian Control in the Suprachiasmatic Nucleus and Functions in the Control of Rhythmic Behavior

Reale, M. E., Webb, I. C., Wang, X., Baltazar, R. M., Coolen, L. M., & Lehman, M. N. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054317 · Cited by 42 · see citing works

The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutation

Rossi, M., Jones, R. L., Norbury, G., Bloch-Zupan, A., & Winter, R. M. (2003) · Clinical Dysmorphology · doi:10.1097/00019605-200310000-00012 · Cited by 42 · see citing works

Microfluidic affinity and ChIP-seq analyses converge on a conserved FOXP2-binding motif in chimp and human, which enables the detection of evolutionarily novel targets

Nelson, C. S., Fuller, C. K., Fordyce, P. M., Greninger, A. L., Li, H., & DeRisi, J. L. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt259 · Cited by 42 · see citing works

Interleukin‐6 induces the lineage commitment of bone marrow‐derived mesenchymal multipotent cells through down‐regulation of Sox2 by osteogenic transcription factors

Yoon, D. S., Kim, Y. H., Lee, S., Lee, K., Park, K. H., Jang, Y., & Lee, J. W. (2014) · The FASEB Journal · doi:10.1096/fj.13-248567 · Cited by 41 · see citing works

Slits affect the timely migration of neural crest cells via robo receptor

Giovannone, D., Reyes, M., Reyes, R., Correa, L., Martinez, D., Ra, H., Gomez, G. A., Kaiser, J., Ma, L., Stein, M., et al. (2012) · Developmental Dynamics · doi:10.1002/dvdy.23817 · Cited by 39 · see citing works

BMP signaling initiates a neural crest differentiation program in embryonic rat CNS stem cells

Gajavelli, S., Wood, P. M., Pennica, D., Whittemore, S. R., & Tsoulfas, P. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.03.026 · Cited by 37 · see citing works

Integrating retinoic acid signaling with brain function.

Luo, T., Wagner, E., & Dräger, U. C. (2009) · Developmental Psychology · doi:10.1037/0012-1649.45.1.139 · Cited by 37 · see citing works

Behavioural Factors Governing Song Complexity in Bengalese Finches

Okanoya, K. (2012) · International Journal of Comparative Psychology · doi:10.46867/ijcp.2012.25.01.02 · Cited by 37 · see citing works

Age-related cognitive impairments in mice with a conditional ablation of the neural cell adhesion moleculePreprint

Bisaz, R., Boadas‐Vaello, P., Genoux, D., & Sandi, C. (2013) · Learning & Memory · doi:10.1101/lm.030064.112 · Cited by 36 · see citing works

Doing with less: Hominin brain atrophy

Bednarik, R. G. (2014) · HOMO · doi:10.1016/j.jchb.2014.06.001 · Cited by 34 · see citing works

Role of Dlx genes in craniofacial morphogenesis: Dlx2 influences skeletal patterning by inducing ectomesenchymal aggregation in ovo

Gordon, C. T., Brinas, I., Rodda, F. A., Bendall, A. J., & Farlie, P. G. (2010) · Evolution & Development · doi:10.1111/j.1525-142x.2010.00432.x · Cited by 33 · see citing works

Coordinated regulation of dorsal bone morphogenetic protein 4 and ventral Sonic hedgehog signaling specifies the dorso‐ventral polarity in the optic vesicle and governs ocular morphogenesis through fibroblast growth factor 8 upregulation

Kobayashi, T., Yasuda, K., & Araki, M. (2010) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2010.01170.x · Cited by 29 · see citing works

Wnt1 and BMP2: two factors recruiting multipotent neural crest progenitors isolated from adult bone marrow

Glejzer, A., Laudet, E., Leprince, P., Hennuy, B., Poulet, C., Shakhova, O., Sommer, L., Rogister, B., & Wislet‐Gendebien, S. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0558-5 · Cited by 29 · see citing works

Dlx5/6‐enhancer directed expression of Cre recombinase in the pharyngeal arches and brain

Ruest, L. B., Hammer, R. E., Yanagisawa, M., & Clouthier, D. E. (2003) · genesis · doi:10.1002/gene.10247 · Cited by 29 · see citing works

The neuronal POU transcription factor Brn-2 interacts with Jab1, a gene involved in the onset of neurodegenerative diseases

Huang, Y.-T., Iwamoto, K., Kurosaki, T., Nasu, M., & Ueda, S. (2005) · Neuroscience Letters · doi:10.1016/j.neulet.2005.03.008 · Cited by 26 · see citing works

Language is an adaptive system: the role of cultural evolution in the origins of structure

Kirby, S. (2011) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780199541119.013.0061 · Cited by 25 · see citing works

Applying Genomic Analysis to Newborn Screening

Solomon, B. D., Pineda‐Alvarez, D., Bear, K. A., Mullikin, J. C., Evans, J. P., & Programc, N. C. S. (2012) · Molecular Syndromology · doi:10.1159/000341253 · Cited by 25 · see citing works

Identification of Putative Target Genes of the Transcription Factor RUNX2

Kuhlwilm, M., Davierwala, A. P., & Pääbo, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083218 · Cited by 25 · see citing works

Bmp and Shh Signaling Mediate the Expression of satb2 in the Pharyngeal Arches

Sheehan‐Rooney, K., Swartz, M. E., Lovely, C. B., Dixon, M. J., & Eberhart, J. K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0059533 · Cited by 24 · see citing works

Implications of Oxytocin in Human Linguistic Cognition: From Genome to Phenome

Theofanopoulou, C. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00271 · Cited by 23 · see citing works

Ecological correlates of song complexity in white-rumped munias

Kagawa, H., Yamada, H., Lin, R., Mizuta, T., Hasegawa, T., & Okanoya, K. (2012) · Interaction Studies Social Behaviour and Communication in Biological and Artificial Systems · doi:10.1075/is.13.2.05kag · Cited by 22 · see citing works

High Intellectual Function in Individuals with Mutation-Positive Microform Holoprosencephaly

Solomon, B. D., Pineda‐Alvarez, D., Gropman, A. L., Willis, M. J. H., Hadley, D. W., & Muenke, M. (2012) · Molecular Syndromology · doi:10.1159/000341373 · Cited by 22 · see citing works

Modulation of WNT signaling activity is key to the formation of the embryonic head

Fossat, N., Jones, V. J., García‐García, M. J., & Tam, P. (2012) · Cell Cycle · doi:10.4161/cc.11.1.18700 · Cited by 21 · see citing works

Hes1 regulates the number and anterior–posterior patterning of mesencephalic dopaminergic neurons at the mid/hindbrain boundary (isthmus)

Kameda, Y., Saitoh, T., & Fujimura, T. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2011.07.016 · Cited by 19 · see citing works

An aetiology of hominin behaviour

Bednarik, R. G. (2012) · HOMO · doi:10.1016/j.jchb.2012.07.004 · Cited by 19 · see citing works

Brain asymmetry in the white matter making and globularity

Theofanopoulou, C. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01355 · Cited by 18 · see citing works

Osteogenesis and neurogenesis: a robust link also for language evolution

Boeckx, C. A., & Benítez‐Burraco, A. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00291 · Cited by 18 · see citing works

An Indonesian child with orofacial duplication and neurocristopathy anomalies: case report

Sjamsudin, J., David, D. J., & Singh, G. D. (2001) · Journal of Cranio-Maxillofacial Surgery · doi:10.1054/jcms.2001.0221 · Cited by 18 · see citing works

Domestication changes innate constraints for birdsong learning

Kagawa, H., Suzuki, K., Takahasi, M., & Okanoya, K. (2014) · Behavioural Processes · doi:10.1016/j.beproc.2014.04.011 · Cited by 18 · see citing works

Tcof1 acts as a modifier of Pax3 during enteric nervous system development and in the pathogenesis of colonic aganglionosis

Barlow, A. J., Dixon, J., Dixon, M. J., & Trainor, P. A. (2013) · Human Molecular Genetics · doi:10.1093/hmg/dds528 · Cited by 18 · see citing works

Foxd3 is an essential Nodal-dependent regulator of zebrafish dorsal mesoderm development

Chang, L. L., & Kessler, D. S. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.03.017 · Cited by 16 · see citing works

Neurocristopathy that manifests right facial cleft and right maxillary duplication

Jian, X.-C., & Chen, X. (1995) · Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology · doi:10.1016/s1079-2104(05)80092-7 · Cited by 15 · see citing works

Self-domestication and language evolution

Thomas, J. (2014) · ERA · Cited by 14 · see citing works

Commentary by Series Editor

Sarnat, H. B. (2001) · Journal of Child Neurology · doi:10.1177/08830738010160111202 · Cited by 12 · see citing works

Postsynaptic activity of metabotropic glutamate receptors in the piriform cortex

Sugitani, M., Sugai, T., & Onoda, N. (2002) · Neuroreport · doi:10.1097/00001756-200208070-00025 · Cited by 11 · see citing works

Regulation of the Mouse Treacher Collins Syndrome Homolog ( Tcof1 ) Promoter Through Differential Repression of Constitutive Expression

Shows, K. H., & Shiang, R. (2008) · DNA and Cell Biology · doi:10.1089/dna.2008.0766 · Cited by 10 · see citing works

FOXP2, retinoic acid, and language: a promising direction

Benítez‐Burraco, A., & Boeckx, C. A. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00387 · Cited by 9 · see citing works

The Immune Syntax Revisited: Opening New Windows on Language Evolution

Benítez‐Burraco, A., & Uriagereka, J. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00084 · Cited by 8 · see citing works

Approaching motor and language deficits in autism from below: a biolinguistic perspective

Benítez‐Burraco, A., & Boeckx, C. A. (2015) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2015.00025 · Cited by 7 · see citing works

Survival of the Friendliest: <i>Homo sapiens</i> Evolved via Selection for Prosociality

Hare, B. (2017) · Annual Review of Psychology · doi:10.1146/annurev-psych-010416-044201 · Cited by 444 · see citing works

Neanderthal language revisited: not only us

Dediu, D., & Levinson, S. C. (2018) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2018.01.001 · Cited by 218 · see citing works

Self-domestication in Homo sapiens: Insights from comparative genomics

Theofanopoulou, C., Gastaldon, S., O’Rourke, T., Samuels, B. D., Messner, A., Martins, P. T., Delogu, F., Alamri, S., & Boeckx, C. (2017) · PLOS ONE · doi:10.1371/journal.pone.0185306 · Cited by 174 · see citing works

Evaluating the self‐domestication hypothesis of human evolution

Sánchez‐Villagra, M. R., & van Schaik, C. P. (2019) · Evolutionary Anthropology: Issues, News, and Reviews · doi:10.1002/evan.21777 · Cited by 115 · see citing works

Self domestication and the evolution of language

Thomas, J., & Kirby, S. (2018) · Biology & Philosophy · doi:10.1007/s10539-018-9612-8 · Cited by 108 · see citing works

Hypotheses for the Evolution of Reduced Reactive Aggression in the Context of Human Self-Domestication

Wrangham, R. W. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.01914 · Cited by 97 · see citing works

Unlocking the origins and biology of domestic animals using ancient DNA and paleogenomics

McHugo, G. P., Dover, M. J., & MacHugh, D. E. (2019) · BMC Biology · doi:10.1186/s12915-019-0724-7 · Cited by 95 · see citing works

Language Impairments in ASD Resulting from a Failed Domestication of the Human Brain

Benítez‐Burraco, A., Lattanzi, W., & Murphy, E. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00373 · Cited by 61 · see citing works

A four-stage model for language evolution under the effects of human self-domestication

Benítez‐Burraco, A., & Progovac, L. (2020) · Language & Communication · doi:10.1016/j.langcom.2020.03.002 · Cited by 64 · see citing works

Subcortical syntax: Reconsidering the neural dynamics of language

Murphy, E., Hoshi, K., & Benítez‐Burraco, A. (2022) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2022.101062 · Cited by 46 · see citing works

The Emergence of Modern Languages: Has Human Self-Domestication Optimized Language Transmission?

Benítez‐Burraco, A., & Kempe, V. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.00551 · Cited by 41 · see citing works

Williams Syndrome, Human Self-Domestication, and Language Evolution

Niego, A., & Benítez‐Burraco, A. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.00521 · Cited by 35 · see citing works

Why Care: Complex Evolutionary History of Human Healthcare Networks

Kessler, S. E. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.00199 · Cited by 35 · see citing works

Domestication Phenotype Linked to Vocal Behavior in Marmoset Monkeys

Ghazanfar, A. A., Kelly, L. M., Takahashi, D. Y., Winters, S., Terrett, R., & Higham, J. P. (2020) · Current Biology · doi:10.1016/j.cub.2020.09.049 · Cited by 26 · see citing works

The Domestication of Humans

Bednarik, R. G. (2020) · Encyclopedia · doi:10.3390/encyclopedia3030067 · Cited by 25 · see citing works

The language-ready head: Evolutionary considerations

Boeckx, C. (2017) · Psychonomic Bulletin &amp; Review · doi:10.3758/s13423-016-1087-5 · Cited by 23 · see citing works

Grammaticalization and language evolution: Focusing the debate

Benítez‐Burraco, A. (2017) · Language Sciences · doi:10.1016/j.langsci.2017.03.003 · Cited by 21 · see citing works

Recent selection of candidate genes for mammal domestication in Europeans and language change in Europe: a hypothesis

Benítez‐Burraco, A., Chekalin, E., Bruskin, S. A., Tatarinova, T. V., & Morozova, I. (2021) · Annals of Human Biology · doi:10.1080/03014460.2021.1936634 · Cited by 18 · see citing works

Evolution and dysfunction of human cognitive and social traits: A transcriptional regulation perspective

Zug, R., & Uller, T. (2022) · Evolutionary Human Sciences · doi:10.1017/ehs.2022.42 · Cited by 16 · see citing works

Language and Cognitive Impairment Associated with a Novel p.Cys63Arg Change in the MED13L Transcriptional Regulator

Jiménez-Romero, M. S., Salas, P. C., & Benítez‐Burraco, A. (2018) · Molecular Syndromology · doi:10.1159/000485638 · Cited by 14 · see citing works

Masculinity and the Mechanisms of Human Self-Domestication

Gleeson, B. T. (2020) · Adaptive Human Behavior and Physiology · doi:10.1007/s40750-019-00126-z · Cited by 15 · see citing works

The Narrative Origins of Language

Ferretti, F. (2021) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780198813781.013.33 · Cited by 12 · see citing works

Language Evolution

Boeckx, C. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804042-3.00133-0 · Cited by 8 · see citing works

Figurative Language, Language Disorders, and Language(s) Evolution

Benítez‐Burraco, A. (2017) · Frontiers in Psychology · doi:10.3389/fpsyg.2017.01713 · Cited by 7 · see citing works

Auto-domestication hypothesis and the rise in mental disorders in modern humans

Bednarik, R. G., Saniotis, A., & Henneberg, M. (2022) · Medical Hypotheses · doi:10.1016/j.mehy.2022.110874 · Cited by 6 · see citing works

Editorial: The Adaptive Value of Languages: Non-linguistic Causes of Language Diversity

Benítez‐Burraco, A., & Moran, S. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.01827 · Cited by 6 · see citing works

Iconic origins of language? An essay review of Steven Mithen’s The Language Puzzle (2024)

van Mazijk, C. (2024) · Biology & Philosophy · doi:10.1007/s10539-024-09952-2 · Cited by 4 · see citing works

There is no place for markedness in biologically-informed phonology

Martins, P. T. (2017) · Linguistik aktuell · doi:10.1075/la.241.09mar · Cited by 3 · see citing works

About the Origins of the Human Ability to Create Constructs of Reality

Bednarik, R. G. (2021) · Axiomathes · doi:10.1007/s10516-021-09537-8 · Cited by 3 · see citing works

Analysis of migration processes in russian education in the context of the ongoing social and cultural transformation development and testing of a model of distance education

Tarasov, A. N., Belyaev, D. A., Fedina, N. V., Kataev, D. V., Komkov, A., & Найденова, Е. А. (2021) · Revista on line de Política e Gestão Educacional · doi:10.22633/rpge.v25i3.15927 · Cited by 2 · see citing works

Integrative and Separationist Perspectives: Understanding the Causal Role of Cultural Transmission in Human Language Evolution

Suman, F. (2018) · Biological Theory · doi:10.1007/s13752-018-0301-2 · Cited by 2 · see citing works

How food fueled language, Part II: language genres, songs in the head, and the coevolution of cooking and language

Young, J. (2022) · Time and Mind · doi:10.1080/1751696x.2022.2103727 · Cited by 1 · see citing works

Sociocultural Transformation as a Factor of Changes in Modern Culture

Tarasov, A., Ivanov, V., & Plekhanov, I. (2023) · Lecture notes in networks and systems · doi:10.1007/978-3-031-36960-5_85 · Cited by 1 · see citing works

Brain and Mind

Tuniz, C., & Vipraio, P. T. (2020) · Springer eBooks · doi:10.1007/978-3-030-36522-6_9 · Cited by 1 · see citing works

A Feedback Loop Between Human Self-Domestication and Dog Domestication Contributing to Language Evolution?Preprint

Benítez‐Burraco, A., Pörtl, D., & Jung, C. (2020) · Preprints.org · doi:10.20944/preprints202003.0238.v1

Revisiting the case for ‘feral’ humans under the light of the human self-domestication hypothesis: focusing on languagePreprint

Niego, A., & Benítez‐Burraco, A. (2021) · Biolinguistics · doi:10.31234/osf.io/wh9qe · Cited by 1 · see citing works

Language and cognitive impairment associated to a novel p.Cys63Arg change in the MED13L genePreprint

Jiménez-Romero, M. S., Salas, P. C., & Benítez‐Burraco, A. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/151688

Références

(2020) · Presses Universitaires de France eBooks · doi:10.3917/puf.lagra.2020.01.0431

Language Evolution

Boeckx, C. A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-820584-6.00038-6

Information management and cultural evolution in Aboriginal Australia (In light of the cultural heterochrony hypothesis)

Steiner, G. F. (2023) · International Journal of Modern Anthropology · doi:10.4314/ijma.v2i20.1

Characteristics and significance of cerebellum`s evolutionary changes, as a part of central nervous system, during the evolution of the human brain:part 1

Nevmerzhytska, N. M., Kharchenko, M., & Prokopiv, M. (2025) · Ukrainian Scientific Medical Youth Journal · doi:10.32345/supplement.2.2025.268-273

The cost of language: functionally over-dominant language circuits in the human brain may limit cognitive abilities and non-verbal executive functions

Lipp, H. (2025) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2025.1654703

No Country for Oldowan Men: Emerging Factors in Language Evolution

Murphy, E. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.01448 · Cited by 17 · see citing works

Recent selection of candidate genes for mammal domestication in Europeans and language change in Europe: a hypothesis

Benítez‐Burraco, A., Chekalin, E., Bruskin, S. A., Tatarinova, T. V., & Morozova, I. (2021) · Annals of Human Biology · doi:10.1080/03014460.2021.1936634 · Cited by 18 · see citing works

How (and why) languages became more complex as we evolved more prosocial: the human self-domestication view

Benítez‐Burraco, A. (2025) · Frontiers in Psychology · doi:10.3389/fpsyg.2024.1499994 · Cited by 7 · see citing works

Human Self-domestication and Language Evolution: Focusing on Disorders

Niego, A. (2022) · idUS (Universidad de Sevilla)

Self-domestication and the Cultural Evolution of Language

Raviv, L., & Kirby, S. (2023) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780198869252.013.60 · Cited by 8 · see citing works