CARTA Member Publications

CARTA encourages transdisciplinary research to advance our understanding of human origins and provides a forum for researchers from disparate fields "to explore and explain the human phenomenon.” This page lists select publications with one or more CARTA member authors.

Displaying 1026 - 1050 of 1207 publications

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2009

Paul, BM, Snyder, AZ, Haist, F, Raichle, ME, Bellugi, U, Stiles, J. Amygdala response to faces parallels social behavior in Williams syndrome. Soc Cogn Affect Neurosci, 2009/07/28. 2009;4:278-85.
Ramchandra, R, Hood, S, Denton, D, Woods, R, McKinley, M, McAllen, R, May, C. Basis for the preferential activation of cardiac sympathetic nerve activity in heart failure. Proc Natl Acad Sci U S A. United States. 2009;106:924-8.
Rosenber, K, Trevathan, W. Der Kaiserschnitt ausentwicklungsgeschichtlicher Sicht. In: Stark, M, eds. Der Kaiserschnitt Indikationen. Hintergründe. Operatives Management der Misgav-Ladach-Methode. München: Urban and Fischer. 2009, p.27-38.
Toleno, DM, Renaud, G, Wolfsberg, TG, Islam, M, Wildman, DE, Siegmund, KD, Hacia, JG. Development and evaluation of new mask protocols for gene expression profiling in humans and chimpanzees. BMC Bioinformatics, 2009/03/07. 2009;10:77.
Pham, T, Gregg, CJ, Karp, F, Chow, R, Padler-Karavani, V, Cao, H, Chen, X, Witztum, JL, Varki, NM, Varki, A. Evidence for a novel human-specific xeno-auto-antibody response against vascular endothelium. Blood, 2009/10/16. 2009;114:5225-35.
Bogin, B. Evolution of Childhood, Biological. In: Shweder, RA, Bidell, TR, eds. The child : an encyclopedic companion. Chicago: The University of Chicago Press. 2009, p.327-329.
Varki, NM, Anderson, D, Herndon, JG, Pham, T, Gregg, CJ, Cheriyan, M, Murphy, J, Strobert, E, Fritz, J, Else, JG, Varki, A. Heart disease is common in humans and chimpanzees, but is caused by different pathological processes. Evol Appl. Wiley-Blackwell. 2009;2(1):101-112.
Konopka, G, Bomar, J, Winden, K, Coppola, G, Jonsson, Z, Gao, F, Peng, S, Preuss, T, Wohlschlegel, J, Geschwind, D. Human-specific transcriptional regulation of CNS development genes by FOXP2. Nature. England. 2009;462:213-7.
Avise, JC, Ayala, FJosé. In the Light of Evolution: Volume III-Two Centuries of Darwin. Sackler Colloquium series. Washington, D.C.: National Academies Press. 2009.
Dai, L, Bellugi, U, Chen, XN, Pulst-Korenberg, AM, Jarvinen-Pasley, A, Tirosh-Wagner, T, Eis, PS, Graham, J, Mills, D, Searcy, Y, Korenberg, JR. Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays. Am J Med Genet A, 2009/02/11. 2009;149A:302-14.
Coufal, NG, Garcia-Perez, JL, Peng, GE, Yeo, GW, Mu, Y, Lovci, MT, Morell, M, O'Shea, KS, Moran, JV, Gage, FH. L1 retrotransposition in human neural progenitor cells. Nature, 2009/08/07. 2009;460:1127-31.
Bogin, B, Varela-Silva, MI. Leg length, proportion, health and beauty: a review. Anthropol Anz, 2010/05/06. 2009;67:439-59.
Goodman, M, Sterner, KN, Islam, M, Uddin, M, Sherwood, CC, Hof, PR, Hou, ZC, Lipovich, L, Jia, H, Grossman, LI, Wildman, DE. Phylogenomic analyses reveal convergent patterns of adaptive evolution in elephant and human ancestries. Proc Natl Acad Sci U S A, 2009/11/21. 2009;106:20824-9.
Di Fiore, A, Disotell, T, Gagneux, P. Primate Malarias. In: Huffman, MA, Chapman, CA, eds. Primate parasite ecology : the dynamics and study of host-parasite relationships. Cambridge, UK ; New York: Cambridge University Press. 2009.
Winn, VD, Gormley, M, Paquet, AC, Kjaer-Sorensen, K, Kramer, A, Rumer, KK, Haimov-Kochman, R, Yeh, RF, Overgaard, MT, Varki, A, Oxvig, C, Fisher, SJ. Severe preeclampsia-related changes in gene expression at the maternal-fetal\ interface include sialic acid-binding immunoglobulin-like lectin-6 and\ pappalysin-2. Endocrinology, 2008/09/27. 2009;150:452-62.
Preuss, TM. The cognitive neuroscience of human uniqueness. In: The cognitive neurosciences, 4th ed. Cambridge, Mass.: MIT Press. 2009, p.49-64.
Denton, D, McKinley, M, Farrell, M, Egan, G. The role of primordial emotions in the evolutionary origin of consciousness. Conscious Cogn. United States. 2009;18:500-14.
Collette, JC, Chen, XN, Mills, DL, Galaburda, AM, Reiss, AL, Bellugi, U, Korenberg, JR. William's syndrome: gene expression is related to parental origin and regional coordinate control. J Hum Genet, 2009/03/14. 2009;54:193-8.

2008

Gothelf, D, Searcy, YM, Reilly, J, Lai, PT, Lanre-Amos, T, Mills, D, Korenberg, JR, Galaburda, A, Bellugi, U, Reiss, AL. Association between cerebral shape and social use of language in Williams syndrome. Am J Med Genet A, 2008/10/17. 2008;146A:2753-61.
Penn, DC, Holyoak, KJ, Povinelli, DJ. Darwin's mistake: explaining the discontinuity between human and nonhuman minds. Behav Brain Sci, 2008/05/16. 2008;31:109-30; discussion 130-178.
Korenberg, JR, Dai, L, Bellugi, U, Jarvinen-Pasley, A, Mills, D, Galaburda, A, Reiss, A, Pober, BR. Deletion of 7q11.23 Genes and Williams Syndrome. In: Epstein, CJ, Erickson, RP, Wynshaw-Boris, AJoseph, eds. Inborn errors of development : the molecular basis of clinical disorders of morphogenesis, 2nd. Oxford ; New York: Oxford University Press. 2008, p.1617 p..

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