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Items: 12


Functional brain imaging predicts public health campaign success.

Falk EB, O'Donnell MB, Tompson S, Gonzalez R, Dal Cin S, Strecher V, Cummings KM, An L.

Soc Cogn Affect Neurosci. 2015 Sep 23. pii: nsv108. [Epub ahead of print]


The dopamine D4 receptor gene (DRD4) moderates cultural difference in independent versus interdependent social orientation.

Kitayama S, King A, Yoon C, Tompson S, Huff S, Liberzon I.

Psychol Sci. 2014 Jun;25(6):1169-77. doi: 10.1177/0956797614528338. Epub 2014 Apr 18.


Mice expressing mutant Trpv4 recapitulate the human TRPV4 disorders.

Weinstein MM, Tompson SW, Chen Y, Lee B, Cohn DH.

J Bone Miner Res. 2014 Aug;29(8):1815-22. doi: 10.1002/jbmr.2220.


Neural mechanisms of dissonance: an fMRI investigation of choice justification.

Kitayama S, Chua HF, Tompson S, Han S.

Neuroimage. 2013 Apr 1;69:206-12. doi: 10.1016/j.neuroimage.2012.11.034. Epub 2012 Dec 11.


Exome sequencing identifies PDE4D mutations in acrodysostosis.

Lee H, Graham JM Jr, Rimoin DL, Lachman RS, Krejci P, Tompson SW, Nelson SF, Krakow D, Cohn DH.

Am J Hum Genet. 2012 Apr 6;90(4):746-51. doi: 10.1016/j.ajhg.2012.03.004. Epub 2012 Mar 29.


Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2.

Tompson SW, Faqeih EA, Ala-Kokko L, Hecht JT, Miki R, Funari T, Funari VA, Nevarez L, Krakow D, Cohn DH.

Am J Med Genet A. 2012 Feb;158A(2):309-14. doi: 10.1002/ajmg.a.34406. Epub 2012 Jan 13.


Evc2 is a positive modulator of Hedgehog signalling that interacts with Evc at the cilia membrane and is also found in the nucleus.

Blair HJ, Tompson S, Liu YN, Campbell J, MacArthur K, Ponting CP, Ruiz-Perez VL, Goodship JA.

BMC Biol. 2011 Feb 28;9:14. doi: 10.1186/1741-7007-9-14.


Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene.

Tompson SW, Bacino CA, Safina NP, Bober MB, Proud VK, Funari T, Wangler MF, Nevarez L, Ala-Kokko L, Wilcox WR, Eyre DR, Krakow D, Cohn DH.

Am J Hum Genet. 2010 Nov 12;87(5):708-12. doi: 10.1016/j.ajhg.2010.10.009. Epub 2010 Oct 28.


A recessive skeletal dysplasia, SEMD aggrecan type, results from a missense mutation affecting the C-type lectin domain of aggrecan.

Tompson SW, Merriman B, Funari VA, Fresquet M, Lachman RS, Rimoin DL, Nelson SF, Briggs MD, Cohn DH, Krakow D.

Am J Hum Genet. 2009 Jan;84(1):72-9. doi: 10.1016/j.ajhg.2008.12.001. Epub 2008 Dec 24.


Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis-van Creveld syndrome patients.

Tompson SW, Ruiz-Perez VL, Blair HJ, Barton S, Navarro V, Robson JL, Wright MJ, Goodship JA.

Hum Genet. 2007 Jan;120(5):663-70. Epub 2006 Sep 21.


Mutations in two nonhomologous genes in a head-to-head configuration cause Ellis-van Creveld syndrome.

Ruiz-Perez VL, Tompson SW, Blair HJ, Espinoza-Valdez C, Lapunzina P, Silva EO, Hamel B, Gibbs JL, Young ID, Wright MJ, Goodship JA.

Am J Hum Genet. 2003 Mar;72(3):728-32. Epub 2003 Feb 4.


Ellis-van Creveld syndrome resulting from segmental uniparental disomy of chromosome 4.

Tompson SW, Ruiz-Perez VL, Wright MJ, Goodship JA.

J Med Genet. 2001 Jun;38(6):E18. No abstract available.

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