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Items: 33

1.

Functional brain network architecture supporting the learning of social networks in humans.

Tompson SH, Kahn AE, Falk EB, Vettel JM, Bassett DS.

Neuroimage. 2020 Jan 7;210:116498. doi: 10.1016/j.neuroimage.2019.116498. [Epub ahead of print]

2.

Correction: Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium.

Wong YL, Hysi P, Cheung G, Tedja M, Hoang QV, Tompson SWJ, Whisenhunt KN, Verhoeven VJM, Zhao W, Hess M, Wong CW, Kifley A, Hosoda Y, Haarman AEG, Hopf S, Laspas P, Sensaki S, Sim X, Miyake M, Tsujikawa A, Lamoureux E, Ohno-Matsui K, Nickels S, Mitchell P, Wong TY, Wang JJ, Hammond CJ, Barathi VA, Cheng CY, Yamashiro K, Young TL, Klaver CCW, Saw SM; Consortium of Refractive Error, Myopia (CREAM).

PLoS One. 2019 Oct 10;14(10):e0223942. doi: 10.1371/journal.pone.0223942. eCollection 2019.

3.

Self-assertive interdependence in Arab culture.

San Martin A, Sinaceur M, Madi A, Tompson S, Maddux WW, Kitayama S.

Nat Hum Behav. 2018 Nov;2(11):830-837. doi: 10.1038/s41562-018-0435-z. Epub 2018 Oct 1.

PMID:
31558808
4.

Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium.

Wong YL, Hysi P, Cheung G, Tedja M, Hoang QV, Tompson SWJ, Whisenhunt KN, Verhoeven V, Zhao W, Hess M, Wong CW, Kifley A, Hosoda Y, Haarman AEG, Hopf S, Laspas P, Sensaki S, Sim X, Miyake M, Tsujikawa A, Lamoureux E, Ohno-Matsui K, Nickels S, Mitchell P, Wong TY, Wang JJ, Hammond CJ, Barathi VA, Cheng CY, Yamashiro K, Young TL, Klaver CCW, Saw SM; Consortium of Refractive Error, Myopia (CREAM).

PLoS One. 2019 Aug 15;14(8):e0220143. doi: 10.1371/journal.pone.0220143. eCollection 2019. Erratum in: PLoS One. 2019 Oct 10;14(10):e0223942.

5.

In-utero epigenetic factors are associated with early-onset myopia in young children.

Seow WJ, Ngo CS, Pan H, Barathi VA, Tompson SW, Whisenhunt KN, Vithana E, Chong YS, Juo SH, Hysi P, Young TL, Karnani N, Saw SM.

PLoS One. 2019 May 17;14(5):e0214791. doi: 10.1371/journal.pone.0214791. eCollection 2019.

6.

Cognitive chimera states in human brain networks.

Bansal K, Garcia JO, Tompson SH, Verstynen T, Vettel JM, Muldoon SF.

Sci Adv. 2019 Apr 3;5(4):eaau8535. doi: 10.1126/sciadv.aau8535. eCollection 2019 Apr.

7.

Time-evolving dynamics in brain networks forecast responses to health messaging.

Cooper N, Garcia JO, Tompson SH, O'Donnell MB, Falk EB, Vettel JM.

Netw Neurosci. 2018 Nov 1;3(1):138-156. doi: 10.1162/netn_a_00058. eCollection 2019.

8.

Neural Mechanisms of Emotion Regulation Moderate the Predictive Value of Affective and Value-Related Brain Responses to Persuasive Messages.

Doré BP, Tompson SH, O'Donnell MB, An LC, Strecher V, Falk EB.

J Neurosci. 2019 Feb 13;39(7):1293-1300. doi: 10.1523/JNEUROSCI.1651-18.2018. Epub 2019 Jan 7.

9.

Network Approaches to Understand Individual Differences in Brain Connectivity: Opportunities for Personality Neuroscience.

Tompson S, Falk EB, Vettel JM, Bassett DS.

Personal Neurosci. 2018 Jul 5;1. pii: e5. doi: 10.1017/pen.2018.4. Epub 2018 Jul 2.

10.

Individual differences in learning social and nonsocial network structures.

Tompson SH, Kahn AE, Falk EB, Vettel JM, Bassett DS.

J Exp Psychol Learn Mem Cogn. 2019 Feb;45(2):253-271. doi: 10.1037/xlm0000580. Epub 2018 Jul 19.

11.

Gene by Culture Effects on Emotional Processing of Social Cues among East Asians and European Americans.

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

Behav Sci (Basel). 2018 Jul 11;8(7). pii: E62. doi: 10.3390/bs8070062.

12.

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.

Tedja MS, Wojciechowski R, Hysi PG, Eriksson N, Furlotte NA, Verhoeven VJM, Iglesias AI, Meester-Smoor MA, Tompson SW, Fan Q, Khawaja AP, Cheng CY, Höhn R, Yamashiro K, Wenocur A, Grazal C, Haller T, Metspalu A, Wedenoja J, Jonas JB, Wang YX, Xie J, Mitchell P, Foster PJ, Klein BEK, Klein R, Paterson AD, Hosseini SM, Shah RL, Williams C, Teo YY, Tham YC, Gupta P, Zhao W, Shi Y, Saw WY, Tai ES, Sim XL, Huffman JE, Polašek O, Hayward C, Bencic G, Rudan I, Wilson JF; CREAM Consortium; 23andMe Research Team; UK Biobank Eye and Vision Consortium, Joshi PK, Tsujikawa A, Matsuda F, Whisenhunt KN, Zeller T, van der Spek PJ, Haak R, Meijers-Heijboer H, van Leeuwen EM, Iyengar SK, Lass JH, Hofman A, Rivadeneira F, Uitterlinden AG, Vingerling JR, Lehtimäki T, Raitakari OT, Biino G, Concas MP, Schwantes-An TH, Igo RP Jr, Cuellar-Partida G, Martin NG, Craig JE, Gharahkhani P, Williams KM, Nag A, Rahi JS, Cumberland PM, Delcourt C, Bellenguez C, Ried JS, Bergen AA, Meitinger T, Gieger C, Wong TY, Hewitt AW, Mackey DA, Simpson CL, Pfeiffer N, Pärssinen O, Baird PN, Vitart V, Amin N, van Duijn CM, Bailey-Wilson JE, Young TL, Saw SM, Stambolian D, MacGregor S, Guggenheim JA, Tung JY, Hammond CJ, Klaver CCW.

Nat Genet. 2018 Jun;50(6):834-848. doi: 10.1038/s41588-018-0127-7. Epub 2018 May 28.

13.

Associations between coherent neural activity in the brain's value system during antismoking messages and reductions in smoking.

Cooper N, Tompson S, O'Donnell MB, Vettel JM, Bassett DS, Falk EB.

Health Psychol. 2018 Apr;37(4):375-384. doi: 10.1037/hea0000574. Epub 2018 Feb 15.

14.

Angiopoietin-1 is required for Schlemm's canal development in mice and humans.

Thomson BR, Souma T, Tompson SW, Onay T, Kizhatil K, Siggs OM, Feng L, Whisenhunt KN, Yanovitch TL, Kalaydjieva L, Azmanov DN, Finzi S, Tanna CE, Hewitt AW, Mackey DA, Bradfield YS, Souzeau E, Javadiyan S, Wiggs JL, Pasutto F, Liu X, John SW, Craig JE, Jin J, Young TL, Quaggin SE.

J Clin Invest. 2017 Dec 1;127(12):4421-4436. doi: 10.1172/JCI95545. Epub 2017 Nov 6.

15.

Assaying the Effects of Splice Site Variants by Exon Trapping in a Mammalian Cell Line.

Tompson SW, Young TL.

Bio Protoc. 2017 May 20;7(10). pii: e2281. doi: 10.21769/BioProtoc.2281.

16.

Predicting behavior change from persuasive messages using neural representational similarity and social network analyses.

Pegors TK, Tompson S, O'Donnell MB, Falk EB.

Neuroimage. 2017 Aug 15;157:118-128. doi: 10.1016/j.neuroimage.2017.05.063. Epub 2017 May 31.

17.

Exome Sequence Analysis of 14 Families With High Myopia.

Kloss BA, Tompson SW, Whisenhunt KN, Quow KL, Huang SJ, Pavelec DM, Rosenberg T, Young TL.

Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):1982-1990. doi: 10.1167/iovs.16-20883.

18.

Reduced penetrance in a large Caucasian pedigree with Stickler syndrome.

Tompson SW, Johnson C, Abbott D, Bakall B, Soler V, Yanovitch TL, Whisenhunt KN, Klemm T, Rozen S, Stone EM, Johnson M, Young TL.

Ophthalmic Genet. 2017 Jan-Feb;38(1):43-50. doi: 10.1080/13816810.2016.1275018. Epub 2017 Jan 17.

19.

Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity.

Souma T, Tompson SW, Thomson BR, Siggs OM, Kizhatil K, Yamaguchi S, Feng L, Limviphuvadh V, Whisenhunt KN, Maurer-Stroh S, Yanovitch TL, Kalaydjieva L, Azmanov DN, Finzi S, Mauri L, Javadiyan S, Souzeau E, Zhou T, Hewitt AW, Kloss B, Burdon KP, Mackey DA, Allen KF, Ruddle JB, Lim SH, Rozen S, Tran-Viet KN, Liu X, John S, Wiggs JL, Pasutto F, Craig JE, Jin J, Quaggin SE, Young TL.

J Clin Invest. 2016 Jul 1;126(7):2575-87. doi: 10.1172/JCI85830. Epub 2016 Jun 6.

20.

Connectivity between mPFC and PCC predicts post-choice attitude change: The self-referential processing hypothesis of choice justification.

Tompson S, Chua HF, Kitayama S.

Hum Brain Mapp. 2016 Nov;37(11):3810-3820. doi: 10.1002/hbm.23277.

21.

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. 2016 Feb;11(2):204-14. doi: 10.1093/scan/nsv108. Epub 2015 Sep 23.

22.

Brain Activity in Self- and Value-Related Regions in Response to Online Antismoking Messages Predicts Behavior Change.

Cooper N, Tompson S, O'Donnell MB, Falk EB.

J Media Psychol. 2015;27:93-109. doi: 10.1027/1864-1105/a000146. Epub 2015 Sep 15.

23.

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.

PMID:
24747168
24.

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):1815-1822. doi: 10.1002/jbmr.2220.

25.

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.

PMID:
23238432
26.

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.

27.

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.

28.

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.

29.

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.

30.

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.

31.

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.

PMID:
17024374
32.

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.

33.

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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