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Results: 1 to 20 of 52

References for PMC Articles for PubMed (Select 22500773)

1.

Predicting white matter integrity from multiple common genetic variants.

Kohannim O, Jahanshad N, Braskie MN, Stein JL, Chiang MC, Reese AH, Hibar DP, Toga AW, McMahon KL, de Zubicaray GI, Medland SE, Montgomery GW, Martin NG, Wright MJ, Thompson PM.

Neuropsychopharmacology. 2012 Aug;37(9):2012-9. doi: 10.1038/npp.2012.49. Epub 2012 Apr 18.

2.

Multilocus genetic analysis of brain images.

Hibar DP, Kohannim O, Stein JL, Chiang MC, Thompson PM.

Front Genet. 2011 Oct 21;2:73. doi: 10.3389/fgene.2011.00073. eCollection 2011.

3.

Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene.

Jahanshad N, Kohannim O, Hibar DP, Stein JL, McMahon KL, de Zubicaray GI, Medland SE, Montgomery GW, Whitfield JB, Martin NG, Wright MJ, Toga AW, Thompson PM.

Proc Natl Acad Sci U S A. 2012 Apr 3;109(14):E851-9. doi: 10.1073/pnas.1105543109. Epub 2012 Jan 9.

4.

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.

Peñagarikano O, Abrahams BS, Herman EI, Winden KD, Gdalyahu A, Dong H, Sonnenblick LI, Gruver R, Almajano J, Bragin A, Golshani P, Trachtenberg JT, Peles E, Geschwind DH.

Cell. 2011 Sep 30;147(1):235-46. doi: 10.1016/j.cell.2011.08.040.

5.

Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults.

Braskie MN, Jahanshad N, Stein JL, Barysheva M, McMahon KL, de Zubicaray GI, Martin NG, Wright MJ, Ringman JM, Toga AW, Thompson PM.

J Neurosci. 2011 May 4;31(18):6764-70. doi: 10.1523/JNEUROSCI.5794-10.2011.

6.

A Hough transform global probabilistic approach to multiple-subject diffusion MRI tractography.

Aganj I, Lenglet C, Jahanshad N, Yacoub E, Harel N, Thompson PM, Sapiro G.

Med Image Anal. 2011 Aug;15(4):414-25. doi: 10.1016/j.media.2011.01.003. Epub 2011 Jan 26.

7.

A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits.

Stein MB, Yang BZ, Chavira DA, Hitchcock CA, Sung SC, Shipon-Blum E, Gelernter J.

Biol Psychiatry. 2011 May 1;69(9):825-31. doi: 10.1016/j.biopsych.2010.11.008. Epub 2010 Dec 30.

8.

Brain graphs: graphical models of the human brain connectome.

Bullmore ET, Bassett DS.

Annu Rev Clin Psychol. 2011;7:113-40. doi: 10.1146/annurev-clinpsy-040510-143934. Review.

PMID:
21128784
9.

Functional connectivity networks in the autistic and healthy brain assessed using Granger causality.

Pollonini L, Patidar U, Situ N, Rezaie R, Papanicolaou AC, Zouridakis G.

Conf Proc IEEE Eng Med Biol Soc. 2010;2010:1730-3. doi: 10.1109/IEMBS.2010.5626702.

PMID:
21096408
10.

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2.

Scott-Van Zeeland AA, Abrahams BS, Alvarez-Retuerto AI, Sonnenblick LI, Rudie JD, Ghahremani D, Mumford JA, Poldrack RA, Dapretto M, Geschwind DH, Bookheimer SY.

Sci Transl Med. 2010 Nov 3;2(56):56ra80. doi: 10.1126/scitranslmed.3001344.

11.

White matter maturation reshapes structural connectivity in the late developing human brain.

Hagmann P, Sporns O, Madan N, Cammoun L, Pienaar R, Wedeen VJ, Meuli R, Thiran JP, Grant PE.

Proc Natl Acad Sci U S A. 2010 Nov 2;107(44):19067-72. doi: 10.1073/pnas.1009073107. Epub 2010 Oct 18.

12.

Genetics of white matter development: a DTI study of 705 twins and their siblings aged 12 to 29.

Chiang MC, McMahon KL, de Zubicaray GI, Martin NG, Hickie I, Toga AW, Wright MJ, Thompson PM.

Neuroimage. 2011 Feb 1;54(3):2308-17. doi: 10.1016/j.neuroimage.2010.10.015. Epub 2010 Oct 13.

13.

Conserved and variable architecture of human white matter connectivity.

Bassett DS, Brown JA, Deshpande V, Carlson JM, Grafton ST.

Neuroimage. 2011 Jan 15;54(2):1262-79. doi: 10.1016/j.neuroimage.2010.09.006. Epub 2010 Sep 17.

PMID:
20850551
14.

Prediction of individual brain maturity using fMRI.

Dosenbach NU, Nardos B, Cohen AL, Fair DA, Power JD, Church JA, Nelson SM, Wig GS, Vogel AC, Lessov-Schlaggar CN, Barnes KA, Dubis JW, Feczko E, Coalson RS, Pruett JR Jr, Barch DM, Petersen SE, Schlaggar BL.

Science. 2010 Sep 10;329(5997):1358-61. doi: 10.1126/science.1194144. Erratum in: Science. 2010 Nov 5;330(6005):756.

15.

A genome-wide scan for common alleles affecting risk for autism.

Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Carson AR, Casallo G, Casey J, Chu SH, Cochrane L, Corsello C, Crawford EL, Crossett A, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Melhem NM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Piven J, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Rickaby J, Roberts W, Roeder K, Roge B, Rutter ML, Bierut LJ, Rice JP, Salt J, Sansom K, Sato D, Segurado R, Senman L, Shah N, Sheffield VC, Soorya L, Sousa I, Stoppioni V, Strawbridge C, Tancredi R, Tansey K, Thiruvahindrapduram B, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Wallace S, Wang K, Wang Z, Wassink TH, Wing K, Wittemeyer K, Wood S, Yaspan BL, Zurawiecki D, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Gallagher L, Geschwind DH, Gill M, Haines JL, Miller J, Monaco AP, Nurnberger JI Jr, Paterson AD, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vicente AM, Vieland VJ, Wijsman EM, Devlin B, Ennis S, Hallmayer J.

Hum Mol Genet. 2010 Oct 15;19(20):4072-82. doi: 10.1093/hmg/ddq307. Epub 2010 Jul 27.

16.

Reconstruction of the orientation distribution function in single- and multiple-shell q-ball imaging within constant solid angle.

Aganj I, Lenglet C, Sapiro G, Yacoub E, Ugurbil K, Harel N.

Magn Reson Med. 2010 Aug;64(2):554-66. doi: 10.1002/mrm.22365.

17.

Genetic influences on brain asymmetry: a DTI study of 374 twins and siblings.

Jahanshad N, Lee AD, Barysheva M, McMahon KL, de Zubicaray GI, Martin NG, Wright MJ, Toga AW, Thompson PM.

Neuroimage. 2010 Aug 15;52(2):455-69. doi: 10.1016/j.neuroimage.2010.04.236. Epub 2010 Apr 27.

18.

Extending genetic linkage analysis to diffusion tensor images to map single gene effects on brain fiber architecture.

Chiang MC, Avedissian C, Barysheva M, Toga AW, McMahon KL, de Zubicaray GI, Wright MJ, Thompson PM.

Med Image Comput Comput Assist Interv. 2009;12(Pt 2):506-13.

PMID:
20426150
19.

Tensor-based analysis of genetic influences on brain integrity using DTI in 100 twins.

Lee AD, Leporé N, Brun C, Chou YY, Barysheva M, Chiang MC, Madsen SK, de Zubicaray GI, McMahon KL, Wright MJ, Toga AW, Thompson PM.

Med Image Comput Comput Assist Interv. 2009;12(Pt 1):967-74.

PMID:
20426082
20.

Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2.

Tan GC, Doke TF, Ashburner J, Wood NW, Frackowiak RS.

Neuroimage. 2010 Nov 15;53(3):1030-42. doi: 10.1016/j.neuroimage.2010.02.018. Epub 2010 Feb 20.

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