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Results: 1 to 20 of 213

1.

Investigating Protein-protein Interactions in Live Cells Using Bioluminescence Resonance Energy Transfer.

Deriziotis P, Graham SA, Estruch SB, Fisher SE.

J Vis Exp. 2014 May 26;(87). doi: 10.3791/51438.

PMID:
24893771
[PubMed - in process]
2.

Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets.

Guadalupe T, Zwiers MP, Teumer A, Wittfeld K, Vasquez AA, Hoogman M, Hagoort P, Fernandez G, Buitelaar J, Hegenscheid K, Völzke H, Franke B, Fisher SE, Grabe HJ, Francks C.

Hum Brain Mapp. 2014 Jul;35(7):3277-89. doi: 10.1002/hbm.22401. Epub 2013 Nov 4.

PMID:
24827550
[PubMed - in process]
3.

A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study.

Baron-Cohen S, Murphy L, Chakrabarti B, Craig I, Mallya U, Lakatošová S, Rehnstrom K, Peltonen L, Wheelwright S, Allison C, Fisher SE, Warrier V.

PLoS One. 2014 May 6;9(5):e96374. doi: 10.1371/journal.pone.0096374. eCollection 2014.

PMID:
24801482
[PubMed - in process]
Free PMC Article
4.

Differences in cerebral cortical anatomy of left- and right-handers.

Guadalupe T, Willems RM, Zwiers MP, Arias Vasquez A, Hoogman M, Hagoort P, Fernandez G, Buitelaar J, Franke B, Fisher SE, Francks C.

Front Psychol. 2014 Mar 28;5:261. doi: 10.3389/fpsyg.2014.00261. eCollection 2014.

PMID:
24734025
[PubMed]
Free PMC Article
5.

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.

Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER; SLI Consortium, Ring SM, Davey Smith G, Francks C, Paracchini S, Monaco AP, Fisher SE, Newbury DF.

Genes Brain Behav. 2014 Apr;13(4):418-29. doi: 10.1111/gbb.12127. Epub 2014 Mar 24.

PMID:
24571439
[PubMed - in process]
6.

On the other hand: including left-handers in cognitive neuroscience and neurogenetics.

Willems RM, Van der Haegen L, Fisher SE, Francks C.

Nat Rev Neurosci. 2014 Mar;15(3):193-201. doi: 10.1038/nrn3679. Epub 2014 Feb 12.

PMID:
24518415
[PubMed - indexed for MEDLINE]
7.

Associations of HLA alleles with specific language impairment.

Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER; SLI Consortium, Monaco AP, Knight JC, Winney B, Fisher SE, Newbury DF.

J Neurodev Disord. 2014 Jan 17;6(1):1. doi: 10.1186/1866-1955-6-1.

PMID:
24433325
[PubMed]
Free PMC Article
8.

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.

Thompson PM, Stein JL, Medland SE, Hibar DP, Vasquez AA, Renteria ME, Toro R, Jahanshad N, Schumann G, Franke B, Wright MJ, Martin NG, Agartz I, Alda M, Alhusaini S, Almasy L, Almeida J, Alpert K, Andreasen NC, Andreassen OA, Apostolova LG, Appel K, Armstrong NJ, Aribisala B, Bastin ME, Bauer M, Bearden CE, Bergmann O, Binder EB, Blangero J, Bockholt HJ, Bøen E, Bois C, Boomsma DI, Booth T, Bowman IJ, Bralten J, Brouwer RM, Brunner HG, Brohawn DG, Buckner RL, Buitelaar J, Bulayeva K, Bustillo JR, Calhoun VD, Cannon DM, Cantor RM, Carless MA, Caseras X, Cavalleri GL, Chakravarty MM, Chang KD, Ching CR, Christoforou A, Cichon S, Clark VP, Conrod P, Coppola G, Crespo-Facorro B, Curran JE, Czisch M, Deary IJ, de Geus EJ, den Braber A, Delvecchio G, Depondt C, de Haan L, de Zubicaray GI, Dima D, Dimitrova R, Djurovic S, Dong H, Donohoe G, Duggirala R, Dyer TD, Ehrlich S, Ekman CJ, Elvsåshagen T, Emsell L, Erk S, Espeseth T, Fagerness J, Fears S, Fedko I, Fernández G, Fisher SE, Foroud T, Fox PT, Francks C, Frangou S, Frey EM, Frodl T, Frouin V, Garavan H, Giddaluru S, Glahn DC, Godlewska B, Goldstein RZ, Gollub RL, Grabe HJ, Grimm O, Gruber O, Guadalupe T, Gur RE, Gur RC, Göring HH, Hagenaars S, Hajek T, Hall GB, Hall J, Hardy J, Hartman CA, Hass J, Hatton SN, Haukvik UK, Hegenscheid K, Heinz A, Hickie IB, Ho BC, Hoehn D, Hoekstra PJ, Hollinshead M, Holmes AJ, Homuth G, Hoogman M, Hong LE, Hosten N, Hottenga JJ, Hulshoff Pol HE, Hwang KS, Jack CR Jr, Jenkinson M, Johnston C, Jönsson EG, Kahn RS, Kasperaviciute D, Kelly S, Kim S, Kochunov P, Koenders L, Krämer B, Kwok JB, Lagopoulos J, Laje G, Landen M, Landman BA, Lauriello J, Lawrie SM, Lee PH, Le Hellard S, Lemaître H, Leonardo CD, Li CS, Liberg B, Liewald DC, Liu X, Lopez LM, Loth E, Lourdusamy A, Luciano M, Macciardi F, Machielsen MW, Macqueen GM, Malt UF, Mandl R, Manoach DS, Martinot JL, Matarin M, Mather KA, Mattheisen M, Mattingsdal M, Meyer-Lindenberg A, McDonald C, McIntosh AM, McMahon FJ, McMahon KL, Meisenzahl E, Melle I, Milaneschi Y, Mohnke S, Montgomery GW, Morris DW, Moses EK, Mueller BA, Muñoz Maniega S, Mühleisen TW, Müller-Myhsok B, Mwangi B, Nauck M, Nho K, Nichols TE, Nilsson LG, Nugent AC, Nyberg L, Olvera RL, Oosterlaan J, Ophoff RA, Pandolfo M, Papalampropoulou-Tsiridou M, Papmeyer M, Paus T, Pausova Z, Pearlson GD, Penninx BW, Peterson CP, Pfennig A, Phillips M, Pike GB, Poline JB, Potkin SG, Pütz B, Ramasamy A, Rasmussen J, Rietschel M, Rijpkema M, Risacher SL, Roffman JL, Roiz-Santiañez R, Romanczuk-Seiferth N, Rose EJ, Royle NA, Rujescu D, Ryten M, Sachdev PS, Salami A, Satterthwaite TD, Savitz J, Saykin AJ, Scanlon C, Schmaal L, Schnack HG, Schork AJ, Schulz SC, Schür R, Seidman L, Shen L, Shoemaker JM, Simmons A, Sisodiya SM, Smith C, Smoller JW, Soares JC, Sponheim SR, Sprooten E, Starr JM, Steen VM, Strakowski S, Strike L, Sussmann J, Sämann PG, Teumer A, Toga AW, Tordesillas-Gutierrez D, Trabzuni D, Trost S, Turner J, Van den Heuvel M, van der Wee NJ, van Eijk K, van Erp TG, van Haren NE, van 't Ent D, van Tol MJ, Valdés Hernández MC, Veltman DJ, Versace A, Völzke H, Walker R, Walter H, Wang L, Wardlaw JM, Weale ME, Weiner MW, Wen W, Westlye LT, Whalley HC, Whelan CD, White T, Winkler AM, Wittfeld K, Woldehawariat G, Wolf C, Zilles D, Zwiers MP, Thalamuthu A, Schofield PR, Freimer NB, Lawrence NS, Drevets W; Alzheimer’s Disease Neuroimaging Initiative, EPIGEN Consortium, IMAGEN Consortium, Saguenay Youth Study (SYS) Group.

Brain Imaging Behav. 2014 Jun;8(2):153-82. doi: 10.1007/s11682-013-9269-5.

PMID:
24399358
[PubMed - in process]
Free PMC Article
9.

Is synaesthesia more common in autism?

Baron-Cohen S, Johnson D, Asher J, Wheelwright S, Fisher SE, Gregersen PK, Allison C.

Mol Autism. 2013 Nov 20;4(1):40. doi: 10.1186/2040-2392-4-40.

PMID:
24252644
[PubMed]
Free PMC Article
10.

Molecular genetics of dyslexia: an overview.

Carrion-Castillo A, Franke B, Fisher SE.

Dyslexia. 2013 Nov;19(4):214-40. doi: 10.1002/dys.1464. Review.

PMID:
24133036
[PubMed - indexed for MEDLINE]
11.

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.

Simpson NH, Addis L, Brandler WM, Slonims V, Clark A, Watson J, Scerri TS, Hennessy ER, Bolton PF, Conti-Ramsden G, Fairfax BP, Knight JC, Stein J, Talcott JB, O'Hare A, Baird G, Paracchini S, Fisher SE, Newbury DF; SLI Consortium.

Dev Med Child Neurol. 2014 Apr;56(4):346-53. doi: 10.1111/dmcn.12294. Epub 2013 Oct 9.

PMID:
24117048
[PubMed - indexed for MEDLINE]
12.

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.

Brandler WM, Morris AP, Evans DM, Scerri TS, Kemp JP, Timpson NJ, St Pourcain B, Smith GD, Ring SM, Stein J, Monaco AP, Talcott JB, Fisher SE, Webber C, Paracchini S.

PLoS Genet. 2013;9(9):e1003751. doi: 10.1371/journal.pgen.1003751. Epub 2013 Sep 12.

PMID:
24068947
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Evolution. Culture, genes, and the human revolution.

Fisher SE, Ridley M.

Science. 2013 May 24;340(6135):929-30. doi: 10.1126/science.1236171. No abstract available.

PMID:
23704558
[PubMed - indexed for MEDLINE]
14.

FOXP2 targets show evidence of positive selection in European populations.

Ayub Q, Yngvadottir B, Chen Y, Xue Y, Hu M, Vernes SC, Fisher SE, Tyler-Smith C.

Am J Hum Genet. 2013 May 2;92(5):696-706. doi: 10.1016/j.ajhg.2013.03.019. Epub 2013 Apr 18.

PMID:
23602712
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Neurogenomics of speech and language disorders: the road ahead.

Deriziotis P, Fisher SE.

Genome Biol. 2013 Apr 18;14(4):204. [Epub ahead of print]

PMID:
23597266
[PubMed - as supplied by publisher]
Free PMC Article
16.

Absolute pitch exhibits phenotypic and genetic overlap with synesthesia.

Gregersen PK, Kowalsky E, Lee A, Baron-Cohen S, Fisher SE, Asher JE, Ballard D, Freudenberg J, Li W.

Hum Mol Genet. 2013 May 15;22(10):2097-104. doi: 10.1093/hmg/ddt059. Epub 2013 Feb 12.

PMID:
23406871
[PubMed - indexed for MEDLINE]
Free Article
17.

Persistence and transmission of recessive deafness and sign language: new insights from village sign languages.

Gialluisi A, Dediu D, Francks C, Fisher SE.

Eur J Hum Genet. 2013 Sep;21(9):894-6. doi: 10.1038/ejhg.2012.292. Epub 2013 Jan 16. No abstract available.

PMID:
23321624
[PubMed - indexed for MEDLINE]
18.

Decoding the genetics of speech and language.

Graham SA, Fisher SE.

Curr Opin Neurobiol. 2013 Feb;23(1):43-51. doi: 10.1016/j.conb.2012.11.006. Epub 2012 Dec 7. Review.

PMID:
23228431
[PubMed - indexed for MEDLINE]
19.

Performance of the EORTC questionnaire for the assessment of quality of life in head and neck cancer patients EORTC QLQ-H&N35: a methodological review.

Singer S, Arraras JI, Chie WC, Fisher SE, Galalae R, Hammerlid E, Nicolatou-Galitis O, Schmalz C, Verdonck-de Leeuw I, Gamper E, Keszte J, Hofmeister D.

Qual Life Res. 2013 Oct;22(8):1927-41. doi: 10.1007/s11136-012-0325-1. Epub 2012 Nov 28. Review.

PMID:
23188134
[PubMed - indexed for MEDLINE]
20.

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.

Newbury DF, Mari F, Sadighi Akha E, Macdermot KD, Canitano R, Monaco AP, Taylor JC, Renieri A, Fisher SE, Knight SJ.

Eur J Hum Genet. 2013 Apr;21(4):361-5. doi: 10.1038/ejhg.2012.166. Epub 2012 Aug 22. No abstract available.

PMID:
22909776
[PubMed - indexed for MEDLINE]
Free PMC Article

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