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Results: 1 to 20 of 235

1.

A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment.

Lozano R, Vino A, Lozano C, Fisher SE, Deriziotis P.

Eur J Hum Genet. 2015 Apr 8. doi: 10.1038/ejhg.2015.66. [Epub ahead of print]

PMID:
25853299
2.

Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.

Villanueva P, Nudel R, Hoischen A, Fernández MA, Simpson NH, Gilissen C, Reader RH, Jara L, Echeverry MM, Francks C, Baird G, Conti-Ramsden G, O'Hare A, Bolton PF, Hennessy ER; SLI Consortium, Palomino H, Carvajal-Carmona L, Veltman JA, Cazier JB, De Barbieri Z, Fisher SE, Newbury DF.

PLoS Genet. 2015 Mar 17;11(3):e1004925. doi: 10.1371/journal.pgen.1004925. eCollection 2015 Mar.

3.

Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.

Pettigrew KA, Fajutrao Valles SF, Moll K, Northstone K, Ring S, Pennell C, Wang C, Leavett R, Hayiou-Thomas ME, Thompson P, Simpson NH, Fisher SE; SLI Consortium, Whitehouse AJ, Snowling MJ, Newbury DF, Paracchini S.

Genes Brain Behav. 2015 Mar 16. doi: 10.1111/gbb.12213. [Epub ahead of print]

PMID:
25778778
4.

A schizophrenia-associated HLA locus affects thalamus volume and asymmetry.

Brucato N, Guadalupe T, Franke B, Fisher SE, Francks C.

Brain Behav Immun. 2015 Feb 26. pii: S0889-1591(15)00063-X. doi: 10.1016/j.bbi.2015.02.021. [Epub ahead of print]

PMID:
25728236
5.

Defining the biological bases of individual differences in musicality.

Gingras B, Honing H, Peretz I, Trainor LJ, Fisher SE.

Philos Trans R Soc Lond B Biol Sci. 2015 Mar 19;370(1664):20140092. doi: 10.1098/rstb.2014.0092.

PMID:
25646515
6.

Common genetic variants influence human subcortical brain structures.

Hibar DP, Stein JL, Renteria ME, Arias-Vasquez A, Desrivières S, Jahanshad N, Toro R, Wittfeld K, Abramovic L, Andersson M, Aribisala BS, Armstrong NJ, Bernard M, Bohlken MM, Boks MP, Bralten J, Brown AA, Chakravarty MM, Chen Q, Ching CR, Cuellar-Partida G, den Braber A, Giddaluru S, Goldman AL, Grimm O, Guadalupe T, Hass J, Woldehawariat G, Holmes AJ, Hoogman M, Janowitz D, Jia T, Kim S, Klein M, Kraemer B, Lee PH, Olde Loohuis LM, Luciano M, Macare C, Mather KA, Mattheisen M, Milaneschi Y, Nho K, Papmeyer M, Ramasamy A, Risacher SL, Roiz-Santiañez R, Rose EJ, Salami A, Sämann PG, Schmaal L, Schork AJ, Shin J, Strike LT, Teumer A, van Donkelaar MM, van Eijk KR, Walters RK, Westlye LT, Whelan CD, Winkler AM, Zwiers MP, Alhusaini S, Athanasiu L, Ehrlich S, Hakobjan MM, Hartberg CB, Haukvik UK, Heister AJ, Hoehn D, Kasperaviciute D, Liewald DC, Lopez LM, Makkinje RR, Matarin M, Naber MA, McKay DR, Needham M, Nugent AC, Pütz B, Royle NA, Shen L, Sprooten E, Trabzuni D, van der Marel SS, van Hulzen KJ, Walton E, Wolf C, Almasy L, Ames D, Arepalli S, Assareh AA, Bastin ME, Brodaty H, Bulayeva KB, Carless MA, Cichon S, Corvin A, Curran JE, Czisch M, de Zubicaray GI, Dillman A, Duggirala R, Dyer TD, Erk S, Fedko IO, Ferrucci L, Foroud TM, Fox PT, Fukunaga M, Gibbs JR, Göring HH, Green RC, Guelfi S, Hansell NK, Hartman CA, Hegenscheid K, Heinz A, Hernandez DG, Heslenfeld DJ, Hoekstra PJ, Holsboer F, Homuth G, Hottenga JJ, Ikeda M, Jack CR Jr, Jenkinson M, Johnson R, Kanai R, Keil M, Kent JW Jr, Kochunov P, Kwok JB, Lawrie SM, Liu X, Longo DL, McMahon KL, Meisenzahl E, Melle I, Mohnke S, Montgomery GW, Mostert JC, Mühleisen TW, Nalls MA, Nichols TE, Nilsson LG, Nöthen MM, Ohi K, Olvera RL, Perez-Iglesias R, Pike GB, Potkin SG, Reinvang I, Reppermund S, Rietschel M, Romanczuk-Seiferth N, Rosen GD, Rujescu D, Schnell K, Schofield PR, Smith C, Steen VM, Sussmann JE, Thalamuthu A, Toga AW, Traynor BJ, Troncoso J, Turner JA, Valdés Hernández MC, van 't Ent D, van der Brug M, van der Wee NJ, van Tol MJ, Veltman DJ, Wassink TH, Westman E, Zielke RH, Zonderman AB, Ashbrook DG, Hager R, Lu L, McMahon FJ, Morris DW, Williams RW, Brunner HG, Buckner RL, Buitelaar JK, Cahn W, Calhoun VD, Cavalleri GL, Crespo-Facorro B, Dale AM, Davies GE, Delanty N, Depondt C, Djurovic S, Drevets WC, Espeseth T, Gollub RL, Ho BC, Hoffmann W, Hosten N, Kahn RS, Le Hellard S, Meyer-Lindenberg A, Müller-Myhsok B, Nauck M, Nyberg L, Pandolfo M, Penninx BW, Roffman JL, Sisodiya SM, Smoller JW, van Bokhoven H, van Haren NE, Völzke H, Walter H, Weiner MW, Wen W, White T, Agartz I, Andreassen OA, Blangero J, Boomsma DI, Brouwer RM, Cannon DM, Cookson MR, de Geus EJ, Deary IJ, Donohoe G, Fernández G, Fisher SE, Francks C, Glahn DC, Grabe HJ, Gruber O, Hardy J, Hashimoto R, Hulshoff Pol HE, Jönsson EG, Kloszewska I, Lovestone S, Mattay VS, Mecocci P, McDonald C, McIntosh AM, Ophoff RA, Paus T, Pausova Z, Ryten M, Sachdev PS, Saykin AJ, Simmons A, Singleton A, Soininen H, Wardlaw JM, Weale ME, Weinberger DR, Adams HH, Launer LJ, Seiler S, Schmidt R, Chauhan G, Satizabal CL, Becker JT, Yanek L, van der Lee SJ, Ebling M, Fischl B, Longstreth WT Jr, Greve D, Schmidt H, Nyquist P, Vinke LN, van Duijn CM, Xue L, Mazoyer B, Bis JC, Gudnason V, Seshadri S, Ikram MA; Alzheimer’s Disease Neuroimaging Initiative; CHARGE Consortium; EPIGEN; IMAGEN; SYS, Martin NG, Wright MJ, Schumann G, Franke B, Thompson PM, Medland SE.

Nature. 2015 Apr 9;520(7546):224-9. doi: 10.1038/nature14101. Epub 2015 Jan 21.

7.

Insights into the genetic foundations of human communication.

Graham SA, Deriziotis P, Fisher SE.

Neuropsychol Rev. 2015 Mar;25(1):3-26. doi: 10.1007/s11065-014-9277-2. Epub 2015 Jan 18.

PMID:
25597031
8.

Genome-wide analysis identifies a role for common copy number variants in specific language impairment.

Simpson NH, Ceroni F, Reader RH, Covill LE, Knight JC; the SLI Consortium, Hennessy ER, Bolton PF, Conti-Ramsden G, O'Hare A, Baird G, Fisher SE, Newbury DF.

Eur J Hum Genet. 2015 Jan 14. doi: 10.1038/ejhg.2014.296. [Epub ahead of print]

PMID:
25585696
9.

Patterns of Gray Matter Abnormalities in Schizophrenia Based on an International Mega-analysis.

Gupta CN, Calhoun VD, Rachakonda S, Chen J, Patel V, Liu J, Segall J, Franke B, Zwiers MP, Arias-Vasquez A, Buitelaar J, Fisher SE, Fernandez G, van Erp TG, Potkin S, Ford J, Mathalon D, McEwen S, Lee HJ, Mueller BA, Greve DN, Andreassen O, Agartz I, Gollub RL, Sponheim SR, Ehrlich S, Wang L, Pearlson G, Glahn DC, Sprooten E, Mayer AR, Stephen J, Jung RE, Canive J, Bustillo J, Turner JA.

Schizophr Bull. 2014 Dec 28. pii: sbu177. [Epub ahead of print]

PMID:
25548384
10.

Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'

Ceroni F, Simpson NH, Francks C, Baird G, Conti-Ramsden G, Clark A, Bolton PF, Hennessy ER, Donnelly P, Bentley DR, Martin H; IMGSAC; SLI Consortium; WGS500 Consortium, Parr J, Pagnamenta AT, Maestrini E, Bacchelli E, Fisher SE, Newbury DF.

Eur J Hum Genet. 2014 Dec 24. doi: 10.1038/ejhg.2014.275. [Epub ahead of print] No abstract available.

PMID:
25537359
11.

Foxp1/2/4 regulate endochondral ossification as a suppresser complex.

Zhao H, Zhou W, Yao Z, Wan Y, Cao J, Zhang L, Zhao J, Li H, Zhou R, Li B, Wei G, Zhang Z, French CA, Dekker JD, Yang Y, Fisher SE, Tucker HO, Guo X.

Dev Biol. 2015 Feb 15;398(2):242-54. doi: 10.1016/j.ydbio.2014.12.007. Epub 2014 Dec 17.

PMID:
25527076
12.

Asymmetry within and around the human planum temporale is sexually dimorphic and influenced by genes involved in steroid hormone receptor activity.

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

Cortex. 2015 Jan;62:41-55. doi: 10.1016/j.cortex.2014.07.015. Epub 2014 Aug 7.

PMID:
25239853
13.

De novo TBR1 mutations in sporadic autism disrupt protein functions.

Deriziotis P, O'Roak BJ, Graham SA, Estruch SB, Dimitropoulou D, Bernier RA, Gerdts J, Shendure J, Eichler EE, Fisher SE.

Nat Commun. 2014 Sep 18;5:4954. doi: 10.1038/ncomms5954.

14.

Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance.

Schreiweis C, Bornschein U, Burguière E, Kerimoglu C, Schreiter S, Dannemann M, Goyal S, Rea E, French CA, Puliyadi R, Groszer M, Fisher SE, Mundry R, Winter C, Hevers W, Pääbo S, Enard W, Graybiel AM.

Proc Natl Acad Sci U S A. 2014 Sep 30;111(39):14253-8. doi: 10.1073/pnas.1414542111. Epub 2014 Sep 15.

15.

No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structure.

Cousijn H, Eissing M, Fernández G, Fisher SE, Franke B, Zwiers M, Harrison PJ, Arias-Vásquez A.

Schizophr Res. 2014 Nov;159(2-3):329-32. doi: 10.1016/j.schres.2014.08.007. Epub 2014 Sep 10.

16.

The liver in pediatric gastrointestinal disease.

Vo HD, Xu J, Rabinowitz SS, Fisher SE, Schwarz SM.

J Pediatr Gastroenterol Nutr. 2014 Sep;59(3):288-99. doi: 10.1097/MPG.0000000000000444.

PMID:
25144777
17.

A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus.

Cai DC, Fonteijn H, Guadalupe T, Zwiers M, Wittfeld K, Teumer A, Hoogman M, Arias-Vásquez A, Yang Y, Buitelaar J, Fernández G, Brunner HG, van Bokhoven H, Franke B, Hegenscheid K, Homuth G, Fisher SE, Grabe HJ, Francks C, Hagoort P.

Genes Brain Behav. 2014 Sep;13(7):675-85. doi: 10.1111/gbb.12157. Epub 2014 Aug 29.

PMID:
25130324
18.

Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia.

Brucato N, DeLisi LE, Fisher SE, Francks C.

Am J Med Genet B Neuropsychiatr Genet. 2014 Oct;165B(7):555-63. doi: 10.1002/ajmg.b.32258. Epub 2014 Aug 11.

PMID:
25111784
19.

Genome-wide screening for DNA variants associated with reading and language traits.

Gialluisi A, Newbury DF, Wilcutt EG, Olson RK, DeFries JC, Brandler WM, Pennington BF, Smith SD, Scerri TS, Simpson NH; SLI Consortium, Luciano M, Evans DM, Bates TC, Stein JF, Talcott JB, Monaco AP, Paracchini S, Francks C, Fisher SE.

Genes Brain Behav. 2014 Sep;13(7):686-701. doi: 10.1111/gbb.12158. Epub 2014 Aug 29.

20.

What can mice tell us about Foxp2 function?

French CA, Fisher SE.

Curr Opin Neurobiol. 2014 Oct;28:72-9. doi: 10.1016/j.conb.2014.07.003. Epub 2014 Jul 19.

PMID:
25048596
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