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Items: 1 to 20 of 249

1.

The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers.

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

Sci Rep. 2016 Feb 12;6:20911. doi: 10.1038/srep20911.

PMID:
26867680
2.

A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.

Fedorenko E, Morgan A, Murray E, Cardinaux A, Mei C, Tager-Flusberg H, Fisher SE, Kanwisher N.

Eur J Hum Genet. 2016 Feb;24(2):310. doi: 10.1038/ejhg.2015.230. No abstract available.

3.

ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide.

Thompson PM, Andreassen OA, Arias-Vasquez A, Bearden CE, Boedhoe PS, Brouwer RM, Buckner RL, Buitelaar JK, Bulaeva KB, Cannon DM, Cohen RA, Conrod PJ, Dale AM, Deary IJ, Dennis EL, de Reus MA, Desrivieres S, Dima D, Donohoe G, Fisher SE, Fouche JP, Francks C, Frangou S, Franke B, Ganjgahi H, Garavan H, Glahn DC, Grabe HJ, Guadalupe T, Gutman BA, Hashimoto R, Hibar DP, Holland D, Hoogman M, Pol HE, Hosten N, Jahanshad N, Kelly S, Kochunov P, Kremen WS, Lee PH, Mackey S, Martin NG, Mazoyer B, McDonald C, Medland SE, Morey RA, Nichols TE, Paus T, Pausova Z, Schmaal L, Schumann G, Shen L, Sisodiya SM, Smit DJ, Smoller JW, Stein DJ, Stein JL, Toro R, Turner JA, van den Heuvel M, van den Heuvel OA, van Erp TG, van Rooij D, Veltman DJ, Walter H, Wang Y, Wardlaw JM, Whelan CD, Wright MJ, Ye J; ENIGMA Consortium.

Neuroimage. 2015 Dec 4. pii: S1053-8119(15)01081-2. doi: 10.1016/j.neuroimage.2015.11.057. [Epub ahead of print]

4.

Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.

Sollis E, Graham SA, Vino A, Froehlich H, Vreeburg M, Dimitropoulou D, Gilissen C, Pfundt R, Rappold GA, Brunner HG, Deriziotis P, Fisher SE.

Hum Mol Genet. 2015 Dec 8. pii: ddv495. [Epub ahead of print]

PMID:
26647308
5.

Ultrasonic vocalizations of adult male Foxp2-mutant mice: behavioral contexts of arousal and emotion.

Gaub S, Fisher SE, Ehret G.

Genes Brain Behav. 2016 Feb;15(2):243-59. doi: 10.1111/gbb.12274. Epub 2016 Jan 13.

PMID:
26566793
6.

Understanding Language from a Genomic Perspective.

Graham SA, Fisher SE.

Annu Rev Genet. 2015 Nov 23;49:131-60. doi: 10.1146/annurev-genet-120213-092236. Epub 2015 Oct 5.

PMID:
26442845
7.

A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer.

Becker M, Devanna P, Fisher SE, Vernes SC.

Mol Cytogenet. 2015 Aug 20;8:69. doi: 10.1186/s13039-015-0173-0. eCollection 2015.

8.

G-protein genomic association with normal variation in gray matter density.

Chen J, Calhoun VD, Arias-Vasquez A, Zwiers MP, van Hulzen K, Fernández G, Fisher SE, Franke B, Turner JA, Liu J.

Hum Brain Mapp. 2015 Nov;36(11):4272-86. doi: 10.1002/hbm.22916. Epub 2015 Aug 7.

PMID:
26248772
9.

A Pooled Genome-Wide Association Study of Asperger Syndrome.

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

PLoS One. 2015 Jul 15;10(7):e0131202. doi: 10.1371/journal.pone.0131202. eCollection 2015.

10.

A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.

Fedorenko E, Morgan A, Murray E, Cardinaux A, Mei C, Tager-Flusberg H, Fisher SE, Kanwisher N.

Eur J Hum Genet. 2016 Feb;24(2):302-6. doi: 10.1038/ejhg.2015.149. Epub 2015 Jul 15.

PMID:
26173965
11.

The prebiotics 3'Sialyllactose and 6'Sialyllactose diminish stressor-induced anxiety-like behavior and colonic microbiota alterations: Evidence for effects on the gut-brain axis.

Tarr AJ, Galley JD, Fisher SE, Chichlowski M, Berg BM, Bailey MT.

Brain Behav Immun. 2015 Nov;50:166-77. doi: 10.1016/j.bbi.2015.06.025. Epub 2015 Jul 2.

PMID:
26144888
12.

Correction: 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, Magdalena Echeverry M, 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 Jun 26;11(6):e1005336. doi: 10.1371/journal.pgen.1005336. eCollection 2015 Jun. No abstract available.

13.

The Forkhead Transcription Factor FOXP2 Is Required for Regulation of p21WAF1/CIP1 in 143B Osteosarcoma Cell Growth Arrest.

Gascoyne DM, Spearman H, Lyne L, Puliyadi R, Perez-Alcantara M, Coulton L, Fisher SE, Croucher PI, Banham AH.

PLoS One. 2015 Jun 2;10(6):e0128513. doi: 10.1371/journal.pone.0128513. eCollection 2015.

14.

The FOXP1, FOXP2 and FOXP4 transcription factors are required for islet alpha cell proliferation and function in mice.

Spaeth JM, Hunter CS, Bonatakis L, Guo M, French CA, Slack I, Hara M, Fisher SE, Ferrer J, Morrisey EE, Stanger BZ, Stein R.

Diabetologia. 2015 Aug;58(8):1836-44. doi: 10.1007/s00125-015-3635-3. Epub 2015 May 29.

PMID:
26021489
15.

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 Dec;23(12):1702-7. doi: 10.1038/ejhg.2015.66. Epub 2015 Apr 8.

PMID:
25853299
16.

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. Erratum in: PLoS Genet. 2015 Jun;11(6):e1005336. Echeverry, Maria Magdalena [corrected to Echeverry, María Magdalena].

17.

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 Apr;14(4):369-76. doi: 10.1111/gbb.12213. Epub 2015 Apr 1.

18.

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

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

Brain Behav Immun. 2015 May;46:311-8. doi: 10.1016/j.bbi.2015.02.021. Epub 2015 Feb 26.

PMID:
25728236
19.

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. Review.

PMID:
25646515
20.

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.

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