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Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.
Vernes SC, Oliver PL, Spiteri E, Lockstone HE, Puliyadi R, Taylor JM, Ho J, Mombereau C, Brewer A, Lowy E, Nicod J, Groszer M, Baban D, Sahgal N, Cazier JB, Ragoussis J, Davies KE, Geschwind DH, Fisher SE. Vernes SC, et al. Among authors: groszer m. PLoS Genet. 2011 Jul;7(7):e1002145. doi: 10.1371/journal.pgen.1002145. Epub 2011 Jul 7. PLoS Genet. 2011. PMID: 21765815 Free PMC article.
A functional genetic link between distinct developmental language disorders.
Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE. Vernes SC, et al. Among authors: groszer m. N Engl J Med. 2008 Nov 27;359(22):2337-45. doi: 10.1056/NEJMoa0802828. Epub 2008 Nov 5. N Engl J Med. 2008. PMID: 18987363 Free PMC article.
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.
Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SD, Nolan PM, Pääbo S, Channon KM, Costa RM, Eilers J, Ehret G, Rawlins JN, Fisher SE. Groszer M, et al. Curr Biol. 2008 Mar 11;18(5):354-62. doi: 10.1016/j.cub.2008.01.060. Curr Biol. 2008. PMID: 18328704 Free PMC article.
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. Schreiweis C, et al. Among authors: groszer m. Proc Natl Acad Sci U S A. 2014 Sep 30;111(39):14253-8. doi: 10.1073/pnas.1414542111. Epub 2014 Sep 15. Proc Natl Acad Sci U S A. 2014. PMID: 25225386 Free PMC article.
Generation of mice with a conditional Foxp2 null allele.
French CA, Groszer M, Preece C, Coupe AM, Rajewsky K, Fisher SE. French CA, et al. Among authors: groszer m. Genesis. 2007 Jul;45(7):440-6. doi: 10.1002/dvg.20305. Genesis. 2007. PMID: 17619227 Free PMC article.
Altered social behavior in mice carrying a cortical Foxp2 deletion.
Medvedeva VP, Rieger MA, Vieth B, Mombereau C, Ziegenhain C, Ghosh T, Cressant A, Enard W, Granon S, Dougherty JD, Groszer M. Medvedeva VP, et al. Among authors: groszer m. Hum Mol Genet. 2019 Mar 1;28(5):701-717. doi: 10.1093/hmg/ddy372. Hum Mol Genet. 2019. PMID: 30357341 Free PMC article.
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.
Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, Nicod J, Xiong L, Joober R, Enard W, Krinsky B, Nanba E, Richardson AJ, Riley BP, Martin NG, Strittmatter SM, Möller HJ, Rujescu D, St Clair D, Muglia P, Roos JL, Fisher SE, Wade-Martins R, Rouleau GA, Stein JF, Karayiorgou M, Geschwind DH, Ragoussis J, Kendler KS, Airaksinen MS, Oshimura M, DeLisi LE, Monaco AP. Francks C, et al. Among authors: groszer m. Mol Psychiatry. 2007 Dec;12(12):1129-39, 1057. doi: 10.1038/sj.mp.4002053. Epub 2007 Jul 31. Mol Psychiatry. 2007. PMID: 17667961 Free PMC article.
40 results