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Items: 1 to 20 of 83

1.
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2
Lottie D Morison, Elisabeth Meffert, Miriam Stampfer, Irene Steiner-Wilke, Brigitte Vollmer, Katrin Schulze, Tracy Briggs, Ruth Braden, Adam Vogel, Daisy Thompson-Lake, Chirag Patel, Edward Blair, Himanshu Goel, Samantha Turner, Ute Moog, Angelika Riess, Frederique Liegeois, David A Koolen, David J Amor, Tjitske Kleefstra, Simon E Fisher, Christiane Zweier, Angela T Morgan
J Med Genet. 2023 Jun; 60(6): 597–607. Published online 2022 Nov 3. doi: 10.1136/jmg-2022-108734
PMCID:
PMC10314088
AbstractArticlePDF–691K
2.
Functional dissection of two amino acid substitutions unique to the human FOXP2 protein
Ulrich Bornschein, Hugo Zeberg, Wolfgang Enard, Wulf Hevers, Svante Pääbo
Sci Rep. 2023; 13: 3747. Published online 2023 Mar 6. doi: 10.1038/s41598-023-30663-3
PMCID:
PMC9988825
AbstractArticlePDF–985K
3.
A comprehensive in silico analysis of the deleterious nonsynonymous SNPs of human FOXP2 protein
Mahmuda Akter, Sumaiya Farah Khan, Abu Ashfaqur Sajib, Fahmida Sultana Rima
PLoS One. 2022; 17(8): e0272625. Published online 2022 Aug 9. doi: 10.1371/journal.pone.0272625
PMCID:
PMC9362936
AbstractArticlePDF–1.1M
4.
Molecular networks of the FOXP2 transcription factor in the brain
Joery den Hoed, Karthikeyan Devaraju, Simon E Fisher
EMBO Rep. 2021 Aug 4; 22(8): e52803. Published online 2021 Jul 14. doi: 10.15252/embr.202152803
PMCID:
PMC8339667
AbstractArticlePDF–1.2M
5.
FOXP2 expression and gray matter density in the male brains of patients with schizophrenia
Julio Sanjuán, Xochitl Helga Castro-Martínez, Gracián García-Martí, Javier González-Fernández, Roberto Sanz-Requena, Josep María Haro, J. Javier Meana, Luis Martí-Bonmatí, Juan Nacher, Noelia Sebastiá-Ortega, Javier Gilabert-Juan, María Dolores Moltó
Brain Imaging Behav. 2021; 15(3): 1403–1411. Published online 2020 Jul 30. doi: 10.1007/s11682-020-00339-x
PMCID:
PMC8286223
AbstractArticlePDF–498K
6.
Toward Robust Functional Neuroimaging Genetics of Cognition
Julia Uddén, Annika Hultén, Katarina Bendtz, Zachary Mineroff, Katerina S. Kucera, Arianna Vino, Evelina Fedorenko, Peter Hagoort, Simon E. Fisher
J Neurosci. 2019 Oct 30; 39(44): 8778–8787. doi: 10.1523/JNEUROSCI.0888-19.2019
PMCID:
PMC6820208
AbstractArticlePDF–775K
7.
Chromatin decondensation by FOXP2 promotes human neuron maturation and expression of neurodevelopmental disease genes
Stephanie L. Hickey, Stefano Berto, Genevieve Konopka
Cell Rep. Author manuscript; available in PMC 2019 Oct 15.
Published in final edited form as: Cell Rep. 2019 May 7; 27(6): 1699–1711.e9. doi: 10.1016/j.celrep.2019.04.044
PMCID:
PMC6794152
AbstractArticlePDF–2.1M
8.
FOXP2 contributes to the cognitive impairment in chronic patients with schizophrenia
Xiaoe Lang, Wenzhong Zhang, Xinxin Song, Guangya Zhang, Xiangdong Du, Yongjie Zhou, Zezhi Li, Xiang Yang Zhang
Aging (Albany NY) 2019 Aug 31; 11(16): 6440–6448. Published online 2019 Aug 19. doi: 10.18632/aging.102198
PMCID:
PMC6738427
AbstractArticlePDF–360K
9.
Functional characterization of two enhancers located downstream FOXP2
Raúl Torres-Ruiz, Antonio Benítez-Burraco, Marta Martínez-Lage, Sandra Rodríguez-Perales, Paloma García-Bellido
BMC Med Genet. 2019; 20: 65. Published online 2019 May 2. doi: 10.1186/s12881-019-0810-2
PMCID:
PMC6498672
AbstractArticlePDF–2.1M
10.
Phonological Working Memory and FOXP2
Katrin Schulze, Faraneh Vargha-Khadem, Mortimer Mishkin
Neuropsychologia. Author manuscript; available in PMC 2019 Jan 8.
Published in final edited form as: Neuropsychologia. 2018 Jan 8; 108: 147–152. Published online 2017 Nov 22. doi: 10.1016/j.neuropsychologia.2017.11.027
PMCID:
PMC5802403
AbstractArticlePDF–774K
11.
The Key Regulator for Language and Speech Development, FOXP2, is a Novel Substrate for SUMOylation
Leslie J. Meredith, Chiung-Min Wang, Leticia Nascimento, Runhua Liu, Lizhong Wang, Wei-Hsiung Yang
J Cell Biochem. Author manuscript; available in PMC 2017 Nov 21.
Published in final edited form as: J Cell Biochem. 2016 Feb; 117(2): 426–438. doi: 10.1002/jcb.25288
PMCID:
PMC5696654
AbstractArticlePDF–1.6M
12.
Early neuroimaging markers of FOXP2 intragenic deletion
Frédérique J. Liégeois, Michael S. Hildebrand, Alexandra Bonthrone, Samantha J. Turner, Ingrid E. Scheffer, Melanie Bahlo, Alan Connelly, Angela T. Morgan
Sci Rep. 2016; 6: 35192. Published online 2016 Oct 13. doi: 10.1038/srep35192
PMCID:
PMC5062117
AbstractArticlePDF–821K
13.
Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development
Kathryn L. Mueller, Jeffrey C. Murray, Jacob J. Michaelson, Morten H. Christiansen, Sheena Reilly, J. Bruce Tomblin
PLoS One. 2016; 11(4): e0152576. Published online 2016 Apr 11. doi: 10.1371/journal.pone.0152576
PMCID:
PMC4827837
AbstractArticlePDF–1.0M
14.
Monoallelic expression of the human FOXP2 speech gene
Abidemi A. Adegbola, Gerald F. Cox, Elizabeth M. Bradshaw, David A. Hafler, Alexander Gimelbrant, Andrew Chess
Proc Natl Acad Sci U S A. 2015 Jun 2; 112(22): 6848–6854. Published online 2014 Nov 24. doi: 10.1073/pnas.1411270111
PMCID:
PMC4460484
AbstractArticlePDF–1.1M
15.
Enhanced Procedural Learning of Speech Sound Categories in a Genetic Variant of FOXP2
Bharath Chandrasekaran, Han-Gyol Yi, Nathaniel J. Blanco, John E. McGeary, W. Todd Maddox
J Neurosci. 2015 May 20; 35(20): 7808–7812. doi: 10.1523/JNEUROSCI.4706-14.2015
PMCID:
PMC4438127
AbstractArticlePDF–538K
16.
FOXF2 deficiency promotes epithelial-mesenchymal transition and metastasis of basal-like breast cancer
Qing-Shan Wang, Peng-Zhou Kong, Xiao-Qing Li, Fan Yang, Yu-Mei Feng
Breast Cancer Res. 2015; 17(1): 30. Published online 2015 Feb 26. doi: 10.1186/s13058-015-0531-1
PMCID:
PMC4361145
AbstractArticlePDF–2.1M
17.
Multiple microRNAs regulate human FOXP2 gene expression by targeting sequences in its 3′ untranslated region
Lijuan Fu, Zhimin Shi, Guanzheng Luo, Weihong Tu, XiuJie Wang, Zhide Fang, XiaoChing Li
Mol Brain. 2014; 7: 71. Published online 2014 Oct 1. doi: 10.1186/s13041-014-0071-0
PMCID:
PMC4189591
AbstractArticlePDF–1.3M
18.
Language features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2
J. Bruce Tomblin, Marlea O'Brien, Larry Shriberg, Charles Williams, Jeff Murray, Shivanand Patil, Jonathan Bjork, Steve Anderson, Kirrie Ballard
J Speech Lang Hear Res. Author manuscript; available in PMC 2010 Apr 1.
Published in final edited form as: J Speech Lang Hear Res. 2009 Oct; 52(5): 1157–1174. doi: 10.1044/1092-4388(2009/07-0162)
PMCID:
PMC2760059
ArticlePDF–403K
19.
The Timing of Selection at the Human FOXP2 Gene
Graham Coop, Kevin Bullaughey, Francesca Luca, Molly Przeworski
Mol Biol Evol. 2008 Jul; 25(7): 1257–1259. Published online 2008 Apr 15. doi: 10.1093/molbev/msn091
PMCID:
PMC2429961
AbstractArticlePDF–224K
20.
Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain
Elizabeth  Spiteri, Genevieve  Konopka, Giovanni  Coppola, Jamee  Bomar, Michael  Oldham, Jing  Ou, Sonja C.  Vernes, Simon E.  Fisher, Bing  Ren, Daniel H.  Geschwind
Am J Hum Genet. 2007 Dec; 81(6): 1144–1157. Published online 2007 Oct 31. doi: 10.1086/522237
PMCID:
PMC2276350
AbstractArticlePDF–717K

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