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Select item 103140881.

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

Abstract Article PDF–691K

Select item 99888252.

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

Abstract Article PDF–985K

Select item 93629363.

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

Abstract Article PDF–1.1M

Select item 83396674.

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

Abstract Article PDF–1.2M

Select item 82862235.

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

Abstract Article PDF–498K

Select item 68202086.

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

Abstract Article PDF–775K

Select item 67941527.

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

Abstract Article PDF–2.1M

Select item 67384278.

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

Abstract Article PDF–360K

Select item 64986729.

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

Abstract Article PDF–2.1M

Select item 580240310.

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

Abstract Article PDF–774K

Select item 569665411.

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

Abstract Article PDF–1.6M

Select item 506211712.

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

Abstract Article PDF–821K

Select item 482783713.

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

Abstract Article PDF–1.0M

Select item 446048414.

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

Abstract Article PDF–1.1M

Select item 443812715.

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

Abstract Article PDF–538K

Select item 436114516.

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

Abstract Article PDF–2.1M

Select item 418959117.

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

Abstract Article PDF–1.3M

Select item 276005918.

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

Article PDF–403K

Select item 242996119.

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

Abstract Article PDF–224K

Select item 227635020.

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

Abstract Article PDF–717K

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