Rappold GA - Search Results

1

Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome.

Wang J, Fröhlich H, Torres FB, Silva RL, Poschet G, Agarwal A, Rappold GA. Wang J, et al. Among authors: rappold ga. Proc Natl Acad Sci U S A. 2022 Feb 22;119(8):e2112852119. doi: 10.1073/pnas.2112852119. Proc Natl Acad Sci U S A. 2022. PMID: 35165191 Free PMC article.

2

Gastrointestinal dysfunction in autism displayed by altered motility and achalasia in Foxp1^+/- mice.

Fröhlich H, Kollmeyer ML, Linz VC, Stuhlinger M, Groneberg D, Reigl A, Zizer E, Friebe A, Niesler B, Rappold G. Fröhlich H, et al. Proc Natl Acad Sci U S A. 2019 Oct 29;116(44):22237-22245. doi: 10.1073/pnas.1911429116. Epub 2019 Oct 14. Proc Natl Acad Sci U S A. 2019. PMID: 31611379 Free PMC article.

3

Disrupted Mitochondrial Network Drives Deficits of Learning and Memory in a Mouse Model of FOXP1 Haploinsufficiency.

Wang J, Rappold GA, Fröhlich H. Wang J, et al. Among authors: rappold ga. Genes (Basel). 2022 Jan 11;13(1):127. doi: 10.3390/genes13010127. Genes (Basel). 2022. PMID: 35052467 Free PMC article.

4

Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalization.

Fröhlich H, Rafiullah R, Schmitt N, Abele S, Rappold GA. Fröhlich H, et al. Among authors: rappold ga. Hum Mol Genet. 2017 Apr 15;26(8):1511-1521. doi: 10.1093/hmg/ddx055. Hum Mol Genet. 2017. PMID: 28204507

5

Foxp1 regulates cortical radial migration and neuronal morphogenesis in developing cerebral cortex.

Li X, Xiao J, Fröhlich H, Tu X, Li L, Xu Y, Cao H, Qu J, Rappold GA, Chen JG. Li X, et al. Among authors: rappold ga. PLoS One. 2015 May 26;10(5):e0127671. doi: 10.1371/journal.pone.0127671. eCollection 2015. PLoS One. 2015. PMID: 26010426 Free PMC article.

6

Sex Hormones Regulate SHANK Expression.

Berkel S, Eltokhi A, Fröhlich H, Porras-Gonzalez D, Rafiullah R, Sprengel R, Rappold GA. Berkel S, et al. Among authors: rappold ga. Front Mol Neurosci. 2018 Sep 25;11:337. doi: 10.3389/fnmol.2018.00337. eCollection 2018. Front Mol Neurosci. 2018. PMID: 30319350 Free PMC article.

7

The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders.

Bacon C, Rappold GA. Bacon C, et al. Among authors: rappold ga. Hum Genet. 2012 Nov;131(11):1687-98. doi: 10.1007/s00439-012-1193-z. Epub 2012 Jun 27. Hum Genet. 2012. PMID: 22736078 Free PMC article. Review.

8

Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour.

Bacon C, Schneider M, Le Magueresse C, Froehlich H, Sticht C, Gluch C, Monyer H, Rappold GA. Bacon C, et al. Among authors: rappold ga. Mol Psychiatry. 2015 May;20(5):632-9. doi: 10.1038/mp.2014.116. Epub 2014 Sep 30. Mol Psychiatry. 2015. PMID: 25266127 Free PMC article.

9

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.

Horn D, Kapeller J, Rivera-Brugués N, Moog U, Lorenz-Depiereux B, Eck S, Hempel M, Wagenstaller J, Gawthrope A, Monaco AP, Bonin M, Riess O, Wohlleber E, Illig T, Bezzina CR, Franke A, Spranger S, Villavicencio-Lorini P, Seifert W, Rosenfeld J, Klopocki E, Rappold GA, Strom TM. Horn D, et al. Among authors: rappold ga. Hum Mutat. 2010 Nov;31(11):E1851-60. doi: 10.1002/humu.21362. Hum Mutat. 2010. PMID: 20848658 Free PMC article.

10

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. Sollis E, et al. Among authors: rappold ga. Hum Mol Genet. 2016 Feb 1;25(3):546-57. doi: 10.1093/hmg/ddv495. Epub 2015 Dec 8. Hum Mol Genet. 2016. PMID: 26647308

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