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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1976 1
1978 1
1982 2
1984 2
1985 2
1987 3
1988 1
1989 3
1990 2
1991 3
1992 1
1993 4
1994 1
1995 5
1997 2
1999 2
2000 1
2001 4
2002 5
2003 6
2004 5
2005 11
2006 3
2007 7
2008 3
2009 3
2010 6
2011 7
2012 5
2013 8
2014 10
2015 17
2016 11
2017 24
2018 13
2019 8
2020 13
2021 20
2022 16
2023 13

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Article type

Publication date

PubMed for id: 862872

233 results

Results by year

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Page 1
AUTS2 Syndrome: Molecular Mechanisms and Model Systems.
Biel A, Castanza AS, Rutherford R, Fair SR, Chifamba L, Wester JC, Hester ME, Hevner RF. Biel A, et al. Front Mol Neurosci. 2022 Mar 31;15:858582. doi: 10.3389/fnmol.2022.858582. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35431798 Free PMC article. Review.
Attention Deficit Hyperactivity and Autism Spectrum Disorders as the Core Symptoms of AUTS2 Syndrome: Description of Five New Patients and Update of the Frequency of Manifestations and Genotype-Phenotype Correlation.
Sanchez-Jimeno C, Blanco-Kelly F, López-Grondona F, Losada-Del Pozo R, Moreno B, Rodrigo-Moreno M, Martinez-Cayuelas E, Riveiro-Alvarez R, Fenollar-Cortés M, Ayuso C, Rodríguez de Alba M, Lorda-Sanchez I, Almoguera B. Sanchez-Jimeno C, et al. Genes (Basel). 2021 Aug 30;12(9):1360. doi: 10.3390/genes12091360. Genes (Basel). 2021. PMID: 34573342 Free PMC article. Review.
Neuronal Migration and AUTS2 Syndrome.
Hori K, Hoshino M. Hori K, et al. Brain Sci. 2017 May 14;7(5):54. doi: 10.3390/brainsci7050054. Brain Sci. 2017. PMID: 28505103 Free PMC article. Review.
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype.
Beunders G, van de Kamp J, Vasudevan P, Morton J, Smets K, Kleefstra T, de Munnik SA, Schuurs-Hoeijmakers J, Ceulemans B, Zollino M, Hoffjan S, Wieczorek S, So J, Mercer L, Walker T, Velsher L; DDD study; Parker MJ, Magee AC, Elffers B, Kooy RF, Yntema HG, Meijers-Heijboer EJ, Sistermans EA. Beunders G, et al. J Med Genet. 2016 Aug;53(8):523-32. doi: 10.1136/jmedgenet-2015-103601. Epub 2016 Apr 13. J Med Genet. 2016. PMID: 27075013
Germ cell mosaicism for AUTS2 exon 6 deletion.
Gieldon L, Jauch A, Obeid K, Kaufmann L, Hinderhofer K, Haug U, Moog U. Gieldon L, et al. Am J Med Genet A. 2021 Apr;185(4):1261-1265. doi: 10.1002/ajmg.a.62091. Epub 2021 Feb 12. Am J Med Genet A. 2021. PMID: 33577136
De novo small deletion affecting transcription start site of short isoform of AUTS2 gene in a patient with syndromic neurodevelopmental defects.
Martinez-Delgado B, Lopez-Martin E, Lara-Herguedas J, Monzon S, Cuesta I, Juliá M, Aquino V, Rodriguez-Martin C, Damian A, Gonzalo I, Gomez-Mariano G, Baladron B, Cazorla R, Iglesias G, Roman E, Ros P, Tutor P, Mellor S, Jimenez C, Cabrejas MJ, Gonzalez-Vioque E, Alonso J, Bermejo-Sánchez E, Posada M. Martinez-Delgado B, et al. Am J Med Genet A. 2021 Mar;185(3):877-883. doi: 10.1002/ajmg.a.62017. Epub 2020 Dec 21. Am J Med Genet A. 2021. PMID: 33346930
233 results