Similar articles for PMID: 22865819

Year	Number of Results
2000	1
2006	2
2008	3
2009	2
2010	1
2011	8
2012	13
2013	8
2014	12
2015	11
2016	10
2017	9
2018	3
2019	5
2020	8
2021	4
2022	2
2024	0

1

Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility.

Bi C, Wu J, Jiang T, Liu Q, Cai W, Yu P, Cai T, Zhao M, Jiang YH, Sun ZS. Bi C, et al. Hum Mutat. 2012 Dec;33(12):1635-8. doi: 10.1002/humu.22174. Epub 2012 Aug 24. Hum Mutat. 2012. PMID: 22865819

2

First de novo ANK3 nonsense mutation in a boy with intellectual disability, speech impairment and autistic features.

Kloth K, Denecke J, Hempel M, Johannsen J, Strom TM, Kubisch C, Lessel D. Kloth K, et al. Eur J Med Genet. 2017 Sep;60(9):494-498. doi: 10.1016/j.ejmg.2017.07.001. Epub 2017 Jul 4. Eur J Med Genet. 2017. PMID: 28687526

3

Identification of autism-related MECP2 mutations by whole-exome sequencing and functional validation.

Wen Z, Cheng TL, Li GZ, Sun SB, Yu SY, Zhang Y, Du YS, Qiu Z. Wen Z, et al. Mol Autism. 2017 Aug 3;8:43. doi: 10.1186/s13229-017-0157-5. eCollection 2017. Mol Autism. 2017. PMID: 28785396 Free PMC article.

4

Using whole-exome sequencing to identify inherited causes of autism.

Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, Sunu CM, Felie JM, Rodriguez J, Nasir RH, Ware J, Joseph RM, Hill RS, Kwan BY, Al-Saffar M, Mukaddes NM, Hashmi A, Balkhy S, Gascon GG, Hisama FM, LeClair E, Poduri A, Oner O, Al-Saad S, Al-Awadi SA, Bastaki L, Ben-Omran T, Teebi AS, Al-Gazali L, Eapen V, Stevens CR, Rappaport L, Gabriel SB, Markianos K, State MW, Greenberg ME, Taniguchi H, Braverman NE, Morrow EM, Walsh CA. Yu TW, et al. Neuron. 2013 Jan 23;77(2):259-73. doi: 10.1016/j.neuron.2012.11.002. Neuron. 2013. PMID: 23352163 Free PMC article.

5

De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia.

Takata A, Ionita-Laza I, Gogos JA, Xu B, Karayiorgou M. Takata A, et al. Neuron. 2016 Mar 2;89(5):940-7. doi: 10.1016/j.neuron.2016.02.024. Neuron. 2016. PMID: 26938441 Free PMC article.

6

A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.

Toma C, Shaw AD, Heath A, Pierce KD, Mitchell PB, Schofield PR, Fullerton JM. Toma C, et al. J Psychiatry Neurosci. 2021 Mar 17;46(2):E247-E257. doi: 10.1503/jpn.200083. J Psychiatry Neurosci. 2021. PMID: 33729739 Free PMC article.

7

Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.

Chen R, Davis LK, Guter S, Wei Q, Jacob S, Potter MH, Cox NJ, Cook EH, Sutcliffe JS, Li B. Chen R, et al. Mol Autism. 2017 Mar 21;8:14. doi: 10.1186/s13229-017-0130-3. eCollection 2017. Mol Autism. 2017. PMID: 28344757 Free PMC article.

8

Sequencing of the ANKYRIN 3 gene (ANK3) encoding ankyrin G in bipolar disorder reveals a non-conservative amino acid change in a short isoform of ankyrin G.

Dedman A, McQuillin A, Kandaswamy R, Sharp S, Anjorin A, Gurling H. Dedman A, et al. Am J Med Genet B Neuropsychiatr Genet. 2012 Apr;159B(3):328-35. doi: 10.1002/ajmg.b.32030. Epub 2012 Feb 10. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22328486

9

Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.

Iqbal Z, Vandeweyer G, van der Voet M, Waryah AM, Zahoor MY, Besseling JA, Roca LT, Vulto-van Silfhout AT, Nijhof B, Kramer JM, Van der Aa N, Ansar M, Peeters H, Helsmoortel C, Gilissen C, Vissers LE, Veltman JA, de Brouwer AP, Frank Kooy R, Riazuddin S, Schenck A, van Bokhoven H, Rooms L. Iqbal Z, et al. Hum Mol Genet. 2013 May 15;22(10):1960-70. doi: 10.1093/hmg/ddt043. Epub 2013 Feb 5. Hum Mol Genet. 2013. PMID: 23390136 Free article.

10

Whole-genome sequencing in a family with twin boys with autism and intellectual disability suggests multimodal polygenic risk.

McKenna B, Koomar T, Vervier K, Kremsreiter J, Michaelson JJ. McKenna B, et al. Cold Spring Harb Mol Case Stud. 2018 Dec 17;4(6):a003285. doi: 10.1101/mcs.a003285. Print 2018 Dec. Cold Spring Harb Mol Case Stud. 2018. PMID: 30559312 Free PMC article.

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