237 related articles for article (PubMed ID: 31871231)
1. Connecting Genotype with Behavioral Phenotype in Mouse Models of Autism Associated with
Clipperton-Allen AE; Page DT
Cold Spring Harb Perspect Med; 2020 Sep; 10(9):. PubMed ID: 31871231
[TBL] [Abstract][Full Text] [Related]
2. Prevalence and clinical/molecular characteristics of PTEN mutations in Turkish children with autism spectrum disorders and macrocephaly.
Kaymakcalan H; Kaya İ; Cevher Binici N; Nikerel E; Özbaran B; Görkem Aksoy M; Erbilgin S; Özyurt G; Jahan N; Çelik D; Yararbaş K; Yalçınkaya L; Köse S; Durak S; Ercan-Sencicek AG
Mol Genet Genomic Med; 2021 Aug; 9(8):e1739. PubMed ID: 34268892
[TBL] [Abstract][Full Text] [Related]
3. Balancing Proliferation and Connectivity in PTEN-associated Autism Spectrum Disorder.
Tilot AK; Frazier TW; Eng C
Neurotherapeutics; 2015 Jul; 12(3):609-19. PubMed ID: 25916396
[TBL] [Abstract][Full Text] [Related]
4. Toward better characterization of restricted and repetitive behaviors in individuals with germline heterozygous PTEN mutations.
Uljarević M; Frazier TW; Rached G; Busch RM; Klaas P; Srivastava S; Martinez-Agosto JA; Sahin M; Eng C; Hardan AY;
Am J Med Genet A; 2021 Nov; 185(11):3401-3410. PubMed ID: 34423884
[TBL] [Abstract][Full Text] [Related]
5. Identification of a PTEN mutation with reduced protein stability, phosphatase activity, and nuclear localization in Hong Kong patients with autistic features, neurodevelopmental delays, and macrocephaly.
Wong CW; Or PMY; Wang Y; Li L; Li J; Yan M; Cao Y; Luk HM; Tong TMF; Leslie NR; Lo IF; Choy KW; Chan AML
Autism Res; 2018 Aug; 11(8):1098-1109. PubMed ID: 29608813
[TBL] [Abstract][Full Text] [Related]
6. Dynamics and structural stability effects of germline PTEN mutations associated with cancer versus autism phenotypes.
Smith IN; Thacker S; Jaini R; Eng C
J Biomol Struct Dyn; 2019 Apr; 37(7):1766-1782. PubMed ID: 29663862
[TBL] [Abstract][Full Text] [Related]
7. Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort.
Wu H; Li H; Bai T; Han L; Ou J; Xun G; Zhang Y; Wang Y; Duan G; Zhao N; Chen B; Du X; Yao M; Zou X; Zhao J; Hu Z; Eichler EE; Guo H; Xia K
Clin Genet; 2020 Feb; 97(2):338-346. PubMed ID: 31674007
[TBL] [Abstract][Full Text] [Related]
8. Neurodevelopmental disorders in children with macrocephaly: A prevalence study and PTEN gene analysis.
Kurata H; Shirai K; Saito Y; Okazaki T; Ohno K; Oguri M; Adachi K; Nanba E; Maegaki Y
Brain Dev; 2018 Jan; 40(1):36-41. PubMed ID: 28774669
[TBL] [Abstract][Full Text] [Related]
9. Neurobehavioral phenotype of autism spectrum disorder associated with germline heterozygous mutations in PTEN.
Busch RM; Srivastava S; Hogue O; Frazier TW; Klaas P; Hardan A; Martinez-Agosto JA; Sahin M; Eng C;
Transl Psychiatry; 2019 Oct; 9(1):253. PubMed ID: 31594918
[TBL] [Abstract][Full Text] [Related]
10. Clinical spectrum of PTEN mutation in pediatric patients. A bicenter experience.
Ciaccio C; Saletti V; D'Arrigo S; Esposito S; Alfei E; Moroni I; Tonduti D; Chiapparini L; Pantaleoni C; Milani D
Eur J Med Genet; 2019 Dec; 62(12):103596. PubMed ID: 30528446
[TBL] [Abstract][Full Text] [Related]
11. Autism-epilepsy phenotype with macrocephaly suggests PTEN, but not GLIALCAM, genetic screening.
Marchese M; Conti V; Valvo G; Moro F; Muratori F; Tancredi R; Santorelli FM; Guerrini R; Sicca F
BMC Med Genet; 2014 Feb; 15():26. PubMed ID: 24580998
[TBL] [Abstract][Full Text] [Related]
12. Cross-level analysis of molecular and neurobehavioral function in a prospective series of patients with germline heterozygous PTEN mutations with and without autism.
Frazier TW; Jaini R; Busch RM; Wolf M; Sadler T; Klaas P; Hardan AY; Martinez-Agosto JA; Sahin M; Eng C;
Mol Autism; 2021 Jan; 12(1):5. PubMed ID: 33509259
[TBL] [Abstract][Full Text] [Related]
13. Autism Spectrum Disorder Associated with Germline Heterozygous
Frazier TW
Cold Spring Harb Perspect Med; 2019 Oct; 9(10):. PubMed ID: 31307976
[TBL] [Abstract][Full Text] [Related]
14. Genetic Suppression of mTOR Rescues Synaptic and Social Behavioral Abnormalities in a Mouse Model of Pten Haploinsufficiency.
Huang WC; Chen Y; Page DT
Autism Res; 2019 Oct; 12(10):1463-1471. PubMed ID: 31441226
[TBL] [Abstract][Full Text] [Related]
15. Clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndrome.
Busa T; Milh M; Degardin N; Girard N; Sigaudy S; Longy M; Olshchwang S; Sobol H; Chabrol B; Philip N
Eur J Paediatr Neurol; 2015 Mar; 19(2):188-92. PubMed ID: 25549896
[TBL] [Abstract][Full Text] [Related]
16. Inherited PTEN mutations and the prediction of phenotype.
Leslie NR; Longy M
Semin Cell Dev Biol; 2016 Apr; 52():30-8. PubMed ID: 26827793
[TBL] [Abstract][Full Text] [Related]
17. Biochemical screening and PTEN mutation analysis in individuals with autism spectrum disorders and macrocephaly.
Hobert JA; Embacher R; Mester JL; Frazier TW; Eng C
Eur J Hum Genet; 2014 Feb; 22(2):273-6. PubMed ID: 23695273
[TBL] [Abstract][Full Text] [Related]
18. Constitutional mislocalization of Pten drives precocious maturation in oligodendrocytes and aberrant myelination in model of autism spectrum disorder.
Lee H; Thacker S; Sarn N; Dutta R; Eng C
Transl Psychiatry; 2019 Jan; 9(1):13. PubMed ID: 30664625
[TBL] [Abstract][Full Text] [Related]
19. Autism-relevant behaviors are minimally impacted by conditional deletion of Pten in oxytocinergic neurons.
Clipperton-Allen AE; Chen Y; Page DT
Autism Res; 2016 Dec; 9(12):1248-1262. PubMed ID: 27220363
[TBL] [Abstract][Full Text] [Related]
20. Alternative splicing landscape of the neural transcriptome in a cytoplasmic-predominant Pten expression murine model of autism-like Behavior.
Thacker S; Sefyi M; Eng C
Transl Psychiatry; 2020 Nov; 10(1):380. PubMed ID: 33159038
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
