Similar articles for PMID: 26204995

Year	Number of Results
2000	1
2003	1
2004	1
2010	1
2011	2
2012	4
2013	4
2014	6
2015	17
2016	20
2017	18
2018	8
2019	16
2020	14
2021	6
2022	10
2023	3
2024	0

1

Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.

Chapman NH, Nato AQ Jr, Bernier R, Ankenman K, Sohi H, Munson J, Patowary A, Archer M, Blue EM, Webb SJ, Coon H, Raskind WH, Brkanac Z, Wijsman EM. Chapman NH, et al. Hum Genet. 2015 Oct;134(10):1055-68. doi: 10.1007/s00439-015-1585-y. Epub 2015 Jul 24. Hum Genet. 2015. PMID: 26204995 Free PMC article.

2

Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder.

Chapman NH, Bernier RA, Webb SJ, Munson J, Blue EM, Chen DH, Heigham E, Raskind WH, Wijsman EM. Chapman NH, et al. Hum Genet. 2018 Oct;137(10):807-815. doi: 10.1007/s00439-018-1939-3. Epub 2018 Oct 1. Hum Genet. 2018. PMID: 30276537 Free PMC article.

3

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.

4

Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder.

Kim N, Kim KH, Lim WJ, Kim J, Kim SA, Yoo HJ. Kim N, et al. Genes (Basel). 2020 Dec 22;12(1):1. doi: 10.3390/genes12010001. Genes (Basel). 2020. PMID: 33374967 Free PMC article.

5

An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray.

Bacchelli E, Cameli C, Viggiano M, Igliozzi R, Mancini A, Tancredi R, Battaglia A, Maestrini E. Bacchelli E, et al. Sci Rep. 2020 Feb 21;10(1):3198. doi: 10.1038/s41598-020-59922-3. Sci Rep. 2020. PMID: 32081867 Free PMC article.

6

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. Wu H, et al. Clin Genet. 2020 Feb;97(2):338-346. doi: 10.1111/cge.13665. Epub 2019 Nov 14. Clin Genet. 2020. PMID: 31674007 Free PMC article.

7

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.

Cukier HN, Dueker ND, Slifer SH, Lee JM, Whitehead PL, Lalanne E, Leyva N, Konidari I, Gentry RC, Hulme WF, Booven DV, Mayo V, Hofmann NK, Schmidt MA, Martin ER, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Cukier HN, et al. Mol Autism. 2014 Jan 10;5(1):1. doi: 10.1186/2040-2392-5-1. Mol Autism. 2014. PMID: 24410847 Free PMC article.

8

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I. Muhle R, et al. Pediatrics. 2004 May;113(5):e472-86. doi: 10.1542/peds.113.5.e472. Pediatrics. 2004. PMID: 15121991 Review.

9

Chromosomal microarray and whole-exome sequence analysis in Taiwanese patients with autism spectrum disorder.

Chang YS, Lin CY, Huang HY, Chang JG, Kuo HT. Chang YS, et al. Mol Genet Genomic Med. 2019 Dec;7(12):e996. doi: 10.1002/mgg3.996. Epub 2019 Oct 8. Mol Genet Genomic Med. 2019. PMID: 31595719 Free PMC article.

10

Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.

Callaghan DB, Rogic S, Tan PPC, Calli K, Qiao Y, Baldwin R, Jacobson M, Belmadani M, Holmes N, Yu C, Li Y, Li Y, Kurtzke FE, Kuzeljevic B, Yu AY, Hudson M, Mcaughton AJM, Xu Y, Dionne-Laporte A, Girard S, Liang P, Separovic ER, Liu X, Rouleau G, Pavlidis P, Lewis MES. Callaghan DB, et al. Clin Genet. 2019 Sep;96(3):199-206. doi: 10.1111/cge.13556. Epub 2019 May 30. Clin Genet. 2019. PMID: 31038196

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