305 related articles for article (PubMed ID: 33921431)
21. Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving
Mak ASL; Chiu ATG; Leung GKC; Mak CCY; Chu YWY; Mok GTK; Tang WF; Chan KYK; Tang MHY; Lau Yim ET; So KW; Tao VQ; Fung CW; Wong VCN; Uddin M; Lee SL; Marshall CR; Scherer SW; Kan ASY; Chung BHY
Mol Autism; 2017; 8():31. PubMed ID: 28670437
[TBL] [Abstract][Full Text] [Related]
22. Double Genetic Hit: Fragile X Syndrome and Partial Deletion of Protein Patched Homolog 1 Antisense as Cause of Severe Autism Spectrum Disorder.
Saldarriaga W; Payán-Gómez C; González-Teshima LY; Rosa L; Tassone F; Hagerman RJ
J Dev Behav Pediatr; 2020 Dec; 41(9):724-728. PubMed ID: 32947579
[TBL] [Abstract][Full Text] [Related]
23. Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder.
Masson J; Demily C; Chatron N; Labalme A; Rollat-Farnier PA; Schluth-Bolard C; Gilbert-Dussardier B; Giuliano F; Touraine R; Tordjman S; Verloes A; Testa G; Sanlaville D; Edery P; Lesca G; Rossi M
Orphanet J Rare Dis; 2019 May; 14(1):121. PubMed ID: 31151468
[TBL] [Abstract][Full Text] [Related]
24. A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorder.
Tsiplova K; Zur RM; Marshall CR; Stavropoulos DJ; Pereira SL; Merico D; Young EJ; Sung WWL; Scherer SW; Ungar WJ
Genet Med; 2017 Nov; 19(11):1268-1275. PubMed ID: 28471434
[TBL] [Abstract][Full Text] [Related]
25. Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications.
Oikonomakis V; Kosma K; Mitrakos A; Sofocleous C; Pervanidou P; Syrmou A; Pampanos A; Psoni S; Fryssira H; Kanavakis E; Kitsiou-Tzeli S; Tzetis M
Clin Genet; 2016 Jun; 89(6):708-18. PubMed ID: 26777411
[TBL] [Abstract][Full Text] [Related]
26. Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications.
Kalsner L; Twachtman-Bassett J; Tokarski K; Stanley C; Dumont-Mathieu T; Cotney J; Chamberlain S
Mol Genet Genomic Med; 2018 Mar; 6(2):171-185. PubMed ID: 29271092
[TBL] [Abstract][Full Text] [Related]
27. Comprehensive molecular testing in patients with high functioning autism spectrum disorder.
Alvarez-Mora MI; Calvo Escalona R; Puig Navarro O; Madrigal I; Quintela I; Amigo J; Martinez-Elurbe D; Linder-Lucht M; Aznar Lain G; Carracedo A; Mila M; Rodriguez-Revenga L
Mutat Res; 2016; 784-785():46-52. PubMed ID: 26845707
[TBL] [Abstract][Full Text] [Related]
28. Clinical genetic testing for patients with autism spectrum disorders.
Shen Y; Dies KA; Holm IA; Bridgemohan C; Sobeih MM; Caronna EB; Miller KJ; Frazier JA; Silverstein I; Picker J; Weissman L; Raffalli P; Jeste S; Demmer LA; Peters HK; Brewster SJ; Kowalczyk SJ; Rosen-Sheidley B; McGowan C; Duda AW; Lincoln SA; Lowe KR; Schonwald A; Robbins M; Hisama F; Wolff R; Becker R; Nasir R; Urion DK; Milunsky JM; Rappaport L; Gusella JF; Walsh CA; Wu BL; Miller DT;
Pediatrics; 2010 Apr; 125(4):e727-35. PubMed ID: 20231187
[TBL] [Abstract][Full Text] [Related]
29. Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.
Lowther C; Valkanas E; Giordano JL; Wang HZ; Currall BB; O'Keefe K; Pierce-Hoffman E; Kurtas NE; Whelan CW; Hao SP; Weisburd B; Jalili V; Fu J; Wong I; Collins RL; Zhao X; Austin-Tse CA; Evangelista E; Lemire G; Aggarwal VS; Lucente D; Gauthier LD; Tolonen C; Sahakian N; Stevens C; An JY; Dong S; Norton ME; MacKenzie TC; Devlin B; Gilmore K; Powell BC; Brandt A; Vetrini F; DiVito M; Sanders SJ; MacArthur DG; Hodge JC; O'Donnell-Luria A; Rehm HL; Vora NL; Levy B; Brand H; Wapner RJ; Talkowski ME
Am J Hum Genet; 2023 Sep; 110(9):1454-1469. PubMed ID: 37595579
[TBL] [Abstract][Full Text] [Related]
30. Whole Genome Sequencing in the Evaluation of Fetal Structural Anomalies: A Parallel Test with Chromosomal Microarray Plus Whole Exome Sequencing.
Zhou J; Yang Z; Sun J; Liu L; Zhou X; Liu F; Xing Y; Cui S; Xiong S; Liu X; Yang Y; Wei X; Zou G; Wang Z; Wei X; Wang Y; Zhang Y; Yan S; Wu F; Zeng F; Wang J; Duan T; Peng Z; Sun L
Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33800913
[TBL] [Abstract][Full Text] [Related]
31. Do the data really support ordering fragile X testing as a first-tier test without clinical features?
Weinstein V; Tanpaiboon P; Chapman KA; Ah Mew N; Hofherr S
Genet Med; 2017 Dec; 19(12):1317-1322. PubMed ID: 28541279
[TBL] [Abstract][Full Text] [Related]
32. Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
Ho KS; Twede H; Vanzo R; Harward E; Hensel CH; Martin MM; Page S; Peiffer A; Mowery-Rushton P; Serrano M; Wassman ER
Biomed Res Int; 2016; 2016():3284534. PubMed ID: 27975050
[TBL] [Abstract][Full Text] [Related]
33. Rare copy number variants are common in young children with autism spectrum disorder.
Eriksson MA; Liedén A; Westerlund J; Bremer A; Wincent J; Sahlin E; Gillberg C; Fernell E; Anderlid BM
Acta Paediatr; 2015 Jun; 104(6):610-8. PubMed ID: 25661985
[TBL] [Abstract][Full Text] [Related]
34. Implications of Provider Specialty, Test Type, and Demographic Factors on Genetic Testing Outcomes for Patients with Autism Spectrum Disorder.
Harrington CN; Morales A; Bernstein JA; Calderwood L
J Autism Dev Disord; 2024 Jun; ():. PubMed ID: 38858309
[TBL] [Abstract][Full Text] [Related]
35. The diagnostic yield of intellectual disability: combined whole genome low-coverage sequencing and medical exome sequencing.
Wang J; Wang Y; Wang L; Chen WY; Sheng M
BMC Med Genomics; 2020 May; 13(1):70. PubMed ID: 32429945
[TBL] [Abstract][Full Text] [Related]
36. Genetic Testing in Patients with Neurodevelopmental Disorders: Experience of 511 Patients at Cincinnati Children's Hospital Medical Center.
Du X; Glass JE; Balow S; Dyer LM; Rathbun PA; Guan Q; Liu J; Wu Y; Dawson DB; Walters-Sen L; Smolarek TA; Zhang W
J Autism Dev Disord; 2022 Nov; 52(11):4828-4842. PubMed ID: 34773222
[TBL] [Abstract][Full Text] [Related]
37. Clinical sequencing yield in epilepsy, autism spectrum disorder, and intellectual disability: A systematic review and meta-analysis.
Stefanski A; Calle-López Y; Leu C; Pérez-Palma E; Pestana-Knight E; Lal D
Epilepsia; 2021 Jan; 62(1):143-151. PubMed ID: 33200402
[TBL] [Abstract][Full Text] [Related]
38. Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features.
Battaglia A; Doccini V; Bernardini L; Novelli A; Loddo S; Capalbo A; Filippi T; Carey JC
Eur J Paediatr Neurol; 2013 Nov; 17(6):589-99. PubMed ID: 23711909
[TBL] [Abstract][Full Text] [Related]
39. De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.
Mirzaa GM; Chong JX; Piton A; Popp B; Foss K; Guo H; Harripaul R; Xia K; Scheck J; Aldinger KA; Sajan SA; Tang S; Bonneau D; Beck A; White J; Mahida S; Harris J; Smith-Hicks C; Hoyer J; Zweier C; Reis A; Thiel CT; Jamra RA; Zeid N; Yang A; Farach LS; Walsh L; Payne K; Rohena L; Velinov M; Ziegler A; Schaefer E; Gatinois V; Geneviève D; Simon MEH; Kohler J; Rotenberg J; Wheeler P; Larson A; Ernst ME; Akman CI; Westman R; Blanchet P; Schillaci LA; Vincent-Delorme C; Gripp KW; Mattioli F; Guyader GL; Gerard B; Mathieu-Dramard M; Morin G; Sasanfar R; Ayub M; Vasli N; Yang S; Person R; Monaghan KG; Nickerson DA; van Binsbergen E; Enns GM; Dries AM; Rowe LJ; Tsai ACH; Svihovec S; Friedman J; Agha Z; Qamar R; Rodan LH; Martinez-Agosto J; Ockeloen CW; Vincent M; Sunderland WJ; Bernstein JA; ; Eichler EE; Vincent JB; ; Bamshad MJ
Genet Med; 2020 Mar; 22(3):538-546. PubMed ID: 31723249
[TBL] [Abstract][Full Text] [Related]
40. Dendritic Spine in Autism Genetics: Whole-Exome Sequencing Identifying De Novo Variant of
Xie Y; Wang H; Hu B; Zhang X; Liu A; Cai C; Li S; Chen C; Wang Z; Yin Z; Wang M
Children (Basel); 2022 Dec; 10(1):. PubMed ID: 36670631
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
