These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
159 related articles for article (PubMed ID: 30619482)
1. Rare Copy Number Variations in a Chinese Cohort of Autism Spectrum Disorder. Fan Y; Du X; Liu X; Wang L; Li F; Yu Y Front Genet; 2018; 9():665. PubMed ID: 30619482 [TBL] [Abstract][Full Text] [Related]
2. MLPA is a practical and complementary alternative to CMA for diagnostic testing in patients with autism spectrum disorders and identifying new candidate CNVs associated with autism. Capkova P; Srovnal J; Capkova Z; Staffova K; Becvarova V; Trkova M; Adamova K; Santava A; Curtisova V; Hajduch M; Prochazka M PeerJ; 2019; 6():e6183. PubMed ID: 30647996 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders. Akter H; Rahman MM; Sarker S; Basiruzzaman M; Islam MM; Rahaman MA; Rahaman MA; Eshaque TB; Dity NJ; Sarker S; Amin MR; Hossain MM; Lopa M; Jahan N; Hossain S; Islam A; Mondol A; Faruk MO; Saha N; Kundu GK; Kanta SI; Kazal RK; Fatema K; Rahman MA; Hasan M; Hossain Mollah MA; Hosen MI; Karuvantevida N; Begum G; Zehra B; Nassir N; Nabi AHMN; Uddin KMF; Uddin M Front Genet; 2023; 14():955631. PubMed ID: 36959829 [No Abstract] [Full Text] [Related]
5. Copy number variation in Han Chinese individuals with autism spectrum disorder. Gazzellone MJ; Zhou X; Lionel AC; Uddin M; Thiruvahindrapuram B; Liang S; Sun C; Wang J; Zou M; Tammimies K; Walker S; Selvanayagam T; Wei J; Wang Z; Wu L; Scherer SW J Neurodev Disord; 2014; 6(1):34. PubMed ID: 25170348 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder. Yin CL; Chen HI; Li LH; Chien YL; Liao HM; Chou MC; Chou WJ; Tsai WC; Chiu YN; Wu YY; Lo CZ; Wu JY; Chen YT; Gau SS Mol Autism; 2016; 7():23. PubMed ID: 27042285 [TBL] [Abstract][Full Text] [Related]
8. Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families. Leppa VM; Kravitz SN; Martin CL; Andrieux J; Le Caignec C; Martin-Coignard D; DyBuncio C; Sanders SJ; Lowe JK; Cantor RM; Geschwind DH Am J Hum Genet; 2016 Sep; 99(3):540-554. PubMed ID: 27569545 [TBL] [Abstract][Full Text] [Related]
9. A discovery resource of rare copy number variations in individuals with autism spectrum disorder. Prasad A; Merico D; Thiruvahindrapuram B; Wei J; Lionel AC; Sato D; Rickaby J; Lu C; Szatmari P; Roberts W; Fernandez BA; Marshall CR; Hatchwell E; Eis PS; Scherer SW G3 (Bethesda); 2012 Dec; 2(12):1665-85. PubMed ID: 23275889 [TBL] [Abstract][Full Text] [Related]
10. High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families. AlAyadhi LY; Hashmi JA; Iqbal M; Albalawi AM; Samman MI; Elamin NE; Bashir S; Basit S Neuroscience; 2016 Dec; 339():561-570. PubMed ID: 27771533 [TBL] [Abstract][Full Text] [Related]
11. Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder. Hnoonual A; Thammachote W; Tim-Aroon T; Rojnueangnit K; Hansakunachai T; Sombuntham T; Roongpraiwan R; Worachotekamjorn J; Chuthapisith J; Fucharoen S; Wattanasirichaigoon D; Ruangdaraganon N; Limprasert P; Jinawath N Sci Rep; 2017 Sep; 7(1):12096. PubMed ID: 28935972 [TBL] [Abstract][Full Text] [Related]
12. The landscape of copy number variations in Finnish families with autism spectrum disorders. Kanduri C; Kantojärvi K; Salo PM; Vanhala R; Buck G; Blancher C; Lähdesmäki H; Järvelä I Autism Res; 2016 Jan; 9(1):9-16. PubMed ID: 26052927 [TBL] [Abstract][Full Text] [Related]
13. The phenotypic manifestations of rare genic CNVs in autism spectrum disorder. Merikangas AK; Segurado R; Heron EA; Anney RJ; Paterson AD; Cook EH; Pinto D; Scherer SW; Szatmari P; Gill M; Corvin AP; Gallagher L Mol Psychiatry; 2015 Nov; 20(11):1366-72. PubMed ID: 25421404 [TBL] [Abstract][Full Text] [Related]
14. Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay. Liu Y; Lv Y; Zarrei M; Dong R; Yang X; Higginbotham EJ; Li Y; Zhao D; Song F; Yang Y; Zhang H; Wang Y; Scherer SW; Gai Z NPJ Genom Med; 2022 Jan; 7(1):1. PubMed ID: 35022430 [TBL] [Abstract][Full Text] [Related]
15. Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders. Ho KS; Wassman ER; Baxter AL; Hensel CH; Martin MM; Prasad A; Twede H; Vanzo RJ; Butler MG Int J Mol Sci; 2016 Dec; 17(12):. PubMed ID: 27941670 [TBL] [Abstract][Full Text] [Related]
16. Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier test. Sheth F; Shah J; Jain D; Shah S; Patel H; Patel K; Solanki DI; Iyer AS; Menghani B; Mhatre P; Mehta S; Bajaj S; Patel V; Pandya M; Dhami D; Patel D; Sheth J; Sheth H BMC Neurol; 2023 Aug; 23(1):292. PubMed ID: 37543562 [TBL] [Abstract][Full Text] [Related]
17. Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohort. Nassir N; Sati I; Al Shaibani S; Ahmed A; Almidani O; Akter H; Woodbury-Smith M; Tayoun AA; Uddin M; Albanna A Neurogenetics; 2022 Apr; 23(2):137-149. PubMed ID: 35325322 [TBL] [Abstract][Full Text] [Related]
18. Chromosomal Microarray in Patients with Non-Syndromic Autism Spectrum Disorders in the Clinical Routine of a Tertiary Hospital. Sandoval-Talamantes AK; Mori MÁ; Santos-Simarro F; García-Miñaur S; Mansilla E; Tenorio JA; Peña C; Adan C; Fernández-Elvira M; Rueda I; Lapunzina P; Nevado J Genes (Basel); 2023 Mar; 14(4):. PubMed ID: 37107578 [TBL] [Abstract][Full Text] [Related]
19. Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum Disorder. Kushima I; Nakatochi M; Aleksic B; Okada T; Kimura H; Kato H; Morikawa M; Inada T; Ishizuka K; Torii Y; Nakamura Y; Tanaka S; Imaeda M; Takahashi N; Yamamoto M; Iwamoto K; Nawa Y; Ogawa N; Iritani S; Hayashi Y; Lo T; Otgonbayar G; Furuta S; Iwata N; Ikeda M; Saito T; Ninomiya K; Okochi T; Hashimoto R; Yamamori H; Yasuda Y; Fujimoto M; Miura K; Itokawa M; Arai M; Miyashita M; Toriumi K; Ohi K; Shioiri T; Kitaichi K; Someya T; Watanabe Y; Egawa J; Takahashi T; Suzuki M; Sasaki T; Tochigi M; Nishimura F; Yamasue H; Kuwabara H; Wakuda T; Kato TA; Kanba S; Horikawa H; Usami M; Kodaira M; Watanabe K; Yoshikawa T; Toyota T; Yokoyama S; Munesue T; Kimura R; Funabiki Y; Kosaka H; Jung M; Kasai K; Ikegame T; Jinde S; Numata S; Kinoshita M; Kato T; Kakiuchi C; Yamakawa K; Suzuki T; Hashimoto N; Ishikawa S; Yamagata B; Nio S; Murai T; Son S; Kunii Y; Yabe H; Inagaki M; Goto YI; Okumura Y; Ito T; Arioka Y; Mori D; Ozaki N Biol Psychiatry; 2022 Sep; 92(5):362-374. PubMed ID: 35667888 [TBL] [Abstract][Full Text] [Related]
20. Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN Mutations. Yehia L; Seyfi M; Niestroj LM; Padmanabhan R; Ni Y; Frazier TW; Lal D; Eng C JAMA Netw Open; 2020 Jan; 3(1):e1920415. PubMed ID: 32003824 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]