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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 35898556)

  • 1. Multiple Recurrent Copy Number Variations (CNVs) in Chromosome 22 Including 22q11.2 Associated with Autism Spectrum Disorder.
    Alhazmi S; Alzahrani M; Farsi R; Alharbi M; Algothmi K; Alburae N; Ganash M; Azhari S; Basingab F; Almuhammadi A; Alqosaibi A; Alkhatabi H; Elaimi A; Jan M; Aldhalaan HM; Alrafiah A; Alrofaidi A
    Pharmgenomics Pers Med; 2022; 15():705-720. PubMed ID: 35898556
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Copy number variations in autistic children.
    Alhazmi S; Alharthi M; Alzahrani M; Alrofaidi A; Basingab F; Almuhammadi A; Alkhatabi H; Ashi A; Chaudhary A; Elaimi A
    Biomed Rep; 2024 Jul; 21(1):107. PubMed ID: 38868529
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The correlation between copy number variation in Chromosome 14 and DNA methylation in Saudi autistic children.
    Alhazmi S; Aljahdli B; Farsi R; Alharbi M; Algothmi K; Alburae N; Ganash M; Azhari S; Basingab F; Almuhammadi A; Alqosaibi A; Alkhatabi H; Elaimi A; Jan M; Aldhalaan H; Alyoubi R; Alrafiah A; Alrofaidi A
    Eur Rev Med Pharmacol Sci; 2022 Nov; 26(21):7866-7882. PubMed ID: 36394735
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Reciprocal Copy Number Variations at 22q11.2 Produce Distinct and Convergent Neurobehavioral Impairments Relevant for Schizophrenia and Autism Spectrum Disorder.
    Lin A; Vajdi A; Kushan-Wells L; Helleman G; Hansen LP; Jonas RK; Jalbrzikowski M; Kingsbury L; Raznahan A; Bearden CE
    Biol Psychiatry; 2020 Aug; 88(3):260-272. PubMed ID: 32143830
    [TBL] [Abstract][Full Text] [Related]  

  • 5. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
    Cappuccio G; Vitiello F; Casertano A; Fontana P; Genesio R; Bruzzese D; Ginocchio VM; Mormile A; Nitsch L; Andria G; Melis D
    Ital J Pediatr; 2016 Apr; 42():39. PubMed ID: 27072107
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Application of copy number variation sequencing in patients with intellectual disability/developmental delay and autistic spectrum disorder].
    Lei J; Zhao G; Huang Y; Long M; Li W; Deng X; Xiu Z; Xiao Y; Zeng S; Zhang J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Mar; 40(3):308-316. PubMed ID: 36854406
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Clinical and molecular characterization of three genomic rearrangements at chromosome 22q13.3 associated with autism spectrum disorder.
    Chen CH; Chen HI; Liao HM; Chen YJ; Fang JS; Lee KF; Gau SS
    Psychiatr Genet; 2017 Feb; 27(1):23-33. PubMed ID: 27846046
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. De novo copy number variations in candidate genomic regions in patients of severe autism spectrum disorder in Vietnam.
    Bui HTP; Huy Do D; Ly HTT; Tran KT; Le HTT; Nguyen KT; Pham LTD; Le HD; Le VS; Mukhopadhyay A; Nguyen LT
    PLoS One; 2024; 19(3):e0290936. PubMed ID: 38451970
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CGH Findings in Children with Complex and Essential Autistic Spectrum Disorder.
    Annunziata S; Bulgheroni S; D'Arrigo S; Esposito S; Taddei M; Saletti V; Alfei E; Sciacca FL; Rizzo A; Pantaleoni C; Riva D
    J Autism Dev Disord; 2023 Feb; 53(2):615-623. PubMed ID: 33394245
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Yield of array-CGH analysis in Tunisian children with autism spectrum disorder.
    Chehbani F; Tomaiuolo P; Picinelli C; Baccarin M; Castronovo P; Scattoni ML; Gaddour N; Persico AM
    Mol Genet Genomic Med; 2022 Aug; 10(8):e1939. PubMed ID: 35762097
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nexus between genome-wide copy number variations and autism spectrum disorder in Northeast Han Chinese population.
    Qiu S; Qiu Y; Li Y; Zhu X; Liu Y; Qiao Y; Cheng Y; Liu Y
    BMC Psychiatry; 2023 Feb; 23(1):96. PubMed ID: 36750796
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Further evidence of GABRA4 and TOP3B as autism susceptibility genes.
    Riley JD; Delahunty C; Alsadah A; Mazzola S; Astbury C
    Eur J Med Genet; 2020 May; 63(5):103876. PubMed ID: 32028044
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.
    Cho SC; Yim SH; Yoo HK; Kim MY; Jung GY; Shin GW; Kim BN; Hwang JW; Kang JJ; Kim TM; Chung YJ
    Psychiatr Genet; 2009 Aug; 19(4):177-85. PubMed ID: 19407672
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers.
    Hudac CM; Bove J; Barber S; Duyzend M; Wallace A; Martin CL; Ledbetter DH; Hanson E; Goin-Kochel RP; Green-Snyder L; Chung WK; Eichler EE; Bernier RA
    Autism Res; 2020 Aug; 13(8):1300-1310. PubMed ID: 32597026
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Copy number variations in Japanese children with autism spectrum disorder.
    Sakamoto Y; Shimoyama S; Furukawa T; Adachi M; Takahashi M; Mikami T; Kuribayashi M; Osato A; Tsushima D; Saito M; Ueno S; Nakamura K
    Psychiatr Genet; 2021 Jun; 31(3):79-87. PubMed ID: 33591083
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Investigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders.
    Görker I; Gürkan H; Ulusal S; Atli E; Ayaz G; Ceylan C; Tozkir H; Altay MA; Erol A; Yildiz N; Direk C; Akköprü H; Kilit N; Aykutlu HC; Bozatli L; Çelik Z; Berberoğlu KK
    Noro Psikiyatr Ars; 2018 Sep; 55(3):215-219. PubMed ID: 30224866
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.