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 *

300 related articles for article (PubMed ID: 31602316)

  • 1. A large data resource of genomic copy number variation across neurodevelopmental disorders.
    Zarrei M; Burton CL; Engchuan W; Young EJ; Higginbotham EJ; MacDonald JR; Trost B; Chan AJS; Walker S; Lamoureux S; Heung T; Mojarad BA; Kellam B; Paton T; Faheem M; Miron K; Lu C; Wang T; Samler K; Wang X; Costain G; Hoang N; Pellecchia G; Wei J; Patel RV; Thiruvahindrapuram B; Roifman M; Merico D; Goodale T; Drmic I; Speevak M; Howe JL; Yuen RKC; Buchanan JA; Vorstman JAS; Marshall CR; Wintle RF; Rosenberg DR; Hanna GL; Woodbury-Smith M; Cytrynbaum C; Zwaigenbaum L; Elsabbagh M; Flanagan J; Fernandez BA; Carter MT; Szatmari P; Roberts W; Lerch J; Liu X; Nicolson R; Georgiades S; Weksberg R; Arnold PD; Bassett AS; Crosbie J; Schachar R; Stavropoulos DJ; Anagnostou E; Scherer SW
    NPJ Genom Med; 2019; 4():26. PubMed ID: 31602316
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.
    Glessner JT; Khan ME; Chang X; Liu Y; Otieno FG; Lemma M; Slaby I; Hain H; Mentch F; Li J; Kao C; Sleiman PMA; March ME; Connolly J; Hakonarson H
    J Neurodev Disord; 2023 Apr; 15(1):14. PubMed ID: 37120522
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. A Diffusion Tensor Imaging Study in Children With ADHD, Autism Spectrum Disorder, OCD, and Matched Controls: Distinct and Non-Distinct White Matter Disruption and Dimensional Brain-Behavior Relationships.
    Ameis SH; Lerch JP; Taylor MJ; Lee W; Viviano JD; Pipitone J; Nazeri A; Croarkin PE; Voineskos AN; Lai MC; Crosbie J; Brian J; Soreni N; Schachar R; Szatmari P; Arnold PD; Anagnostou E
    Am J Psychiatry; 2016 Dec; 173(12):1213-1222. PubMed ID: 27363509
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank.
    Birnbaum R; Mahjani B; Loos RJF; Sharp AJ
    JAMA Psychiatry; 2022 Mar; 79(3):250-259. PubMed ID: 35080590
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
    Williams NM; Zaharieva I; Martin A; Langley K; Mantripragada K; Fossdal R; Stefansson H; Stefansson K; Magnusson P; Gudmundsson OO; Gustafsson O; Holmans P; Owen MJ; O'Donovan M; Thapar A
    Lancet; 2010 Oct; 376(9750):1401-8. PubMed ID: 20888040
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of novel driver risk genes in CNV loci associated with neurodevelopmental disorders.
    Azidane S; Gallego X; Durham L; Cáceres M; Guney E; Pérez-Cano L
    HGG Adv; 2024 Jul; 5(3):100316. PubMed ID: 38850022
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD.
    Chaves TF; Ocampos M; Barbato IT; de Camargo Pinto LL; de Luca GR; Barbato Filho JH; Bernardi P; Costa Netto Muniz Y; Francesca Maris A
    Sci Rep; 2024 Feb; 14(1):3762. PubMed ID: 38355898
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder.
    Ramos-Quiroga JA; Sánchez-Mora C; Casas M; Garcia-Martínez I; Bosch R; Nogueira M; Corrales M; Palomar G; Vidal R; Coll-Tané M; Bayés M; Cormand B; Ribasés M
    J Psychiatr Res; 2014 Feb; 49():60-7. PubMed ID: 24269040
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Inherited duplication of the pseudoautosomal region Xq28 in a subject with Gilles de la Tourette syndrome and intellectual disability: a case report.
    Maccarini S; Cipani A; Bertini V; Skripac J; Salvi A; Borsani G; Marchina E
    Mol Cytogenet; 2020; 13():23. PubMed ID: 32582378
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection and characterization of copy number variation in autism spectrum disorder.
    Marshall CR; Scherer SW
    Methods Mol Biol; 2012; 838():115-35. PubMed ID: 22228009
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Association of copy number variation across the genome with neuropsychiatric traits in the general population.
    Guyatt AL; Stergiakouli E; Martin J; Walters J; O'Donovan M; Owen M; Thapar A; Kirov G; Rodriguez S; Rai D; Zammit S; Gaunt TR
    Am J Med Genet B Neuropsychiatr Genet; 2018 Jul; 177(5):489-502. PubMed ID: 29687944
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders.
    Glessner JT; Li J; Wang D; March M; Lima L; Desai A; Hadley D; Kao C; Gur RE; Cohen N; Sleiman PMA; Li Q; Hakonarson H;
    Genome Med; 2017 Nov; 9(1):106. PubMed ID: 29191242
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Large-scale discovery of novel neurodevelopmental disorder-related genes through a unified analysis of single-nucleotide and copy number variants.
    Hamanaka K; Miyake N; Mizuguchi T; Miyatake S; Uchiyama Y; Tsuchida N; Sekiguchi F; Mitsuhashi S; Tsurusaki Y; Nakashima M; Saitsu H; Yamada K; Sakamoto M; Fukuda H; Ohori S; Saida K; Itai T; Azuma Y; Koshimizu E; Fujita A; Erturk B; Hiraki Y; Ch'ng GS; Kato M; Okamoto N; Takata A; Matsumoto N
    Genome Med; 2022 Apr; 14(1):40. PubMed ID: 35468861
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.
    Jarick I; Volckmar AL; Pütter C; Pechlivanis S; Nguyen TT; Dauvermann MR; Beck S; Albayrak Ö; Scherag S; Gilsbach S; Cichon S; Hoffmann P; Degenhardt F; Nöthen MM; Schreiber S; Wichmann HE; Jöckel KH; Heinrich J; Tiesler CM; Faraone SV; Walitza S; Sinzig J; Freitag C; Meyer J; Herpertz-Dahlmann B; Lehmkuhl G; Renner TJ; Warnke A; Romanos M; Lesch KP; Reif A; Schimmelmann BG; Hebebrand J; Scherag A; Hinney A
    Mol Psychiatry; 2014 Jan; 19(1):115-21. PubMed ID: 23164820
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.
    Nguyen HT; Bryois J; Kim A; Dobbyn A; Huckins LM; Munoz-Manchado AB; Ruderfer DM; Genovese G; Fromer M; Xu X; Pinto D; Linnarsson S; Verhage M; Smit AB; Hjerling-Leffler J; Buxbaum JD; Hultman C; Sklar P; Purcell SM; Lage K; He X; Sullivan PF; Stahl EA
    Genome Med; 2017 Dec; 9(1):114. PubMed ID: 29262854
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.