BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 37981655)

  • 1. Allelic hierarchy for USH2A influences auditory and visual phenotypes in South Korean patients.
    Nam DW; Song YK; Kim JH; Lee EK; Park KH; Cha J; Choi BY; Lee JH; Oh SH; Jo DH; Lee SY
    Sci Rep; 2023 Nov; 13(1):20239. PubMed ID: 37981655
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Tissue-specific genotype-phenotype correlations among USH2A-related disorders in the RUSH2A study.
    Hufnagel RB; Liang W; Duncan JL; Brewer CC; Audo I; Ayala AR; Branham K; Cheetham JK; Daiger SP; Durham TA; Guan B; Heon E; Hoyng CB; Iannaccone A; Kay CN; Michaelides M; Pennesi ME; Singh MS; Ullah E;
    Hum Mutat; 2022 May; 43(5):613-624. PubMed ID: 35266249
    [TBL] [Abstract][Full Text] [Related]  

  • 3.
    Zhu T; Chen DF; Wang L; Wu S; Wei X; Li H; Jin ZB; Sui R
    Br J Ophthalmol; 2021 May; 105(5):694-703. PubMed ID: 32675063
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants.
    Lenassi E; Vincent A; Li Z; Saihan Z; Coffey AJ; Steele-Stallard HB; Moore AT; Steel KP; Luxon LM; Héon E; Bitner-Glindzicz M; Webster AR
    Eur J Hum Genet; 2015 Oct; 23(10):1318-27. PubMed ID: 25649381
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Auditory and olfactory findings in patients with USH2A-related retinal degeneration-Findings at baseline from the rate of progression in USH2A-related retinal degeneration natural history study (RUSH2A).
    Iannaccone A; Brewer CC; Cheng P; Duncan JL; Maguire MG; Audo I; Ayala AR; Bernstein PS; Bidelman GM; Cheetham JK; Doty RL; Durham TA; Hufnagel RB; Myers MH; Stingl K; Zein WM;
    Am J Med Genet A; 2021 Dec; 185(12):3717-3727. PubMed ID: 34331386
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Correlation between Genotype and Phenotype in 69 Chinese Patients with USH2A Mutations: A comparative study of the patients with Usher Syndrome and Nonsyndromic Retinitis Pigmentosa.
    Meng X; Liu X; Li Y; Guo T; Yang L
    Acta Ophthalmol; 2021 Jun; 99(4):e447-e460. PubMed ID: 33124170
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Electroretinography Reveals Difference in Cone Function between Syndromic and Nonsyndromic USH2A Patients.
    Sengillo JD; Cabral T; Schuerch K; Duong J; Lee W; Boudreault K; Xu Y; Justus S; Sparrow JR; Mahajan VB; Tsang SH
    Sci Rep; 2017 Sep; 7(1):11170. PubMed ID: 28894305
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical aspects of Usher syndrome and the USH2A gene in a cohort of 433 patients.
    Blanco-Kelly F; Jaijo T; Aller E; Avila-Fernandez A; López-Molina MI; Giménez A; García-Sandoval B; Millán JM; Ayuso C
    JAMA Ophthalmol; 2015 Feb; 133(2):157-64. PubMed ID: 25375654
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa.
    Pierrache LH; Hartel BP; van Wijk E; Meester-Smoor MA; Cremers FP; de Baere E; de Zaeytijd J; van Schooneveld MJ; Cremers CW; Dagnelie G; Hoyng CB; Bergen AA; Leroy BP; Pennings RJ; van den Born LI; Klaver CC
    Ophthalmology; 2016 May; 123(5):1151-60. PubMed ID: 26927203
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Establishing Genotype-phenotype Correlation in USH2A-related Disorders to Personalize Audiological Surveillance and Rehabilitation.
    Molina-Ramírez LP; Lenassi E; Ellingford JM; Sergouniotis PI; Ramsden SC; Bruce IA; Black GCM
    Otol Neurotol; 2020 Apr; 41(4):431-437. PubMed ID: 32176120
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phenotypic and Genetic Characteristics in a Cohort of Patients with Usher Genes.
    Feenstra HM; Al-Khuzaei S; Shah M; Broadgate S; Shanks M; Kamath A; Yu J; Jolly JK; MacLaren RE; Clouston P; Halford S; Downes SM
    Genes (Basel); 2022 Aug; 13(8):. PubMed ID: 36011334
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spectral-Domain Optical Coherence Tomography Analysis in Syndromic and Nonsyndromic Forms of Retinitis Pigmentosa due to USH2A Genetic Variants.
    Colombo L; Maltese PE; Romano D; Fogagnolo P; Castori M; Marceddu G; Cristofoli F; Percio M; Piteková B; Modarelli AM; Bertelli M; Rossetti L
    Ophthalmic Res; 2022; 65(2):180-195. PubMed ID: 34781295
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Targeted next-generation sequencing reveals novel USH2A mutations associated with diverse disease phenotypes: implications for clinical and molecular diagnosis.
    Chen X; Sheng X; Liu X; Li H; Liu Y; Rong W; Ha S; Liu W; Kang X; Zhao K; Zhao C
    PLoS One; 2014; 9(8):e105439. PubMed ID: 25133613
    [TBL] [Abstract][Full Text] [Related]  

  • 14. USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families.
    Ahmed AN; Tahir R; Khan N; Ahmad M; Dawood M; Basit A; Yasin M; Nowshid M; Marwan M; Sultan K; Saleha S
    BMC Ophthalmol; 2021 Apr; 21(1):191. PubMed ID: 33926394
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Severe or Profound Sensorineural Hearing Loss Caused by Novel USH2A Variants in Korea: Potential Genotype-Phenotype Correlation.
    Lee SY; Joo K; Oh J; Han JH; Park HR; Lee S; Oh DY; Woo SJ; Choi BY
    Clin Exp Otorhinolaryngol; 2020 May; 13(2):113-122. PubMed ID: 31674169
    [TBL] [Abstract][Full Text] [Related]  

  • 16.
    Ordoñez-Labastida V; Chacon-Camacho OF; Lopez-Rodriguez VR; Zenteno JC
    Mol Vis; 2023; 29():31-38. PubMed ID: 37287646
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Truncating Variants Contribute to Hearing Loss and Severe Retinopathy in
    Inaba A; Maeda A; Yoshida A; Kawai K; Hirami Y; Kurimoto Y; Kosugi S; Takahashi M
    Int J Mol Sci; 2020 Oct; 21(21):. PubMed ID: 33105608
    [No Abstract]   [Full Text] [Related]  

  • 18. Novel USH2A mutations in Israeli patients with retinitis pigmentosa and Usher syndrome type 2.
    Kaiserman N; Obolensky A; Banin E; Sharon D
    Arch Ophthalmol; 2007 Feb; 125(2):219-24. PubMed ID: 17296898
    [TBL] [Abstract][Full Text] [Related]  

  • 19. USH2A Gene Mutations in Rabbits Lead to Progressive Retinal Degeneration and Hearing Loss.
    Nguyen VP; Song J; Prieskorn D; Zou J; Li Y; Dolan D; Xu J; Zhang J; Jayasundera KT; Yang J; Raphael Y; Khan N; Iannuzzi M; Bisgaier C; Chen YE; Paulus YM; Yang D
    Transl Vis Sci Technol; 2023 Feb; 12(2):26. PubMed ID: 36795064
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II.
    Yan D; Ouyang X; Patterson DM; Du LL; Jacobson SG; Liu XZ
    J Hum Genet; 2009 Dec; 54(12):732-8. PubMed ID: 19881469
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.