BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 30109564)

  • 1. Identification of pathways and genes associated with cerebral palsy.
    Zhu Q; Ni Y; Wang J; Yin H; Zhang Q; Zhang L; Bian W; Liang B; Kong L; Xuan L; Lu N
    Genes Genomics; 2018 Dec; 40(12):1339-1349. PubMed ID: 30109564
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Genetic analysis of 10 children with cerebral palsy].
    Zhu Q; Ni Y; Wang J; Yin H; Zhang Q; Bian W; Zhang L; Lin M; Liu J; Zhou J; Sha C; Zhou X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Mar; 36(3):229-233. PubMed ID: 30835352
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy.
    Wang Y; Xu Y; Zhou C; Cheng Y; Qiao N; Shang Q; Xia L; Song J; Gao C; Qiao Y; Zhang X; Li M; Ma C; Fan Y; Peng X; Wu S; Lv N; Li B; Sun Y; Zhang B; Li T; Li H; Zhang J; Su Y; Li Q; Yuan J; Liu L; Moreno-De-Luca A; MacLennan AH; Gecz J; Zhu D; Wang X; Zhu C; Xing Q
    Nat Med; 2024 May; 30(5):1395-1405. PubMed ID: 38693247
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Predictors of whole exome sequencing in dystonic cerebral palsy and cerebral palsy-like disorders.
    Pavelekova P; Necpal J; Jech R; Havrankova P; Svantnerova J; Jurkova V; Gdovinova Z; Lackova A; Han V; Winkelmann J; Zech M; Skorvanek M
    Parkinsonism Relat Disord; 2023 Jun; 111():105352. PubMed ID: 36997436
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hidden etiology of cerebral palsy: genetic and clinical heterogeneity and efficient diagnosis by next-generation sequencing.
    Rosello M; Caro-Llopis A; Orellana C; Oltra S; Alemany-Albert M; Marco-Hernandez AV; Monfort S; Pedrola L; Martinez F; Tomás M
    Pediatr Res; 2021 Aug; 90(2):284-288. PubMed ID: 33177673
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mendelian etiologies identified with whole exome sequencing in cerebral palsy.
    Chopra M; Gable DL; Love-Nichols J; Tsao A; Rockowitz S; Sliz P; Barkoudah E; Bastianelli L; Coulter D; Davidson E; DeGusmao C; Fogelman D; Huth K; Marshall P; Nimec D; Sanders JS; Shore BJ; Snyder B; Stone SSD; Ubeda A; Watkins C; Berde C; Bolton J; Brownstein C; Costigan M; Ebrahimi-Fakhari D; Lai A; O'Donnell-Luria A; Paciorkowski AR; Pinto A; Pugh J; Rodan L; Roe E; Swanson L; Zhang B; Kruer MC; Sahin M; Poduri A; Srivastava S
    Ann Clin Transl Neurol; 2022 Feb; 9(2):193-205. PubMed ID: 35076175
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy.
    Moreno-De-Luca A; Millan F; Pesacreta DR; Elloumi HZ; Oetjens MT; Teigen C; Wain KE; Scuffins J; Myers SM; Torene RI; Gainullin VG; Arvai K; Kirchner HL; Ledbetter DH; Retterer K; Martin CL
    JAMA; 2021 Feb; 325(5):467-475. PubMed ID: 33528536
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy.
    McMichael G; Bainbridge MN; Haan E; Corbett M; Gardner A; Thompson S; van Bon BW; van Eyk CL; Broadbent J; Reynolds C; O'Callaghan ME; Nguyen LS; Adelson DL; Russo R; Jhangiani S; Doddapaneni H; Muzny DM; Gibbs RA; Gecz J; MacLennan AH
    Mol Psychiatry; 2015 Feb; 20(2):176-82. PubMed ID: 25666757
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy.
    Zarrei M; Fehlings DL; Mawjee K; Switzer L; Thiruvahindrapuram B; Walker S; Merico D; Casallo G; Uddin M; MacDonald JR; Gazzellone MJ; Higginbotham EJ; Campbell C; deVeber G; Frid P; Gorter JW; Hunt C; Kawamura A; Kim M; McCormick A; Mesterman R; Samdup D; Marshall CR; Stavropoulos DJ; Wintle RF; Scherer SW
    Genet Med; 2018 Feb; 20(2):172-180. PubMed ID: 28771244
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cerebral palsy and related neuromotor disorders: Overview of genetic and genomic studies.
    Friedman JM; van Essen P; van Karnebeek CDM
    Mol Genet Metab; 2022 Dec; 137(4):399-419. PubMed ID: 34872807
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autism.
    van Eyk CL; Corbett MA; Gardner A; van Bon BW; Broadbent JL; Harper K; MacLennan AH; Gecz J
    Transl Psychiatry; 2018 Apr; 8(1):88. PubMed ID: 29681622
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic testing in individuals with cerebral palsy.
    May HJ; Fasheun JA; Bain JM; Baugh EH; Bier LE; Revah-Politi A; ; Roye DP; Goldstein DB; Carmel JB
    Dev Med Child Neurol; 2021 Dec; 63(12):1448-1455. PubMed ID: 34114234
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic Spectrum Identified by Exome Sequencing in a Chinese Pediatric Cerebral Palsy Cohort.
    Mei H; Yang L; Xiao T; Wang S; Wu B; Wang H; Lu Y; Dong X; Yang H; Zhou W
    J Pediatr; 2022 Mar; 242():206-212.e6. PubMed ID: 34788679
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
    Jin SC; Lewis SA; Bakhtiari S; Zeng X; Sierant MC; Shetty S; Nordlie SM; Elie A; Corbett MA; Norton BY; van Eyk CL; Haider S; Guida BS; Magee H; Liu J; Pastore S; Vincent JB; Brunstrom-Hernandez J; Papavasileiou A; Fahey MC; Berry JG; Harper K; Zhou C; Zhang J; Li B; Zhao H; Heim J; Webber DL; Frank MSB; Xia L; Xu Y; Zhu D; Zhang B; Sheth AH; Knight JR; Castaldi C; Tikhonova IR; López-Giráldez F; Keren B; Whalen S; Buratti J; Doummar D; Cho M; Retterer K; Millan F; Wang Y; Waugh JL; Rodan L; Cohen JS; Fatemi A; Lin AE; Phillips JP; Feyma T; MacLennan SC; Vaughan S; Crompton KE; Reid SM; Reddihough DS; Shang Q; Gao C; Novak I; Badawi N; Wilson YA; McIntyre SJ; Mane SM; Wang X; Amor DJ; Zarnescu DC; Lu Q; Xing Q; Zhu C; Bilguvar K; Padilla-Lopez S; Lifton RP; Gecz J; MacLennan AH; Kruer MC
    Nat Genet; 2020 Oct; 52(10):1046-1056. PubMed ID: 32989326
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy.
    Yechieli M; Gulsuner S; Ben-Pazi H; Fattal A; Aran A; Kuzminsky A; Sagi L; Guttman D; Schneebaum Sender N; Gross-Tsur V; Klopstock T; Walsh T; Renbaum P; Zeligson S; Shemer Meiri L; Lev D; Shmueli D; Blumkin L; Lahad A; King MC; Levy EL; Segel R
    J Med Genet; 2022 Aug; 59(8):759-767. PubMed ID: 34321325
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Whole‑genome scale identification of methylation markers specific for cerebral palsy in monozygotic discordant twins.
    Jiao Z; Jiang Z; Wang J; Xu H; Zhang Q; Liu S; Du N; Zhang Y; Qiu H
    Mol Med Rep; 2017 Dec; 16(6):9423-9430. PubMed ID: 29039597
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cerebral palsy: causes, pathways, and the role of genetic variants.
    MacLennan AH; Thompson SC; Gecz J
    Am J Obstet Gynecol; 2015 Dec; 213(6):779-88. PubMed ID: 26003063
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The genetic basis of cerebral palsy.
    Fahey MC; Maclennan AH; Kretzschmar D; Gecz J; Kruer MC
    Dev Med Child Neurol; 2017 May; 59(5):462-469. PubMed ID: 28042670
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic variants in the HLA region contribute to the risk of cerebral palsy.
    Cheng Y; Xu Y; Li H; Qiao Y; Wang Y; Su Y; Zhang J; Wang X; Song L; Ding J; Wang D; Zhu C; Xing Q
    Biochim Biophys Acta Mol Basis Dis; 2024 Mar; 1870(3):167008. PubMed ID: 38163449
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Gene expressions in cerebral palsy subjects reveal structural and functional changes in the gastrocnemius muscle that are closely associated with passive muscle stiffness.
    Pingel J; Kampmann ML; Andersen JD; Wong C; Døssing S; Børsting C; Nielsen JB
    Cell Tissue Res; 2021 May; 384(2):513-526. PubMed ID: 33515289
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.