BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

343 related articles for article (PubMed ID: 25666757)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies.
    Waldmüller S; Schroeder C; Sturm M; Scheffold T; Imbrich K; Junker S; Frische C; Hofbeck M; Bauer P; Bonin M; Gawaz M; Gramlich M
    Mol Cell Probes; 2015 Oct; 29(5):308-14. PubMed ID: 25979592
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Targeted resequencing identifies genes with recurrent variation in cerebral palsy.
    van Eyk CL; Corbett MA; Frank MSB; Webber DL; Newman M; Berry JG; Harper K; Haines BP; McMichael G; Woenig JA; MacLennan AH; Gecz J
    NPJ Genom Med; 2019; 4():27. PubMed ID: 31700678
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. The emerging genetic landscape of cerebral palsy.
    van Eyk CL; Corbett MA; Maclennan AH
    Handb Clin Neurol; 2018; 147():331-342. PubMed ID: 29325622
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.
    Kelsen JR; Dawany N; Moran CJ; Petersen BS; Sarmady M; Sasson A; Pauly-Hubbard H; Martinez A; Maurer K; Soong J; Rappaport E; Franke A; Keller A; Winter HS; Mamula P; Piccoli D; Artis D; Sonnenberg GF; Daly M; Sullivan KE; Baldassano RN; Devoto M
    Gastroenterology; 2015 Nov; 149(6):1415-24. PubMed ID: 26193622
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
    Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
    Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients.
    Lim EC; Brett M; Lai AH; Lee SP; Tan ES; Jamuar SS; Ng IS; Tan EC
    Hum Genomics; 2015 Dec; 9():33. PubMed ID: 26666243
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The genetic landscape of infantile spasms.
    Michaud JL; Lachance M; Hamdan FF; Carmant L; Lortie A; Diadori P; Major P; Meijer IA; Lemyre E; Cossette P; Mefford HC; Rouleau GA; Rossignol E
    Hum Mol Genet; 2014 Sep; 23(18):4846-58. PubMed ID: 24781210
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations.
    Kataoka M; Matoba N; Sawada T; Kazuno AA; Ishiwata M; Fujii K; Matsuo K; Takata A; Kato T
    Mol Psychiatry; 2016 Jul; 21(7):885-93. PubMed ID: 27217147
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fetal and maternal candidate single nucleotide polymorphism associations with cerebral palsy: a case-control study.
    O'Callaghan ME; Maclennan AH; Gibson CS; McMichael GL; Haan EA; Broadbent JL; Goldwater PN; Painter JN; Montgomery GW; Dekker GA;
    Pediatrics; 2012 Feb; 129(2):e414-23. PubMed ID: 22291124
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy.
    Fehlings DL; Zarrei M; Engchuan W; Sondheimer N; Thiruvahindrapuram B; MacDonald JR; Higginbotham EJ; Thapa R; Behlim T; Aimola S; Switzer L; Ng P; Wei J; Danthi PS; Pellecchia G; Lamoureux S; Ho K; Pereira SL; de Rijke J; Sung WWL; Mowjoodi A; Howe JL; Nalpathamkalam T; Manshaei R; Ghaffari S; Whitney J; Patel RV; Hamdan O; Shaath R; Trost B; Knights S; Samdup D; McCormick A; Hunt C; Kirton A; Kawamura A; Mesterman R; Gorter JW; Dlamini N; Merico D; Hilali M; Hirschfeld K; Grover K; Bautista NX; Han K; Marshall CR; Yuen RKC; Subbarao P; Azad MB; Turvey SE; Mandhane P; Moraes TJ; Simons E; Maxwell G; Shevell M; Costain G; Michaud JL; Hamdan FF; Gauthier J; Uguen K; Stavropoulos DJ; Wintle RF; Oskoui M; Scherer SW
    Nat Genet; 2024 Apr; 56(4):585-594. PubMed ID: 38553553
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.