BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 34389249)

  • 1. Genetic counseling considerations in cerebral palsy.
    Elliott AM; Guimond C
    Mol Genet Metab; 2022 Dec; 137(4):428-435. PubMed ID: 34389249
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A diagnostic approach for cerebral palsy in the genomic era.
    Lee RW; Poretti A; Cohen JS; Levey E; Gwynn H; Johnston MV; Hoon AH; Fatemi A
    Neuromolecular Med; 2014 Dec; 16(4):821-44. PubMed ID: 25280894
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Shortened consent forms for genome-wide sequencing: Parent and provider perspectives.
    Hitchcock EC; Study C; Elliott AM
    Mol Genet Genomic Med; 2020 Jul; 8(7):e1254. PubMed ID: 32383361
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genomics in Cerebral Palsy phenotype across the lifespan: Comparison of diagnostic yield between children and adult population.
    Al Zahrani H; Siriwardena K; Young D; Lehman A; Horvath GA; Goez H
    Mol Genet Metab; 2022 Dec; 137(4):420-427. PubMed ID: 34364746
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Etiology and Ontogeny of Cerebral Palsy: Implications for Practice and Research.
    Evans MI; Britt DW; Devoe LD
    Reprod Sci; 2024 May; 31(5):1179-1189. PubMed ID: 38133768
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The long-term impact of receiving incidental findings on parents undergoing genome-wide sequencing.
    Cheung F; Birch P; Friedman JM; ; ; Elliott AM; Adam S
    J Genet Couns; 2022 Aug; 31(4):887-900. PubMed ID: 35128755
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Diagnostic Yield of Exome Sequencing in Cerebral Palsy and Implications for Genetic Testing Guidelines: A Systematic Review and Meta-analysis.
    Gonzalez-Mantilla PJ; Hu Y; Myers SM; Finucane BM; Ledbetter DH; Martin CL; Moreno-De-Luca A
    JAMA Pediatr; 2023 May; 177(5):472-478. PubMed ID: 36877506
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic counseling considerations with rapid genome-wide sequencing in a neonatal intensive care unit.
    Smith EE; du Souich C; Dragojlovic N; ; ; Elliott AM
    J Genet Couns; 2019 Apr; 28(2):263-272. PubMed ID: 30964583
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Genetic Counseling and Genome Sequencing in Pediatric Rare Disease.
    Elliott AM
    Cold Spring Harb Perspect Med; 2020 Mar; 10(3):. PubMed ID: 31501267
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic counseling for consumer-driven whole exome and whole genome sequencing: A commentary on early experiences.
    Schmidt JL; Maas R; Altmeyer SR
    J Genet Couns; 2019 Apr; 28(2):449-455. PubMed ID: 30861266
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. Genetic or Other Causation Should Not Change the Clinical Diagnosis of Cerebral Palsy.
    MacLennan AH; Lewis S; Moreno-De-Luca A; Fahey M; Leventer RJ; McIntyre S; Ben-Pazi H; Corbett M; Wang X; Baynam G; Fehlings D; Kurian MA; Zhu C; Himmelmann K; Smithers-Sheedy H; Wilson Y; Ocaña CS; van Eyk C; Badawi N; Wintle RF; Jacobsson B; Amor DJ; Mallard C; Pérez-Jurado LA; Hallman M; Rosenbaum PJ; Kruer MC; Gecz J
    J Child Neurol; 2019 Jul; 34(8):472-476. PubMed ID: 30963790
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Atypical cerebral palsy: genomics analysis enables precision medicine.
    Matthews AM; Blydt-Hansen I; Al-Jabri B; Andersen J; Tarailo-Graovac M; Price M; Selby K; Demos M; Connolly M; Drögemoller B; Shyr C; Mwenifumbo J; Elliott AM; Lee J; Ghani A; Stöckler S; Salvarinova R; Vallance H; Sinclair G; Ross CJ; Wasserman WW; McKinnon ML; Horvath GA; Goez H; van Karnebeek CD;
    Genet Med; 2019 Jul; 21(7):1621-1628. PubMed ID: 30542205
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study.
    Elliott AM; Adam S; du Souich C; Lehman A; Nelson TN; van Karnebeek C; Alderman E; Armstrong L; Aubertin G; Blood K; Boelman C; Boerkoel C; Bretherick K; Brown L; Chijiwa C; Clarke L; Couse M; Creighton S; Watts-Dickens A; Gibson WT; Gill H; Tarailo-Graovac M; Hamilton S; Heran H; Horvath G; Huang L; Hulait GK; Koehn D; Lee HK; Lewis S; Lopez E; Louie K; Niederhoffer K; Matthews A; Meagher K; Peng JJ; Patel MS; Race S; Richmond P; Rupps R; Salvarinova R; Seath K; Selby K; Steinraths M; Stockler S; Tang K; Tyson C; van Allen M; Wasserman W; Mwenifumbo J; Friedman JM
    HGG Adv; 2022 Jul; 3(3):100108. PubMed ID: 35599849
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.