BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 28513615)

  • 1. Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type I reveals candidate genes for cranio-facial development.
    Merello E; Tattini L; Magi A; Accogli A; Piatelli G; Pavanello M; Tortora D; Cama A; Kibar Z; Capra V; De Marco P
    Eur J Hum Genet; 2017 Aug; 25(8):952-959. PubMed ID: 28513615
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Three sisters with Chiari I malformation with and without associated syringomyelia.
    Weisfeld-Adams JD; Carter MR; Likeman MJ; Rankin J
    Pediatr Neurosurg; 2007; 43(6):533-8. PubMed ID: 17992048
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial Chiari type I malformation with syringomyelia in two siblings: case report and review of the literature.
    Mavinkurve GG; Sciubba D; Amundson E; Jallo GI
    Childs Nerv Syst; 2005 Nov; 21(11):955-9. PubMed ID: 15821947
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chiari malformation type I: what information from the genetics?
    Capra V; Iacomino M; Accogli A; Pavanello M; Zara F; Cama A; De Marco P
    Childs Nerv Syst; 2019 Oct; 35(10):1665-1671. PubMed ID: 31385087
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Genetic analysis of posterior cranial fossa morphology in families of Chiari malformation type Ⅰ].
    Yuan XX; Li Y; Sha SF; Sun WX; Qiu Y; Liu Z; Zhu WG; Zhu ZZ
    Zhonghua Yi Xue Za Zhi; 2017 Apr; 97(15):1140-1144. PubMed ID: 28427119
    [No Abstract]   [Full Text] [Related]  

  • 6. Chiari malformation type I: a case-control association study of 58 developmental genes.
    Urbizu A; Toma C; Poca MA; Sahuquillo J; Cuenca-León E; Cormand B; Macaya A
    PLoS One; 2013; 8(2):e57241. PubMed ID: 23437350
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chiari Type I malformation and syringomyelia in unrelated patients with blepharophimosis. Report of two cases.
    Paquis P; Lonjon M; Brunet M; Lambert JC; Grellier P
    J Neurosurg; 1998 Nov; 89(5):835-8. PubMed ID: 9817424
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel LRP5 missense mutation in a patient with a high bone mass phenotype results in decreased DKK1-mediated inhibition of Wnt signaling.
    Balemans W; Devogelaer JP; Cleiren E; Piters E; Caussin E; Van Hul W
    J Bone Miner Res; 2007 May; 22(5):708-16. PubMed ID: 17295608
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel fibroblast growth factor receptor 2 mutation in Crouzon syndrome associated with Chiari type I malformation and syringomyelia.
    Fujisawa H; Hasegawa M; Kida S; Yamashita J
    J Neurosurg; 2002 Aug; 97(2):396-400. PubMed ID: 12186468
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15.
    Boyles AL; Enterline DS; Hammock PH; Siegel DG; Slifer SH; Mehltretter L; Gilbert JR; Hu-Lince D; Stephan D; Batzdorf U; Benzel E; Ellenbogen R; Green BA; Kula R; Menezes A; Mueller D; Oro' JJ; Iskandar BJ; George TM; Milhorat TH; Speer MC
    Am J Med Genet A; 2006 Dec; 140(24):2776-85. PubMed ID: 17103432
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation.
    Markunas CA; Enterline DS; Dunlap K; Soldano K; Cope H; Stajich J; Grant G; Fuchs H; Gregory SG; Ashley-Koch AE
    Ann Hum Genet; 2014 Jan; 78(1):1-12. PubMed ID: 24359474
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dkk1-induced inhibition of Wnt signaling in osteoblast differentiation is an underlying mechanism of bone loss in multiple myeloma.
    Qiang YW; Barlogie B; Rudikoff S; Shaughnessy JD
    Bone; 2008 Apr; 42(4):669-80. PubMed ID: 18294945
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.
    Markunas CA; Soldano K; Dunlap K; Cope H; Asiimwe E; Stajich J; Enterline D; Grant G; Fuchs H; Gregory SG; Ashley-Koch AE
    PLoS One; 2013; 8(4):e61521. PubMed ID: 23620759
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rare and de novo coding variants in chromodomain genes in Chiari I malformation.
    Sadler B; Wilborn J; Antunes L; Kuensting T; Hale AT; Gannon SR; McCall K; Cruchaga C; Harms M; Voisin N; Reymond A; Cappuccio G; Brunetti-Pierri N; Tartaglia M; Niceta M; Leoni C; Zampino G; Ashley-Koch A; Urbizu A; Garrett ME; Soldano K; Macaya A; Conrad D; Strahle J; Dobbs MB; Turner TN; Shannon CN; Brockmeyer D; Limbrick DD; Gurnett CA; Haller G
    Am J Hum Genet; 2021 Jan; 108(1):100-114. PubMed ID: 33352116
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and radiological findings in Arnold Chiari malformation.
    Khan AA; Bhatti SN; Khan G; Ahmed E; Aurangzeb A; Ali A; Khan A; Afzal S
    J Ayub Med Coll Abbottabad; 2010; 22(2):75-8. PubMed ID: 21702272
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of association of LRP5, LRP6, SOST, DKK1, and CTNNB1 genes with bone mineral density in a Slovenian population.
    Mencej-Bedrac S; Prezelj J; Kocjan T; Komadina R; Marc J
    Calcif Tissue Int; 2009 Dec; 85(6):501-6. PubMed ID: 19898734
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chiari 1 malformation and exome sequencing in 51 trios: the emerging role of rare missense variants in chromatin-remodeling genes.
    Provenzano A; La Barbera A; Scagnet M; Pagliazzi A; Traficante G; Pantaleo M; Tiberi L; Vergani D; Kurtas NE; Guarducci S; Bargiacchi S; Forzano G; Artuso R; Palazzo V; Kura A; Giordano F; di Feo D; Mortilla M; De Filippi C; Mattei G; Garavelli L; Giusti B; Genitori L; Zuffardi O; Giglio S
    Hum Genet; 2021 Apr; 140(4):625-647. PubMed ID: 33337535
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A genetic hypothesis for Chiari I malformation with or without syringomyelia.
    Speer MC; George TM; Enterline DS; Franklin A; Wolpert CM; Milhorat TH
    Neurosurg Focus; 2000 Mar; 8(3):E12. PubMed ID: 16676924
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in the fourth β-propeller domain of LRP4 are associated with isolated syndactyly with fusion of the third and fourth fingers.
    Sukenik Halevy R; Chien HC; Heinz B; Bamshad MJ; Nickerson DA; ; Kircher M; Ahituv N
    Hum Mutat; 2018 Jun; 39(6):811-815. PubMed ID: 29524275
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing.
    Musolf AM; Ho WSC; Long KA; Zhuang Z; Argersinger DP; Sun H; Moiz BA; Simpson CL; Mendelevich EG; Bogdanov EI; Bailey-Wilson JE; Heiss JD
    Eur J Hum Genet; 2019 Oct; 27(10):1599-1610. PubMed ID: 31227808
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.