43 related articles for article (PubMed ID: 31227808)
1. 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]
2. 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]
3. Noonan syndrome and type 1 Chiari malformation: Possible association.
Samuels M; Northrup H
Am J Med Genet A; 2024 Jun; ():e63776. PubMed ID: 38847235
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Evaluation and Treatment of Patients with Small Posterior Cranial Fossa and Chiari Malformation, Types 0 and 1.
Bogdanov EI; Heiss JD
Adv Tech Stand Neurosurg; 2024; 50():307-334. PubMed ID: 38592536
[TBL] [Abstract][Full Text] [Related]
6. A genetic component in Chiari I malformation: Chiari 1 malformation in all five family members.
Hassan TF; Morgan RD; Psaromatis KM; Baronia BC
Radiol Case Rep; 2024 Apr; 19(4):1445-1451. PubMed ID: 38292805
[TBL] [Abstract][Full Text] [Related]
7. Chiari Syndrome: Advances in Epidemiology and Pathogenesis: A Systematic Review.
Rodríguez-Blanque R; Almazán-Soto C; Piqueras-Sola B; Sánchez-García JC; Reinoso-Cobo A; Menor-Rodríguez MJ; Cortés-Martín J
J Clin Med; 2023 Oct; 12(20):. PubMed ID: 37892831
[TBL] [Abstract][Full Text] [Related]
8. The Small Posterior Cranial Fossa Syndrome and Chiari Malformation Type 0.
Bogdanov EI; Faizutdinova AT; Heiss JD
J Clin Med; 2022 Sep; 11(18):. PubMed ID: 36143119
[TBL] [Abstract][Full Text] [Related]
9. Sequencing-based genome-wide association studies reporting standards.
McMahon A; Lewis E; Buniello A; Cerezo M; Hall P; Sollis E; Parkinson H; Hindorff LA; Harris LW; MacArthur JAL
Cell Genom; 2021 Oct; 1(1):. PubMed ID: 34870259
[TBL] [Abstract][Full Text] [Related]
10. Posterior cranial fossa and cervical spine morphometric abnormalities in symptomatic Chiari type 0 and Chiari type 1 malformation patients with and without syringomyelia.
Bogdanov EI; Faizutdinova AT; Heiss JD
Acta Neurochir (Wien); 2021 Nov; 163(11):3051-3064. PubMed ID: 34448046
[TBL] [Abstract][Full Text] [Related]
11. Functional and morphological changes in hypoplasic posterior fossa.
Bianchi F; Benato A; Frassanito P; Tamburrini G; Massimi L
Childs Nerv Syst; 2021 Oct; 37(10):3093-3104. PubMed ID: 34169386
[TBL] [Abstract][Full Text] [Related]
12. Rare functional genetic variants in COL7A1, COL6A5, COL1A2 and COL5A2 frequently occur in Chiari Malformation Type 1.
Urbizu A; Garrett ME; Soldano K; Drechsel O; Loth D; Marcé-Grau A; Mestres I Soler O; Poca MA; Ossowski S; Macaya A; Loth F; Labuda R; Ashley-Koch A
PLoS One; 2021; 16(5):e0251289. PubMed ID: 33974636
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
Ma DQ; Cuccaro ML; Jaworski JM; Haynes CS; Stephan DA; Parod J; Abramson RK; Wright HH; Gilbert JR; Haines JL; Pericak-Vance MA
Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Neuroradiological diagnosis of Chiari malformations.
Chiapparini L; Saletti V; Solero CL; Bruzzone MG; Valentini LG
Neurol Sci; 2011 Dec; 32 Suppl 3():S283-6. PubMed ID: 21800079
[TBL] [Abstract][Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]