139 related articles for article (PubMed ID: 31227808)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q.
Musolf AM; Moiz BA; Sun H; Pikielny CW; Bossé Y; Mandal D; de Andrade M; Gaba C; Yang P; Li Y; You M; Govindan R; Wilson RK; Kupert EY; Anderson MW; Schwartz AG; Pinney SM; Amos CI; Bailey-Wilson JE
Cancer Epidemiol Biomarkers Prev; 2020 Feb; 29(2):434-442. PubMed ID: 31826912
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Familial Chiari malformation: case series.
Schanker BD; Walcott BP; Nahed BV; Kahle KT; Li YM; Coumans JV
Neurosurg Focus; 2011 Sep; 31(3):E1. PubMed ID: 21882906
[TBL] [Abstract][Full Text] [Related]
9. A genome-wide association study identifies candidate loci associated to syringomyelia secondary to Chiari-like malformation in Cavalier King Charles Spaniels.
Ancot F; Lemay P; Knowler SP; Kennedy K; Griffiths S; Cherubini GB; Sykes J; Mandigers PJJ; Rouleau GA; Rusbridge C; Kibar Z
BMC Genet; 2018 Mar; 19(1):16. PubMed ID: 29566674
[TBL] [Abstract][Full Text] [Related]
10. Pathogenesis of Chiari malformation: a morphometric study of the posterior cranial fossa.
Nishikawa M; Sakamoto H; Hakuba A; Nakanishi N; Inoue Y
J Neurosurg; 1997 Jan; 86(1):40-7. PubMed ID: 8988080
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Analysis of the volumes of the posterior cranial fossa, cerebellum, and herniated tonsils using the stereological methods in patients with Chiari type I malformation.
Vurdem ÜE; Acer N; Ertekin T; Savranlar A; Inci MF
ScientificWorldJournal; 2012; 2012():616934. PubMed ID: 22629166
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients.
Milhorat TH; Chou MW; Trinidad EM; Kula RW; Mandell M; Wolpert C; Speer MC
Neurosurgery; 1999 May; 44(5):1005-17. PubMed ID: 10232534
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families.
Simpson CL; Musolf AM; Li Q; Portas L; Murgia F; Cordero RY; Cordero JB; Moiz BA; Holzinger ER; Middlebrooks CD; Lewis DD; Bailey-Wilson JE; Stambolian D
BMC Med Genet; 2019 Jan; 20(1):27. PubMed ID: 30704416
[TBL] [Abstract][Full Text] [Related]
17. Volumetric analysis of the posterior cranial fossa in a family with four generations of the Chiari malformation Type I.
Tubbs RS; Hill M; Loukas M; Shoja MM; Oakes WJ
J Neurosurg Pediatr; 2008 Jan; 1(1):21-4. PubMed ID: 18352798
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Evidence of posterior fossa hypoplasia in the familial variant of adult Chiari I malformation: case report.
Atkinson JL; Kokmen E; Miller GM
Neurosurgery; 1998 Feb; 42(2):401-3; discussion 404. PubMed ID: 9482195
[TBL] [Abstract][Full Text] [Related]
20. Analysis of the posterior fossa in children with the Chiari 0 malformation.
Tubbs RS; Elton S; Grabb P; Dockery SE; Bartolucci AA; Oakes WJ
Neurosurgery; 2001 May; 48(5):1050-4; discussion 1054-5. PubMed ID: 11334271
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
