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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2012 | 1 |
2013 | 2 |
2014 | 2 |
2015 | 1 |
2021 | 1 |
2024 | 0 |
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Page 1
Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations.
J Neurosurg Pediatr. 2012 Apr;9(4):372-8. doi: 10.3171/2011.12.PEDS11113.
J Neurosurg Pediatr. 2012.
PMID: 22462700
Free PMC article.
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.
Urbizu A, et al.
PLoS One. 2021 May 11;16(5):e0251289. doi: 10.1371/journal.pone.0251289. eCollection 2021.
PLoS One. 2021.
PMID: 33974636
Free PMC article.
Item in Clipboard
Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation.
Lock EF, Soldano KL, Garrett ME, Cope H, Markunas CA, Fuchs H, Grant G, Dunson DB, Gregory SG, Ashley-Koch AE.
Lock EF, et al.
BMC Genomics. 2015 Jan 22;16(1):11. doi: 10.1186/s12864-014-1211-8.
BMC Genomics. 2015.
PMID: 25609184
Free PMC article.
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Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics.
Markunas CA, Lock E, Soldano K, Cope H, Ding CK, Enterline DS, Grant G, Fuchs H, Ashley-Koch AE, Gregory SG.
Markunas CA, et al.
BMC Med Genomics. 2014 Jun 25;7:39. doi: 10.1186/1755-8794-7-39.
BMC Med Genomics. 2014.
PMID: 24962150
Free PMC article.
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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.
Markunas CA, et al.
Ann Hum Genet. 2014 Jan;78(1):1-12. doi: 10.1111/ahg.12041. Epub 2013 Oct 6.
Ann Hum Genet. 2014.
PMID: 24359474
Free PMC article.
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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.
Markunas CA, et al.
PLoS One. 2013 Apr 19;8(4):e61521. doi: 10.1371/journal.pone.0061521. Print 2013.
PLoS One. 2013.
PMID: 23620759
Free PMC article.
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