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Page 1
KIAA1217: A novel candidate gene associated with isolated and syndromic vertebral malformations.
Al Dhaheri N, Wu N, Zhao S, Wu Z, Blank RD, Zhang J, Raggio C, Halanski M, Shen J, Noonan K, Qiu G, Nemeth B, Sund S, Dunwoodie SL, Chapman G, Glurich I, Steiner RD, Wohler E, Martin R, Sobreira NL, Giampietro PF. Al Dhaheri N, et al. Among authors: glurich i. Am J Med Genet A. 2020 Jul;182(7):1664-1672. doi: 10.1002/ajmg.a.61607. Epub 2020 May 5. Am J Med Genet A. 2020. PMID: 32369272 Free PMC article.
Evaluation of SLC35A3 as a candidate gene for human vertebral malformations.
Ghebranious N, Burmester JK, Glurich I, McPherson E, Ivacic L, Kislow J, Rasmussen K, Kumar V, Raggio CL, Blank RD, Jacobsen FS, Faciszewski T, Womack J, Giampietro PF. Ghebranious N, et al. Among authors: glurich i. Am J Med Genet A. 2006 Jun 15;140(12):1346-8. doi: 10.1002/ajmg.a.31307. Am J Med Genet A. 2006. PMID: 16691598 No abstract available.
DLL3 as a candidate gene for vertebral malformations.
Giampietro PF, Raggio CL, Reynolds C, Ghebranious N, Burmester JK, Glurich I, Rasmussen K, McPherson E, Pauli RM, Shukla SK, Merchant S, Jacobsen FS, Faciszewski T, Blank RD. Giampietro PF, et al. Among authors: glurich i. Am J Med Genet A. 2006 Nov 15;140(22):2447-53. doi: 10.1002/ajmg.a.31509. Am J Med Genet A. 2006. PMID: 17041936
An analysis of PAX1 in the development of vertebral malformations.
Giampietro PF, Raggio CL, Reynolds CE, Shukla SK, McPherson E, Ghebranious N, Jacobsen FS, Kumar V, Faciszewski T, Pauli RM, Rasmussen K, Burmester JK, Zaleski C, Merchant S, David D, Weber JL, Glurich I, Blank RD. Giampietro PF, et al. Among authors: glurich i. Clin Genet. 2005 Nov;68(5):448-53. doi: 10.1111/j.1399-0004.2005.00520.x. Clin Genet. 2005. PMID: 16207213
A missense T (Brachyury) mutation contributes to vertebral malformations.
Ghebranious N, Blank RD, Raggio CL, Staubli J, McPherson E, Ivacic L, Rasmussen K, Jacobsen FS, Faciszewski T, Burmester JK, Pauli RM, Boachie-Adjei O, Glurich I, Giampietro PF. Ghebranious N, et al. Among authors: glurich i. J Bone Miner Res. 2008 Oct;23(10):1576-83. doi: 10.1359/jbmr.080503. J Bone Miner Res. 2008. PMID: 18466071 Free article.
Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations.
Ghebranious N, Raggio CL, Blank RD, McPherson E, Burmester JK, Ivacic L, Rasmussen K, Kislow J, Glurich I, Jacobsen FS, Faciszewski T, Pauli RM, Boachie-Adjei O, Giampietro PF. Ghebranious N, et al. Among authors: glurich i. Scoliosis. 2007 Sep 23;2:13. doi: 10.1186/1748-7161-2-13. Scoliosis. 2007. PMID: 17888180 Free PMC article.
Molecular diagnosis of vertebral segmentation disorders in humans.
Giampietro PF, Dunwoodie SL, Kusumi K, Pourquié O, Tassy O, Offiah AC, Cornier AS, Alman BA, Blank RD, Raggio CL, Glurich I, Turnpenny PD. Giampietro PF, et al. Among authors: glurich i. Expert Opin Med Diagn. 2008 Oct;2(10):1107-21. doi: 10.1517/17530059.2.10.1107. Expert Opin Med Diagn. 2008. PMID: 23496422
A randomized controlled trial of genotype-based Coumadin initiation.
Burmester JK, Berg RL, Yale SH, Rottscheit CM, Glurich IE, Schmelzer JR, Caldwell MD. Burmester JK, et al. Genet Med. 2011 Jun;13(6):509-18. doi: 10.1097/GIM.0b013e31820ad77d. Genet Med. 2011. PMID: 21423021 Free article. Clinical Trial.
88 results