Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

38 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
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. 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. 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
Clinical genetics provider real-time workflow study.
McPherson E, Zaleski C, Benishek K, McCarty CA, Giampietro PF, Reynolds K, Rasmussen K. McPherson E, et al. Genet Med. 2008 Sep;10(9):699-706. doi: 10.1097/gim.0b013e318182206f. Genet Med. 2008. PMID: 18978682
Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromes.
Giampietro PF, Armstrong L, Stoddard A, Blank RD, Livingston J, Raggio CL, Rasmussen K, Pickart M, Lorier R, Turner A, Sund S, Sobrera N, Neptune E, Sweetser D, Santiago-Cornier A, Broeckel U. Giampietro PF, et al. Am J Med Genet A. 2015 Jan;167A(1):95-102. doi: 10.1002/ajmg.a.36799. Epub 2014 Oct 27. Am J Med Genet A. 2015. PMID: 25348728
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. 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. J Bone Miner Res. 2008 Oct;23(10):1576-83. doi: 10.1359/jbmr.080503. J Bone Miner Res. 2008. PMID: 18466071 Free article.
Analysis of maternal risk factors associated with congenital vertebral malformations.
Hesemann J, Lauer E, Ziska S, Noonan K, Nemeth B, Scott-Schwoerer J, McCarty C, Rasmussen K, Goldberg JM, Sund S, Eickhoff J, Raggio CL, Giampietro PF. Hesemann J, et al. Spine (Phila Pa 1976). 2013 Mar 1;38(5):E293-8. doi: 10.1097/BRS.0b013e318283be6e. Spine (Phila Pa 1976). 2013. PMID: 23446706 Free PMC 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. Scoliosis. 2007 Sep 23;2:13. doi: 10.1186/1748-7161-2-13. Scoliosis. 2007. PMID: 17888180 Free PMC article.
38 results