Rhodenizer D[Author] - Search Results

Year	Number of Results
2008	1
2009	2
2011	1
2012	2
2013	2
2014	1
2024	0

1

DDOST mutations identified by whole-exome sequencing are implicated in congenital disorders of glycosylation.

Jones MA, Ng BG, Bhide S, Chin E, Rhodenizer D, He P, Losfeld ME, He M, Raymond K, Berry G, Freeze HH, Hegde MR. Jones MA, et al. Among authors: rhodenizer d. Am J Hum Genet. 2012 Feb 10;90(2):363-8. doi: 10.1016/j.ajhg.2011.12.024. Epub 2012 Feb 2. Am J Hum Genet. 2012. PMID: 22305527 Free PMC article.

2

Comprehensive mutation analysis for congenital muscular dystrophy: a clinical PCR-based enrichment and next-generation sequencing panel.

Valencia CA, Ankala A, Rhodenizer D, Bhide S, Littlejohn MR, Keong LM, Rutkowski A, Sparks S, Bonnemann C, Hegde M. Valencia CA, et al. Among authors: rhodenizer d. PLoS One. 2013;8(1):e53083. doi: 10.1371/journal.pone.0053083. Epub 2013 Jan 11. PLoS One. 2013. PMID: 23326386 Free PMC article.

3

A forward genetic screen in Drosophila implicates insulin signaling in age-related locomotor impairment.

Jones MA, Gargano JW, Rhodenizer D, Martin I, Bhandari P, Grotewiel M. Jones MA, et al. Among authors: rhodenizer d. Exp Gerontol. 2009 Aug;44(8):532-40. doi: 10.1016/j.exger.2009.05.007. Epub 2009 May 28. Exp Gerontol. 2009. PMID: 19481596 Free PMC article.

4

Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophy.

Valencia CA, Rhodenizer D, Bhide S, Chin E, Littlejohn MR, Keong LM, Rutkowski A, Bonnemann C, Hegde M. Valencia CA, et al. Among authors: rhodenizer d. J Mol Diagn. 2012 May-Jun;14(3):233-46. doi: 10.1016/j.jmoldx.2012.01.009. Epub 2012 Mar 16. J Mol Diagn. 2012. PMID: 22426012 Free PMC article.

5

Targeted polymerase chain reaction-based enrichment and next generation sequencing for diagnostic testing of congenital disorders of glycosylation.

Jones MA, Bhide S, Chin E, Ng BG, Rhodenizer D, Zhang VW, Sun JJ, Tanner A, Freeze HH, Hegde MR. Jones MA, et al. Among authors: rhodenizer d. Genet Med. 2011 Nov;13(11):921-32. doi: 10.1097/GIM.0b013e318226fbf2. Genet Med. 2011. PMID: 21811164 Free PMC article.

6

Molecular diagnostic testing for congenital disorders of glycosylation (CDG): detection rate for single gene testing and next generation sequencing panel testing.

Jones MA, Rhodenizer D, da Silva C, Huff IJ, Keong L, Bean LJ, Coffee B, Collins C, Tanner AK, He M, Hegde MR. Jones MA, et al. Among authors: rhodenizer d. Mol Genet Metab. 2013 Sep-Oct;110(1-2):78-85. doi: 10.1016/j.ymgme.2013.05.012. Epub 2013 May 28. Mol Genet Metab. 2013. PMID: 23806237

7

Sod2 knockdown in the musculature has whole-organism consequences in Drosophila.

Martin I, Jones MA, Rhodenizer D, Zheng J, Warrick JM, Seroude L, Grotewiel M. Martin I, et al. Among authors: rhodenizer d. Free Radic Biol Med. 2009 Sep 15;47(6):803-13. doi: 10.1016/j.freeradbiomed.2009.06.021. Epub 2009 Jun 21. Free Radic Biol Med. 2009. PMID: 19545620 Free PMC article.

8

Genetic and environmental factors impact age-related impairment of negative geotaxis in Drosophila by altering age-dependent climbing speed.

Rhodenizer D, Martin I, Bhandari P, Pletcher SD, Grotewiel M. Rhodenizer D, et al. Exp Gerontol. 2008 Aug;43(8):739-48. doi: 10.1016/j.exger.2008.04.011. Epub 2008 Apr 27. Exp Gerontol. 2008. PMID: 18515028 Free PMC article.

9

Development and performance of a comprehensive targeted sequencing assay for pan-ethnic screening of carrier status.

Tanner AK, Valencia CA, Rhodenizer D, Espirages M, Da Silva C, Borsuk L, Caldwell S, Gregg E, Grimes E, Lichanska AM, Morris L, Purkayastha A, Weslowski B, Tibbetts C, Lorence MC, Hegde M. Tanner AK, et al. Among authors: rhodenizer d. J Mol Diagn. 2014 May;16(3):350-60. doi: 10.1016/j.jmoldx.2013.12.003. Epub 2014 Feb 8. J Mol Diagn. 2014. PMID: 24517888 Free article.

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