Latham GJ - Search Results

1

Validation of Fragile X Screening in the Newborn Population Using a Fit-for-Purpose FMR1 PCR Assay System.

Lee S, Taylor JL, Redmond C, Hadd AG, Kemppainen JA, Haynes BC, Shone S, Bailey DB Jr, Latham GJ. Lee S, et al. Among authors: latham gj. J Mol Diagn. 2020 Mar;22(3):346-354. doi: 10.1016/j.jmoldx.2019.11.002. Epub 2019 Dec 19. J Mol Diagn. 2020. PMID: 31866572 Free PMC article.

2

An information-rich CGG repeat primed PCR that detects the full range of fragile X expanded alleles and minimizes the need for southern blot analysis.

Chen L, Hadd A, Sah S, Filipovic-Sadic S, Krosting J, Sekinger E, Pan R, Hagerman PJ, Stenzel TT, Tassone F, Latham GJ. Chen L, et al. Among authors: latham gj. J Mol Diagn. 2010 Sep;12(5):589-600. doi: 10.2353/jmoldx.2010.090227. Epub 2010 Jul 8. J Mol Diagn. 2010. PMID: 20616364 Free PMC article.

3

Targeted, high-depth, next-generation sequencing of cancer genes in formalin-fixed, paraffin-embedded and fine-needle aspiration tumor specimens.

Hadd AG, Houghton J, Choudhary A, Sah S, Chen L, Marko AC, Sanford T, Buddavarapu K, Krosting J, Garmire L, Wylie D, Shinde R, Beaudenon S, Alexander EK, Mambo E, Adai AT, Latham GJ. Hadd AG, et al. Among authors: latham gj. J Mol Diagn. 2013 Mar;15(2):234-47. doi: 10.1016/j.jmoldx.2012.11.006. Epub 2013 Jan 13. J Mol Diagn. 2013. PMID: 23321017 Free article.

4

A novel methylation PCR that offers standardized determination of FMR1 methylation and CGG repeat length without southern blot analysis.

Grasso M, Boon EM, Filipovic-Sadic S, van Bunderen PA, Gennaro E, Cao R, Latham GJ, Hadd AG, Coviello DA. Grasso M, et al. Among authors: latham gj. J Mol Diagn. 2014 Jan;16(1):23-31. doi: 10.1016/j.jmoldx.2013.09.004. Epub 2013 Oct 29. J Mol Diagn. 2014. PMID: 24177047 Free PMC article.

5

A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome.

Filipovic-Sadic S, Sah S, Chen L, Krosting J, Sekinger E, Zhang W, Hagerman PJ, Stenzel TT, Hadd AG, Latham GJ, Tassone F. Filipovic-Sadic S, et al. Among authors: latham gj. Clin Chem. 2010 Mar;56(3):399-408. doi: 10.1373/clinchem.2009.136101. Epub 2010 Jan 7. Clin Chem. 2010. PMID: 20056738 Free PMC article.

6

High-resolution methylation polymerase chain reaction for fragile X analysis: evidence for novel FMR1 methylation patterns undetected in Southern blot analyses.

Chen L, Hadd A, Sah S, Houghton JF, Filipovic-Sadic S, Zhang W, Hagerman PJ, Tassone F, Latham GJ. Chen L, et al. Among authors: latham gj. Genet Med. 2011 Jun;13(6):528-538. doi: 10.1097/GIM.0b013e31820a780f. Genet Med. 2011. PMID: 21430544 Free PMC article.

7

Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers.

Nolin SL, Glicksman A, Ersalesi N, Dobkin C, Brown WT, Cao R, Blatt E, Sah S, Latham GJ, Hadd AG. Nolin SL, et al. Among authors: latham gj. Genet Med. 2015 May;17(5):358-64. doi: 10.1038/gim.2014.106. Epub 2014 Sep 11. Genet Med. 2015. PMID: 25210937 Free article.

8

Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies.

Houghton J, Hadd AG, Zeigler R, Haynes BC, Latham GJ. Houghton J, et al. Among authors: latham gj. J Vis Exp. 2016 Apr 11;(110):e53836. doi: 10.3791/53836. J Vis Exp. 2016. PMID: 27166994 Free PMC article.

9

A methylation PCR method determines FMR1 activation ratios and differentiates premutation allele mosaicism in carrier siblings.

Hadd AG, Filipovic-Sadic S, Zhou L, Williams A, Latham GJ, Berry-Kravis E, Hall DA. Hadd AG, et al. Among authors: latham gj. Clin Epigenetics. 2016 Dec 1;8:130. doi: 10.1186/s13148-016-0280-8. eCollection 2016. Clin Epigenetics. 2016. PMID: 27980694 Free PMC article.

10

Comprehensive genotyping of the C9orf72 hexanucleotide repeat region in 2095 ALS samples from the NINDS collection using a two-mode, long-read PCR assay.

Bram E, Javanmardi K, Nicholson K, Culp K, Thibert JR, Kemppainen J, Le V, Schlageter A, Hadd A, Latham GJ. Bram E, et al. Among authors: latham gj. Amyotroph Lateral Scler Frontotemporal Degener. 2019 Feb;20(1-2):107-114. doi: 10.1080/21678421.2018.1522353. Epub 2018 Nov 15. Amyotroph Lateral Scler Frontotemporal Degener. 2019. PMID: 30430876 Free PMC article.

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