Latham GJ - Search Results

1

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.

2

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.

3

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.

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

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.

6

CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles.

Pretto DI, Mendoza-Morales G, Lo J, Cao R, Hadd A, Latham GJ, Durbin-Johnson B, Hagerman R, Tassone F. Pretto DI, et al. Among authors: latham gj. J Med Genet. 2014 May;51(5):309-18. doi: 10.1136/jmedgenet-2013-102021. Epub 2014 Mar 3. J Med Genet. 2014. PMID: 24591415 Free PMC article.

7

AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission.

Yrigollen CM, Martorell L, Durbin-Johnson B, Naudo M, Genoves J, Murgia A, Polli R, Zhou L, Barbouth D, Rupchock A, Finucane B, Latham GJ, Hadd A, Berry-Kravis E, Tassone F. Yrigollen CM, et al. Among authors: latham gj. J Neurodev Disord. 2014;6(1):24. doi: 10.1186/1866-1955-6-24. Epub 2014 Jul 30. J Neurodev Disord. 2014. PMID: 25110527 Free PMC article.

8

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.

9

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.

10

Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles.

Nolin SL, Glicksman A, Tortora N, Allen E, Macpherson J, Mila M, Vianna-Morgante AM, Sherman SL, Dobkin C, Latham GJ, Hadd AG. Nolin SL, et al. Among authors: latham gj. Am J Med Genet A. 2019 Jul;179(7):1148-1156. doi: 10.1002/ajmg.a.61165. Epub 2019 May 2. Am J Med Genet A. 2019. PMID: 31050164 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

94 results

Search Page