Hadd A[au] - Search Results

Year	Number of Results
1996	1
1997	1
2000	4
2004	1
2005	1
2006	1
2010	3
2011	2
2012	2
2013	4
2014	10
2015	1
2016	3
2017	1
2018	2
2019	4
2020	3
2022	0

1

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: hadd ag. 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.

2

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: hadd ag. 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.

3

Structural diversity and protein engineering of the aminoacyl-tRNA synthetases.

Perona JJ, Hadd A. Perona JJ, et al. Among authors: hadd a. Biochemistry. 2012 Nov 6;51(44):8705-29. doi: 10.1021/bi301180x. Epub 2012 Oct 26. Biochemistry. 2012. PMID: 23075299 Review.

4

A Genotype-Phenotype Study of High-Resolution FMR1 Nucleic Acid and Protein Analyses in Fragile X Patients with Neurobehavioral Assessments.

Budimirovic DB, Schlageter A, Filipovic-Sadic S, Protic DD, Bram E, Mahone EM, Nicholson K, Culp K, Javanmardi K, Kemppainen J, Hadd A, Sharp K, Adayev T, LaFauci G, Dobkin C, Zhou L, Brown WT, Berry-Kravis E, Kaufmann WE, Latham GJ. Budimirovic DB, et al. Among authors: hadd a. Brain Sci. 2020 Sep 30;10(10):694. doi: 10.3390/brainsci10100694. Brain Sci. 2020. PMID: 33008014 Free PMC article.

5

The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective.

Latham GJ, Coppinger J, Hadd AG, Nolin SL. Latham GJ, et al. Among authors: hadd ag. Front Genet. 2014 Jul 29;5:244. doi: 10.3389/fgene.2014.00244. eCollection 2014. Front Genet. 2014. PMID: 25120560 Free PMC article. Review.

6

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: hadd ag. 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.

7

Absence of AGG Interruptions Is a Risk Factor for Full Mutation Expansion Among Israeli FMR1 Premutation Carriers.

Domniz N, Ries-Levavi L, Cohen Y, Marom-Haham L, Berkenstadt M, Pras E, Glicksman A, Tortora N, Latham GJ, Hadd AG, Nolin SL, Elizur SE. Domniz N, et al. Among authors: hadd ag. Front Genet. 2018 Dec 13;9:606. doi: 10.3389/fgene.2018.00606. eCollection 2018. Front Genet. 2018. PMID: 30619448 Free PMC article.

8

Adoption of array technologies into the clinical laboratory.

Hadd AG, Brown JT, Andruss BF, Ye F, WalkerPeach CR. Hadd AG, et al. Expert Rev Mol Diagn. 2005 May;5(3):409-20. doi: 10.1586/14737159.5.3.409. Expert Rev Mol Diagn. 2005. PMID: 15934817 Review.

9

Fungible Correlation Matrices.

Hadd A. Hadd A. Multivariate Behav Res. 2019 Jan-Feb;54(1):156. doi: 10.1080/00273171.2018.1562323. Epub 2019 Feb 8. Multivariate Behav Res. 2019. PMID: 30736702 No abstract available.

10

X-inactivation in the clinical phenotype of fragile X premutation carrier sisters.

Hall DA, Robertson-Dick EE, O'Keefe JA, Hadd AG, Zhou L, Berry-Kravis E. Hall DA, et al. Among authors: hadd ag. Neurol Genet. 2016 Feb 3;2(1):e45. doi: 10.1212/NXG.0000000000000045. eCollection 2016 Feb. Neurol Genet. 2016. PMID: 27066582 Free PMC article.

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