Publications by authors named "Andrew Hadd"

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Establishing a Common Lexicon for Circulating Tumor DNA Analysis and Molecular Residual Disease: Insights From the BLOODPAC Consortium.
Andrew G Hadd, Angela Silvestro, Brittany Avin McKelvey, Jonathan Baden, Christina Bormann Chung

Clin Transl Sci· March 2025

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A Genotype-Phenotype Study of High-Resolution Nucleic Acid and Protein Analyses in Fragile X Patients with Neurobehavioral Assessments.
Dejan B Budimirovic, Annette Schlageter, Stela Filipovic-Sadic, Dragana D Protic, Eran Bram, Andrew Hadd

Brain Sci· September 2020

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Correction: Novel Insight into Mutational Landscape of Head and Neck Squamous Cell Carcinoma.
Daria A Gaykalova, Elizabeth Mambo, Ashish Choudhary, Jeffery Houghton, Kalyan Buddavarapu, Andrew Hadd

PLoS One· May 2020

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Validation of Fragile X Screening in the Newborn Population Using a Fit-for-Purpose FMR1 PCR Assay System.
Stacey Lee, Jennifer L Taylor, Charles Redmond, Andrew G Hadd, Jon A Kemppainen

J Mol Diagn· March 2020

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Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles.
Sarah L Nolin, Anne Glicksman, Nicole Tortora, Emily Allen, James Macpherson, Andrew G Hadd

Am J Med Genet A· July 2019

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Comprehensive genotyping of the C9orf72 hexanucleotide repeat region in 2095 ALS samples from the NINDS collection using a two-mode, long-read PCR assay.
Eran Bram, Kamyab Javanmardi, Kimberly Nicholson, Kristen Culp, Julie R Thibert, Andrew Hadd

Amyotroph Lateral Scler Frontotemporal Degener· February 2019

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Absence of AGG Interruptions Is a Risk Factor for Full Mutation Expansion Among Israeli FMR1 Premutation Carriers.
Noam Domniz, Liat Ries-Levavi, Yoram Cohen, Lilach Marom-Haham, Michal Berkenstadt, Andrew G Hadd

Front Genet· December 2018

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A methylation PCR method determines activation ratios and differentiates premutation allele mosaicism in carrier siblings.
Andrew G Hadd, Stela Filipovic-Sadic, Lili Zhou, Arianna Williams, Gary J Latham

Clin Epigenetics· March 2017

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Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies.
Jeffrey Houghton, Andrew G Hadd, Robert Zeigler, Brian C Haynes, Gary J Latham

J Vis Exp· April 2016

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X-inactivation in the clinical phenotype of fragile X premutation carrier sisters.
Deborah A Hall, Erin E Robertson-Dick, Joan A O'Keefe, Andrew G Hadd, Lili Zhou

Neurol Genet· February 2016

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Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers.
Sarah L Nolin, Anne Glicksman, Nicole Ersalesi, Carl Dobkin, W Ted Brown, Andrew G Hadd

Genet Med· May 2015

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Recoding aminoacyl-tRNA synthetases for synthetic biology by rational protein-RNA engineering.
Andrew Hadd, John J Perona

ACS Chem Biol· December 2014

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Novel insight into mutational landscape of head and neck squamous cell carcinoma.
Daria A Gaykalova, Elizabeth Mambo, Ashish Choudhary, Jeffery Houghton, Kalyan Buddavarapu, Andrew Hadd

PLoS One· November 2014

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Evaluation of an integrated clinical workflow for targeted next-generation sequencing of low-quality tumor DNA using a 51-gene enrichment panel.
Ashish Choudhary, Elizabeth Mambo, Tiffany Sanford, Michael Boedigheimer, Brian Twomey, Andrew Hadd

BMC Med Genomics· November 2014

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Coevolution of specificity determinants in eukaryotic glutamyl- and glutaminyl-tRNA synthetases.
Andrew Hadd, John J Perona

J Mol Biol· October 2014

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AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission.
Carolyn M Yrigollen, Loreto Martorell, Blythe Durbin-Johnson, Montserrat Naudo, Jordi Genoves, Andrew Hadd

J Neurodev Disord· August 2014

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The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective.
Gary J Latham, Justine Coppinger, Andrew G Hadd, Sarah L Nolin

Front Genet· August 2014

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Intermediate CGG repeat length at the FMR1 locus is not associated with hormonal indicators of ovarian age.
Jennie K Kline, Ann M Kinney, Bruce Levin, Stephen A Brown, Andrew G Hadd

Menopause· July 2014

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CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles.
Dalyir I Pretto, Guadalupe Mendoza-Morales, Joyce Lo, Ru Cao, Andrew Hadd

J Med Genet· May 2014

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A novel methylation PCR that offers standardized determination of FMR1 methylation and CGG repeat length without southern blot analysis.
Marina Grasso, Elles M J Boon, Stela Filipovic-Sadic, Patrick A van Bunderen, Elena Gennaro, Andrew G Hadd

J Mol Diagn· January 2014

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Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles.
Sarah L Nolin, Sachin Sah, Anne Glicksman, Stephanie L Sherman, Emily Allen, Andrew G Hadd

Am J Med Genet A· April 2013

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Targeted, high-depth, next-generation sequencing of cancer genes in formalin-fixed, paraffin-embedded and fine-needle aspiration tumor specimens.
Andrew G Hadd, Jeff Houghton, Ashish Choudhary, Sachin Sah, Liangjing Chen

J Mol Diagn· March 2013

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A dual-mode single-molecule fluorescence assay for the detection of expanded CGG repeats in Fragile X syndrome.
Brian Cannon, Cynthia Pan, Liangjing Chen, Andrew G Hadd, Rick Russell

Mol Biotechnol· January 2013

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Structural diversity and protein engineering of the aminoacyl-tRNA synthetases.
John J Perona, Andrew Hadd

Biochemistry· November 2012

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Structural conservation of an ancient tRNA sensor in eukaryotic glutaminyl-tRNA synthetase.
Thomas D Grant, Edward H Snell, Joseph R Luft, Erin Quartley, Stephanie Corretore, Andrew Hadd

Nucleic Acids Res· April 2012

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