Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers
Nolin, Sarah L., Glicksman, Anne, Ersalesi, Nicole, Dobkin, Carl, Ted Brown, W., Cao, Ru, Blatt, Eliot, Sah, Sachin, Latham, Gary J., Hadd, Andrew G.
Published in Genetics in medicine (01.05.2015)
Published in Genetics in medicine (01.05.2015)
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A Novel FMR1 PCR Method for the Routine Detection of Low Abundance Expanded Alleles and Full Mutations in Fragile X Syndrome
Filipovic-Sadic, Stela, Sah, Sachin, Chen, Liangjing, Krosting, Julie, Sekinger, Edward, Zhang, Wenting, Hagerman, Paul J, Stenzel, Timothy T, Hadd, Andrew G, Latham, Gary J, Tassone, Flora
Published in Clinical chemistry (Baltimore, Md.) (01.03.2010)
Published in Clinical chemistry (Baltimore, Md.) (01.03.2010)
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Targeted, High-Depth, Next-Generation Sequencing of Cancer Genes in Formalin-Fixed, Paraffin-Embedded and Fine-Needle Aspiration Tumor Specimens
Hadd, Andrew G, Houghton, Jeff, Choudhary, Ashish, Sah, Sachin, Chen, Liangjing, Marko, Adam C, Sanford, Tiffany, Buddavarapu, Kalyan, Krosting, Julie, Garmire, Lana, Wylie, Dennis, Shinde, Rupali, Beaudenon, Sylvie, Alexander, Erik K, Mambo, Elizabeth, Adai, Alex T, Latham, Gary J
Published in The Journal of molecular diagnostics : JMD (01.03.2013)
Published in The Journal of molecular diagnostics : JMD (01.03.2013)
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Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles
Nolin, Sarah L., Glicksman, Anne, Tortora, Nicole, Allen, Emily, Macpherson, James, Mila, Montserrat, Vianna‐Morgante, Angela M., Sherman, Stephanie L., Dobkin, Carl, Latham, Gary J., Hadd, Andrew G.
Published in American journal of medical genetics. Part A (01.07.2019)
Published in American journal of medical genetics. Part A (01.07.2019)
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Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles
Nolin, Sarah L., Sah, Sachin, Glicksman, Anne, Sherman, Stephanie L., Allen, Emily, Berry-Kravis, Elizabeth, Tassone, Flora, Yrigollen, Carolyn, Cronister, Amy, Jodah, Marcia, Ersalesi, Nicole, Dobkin, Carl, Brown, W. Ted, Shroff, Raghav, Latham, Gary J., Hadd, Andrew G.
Published in American journal of medical genetics. Part A (01.04.2013)
Published in American journal of medical genetics. Part A (01.04.2013)
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High-resolution methylation polymerase chain reaction for fragile X analysis: Evidence for novel FMR1 methylation patterns undetected in Southern blot analyses
Chen, Liangjing, Hadd, Andrew G., Sah, Sachin, Houghton, Jeffrey F., Filipovic-Sadic, Stela, Zhang, Wenting, Hagerman, Paul J., Tassone, Flora, Latham, Gary J.
Published in Genetics in medicine (01.06.2011)
Published in Genetics in medicine (01.06.2011)
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Novel insight into mutational landscape of head and neck squamous cell carcinoma
Gaykalova, Daria A, Mambo, Elizabeth, Choudhary, Ashish, Houghton, Jeffery, Buddavarapu, Kalyan, Sanford, Tiffany, Darden, Will, Adai, Alex, Hadd, Andrew, Latham, Gary, Danilova, Ludmila V, Bishop, Justin, Li, Ryan J, Westra, William H, Hennessey, Patrick, Koch, Wayne M, Ochs, Michael F, Califano, Joseph A, Sun, Wenyue
Published in PloS one (25.03.2014)
Published in PloS one (25.03.2014)
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A Genotype-Phenotype Study of High-Resolution FMR1 Nucleic Acid and Protein Analyses in Fragile X Patients with Neurobehavioral Assessments
Budimirovic, Dejan B, Schlageter, Annette, Filipovic-Sadic, Stela, Protic, Dragana D, Bram, Eran, Mahone, E Mark, Nicholson, Kimberly, Culp, Kristen, Javanmardi, Kamyab, Kemppainen, Jon, Hadd, Andrew, Sharp, Kevin, Adayev, Tatyana, LaFauci, Giuseppe, Dobkin, Carl, Zhou, Lili, Brown, William Ted, Berry-Kravis, Elizabeth, Kaufmann, Walter E, Latham, Gary J
Published in Brain sciences (01.10.2020)
Published in Brain sciences (01.10.2020)
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The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective
Latham, Gary J, Coppinger, Justine, Hadd, Andrew G, Nolin, Sarah L
Published in Frontiers in genetics (29.07.2014)
Published in Frontiers in genetics (29.07.2014)
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Validation of Fragile X Screening in the Newborn Population Using a Fit-for-Purpose FMR1 PCR Assay System
Lee, Stacey, Taylor, Jennifer L., Redmond, Charles, Hadd, Andrew G., Kemppainen, Jon A., Haynes, Brian C., Shone, Scott, Bailey, Donald B., Latham, Gary J.
Published in The Journal of molecular diagnostics : JMD (01.03.2020)
Published in The Journal of molecular diagnostics : JMD (01.03.2020)
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AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission
Yrigollen, Carolyn M, Martorell, Loreto, Durbin-Johnson, Blythe, Naudo, Montserrat, Genoves, Jordi, Murgia, Alessandra, Polli, Roberta, Zhou, Lili, Barbouth, Deborah, Rupchock, Abigail, Finucane, Brenda, Latham, Gary J, Hadd, Andrew, Berry-Kravis, Elizabeth, Tassone, Flora
Published in Journal of neurodevelopmental disorders (30.07.2014)
Published in Journal of neurodevelopmental disorders (30.07.2014)
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Absence of AGG Interruptions Is a Risk Factor for Full Mutation Expansion Among Israeli FMR1 Premutation Carriers
Domniz, Noam, Ries-Levavi, Liat, Cohen, Yoram, Marom-Haham, Lilach, Berkenstadt, Michal, Pras, Elon, Glicksman, Anne, Tortora, Nicole, Latham, Gary J, Hadd, Andrew G, Nolin, Sarah L, Elizur, Shai E
Published in Frontiers in genetics (13.12.2018)
Published in Frontiers in genetics (13.12.2018)
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Correction: Novel Insight into Mutational Landscape of Head and Neck Squamous Cell Carcinoma
Gaykalova, Daria A, Mambo, Elizabeth, Choudhary, Ashish, Houghton, Jeffery, Buddavarapu, Kalyan, Sanford, Tiffany, Darden, Will, Adai, Alex, Hadd, Andrew, Latham, Gary, Danilova, Ludmila V, Bishop, Justin, Li, Ryan J, Westra, William H, Hennessey, Patrick, Koch, Wayne M, Ochs, Michael F, Califano, Joseph A, Sun, Wenyue
Published in PloS one (13.05.2020)
Published in PloS one (13.05.2020)
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A Novel Methylation PCR that Offers Standardized Determination of FMR1 Methylation and CGG Repeat Length without Southern Blot Analysis
Grasso, Marina, Boon, Elles M.J, Filipovic-Sadic, Stela, van Bunderen, Patrick A, Gennaro, Elena, Cao, Ru, Latham, Gary J, Hadd, Andrew G, Coviello, Domenico A
Published in The Journal of molecular diagnostics : JMD (2014)
Published in The Journal of molecular diagnostics : JMD (2014)
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A methylation PCR method determines FMR1 activation ratios and differentiates premutation allele mosaicism in carrier siblings
Hadd, Andrew G, Filipovic-Sadic, Stela, Zhou, Lili, Williams, Arianna, Latham, Gary J, Berry-Kravis, Elizabeth, Hall, Deborah A
Published in Clinical epigenetics (01.12.2016)
Published in Clinical epigenetics (01.12.2016)
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Bacterial Rhodopsin: Evidence for a New Type of Phototrophy in the Sea
Béjà, Oded, Aravind, L., Koonin, Eugene V., Suzuki, Marcelino T., Hadd, Andrew, Nguyen, Linh P., Jovanovich, Stevan B., Gates, Christian M., Feldman, Robert A., Spudich, John L., Spudich, Elena N., DeLong, Edward F.
Published in Science (American Association for the Advancement of Science) (15.09.2000)
Published in Science (American Association for the Advancement of Science) (15.09.2000)
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Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies
Houghton, Jeffrey, Hadd, Andrew G, Zeigler, Robert, Haynes, Brian C, Latham, Gary J
Published in Journal of visualized experiments (11.04.2016)
Published in Journal of visualized experiments (11.04.2016)
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X-inactivation in the clinical phenotype of fragile X premutation carrier sisters
Hall, Deborah A, Robertson-Dick, Erin E, O'Keefe, Joan A, Hadd, Andrew G, Zhou, Lili, Berry-Kravis, Elizabeth
Published in Neurology. Genetics (01.02.2016)
Published in Neurology. Genetics (01.02.2016)
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