Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers von Nolin, Sarah L., Glicksman, Anne, Ersalesi, Nicole, Dobkin, Carl, Ted Brown, W., Cao, Ru, Blatt, Eliot, Sah, Sachin, Latham, Gary J., Hadd, Andrew G.

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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 von 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

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Targeted, High-Depth, Next-Generation Sequencing of Cancer Genes in Formalin-Fixed, Paraffin-Embedded and Fine-Needle Aspiration Tumor Specimens von 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

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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 von Chen, Liangjing, Hadd, Andrew G., Sah, Sachin, Houghton, Jeffrey F., Filipovic-Sadic, Stela, Zhang, Wenting, Hagerman, Paul J., Tassone, Flora, Latham, Gary J.

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

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Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles von 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.

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

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

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Novel insight into mutational landscape of head and neck squamous cell carcinoma von 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

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

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Validation of Fragile X Screening in the Newborn Population Using a Fit-for-Purpose FMR1 PCR Assay System von Lee, Stacey, Taylor, Jennifer L., Redmond, Charles, Hadd, Andrew G., Kemppainen, Jon A., Haynes, Brian C., Shone, Scott, Bailey, Donald B., Latham, Gary J.

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

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Bacterial Rhodopsin: Evidence for a New Type of Phototrophy in the Sea von 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.

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Microchip Device for Performing Enzyme Assays von Hadd, Andrew G, Raymond, Daniel E, Halliwell, John W, Jacobson, Stephen C, Ramsey, J. Michael

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Correction: Novel Insight into Mutational Landscape of Head and Neck Squamous Cell Carcinoma von 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

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A Novel Methylation PCR that Offers Standardized Determination of FMR1 Methylation and CGG Repeat Length without Southern Blot Analysis von 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

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Microfluidic Assays of Acetylcholinesterase Inhibitors von Hadd, Andrew G, Jacobson, Stephen C, Ramsey, J. Michael

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A methylation PCR method determines FMR1 activation ratios and differentiates premutation allele mosaicism in carrier siblings von Hadd, Andrew G, Filipovic-Sadic, Stela, Zhou, Lili, Williams, Arianna, Latham, Gary J, Berry-Kravis, Elizabeth, Hall, Deborah A

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Dual-Mode Single-Molecule Fluorescence Assay for the Detection of Expanded CGG Repeats in Fragile X Syndrome von Cannon, Brian, Pan, Cynthia, Chen, Liangjing, Hadd, Andrew G, Russell, Rick

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

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