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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Deficits in Prenatal Serine Biosynthesis Underlie the Mitochondrial Dysfunction Associated with the Autism-Linked FMR1 Gene von Nolin, Sarah L., Napoli, Eleonora, Flores, Amanda, Hagerman, Randi J., Giulivi, Cecilia

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FMR1 allelic complexity in premutation carriers provides no evidence for a correlation with age at amenorrhea von Rodrigues, Bárbara, Sousa, Vanessa, Yrigollen, Carolyn M, Tassone, Flora, Villate, Olatz, Allen, Emily G, Glicksman, Anne, Tortora, Nicole, Nolin, Sarah L, Nogueira, António J A, Jorge, Paula

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Cis-acting DNA sequence at a replication origin promotes repeat expansion to fragile X full mutation von Gerhardt, Jeannine, Zaninovic, Nikica, Zhan, Qiansheng, Madireddy, Advaitha, Nolin, Sarah L, Ersalesi, Nicole, Yan, Zi, Rosenwaks, Zev, Schildkraut, Carl L

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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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Fragile X analysis of 1112 prenatal samples from 1991 to 2010 von Nolin, Sarah L., Glicksman, Anne, Ding, Xiaohua, Ersalesi, Nicole, Brown, W. Ted, Sherman, Stephanie L., Dobkin, Carl

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Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles von Nolin, Sarah L., Brown, W. Ted, Glicksman, Anne, Houck, Jr, George E., Gargano, Alice D., Sullivan, Amy, Biancalana, Valérie, Bröndum-Nielsen, Karen, Hjalgrim, Helle, Holinski-Feder, Elke, Kooy, Frank, Longshore, John, Macpherson, James, Mandel, Jean-Louis, Matthijs, Gert, Rousseau, Francois, Steinbach, Peter, Väisänen, Marja-Leena, von Koskull, Harriet, Sherman, Stephanie L.

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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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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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FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation von Allen, Emily G, Glicksman, Anne, Tortora, Nicole, Charen, Krista, He, Weiya, Amin, Ashima, Hipp, Heather, Shubeck, Lisa, Nolin, Sarah L, Sherman, Stephanie L

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The Fragile X Mental Retardation Protein FMRP Binds Elongation Factor 1A mRNA and Negatively Regulates Its Translation in Vivo von Sung, Ying Ju, Dolzhanskaya, Natalia, Nolin, Sarah L., Brown, Ted, Currie, Julia R., Denman, Robert B.

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Refining the risk for fragile X–associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size von Allen, Emily Graves, Charen, Krista, Hipp, Heather S., Shubeck, Lisa, Amin, Ashima, He, Weiya, Nolin, Sarah L., Glicksman, Anne, Tortora, Nicole, McKinnon, Bonnie, Shelly, Katharine E., Sherman, Stephanie L.

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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 syndrome in a male with methylated premutation alleles and no detectable methylated full mutation alleles von Hayward, Bruce, Loutaev, Inna, Ding, Xiaohua, Nolin, Sarah L., Thurm, Audrey, Usdin, Karen, Smith, Carolyn B.

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Orientation Specificity in Representations of Place von Sholl, M. Jeanne, Nolin, Tina L

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Familial transmission of the FMR1 CGG repeat von NOLIN, S. L, LEWIS, F. A, SHERMAN, S. L, BROWN, W. T, LING LING YE, HOUCK, G. E, GLICKSMAN, A. E, LIMPRASERT, P, SHU YUN LI, ZHONG, N, ASHLEY, A. E, FEINGOLD, E

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Global transcriptome dysregulation in second trimester fetuses with FMR1 expansions von Zwemer, Lillian M., Nolin, Sarah L., Okamoto, Patricia M., Eisenberg, Marcia, Wick, Heather C., Bianchi, Diana W.

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Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis von Qiao, Ying, Liu, Xudong, Harvard, Chansonette, Nolin, Sarah L, Brown, W Ted, Koochek, Maryam, Holden, Jeanette J A, Lewis, M E Suzanne, Rajcan-Separovic, Evica

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Fragile X protein in newborn dried blood spots von Adayev, Tatyana, LaFauci, Giuseppe, Dobkin, Carl, Caggana, Michele, Wiley, Veronica, Field, Michael, Wotton, Tiffany, Kascsak, Richard, Nolin, Sarah L, Glicksman, Anne, Hosmer, Nicole, Brown, W Ted

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Stoichiometry of dissolved organic matter dynamics on the continental shelf of the northeastern U.S.A von Hopkinson, Charles S., Fry, Brian, Nolin, Amy L.

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