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Reduced RNA expression of the FMR1 gene in women with low (CGGn<26) repeats
Wang, Qi, Barad, David H., Darmon, Sarah K., Kushnir, Vitaly A., Wu, Yan-Guang, Lazzaroni-Tealdi, Emanuela, Zhang, Lin, Albertini, David F., Gleicher, Norbert
Published in PloS one (21.12.2018)
Published in PloS one (21.12.2018)
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Clinical implications of somatic allele expansion in female FMR1 premutation carriers
Aishworiya, Ramkumar, Hwang, Ye Hyun, Santos, Ellery, Hayward, Bruce, Usdin, Karen, Durbin-Johnson, Blythe, Hagerman, Randi, Tassone, Flora
Published in Scientific reports (29.04.2023)
Published in Scientific reports (29.04.2023)
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Fmr1 and Nlgn3 knockout rats: novel tools for investigating autism spectrum disorders
Hamilton, Shannon M, Green, Jennie R, Veeraragavan, Surabi, Yuva, Lisa, McCoy, Aaron, Wu, Yumei, Warren, Joe, Little, Lara, Ji, Diana, Cui, Xiaoxia, Weinstein, Edward, Paylor, Richard
Published in Behavioral neuroscience (01.04.2014)
Published in Behavioral neuroscience (01.04.2014)
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Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056
Jacquemont, Sébastien, Curie, Aurore, des Portes, Vincent, Torrioli, Maria Giulia, Berry-Kravis, Elizabeth, Hagerman, Randi J, Ramos, Feliciano J, Cornish, Kim, He, Yunsheng, Paulding, Charles, Neri, Giovanni, Chen, Fei, Hadjikhani, Nouchine, Martinet, Danielle, Meyer, Joanne, Beckmann, Jacques S, Delange, Karine, Brun, Amandine, Bussy, Gerald, Gasparini, Fabrizio, Hilse, Talita, Floesser, Annette, Branson, Janice, Bilbe, Graeme, Johns, Donald, Gomez-Mancilla, Baltazar
Published in Science translational medicine (05.01.2011)
Published in Science translational medicine (05.01.2011)
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Deletion of Fmr1 results in sex‐specific changes in behavior
Nolan, Suzanne O., Reynolds, Conner D., Smith, Gregory D., Holley, Andrew J., Escobar, Brianna, Chandler, Matthew A., Volquardsen, Megan, Jefferson, Taylor, Pandian, Ashvini, Smith, Tileena, Huebschman, Jessica, Lugo, Joaquin N.
Published in Brain and behavior (01.10.2017)
Published in Brain and behavior (01.10.2017)
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Involvement of the Cerebellar Peduncles in FMR1 Premutation Carriers: A Pictorial Review of Their Anatomy, Imaging, and Pathology
Paracuellos-Ayala, Irene, Caruana, Giovanni, Reyes Ortega, Macarena Maria, Hagerman, Randi J., Wang, Jun Yi, Rodriguez-Revenga, Laia, Elias-Mas, Andrea
Published in International journal of molecular sciences (06.05.2025)
Published in International journal of molecular sciences (06.05.2025)
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Effects of Fmr1 Gene Mutations on Sex Differences in Autism-Like Behavior and Dendritic Spine Development in Mice and Transcriptomic Studies
Wang, Zhao, Qiao, Dan, Chen, Huan, Zhang, Shihua, Zhang, Bohan, Zhang, Jingbao, Hu, Xiangting, Wang, Chang, Cui, Huixian, Wang, Xia, Li, Sha
Published in Neuroscience (01.12.2023)
Published in Neuroscience (01.12.2023)
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Fragile-X–Associated Tremor/Ataxia Syndrome (FXTAS) in Females with the FMR1 Premutation
Hagerman, R.J., Leavitt, B.R., Farzin, F., Jacquemont, S., Greco, C.M., Brunberg, J.A., Tassone, F., Hessl, D., Harris, S.W., Zhang, L., Jardini, T., Gane, L.W., Ferranti, J., Ruiz, L., Leehey, M.A., Grigsby, J., Hagerman, P.J.
Published in American journal of human genetics (01.05.2004)
Published in American journal of human genetics (01.05.2004)
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A single early-life seizure results in long-term behavioral changes in the adult Fmr1 knockout mouse
Hodges, Samantha L., Reynolds, Conner D., Nolan, Suzanne O., Huebschman, Jessica L., Okoh, James T., Binder, Matthew S., Lugo, Joaquin N.
Published in Epilepsy research (01.11.2019)
Published in Epilepsy research (01.11.2019)
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FMR1 and the fragile X syndrome: Human genome epidemiology review
Crawford, Dana C., Acuña, Juan M., Sherman, Stephanie L.
Published in Genetics in medicine (01.09.2001)
Published in Genetics in medicine (01.09.2001)
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FMR1 gray-zone alleles: Association with Parkinson's disease in women?
Hall, Deborah A., Berry-Kravis, Elizabeth, Zhang, Wenting, Tassone, Flora, Spector, Elaine, Zerbe, Gary, Hagerman, Paul J., Ouyang, Bichun, Leehey, Maureen A.
Published in Movement disorders (15.08.2011)
Published in Movement disorders (15.08.2011)
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