photo of Ruth Braden

Ruth Braden

Ruth Braden

Details

Role Research Coordinator
Research area Genetics

Top Publications

  • Morison, L, Meffert, E, Stampfer, M, Steiner-Wilke, I, Vollmer, B, Schulze, K, Briggs, T, Braden, R, Vogel, AP, Thompson-Lake, D, et al. Indepth characterization of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2. 2022
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  • Braden, RO, Amor, DJ, Fisher, SE, Mei, C, Myers, CT, Mefford, H, Gill, D, Srivastava, S, Swanson, LC, Goel, H, et al. Severe speech impairment is a distinguishing feature of FOXP1‐related disorder. Developmental Medicine & Child Neurology 63(12) : 1417 -1426 2021
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  • Morgan, A, Braden, R, Wong, MMK, Colin, E, Amor, D, Liégeois, F, Srivastava, S, Vogel, A, Bizaoui, V, Ranguin, K, et al. Speech and language deficits are central to SETBP1 haploinsufficiency disorder. European Journal of Human Genetics 29(8) : 1216 -1225 2021
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  • Jansen, NA, Braden, RO, Srivastava, S, Otness, EF, Lesca, G, Rossi, M, Nizon, M, Bernier, RA, Quelin, C, van Haeringen, A, et al. Clinical delineation of SETBP1 haploinsufficiency disorder. European Journal of Human Genetics 29(8) : 1198 -1205 2021
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  • Braden, RO, Boyce, JO, Stutterd, CA, Pope, K, Goel, H, Leventer, RJ, Scheffer, IE, Morgan, AT. Speech, Language, and Oromotor Skills in Patients With Polymicrogyria.. Neurology 96(14) : e1898 -e1912 2021
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