Selected Publications

Garvey MH, Nash T, Kippenhan JS, Kohn P, Mervis CB, Eisenberg DP, Ye J, Gregory MD, Berman KF. : Contrasting neurofunctional correlates of face- and visuospatial-processing in children and adolescents with Williams syndrome: convergent results from four fMRI paradigms. Sci Rep. 14(1): 10304, May 2024.

S.-M. Wei, Gregory, M. D., Nash, T., Gouvea, A. deA. E., Mervis, C. B., Garvey, M. H., Cole, K. M., Kippenhan, J. S., Eisenberg, D. P., Kolachana, B., Schmidt, P. J., & Berman, K. F. : Altered pubertal timing in 7q11.23 copy number variations and associated genetic mechanisms. iScience. 27(3), Mar 2024.

Iadarola, M. J., Sapio, M. R., Loydpierson, A. J., Mervis, C. B., Fehrenbacher, J. C., Vasko. M. R., Maric, D., Eisenberg, D. P., Nash, T. A., Kippenhan, J. S., Garvey, M. H., Mannes, A. J., Gregory, M. D., & Berman, K. F. : Syntaxin1A overexpression and pain insensitivity in individuals with 7q11.23 duplication syndrome. JCI Insight. 22(4): e176147, Feb 2024.

Liu, D., Billington, C. J. Jr., Raja, N., Wong, Z. C., Levin, M.D., Resch, W., Alba, C., Hupalo, D. N., Biamino, E., Bedeschi, M. F., Digilio, M. C., Squeo, G. M., Villa, R., Parrish, P.C. R., Knutsen, R. H., Osgood, S., Freeman, J. A., Dalgard, C. L., Merla, G., Pober, B. R., Mervis, C. B., Roberts, A. E., Morris, C. A., Osborne, L. R., & Kozel, B. A. : Matrisome and immune pathways contribute to extreme vascular outcomes in Williams-Beuren syndrome. J Am Heart Assoc. 13(3): e031377, Feb 2024.

Guimaraes VN, Mervis CB. : Concurrent predictors of mathematics achievement for 9-year-old children with Williams syndrome. Sci Rep. 14(1): 2454, Jan 2024.

Gregory, M. D., Jabbi, M., Kippenhan, J. S., Nash, T., Garvey, M. H., Eisenberg, D. P., Wei, S.-M., Kohn, P., Kolachana, B., Mervis, C. B., & Berman: Williams syndrome hemideletion and GTF2I sequence variation relate to insula structure and function. Proc OHBM 2024 Notes: Poster.

Kippenhan, J. S., Gregory, M. D., Eisenberg, D. P., Nash, T. A,, Mervis, C. B., Kolachana, B., Wright, D., Garvey, M. H., Kohn, P., & Berman, K. F.: Prefrontal cortex-based schizophrenia phenotypes linked to variation in Williams syndrome gene LIMK1. Proc OHBM 2024 Notes: Poster.

Garvey, M. H., Nash, T., Kippenhan, J. S., Kohn, P., Mervis, C. B., Eisenberg, D. P., Ilsley, A., Keleman, A., Spurney, M., Chavannes, A., Gregory, M. D., & Berman, K. F, : Impact of copy number variation of the 7q11.23 Williams syndrome critical region on brain structure. Proc OHBM 2024 Notes: Poster.

Bookless, M., Severance, B., Simons, K., Guimaraes, V. N., Becerra, A. M., Velleman, S. L., & Mervis, C. B. : Mean babble level and canonical babble ratio: Relationships to vocabulary in Williams syndrome. Proc ASLHA Proc ASLHA 2024 Notes: Poster.

Keleman, A. G., Nash, T. A., Kippenhan, J. S., Gregory, M. D,, Raymond, C. B.,, Garvey, M. H., Kohn, P.D., Eisenberg, D. P., Wei, S.-M., Mervis, C. B., & Berman, K. F. : Changes in myelination of the human brain from childhood through early adulthood in people with rare 7q11.23 copy number variations as measured with quantitative myelin water imaging. Proc Flux 2024 Notes: Poster.