Genila M Bibat

Research Associate

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Fingerprint Dive into the research topics where Genila M Bibat is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Rett Syndrome Medicine & Life Sciences
Facioscapulohumeral Muscular Dystrophy Medicine & Life Sciences
Mutation Medicine & Life Sciences
Methyl-CpG-Binding Protein 2 Medicine & Life Sciences
Leukoencephalopathies Medicine & Life Sciences
Duchenne Muscular Dystrophy Medicine & Life Sciences
Genotype Medicine & Life Sciences
Genes Medicine & Life Sciences

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Research Output 2001 2019

Clinical trial readiness to solve barriers to drug development in FSHD (ReSolve): Protocol of a large, international, multi-center prospective study

Lorusso, S., Johnson, N. E., McDermott, M. P., Eichinger, K., Butterfield, R. J., Carraro, E., Higgs, K., Lewis, L., Mul, K., Sacconi, S., Sansone, V. A., Shieh, P., Van Engelen, B., Wagner, K., Wang, L., Statland, J. M., Tawil, R., Dimachkie, M., Pasnoor, M., Roath, K. & 32 others, McCalley, A., Currence, M., Herbelin, L., Hamel, J., Arnold, W. D., Alexander, T., Yankie, M., Kelly, K., Holmberg, B., Diaz, L., Jones, A., Butler, A., Moldt, S., Wilson, A., McIntyre, M., Leung, D., Bibat, G., Yep, M., Stinson, N., Jaworek, A., Sissons-Ross, L., Johnstone, L., Skura, C., Deguzman, D., Cornelissen, Y., Villa, L., Puma, A., Gambella, M., Shi, Y., Garcia, J., Beshiri, F. & Mauro, L., Sep 10 2019, In : BMC neurology. 19, 1, 224.

Research output: Contribution to journalArticle

Open Access
Facioscapulohumeral Muscular Dystrophy
Clinical Trials
Prospective Studies
Pharmaceutical Preparations
Outcome Assessment (Health Care)

The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy

Thangarajh, M., Kaat, A. J., Bibat, G. M., Mansour, J., Summerton, K., Gioia, A., Berger, C., Hardy, K. K. & Wagner, K. R., Jan 1 2019, (Accepted/In press) In : Annals of Clinical and Translational Neurology.

Research output: Contribution to journalArticle

Open Access
Duchenne Muscular Dystrophy
National Institutes of Health (U.S.)
Equipment and Supplies

Are dopamine receptor and transporter changes in Rett syndrome reflected in Mecp2-deficient mice?

Wong, D. F., Blue, M. E., Brasic, J. R., Nandi, A., Valentine, H., Stansfield, K. H., Rousset, O., Bibat, G. M., Yablonski, M. E., Johnston, M. V., Gjedde, A. & Naidu, S., Sep 1 2018, In : Experimental Neurology. 307, p. 74-81 8 p.

Research output: Contribution to journalArticle

Rett Syndrome
Dopamine Plasma Membrane Transport Proteins
Dopamine Receptors
Positron-Emission Tomography

Bone health in facioscapulohumeral muscular dystrophy: A cross-sectional study

Chagarlamudi, H., Corbett, A., Stoll, M., Bibat, G. M., Grosmann, C., Matichak Stock, C., Stinson, N., Shapiro, J. & Wagner, K. R., Dec 1 2017, In : Muscle and Nerve. 56, 6, p. 1108-1113 6 p.

Research output: Contribution to journalArticle

Facioscapulohumeral Muscular Dystrophy
Bone Density
Cross-Sectional Studies
Bone and Bones

Evaluation of QTc in Rett syndrome: Correlation with age, severity, and genotype

Crosson, J., Srivastava, S., Bibat, G. M., Gupta, S., Kantipuly, A., Smith-Hicks, C. L., Myers, S. M., Sanyal, A., Yenokyan, G., Brenner, J. & Naidu, S., 2017, (Accepted/In press) In : American Journal of Medical Genetics, Part A.

Research output: Contribution to journalArticle

Rett Syndrome
Sudden Death