Tartaglia, Nicole
Children's Hospital Colorado · University of Colorado Anschutz
7 papers on CoChatORCID 0000-0002-8529-6722
Most cited papers
- Verified
Advances in the Treatment of Fragile X Syndrome
Hagerman, R. J., Berry-Kravis, E., Kaufmann, W. E., Ono, M. Y., Tartaglia, N., Lachiewicz, A., Kronk, R., Delahunty, C., Hessl, D., Visootsak, J., et al. (2009) · Pediatrics
Genetics and Neurodevelopmental DisordersGenetic Neurodegenerative Diseases
Cited by 596
- Verified
Blockade of interleukin-1 induced hyperthermia by subdiaphragmatic vagotomy: evidence for vagal mediation of immune-brain communication
Watkins, L. R., Goehler, L. E., Relton, J. K., Tartaglia, N., Silbert, L., Martin, D., & Maier, S. F. (1995) · Neuroscience Letters
Vagus Nerve Stimulation ResearchThermal Regulation in Medicine
Cited by 516
- Verified
Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy
Ottesen, A. M., Aksglaede, L., Garn, I., Tartaglia, N., Tassone, F., Gravholt, C. H., Bojesen, A., Sørensen, K., Jørgensen, N., Rajpert‐De Meyts, E., et al. (2010) · American Journal of Medical Genetics Part A
Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesSexual Differentiation and Disorders
Cited by 219
- Verified
Behavioral and Social Phenotypes in Boys With 47,XYY Syndrome or 47,XXY Klinefelter Syndrome
Ross, J. L., Roeltgen, D. P., Kushner, H., Zinn, A. R., Reiss, A., Bardsley, M. Z., McCauley, E., & Tartaglia, N. (2012) · Pediatrics
Sexual Differentiation and DisordersGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Cited by 185
- Verified
Metformin as targeted treatment in fragile X syndrome
Dy, A. B. C., Tassone, F., Eldeeb, M., Salcedo‐Arellano, M. J., Tartaglia, N., & Hagerman, R. (2018) · Clinical Genetics
Genetics and Neurodevelopmental DisordersGenetic Syndromes and Imprinting
Cited by 124
- Verified
A double-blind, randomized, placebo-controlled clinical study of trofinetide in the treatment of fragile X syndrome
Berry-Kravis, E., Horrigan, J. P., Tartaglia, N., Hagerman, R., Kolevzon, A., Erickson, C. A., Hatti, S., Snape, M., Yaroshinsky, A., Stoms, G., et al. (2020) · Pediatric Neurology
Genetics and Neurodevelopmental DisordersAlzheimer's disease research and treatments
Cited by 102
- Verified
Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder
García‐Nonell, C., Ratera, E. R., Harris, S., Hessl, D., Ono, M. Y., Tartaglia, N., Marvin, E., Tassone, F., & Hagerman, R. J. (2008) · American Journal of Medical Genetics Part A
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 76
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