Morissette, Rachel
National Institutes of Health · National Institutes of Health Clinical Center
7 papers on CoChatORCID 0000-0002-1591-5364
Most cited papers
- VerifiedRetracted
RETRACTED ARTICLE: sFRP2 in the aged microenvironment drives melanoma metastasis and therapy resistance
Kaur, A., Webster, M. R., Marchbank, K., Behera, R., Ndoye, A., Kugel, C. H., Dang, V. M., Appleton, J., O’Connell, M. P., Cheng, P., et al. (2016) · Nature
Melanoma and MAPK PathwaysWnt/β-catenin signaling in development and cancer
Cited by 398
- Verified
Revisiting the prevalence of nonclassic congenital adrenal hyperplasia in US Ashkenazi Jews and Caucasians
Hannah-Shmouni, F., Morissette, R., Sinaii, N., Elman, M., Prezant, T. R., Chen, W., Pulver, A., & Merke, D. P. (2017) · Genetics in Medicine
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 141
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Tenascin-X Haploinsufficiency Associated with Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia
Merke, D. P., Chen, W., Morissette, R., Xu, Z., Van Ryzin, C., Sachdev, V., Hannoush, H., Shanbhag, S. M., Acevedo, A. T., Nishitani, M., et al. (2013) · The Journal of Clinical Endocrinology & Metabolism
Sexual Differentiation and DisordersConnective tissue disorders research
Cited by 82
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Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia
Morissette, R., Chen, W., Perritt, A. F., Dreiling, J. L., Arai, A. E., Sachdev, V., Hannoush, H., Mallappa, A., Xu, Z., McDonnell, N. B., et al. (2015) · The Journal of Clinical Endocrinology & Metabolism
Connective tissue disorders researchSexual Differentiation and Disorders
Cited by 68
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Transforming growth factor-β and inflammation in vascular (type IV) Ehlers-Danlos syndrome
Morissette, R., Schoenhoff, F., Xu, Z., Shilane, D. A., Griswold, B. F., Chen, W., Yang, J., Zhu, J., Fert-Bober, J., Sloper, L., et al. (2014) · Circulation: Cardiovascular Genetics
Connective tissue disorders researchTGF-β signaling in diseases
Cited by 51
- Verified
Ehlers-Danlos Syndrome Caused by Biallelic TNXB Variants in Patients with Congenital Adrenal Hyperplasia
Chen, W., Perritt, A. F., Morissette, R., Dreiling, J. L., Bohn, M.-F., Mallappa, A., Xu, Z., Quezado, M., & Merke, D. P. (2016) · Human Mutation
Connective tissue disorders researchGenomics and Rare Diseases
Cited by 45
- Verified
The soluble domains of Gpi8 and Gaa1, two subunits of glycosylphosphatidylinositol transamidase (GPI-T), assemble into a complex
Gamage, D. G., Varma, Y., Meitzler, J. L., Morissette, R., Ness, T. J., & Hendrickson, T. L. (2017) · Archives of Biochemistry and Biophysics
Glycosylation and Glycoproteins ResearchFungal and yeast genetics research
Cited by 8
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