Merke, Deborah P.
National Institutes of Health · Eunice Kennedy Shriver National Institute of Child Health and Human Development · National Institutes of Health Clinical Center
66 papers on CoChatORCID 0000-0002-3746-0460
Most cited papers
- Verified
A Phase 2, Multicenter Study of Nevanimibe for the Treatment of Congenital Adrenal Hyperplasia
El-Maouche, D., Merke, D. P., Vogiatzi, M. G., Chang, A. Y., Turcu, A. F., Joyal, E. G., Lin, V. H., Weintraub, L., Plaunt, M. R., Mohideen, P., et al. (2020) · The Journal of Clinical Endocrinology & Metabolism
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 34
- Verified
Androgen excess and diagnostic steroid biomarkers for nonclassic 21-hydroxylase deficiency without cosyntropin stimulation
Turcu, A. F., El-Maouche, D., Zhao, L., Nanba, A. T., Gaynor, A., Veeraraghavan, P., Auchus, R. J., & Merke, D. P. (2020) · European Journal of Endocrinology
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 33
- Verified
Hypoglycemia during acute illness in children with classic congenital adrenal hyperplasia
Keil, M. F., Bosmans, C., Van Ryzin, C., & Merke, D. P. (2010) · Journal of Pediatric Nursing
Adrenal Hormones and DisordersSexual Differentiation and Disorders
Cited by 30
- Verified
High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia.
Lao, Q., Brookner, B., & Merke, D. P. (2019) · The Journal of Molecular Diagnostics
Sexual Differentiation and DisordersConnective tissue disorders research
Cited by 29
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Adrenomedullary Function in Patients with Nonclassic Congenital Adrenal Hyperplasia
Verma, S., Green-Golan, L., VanRyzin, C., Drinkard, B., Mehta, S. P., Weise, M., Eisenhofer, G., & Merke, D. P. (2010) · Hormone and Metabolic Research
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 24
- Verified
Androgens correlate with increased erythropoiesis in women with congenital adrenal hyperplasia
Karunasena, N., Han, T. S., Mallappa, A., Elman, M., Merke, D. P., Ross, R. J. M., & Daniel, E. (2017) · Clinical Endocrinology
Sexual Differentiation and DisordersHormonal and reproductive studies
Cited by 23
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24-Hour Profiles of 11-Oxygenated C19 Steroids and Δ5-Steroid Sulfates during Oral and Continuous Subcutaneous Glucocorticoids in 21-Hydroxylase Deficiency
Turcu, A. F., Mallappa, A., Nella, A. A., Chen, X., Zhao, L., Nanba, A. T., Byrd, J. B., Auchus, R. J., & Merke, D. P. (2021) · Frontiers in Endocrinology
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 20
- Verified
Adrenal morphology and associated comorbidities in congenital adrenal hyperplasia
El‐Maouche, D., Hannah‐Shmouni, F., Mallappa, A., Hargreaves, C. J., Avila, N. A., & Merke, D. P. (2019) · Clinical Endocrinology
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 20
- Verified
Adrenocorticotropin hypersecretion and pituitary microadenoma following bilateral adrenalectomy in a patient with classic 21-hydroxylase deficiency
Charmandari, E., Chrousos, G. P., & Merke, D. P. (2005) · Journal of Pediatric Endocrinology and Metabolism
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 20
- Verified
Complement component 4 copy number variation and CYP21A2 genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Chen, W., Xu, Z., Nishitani, M., Van Ryzin, C., McDonnell, N. B., & Merke, D. P. (2012) · Human Genetics
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 18
- Verified
Alterations in Hydrocortisone Pharmacokinetics in a Patient With Congenital Adrenal Hyperplasia Following Bariatric Surgery
Mallappa, A., Nella, A. A., Kumar, P., Brooks, K. M., Perritt, A. F., Ling, A., Liu, C.-Y., & Merke, D. P. (2017) · Journal of the Endocrine Society
Adrenal Hormones and DisordersSexual Differentiation and Disorders
Cited by 16
- Verified
Complement component 4 variations may influence psychopathology risk in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Lao, Q., Jardin, M. D., Jayakrishnan, R., Ernst, M., & Merke, D. P. (2018) · Human Genetics
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 12
- Verified
Positive fertility outcomes in a female with classic congenital adrenal hyperplasia following bilateral adrenalectomy
Dagalakis, U., Mallappa, A., Elman, M., Quezado, M., & Merke, D. P. (2016) · International Journal of Pediatric Endocrinology
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 10
- Verified
Congenital Adrenal Hyperplasia
Mallappa, A., & Merke, D. P. (2017) · Management of Adrenal Masses in Children and Adults
Sexual Differentiation and DisordersAdrenal and Paraganglionic Tumors
Cited by 8
- Verified
Congenital adrenal hyperplasia due to two rare CYP21A2 variant alleles, including a novel attenuated CYP21A1P/CYP21A2 chimera
Lao, Q., Burkardt, D. D., Kollender, S., Faucz, F. R., & Merke, D. P. (2023) · Molecular Genetics & Genomic Medicine
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 8
- Verified
Design of a Phase 1/2 Open-Label, Dose-Escalation Study of the Safety and Efficacy of Gene Therapy in Adults With Classic Congenital Adrenal Hyperplasia (CAH) Due to 21-hydroxylase Deficiency Through Administration of an Adeno-Associated Virus (AAV) Serotype 5-Based Recombinant Vector Encoding the Human CYP21A2 Gene
Merke, D. P., Auchus, R. J., Sarafoglou, K., Geffner, M. E., Kim, M. S., Escandon, R. D., Bharucha, K. N., Shaywitz, A. J., Eclov, R., Beard, C. W., et al. (2021) · Journal of the Endocrine Society
Virus-based gene therapy researchAdrenal Hormones and Disorders
Cited by 7
- Verified
OR25-02 A Phase 3 study of a modified-release hydrocortisone in the treatment of congenital adrenal hyperplasia
Merke, D. P., Mallappa, A., Arlt, W., de la Perriere, A. B., Hirschberg, A. L., Juul, A., Newell-Price, J. D. C., Perry, C. G., Prete, A., Rees, A., et al. (2020) · Journal of the Endocrine Society
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 4
- Verified
Pseudogene TNXA Variants May Interfere with the Genetic Testing of CAH-X
Lao, Q., Zhou, K., Parker, M., Faucz, F. R., & Merke, D. P. (2023) · Genes
Sexual Differentiation and DisordersConnective tissue disorders research
Cited by 1
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