| Diagnosis and treatment of primary adrenal insufficiency: an endocrine society clinical practice guideline SR Bornstein, B Allolio, W Arlt, A Barthel, A Don-Wauchope, GD Hammer, ... The Journal of Clinical Endocrinology & Metabolism 101 (2), 364-389, 2016 | 1348 | 2016 |
| Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST) W Balemans, M Ebeling, N Patel, E Van Hul, P Olson, M Dioszegi, ... Human molecular genetics 10 (5), 537-544, 2001 | 1257 | 2001 |
| Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex LS Kirschner, JA Carney, SD Pack, SE Taymans, C Giatzakis, YS Cho, ... Nature genetics 26 (1), 89-92, 2000 | 1186 | 2000 |
| Neuroendocrinology and pathophysiology of the stress system CA Stratakis, GP Chrousos ANNALS-NEW YORK ACADEMY OF SCIENCES 771, 1-18, 1995 | 842 | 1995 |
| Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation CA Stratakis, LS Kirschner, JA Carney The Journal of Clinical Endocrinology & Metabolism 86 (9), 4041-4046, 2001 | 831 | 2001 |
| Cushing's syndrome A Lacroix, RA Feelders, CA Stratakis, LK Nieman The lancet 386 (9996), 913-927, 2015 | 799 | 2015 |
| Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations KA Janeway, SY Kim, M Lodish, V Nosé, P Rustin, J Gaal, PLM Dahia, ... Proceedings of the National Academy of Sciences 108 (1), 314-318, 2011 | 634 | 2011 |
| Bone mineral density in women with depression D Michelson, C Stratakis, L Hill, J Reynolds, E Galliven, G Chrousos, ... New England Journal of Medicine 335 (16), 1176-1181, 1996 | 611 | 1996 |
| An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma RC Ribeiro, F Sandrini, B Figueiredo, GP Zambetti, E Michalkiewicz, ... Proceedings of the National Academy of Sciences 98 (16), 9330-9335, 2001 | 587 | 2001 |
| Clinical and molecular genetics of patients with the Carney–Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC … B Pasini, SR McWhinney, T Bei, L Matyakhina, S Stergiopoulos, ... European Journal of Human Genetics 16 (1), 79-88, 2008 | 503 | 2008 |
| Chronic insomnia and activity of the stress system: a preliminary study AN Vgontzas, C Tsigos, EO Bixler, CA Stratakis, K Zachman, A Kales, ... Journal of psychosomatic research 45 (1), 21-31, 1998 | 496 | 1998 |
| Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2. CA Stratakis, JA Carney, JP Lin, DA Papanicolaou, M Karl, DL Kastner, ... The Journal of clinical investigation 97 (3), 699-705, 1996 | 493 | 1996 |
| SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexes RG Ruf, PX Xu, D Silvius, EA Otto, F Beekmann, UT Muerb, S Kumar, ... Proceedings of the National Academy of Sciences 101 (21), 8090-8095, 2004 | 458 | 2004 |
| Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex LS Kirschner, F Sandrini, J Monbo, JP Lin, JA Carney, CA Stratakis Human molecular genetics 9 (20), 3037-3046, 2000 | 452 | 2000 |
| Point mutation causing a single amino acid substitution in the hormone binding domain of the glucocorticoid receptor in familial glucocorticoid resistance. DM Hurley, D Accili, CA Stratakis, M Karl, N Vamvakopoulos, E Rorer, ... The Journal of clinical investigation 87 (2), 680-686, 1991 | 428 | 1991 |
| Mutations in Regulatory Subunit Type 1A of Cyclic Adenosine 5′-Monophosphate-Dependent Protein Kinase (PRKAR1A): Phenotype Analysis in 353 Patients … J Bertherat, A Horvath, L Groussin, S Grabar, S Boikos, L Cazabat, R Libe, ... The Journal of Clinical Endocrinology & Metabolism 94 (6), 2085-2091, 2009 | 401 | 2009 |
| Familial paraganglioma and gastric stromal sarcoma: a new syndrome distinct from the Carney triad JA Carney, CA Stratakis American journal of medical genetics 108 (2), 132-139, 2002 | 384 | 2002 |
| Somatic HIF2A Gain-of-Function Mutations in Paraganglioma with Polycythemia Z Zhuang, C Yang, F Lorenzo, M Merino, T Fojo, E Kebebew, V Popovic, ... New England Journal of Medicine 367 (10), 922-930, 2012 | 383 | 2012 |
| Constitutive activation of PKA catalytic subunit in adrenal Cushing's syndrome F Beuschlein, M Fassnacht, G Assié, D Calebiro, CA Stratakis, A Osswald, ... New England Journal of Medicine 370 (11), 1019-1028, 2014 | 377 | 2014 |
| Sex hormones, acting on the TERT gene, increase telomerase activity in human primary hematopoietic cells RT Calado, WT Yewdell, KL Wilkerson, JA Regal, S Kajigaya, ... Blood, The Journal of the American Society of Hematology 114 (11), 2236-2243, 2009 | 377 | 2009 |
Fabio Rueda FauczNational Institutes of HealthVerifierad e-postadress på nih.gov
