29 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Shetty I, Fuller S, Raygada M, Merino MJ, Thomas BJ, Widemann BC, Reilly KM, Pacak K, Del Rivero J. Adrenocortical carcinoma masquerading as pheochromocytoma: a histopathologic dilemma. Endocrinology, Diabetes & Metabolism Case Reports. 2020. PMID 31917677 DOI: 10.1530/Edm-19-0147  0.313
2019 Ilanchezhian M, Fuller SN, Raygada M, Stratakis CA, Meltzer PS, Miettinen M, Glod J, Killian K, Arnaldez FI. Clinical characterization of patients with SDHC epimutation in gastrointestinal stromal tumors. Journal of Clinical Oncology. 37: 11033-11033. DOI: 10.1200/Jco.2019.37.15_Suppl.11033  0.357
2019 Siegel C, Raygada M, Acquaye A, Stearn S, Wall K, Crandon S, Stevens-Brown K, Wu J, Vera L, Theeler B, Reyes J, Leggiero N, Cordova C, Bryla C, Burton E, et al. RARE-10. IMPROVING CARE FOR ADULT PATIENTS WITH RARE CNS TUMORS: THE NATIONAL CANCER INSTITUTE-COMPREHENSIVE ONCOLOGY NETWORK EVALUATING RARE CNS TUMORS (NCI-CONNECT) PROGRAM AND CLINIC Neuro-Oncology. 21: vi223-vi223. DOI: 10.1093/Neuonc/Noz175.933  0.323
2018 Barakat AJ, Raygada M, Rennert OM. Barakat syndrome revisited. American Journal of Medical Genetics. Part A. PMID 29663634 DOI: 10.1002/Ajmg.A.38693  0.314
2017 Jochmanova I, Wolf KI, King KS, Nambuba J, Wesley R, Martucci V, Raygada M, Adams KT, Prodanov T, Fojo AT, Lazurova I, Pacak K. SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations. Journal of Cancer Research and Clinical Oncology. PMID 28374168 DOI: 10.1007/S00432-017-2397-3  0.33
2017 Lyssikatos C, Pavithran PV, Tirosh A, Faucz FR, Vasukutty JR, Belyavskaya E, Ahamed A, Raygada M, Stratakis CA. NEWLY DIAGNOSED CARNEY COMPLEX IN 3 YOUNG ADULTS WITH PRIMARY ADRENAL CUSHING SYNDROME – A CASE SERIES AND REVIEW OF THE LITERATURE Aace Clinical Case Reports. 3: e326-e330. DOI: 10.4158/Ep161541.Cr  0.322
2016 Boikos SA, Pappo AS, Killian JK, LaQuaglia MP, Weldon CB, George S, Trent JC, von Mehren M, Wright JA, Schiffman JD, Raygada M, Pacak K, Meltzer PS, Miettinen MM, Stratakis C, et al. Molecular Subtypes of KIT/PDGFRA Wild-Type Gastrointestinal Stromal Tumors: A Report From the National Institutes of Health Gastrointestinal Stromal Tumor Clinic. Jama Oncology. PMID 27011036 DOI: 10.1001/Jamaoncol.2016.0256  0.359
2016 Nobel YR, Lodish MB, Raygada M, Rivero JD, Faucz FR, Abraham SB, Lyssikatos C, Belyavskaya E, Stratakis CA, Zilbermint M. Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene. Endocrinology, Diabetes & Metabolism Case Reports. 2016: 150104. PMID 26807262 DOI: 10.1530/Edm-15-0104  0.31
2016 Schernthaner-Reiter MH, Adams D, Trivellin G, Ramnitz MS, Raygada M, Golas G, Faucz FR, Nilsson O, Nella AA, Dileepan K, Lodish M, Lee P, Tifft C, Markello T, Gahl W, et al. A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothers. European Journal of Pediatrics. PMID 26795631 DOI: 10.1007/S00431-015-2684-4  0.319
2016 Boikos SA, Xekouki P, Fumagalli E, Faucz FR, Raygada M, Szarek E, Ball E, Kim SY, Miettinen M, Helman LJ, Carney JA, Pacak K, Stratakis CA. Carney triad can be (rarely) associated with germline succinate dehydrogenase defects. European Journal of Human Genetics : Ejhg. 24: 569-73. PMID 26173966 DOI: 10.1038/Ejhg.2015.142  0.382
2015 Lodish MB, Yuan B, Levy I, Braunstein GD, Lyssikatos C, Salpea P, Szarek E, Karageorgiadis AS, Belyavskaya E, Raygada M, Faucz FR, Izatt L, Brain C, Gardner J, Quezado M, et al. Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentations. European Journal of Endocrinology / European Federation of Endocrine Societies. 172: 803-11. PMID 25924874 DOI: 10.1530/Eje-14-1154  0.301
2015 Xekouki P, Szarek E, Bullova P, Giubellino A, Quezado M, Mastroyannis SA, Mastorakos P, Wassif CA, Raygada M, Rentia N, Dye L, Cougnoux A, Koziol D, Sierra Mde L, Lyssikatos C, et al. Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice. The Journal of Clinical Endocrinology and Metabolism. 100: E710-9. PMID 25695889 DOI: 10.1210/Jc.2014-4297  0.347
2014 Raygada M, King KS, Adams KT, Stratakis CA, Pacak K. Counseling patients with succinate dehydrogenase subunit defects: genetics, preventive guidelines, and dealing with uncertainty. Journal of Pediatric Endocrinology & Metabolism : Jpem. 27: 837-44. PMID 24854530 DOI: 10.1515/Jpem-2013-0369  0.377
2014 Boikos SA, Xekouki P, Faucz FR, Pacak K, Raygada M, Adams K, Szarek E, Ball E, Kim SY, Fumagalli E, Helman LJ, Carney JA, Stratakis CA. Abstract 568: Few Carney's Triad patients have mutations in two subunits of the succinate dehydrogenase enzyme (SDHB, SDHC) Cancer Research. 74: 568-568. DOI: 10.1158/1538-7445.Am2014-568  0.368
2011 King KS, Prodanov T, Kantorovich V, Fojo T, Hewitt JK, Zacharin M, Wesley R, Lodish M, Raygada M, Gimenez-Roqueplo AP, McCormack S, Eisenhofer G, Milosevic D, Kebebew E, Stratakis CA, et al. Metastatic pheochromocytoma/paraganglioma related to primary tumor development in childhood or adolescence: significant link to SDHB mutations. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 29: 4137-42. PMID 21969497 DOI: 10.1200/Jco.2011.34.6353  0.319
2011 Janeway KA, Kim SY, Lodish M, Nosé V, Rustin P, Gaal J, Dahia PL, Liegl B, Ball ER, Raygada M, Lai AH, Kelly L, Hornick JL, O'Sullivan M, et al. Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations. Proceedings of the National Academy of Sciences of the United States of America. 108: 314-8. PMID 21173220 DOI: 10.1073/Pnas.1009199108  0.339
2010 Johnston JJ, Sapp JC, Turner JT, Amor D, Aftimos S, Aleck KA, Bocian M, Bodurtha JN, Cox GF, Curry CJ, Day R, Donnai D, Field M, Fujiwara I, Gabbett M, ... ... Raygada M, et al. Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations. Human Mutation. 31: 1142-54. PMID 20672375 DOI: 10.1002/Humu.21328  0.312
2010 Stratakis CA, Tichomirowa MA, Boikos S, Azevedo MF, Lodish M, Martari M, Verma S, Daly AF, Raygada M, Keil MF, Papademetriou J, Drori-Herishanu L, Horvath A, Tsang KM, Nesterova M, et al. The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes Clinical Genetics. 78: 457-463. PMID 20507346 DOI: 10.1111/J.1399-0004.2010.01406.X  0.345
2007 Timmers HJ, Kozupa A, Eisenhofer G, Raygada M, Adams KT, Solis D, Lenders JW, Pacak K. Clinical presentations, biochemical phenotypes, and genotype-phenotype correlations in patients with succinate dehydrogenase subunit B-associated pheochromocytomas and paragangliomas. The Journal of Clinical Endocrinology and Metabolism. 92: 779-86. PMID 17200167 DOI: 10.1210/Jc.2006-2315  0.341
2005 Nwosu BU, Raygada M, Tsilou ET, Rennert OM, Stratakis CA. Rieger's anomaly and other ocular abnormalities in association with osteogenesis imperfecta and a COL1A1 mutation Ophthalmic Genetics. 26: 135-138. PMID 16272059 DOI: 10.1080/13816810500228993  0.33
2005 Raygada M, Rennert O. Congenital generalized lipodystrophy: Profile of the disease and gender differences in two siblings Clinical Genetics. 67: 98-101. PMID 15617555 DOI: 10.1111/J.1399-0004.2004.00372.X  0.358
1999 Hilakivi-Clarke L, Cho E, Onojafe I, Raygada M, Clarke R. Maternal exposure to genistein during pregnancy increases carcinogen-induced mammary tumorigenesis in female rat offspring Oncology Reports. 6: 1089-1095. PMID 10425307 DOI: 10.3892/Or.6.5.1089  0.322
1997 Hilakivi-Clarke L, Clarke R, Onojafe I, Raygada M, Cho E, Lippman M. A maternal diet high in n - 6 polyunsaturated fats alters mammary gland development, puberty onset, and breast cancer risk among female rat offspring Proceedings of the National Academy of Sciences of the United States of America. 94: 9372-9377. PMID 9256489 DOI: 10.1073/Pnas.94.17.9372  0.317
1996 Hilakivi-Clarke L, Onojafe I, Raygada M, Cho E, Clarke R, Lippman ME. Breast cancer risk in rats fed a diet high in n-6 polyunsaturated fatty acids during pregnancy Journal of the National Cancer Institute. 88: 1821-1827. PMID 8961971 DOI: 10.1093/Jnci/88.24.1821  0.32
1996 Wang Y, Montrose-Rafizadeh C, Adams L, Raygada M, Nadiv O, Egan JM. GIP regulates glucose transporters, hexokinases, and glucose-induced insulin secretion in RIN 1046-38 cells Molecular and Cellular Endocrinology. 116: 81-87. PMID 8822268 DOI: 10.1016/0303-7207(95)03701-2  0.321
1995 Wang Y, Egan JM, Raygada M, Nadiv O, Roth J, Montrose-Rafizadeh C. Glucagon-like peptide-1 affects gene transcription and messenger ribonucleic acid stability of components of the insulin secretory system in RIN 1046-38 cells Endocrinology. 136: 4910-4917. PMID 7588224 DOI: 10.1210/Endo.136.11.7588224  0.336
1994 Saah MI, Raygada M, Grunberg NE. Effects of nicotine on body weight and plasma insulin in female and male rats. Life Sciences. 55: 925-31. PMID 8057754 DOI: 10.1016/0024-3205(94)00538-9  0.552
1992 Raygada M, Shaham Y, Nespor SM, Kant GJ, Grunberg NE. Effect of stress on hypothalamic insulin in rats. Brain Research Bulletin. 29: 129-34. PMID 1326377 DOI: 10.1016/0361-9230(92)90017-R  0.59
1989 Raygada M, Nespor SM, Grunberg NE. Nicotine alters insulin levels in rat hypothalami Pharmacology Biochemistry and Behavior. 32: 1085. DOI: 10.1016/0091-3057(89)90113-5  0.548
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