| Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma BE Baysal, RE Ferrell, JE Willett-Brozick, EC Lawrence, D Myssiorek, ... Science 287 (5454), 848-851, 2000 | 1997 | 2000 |
| Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas BE Baysal, JE Willett-Brozick, EC Lawrence, CM Drovdlic, SA Savul, ... Journal of medical genetics 39 (3), 178-183, 2002 | 426 | 2002 |
| Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene F Schiavi, CC Boedeker, B Bausch, M Peçzkowska, CF Gomez, ... Jama 294 (16), 2057-2063, 2005 | 415 | 2005 |
| Hereditary paraganglioma targets diverse paraganglia BE Baysal Journal of medical genetics 39 (9), 617-622, 2002 | 296 | 2002 |
| Revisiting the TCA cycle: signaling to tumor formation N Raimundo, BE Baysal, GS Shadel Trends in molecular medicine 17 (11), 641-649, 2011 | 279 | 2011 |
| APOBEC3A cytidine deaminase induces RNA editing in monocytes and macrophages S Sharma, SK Patnaik, R Thomas Taggart, ED Kannisto, SM Enriquez, ... Nature communications 6 (1), 6881, 2015 | 259 | 2015 |
| Centrifugal enhancement of retroviral mediated gene transfer AB Bahnson, JT Dunigan, BE Baysal, T Mohney, RW Atchison, ... Journal of virological methods 54 (2-3), 131-143, 1995 | 237 | 1995 |
| Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect K Astrom, JE Cohen, JE Willett-Brozick, CE Aston, BE Baysal Human genetics 113, 228-237, 2003 | 234 | 2003 |
| Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene PEM Taschner, JC Jansen, BE Baysal, A Bosch, EH Rosenberg, ... Genes, Chromosomes and Cancer 31 (3), 274-281, 2001 | 204 | 2001 |
| Genetics of carney triad: recurrent losses at chromosome 1 but lack of germline mutations in genes associated with paragangliomas and gastrointestinal stromal tumors L Matyakhina, TA Bei, SR McWhinney, B Pasini, S Cameron, B Gunawan, ... The Journal of Clinical Endocrinology & Metabolism 92 (8), 2938-2943, 2007 | 168 | 2007 |
| Biochemically Silent Abdominal Paragangliomas in Patients with Mutations in the Succinate Dehydrogenase Subunit B Gene HJLM Timmers, K Pacak, TT Huynh, M Abu-Asab, M Tsokos, MJ Merino, ... The journal of clinical endocrinology & metabolism 93 (12), 4826-4832, 2008 | 149 | 2008 |
| On the association of succinate dehydrogenase mutations with hereditary paraganglioma BE Baysal Trends in Endocrinology & Metabolism 14 (10), 453-459, 2003 | 143 | 2003 |
| Familial malignant catecholamine-secreting paraganglioma with prolonged survival associated with mutation in the succinate dehydrogenase B gene AL Young, BE Baysal, A Deb, WF Young Jr The Journal of Clinical Endocrinology & Metabolism 87 (9), 4101-4105, 2002 | 142 | 2002 |
| Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23. BE Baysal, JE Farr, WS Rubinstein, RA Galus, KA Johnson, CE Aston, ... American journal of human genetics 60 (1), 121, 1997 | 122 | 1997 |
| Loss of distal 11q is associated with DNA repair deficiency and reduced sensitivity to ionizing radiation in head and neck squamous cell carcinoma RA Parikh, JS White, X Huang, DW Schoppy, BE Baysal, R Baskaran, ... Genes, Chromosomes and Cancer 46 (8), 761-775, 2007 | 117 | 2007 |
| Clinical and molecular progress in hereditary paraganglioma BE Baysal Journal of medical genetics 45 (11), 689-694, 2008 | 109 | 2008 |
| Etiopathogenesis and clinical presentation of carotid body tumors BE Baysal, EN Myers Microscopy research and technique 59 (3), 256-261, 2002 | 109 | 2002 |
| Phenotypic dichotomy in mitochondrial complex II genetic disorders BE Baysal, WS Rubinstein, PE Taschner Journal of molecular medicine 79, 495-503, 2001 | 106 | 2001 |
| Proportion of heritable paraganglioma cases and associated clinical characteristics CM Drovdlic, EN Myers, JA Peters, BE Baysal, DE Brackmann, ... The Laryngoscope 111 (10), 1822-1827, 2001 | 105 | 2001 |
| An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma BE Baysal, JE Willett-Brozick, EC Lawrence, EN Myers, RE Ferrell Journal of medical genetics 41 (9), 703-709, 2004 | 104 | 2004 |
Wendy Rubinstein, MD, PhDSenior Scientific Officer, National Cancer Institute在 nih.gov 的电子邮件经过验证
