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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
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Last data update: May 02, 2024
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Germline genetic variants in pheochromocytoma/paraganglioma: single-center experience.
José V Lima et al. Endocr Oncol 2023 3(1) e220091
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Metastatic pheochromocytoma and paraganglioma: Somatostatin receptor 2 expression, genetics and therapeutic responses.
Alessa Fischer et al. The Journal of clinical endocrinology and metabolism 2023
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Genetic Testing for Adrenal Tumors-What the Contemporary Surgeon Should Know.
Maria F Bates et al. Surgical oncology clinics of North America 2023 32(2) 303-313
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Genetic study in pheochromocytoma ¿is it possible to stratify the risk of hereditary pheochromocytoma?
Marta Araujo-Castro et al. Neuroendocrinology 2023
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An integrated somatic and germline approach to aid interpretation of germline variants of uncertain significance in cancer susceptibility genes.
Schwartz Alison et al. Frontiers in oncology 2022 12942741
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Mutational Profile and Potential Molecular Therapeutic Targets of Pheochromocytoma.
Ma Xiaosen et al. Frontiers in endocrinology 2022 13921645
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Surveillance improves outcomes for carriers of SDHB pathogenic variants: a multi-center study.
Davidoff Dahlia F et al. The Journal of clinical endocrinology and metabolism 2022
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Universal Germline Panel Testing for Individuals with Pheochromocytoma and Paraganglioma Produces High Diagnostic Yield.
Horton Carolyn et al. The Journal of clinical endocrinology and metabolism 2022
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SDHB-Associated Paraganglioma Syndrome in Africa-A Need for Greater Genetic Testing.
Siddiqui Nida et al. Journal of the Endocrine Society 2021 5(10) bvab111
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Cost-minimization analysis of sequential genetic testing versus targeted next-generation sequencing gene panels in patients with pheochromocytoma and paraganglioma.
Pipitprapat Weenita et al. Annals of medicine 2021 53(1) 1243-1255
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Non-medullary Thyroid Cancer Susceptibility Genes: Evidence and Disease Spectrum.
Zhou Jingan et al. Annals of surgical oncology 2021
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Genetic testing for pheochromocytoma and paraganglioma: SDHx carriers' experiences.
Martins Raquel Gomes et al. Journal of genetic counseling 2021 Feb
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Genetic evaluation of patients and families with concern for hereditary endocrine tumor syndromes.
Anderson Jennifer L et al. Familial cancer 2021 Jan
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Screening of a large cohort of asymptomatic SDHx mutation carriers in routine practice.
Saie Clotilde et al. The Journal of clinical endocrinology and metabolism 2020 Nov
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Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paraganglioma.
Ben Aim Laurène et al. Journal of medical genetics 2019 56(8) 513-520
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Pheochromocytoma Due to TMEM127 Mutation - The Importance of Genetic Testing for Clinical Decision.
Paredes Sílvia Cristina de Sousa et al. European endocrinology 2020 Apr 16(1) 72-74
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Pheochromocytoma and paraganglioma genetic testing: Psychological impact.
Martins Raquel Gomes et al. Health psychology : official journal of the Division of Health Psychology, American Psychological Association 2020 Jul
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Genetic screening for monogenic hypertension in hypertensive individuals in a clinical setting.
Bao Minghui et al. Journal of medical genetics 2020 Jun
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Clinical and genetic features of pediatric PCCs/PGLs patients: a single-center experience in China.
Li Minghao et al. Translational andrology and urology 2020 Apr 9(2) 267-275
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Dataset for the Reporting of Pheochromocytoma and Paraganglioma: Explanations and Recommendations of the Guidelines from the International Collaboration on Cancer Reporting (ICCR).
Thompson Lester D R et al. Human pathology 2020 May
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An overview of 20 years of genetic studies in pheochromocytoma and paraganglioma.
Buffet Alexandre et al. Best practice & research. Clinical endocrinology & metabolism 2020 Mar 101416
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A primer on the genetics of medullary thyroid cancer.
Larouche V et al. Current oncology (Toronto, Ont.) 2019 Dec 26(6) 389-394
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Genetic Profile of Indian Pheochromocytoma and Paraganglioma Patients - A Single Institutional Study.
Agarwal Gaurav et al. Indian journal of endocrinology and metabolism 23(4) 486-490
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Structured assessment and followup for patients with hereditary kidney tumour syndromes.
Lattouf Jean-Baptiste et al. Canadian Urological Association journal = Journal de l'Association des urologues du Canada 10(7-8) E214-E222
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Imaging Features of Succinate Dehydrogenase-deficient Pheochromocytoma-Paraganglioma Syndromes.
Withey Samuel Joseph et al. Radiographics : a review publication of the Radiological Society of North America, Inc 39(5) 1393-1410
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Pheochromocytoma and paraganglioma: implications of germline mutation investigation for treatment, screening, and surveillance.
Gómez Ana Milena et al. Archives of endocrinology and metabolism 2019 Jul
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Pheochromocytoma/Paraganglioma: Is This a Genetic Disorder?
Fishbein Lauren et al. Current cardiology reports 2019 Jul 21(9) 104
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Metabolome-guided genomics to identify pathogenic variants in isocitrate dehydrogenase, fumarate hydratase, and succinate dehydrogenase genes in pheochromocytoma and paraganglioma.
Richter Susan et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 21(3) 705-717
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 02, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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