Clinical and Molecular Features of Renal and Pheochromocytoma/Paraganglioma Tumor Association Syndrome (RAPTAS): Case Series and Literature Review

Prevalence and Characteristics of Patients with Suspected Inherited Renal Cell Cancer: Application of the ACMG/NSGC Genetic Referral Guidelines to Patient Cohorts

(2017) Hong Truong et al.   Journal of Genetic Counseling

European Society of Endocrinology Clinical Practice Guideline for long-term follow-up of patients operated on for a phaeochromocytoma or a paraganglioma: Table 1

(2016) P F Plouin et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

The 2016 WHO Classification of Tumours of the Urinary System and Male Genital Organs—Part A: Renal, Penile, and Testicular Tumours

(2016) Holger Moch et al.   EUROPEAN UROLOGY

Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and Erythrocytosis

(2016) Esther Korpershoek et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Renal carcinoma associated with a novel succinate dehydrogenase A mutation: a case report and review of literature of a rare subtype of renal carcinoma

(2015) Yasemin Ozluk et al.   HUMAN PATHOLOGY

SDHB/SDHA immunohistochemistry in pheochromocytomas and paragangliomas: a multicenter interobserver variation analysis using virtual microscopy: a Multinational Study of the European Network for the Study of Adrenal Tumors (ENS@T)

(2015) Thomas G Papathomas et al.   MODERN PATHOLOGY

Familial pheochromocytoma and renal cell carcinoma syndrome: TMEM127 as a novel candidate gene for the association

(2015) Karen Gomez Hernandez et al.   VIRCHOWS ARCHIV

Succinate Dehydrogenase (SDH)-deficient Renal Carcinoma

(2014) Anthony J. Gill et al.   AMERICAN JOURNAL OF SURGICAL PATHOLOGY

A clinical and genetic analysis of multiple primary cancer referrals to genetics services

(2014) James Whitworth et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

GermlineFHMutations Presenting With Pheochromocytoma

(2014) Graeme R. Clark et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Succinate dehydrogenase-deficient renal cell carcinoma: detailed characterization of 11 tumors defining a unique subtype of renal cell carcinoma

(2014) Sean R Williamson et al.   MODERN PATHOLOGY

SDH Mutations Establish a Hypermethylator Phenotype in Paraganglioma

(2013) Eric Letouzé et al.   CANCER CELL

Canadian guideline on genetic screening for hereditary renal cell cancers

(2013) M. Neil Reaume et al.   CUAJ-Canadian Urological Association Journal

The tumor susceptibility gene TMEM127  is mutated in renal cell carcinomas and modulates endolysosomal function

(2013) Y. Qin et al.   HUMAN MOLECULAR GENETICS

A Comprehensive Next Generation Sequencing–Based Genetic Testing Strategy To Improve Diagnosis of Inherited Pheochromocytoma and Paraganglioma

(2013) Eleanor Rattenberry et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Germline SDHC mutation presenting as recurrent SDH deficient GIST and renal carcinoma

(2013) Anthony J. Gill et al.   PATHOLOGY

Myc and mTOR converge on a common node in protein synthesis control that confers synthetic lethality in Myc-driven cancers

(2013) M. Pourdehnad et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

(2012) N. Burnichon et al.   CLINICAL CANCER RESEARCH

Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3

(2012) Angelica Malinoc et al.   ENDOCRINE-RELATED CANCER

Staging and Functional Characterization of Pheochromocytoma and Paraganglioma by 18F-Fluorodeoxyglucose (18F-FDG) Positron Emission Tomography

(2012) Henri J. L. M. Timmers et al.   JNCI-Journal of the National Cancer Institute

Succinate Dehydrogenase Kidney Cancer: An Aggressive Example of the Warburg Effect in Cancer

(2012) Christopher J. Ricketts et al.   JOURNAL OF UROLOGY

GENETICS IN ENDOCRINOLOGY: The genetics of phaeochromocytoma: using clinical features to guide genetic testing

(2011) Mariam Jafri et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

von Hippel–Lindau disease: A clinical and scientific review

(2011) Eamonn R Maher et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Renal Tumors and Hereditary Pheochromocytoma-Paraganglioma Syndrome Type 4

(2011) Anthony J. Gill et al.   NEW ENGLAND JOURNAL OF MEDICINE

SDHA is a tumor suppressor gene causing paraganglioma

(2010) Nelly Burnichon et al.   HUMAN MOLECULAR GENETICS

Genetics of Familial Renal Cancers

(2010) Eamonn R. Maher   NEPHRON EXPERIMENTAL NEPHROLOGY

Tumor risks and genotype–phenotype–proteotype analysis in 358 patients with germline mutations inSDHBandSDHD

(2009) Christopher J. Ricketts et al.   HUMAN MUTATION

Germline SDHB Mutations and Familial Renal Cell Carcinoma

(2008) C. Ricketts et al.   JNCI-Journal of the National Cancer Institute