Genetic Testing by Cancer Site

Lifetime Cancer Risks in Individuals with Germline PTEN Mutations

(2012) M.-H. Tan et al.   CLINICAL CANCER RESEARCH

Role of Multiple Endocrine Neoplasia Type 1 Mutational Analysis in Clinical Practice

(2011) Paul Newey et al.   Endocrine Practice

Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas

(2011) Jenny Welander et al.   ENDOCRINE-RELATED CANCER

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

Germline Mutations of theTMEM127Gene in Patients with Paraganglioma of Head and Neck and Extraadrenal Abdominal Sites

(2011) Hartmut P. H. Neumann et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Molecular Analysis of Pheochromocytoma after Maternal Transmission of SDHD Mutation Elucidates Mechanism of Parent-of-Origin Effect

(2011) Phey M. Yeap et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

SDHA Immunohistochemistry Detects GermlineSDHAGene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas

(2011) Esther Korpershoek et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Metastatic Pheochromocytoma/Paraganglioma Related to Primary Tumor Development in Childhood or Adolescence: Significant Link toSDHBMutations

(2011) Kathryn S. King et al.   JOURNAL OF CLINICAL ONCOLOGY

Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome clinical features

(2011) R. Pilarski et al.   JOURNAL OF MEDICAL GENETICS

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

(2011) Iñaki Comino-Méndez et al.   NATURE GENETICS

The Cowden syndrome: a clinical and genetic study in 21 patients

(2010) Th. M. Starink et al.   CLINICAL GENETICS

Frequent Gastrointestinal Polyps and Colorectal Adenocarcinomas in a Prospective Series of PTEN Mutation Carriers

(2010) Brandie Heald et al.   GASTROENTEROLOGY

Endocrine Cancer Predisposition Syndromes: Hereditary Paraganglioma, Multiple Endocrine Neoplasia Type 1, Multiple Endocrine Neoplasia Type 2, and Hereditary Thyroid Cancer

(2010) Wendy S. Rubinstein   HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA

SDHA is a tumor suppressor gene causing paraganglioma

(2010) Nelly Burnichon et al.   HUMAN MOLECULAR GENETICS

Spectrum and Prevalence of FP/TMEM127 Gene Mutations in Pheochromocytomas and Paragangliomas

(2010) Li Yao et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Germline Epigenetic Regulation of KILLIN in Cowden and Cowden-like Syndrome

(2010) Kristi L. Bennett   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

(2010) Jean-Pierre Bayley et al.   LANCET ONCOLOGY

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

(2010) Yuejuan Qin et al.   NATURE GENETICS

Clinical Predictors and Algorithm for the Genetic Diagnosis of Pheochromocytoma Patients

(2009) Z. Erlic et al.   CLINICAL CANCER RESEARCH

Parathyroid Carcinoma in Multiple Endocrine Neoplasia Type 1 with a Classic Germline Mutation

(2009) Roger Shih et al.   Endocrine Practice

SDHB-associated renal oncocytoma suggests a broadening of the renal phenotype in hereditary paragangliomatosis

(2009) Alex Henderson et al.   Familial Cancer

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

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

The Succinate Dehydrogenase Genetic Testing in a Large Prospective Series of Patients with Paragangliomas

(2009) Nelly Burnichon et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

SDH5, a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma

(2009) H.-X. Hao et al.   SCIENCE

Medullary Thyroid Cancer: Management Guidelines of the American Thyroid Association

(2009) Richard T. Kloos (Chair) et al.   THYROID

Germline Mutations and Variants in the Succinate Dehydrogenase Genes in Cowden and Cowden-like Syndromes

(2008) Ying Ni et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Multiple endocrine neoplasia type 1 (MEN1): its manifestations and effect of genetic screening on clinical outcome

(2008) C. R. C. Pieterman et al.   CLINICAL ENDOCRINOLOGY

Paraganglioma after Maternal Transmission of a Succinate Dehydrogenase Gene Mutation

(2008) Pascal Pigny et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Cowden Syndrome: A Critical Review of the Clinical Literature

(2008) Robert Pilarski   Journal of Genetic Counseling

Germline SDHB Mutations and Familial Renal Cell Carcinoma

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

Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene

(2007) Manuel C. Lemos et al.   HUMAN MUTATION