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Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

Nature genetics, 2010-03, Vol.42 (3), p.229-233

2010

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Recurrent Mutations of Chromatin-Remodeling Genes and Kinase Receptors in Pheochromocytomas and Paragangliomas

Clinical cancer research, 2016-05, Vol.22 (9), p.2301-2310

2016

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In vivo and in vitro oncogenic effects of HIF2A mutations in pheochromocytomas and paragangliomas

Endocrine-related cancer, 2013-06, Vol.20 (3), p.349-359

2013

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Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas

JAMA : the journal of the American Medical Association, 2010-12, Vol.304 (23), p.2611

2010

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EPAS1 Mutations and Paragangliomas in Cyanotic Congenital Heart Disease

The New England journal of medicine, 2018-03, Vol.378 (13), p.1259-1261

2018

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Recognizing hypoxia in phaeochromocytomas and paragangliomas

Nature reviews. Endocrinology, 2020-04, Vol.16 (4), p.191-192

2020

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Endocrine and Neuroendocrine Tumors Special Issue-Checkpoint Inhibitors for Adrenocortical Carcinoma and Metastatic Pheochromocytoma and Paraganglioma: Do They Work?

Cancers, 2022-01, Vol.14 (3), p.467

2022

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Next-generation sequencing for the diagnosis of hereditary pheochromocytoma and paraganglioma syndromes

Current opinion in endocrinology, diabetes, and obesity, 2015-06, Vol.22 (3), p.169-179

2015

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Assessment of Depression, Anxiety, Quality of Life, and Coping in Long-Standing Multiple Endocrine Neoplasia Type 2 Patients

Thyroid (New York, N.Y.), 2017-05, Vol.27 (5), p.693

2017

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ACT-Discover: identifying karyotype heterogeneity in pancreatic cancer evolution using ctDNA

Genome medicine, 2023-04, Vol.15 (1), p.27-27, Article 27

2023

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Combined Targeting of Pathogenetic Mechanisms in Pancreatic Neuroendocrine Tumors Elicits Synergistic Antitumor Effects

Cancers, 2022-11, Vol.14 (22), p.5481

2022

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Early‐onset, progressive, frequent, extensive, and severe bone mineral and renal complications in multiple endocrine neoplasia type 1–associated primary hyperparathyroidism

Journal of bone and mineral research, 2010-11, Vol.25 (11), p.2382-2391

2010

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Inflated pathogenic variant profiles in the ClinVar database

Nature reviews. Endocrinology, 2018-07, Vol.14 (7), p.387

Toledo, Rodrigo A

2018

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Hypercalcitoninemia is not Pathognomonic of Medullary Thyroid Carcinoma

Clinics (São Paulo, Brazil), 2009-01, Vol.64 (7), p.699-706

2009

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Germline Mutation in the Aryl Hydrocarbon Receptor Interacting Protein Gene in Familial Somatotropinoma

The journal of clinical endocrinology and metabolism, 2007-05, Vol.92 (5), p.1934-1937

2007

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Hypoxia-Inducible Factor 2 Alpha (HIF2α) Inhibitors: Targeting Genetically Driven Tumor Hypoxia

Endocrine reviews, 2023-04, Vol.44 (2), p.312-322

2023

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Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas

Nature reviews. Endocrinology, 2017-04, Vol.13 (4), p.233

2017

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Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS

The journal of clinical endocrinology and metabolism, 2013-02, Vol.98 (2), p.E364-E369

2013

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Pituitary tumors in patients with MEN1 syndrome

Clinics (São Paulo, Brazil), 2012-01, Vol.67 (Suppl 1), p.43-48

2012

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Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study

The journal of clinical endocrinology and metabolism, 2010-11, Vol.95 (11), p.E373-E383

2010

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A differential diagnosis of inherited endocrine tumors and their tumor counterparts

Clinics (São Paulo, Brazil), 2013-07, Vol.68 (7), p.1039-1056

2013

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RET Y791F: alone or accompanied?

Archives of endocrinology and metabolism, 2015-10, Vol.59 (5), p.476

2015

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Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

Recurrent Mutations of Chromatin-Remodeling Genes and Kinase Receptors in Pheochromocytomas and Paragangliomas

In vivo and in vitro oncogenic effects of HIF2A mutations in pheochromocytomas and paragangliomas

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas

EPAS1 Mutations and Paragangliomas in Cyanotic Congenital Heart Disease

Recognizing hypoxia in phaeochromocytomas and paragangliomas

Endocrine and Neuroendocrine Tumors Special Issue-Checkpoint Inhibitors for Adrenocortical Carcinoma and Metastatic Pheochromocytoma and Paraganglioma: Do They Work?

Exome Sequencing of Plasma DNA Portrays the Mutation Landscape of Colorectal Cancer and Discovers Mutated VEGFR2 Receptors as Modulators of Antiangiogenic Therapies

Next-generation sequencing for the diagnosis of hereditary pheochromocytoma and paraganglioma syndromes

Assessment of Depression, Anxiety, Quality of Life, and Coping in Long-Standing Multiple Endocrine Neoplasia Type 2 Patients

ACT-Discover: identifying karyotype heterogeneity in pancreatic cancer evolution using ctDNA

Combined Targeting of Pathogenetic Mechanisms in Pancreatic Neuroendocrine Tumors Elicits Synergistic Antitumor Effects

Early‐onset, progressive, frequent, extensive, and severe bone mineral and renal complications in multiple endocrine neoplasia type 1–associated primary hyperparathyroidism

Inflated pathogenic variant profiles in the ClinVar database

Hypercalcitoninemia is not Pathognomonic of Medullary Thyroid Carcinoma

Germline Mutation in the Aryl Hydrocarbon Receptor Interacting Protein Gene in Familial Somatotropinoma

Hypoxia-Inducible Factor 2 Alpha (HIF2α) Inhibitors: Targeting Genetically Driven Tumor Hypoxia

p27 variant and corticotropinoma susceptibility: a genetic and in vitro study

RNF43 mutations predict response to anti-BRAF/EGFR combinatory therapies in BRAFV600E metastatic colorectal cancer

Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas

Exomic Sequencing of Medullary Thyroid Cancer Reveals Dominant and Mutually Exclusive Oncogenic Mutations in RET and RAS

Pituitary tumors in patients with MEN1 syndrome

Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study

A differential diagnosis of inherited endocrine tumors and their tumor counterparts

RET Y791F: alone or accompanied?

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