Integrative genetic characterization and phenotype correlations in pheochromocytoma and paraganglioma tumours (Q37505830)

20 August 2017

Integrative genetic characterization and phenotype correlations in pheochromocytoma and paraganglioma tumours (English)

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20 August 2017

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Peter Stålberg

5

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author name string

Joakim Crona

1

1 reference

20 August 2017

Margareta Nordling

2

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20 August 2017

Rajani Maharjan

3

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20 August 2017

Dan Granberg

4

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20 August 2017

Per Hellman

6

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20 August 2017

Peyman Björklund

7

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20 August 2017

language of work or name

English

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publication date

22 January 2014

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20 August 2017

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20 August 2017

9

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20 August 2017

1

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20 August 2017

e86756

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Creative Commons Attribution 4.0 International

20 August 2017

start time

22 January 2014

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Novel HIF2A mutations disrupt oxygen sensing, leading to polycythemia, paragangliomas, and somatostatinomas

23 August 2017

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Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases

23 August 2017

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Pheochromocytoma - update on disease management

23 August 2017

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Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemia

23 August 2017

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Comprehensive re-sequencing of adrenal aldosterone producing lesions reveal three somatic mutations near the KCNJ5 potassium channel selectivity filter

23 August 2017

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Prevalence of germline mutations in patients with pheochromocytoma or abdominal paraganglioma and sporadic presentation: a population-based study in Western Sweden

23 August 2017

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Vandetanib in patients with locally advanced or metastatic medullary thyroid cancer: a randomized, double-blind phase III trial

23 August 2017

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Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

23 August 2017

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COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

23 August 2017

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A method and server for predicting damaging missense mutations

23 August 2017

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Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

23 August 2017

1 reference

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Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome

23 August 2017

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SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma

23 August 2017

1 reference

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Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

23 August 2017

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Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas

23 August 2017

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A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes

23 August 2017

1 reference

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Germ-line mutations in nonsyndromic pheochromocytoma

23 August 2017

1 reference

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Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

23 August 2017

1 reference

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Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

23 August 2017

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Next-generation sequencing in the clinical genetic screening of patients with pheochromocytoma and paraganglioma

23 August 2017

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A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma

6 September 2017

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Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas

6 September 2017

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The genomic landscape of small intestine neuroendocrine tumors

6 September 2017

1 reference

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Rationale for anti-angiogenic therapy in pheochromocytoma and paraganglioma.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899286

MAX mutations status in Swedish patients with pheochromocytoma and paraganglioma tumours.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899286

Somatic mutations in H-RAS in sporadic pheochromocytoma and paraganglioma identified by exome sequencing.

2 September 2018

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Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome

2 September 2018

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Somatic mutation analysis of the SDHB, SDHC, SDHD, and RET genes in the clinical assessment of sporadic and hereditary pheochromocytoma.

2 September 2018

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Size of the tumor and pheochromocytoma of the adrenal gland scaled score (PASS): can they predict malignancy?

2 September 2018

1 reference

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Local-regional recurrence of sporadic or syndromic abdominal extra-adrenal paraganglioma: incidence, characteristics, and outcome

2 September 2018

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RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest.

2 September 2018

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PHD2 mutation and congenital erythrocytosis with paraganglioma.

2 September 2018

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Year of diagnosis, features at presentation, and risk of recurrence in patients with pheochromocytoma or secreting paraganglioma

2 September 2018

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Human Gene Mutation Database (HGMD): 2003 update.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899286

Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899286

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899286

Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma

2 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0086756

Succinate Dehydrogenase B Gene Mutations Predict Survival in Patients with Malignant Pheochromocytomas or Paragangliomas

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0086756

Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899286

Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899286

Long-term evaluation following resection of apparently benign pheochromocytoma(s)/paraganglioma(s)

3 December 2018

1 reference

12 December 2020

Multiplex ligation-dependent probe amplification improves diagnostics in spinal muscular atrophy

1 reference

12 December 2020

Oncologic aspects of pheochromocytoma: the importance of follow-up

1 reference

12 December 2020

HIF2AMutations in Paraganglioma with Polycythemia

1 reference

12 December 2020

Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosis

1 reference

12 December 2020

Pheochromocytoma of the Adrenal gland Scaled Score (PASS) to separate benign from malignant neoplasms: a clinicopathologic and immunophenotypic study of 100 cases

1 reference

12 December 2020

Dysregulation of the HIF pathway due to VHL mutation causing severe erythrocytosis and pulmonary arterial hypertension

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0086756

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DOI

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20 August 2017

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20 August 2017

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