×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study.
30763276 2019
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
p.Ser891Ala RET gene mutations in medullary thyroid cancer: Phenotypical and genealogical characterization of 28 apparently unrelated kindreds and founder effect uncovering in Northern Italy.
30927507 2019
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
The RET C611Y mutation causes MEN 2A and associated cutaneous
30300539 2018
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Different RET gene mutation-induced multiple endocrine neoplasia type 2A in 3 Chinese families.
28099363 2017
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Nationwide French Study of RET Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as Modifiers.
28946813 2017
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
GeneticVariation
CLINVAR
Nationwide French Study of RET Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as Modifiers.
28946813 2017
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Founder Effect of the RETC611Y Mutation in Multiple Endocrine Neoplasia 2A in Denmark: A Nationwide Study.
29020875 2017
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
GeneticVariation
CLINVAR
Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation.
27673361 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
GeneticVariation
CLINVAR
Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
27539324 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
27539324 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
GeneticVariation
CLINVAR
M918V RET mutation causes familial medullary thyroid carcinoma: study of 8 affected kindreds.
27807060 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
A cohort study on 10-year survival of sporadic medullary thyroid carcinoma with somatic RET mutation.
27847096 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
M918V RET mutation causes familial medullary thyroid carcinoma: study of 8 affected kindreds.
27807060 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Diversity of mutations in the RET proto-oncogene and its oncogenic mechanism in medullary thyroid cancer.
26678667 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Surgery in MEN 2A Patients Older Than 5 Years with Micro-MTC: Outcome at Long-term Follow-up.
27406704 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Comprehensive Genomic Profiling of Clinically Advanced Medullary Thyroid Carcinoma.
27207748 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Genetic analysis and clinical investigation of a pedigree with multiple endocrine neoplasia type 2A: A case report.
27698838 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation.
27673361 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Molecular diagnosis and comprehensive treatment of multiple endocrine neoplasia type 2 in Southeastern Chinese.
25628771 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Identification of Novel Small Molecule Inhibitors of Oncogenic RET Kinase.
26046350 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
25810047 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
RET mutation p.S891A in a Chinese family with familial medullary thyroid carcinoma and associated cutaneous amyloidosis binding OSMR variant p.G513D.
26356818 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
High Discrepancy of Driver Mutations in Patients with NSCLC and Synchronous Multiple Lung Ground-Glass Nodules.
25629635 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
RET Cys634Arg mutation confers a more aggressive multiple endocrine neoplasia type 2A phenotype than Cys634Tyr mutation.
25515555 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Multiple endocrine neoplasia Type 2
0.200
CausalMutation
CLINVAR
Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.
26269449 2015