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A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.

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22 February 2020

A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment (English)

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22 February 2020

medical genetics

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Rachel Pearlman

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22 February 2020

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Heather Hampel

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22 February 2020

Robin L Bennett

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22 February 2020

Adam Buchanan

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22 February 2020

Georgia L Wiesner

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22 February 2020

Guideline Development Group, American College of Medical Genetics and Genomics Professional Practice and Guidelines Committee and National Society of Genetic Counselors Practice Guidelines Committee

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22 February 2020

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13 November 2014

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22 February 2020

Genetics in Medicine

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22 February 2020

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22 February 2020

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22 February 2020

70-87

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22 February 2020

Adverse events in cancer genetic testing: medical, ethical, legal, and financial implications

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21 January 2018

American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer Susceptibility

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21 January 2018

Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: recommendation statement

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21 January 2018

Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives

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Referral for cancer genetics consultation: a review and compilation of risk assessment criteria

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21 January 2018

Lung cysts, spontaneous pneumothorax, and genetic associations in 89 families with Birt-Hogg-Dubé syndrome

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21 January 2018

Familial spontaneous pneumothorax

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Mutations in regulatory subunit type 1A of cyclic adenosine 5'-monophosphate-dependent protein kinase (PRKAR1A): phenotype analysis in 353 patients and 80 different genotypes

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21 January 2018

Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease

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21 January 2018

Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysio

1 reference

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21 January 2018

Clinical and Molecular Features of the Carney Complex: Diagnostic Criteria and Recommendations for Patient Evaluation

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21 January 2018

Constitutional mismatch repair deficiency and childhood leukemia/lymphoma--report on a novel biallelic MSH6 mutation

1 reference

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21 January 2018

Constitutional mismatch repair-deficiency syndrome

1 reference

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21 January 2018

High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Lifetime cancer risks in individuals with germline PTEN mutations.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Frequent gastrointestinal polyps and colorectal adenocarcinomas in a prospective series of PTEN mutation carriers

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germline Inactivation of PTEN and Dysregulation of the Phosphoinositol-3-Kinase/Akt Pathway Cause Human Lhermitte-Duclos Disease in Adults

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Will the real Cowden syndrome please stand up: revised diagnostic criteria

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

American founder mutation for attenuated familial adenomatous polyposis

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Papillary thyroid carcinoma and familial adenomatous polyposis of the colon

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Familial adenomatous polyposis associated thyroid carcinoma: a distinct type of follicular cell neoplasm

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Hepatoblastoma and APC gene mutation in familial adenomatous polyposis.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): a review of the literature.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Prevalence of BRCA2 and CDKN2a mutations in German familial pancreatic cancer families

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

BRCA germline mutations in Jewish patients with pancreatic adenocarcinoma

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germline BRCA2 6174delT mutations in Ashkenazi Jewish pancreatic cancer patients

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Analysis of the gene coding for the BRCA2-interacting protein PALB2 in familial and sporadic pancreatic cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

ATM mutations in patients with hereditary pancreatic cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germline mutations in HOXB13 and prostate-cancer risk

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

A population-based assessment of germline HOXB13 G84E mutation and prostate cancer risk

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

The prevalence of BRCA1 mutations among young women with triple-negative breast cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Prevalence of BRCA1 mutations among 403 women with triple-negative breast cancer: implications for genetic screening selection criteria: a Hellenic Cooperative Oncology Group Study.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Prevalence of BRCA mutations among women with triple-negative breast cancer (TNBC) in a genetic counseling cohort

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Cancer risks for male carriers of germline mutations in BRCA1 or BRCA2: a review of the literature

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Evidence for common ancestral origin of a recurring BRCA1 genomic rearrangement identified in high-risk Hispanic families

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Prostate cancer in male BRCA1 and BRCA2 mutation carriers has a more aggressive phenotype

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

A systematic review of the indications for genetic testing and prophylactic gastrectomy among patients with hereditary diffuse gastric cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Hereditary diffuse gastric cancer: updated consensus guidelines for clinical management and directions for future research

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germline Fumarate Hydratase Mutations in Families with Multiple Cutaneous and Uterine Leiomyomata

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer

1 reference

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21 January 2018

Cancer-associated genodermatoses: skin neoplasms as clues to hereditary tumor syndromes.

1 reference

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21 January 2018

Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma

1 reference

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21 January 2018

Fumarate hydratase mutations and predisposition to cutaneous leiomyomas, uterine leiomyomas and renal cancer

1 reference

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21 January 2018

Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample

1 reference

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21 January 2018

Geographical variation in the penetrance of CDKN2A mutations for melanoma

1 reference

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21 January 2018

High-risk Melanoma Susceptibility Genes and Pancreatic Cancer, Neural System Tumors, and Uveal Melanoma across GenoMEL

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Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide high-density single nucleotide polymorphism (SNP) scan and identification of BMPR1A loss of function

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germline bone morphogenesis protein receptor 1A mutation causes colorectal tumorigenesis in hereditary mixed polyposis syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Hereditary mixed polyposis syndrome due to a BMPR1A mutation

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Novel mutations of the MET proto-oncogene in papillary renal carcinomas.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Genetic testing in pheochromocytoma or functional paraganglioma

1 reference

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21 January 2018

The prevalence of SDHB, SDHC, and SDHD mutations in patients with head and neck paraganglioma and association of mutations with clinical features.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

When should genetic testing be obtained in a patient with phaeochromocytoma or paraganglioma?

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Biochemistry, genetics and therapy of malignant pheochromocytomas.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Patterns of risk of hereditary retinoblastoma and applications to genetic counselling

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Second primary tumors in patients with retinoblastoma. A review of the literature

1 reference

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21 January 2018

Mutations in the SMAD4/DPC4 gene in juvenile polyposis

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Juvenile polyposis syndrome: a study of genotype, phenotype, and long-term outcome

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4).

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Colorectal neoplasia in juvenile polyposis or juvenile polyps

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Sarcomas in TP53 germline mutation carriers: a review of the IARC TP53 database

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Molecular genetics of adrenocortical tumours, from familial to sporadic diseases

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germline p53 mutations in a cohort with childhood sarcoma: sex differences in cancer risk

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Sensitivity and predictive value of criteria for p53 germline mutation screening

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Cancer risk in mutation carriers of DNA-mismatch-repair genes

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Cancer Risks For Mismatch Repair Gene Mutation Carriers: A Population-Based Early Onset Case-Family Study

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Feasibility of screening for Lynch syndrome among patients with colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Guidelines for diagnosis and therapy of MEN type 1 and type 2.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Contribution of genetic analysis in screening for MEN1 among patients with sporadic disease and one or more typical manifestation

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Should routine analysis of the MEN1 gene be performed in all patients with primary hyperparathyroidism under 40 years of age?

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Pheochromocytoma and paraganglioma syndromes: genetics and management update.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Thyroid cancer genetics: multiple endocrine neoplasia type 2, non-medullary familial thyroid cancer, and familial syndromes associated with thyroid cancer

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Ret proto-oncogene mutations in apparently sporadic Turkish medullary thyroid carcinoma patients: Turkmen study

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma: an update

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Medullary thyroid cancer: management guidelines of the American Thyroid Association

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Lynch syndrome and MYH-associated polyposis: review and testing strategy.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Identification of MYH mutation carriers in colorectal cancer: a multicenter, case-control, population-based study.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Clinical Implications of the Colorectal Cancer Risk Associated With MUTYH Mutation

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Complications of the naevoid basal cell carcinoma syndrome: results of a population based study

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Very high risk of cancer in familial Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Frequent hSNF5/INI1 Germline Mutations in Patients with Rhabdoid Tumor

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germline and somatic SMARCA4 mutations characterize small cell carcinoma of the ovary, hypercalcemic type

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Tuberous sclerosis complex consensus conference: revised clinical diagnostic criteria

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

The tuberous sclerosis complex: a comprehensive review

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Central nervous system hemangioblastomas, endolymphatic sac tumors, and von Hippel-Lindau disease

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Germline mutations in the vhl gene in patients presenting with phaeochromocytomas

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Should endolymphatic sac tumors be considered part of the von Hippel-Lindau complex? Pathology case report

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Endolymphatic sac tumors: Histopathologic confirmation, clinical characterization, and implication in von hippel‐lindau disease

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2014.147

21 January 2018

MEN1 gene analysis in patients with primary hyperparathyroidism: 10-year experience of a single institution for thyroid and parathyroid care in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

American Gastroenterological Association medical position statement: hereditary colorectal cancer and genetic testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary prostate cancer: epidemiologic and clinical features

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trilateral retinoblastoma: a meta-analysis of hereditary retinoblastoma associated with primary ectopic intracranial retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic analysis of 18 pancreatic carcinoma/melanoma-prone families

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carcinogenesis in MYH-associated polyposis follows a distinct genetic pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PALB2 mutations in European familial pancreatic cancer families

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aggressive papillary tumors of temporal bone

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolution of cardiac rhabdomyoma in tuberous sclerosis complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family history-taking in community family practice: implications for genetic screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer: deleterious BRCA2 mutations in 17%.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRCA2 germline mutations in familial pancreatic carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prevalence of BRCA2 mutations in familial pancreatic cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sporadic pheochromocytomas are rarely associated with germline mutations in the vhl tumor suppressor gene or the ret protooncogene

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk of Soft Tissue Sarcomas by Individual Subtype in Survivors of Hereditary Retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation analysis of the RET proto-oncogene and early thyroidectomy: results of a Portuguese cancer centre

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Solitary retinal capillary hemangioma: hereditary (von Hippel-Lindau disease) or nonhereditary?

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular pathology of tumours of the ear and temporal bone

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family history: the three-generation pedigree.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population-based molecular detection of hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Concise handbook of familial cancer susceptibility syndromes - second edition

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

What's the harm? Genetic counselor perceptions of adverse effects of genetics service provision by non-genetics professionals

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening of the Men1 gene and discovery of germ-line and somatic mutations in apparently sporadic parathyroid tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic screening for multiple endocrine neoplasia syndrome type 1 (MEN-1): when and how

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ACOG Practice Bulletin No. 103: Hereditary breast and ovarian cancer syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile polyposis--a precancerous condition.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aggressive papillary tumor of middle ear/temporal bone and adnexal papillary cystadenoma. Manifestations of von Hippel-Lindau disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Solitary juvenile polyps: not a marker for subsequent malignancy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS families

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the MEN1 gene in sporadic pituitary adenomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SDHA mutations in adult and pediatric wild-type gastrointestinal stromal tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline BRCA1 185delAG mutations in Jewish women with breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High incidence of fundus hamartomas and clinical significance of a fundus score in tuberous sclerosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence, morphology and biology of renal cell carcinoma in von Hippel-Lindau disease compared to sporadic renal cell carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The value of MUTYH testing in patients with early onset microsatellite stable colorectal cancer referred for hereditary nonpolyposis colon cancer syndrome testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of tuberous sclerosis complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The duration of ambulatory visits to physicians

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Penetrance and expressivity of the chromosome 9p melanoma susceptibility locus (MLM)

1 reference

https://pubmed.ncbi.nlm.nih.gov/25394175

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/GIM.2014.147

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25394175%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

Microsoft Academic ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25394175%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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