×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Development of a high risk pancreatic screening clinic using 3.0 T MRI.
29101607 2018
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Pathogenic Germline Variants in 10,389 Adult Cancers.
29625052 2018
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Genetic variants in ATM, H2AFX and MRE11 genes and susceptibility to breast cancer in the polish population.
29678143 2018
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Characteristics of African American women at high-risk for ovarian cancer in the southeast: Results from a Gynecologic Cancer Risk Assessment Clinic.
29486991 2018
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Intraductal/ductal histology and lymphovascular invasion are associated with germline DNA-repair gene mutations in prostate cancer.
29368341 2018
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Rare germline variants in ATM are associated with chronic lymphocytic leukemia.
28652578 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results.
28008555 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
28152038 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Germline Mutations in ATM and BRCA1/2 Distinguish Risk for Lethal and Indolent Prostate Cancer and are Associated with Early Age at Death.
27989354 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
The Clinical Utility of Next Generation Sequencing Results in a Community-Based Hereditary Cancer Risk Program.
27276934 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
27978560 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Molecular and Functional Characterization of a Cohort of Spanish Patients with Ataxia-Telangiectasia.
27664052 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
27978560 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Deleterious Germline Mutations in Patients With Apparently Sporadic Pancreatic Adenocarcinoma.
28767289 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients.
28281021 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients.
28724667 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Rare, protein-truncating variants in ATM , CHEK2 and PALB2 , but not XRCC2 , are associated with increased breast cancer risks.
28779002 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Presented Abstracts from the Thirty Sixth Annual Conference of the National Society of Genetic Counselors (Columbus, OH, September 2017).
28956312 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.
28195393 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Multigene panels in Ashkenazi Jewish patients yield high rates of actionable mutations in multiple non-BRCA cancer-associated genes.
28495237 2017
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
27153395 2016
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
GeneticVariation
CLINVAR
Identification of Gene Mutations and Fusion Genes in Patients with Sézary Syndrome.
27039262 2016
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Ataxia Telangiectasia Masquerading as Hyper IgM Syndrome.
26220245 2016
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer.
26976419 2016
×
Entrez Id: 472
Gene Symbol: ATM
ATM
Neoplastic Syndromes, Hereditary
0.100
CausalMutation
CLINVAR
Gene mutations responsible for primary immunodeficiency disorders: A report from the first primary immunodeficiency biobank in Iran.
27980538 2016