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BayesMendel: an R environment for Mendelian risk prediction

BayesMendel: an R environment for Mendelian risk prediction

http://www.wikidata.org/entity/Q33241509

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Meta-analysis of BRCA1 and BRCA2 penetrance Recent Enhancements to the Genetic Risk Prediction Model BRCAPRO Characterization of BRCA1 and BRCA2 mutations in a large United States sample Incorporating medical interventions into carrier probability estimation for genetic counseling.Recent BRCAPRO upgrades significantly improve calibration.Estimating CDKN2A carrier probability and personalizing cancer risk assessments in hereditary melanoma using MelaPRO.The BRCAPRO 5.0 model is a useful tool in genetic counseling and clinical management of male breast cancer cases.Breast cancer risk among male BRCA1 and BRCA2 mutation carriers Providing access to risk prediction tools via the HL7 XML-formatted risk web service.Performance of PREMM(1,2,6), MMRpredict, and MMRpro in detecting Lynch syndrome among endometrial cancer cases PancPRO: risk assessment for individuals with a family history of pancreatic cancer.A recessive Mendelian model to predict carrier probabilities of DFNB1 for nonsyndromic deafness.Accuracy of MSI testing in predicting germline mutations of MSH2 and MLH1: a case study in Bayesian meta-analysis of diagnostic tests without a gold standard.Effect of misreported family history on Mendelian mutation prediction models A two-stage approach to genetic risk assessment in primary care.Breast Cancer Risk Prediction Using Clinical Models and 77 Independent Risk-Associated SNPs for Women Aged Under 50 Years: Australian Breast Cancer Family Registry Incorporating tumor immunohistochemical markers in BRCA1 and BRCA2 carrier prediction.Validity of models for predicting BRCA1 and BRCA2 mutations Identifying people at a high risk of developing pancreatic cancer Prediction of germline mutations and cancer risk in the Lynch syndrome Multiple diseases in carrier probability estimation: accounting for surviving all cancers other than breast and ovary in BRCAPRO.Simplifying clinical use of the genetic risk prediction model BRCAPRO.Prediction of BRCA Mutations Using the BRCAPRO Model in Clinic-Based African American, Hispanic, and Other Minority Families in the United States The penetrance of ductal carcinoma in situ among BRCA1 and BRCA2 mutation carriers Penetrance of HNPCC-related cancers in a retrolective cohort of 12 large Newfoundland families carrying a MSH2 founder mutation: an evaluation using modified segregation models.Frailty Models for Familial Risk with Application to Breast Cancer.Characteristics of BRCA1/2 mutations carriers including large genomic rearrangements in high risk breast cancer patients Estimating TP53 Mutation Carrier Probability in Families with Li-Fraumeni Syndrome Using LFSPRO.Large genomic rearrangements in the familial breast and ovarian cancer gene BRCA1 are associated with an increased frequency of high risk features.Tailoring BRCAPRO to Asian-Americans.

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BayesMendel: an R environment for Mendelian risk prediction

http://www.wikidata.org/entity/Q33241509

description

2004 nî lūn-bûn

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2004 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2004 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

@zh-hk

2004年論文

@zh-mo

2004年論文

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2004年论文

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name

BayesMendel: an R environment for Mendelian risk prediction

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BayesMendel: an R environment for Mendelian risk prediction

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BayesMendel: an R environment for Mendelian risk prediction

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BayesMendel: an R environment for Mendelian risk prediction

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BayesMendel: an R environment for Mendelian risk prediction

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BayesMendel: an R environment for Mendelian risk prediction

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Statistical Applications in Genetics and Molecular Biology

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BayesMendel: an R environment for Mendelian risk prediction

@en

P2093

Giovanni Parmigiani

http://www.w3.org/2001/XMLSchema#string

Hormuzd A Katki

http://www.w3.org/2001/XMLSchema#string

Sining Chen

http://www.w3.org/2001/XMLSchema#string

Wenyi Wang

http://www.w3.org/2001/XMLSchema#string

P2860

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews

Inheritance of human breast cancer: evidence for autosomal dominant transmission in high-risk families.

Genetic susceptibility to non-polyposis colorectal cancer.

Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2

Understanding mathematical models for breast cancer risk assessment and counseling.

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

Accuracy of MSI testing in predicting germline mutations of MSH2 and MLH1: a case study in Bayesian meta-analysis of diagnostic tests without a gold standard.

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Article21

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scholarly article

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10.2202/1544-6115.1063

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3

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2004-09-17T00:00:00Z

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