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Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies

Genetic epidemiology, 2016-09, Vol.40 (6), p.461-469

2016

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Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome

Clinical genetics, 2011-06, Vol.79 (6), p.512-522

2011

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Hippocampal volumes in cognitively normal persons at genetic risk for Alzheimer's disease

Annals of neurology, 1998-08, Vol.44 (2), p.288-291

1998

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Frequency of loss of hMLH1 expression in colorectal carcinoma increases with advancing age

Cancer, 2003-03, Vol.97 (6), p.1421-1427

2003

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Absence of PMS2 mutations in colon-CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression

Clinical genetics, 2013-06, Vol.83 (6), p.591-593

2013

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Microsatellite instability in hereditary and sporadic breast cancers

International journal of cancer, 2003-11, Vol.107 (4), p.580-582

2003

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Hippocampal atrophy and apolipoprotein E genotype are independently associated with Alzheimer's disease

Annals of neurology, 1998-03, Vol.43 (3), p.303-310

1998

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Genetic heterogeneity in Peutz-Jeghers syndrome

Human mutation, 2000-07, Vol.16 (1), p.23-30

2000

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Iron overload in cirrhosis—HFE genotypes and outcome after liver transplantation

Hepatology (Baltimore, Md.), 2000-02, Vol.31 (2), p.456-460

2000

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Polymorphisms in genes involved in sex hormone metabolism may increase risk of benign prostatic hyperplasia

The Prostate, 2006-03, Vol.66 (4), p.392-404

2006

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Microsatellite instability and hMLH1/hMSH2 expression in young endometrial carcinoma patients: Associations with family history and histopathology

International journal of cancer, 2000-04, Vol.86 (1), p.60-66

2000

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Genotype‐phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium

Journal of internal medicine, 1995-10, Vol.238 (4), p.343-346

1995

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Genome linkage screen for prostate cancer susceptibility loci: Results from the Mayo Clinic familial prostate cancer study

The Prostate, 2003-12, Vol.57 (4), p.335-346

2003

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High throughput detection of microsatellite instability by denaturing high-performance liquid chromatography

Human mutation, 2003-11, Vol.22 (5), p.388-394

2003

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Polymorphisms in the 5α reductase type 2 gene and urologic measures of BPH

The Prostate, 2005-03, Vol.62 (4), p.380-387

2005

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Candidate-gene association studies with pedigree data: Controlling for environmental covariates

Genetic epidemiology, 2003-05, Vol.24 (4), p.273-283

2003

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DNA mismatch repair genes hMLH1, hMSH2, and hMSH6 are not inactivated in bronchioloalveolar carcinomas of the lung

Cancer, 2001-12, Vol.92 (11), p.2898-2901

2001

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Predictive value of APOE genotyping in incipient Alzheimer's disease

Annals of the New York Academy of Sciences, 1996-12, Vol.802, p.58-69

1996

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Prevalence and clinical significance of HFE gene mutations in patients with iron overload

The American journal of gastroenterology, 2000, Vol.95 (10), p.2910-2914

2000

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Luteinizing hormone β polymorphism and risk of familial and sporadic prostate cancer

The Prostate, 2003-06, Vol.56 (1), p.30-36

2003

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Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism

Clinical genetics, 1996-03, Vol.49 (3), p.124-129

1996

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Current status of adjuvant chemotherapy for colorectal cancer: Can molecular markers play a role in predicting prognosis?

Cancer, 1992-09, Vol.70 (S4), p.1732-1739

1992

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A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repair

Genes chromosomes & cancer, 2001-02, Vol.30 (2), p.181-186

2001

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Microsatellite Instability in Keratoacanthoma

Cancer, 1995-11, Vol.76 (10), p.1765-1771

1995

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High functioning fragile X males: Demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression

American journal of medical genetics, 1994-07, Vol.51 (4), p.298-308

1994

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Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies

Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome

Hippocampal volumes in cognitively normal persons at genetic risk for Alzheimer's disease

Frequency of loss of hMLH1 expression in colorectal carcinoma increases with advancing age

Absence of PMS2 mutations in colon-CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression

Microsatellite instability in hereditary and sporadic breast cancers

Hippocampal atrophy and apolipoprotein E genotype are independently associated with Alzheimer's disease

Genetic heterogeneity in Peutz-Jeghers syndrome

Iron overload in cirrhosis—HFE genotypes and outcome after liver transplantation

Polymorphisms in genes involved in sex hormone metabolism may increase risk of benign prostatic hyperplasia

Microsatellite instability and hMLH1/hMSH2 expression in young endometrial carcinoma patients: Associations with family history and histopathology

Genotype‐phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium

Genome linkage screen for prostate cancer susceptibility loci: Results from the Mayo Clinic familial prostate cancer study

High throughput detection of microsatellite instability by denaturing high-performance liquid chromatography

Polymorphisms in the 5α reductase type 2 gene and urologic measures of BPH

Candidate-gene association studies with pedigree data: Controlling for environmental covariates

DNA mismatch repair genes hMLH1, hMSH2, and hMSH6 are not inactivated in bronchioloalveolar carcinomas of the lung

Predictive value of APOE genotyping in incipient Alzheimer's disease

Prevalence and clinical significance of HFE gene mutations in patients with iron overload

Luteinizing hormone β polymorphism and risk of familial and sporadic prostate cancer

Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism

Current status of adjuvant chemotherapy for colorectal cancer: Can molecular markers play a role in predicting prognosis?

A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repair

Microsatellite Instability in Keratoacanthoma

High functioning fragile X males: Demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression

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