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Met induces mammary tumors with diverse histologies and is associated with poor outcome and human basal breast cancer

Proceedings of the National Academy of Sciences - PNAS, 2009-08, Vol.106 (31), p.12903-12908

2009

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Genome-Wide Association Scan for Diabetic Nephropathy Susceptibility Genes in Type 1 Diabetes

Diabetes (New York, N.Y.), 2009-06, Vol.58 (6), p.1403-1410

2009

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Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification

PLoS genetics, 2013-08, Vol.9 (8), p.e1003609-e1003609

2013

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Tumoral BRD4 expression in lymph node-negative breast cancer: association with T-bet+ tumor-infiltrating lymphocytes and disease-free survival

BMC cancer, 2018-07, Vol.18 (1), p.750-750, Article 750

2018

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Osteosarcoma and soft-tissue sarcomas with an immune infiltrate express PD-L1: relation to clinical outcome and Th1 pathway activation

Oncoimmunology, 2020-01, Vol.9 (1), p.1737385-1737385

2020

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Penalized maximum likelihood inference under the mixture cure model in sparse data

Statistics in medicine, 2023-06, Vol.42 (13), p.2134-2161

2023

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A Genome-Wide Association Study Identifies a Novel Major Locus for Glycemic Control in Type 1 Diabetes, as Measured by Both A1C and Glucose

Diabetes (New York, N.Y.), 2010-02, Vol.59 (2), p.539-549

2010

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Insights From Mixture Cure Modeling of Molecular Markers for Prognosis in Breast Cancer

Journal of clinical oncology, 2013-06, Vol.31 (16), p.2047-2054

2013

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Statistical power in COVID-19 case-control host genomic study design

Genome medicine, 2020-12, Vol.12 (1), p.115-8, Article 115

2020

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gpart: human genome partitioning and visualization of high-density SNP data by identifying haplotype blocks

Bioinformatics, 2019-11, Vol.35 (21), p.4419-4421

2019

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Integrating epigenetic, genetic, and phenotypic data to uncover gene-region associations with triglycerides in the GOLDN study

BMC proceedings, 2018-09, Vol.12 (Suppl 9), p.57-57, Article 57

2018

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Characterization of direct and/or indirect genetic associations for multiple traits in longitudinal studies of disease progression

Genetics (Austin), 2023-08, Vol.225 (1)

2023

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A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits

Frontiers in genetics, 2014-10, Vol.5, p.357-357

2014

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Human leucocyte antigen risk alleles for psoriatic arthritis among patients with psoriasis

Annals of the rheumatic diseases, 2012-01, Vol.71 (1), p.50-55

2012

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A new haplotype block detection method for dense genome sequencing data based on interval graph modeling of clusters of highly correlated SNPs

Bioinformatics, 2018-02, Vol.34 (3), p.388-397

2018

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Prognostic Effect of Basal-Like Breast Cancers Is Time Dependent: Evidence from Tissue Microarray Studies on a Lymph Node–Negative Cohort

Clinical cancer research, 2008-07, Vol.14 (13), p.4168-4174

2008

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Expression profiling of familial breast cancers demonstrates higher expression of FGFR2 in BRCA2-associated tumors

Breast cancer research and treatment, 2009-09, Vol.117 (1), p.183-191

2009

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Gene-based multiple regression association testing for combined examination of common and low frequency variants in quantitative trait analysis

Frontiers in genetics, 2013, Vol.4, p.233-233

2013

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TP53 Mutations and Outcome in Osteosarcoma: A Prospective, Multicenter Study

Journal of clinical oncology, 2005-03, Vol.23 (7), p.1483-1490

2005

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Two‐phase sample selection strategies for design and analysis in post‐genome‐wide association fine‐mapping studies

Statistics in medicine, 2021-12, Vol.40 (30), p.6792-6817

2021

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CK8/18 expression, the basal phenotype, and family history in identifying BRCA1‐associated breast cancer in the Ontario site of the Breast Cancer Family Registry

Cancer, 2011-04, Vol.117 (7), p.1350-1359

2011

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Ethnic Differences in Relative Risk of Idiopathic Calcium Nephrolithiasis in North America

The Journal of urology, 2007-11, Vol.178 (5), p.1992-1997

2007

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Human leukocyte antigen alleles and susceptibility to psoriatic arthritis

Human immunology, 2013-10, Vol.74 (10), p.1333-1338

2013

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The Combination of p53 Mutation and neu/erbB-2 Amplification Is Associated With Poor Survival in Node-Negative Breast Cancer

Journal of clinical oncology, 2004-01, Vol.22 (1), p.86-96

2004

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The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy

Human genetics, 2015-02, Vol.134 (2), p.247-257

2015

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Met induces mammary tumors with diverse histologies and is associated with poor outcome and human basal breast cancer

Genome-Wide Association Scan for Diabetic Nephropathy Susceptibility Genes in Type 1 Diabetes

Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification

Tumoral BRD4 expression in lymph node-negative breast cancer: association with T-bet+ tumor-infiltrating lymphocytes and disease-free survival

Osteosarcoma and soft-tissue sarcomas with an immune infiltrate express PD-L1: relation to clinical outcome and Th1 pathway activation

Penalized maximum likelihood inference under the mixture cure model in sparse data

A Genome-Wide Association Study Identifies a Novel Major Locus for Glycemic Control in Type 1 Diabetes, as Measured by Both A1C and Glucose

Insights From Mixture Cure Modeling of Molecular Markers for Prognosis in Breast Cancer

Statistical power in COVID-19 case-control host genomic study design

gpart: human genome partitioning and visualization of high-density SNP data by identifying haplotype blocks

Integrating epigenetic, genetic, and phenotypic data to uncover gene-region associations with triglycerides in the GOLDN study

Characterization of direct and/or indirect genetic associations for multiple traits in longitudinal studies of disease progression

A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits

Human leucocyte antigen risk alleles for psoriatic arthritis among patients with psoriasis

A new haplotype block detection method for dense genome sequencing data based on interval graph modeling of clusters of highly correlated SNPs

Prognostic Effect of Basal-Like Breast Cancers Is Time Dependent: Evidence from Tissue Microarray Studies on a Lymph Node–Negative Cohort

Expression profiling of familial breast cancers demonstrates higher expression of FGFR2 in BRCA2-associated tumors

Gene-based multiple regression association testing for combined examination of common and low frequency variants in quantitative trait analysis

TP53 Mutations and Outcome in Osteosarcoma: A Prospective, Multicenter Study

Two‐phase sample selection strategies for design and analysis in post‐genome‐wide association fine‐mapping studies

CK8/18 expression, the basal phenotype, and family history in identifying BRCA1‐associated breast cancer in the Ontario site of the Breast Cancer Family Registry

Ethnic Differences in Relative Risk of Idiopathic Calcium Nephrolithiasis in North America

Human leukocyte antigen alleles and susceptibility to psoriatic arthritis

The Combination of p53 Mutation and neu/erbB-2 Amplification Is Associated With Poor Survival in Node-Negative Breast Cancer

The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy

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