The Significance of Not Finding a Gene

Por Province, Michael A.
Publicado em 2001

A Correlated Meta-Analysis Strategy for Data Mining “OMIC” Scans

Por Province, Michael A, Borecki, Ingrid B
Publicado em 2013

Re: CYP2D6 Genotyping and the Use of Tamoxifen in Breast Cancer

Por Province, Michael A., Klein, Teri E.
Publicado em 2014

A Framework for Interpreting Type I Error Rates from a Product‐Term Model of Interaction Applied to Quantitative Traits

Por Rao, Tara J., Province, Michael A.
Publicado no Genet Epidemiol (2015)

Microsatellite linkage analysis, single-nucleotide polymorphisms, and haplotype associations with ECB21 in the COGA data

Por Kraja, Aldi T, Borecki, Ingrid B, Province, Michael A
Publicado em 2005

Use of a random coefficient regression (RCR) model to estimate growth parameters

Por Corbett, Jonathan, Kraja, Aldi, Borecki, Ingrid B, Province, Michael A
Publicado em 2003

Regarding “Testing for Population Subdivision and Association in Four Case-Control Studies”

Por Pankow, James S., Province, Michael A., Hunt, Steven C., Arnett, Donna K.
Publicado em 2002

Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits

Por Zhang, Qunyuan, Chung, Doyoung, Kraja, Aldi, Borecki, Ingrid I, Province, Michael A
Publicado em 2011

Distance-based phenotypic association analysis of DNA sequence data

Por Chung, Doyoung, Zhang, Qunyuan, Kraja, Aldi T, Borecki, Ingrid B, Province, Michael A
Publicado em 2011

Adjusting Family Relatedness in Data-driven Burden Test of Rare Variants

Por Zhang, Qunyuan, Wang, Lihua, Koboldt, Dan, Boreki, Ingrid B., Province, Michael A.
Publicado no Genet Epidemiol (2014)

CANDID: A flexible method for prioritizing candidate genes for complex human traits

Por Hutz, Janna E., Kraja, Aldi T., McLeod, Howard L., Province, Michael A.
Publicado no Genet Epidemiol (2008)

Genomewide Analysis of Inherited Variation Associated with Phosphorylation of PI3K/AKT/mTOR Signaling Proteins

Por Hutz, Janna E., Manning, W. Aaron, Province, Michael A., McLeod, Howard L.
Publicado em 2011

A Data Driven Method for Identifying Rare Variants with Heterogeneous Trait Effects

Por Zhang, Qunyuan, Irvin, Marguerite R., Arnett, Donna K., Province, Michael A., Borecki, Ingrid
Publicado em 2011

Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data

Por Kraja, Aldi T, Czajkowski, Jacek, Feitosa, Mary F, Borecki, Ingrid B, Province, Michael A
Publicado em 2011

Data for GAW20: genome-wide DNA sequence variation and epigenome-wide DNA methylation before and after fenofibrate treatment in a family study of metabolic phenotypes

Por Aslibekyan, Stella, Almasy, Laura, Province, Michael A., Absher, Devin M., Arnett, Donna K.
Publicado no BMC Proc (2018)

LIPC variants in the promoter and intron 1 modify HDL-C levels in a sex-specific fashion

Por Feitosa, Mary F., Myers, Richard H., Pankow, James S., Province, Michael A., Borecki, Ingrid B.
Publicado em 2008

Avoiding the high Bonferroni penalty in genome-wide association studies

Por Gao, Xiaoyi, Becker, Lewis C., Becker, Diane M., Starmer, Joshua D., Province, Michael A.
Publicado em 2010

Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study

Por Gomez, Felicia, Wang, Lihua, Abel, Haley, Zhang, Qunyuan, Province, Michael A, Borecki, Ingrid B
Publicado no BMC Genet (2015)

Genome-wide discovery of loci influencing chemotherapy cytotoxicity

Por Watters, James W., Kraja, Aldi, Meucci, Melissa A., Province, Michael A., McLeod, Howard L.
Publicado em 2004

Common Genetic Variants on 6q24 Associated With Exceptional Episodic Memory Performance in the Elderly

Por Barral, Sandra, Cosentino, Stephanie, Christensen, Kaare, Newman, Anne B., Perls, Thomas T., Province, Michael A., Mayeux, Richard
Publicado no JAMA Neurol (2014)