Detecting and Characterizing Pleiotropy: New Methods for Uncovering the Connection Between the Complexity of Genomic Architecture and Multiple phenotypes

Por Tyler, Anna L., Crawford, Dana C., Pendergrass, Sarah A.
Publicado em 2014

Visualizing genomic information across chromosomes with PhenoGram

Por Wolfe, Daniel, Dudek, Scott, Ritchie, Marylyn D, Pendergrass, Sarah A
Publicado em 2013

Synthesis-View: visualization and interpretation of SNP association results for multi-cohort, multi-phenotype data and meta-analysis

Por Pendergrass Sarah A, Dudek Scott M, Crawford Dana C, Ritchie Marylyn D
Publicado em 2010-12-01

Synthesis-View: visualization and interpretation of SNP association results for multi-cohort, multi-phenotype data and meta-analysis

Por Pendergrass, Sarah A, Dudek, Scott M, Crawford, Dana C, Ritchie, Marylyn D
Publicado em 2010

Visually integrating and exploring high throughput Phenome-Wide Association Study (PheWAS) results using PheWAS-View

Por Pendergrass, Sarah A, Dudek, Scott M, Crawford, Dana C, Ritchie, Marylyn D
Publicado em 2012

Genome-wide analysis of mRNAs bound to the histone stem–loop binding protein

Por Townley-Tilson, W.H. Davin, Pendergrass, Sarah A., Marzluff, William F., Whitfield, Michael L.
Publicado em 2006

USING BIOBIN TO EXPLORE RARE VARIANT POPULATION STRATIFICATION

Por Moore, Carrie B., Wallace, John R., Frase, Alex T., Pendergrass, Sarah A., Ritchie, Marylyn D.
Publicado em 2013

BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge

Por Moore, Carrie B, Wallace, John R, Frase, Alex T, Pendergrass, Sarah A, Ritchie, Marylyn D
Publicado em 2013

ATHENA: the analysis tool for heritable and environmental network associations

Por Holzinger, Emily R., Dudek, Scott M., Frase, Alex T., Pendergrass, Sarah A., Ritchie, Marylyn D.
Publicado em 2014

Intrinsic gene expression subsets of diffuse cutaneous systemic sclerosis are stable in serial skin biopsies

Por Pendergrass, Sarah A., Lemaire, Raphael, Francis, Ian, Mahoney, J. Matthew, Lafyatis, Robert, Whitfield, Michael L.
Publicado em 2012

Knowledge-driven genomic interactions: an application in ovarian cancer

Por Kim, Dokyoon, Li, Ruowang, Dudek, Scott M, Frase, Alex T, Pendergrass, Sarah A, Ritchie, Marylyn D
Publicado em 2014

Genomic analyses with biofilter 2.0: knowledge driven filtering, annotation, and model development

Por Pendergrass, Sarah A, Frase, Alex, Wallace, John, Wolfe, Daniel, Katiyar, Neerja, Moore, Carrie, Ritchie, Marylyn D
Publicado em 2013

Limited Systemic Sclerosis Patients with Pulmonary Arterial Hypertension Show Biomarkers of Inflammation and Vascular Injury

Por Pendergrass, Sarah A., Hayes, Everett, Farina, Giuseppina, Lemaire, Raphael, Farber, Harrison W., Whitfield, Michael L., Lafyatis, Robert
Publicado em 2010

Characterization of mitochondrial haplogroups in a large population-based sample from the United States

Por Mitchell, Sabrina L., Goodloe, Robert, Brown-Gentry, Kristin, Pendergrass, Sarah A., Murdock, Deborah G., Crawford, Dana C.
Publicado em 2014

PHENOME-WIDE INTERACTION STUDY (PheWIS) IN AIDS CLINICAL TRIALS GROUP DATA (ACTG)

Por Verma, Shefali S., Frase, Alex T., Verma, Anurag, Pendergrass, Sarah A., Mahony, Shaun, Haas, David W., Ritchie, Marylyn D.
Publicado no Pac Symp Biocomput (2016)

Antagonistic effect of the matricellular signaling protein CCN3 on TGF-β- and Wnt-mediated fibrillinogenesis in systemic sclerosis and Marfan syndrome

Por Lemaire, Raphael, Farina, Giuseppina, Bayle, Julie, Dimarzio, Michael, Pendergrass, Sarah A., Milano, Ausra, Whitfield, Michael L., Lafyatis, Robert
Publicado em 2010

A Core MYC Gene Expression Signature Is Prominent in Basal-Like Breast Cancer but Only Partially Overlaps the Core Serum Response

Por Chandriani, Sanjay, Frengen, Eirik, Cowling, Victoria H., Pendergrass, Sarah A., Perou, Charles M., Whitfield, Michael L., Cole, Michael D.
Publicado em 2009

Low Frequency Variants, Collapsed Based on Biological Knowledge, Uncover Complexity of Population Stratification in 1000 Genomes Project Data

Por Moore, Carrie B., Wallace, John R., Wolfe, Daniel J., Frase, Alex T., Pendergrass, Sarah A., Weiss, Kenneth M., Ritchie, Marylyn D.
Publicado em 2013

Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry

Por Dumitrescu, Logan, Restrepo, Nicole A., Goodloe, Robert, Boston, Jonathan, Farber-Eger, Eric, Pendergrass, Sarah A., Bush, William S., Crawford, Dana C.
Publicado no BioData Min (2015)

Contrasting Association Results between Existing PheWAS Phenotype Definition Methods and Five Validated Electronic Phenotypes

Por Leader, Joseph B, Pendergrass, Sarah A, Verma, Anurag, Carey, David J, Hartzel, Dustin N, Ritchie, Marylyn D, Kirchner, H. Lester
Publicado no AMIA Annu Symp Proc (2015)