default search action
Google
Google Scholar
Semantic Scholar
Internet Archive Scholar
CiteSeerX
ORCIDSarah A. Pendergrass
Person information
Refine list
refinements active!
zoomed in on ?? of ?? records
view refined list in
export refined list as
2020 – today
- 2021
[j14]Ning Shang
, Atlas Khan, Fernanda Polubriaginof, Francesca Zanoni, Karla Mehl, David Fasel, Paul E. Drawz, Robert J. Carroll, Joshua C. Denny, Matthew A. Hathcock, Adelaide M. Arruda-Olson, Peggy L. Peissig, Richard A. Dart, Murray H. Brilliant, Eric B. Larson, David S. Carrell, Sarah A. Pendergrass, Shefali Setia Verma, Marylyn D. Ritchie, Barbara Benoit, Vivian S. Gainer, Elizabeth W. Karlson, Adam S. Gordon, Gail P. Jarvik, Ian B. Stanaway, David R. Crosslin, Sumit Mohan, Iuliana Ionita-Laza, Nicholas P. Tatonetti, Ali G. Gharavi, George Hripcsak, Chunhua Weng, Krzysztof Kiryluk:
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies. npj Digit. Medicine 4 (2021)
2010 – 2019
- 2019
- [j13]Xinyuan Zhang, Anna Okula Basile, Sarah A. Pendergrass, Marylyn D. Ritchie:
Real world scenarios in rare variant association analysis: the impact of imbalance and sample size on the power in silico. BMC Bioinform. 20(1): 46:1-46:10 (2019) - [c18]William G. La Cava, Christopher R. Bauer, Jason H. Moore, Sarah A. Pendergrass:
Interpretation of machine learning predictions for patient outcomes in electronic health records. AMIA 2019 - [c17]Xinyuan Zhang, Yogasudha Veturi, Shefali Setia Verma, William Bone, Anurag Verma, Anastasia Lucas, Scott J. Hebbring, Joshua C. Denny, Ian B. Stanaway, Gail P. Jarvik, David R. Crosslin, Eric B. Larson, Laura Rasmussen-Torvik, Sarah A. Pendergrass, Jordan W. Smoller, Hakon Hakonarson, Patrick Sleiman, Chunhua Weng, David Fasel, Wei-Qi Wei, Iftikhar J. Kullo, Daniel J. Schaid, Wendy K. Chung, Marylyn D. Ritchie:
Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43, 870 individuals from the eMERGE network. PSB 2019: 272-283 - [i1]William G. La Cava, Christopher R. Bauer, Jason H. Moore, Sarah A. Pendergrass:
Interpretation of machine learning predictions for patient outcomes in electronic health records. CoRR abs/1903.12074 (2019) - 2018
- [j12]Anurag Verma, Yukiko Bradford, Scott M. Dudek, Anastasia Lucas, Shefali S. Verma, Sarah A. Pendergrass, Marylyn D. Ritchie:
A simulation study investigating power estimates in phenome-wide association studies. BMC Bioinform. 19(1): 120:1-120:8 (2018) - 2017
- [c16]Anna Okula Basile, Anurag Verma, Marta Byrska-Bishop, Sarah A. Pendergrass, Christian Darabos, H. Lester Kirchner:
Session Introduction. PSB 2017: 177-183 - [c15]Christopher R. Bauer, Daniel R. Lavage, John Snyder, Joseph B. Leader, J. Matthew Mahoney, Sarah A. Pendergrass:
Opening the Door to the Large Scale Use of Clinical Lab Measures for Association Testing: Exploring Different Methods for Defining Phenotypes. PSB 2017: 356-367 - [c14]Shefali S. Verma, Anastasia Lucas, Daniel R. Lavage, Joseph B. Leader, Raghu Metpally, Sarathbabu Krishnamurthy, Frederick E. Dewey, Ingrid B. Borecki, Alexander E. Lopez, John D. Overton, John Penn, Jeffrey G. Reid, Sarah A. Pendergrass, Gerda Breitwieser, Marylyn D. Ritchie:
Identifying Genetic Associations with Variability in Metabolic Health and Blood Count Laboratory Values: Diving into the Quantitative Traits by Leveraging Longitudinal Data from an EHR. PSB 2017: 533-544 - 2016
- [j11]Anna L. Tyler, Dana C. Crawford, Sarah A. Pendergrass:
The detection and characterization of pleiotropy: discovery, progress, and promise. Briefings Bioinform. 17(1): 13-22 (2016) - [j10]Mariusz Butkiewicz, Jessica Cooke Bailey, Alex T. Frase, Scott M. Dudek, Brian L. Yaspan, Marylyn D. Ritchie, Sarah A. Pendergrass, Jonathan L. Haines:
Pathway analysis by randomization incorporating structure - PARIS: an update. Bioinform. 32(15): 2361-2363 (2016) - [c13]Shefali S. Verma, Alex T. Frase, Anurag Verma, Sarah A. Pendergrass, Shaun Mahony, David W. Haas, Marylyn D. Ritchie:
Phenome-Wide Interaction Study (PheWIS) in Aids Clinical Trials Group Data (ACTG). PSB 2016: 57-68 - [c12]Anurag Verma, Joseph B. Leader, Shefali S. Verma, Alex T. Frase, John R. Wallace, Scott M. Dudek, Daniel R. Lavage, Cristopher V. Van Hout, Frederick E. Dewey, John Penn, Alexander E. Lopez, John D. Overton, David J. Carey, David H. Ledbetter, H. Lester Kirchner, Marylyn D. Ritchie, Sarah A. Pendergrass:
Integrating Clinical Laboratory Measures and ICD-9 Code Diagnoses in Phenome-Wide Association Studies. PSB 2016: 168-179 - 2015
- [j9]Logan Dumitrescu, Nicole A. Restrepo, Robert J. Goodloe, Jonathan Boston, Eric Farber-Eger, Sarah A. Pendergrass, William S. Bush, Dana C. Crawford:
Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry. BioData Min. 8: 35 (2015) - [c11]Joseph B. Leader, Sarah A. Pendergrass, Anurag Verma, David J. Carey, Dustin N. Hartzel, Marylyn D. Ritchie, H. Lester Kirchner:
Contrasting Association Results Between Existing PheWAS Phenotype Definition Methods and Five Validated Electronic Phenotypes. AMIA 2015 - [c10]Molly A. Hall, Shefali S. Verma, Dennis P. Wall, Jason H. Moore, Brendan Keating, Daniel B. Campbell, Gregory Gibson, Folkert W. Asselbergs, Sarah A. Pendergrass:
Session Introduction. Pacific Symposium on Biocomputing 2015: 156-160 - 2014
- [j8]Sabrina L. Mitchell, Jacob B. Hall, Robert J. Goodloe, Jonathan Boston, Eric Farber-Eger, Sarah A. Pendergrass, William S. Bush, Dana C. Crawford:
Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies. BioData Min. 7: 6 (2014) - [j7]Timothy H. Ciesielski, Sarah A. Pendergrass, Marquitta J. White, Nuri Kodaman, Rafal S. Sobota, Minjun Huang, Jacquelaine Bartlett, Jing Li, Qinxin Pan, Jiang Gui, Scott B. Selleck, Christopher I. Amos, Marylyn D. Ritchie, Jason H. Moore, Scott M. Williams:
Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors. BioData Min. 7: 10 (2014) - [j6]Do Kyoon Kim, Ruowang Li, Scott M. Dudek, Alex T. Frase, Sarah A. Pendergrass, Marylyn D. Ritchie:
Knowledge-driven genomic interactions: an application in ovarian cancer. BioData Min. 7: 20 (2014) - [j5]Emily Rose Holzinger, Scott M. Dudek, Alex T. Frase, Sarah A. Pendergrass, Marylyn D. Ritchie:
ATHENA: the analysis tool for heritable and environmental network associations. Bioinform. 30(5): 698-705 (2014) - [c9]Anna L. Tyler, Dana C. Crawford, Sarah A. Pendergrass:
Session introduction. Pacific Symposium on Biocomputing 2014: 183-187 - [c8]Sarah A. Pendergrass, Santhosh Girirajan, Scott B. Selleck:
Uncovering the Etiology of Autism Spectrum Disorders: Genomics, Bioinformatics, Environment, Data Collection and Exploration, and Future Possibilities. Pacific Symposium on Biocomputing 2014: 422-426 - 2013
- [j4]Daniel Wolfe, Scott M. Dudek, Marylyn D. Ritchie, Sarah A. Pendergrass:
Visualizing genomic information across chromosomes with PhenoGram. BioData Min. 6: 18 (2013) - [j3]Sarah A. Pendergrass, Alex T. Frase, John R. Wallace, Daniel Wolfe, Neerja Katiyar, Carrie Moore, Marylyn D. Ritchie:
Genomic analyses with biofilter 2.0: knowledge driven filtering, annotation, and model development. BioData Min. 6: 25 (2013) - [c7]Sarah A. Pendergrass, Shefali S. Verma, Emily Rose Holzinger, Carrie Moore, John R. Wallace, Scott M. Dudek, Wayne Huggins, Terrie E. Kitchner, Carol Waudby, Richard L. Berg, Catherine A. McCarty, Marylyn D. Ritchie:
Next-Generation Analysis of Cataracts: Determining Knowledge Driven Gene-Gene Interactions Using Biofilter, and Gene-Environment Interactions Using the PhenX Toolkit. Pacific Symposium on Biocomputing 2013: 147-158 - [c6]Carrie Moore, John R. Wallace, Alex T. Frase, Sarah A. Pendergrass, Marylyn D. Ritchie:
Using BioBin to Explore Rare Variant Population Stratification. Pacific Symposium on Biocomputing 2013: 332-343 - 2012
- [j2]Sarah A. Pendergrass, Scott M. Dudek, Dana C. Crawford, Marylyn D. Ritchie:
Visually integrating and exploring high throughput Phenome-Wide Association Study (PheWAS) results using PheWAS-View. BioData Min. 5: 5 (2012) - [c5]Carrie C. Buchanan, John R. Wallace, Alex T. Frase, Eric Torstenson, Sarah A. Pendergrass, Marylyn D. Ritchie:
A Biologically Informed Method for Detecting Associations with Rare Variants. EvoBIO 2012: 201-210 - 2011
- [c4]Chun-Nan Hsu, Cheng-Ju Kuo, Congxing Cai, Sarah A. Pendergrass, Marylyn D. Ritchie, José Luis Ambite:
Learning Phenotype Mapping for Integrating Large Genetic Data. BioNLP@ACL 2011: 19-27 - [c3]Sarah A. Pendergrass, Scott M. Dudek, Dan M. Roden, Dana C. Crawford, Marylyn D. Ritchie:
Visual Integration of Results from a Large Dna Biobank (Biovu) Using Synthesis-View. Pacific Symposium on Biocomputing 2011: 265-275 - 2010
- [j1]Sarah A. Pendergrass, Scott M. Dudek, Dana C. Crawford, Marylyn D. Ritchie:
Synthesis-View: visualization and interpretation of SNP association results for multi-cohort, multi-phenotype data and meta-analysis. BioData Min. 3: 10 (2010)
2000 – 2009
- 2004
- [c2]Paul M. Meaney, Qianqian Fang, Margaret Fanning, Sarah A. Pendergrass, Timothy Raynolds, Colleen Fox, Keith D. Paulsen:
Microwave Breast Imaging with an Under-Determined Reconstruction Parameter Mesh. ISBI 2004: 1369-1372 - 2002
- [c1]Dun Li, Paul M. Meaney, Margaret Fanning, Qianqian Fang, Sarah A. Pendergrass, Timothy Raynolds:
Spectrum analysis of microwave breast examination data and reconstructed images. ISBI 2002: 62-65
Coauthor Index
manage site settings
To protect your privacy, all features that rely on external API calls from your browser are turned off by default. You need to opt-in for them to become active. All settings here will be stored as cookies with your web browser. For more information see our F.A.Q.
Unpaywalled article links
Add open access links from 
to the list of external document links (if available).
Privacy notice: By enabling the option above, your browser will contact the API of unpaywall.org to load hyperlinks to open access articles. Although we do not have any reason to believe that your call will be tracked, we do not have any control over how the remote server uses your data. So please proceed with care and consider checking the Unpaywall privacy policy.
Archived links via Wayback Machine
For web page which are no longer available, try to retrieve content from the 
of the Internet Archive (if available).
Privacy notice: By enabling the option above, your browser will contact the API of archive.org to check for archived content of web pages that are no longer available. Although we do not have any reason to believe that your call will be tracked, we do not have any control over how the remote server uses your data. So please proceed with care and consider checking the Internet Archive privacy policy.
Reference lists
Add a list of references from 
, 
, and 
to record detail pages.
load references from crossref.org and opencitations.net
Privacy notice: By enabling the option above, your browser will contact the APIs of crossref.org, opencitations.net, and semanticscholar.org to load article reference information. Although we do not have any reason to believe that your call will be tracked, we do not have any control over how the remote server uses your data. So please proceed with care and consider checking the Crossref privacy policy and the OpenCitations privacy policy, as well as the AI2 Privacy Policy covering Semantic Scholar.
Citation data
Add a list of citing articles from and to record detail pages.
load citations from opencitations.net
Privacy notice: By enabling the option above, your browser will contact the API of opencitations.net and semanticscholar.org to load citation information. Although we do not have any reason to believe that your call will be tracked, we do not have any control over how the remote server uses your data. So please proceed with care and consider checking the OpenCitations privacy policy as well as the AI2 Privacy Policy covering Semantic Scholar.
OpenAlex data
Load additional information about publications from 
.
Privacy notice: By enabling the option above, your browser will contact the API of openalex.org to load additional information. Although we do not have any reason to believe that your call will be tracked, we do not have any control over how the remote server uses your data. So please proceed with care and consider checking the information given by OpenAlex.
last updated on 2024-10-07 22:11 CEST by the dblp team
all metadata released as open data under CC0 1.0 license
see also: Terms of Use | Privacy Policy | Imprint
dblp was originally created in 1993 at:
since 2018, dblp has been operated and maintained by:
the dblp computer science bibliography is funded and supported by:
