The Use of Multiplicity Corrections, Order Statistics and Generalized Family-Wise Statistics with Application to Genome-Wide Studies

Por Schrodi, Steven J.
Publicado no PLoS One (2016)

Reflections on the Field of Human Genetics: A Call for Increased Disease Genetics Theory

Por Schrodi, Steven J.
Publicado no Front Genet (2016)

The Impact of Diagnostic Code Misclassification on Optimizing the Experimental Design of Genetic Association Studies

Por Schrodi, Steven J.
Publicado no J Healthc Eng (2017)

A PheWAS approach in studying HLA-DRB1*1501

Por Hebbring, Scott J., Schrodi, Steven J., Ye, Zhan, Zhou, Zhiyi, Page, David, Brilliant, Murray H
Publicado em 2013

Pro-inflammatory immune responses are associated with clinical signs and symptoms of human anaplasmosis

Por Schotthoefer, Anna M., Schrodi, Steven J., Meece, Jennifer K., Fritsche, Thomas R., Shukla, Sanjay K.
Publicado no PLoS One (2017)

Use of an Electronic Medical Record to Create the Marshfield Clinic Twin/Multiple Birth Cohort

Por Mayer, John, Kitchner, Terrie, Ye, Zhan, Zhou, Zhiyi, He, Min, Schrodi, Steven J., Hebbring, Scott J.
Publicado no Genet Epidemiol (2014)

Differential Lipid Response to Statins is Associated with Variants in the BUD13-APOA5 Gene Region

Por O'Brien, Sarah E, Schrodi, Steven J, Ye, Zhan, Brilliant, Murray H, Virani, Salim S., Brautbar, Ariel
Publicado no J Cardiovasc Pharmacol (2015)

Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections

Por Ye, Zhan, Vasco, Daniel A., Carter, Tonia C., Brilliant, Murray H., Schrodi, Steven J., Shukla, Sanjay K.
Publicado em 2014

Phenome-wide association studies (PheWASs) for functional variants

Por Ye, Zhan, Mayer, John, Ivacic, Lynn, Zhou, Zhiyi, He, Min, Schrodi, Steven J, Page, David, Brilliant, Murray H, Hebbring, Scott J
Publicado no Eur J Hum Genet (2015)

The Decay of Disease Association with Declining Linkage Disequilibrium: A Fine Mapping Theorem

Por Maadooliat, Mehdi, Bansal, Naveen K., Upadhya, Jiblal, Farazi, Manzur R., Li, Xiang, He, Max M., Hebbring, Scott J., Ye, Zhan, Schrodi, Steven J.
Publicado no Front Genet (2016)

Changes in Gut and Plasma Microbiome following Exercise Challenge in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)

Por Shukla, Sanjay K., Cook, Dane, Meyer, Jacob, Vernon, Suzanne D., Le, Thao, Clevidence, Derek, Robertson, Charles E., Schrodi, Steven J., Yale, Steven, Frank, Daniel N.
Publicado no PLoS One (2015)

Neither Replication nor Simulation Supports a Role for the Axon Guidance Pathway in the Genetics of Parkinson's Disease

Por Li, Yonghong, Rowland, Charles, Xiromerisiou, Georgia, Lagier, Robert J., Schrodi, Steven J., Dradiotis, Efthimios, Ross, David, Bui, Nam, Catanese, Joseph, Aggelakis, Konstantinos, Grupe, Andrew, Hadjigeorgiou, Georgios
Publicado em 2008

Validation of a metabolite panel for early diagnosis of type 2 diabetes

Por Carter, Tonia C., Rein, Dietrich, Padberg, Inken, Peter, Erik, Rennefahrt, Ulrike, David, Donna E., McManus, Valerie, Stefanski, Elisha, Martin, Silke, Schatz, Philipp, Schrodi, Steven J.
Publicado no Metabolism (2016)

The 5q31 variants associated with psoriasis and Crohn's disease are distinct

Por Li, Yonghong, Chang, Monica, Schrodi, Steven J., Callis-Duffin, Kristina P., Matsunami, Nori, Civello, Daniel, Bui, Nam, Catanese, Joseph J., Leppert, Mark F., Krueger, Gerald G., Begovich, Ann B.
Publicado em 2008

Genetic and Functional Associations with Decreased Anti-inflammatory Tumor Necrosis Factor Alpha Induced Protein 3 in Macrophages from Subjects with Axial Spondyloarthritis

Por Liu, Yiping, Ye, Zhan, Li, Xiang, Anderson, Jennifer L., Khan, Mike, DaSilva, Douglas, Baron, Marissa, Wilson, Deborah, Bocoun, Vera, Ivacic, Lynn C., Schrodi, Steven J., Smith, Judith A.
Publicado no Front Immunol (2017)

Genetic-based prediction of disease traits: prediction is very difficult, especially about the future(†)

Por Schrodi, Steven J., Mukherjee, Shubhabrata, Shan, Ying, Tromp, Gerard, Sninsky, John J., Callear, Amy P., Carter, Tonia C., Ye, Zhan, Haines, Jonathan L., Brilliant, Murray H., Crane, Paul K., Smelser, Diane T., Elston, Robert C., Weeks, Daniel E.
Publicado em 2014

Further Genetic Evidence for Three Psoriasis-Risk Genes: ADAM33, CDKAL1, and PTPN22

Por Li, Yonghong, Liao, Wilson, Chang, Monica, Schrodi, Steven J., Bui, Nam, Catanese, Joseph J., Poon, Annie, Matsunami, Nori, Callis-Duffin, Kristina P., Leppert, Mark F., Bowcock, Anne M., Kwok, Pui-Yan, Krueger, Gerald G., Begovich, Ann B.
Publicado em 2008

SeqHBase: a big data toolset for family based sequencing data analysis

Por He, Min, Person, Thomas N, Hebbring, Scott J, Heinzen, Ethan, Ye, Zhan, Schrodi, Steven J, McPherson, Elizabeth W, Lin, Simon M, Peissig, Peggy L, Brilliant, Murray H, O'Rawe, Jason, Robison, Reid J, Lyon, Gholson J, Wang, Kai
Publicado no J Med Genet (2015)

Multiple Loci within the Major Histocompatibility Complex Confer Risk of Psoriasis

Por Feng, Bing-Jian, Sun, Liang-Dan, Soltani-Arabshahi, Razieh, Bowcock, Anne M., Nair, Rajan P., Stuart, Philip, Elder, James T., Schrodi, Steven J., Begovich, Ann B., Abecasis, Gonçalo R., Zhang, Xue-Jun, Callis-Duffin, Kristina P., Krueger, Gerald G., Goldgar, David E.
Publicado em 2009

Mining Retrospective Data for Virtual Prospective Drug Repurposing: L-DOPA and Age-related Macular Degeneration

Por Brilliant, Murray H., Vaziri, Kamyar, Connor, Thomas B., Schwartz, Stephen G., Carroll, Joseph J., McCarty, Catherine A., Schrodi, Steven J., Hebbring, Scott J., Kishor, Krishna S., Flynn, Harry W., Moshfeghi, Andrew A., Moshfeghi, Darius M., Fini, M. Elizabeth, McKay, Brian S.
Publicado no Am J Med (2015)