The challenges, advantages and future of phenome-wide association studies

Por Hebbring, Scott J
Publicado em 2014

Sulfotransferase gene copy number variation: pharmacogenetics and function

Por Hebbring, S.J., Moyer, A.M., Weinshilboum, R.M.
Publicado em 2009

Utilizing genotype imputation for the augmentation of sequence data.

Por Brooke L Fridley, Gregory Jenkins, Matthew E Deyo-Svendsen, Scott Hebbring, Robert Freimuth
Publicado em 2010-06-01

Utilizing Genotype Imputation for the Augmentation of Sequence Data

Por Fridley, Brooke L., Jenkins, Gregory, Deyo-Svendsen, Matthew E., Hebbring, Scott, Freimuth, Robert
Publicado em 2010

Application of clinical text data for phenome-wide association studies (PheWASs)

Por Hebbring, Scott J., Rastegar-Mojarad, Majid, Ye, Zhan, Mayer, John, Jacobson, Crystal, Lin, Simon
Publicado no Bioinformatics (2015)

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

Nonparametric Tests of Association of Multiple Genes with Human Disease

Por Schaid, Daniel J., McDonnell, Shannon K., Hebbring, Scott J., Cunningham, Julie M., Thibodeau, Stephen N.
Publicado em 2005

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)

SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies

Por Klein, C, Wu, Y, Kruckeberg, K, Hebbring, S, Anderson, S, Cunningham, J, Dyck, P, Klein, D, Thibodeau, S, Dyck, P
Publicado em 2005

Copy number variation and cytidine analogue cytotoxicity: A genome-wide association approach

Por Wang Liewei, Kocher Jean-Pierre A, Li Liang, Chai High, Hebbring Scott J, Kalari Krishna R, Weinshilboum Richard M
Publicado em 2010-06-01

Copy number variation and cytidine analogue cytotoxicity: A genome-wide association approach

Por Kalari, Krishna R, Hebbring, Scott J, Chai, High Seng, Li, Liang, Kocher, Jean-Pierre A, Wang, Liewei, Weinshilboum, Richard M
Publicado em 2010

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)

RNA-Binding Protein IGF2BP1 in Cutaneous Squamous Cell Carcinoma

Por Kim, TaeWon, Havighurst, Thomas, Kim, KyungMann, Hebbring, Scott J, Ye, Zhan, Aylward, Juliet, Keles, Sunduz, Xu, Yaohui G., Spiegelman, Vladimir S.
Publicado no J Invest Dermatol (2016)

The impact of glucocorticoid polymorphisms on markers of neonatal respiratory disease following antenatal betamethasone administration

Por Haas, David M., Dantzer, Jessica, Lehmann, Amalia S., Philips, Santosh, Skaar, Todd C., McCormick, Catherine L., Hebbring, Scott J., Jung, Jeesun, Li, Lang
Publicado em 2013

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)

The impact of drug metabolizing enzyme polymorphisms on outcomes after antenatal corticosteroid use

Por Haas, David M., Lehmann, Amalia S., Skaar, Todd, Philips, Santosh, McCormick, Catherine L., Beagle, Kyle, Hebbring, Scott J., Dantzer, Jessica, Li, Lang, Jung, Jeesun
Publicado em 2012

Confirmation of Linkage of Prostate Cancer Aggressiveness with Chromosome 19q

Por Slager, S. L., Schaid, D. J., Cunningham, J. M., McDonnell, S. K., Marks, A. F., Peterson, B. J., Hebbring, S. J., Anderson, S., French, A. J., Thibodeau, S. N.
Publicado em 2003

Polymorphisms in mitochondrial genes and prostate cancer risk

Por Wang, Liang, McDonnell, Shannon K., Hebbring, Scott J., Cunningham, Julie M., Sauver, Jennifer St, Cerhan, James R., Isaya, Grazia, Schaid, Daniel J., Thibodeau, Stephen N.
Publicado em 2008

Betaine-homocysteine methyltransferase: human liver genotype-phenotype correlation

Por Feng, Qiping, Kalari, Krishna, Fridley, Brooke L., Jenkins, Gregory, Ji, Yuan, Abo, Ryan, Hebbring, Scott, Zhang, Jianping, Nye, Monica D., Leeder, J. Steven, Weinshilboum, Richard. M.
Publicado em 2010

Serine Hydroxymethyltransferase 1 and 2: Gene Sequence Variation and Functional Genomic Characterization

Por Hebbring, Scott J., Chai, Yubo, Ji, Yuan, Abo, Ryan P., Jenkins, Gregory D., Fridley, Brooke, Zhang, Jianping, Eckloff, Bruce W., Wieben, Eric D., Weinshilboum, Richard M.
Publicado em 2012