The gene for HMSN2C maps to 12q23-24: A region of neuromuscular disorders von KLEIN, C. J, CUNNINGHAM, J. M, DYCK, P. J, ATKINSON, E. J, SCHAID, D. J, HEBBRING, S. J, ANDERSON, S. A, KLEIN, D. M, DYCK, P. J. B, LITCHY, W. J, THIBODEAU, S. N

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A PheWAS approach in studying HLA-DRB11501 von Hebbring, S J, Schrodi, S J, Ye, Z, Zhou, Z, Page, D, Brilliant, M H

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Confirmation of Linkage of Prostate Cancer Aggressiveness with Chromosome 19q von 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.

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SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies von Klein, C J, Wu, Y, Kruckeberg, K E, Hebbring, S J, Anderson, S A, Cunningham, J M, Dyck, P J B, Klein, D M, Thibodeau, S N, Dyck, P J

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Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants von Karnes, JH, Bastarache, L, Shaffer, CM, Gaudieri, S, Xu, YM, Glazer, AM, Mosley, JD, Zhao, SL, Raychaudhuri, S, Mallal, S, Ye, Z, Mayer, JG, Brilliant, MH, Hebbring, SJ, Roden, DM, Phillips, EJ, Denny, JC

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Sulfotransferase gene copy number variation: pharmacogenetics and function von Hebbring, S.J., Moyer, A.M., Weinshilboum, R.M.

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Nonparametric Tests of Association of Multiple Genes with Human Disease von Schaid, Daniel J., McDonnell, Shannon K., Hebbring, Scott J., Cunningham, Julie M., Thibodeau, Stephen N.

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Fine mapping of familial prostate cancer families narrows the interval for a susceptibility locus on chromosome 22q12.3 to 1.36 Mb von Johanneson, Bo, McDonnell, Shannon K., Karyadi, Danielle M., Hebbring, Scott J., Wang, Liang, Deutsch, Kerry, McIntosh, Laura, Kwon, Erika M., Suuriniemi, Miia, Stanford, Janet L., Schaid, Daniel J., Ostrander, Elaine A., Thibodeau, Stephen N.

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Role of SULT1A1 copy number in tamoxifen treated breast cancer: Findings from the North Central Cancer Treatment Group (NCCTG) adjuvant trial 89–30–52 von Goetz, M. P., Moyer, A. M., Weinshilboum, R. M., Suman, V. A., Hebbring, S. J., Ames, M. M., Berg, J. C., Reynolds, C., Perez, E. A., Ingle, J. N.

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Androgen Receptor Gene Polymorphisms and Increased Risk of Urologic Measures of Benign Prostatic Hyperplasia von Roberts, Rosebud O., Bergstralh, Erik J., Cunningham, Julie M., Hebbring, Scott J., Thibodeau, Stephen N., Lieber, Michael M., Jacobsen, Steven J.

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Polymorphisms in genes involved in sex hormone metabolism may increase risk of benign prostatic hyperplasia von Roberts, Rosebud O., Bergstralh, Erik J., Farmer, Sara A., Jacobson, Debra J., Hebbring, Scott J., Cunningham, Julie M., Thibodeau, Stephen N., Lieber, Michael M., Jacobsen, Steven J.

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Growth factor, cytokine, and vitamin D receptor polymorphisms and risk of benign prostatic hyperplasia in a community-based cohort of men von Mullan, Rebecca J., Bergstralh, Eric J., Farmer, Sara A., Jacobson, Debra J., Hebbring, Scott J., Cunningham, Julie M., Thibodeau, Stephen N., Lieber, Michael M., Jacobsen, Steven J., Roberts, Rosebud O.

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Polymorphisms in the 5α reductase type 2 gene and urologic measures of BPH von Roberts, Rosebud O., Bergstralh, Erik J., Farmer, Sara A., Jacobson, Debra J., McGree, Michaela E., Hebbring, Scott J., Cunningham, Julie M., Anderson, Sarah A., Thibodeau, Stephen N., Lieber, Michael M., Jacobsen, Steven J.

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Allelic Imbalance of 8p Indicates Poor Survival in Gastric Cancer von French, Amy J., Petroni, Gina, Thibideau, Stephen N., Smolkin, Mark, Bissonette, Eric, Roviello, Franco, Harper, Jeffrey C., Koch, Benjamin R., Anderson, Sarah A., Hebbring, Scott J., Powell, Steven M.

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Association of Smoking, Alcohol Consumption, Blood Pressure, Body Mass Index, and Glycemic Risk Factors With Age-Related Macular Degeneration: A Mendelian Randomization Study von Kuan, Valerie, Warwick, Alasdair, Hingorani, Aroon, Tufail, Adnan, Cipriani, Valentina, Burgess, Stephen, Sofat, Reecha

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A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration von Strunz, Tobias, Lauwen, Susette, Kiel, Christina, Hollander, Anneke den, Weber, Bernhard H. F.

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Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits von Grassmann, Felix, Kiel, Christina, Zimmermann, Martina E, Gorski, Mathias, Grassmann, Veronika, Stark, Klaus, Heid, Iris M, Weber, Bernhard H F

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Gluthatione-S-transferase P1 polymorphism I105V in familial and sporadic prostate cancer von Debes, Jose D., Yokomizo, Akira, McDonnell, Shannon K., Hebbring, Scott J., Christensen, Gerald B., Cunningham, Julie M., Jacobsen, Steven J., Tindall, Donald J., Liu, Wanguo, Schaid, Daniel J., Thibodeau, Stephen N.

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The challenges, advantages and future of phenome‐wide association studies von Hebbring, Scott J.

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The phenotypic legacy of admixture between modern humans and Neandertals von Simonti, Corinne N., Vernot, Benjamin, Bastarache, Lisa, Bottinger, Erwin, Carrell, David S., Chisholm, Rex L., Crosslin, David R., Hebbring, Scott J., Jarvik, Gail P., Kullo, Iftikhar J., Li, Rongling, Pathak, Jyotishman, Ritchie, Marylyn D., Roden, Dan M., Verma, Shefali S., Tromp, Gerard, Prato, Jeffrey D., Bush, William S., Akey, Joshua M., Denny, Joshua C., Capra, John A.

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