Glycine and a Glycine Dehydrogenase ( ) SNP as Citalopram/Escitalopram Response Biomarkers in Depression: Pharmacometabolomics-Informed Pharmacogenomics by Ji, Y, Hebbring, S, Zhu, H, Jenkins, G D, Biernacka, J, Snyder, K, Drews, M, Fiehn, O, Zeng, Z, Schaid, D, Mrazek, D A, Kaddurah‐Daouk, R, Weinshilboum, R M

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Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants by Karnes, Jason H, Bastarache, Lisa, Shaffer, Christian M, Gaudieri, Silvana, Xu, Yaomin, Glazer, Andrew M, Mosley, Jonathan D, Zhao, Shilin, Raychaudhuri, Soumya, Mallal, Simon, Ye, Zhan, Mayer, John G, Brilliant, Murray H, Hebbring, Scott J, Roden, Dan M, Phillips, Elizabeth J, Denny, Joshua C

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Confirmation of Linkage of Prostate Cancer Aggressiveness with Chromosome 19q by 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 by 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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The All of Us Research Program: Data quality, utility, and diversity by Ramirez, Andrea H., Halvorson, Alese, Qian, Jun, Mayo, Kelsey, Basford, Melissa, Deflaux, Nicole, Muthuraman, Karthik N., Xu, Hua, Wilkins, Consuelo, Anton-Culver, Hoda, Boerwinkle, Eric, Cohn, Elizabeth, Schully, Sheri D., Argos, Maria, Cronin, Robert M., O’Donnell, Christopher, Fouad, Mona, Greenland, Philip, Hebbring, Scott J., Karlson, Elizabeth W., Khatri, Parinda, Korf, Bruce, Sodeke, Stephen, Wilbanks, John, Hentges, Justin, Mockrin, Stephen, Lunt, Christopher, Devaney, Stephanie A., Gebo, Kelly, Denny, Joshua C., Harris, Paul A., Roden, Dan M., Ahmedani, Brian, Cole Johnson, Christine D., Ahsan, Habib, Antoine-LaVigne, Donna, Anton-Culver, Hoda, Topol, Eric, Jain, Praduman, Korf, Bruce, Behringer, Melissa, Gharavi, Ali G., Hripcsak, George, Bier, Louise, Hebbring, Scott Joseph, Burnside, Elizabeth, Drezner, Marc K., Channamsetty, Veena, Montalvo, Wanda, Chinea, Carmen, Jenks, Nancy, Cicek, Mine, Thibodeau, Steve, Collier, Ever, Winkler, Joyce, Corcoran, John, Daviglus, Martha, Denny, Joshua, Doheny, Kim, Eichler, Evan, Lennon, Niall, Gabriel, Stacey, Gibbs, Richard, Gil Rico, Edgar M., Glazer, David, Greenland, Philip, Hogan, William R., Pollan, Cliff, Okun, Sally, Karlson, Elizabeth W., Smoller, Jordan, Ross, Margaret Elizabeth, Kaushal, Rainu, Khatri, Parinda, Kheterpal, Vik, Ojo, Akinlolu, Moreno, Francisco A., Menon, Usha, Malik-Gagnon, Lynda, Mangravite, Lara, Marallo, Adria, Visweswaran, Shyam, Reis, Steven, Moore, John, Talavera, Gregory, O'Donnell, Christopher, Ohno-Machado, Lucila, Randal, Fornessa, Theodorou, Andreas A., Roxas-Murray, Mercedita, Stark, Louisa, Tepp, Ronnie, Topper, Scott, Weidman, Lisa, Weiss, Scott T., Wellis, David, Whittle, Jeffrey, Wilson, Amanda, Zuchner, Stephan, Zwick, Michael E.

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Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network by Venner, Eric, Muzny, Donna M., Abrams, Debra, Albertson-Junkans, Ladia, Ames, Darren C., Aronson, Samuel, Babb, Lawrence J., Balasubramanian, Adithya, Bastarache, Lisa, Behr, Meckenzie, Blout, Carrie, Bowser, Mark, Brilliant, Murray, Brodeur, Wendy, Caraballo, Pedro, Castro, Victor, Chisholm, Rex L., Chung, Wendy, Chute, Christopher G., City, Brittany, Connolly, John J., Crane, Paul, Crew, Katherine, De Andrade, Mariza, Denson, Shawn, Denny, Josh, DeSmet, Tim, Dikilitas, Ozan, Fullerton, Stephanie M., Gabriel, Stacey, Gainer, Vivian, Gharavi, Ali, Glazer, Andrew M., Goehringer, Jessica, Gordon, Adam S., Graham, Chet, Dayal, Jyoti, Hakonarson, Hakon, Harden, Maegan V., Harr, Margaret, Hayes, M. Geoffrey, Henrikson, Nora, Howell, Kayla M., Jiang, Yunyun, Joo, Yoonjung Yoonie, Justice, Anne E., Kalla, Sara E., Kalra, Divya, Kelly, Melissa A., Key, Dustin, Kiryluk, Krzysztof, Kullo, Iftikhar J., Larson, Eric B., Lin, Chiao-Feng, Linder, Jodell, Macbeth, Alyssa, Dinsmore, Michael J., Dodge, Sheila, Fasel, David, Fedotov, Alex, Feng, Qiping, McGowan, Michelle L., Meldrim, Jim, Mosley, Jonathan, Muniz, Jesse, Murdock, David R., Murugan, Mullai, Myers, Melanie F., Namjou, Bahram, Ni, Yizhao, Obeng, Aniwaa Owusu, Taylor, Casey Overby, Peterson, Josh F., Pratap, Siddharth, Prows, Cynthia A., Ralston, James D., Ramaprasan, Arvind, Rasmussen-Torvik, Laura, Schaid, Dan, Sengupta, Soumitra, Singh, Rajbir, Sleiman, Patrick M.A., Smoller, Jordan W., Stanaway, Ian B., Stroud, Mary, Tolwinski, Kasia, Van Driest, Sara L., Veenstra, David, Vicente, Gina, Wagner, Michael, Walunas, Theresa, Wells, Quinn, White, Peter S., Wiley, Ken L., Wilson, Michael W., Woolf, Betty, Yi, Victoria, Zhang, Ge, Zhang, Lan, Gibbs, Richard A.

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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 by Strunz, Tobias, Lauwen, Susette, Kiel, Christina, Hollander, Anneke den, Weber, Bernhard H. F.

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A germline DNA polymorphism enhances alternative splicing of the KLF6 tumor suppressor gene and is associated with increased prostate cancer risk by NARLA, Goutham, DIFEO, Analisa, MCDONNELL, Shannon K, WILEY, Kathleen E, JACOBSEN, Steven J, ISAACS, Sarah D, WALSH, Patrick C, ZHENG, S. Lilly, CHANG, Bao-Li, FRIEDRICHSEN, Danielle M, STANFORD, Janet L, OSTRANDER, Elaine A, REEVES, Helen L, CHINNAIYAN, Arul M, RUBIN, Mark A, JIANFENG XU, THIBODEAU, Stephen N, FRIEDMAN, Scott L, MARTIGNETTI, John A, SCHAID, Daniel J, HIRSHFELD, Jennifer, HOD, Eldad, KATZ, Amanda, ISAACS, William B, HEBBRING, Scott, KOMIYA, Akira

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Comparison of Microsatellites Versus Single-Nucleotide Polymorphisms in a Genome Linkage Screen for Prostate Cancer–Susceptibility Loci by Schaid, Daniel J., Guenther, Jennifer C., Christensen, Gerald B., Hebbring, Scott, Rosenow, Carsten, Hilker, Christopher A., McDonnell, Shannon K., Cunningham, Julie M., Slager, Susan L., Blute, Michael L., Thibodeau, Stephen N.

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Genetic sex validation for sample tracking in next-generation sequencing clinical testing by Hu, Jianhong, Korchina, Viktoriya, Zouk, Hana, Harden, Maegan V, Murdock, David, Macbeth, Alyssa, Harrison, Steven M, Lennon, Niall, Kovar, Christie, Balasubramanian, Adithya, Zhang, Lan, Chandanavelli, Gauthami, Pasham, Divya, Rowley, Robb, Wiley, Ken, Smith, Maureen E, Gordon, Adam, Jarvik, Gail P, Sleiman, Patrick, Kelly, Melissa A, Bland, Harris T, Murugan, Mullai, Venner, Eric, Boerwinkle, Eric, Prows, Cynthia, Mahanta, Lisa, Rehm, Heidi L, Gibbs, Richard A, Muzny, Donna M

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

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The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities by Venner, Eric, Patterson, Karynne, Kalra, Divya, Wheeler, Marsha M., Chen, Yi-Ju, Kalla, Sara E., Yuan, Bo, Karnes, Jason H., Walker, Kimberly, Smith, Joshua D., McGee, Sean, Radhakrishnan, Aparna, Haddad, Andrew, Empey, Philip E., Wang, Qiaoyan, Lichtenstein, Lee, Toledo, Diana, Jarvik, Gail, Musick, Anjene, Gibbs, Richard A.

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Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities by Venner, Eric, Patterson, Karynne, Kalra, Divya, Wheeler, Marsha M., Chen, Yi-Ju, Kalla, Sara E., Yuan, Bo, Karnes, Jason H., Walker, Kimberly, Smith, Joshua D., McGee, Sean, Radhakrishnan, Aparna, Haddad, Andrew, Empey, Philip E., Wang, Qiaoyan, Lichtenstein, Lee, Toledo, Diana, Jarvik, Gail, Musick, Anjene, Gibbs, Richard A.

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

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Glycine and a Glycine Dehydrogenase (GLDC) SNP as Citalopram/Escitalopram Response Biomarkers in Depression: Pharmacometabolomics-Informed Pharmacoqenomics: Sex and Lifestyle Drugs by JI, Y, HEBBRING, S, MRAZEK, D. A, KADDURAH-DAOUK, R, WEINSHILBOUM, R. M, ZHU, H, JENKINS, G. D, BIERNACKA, J, SNYDER, K, DREWS, M, FIEHN, O, ZENG, Z, SCHAID, D

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Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics by Camp, Nicola J., Cannon-Albright, Lisa A., Farnham, James M., Baffoe-Bonnie, Agnes B., George, Asha, Powell, Isaac, Bailey-Wilson, Joan E., Carpten, John D., Giles, Graham G., Hopper, John L., Severi, Gianluca, English, Dallas R., Foulkes, William D., Maehle, Lovise, Moller, Pal, Eeles, Ros, Easton, Douglas, Badzioch, Michael D., Whittemore, Alice S., Oakley-Girvan, Ingrid, Hsieh, Chih-Lin, Dimitrov, Latchezar, Xu, Jianfeng, Stanford, Janet L., Johanneson, Bo, Deutsch, Kerry, McIntosh, Laura, Ostrander, Elaine A., Wiley, Kathleen E., Isaacs, Sarah D., Walsh, Patrick C., Thibodeau, Stephen N., McDonnell, Shannon K., Hebbring, Scott, Schaid, Daniel J., Lange, Ethan M., Cooney, Kathleen A., Tammela, Teuvo L.J., Schleutker, Johanna, Paiss, Thomas, Maier, Christiane, Grönberg, Henrik, Wiklund, Fredrik, Emanuelsson, Monica, Isaacs, William B.

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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 by 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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Genome linkage screen for prostate cancer susceptibility loci: Results from the Mayo Clinic familial prostate cancer study by Cunningham, Julie M., McDonnell, Shannon K., Marks, Angela, Hebbring, Scott, Anderson, Sarah A., Peterson, Brett J., Slager, Susan, French, Amy, Blute, Michael L., Schaid, Daniel J., Thibodeau, Stephen N.

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Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families by Bailey-Wilson, Joan E, Childs, Erica J, Cropp, Cheryl D, Schaid, Daniel J, Xu, Jianfeng, Camp, Nicola J, Cannon-Albright, Lisa A, Farnham, James M, George, Asha, Powell, Isaac, Carpten, John D, Giles, Graham G, Hopper, John L, Severi, Gianluca, English, Dallas R, Foulkes, William D, Mæhle, Lovise, Møller, Pål, Eeles, Rosalind, Easton, Douglas, Guy, Michelle, Edwards, Steve, Badzioch, Michael D, Whittemore, Alice S, Oakley-Girvan, Ingrid, Hsieh, Chih-Lin, Dimitrov, Latchezar, Stanford, Janet L, Karyadi, Danielle M, Deutsch, Kerry, McIntosh, Laura, Ostrander, Elaine A, Wiley, Kathleen E, Isaacs, Sarah D, Walsh, Patrick C, Thibodeau, Stephen N, McDonnell, Shannon K, Hebbring, Scott, Lange, Ethan M, Cooney, Kathleen A, Tammela, Teuvo L J, Schleutker, Johanna, Maier, Christiane, Bochum, Sylvia, Hoegel, Josef, Grönberg, Henrik, Wiklund, Fredrik, Emanuelsson, Monica, Cancel-Tassin, Geraldine, Valeri, Antoine, Cussenot, Olivier, Isaacs, William B

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Polymorphisms in genes involved in sex hormone metabolism and risk of benign prostatic hyperplasia by Roberts, R.O., Bergstralh, E.J., Farmer, S.A., Jacobson, D.J., Hebbring, S.J., Cunningham, J.M., Thibodeau, S.N., Lieber, M.M., Jacobsen, S.J.

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