Pathophysiology of drug hypersensitivity von Elzagallaai, Abdelbaset A., Rieder, Michael J.

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Use of Pharmacogenetic and Clinical Factors to Predict the Therapeutic Dose of Warfarin von Gage, BF, Eby, C, Johnson, JA, Deych, E, Rieder, MJ, Ridker, PM, Milligan, PE, Grice, G, Lenzini, P, Rettie, AE, Aquilante, CL, Grosso, L, Marsh, S, Langaee, T, Farnett, LE, Voora, D, Veenstra, DL, Glynn, RJ, Barrett, A, McLeod, HL

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Hair cortisol analysis: An update on methodological considerations and clinical applications von Greff, Michael J.E., Levine, Jeffrey M., Abuzgaia, Awatif M., Elzagallaai, Abdelbaset A., Rieder, Michael J., van Uum, Stan H.M.

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Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants von Fu, Wenqing, O’Connor, Timothy D., Jun, Goo, Kang, Hyun Min, Abecasis, Goncalo, Leal, Suzanne M., Gabriel, Stacey, Rieder, Mark J., Altshuler, David, Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., NHLBI Exome Sequencing Project, Akey, Joshua M.

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations von O’Roak, Brian J., Vives, Laura, Girirajan, Santhosh, Karakoc, Emre, Krumm, Niklas, Coe, Bradley P., Levy, Roie, Ko, Arthur, Lee, Choli, Smith, Joshua D., Turner, Emily H., Stanaway, Ian B., Vernot, Benjamin, Malig, Maika, Baker, Carl, Reilly, Beau, Akey, Joshua M., Borenstein, Elhanan, Rieder, Mark J., Nickerson, Deborah A., Bernier, Raphael, Shendure, Jay, Eichler, Evan E.

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations von O'Roak, Brian J, Deriziotis, Pelagia, Lee, Choli, Vives, Laura, Schwartz, Jerrod J, Girirajan, Santhosh, Karakoc, Emre, MacKenzie, Alexandra P, Ng, Sarah B, Baker, Carl, Rieder, Mark J, Nickerson, Deborah A, Bernier, Raphael, Fisher, Simon E, Shendure, Jay, Eichler, Evan E

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HLA-A31:01 and HLA-B15:02 as Genetic Markers for Carbamazepine Hypersensitivity in Children von Amstutz, U, Ross, C J D, Castro-Pastrana, L I, Rieder, M J, Shear, N H, Hayden, M R, Carleton, B C

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Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes von Tennessen, Jacob A., Bigham, Abigail W., O'Connor, Timothy D., Fu, Wenqing, Kenny, Eimear E., Gravel, Simon, McGee, Sean, Do, Ron, Liu, Xiaoming, Jun, Goo, Kang, Hyun Min, Jordan, Daniel, Leal, Suzanne M., Gabriel, Stacey, Rieder, Mark J., Abecasis, Goncalo, Altshuler, David, Nickerson, Deborah A., Boerwinkle, Eric, Sunyaev, Shamil, Bustamante, Carlos D., Bamshad, Michael J., Akey, Joshua M.

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Recurrent Gain-of-Function Mutation in PRKG1 Causes Thoracic Aortic Aneurysms and Acute Aortic Dissections von Guo, Dong-chuan, Regalado, Ellen, Casteel, Darren E., Santos-Cortez, Regie L., Gong, Limin, Kim, Jeong Joo, Dyack, Sarah, Horne, S. Gabrielle, Chang, Guijuan, Jondeau, Guillaume, Boileau, Catherine, Coselli, Joseph S., Li, Zhenyu, Leal, Suzanne M., Shendure, Jay, Rieder, Mark J., Bamshad, Michael J., Nickerson, Deborah A., Kim, Choel, Milewicz, Dianna M.

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Using synthetic templates to design an unbiased multiplex PCR assay von Carlson, Christopher S., Emerson, Ryan O., Sherwood, Anna M., Desmarais, Cindy, Chung, Moon-Wook, Parsons, Joseph M., Steen, Michelle S., LaMadrid-Herrmannsfeldt, Marissa A., Williamson, David W., Livingston, Robert J., Wu, David, Wood, Brent L., Rieder, Mark J., Robins, Harlan

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Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy von Norton, Nadine, Li, Duanxiang, Rieder, Mark J., Siegfried, Jill D., Rampersaud, Evadnie, Züchner, Stephan, Mangos, Steve, Gonzalez-Quintana, Jorge, Wang, Libin, McGee, Sean, Reiser, Jochen, Martin, Eden, Nickerson, Deborah A., Hershberger, Ray E.

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Reducing pain during vaccine injections: clinical practice guideline von Taddio, Anna, MSc PhD, McMurtry, C. Meghan, PhD, Shah, Vibhuti, MD MSc, Riddell, Rebecca Pillai, PhD, Chambers, Christine T., PhD, Noel, Melanie, PhD, MacDonald, Noni E., MD, Rogers, Jess, BA, Bucci, Lucie M., MA, Mousmanis, Patricia, MD, Lang, Eddy, MD, Halperin, Scott A., MD, Bowles, Susan, PharmD, Halpert, Christine, RN MA, Ipp, Moshe, MD, Asmundson, Gordon J.G., PhD, Rieder, Michael J., MD PhD, Robson, Kate, MLS, Uleryk, Elizabeth, PhD, Antony, Martin M., MD, Dubey, Vinita, RN, Hanrahan, Anita, PhD, Lockett, Donna, MD, Scott, Jeffrey, PhD, Bleeker, Elizabeth Votta, HELPinkids&Adults

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Recommendations for genetic testing to reduce the incidence of anthracycline‐induced cardiotoxicity von Aminkeng, Folefac, Ross, Colin J. D., Rassekh, Shahrad R., Hwang, Soomi, Rieder, Michael J., Bhavsar, Amit P., Smith, Anne, Sanatani, Shubhayan, Gelmon, Karen A., Bernstein, Daniel, Hayden, Michael R., Amstutz, Ursula, Carleton, Bruce C.

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Recommendations for HLA‐B15:02 and HLA‐A31:01 genetic testing to reduce the risk of carbamazepine‐induced hypersensitivity reactions von Amstutz, Ursula, Shear, Neil H., Rieder, Michael J., Hwang, Soomi, Fung, Vincent, Nakamura, Hidefumi, Connolly, Mary B., Ito, Shinya, Carleton, Bruce C.

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Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue von Innocenti, Federico, Cooper, Gregory M, Stanaway, Ian B, Gamazon, Eric R, Smith, Joshua D, Mirkov, Snezana, Ramirez, Jacqueline, Liu, Wanqing, Lin, Yvonne S, Moloney, Cliona, Aldred, Shelly Force, Trinklein, Nathan D, Schuetz, Erin, Nickerson, Deborah A, Thummel, Ken E, Rieder, Mark J, Rettie, Allan E, Ratain, Mark J, Cox, Nancy J, Brown, Christopher D

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Interrupting the Nazarov reaction: domino and cascade processes utilizing cyclopentenyl cations von Grant, Tina N, Rieder, Curtis J, West, Frederick G

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Genome-wide association of lipid-lowering response to statins in combined study populations von Barber, Mathew J, Mangravite, Lara M, Hyde, Craig L, Chasman, Daniel I, Smith, Joshua D, McCarty, Catherine A, Li, Xiaohui, Wilke, Russell A, Rieder, Mark J, Williams, Paul T, Ridker, Paul M, Chatterjee, Aurobindo, Rotter, Jerome I, Nickerson, Deborah A, Stephens, Matthew, Krauss, Ronald M

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Viruses comprise an extensive pool of mobile genetic elements in eukaryote cell cultures and human clinical samples von Thannesberger, Jakob, Hellinger, Hans-Joerg, Klymiuk, Ingeborg, Kastner, Marie-Theres, Rieder, Franz J. J., Schneider, Martina, Fister, Susanne, Lion, Thomas, Kosulin, Karin, Laengle, Johannes, Bergmann, Michael, Rattei, Thomas, Steininger, Christoph

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Pharmacogenomic Prediction of Anthracycline-Induced Cardiotoxicity in Children von VISSCHER, Henk, ROSS, Colin J. D, DER PAL, Helena J. Van, BROWN, Andrew M. K, ROGERS, Paul C, PHILLIPS, Michael S, RIEDER, Michael J, CARLETON, Bruce C, HAYDEN, Michael R, ROD RASSEKH, S, BARHDADI, Amina, DUBE, Marie-Pierre, AL-SALOOS, Hesham, SANDOR, George S, CARON, Huib N, DALEN, Elvira C. Van, KREMER, Leontien C

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The Risk of Adverse Pregnancy Outcome After First Trimester Exposure to H1 Antihistamines: A Systematic Review and Meta-Analysis von Etwel, Fatma, Faught, Lauren H., Rieder, Michael J., Koren, Gideon

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