Maximizing Cumulative Trypsin Activity with Calcium at Elevated Temperature for Enhanced Bottom-Up Proteome Analysis von Nickerson, Jessica, Doucette, Alan

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Impact of Surfactants on Cumulative Trypsin Activity in Bottom-Up Proteome Analysis von Nickerson, Jessica L., Sheridan, Liam V., Doucette, Alan A.

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Recent advances in top‐down proteome sample processing ahead of MS analysis von Nickerson, Jessica L., Baghalabadi, Venus, Rajendran, Subin R. C. K., Jakubec, Philip J., Said, Hammam, McMillen, Teresa S., Dang, Ziheng, Doucette, Alan A.

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Organic Solvent-Based Protein Precipitation for Robust Proteome Purification Ahead of Mass Spectrometry von Nickerson, Jessica L, Baghalabadi, Venus, Dang, Ziheng, Miller, Victoria A, Little, Sara L, Doucette, Alan A

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Cilastatin Ameliorates Rhabdomyolysis-induced AKI in Mice von Matsushita, Katsuyuki, Mori, Kiyoshi, Saritas, Turgay, Eiwaz, Mahaba B., Funahashi, Yoshio, Nickerson, Megan N., Hebert, Jessica F., Munhall, Adam C., McCormick, James A., Yanagita, Motoko, Hutchens, Michael P.

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Mosaicism of the UDP-Galactose Transporter SLC35A2 Causes a Congenital Disorder of Glycosylation von Ng, Bobby G., Buckingham, Kati J., Raymond, Kimiyo, Kircher, Martin, Turner, Emily H., He, Miao, Smith, Joshua D., Eroshkin, Alexey, Szybowska, Marta, Losfeld, Marie E., Chong, Jessica X., Kozenko, Mariya, Li, Chumei, Patterson, Marc C., Gilbert, Rodney D., Nickerson, Deborah A., Shendure, Jay, Bamshad, Michael J., Freeze, Hudson H.

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Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results von Tabor, Holly K., Auer, Paul L., Jamal, Seema M., Chong, Jessica X., Yu, Joon-Ho, Gordon, Adam S., Graubert, Timothy A., O’Donnell, Christopher J., Rich, Stephen S., Nickerson, Deborah A., Bamshad, Michael J.

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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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Von Hippel-Lindau (VHL) inactivation in sporadic clear cell renal cancer: associations with germline VHL polymorphisms and etiologic risk factors von Moore, Lee E, Nickerson, Michael L, Brennan, Paul, Toro, Jorge R, Jaeger, Erich, Rinsky, Jessica, Han, Summer S, Zaridze, David, Matveev, Vsevolod, Janout, Vladimir, Kollarova, Hellena, Bencko, Vladimir, Navratilova, Marie, Szeszenia-Dabrowska, Neonilia, Mates, Dana, Schmidt, Laura S, Lenz, Petra, Karami, Sara, Linehan, W Marston, Merino, Maria, Chanock, Stephen, Boffetta, Paolo, Chow, Wong-Ho, Waldman, Frederic M, Rothman, Nathaniel

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Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis von Emond, Mary J, Louie, Tin, Emerson, Julia, Chong, Jessica X, Mathias, Rasika A, Knowles, Michael R, Rieder, Mark J, Tabor, Holly K, Nickerson, Debbie A, Barnes, Kathleen C, Go, Lung, Gibson, Ronald L, Bamshad, Michael J

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The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities von Chong, Jessica X., Buckingham, Kati J., Jhangiani, Shalini N., Boehm, Corinne, Sobreira, Nara, Smith, Joshua D., Harrell, Tanya M., McMillin, Margaret J., Wiszniewski, Wojciech, Gambin, Tomasz, Coban Akdemir, Zeynep H., Doheny, Kimberly, Scott, Alan F., Avramopoulos, Dimitri, Chakravarti, Aravinda, Hoover-Fong, Julie, Mathews, Debra, Witmer, P. Dane, Ling, Hua, Hetrick, Kurt, Watkins, Lee, Patterson, Karynne E., Reinier, Frederic, Blue, Elizabeth, Muzny, Donna, Kircher, Martin, Bilguvar, Kaya, López-Giráldez, Francesc, Sutton, V. Reid, Tabor, Holly K., Leal, Suzanne M., Gunel, Murat, Mane, Shrikant, Gibbs, Richard A., Boerwinkle, Eric, Hamosh, Ada, Shendure, Jay, Lupski, James R., Lifton, Richard P., Valle, David, Nickerson, Deborah A., Bamshad, Michael J.

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Controversies and progress on standardization of large-scale brain network nomenclature von Uddin, Lucina Q., Betzel, Richard F., Cohen, Jessica R., Damoiseaux, Jessica S., De Brigard, Felipe, Eickhoff, Simon B., Fornito, Alex, Gratton, Caterina, Gordon, Evan M., Laird, Angela R., Larson-Prior, Linda, McIntosh, A. Randal, Nickerson, Lisa D., Pessoa, Luiz, Pinho, Ana Luísa, Poldrack, Russell A., Razi, Adeel, Sadaghiani, Sepideh, Shine, James M., Yendiki, Anastasia, Yeo, B. T. Thomas, Spreng, R. Nathan

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Remote Household Observation for Noninfluenza Respiratory Viral Illness von Emanuels, Anne, Heimonen, Jessica, O’Hanlon, Jessica, Kim, Ashley E, Wilcox, Naomi, McCulloch, Denise J, Brandstetter, Elisabeth, Wolf, Caitlin R, Logue, Jennifer K, Han, Peter D, Pfau, Brian, Newman, Kira L, Hughes, James P, Jackson, Michael L, Uyeki, Timothy M, Boeckh, Michael, Starita, Lea M, Nickerson, Deborah A, Bedford, Trevor, Englund, Janet A, Chu, Helen Y

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DUOX2 Gene Mutation Manifesting as Resistance to Thyrotropin Phenotype von Srichomkwun, Panudda, Takamatsu, Junta, Nickerson, Deborah A., Bamshad, Michael J., Chong, Jessica X., Refetoff, Samuel

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Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate von Cox, Liza L., Cox, Timothy C., Moreno Uribe, Lina M., Zhu, Ying, Richter, Chika T., Nidey, Nichole, Standley, Jennifer M., Deng, Mei, Blue, Elizabeth, Chong, Jessica X., Yang, Yueqin, Carstens, Russ P., Anand, Deepti, Lachke, Salil A., Smith, Joshua D., Dorschner, Michael O., Bedell, Bruce, Kirk, Edwin, Hing, Anne V., Venselaar, Hanka, Valencia-Ramirez, Luz C., Bamshad, Michael J., Glass, Ian A., Cooper, Jonathan A., Haan, Eric, Nickerson, Deborah A., van Bokhoven, Hans, Zhou, Huiqing, Krahn, Katy N., Buckley, Michael F., Murray, Jeffrey C., Lidral, Andrew C., Roscioli, Tony

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8q24 genetic variation and comprehensive haplotypes altering familial risk of prostate cancer von Dupont, William D., Breyer, Joan P., Plummer, W. Dale, Chang, Sam S., Cookson, Michael S., Smith, Joseph A., Blue, Elizabeth E., Bamshad, Michael J., Smith, Jeffrey R.

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Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features von Chong, Jessica X., Yu, Joon-Ho, Lorentzen, Peter, Park, Karen M., Jamal, Seema M., Tabor, Holly K., Rauch, Anita, Saenz, Margarita Sifuentes, Boltshauser, Eugen, Patterson, Karynne E., Nickerson, Deborah A., Bamshad, Michael J.

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Evaluation of Load-Velocity Relationships and Repetitions-to-Failure Equations in the Presence of Male and Female Spotters von Nickerson, Brett S., Williams, Tyler D., Snarr, Ronald L., Garza, Jessica M., Salinas, Gilberto

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Impact of Spotter Sex on One Repetition Maximum Bench Press Performance von Nickerson, Brett S., Salinas, Gilberto, Garza, Jessica M., Cho, Seongkwan, Snarr, Ronald L.

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Mechanisms of Difference in AKI-CKD Transition due to Acute Cardiorenal Syndrome and Ischemia-Reperfusion Injury: TH-PO086 von Funahashi, Yoshio, Hebert, Jessica F., Munhall, Adam C., Nickerson, Megan N., Hutchens, Michael

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