cis-Platinum-hexamethylmelamine therapy of advanced ovarian cancer von Lopez, JoséA., Krikorian, John G., Dias, Sylvia F., Spiers, Alexander S.D., Finkel, Harvey E., Barnard, Donna E.

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The principal results of the International Immune Tolerance Study: a randomized dose comparison von Hay, Charles R.M., DiMichele, Donna M.

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Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders von Wang, Tianyun, Hoekzema, Kendra, Vecchio, Davide, Wu, Huidan, Sulovari, Arvis, Coe, Bradley P., Gillentine, Madelyn A., Wilfert, Amy B., Perez-Jurado, Luis A., Kvarnung, Malin, Sleyp, Yoeri, Earl, Rachel K., Rosenfeld, Jill A., Geisheker, Madeleine R., Han, Lin, Du, Bing, Barnett, Chris, Thompson, Elizabeth, Shaw, Marie, Carroll, Renee, Friend, Kathryn, Catford, Rachael, Palmer, Elizabeth E., Zou, Xiaobing, Ou, Jianjun, Li, Honghui, Guo, Hui, Gerdts, Jennifer, Avola, Emanuela, Calabrese, Giuseppe, Elia, Maurizio, Greco, Donatella, Lindstrand, Anna, Nordgren, Ann, Anderlid, Britt-Marie, Vandeweyer, Geert, Van Dijck, Anke, Van der Aa, Nathalie, McKenna, Brooke, Hancarova, Miroslava, Bendova, Sarka, Havlovicova, Marketa, Malerba, Giovanni, Bernardina, Bernardo Dalla, Muglia, Pierandrea, van Haeringen, Arie, Hoffer, Mariette J. V., Franke, Barbara, Cappuccio, Gerarda, Delatycki, Martin, Lockhart, Paul J., Manning, Melanie A., Liu, Pengfei, Scheffer, Ingrid E., Brunetti-Pierri, Nicola, Rommelse, Nanda, Amaral, David G., Santen, Gijs W. E., Trabetti, Elisabetta, Sedláček, Zdeněk, Michaelson, Jacob J., Pierce, Karen, Courchesne, Eric, Kooy, R. Frank, Nordenskjöld, Magnus, Romano, Corrado, Peeters, Hilde, Bernier, Raphael A., Gecz, Jozef, Xia, Kun, Eichler, Evan E.

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Clonal haematopoiesis and risk of chronic liver disease von Wong, Waihay J., Emdin, Connor, Bick, Alexander G., Zekavat, Seyedeh M., Niroula, Abhishek, Pirruccello, James P., Dichtel, Laura, Griffin, Gabriel, Uddin, Md Mesbah, Gibson, Christopher J., Kovalcik, Veronica, Lin, Amy E., McConkey, Marie E., Vromman, Amelie, Sellar, Rob S., Kim, Peter G., Agrawal, Mridul, Weinstock, Joshua, Long, Michelle T., Yu, Bing, Banerjee, Rajarshi, Nicholls, Rowan C., Dennis, Andrea, Kelly, Matt, Loh, Po-Ru, McCarroll, Steve, Boerwinkle, Eric, Vasan, Ramachandran S., Jaiswal, Siddhartha, Johnson, Andrew D., Chung, Raymond T., Corey, Kathleen, Levy, Daniel, Ballantyne, Christie, Ebert, Benjamin L., Natarajan, Pradeep

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Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders von Wang, Tianyun, Kim, Chang N., Bakken, Trygve E., Gillentine, Madelyn A., Henning, Barbara, Mao, Yafei, Gilissen, Christian, Nowakowski, Tomasz J., Eichler, Evan E.

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Performance of commercial PCR assays to detect toxigenic Clostridioides difficile in the feces of puppies von Anis, Eman, Barnart, Denise, Barnard, Amanda, Kelly, Donna J., Redding, Laurel E.

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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders von Gillentine, Madelyn A, Wang, Tianyun, Hoekzema, Kendra, Rosenfeld, Jill, Liu, Pengfei, Guo, Hui, Kim, Chang N, De Vries, Bert B A, Vissers, Lisenka E L M, Nordenskjold, Magnus, Kvarnung, Malin, Lindstrand, Anna, Nordgren, Ann, Gecz, Jozef, Iascone, Maria, Cereda, Anna, Scatigno, Agnese, Maitz, Silvia, Zanni, Ginevra, Bertini, Enrico, Zweier, Christiane, Schuhmann, Sarah, Wiesener, Antje, Pepper, Micah, Panjwani, Heena, Torti, Erin, Abid, Farida, Anselm, Irina, Srivastava, Siddharth, Atwal, Paldeep, Bacino, Carlos A, Bhat, Gifty, Cobian, Katherine, Bird, Lynne M, Friedman, Jennifer, Wright, Meredith S, Callewaert, Bert, Petit, Florence, Mathieu, Sophie, Afenjar, Alexandra, Christensen, Celenie K, White, Kerry M, Elpeleg, Orly, Berger, Itai, Espineli, Edward J, Fagerberg, Christina, Brasch-Andersen, Charlotte, Hansen, Lars Kjærsgaard, Feyma, Timothy, Hughes, Susan, Thiffault, Isabelle, Sullivan, Bonnie, Yan, Shuang, Keller, Kory, Keren, Boris, Mignot, Cyril, Kooy, Frank, Meuwissen, Marije, Basinger, Alice, Kukolich, Mary, Philips, Meredith, Ortega, Lucia, Drummond-Borg, Margaret, Lauridsen, Mathilde, Sorensen, Kristina, Lehman, Anna, Lopez-Rangel, Elena, Levy, Paul, Lessel, Davor, Lotze, Timothy, Madan-Khetarpal, Suneeta, Sebastian, Jessica, Vento, Jodie, Vats, Divya, Benman, L Manace, Mckee, Shane, Mirzaa, Ghayda M, Muss, Candace, Pappas, John, Peeters, Hilde, Romano, Corrado, Elia, Maurizio, Galesi, Ornella, Simon, Marleen E H, van Gassen, Koen L I, Simpson, Kara, Stratton, Robert, Syed, Sabeen, Thevenon, Julien, Palafoll, Irene Valenzuela, Vitobello, Antonio, Bournez, Marie, Faivre, Laurence, Xia, Kun, Earl, Rachel K, Nowakowski, Tomasz, Bernier, Raphael A, Eichler, Evan E

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Psychiatric and Medical Profiles of Autistic Adults in the SPARK Cohort von Fombonne, Eric, Green Snyder, LeeAnne, Daniels, Amy, Feliciano, Pamela, Chung, Wendy

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Genome sequencing unveils a regulatory landscape of platelet reactivity von Keramati, Ali R., Chen, Ming-Huei, Rodriguez, Benjamin A. T., Yanek, Lisa R., Bhan, Arunoday, Gaynor, Brady J., Ryan, Kathleen, Brody, Jennifer A., Zhong, Xue, Wei, Qiang, Kammers, Kai, Kanchan, Kanika, Iyer, Kruthika, Kowalski, Madeline H., Pitsillides, Achilleas N., Cupples, L. Adrienne, Li, Bingshan, Schlaeger, Thorsten M., Shuldiner, Alan R., O’Connell, Jeffrey R., Ruczinski, Ingo, Mitchell, Braxton D., Faraday, Nauder, Taub, Margaret A., Becker, Lewis C., Lewis, Joshua P., Mathias, Rasika A., Johnson, Andrew D.

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Physician and Nurse Well-Being and Preferred Interventions to Address Burnout in Hospital Practice: Factors Associated With Turnover, Outcomes, and Patient Safety von Aiken, Linda H, Lasater, Karen B, Sloane, Douglas M, Pogue, Colleen A, Fitzpatrick Rosenbaum, Kathleen E, Muir, K Jane, McHugh, Matthew D

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A Circulating MicroRNA Signature Serves as a Diagnostic and Prognostic Indicator in Sarcoidosis von Ascoli, Christian, Huang, Yue, Schott, Cody, Turturice, Benjamin A, Metwally, Ahmed, Perkins, David L, Finn, Patricia W

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Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders von Wang, Tianyun, Hoekzema, Kendra, Vecchio, Davide, Wu, Huidan, Sulovari, Arvis, Coe, Bradley P., Gillentine, Madelyn A., Wilfert, Amy B., Perez-Jurado, Luis A., Kvarnung, Malin, Sleyp, Yoeri, Earl, Rachel K., Rosenfeld, Jill A., Geisheker, Madeleine R., Han, Lin, Du, Bing, Barnett, Chris, Thompson, Elizabeth, Shaw, Marie, Carroll, Renee, Friend, Kathryn, Catford, Rachael, Palmer, Elizabeth E., Zou, Xiaobing, Ou, Jianjun, Li, Honghui, Guo, Hui, Gerdts, Jennifer, Avola, Emanuela, Calabrese, Giuseppe, Elia, Maurizio, Greco, Donatella, Lindstrand, Anna, Nordgren, Ann, Anderlid, Britt-Marie, Vandeweyer, Geert, Van Dijck, Anke, Van der Aa, Nathalie, McKenna, Brooke, Hancarova, Miroslava, Bendova, Sarka, Havlovicova, Marketa, Malerba, Giovanni, Bernardina, Bernardo Dalla, Muglia, Pierandrea, van Haeringen, Arie, Hoffer, Mariette J. V., Franke, Barbara, Cappuccio, Gerarda, Delatycki, Martin, Lockhart, Paul J., Manning, Melanie A., Liu, Pengfei, Scheffer, Ingrid E., Brunetti-Pierri, Nicola, Rommelse, Nanda, Amaral, David G., Santen, Gijs W. E., Trabetti, Elisabetta, Sedláček, Zdeněk, Michaelson, Jacob J., Pierce, Karen, Courchesne, Eric, Kooy, R. Frank, Nordenskjöld, Magnus, Romano, Corrado, Peeters, Hilde, Bernier, Raphael A., Gecz, Jozef, Xia, Kun, Eichler, Evan E.

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Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program von Cade, Brian E, Lee, Jiwon, Sofer, Tamar, Wang, Heming, Zhang, Man, Chen, Han, Gharib, Sina A, Gottlieb, Daniel J, Guo, Xiuqing, Lane, Jacqueline M, Liang, Jingjing, Lin, Xihong, Mei, Hao, Patel, Sanjay R, Purcell, Shaun M, Saxena, Richa, Shah, Neomi A, Evans, Daniel S, Hanis, Craig L, Hillman, David R, Mukherjee, Sutapa, Palmer, Lyle J, Stone, Katie L, Tranah, Gregory J, Abecasis, Gonçalo R, Boerwinkle, Eric A, Correa, Adolfo, Cupples, L Adrienne, Kaplan, Robert C, Nickerson, Deborah A, North, Kari E, Psaty, Bruce M, Rotter, Jerome I, Rich, Stephen S, Tracy, Russell P, Vasan, Ramachandran S, Wilson, James G, Zhu, Xiaofeng, Redline, Susan

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Development of a web-based toolkit to support improvement of care coordination in primary care von Ganz, David A, Barnard, Jenny M, Smith, Nina Z Y, Miake-Lye, Isomi M, Delevan, Deborah M, Simon, Alissa, Rose, Danielle E, Stockdale, Susan E, Chang, Evelyn T, Noël, Polly H, Finley, Erin P, Lee, Martin L, Zulman, Donna M, Cordasco, Kristina M, Rubenstein, Lisa V

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Common Coding Variants in SCN10A Are Associated With the Nav1.8 Late Current and Cardiac Conduction von Macri, Vincenzo, Brody, Jennifer A, Arking, Dan E, Hucker, William J, Yin, Xiaoyan, Lin, Honghuang, Mills, Robert W, Sinner, Moritz F, Lubitz, Steven A, Liu, Ching-Ti, Morrison, Alanna C, Alonso, Alvaro, Li, Ning, Fedorov, Vadim V, Janssen, Paul M, Bis, Joshua C, Heckbert, Susan R, Dolmatova, Elena V, Lumley, Thomas, Sitlani, Colleen M, Cupples, L Adrienne, Pulit, Sara L, Newton-Cheh, Christopher, Barnard, John, Smith, Jonathan D, Van Wagoner, David R, Chung, Mina K, Vlahakes, Gus J, O'Donnell, Christopher J, Rotter, Jerome I, Margulies, Kenneth B, Morley, Michael P, Cappola, Thomas P, Benjamin, Emelia J, Muzny, Donna, Gibbs, Richard A, Jackson, Rebecca D, Magnani, Jared W, Herndon, Caroline N, Rich, Stephen S, Psaty, Bruce M, Milan, David J, Boerwinkle, Eric, Mohler, Peter J, Sotoodehnia, Nona, Ellinor, Patrick T

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TGF-β1 Variants in Chronic Beryllium Disease and Sarcoidosis von Jonth, Alexas C., Silveira, Lori, Fingerlin, Tasha E., Sato, Hiroe, Luby, Julie C., Welsh, Kenneth I., Rose, Cecile S., Newman, Lee S., du Bois, Roland M., Maier, Lisa A.

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HLA and environmental interactions in sarcoidosis von Rossman, M D, Thompson, B, Frederick, M, Iannuzzi, M C, Rybicki, B A, Pandey, J P, Newman, L S, Rose, C, Magira, E, Monos, D

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Robust trend tests for genetic association using matched case-control design von Zheng, Gang, Tian, Xin

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DC: 0-3 Assessment Protocol Project: Defining a comprehensive information set to support DC: 0-3 diagnostic formulation von Weston, Donna R., Thomas, Jean M., Barnard, Kathryn E., Wieder, Serena, Clark, Roseanne, Carter, Alice S., Fenichel, Emily

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DC: 0-3 assessment protocol project: Defining a comprehensive information set to support DC: 0-3 diagnostic formulation: The Use of the Diagnostic Classification 0-3 von WESTON, Donna R, THOMAS, Jean M, BARNARD, Kathryn E, WIEDER, Serena, CLARK, Roseanne, CARTER, Alice S, FENICHEL, Emily

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