Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource von Strande, Natasha T., Riggs, Erin Rooney, Buchanan, Adam H., Ceyhan-Birsoy, Ozge, DiStefano, Marina, Dwight, Selina S., Goldstein, Jenny, Ghosh, Rajarshi, Seifert, Bryce A., Sneddon, Tam P., Wright, Matt W., Milko, Laura V., Cherry, J. Michael, Giovanni, Monica A., Murray, Michael F., O’Daniel, Julianne M., Ramos, Erin M., Santani, Avni B., Scott, Alan F., Plon, Sharon E., Rehm, Heidi L., Martin, Christa L., Berg, Jonathan S.

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Antimicrobial Resistance in Gram-Negative Rods Causing Bacteremia in Hematopoietic Stem Cell Transplant Recipients: Intercontinental Prospective Study of the Infectious Diseases Wo... von Averbuch, Diana, Tridello, Gloria, Hoek, Jennifer, Mikulska, Malgorzata, Akan, Hamdi, San Segundo, Lucrecia Yaňez, Pabst, Thomas, Özçelik, Tülay, Klyasova, Galina, Donnini, Irene, Wu, Depei, Gülbas, Zafer, Zuckerman, Tsila, de Sousa, Aida Botelho, Beguin, Yves, Xhaard, Aliénor, Bachy, Emmanuel, Ljungman, Per, de la Camara, Rafael, Rascon, Jelena, Camps, Isabel Ruiz, Vitek, Antonin, Patriarca, Francesca, Cudillo, Laura, Vrhovac, Radovan, Shaw, Peter J., Wolfs, Tom, O’Brien, Tracey, Avni, Batia, Silling, Gerda, Sabty, Firas Al, Graphakos, Stelios, Sankelo, Marja, Sengeloev, Henrik, Pillai, Srinivas, Matthes, Susanne, Melanthiou, Frederiki, Iacobelli, Simona, Styczynski, Jan, Engelhard, Dan, Cesaro, Simone

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Automated Clinical Exome Reanalysis Reveals Novel Diagnoses von Baker, Samuel W., Murrell, Jill R., Nesbitt, Addie I., Pechter, Kieran B., Balciuniene, Jorune, Zhao, Xiaonan, Yu, Zhenming, Denenberg, Elizabeth H., DeChene, Elizabeth T., Wilkens, Alisha B., Bhoj, Elizabeth J., Guan, Qiaoning, Dulik, Matthew C., Conlin, Laura K., Abou Tayoun, Ahmad N., Luo, Minjie, Wu, Chao, Cao, Kajia, Sarmady, Mahdi, Bedoukian, Emma C., Tarpinian, Jennifer, Medne, Livija, Skraban, Cara M., Deardorff, Matthew A., Krantz, Ian D., Krock, Bryan L., Santani, Avni B.

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Scaling resolution of variant classification differences in ClinVar between 41 clinical laboratories through an outlier approach von Harrison, Steven M., Dolinksy, Jill S., Chen, Wenjie, Collins, Christin D., Das, Soma, Deignan, Joshua L., Garber, Kathryn B., Garcia, John, Jarinova, Olga, Knight Johnson, Amy E., Koskenvuo, Juha W., Lee, Hane, Mao, Rong, Mar‐Heyming, Rebecca, McFaddin, Andrew S., Moyer, Krista, Nagan, Narasimhan, Rentas, Stefan, Santani, Avni B., Seppälä, Eija H., Shirts, Brian H., Tidwell, Timothy, Topper, Scott, Vincent, Lisa M., Vinette, Kathy, Rehm, Heidi L.

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Correction to: Regional intra-arterial steroid treatment in 120 patients with steroid-resistant or -dependent GvHD von Shapira, M. Y., Klimov, A., Sheth, V., Grisariu, S., Avni, B. R., Or, R., Bloom, A. I.

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Early lymphocyte collection for anti‐CD19 CART production improves T‐cell fitness in patients with relapsed/refractory diffuse large B‐cell lymphoma von Dubnikov Sharon, T., Assayag, M., Avni, B., Kfir‐Erenfeld, S., Lebel, E., Gatt, M. E., Goldschmidt, N., Stepensky, P., Asherie, N., Grisariu, S.

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Incidence and risk factors for moderate-to-severe veno-occlusive disease of the liver after allogeneic stem cell transplantation using a reduced intensity conditioning regimen von Tsirigotis, P D, Resnick, I B, Avni, B, Grisariu, S, Stepensky, P, Or, R, Shapira, M Y

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Genomic Reporting Practices Across 5 Molecular Disciplines: A Study From the College of American Pathologists von Furtado, Larissa V, Kim, Annette S, Moyer, Ann M, Moncur, Joel T, Xian, Rena R, Roy, Angshumoy, Santani, Avni B, Akkari, Yassmine, Voelkerding, Karl V, Souers, Rhona J, Halley, Jaimie, Palomaki, Glenn E

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Validation of association of the apolipoprotein E ε2 allele with neurodevelopmental dysfunction after cardiac surgery in neonates and infants von Gaynor, J. William, MD, Kim, Daniel Seung, BS, Arrington, Cammon B., MD, PhD, Atz, Andrew M., MD, Bellinger, David C., PhD, Burt, Amber A., MSPH, Ghanayem, Nancy S., MD, Jacobs, Jeffery P., MD, Lee, Teresa M., MD, Lewis, Alan B., MD, Mahle, William T., MD, Marino, Bradley S., MD, Miller, Stephen G., MD, Newburger, Jane W., MD, MPH, Pizarro, Christian, MD, Ravishankar, Chitra, MD, Santani, Avni B., PhD, Wilder, Nicole S., MD, Jarvik, Gail P., MD, PhD, Mital, Seema, MD, Russell, Mark W., MD

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Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach von Wu, Chao, Devkota, Batsal, Evans, Perry, Zhao, Xiaonan, Baker, Samuel W, Niazi, Rojeen, Cao, Kajia, Gonzalez, Michael A, Jayaraman, Pushkala, Conlin, Laura K, Krock, Bryan L, Deardorff, Matthew A, Spinner, Nancy B, Krantz, Ian D, Santani, Avni B, Tayoun, Ahmad N Abou, Sarmady, Mahdi

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De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder von Gregor, Anne, Sadleir, Lynette G., Asadollahi, Reza, Azzarello-Burri, Silvia, Battaglia, Agatino, Ousager, Lilian Bomme, Boonsawat, Paranchai, Bruel, Ange-Line, Buchert, Rebecca, Calpena, Eduardo, Cogné, Benjamin, Dallapiccola, Bruno, Distelmaier, Felix, Elmslie, Frances, Faivre, Laurence, Haack, Tobias B., Harrison, Victoria, Henderson, Alex, Hunt, David, Isidor, Bertrand, Joset, Pascal, Kumada, Satoko, Lachmeijer, Augusta M.A., Lees, Melissa, Lynch, Sally Ann, Martinez, Francisco, Matsumoto, Naomichi, McDougall, Carey, Mefford, Heather C., Miyake, Noriko, Myers, Candace T., Moutton, Sébastien, Nesbitt, Addie, Novelli, Antonio, Orellana, Carmen, Rauch, Anita, Rosello, Monica, Saida, Ken, Santani, Avni B., Sarkar, Ajoy, Scheffer, Ingrid E., Shinawi, Marwan, Steindl, Katharina, Symonds, Joseph D., Zackai, Elaine H., Reis, André, Sticht, Heinrich, Zweier, Christiane

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NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly von Schanze, Ina, Bunt, Jens, Lim, Jonathan W.C., Schanze, Denny, Dean, Ryan J., Alders, Marielle, Blanchet, Patricia, Attié-Bitach, Tania, Berland, Siren, Boogert, Steven, Boppudi, Sangamitra, Bridges, Caitlin J., Cho, Megan T., Dobyns, William B., Donnai, Dian, Douglas, Jessica, Earl, Dawn L., Edwards, Timothy J., Faivre, Laurence, Fregeau, Brieana, Genevieve, David, Gérard, Marion, Gatinois, Vincent, Holder-Espinasse, Muriel, Huth, Samuel F., Izumi, Kosuke, Kerr, Bronwyn, Lacaze, Elodie, Lakeman, Phillis, Mahida, Sonal, Mirzaa, Ghayda M., Morgan, Sian M., Nowak, Catherine, Peeters, Hilde, Petit, Florence, Pilz, Daniela T., Puechberty, Jacques, Reinstein, Eyal, Rivière, Jean-Baptiste, Santani, Avni B., Schneider, Anouck, Sherr, Elliott H., Smith-Hicks, Constance, Wieland, Ilse, Zackai, Elaine, Zhao, Xiaonan, Gronostajski, Richard M., Zenker, Martin, Richards, Linda J.

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A Framework of Critical Considerations in Clinical Exome Reanalyses by Clinical and Laboratory Standards Institute von Leung, Marco L., Ji, Jianling, Baker, Samuel, Buchan, Jillian G., Sivakumaran, Theru A., Krock, Bryan L., Hutchins, Rebecca, Bayrak-Toydemir, Pinar, Pfeifer, John, Cremona, Maria Laura, Funke, Birgit, Santani, Avni B.

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Phenotypic predictors and final diagnoses in patients referred for RASopathy testing by targeted next-generation sequencing von Bhoj, Elizabeth J., Yu, Zhenming, Guan, Qiaoning, Ahrens-Nicklas, Rebecca, Cao, Kajia, Luo, Minjie, Tischler, Tanya, Deardorff, Matthew A., Zackai, Elaine, Santani, Avni B.

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Mung bean nuclease treatment increases capture specificity of microdroplet-PCR based targeted DNA enrichment von Yu, Zhenming, Cao, Kajia, Tischler, Tanya, Stolle, Catherine A, Santani, Avni B

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Enteroviral infection in patients treated with rituximab for non‐Hodgkin lymphoma: a case series and review of the literature von Grisariu, S., Vaxman, I., Gatt, M., Elias, S., Avni, B., Arad, A., Pasvolsky, O., Raanani, P., Paltiel, O.

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Congenital polyvalvular disease expands the cardiac phenotype of the RASopathies von Matalon, Dena R., Stevenson, David A., Bhoj, Elizabeth J., Santani, Avni B., Keena, Beth, Cohen, Meryl S., Lin, Angela E., Sheppard, Sarah E., Zackai, Elaine H.

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Variable Clinical Manifestations of Xia‐Gibbs syndrome: Findings of Consecutively Identified Cases at a Single Children's Hospital von Ritter, Alyssa L., McDougall, Carey, Skraban, Cara, Medne, Livija, Bedoukian, Emma C., Asher, Stephanie B., Balciuniene, Jorune, Campbell, Colleen D., Baker, Samuel W., Denenberg, Elizabeth H., Mazzola, Sarah, Fiordaliso, Sarah K., Krantz, Ian D., Kaplan, Paige, Ierardi‐Curto, Lynne, Santani, Avni B., Zackai, Elaine H., Izumi, Kosuke

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Molecular Diagnostic Outcomes from 700 Cases: What Can We Learn from a Retrospective Analysis of Clinical Exome Sequencing? von Murrell, Jill R, Nesbitt, Addie May I, Baker, Samuel W, Pechter, Kieran B, Balciuniene, Jorune, Zhao, Xiaonan, Denenberg, Elizabeth H, DeChene, Elizabeth T, Wu, Chao, Jayaraman, Pushkala, Cao, Kajia, Gonzalez, Michael, Devoto, Marcella, Testori, Alessandro, Monos, John D, Dulik, Matthew C, Conlin, Laura K, Luo, Minjie, McDonald Gibson, Kristin, Guan, Qiaoning, Sarmady, Mahdi, Bhoj, Elizabeth, Helbig, Ingo, Zackai, Elaine H, Bedoukian, Emma C, Wilkens, Alisha, Tarpinian, Jennifer, Izumi, Kosuke, Skraban, Cara M, Deardorff, Matthew A, Medne, Livija, Krantz, Ian D, Krock, Bryan L, Santani, Avni B

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Regional intra-arterial steroid treatment in 120 patients with steroid-resistant or -dependent GvHD von Shapira, M Y, Klimov, A, Sheth, V, Grisariu, S, Avni, B R, Or, R, Bloom, A I

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