Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly von Li, Dong, Wenger, Tara L, Seiler, Christoph, March, Michael E, Gutierrez-Uzquiza, Alvaro, Kao, Charlly, Bhoj, Elizabeth, Tian, Lifeng, Rosenbach, Misha, Liu, Yichuan, Robinson, Nora, Behr, Mechenzie, Chiavacci, Rosetta, Hou, Cuiping, Wang, Tiancheng, Bakay, Marina, Pellegrino da Silva, Renata, Perkins, Jonathan A, Sleiman, Patrick, Levine, Michael A, Hicks, Patricia J, Itkin, Maxim, Dori, Yoav, Hakonarson, Hakon

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Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapy von Wenger, Tara L., Bly, Randall A., Wu, Natalie, Albert, Catherine M., Park, Julie, Shieh, Joseph, Chenbhanich, Jirat, Heike, Carrie L., Adam, Margaret P., Chang, Irene, Sun, Angela, Miller, Danny E., Beck, Anita E., Gupta, Deepti, Boos, Markus D., Zackai, Elaine H., Everman, David, Ganapathi, Shireen, Wilson, Meredith, Christodoulou, John, Zarate, Yuri A., Curry, Cynthia, Li, Dong, Guimier, Anne, Amiel, Jeanne, Hakonarson, Hakon, Webster, Richard, Bhoj, Elizabeth J., Perkins, Jonathan A., Dahl, John P., Dobyns, William B.

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Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients von Levin, Mark D., Saitta, Sulagna C., Gripp, Karen W., Wenger, Tara L., Ganesh, Jaya, Kalish, Jennifer M., Epstein, Michael R., Smith, Rosemarie, Czosek, Richard J., Ware, Stephanie M., Goldenberg, Paula, Myers, Angela, Chatfield, Kathryn C., Gillespie, Matthew J., Zackai, Elaine H., Lin, Angela E.

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Critical region within 22q11.2 linked to higher rate of autism spectrum disorder von Clements, Caitlin C, Wenger, Tara L, Zoltowski, Alisa R, Bertollo, Jennifer R, Miller, Judith S, de Marchena, Ashley B, Mitteer, Lauren M, Carey, John C, Yerys, Benjamin E, Zackai, Elaine H, Emanuel, Beverly S, McDonald-McGinn, Donna M, Schultz, Robert T

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Role of Pediatric Geneticists in Craniofacial Teams: The Identification of Craniofacial Conditions with Cancer Predisposition von Wenger, Tara L., MD, PhD, Earl, Dawn, ARNP, Chow, Penny, MS, CGC, Sanchez-Lara, Pedro A., MD, MSCE

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Avoidance of surgery for head and neck infantile myofibromatosis using imatinib monotherapy von Pattisapu, Prasanth, Wenger, Tara L., Dahl, John P., Bly, Randall A., Bonilla‐Velez, Juliana, Wu, Natalie, Hall, Anurekha, Rudzinski, Erin R., Perkins, Jonathan A.

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ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor von Li, Dong, March, Michael E., Gutierrez-Uzquiza, Alvaro, Kao, Charlly, Seiler, Christoph, Pinto, Erin, Matsuoka, Leticia S., Battig, Mark R., Bhoj, Elizabeth J., Wenger, Tara L., Tian, Lifeng, Robinson, Nora, Wang, Tiancheng, Liu, Yichuan, Weinstein, Brant M., Swift, Matthew, Jung, Hyun Min, Kaminski, Courtney N., Chiavacci, Rosetta, Perkins, Jonathan A., Levine, Michael A., Sleiman, Patrick M. A., Hicks, Patricia J., Strausbaugh, Janet T., Belasco, Jean B., Dori, Yoav, Hakonarson, Hakon

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Targeted long-read sequencing identifies missing disease-causing variation von Miller, Danny E., Sulovari, Arvis, Wang, Tianyun, Loucks, Hailey, Hoekzema, Kendra, Munson, Katherine M., Lewis, Alexandra P., Fuerte, Edith P. Almanza, Paschal, Catherine R., Walsh, Tom, Thies, Jenny, Bennett, James T., Glass, Ian, Dipple, Katrina M., Patterson, Karynne, Bonkowski, Emily S., Nelson, Zoe, Squire, Audrey, Sikes, Megan, Beckman, Erika, Bennett, Robin L., Earl, Dawn, Lee, Winston, Allikmets, Rando, Perlman, Seth J., Chow, Penny, Hing, Anne V., Wenger, Tara L., Adam, Margaret P., Sun, Angela, Lam, Christina, Chang, Irene, Zou, Xue, Austin, Stephanie L., Huggins, Erin, Safi, Alexias, Iyengar, Apoorva K., Reddy, Timothy E., Majoros, William H., Allen, Andrew S., Crawford, Gregory E., Kishnani, Priya S., King, Mary-Claire, Cherry, Tim, Chong, Jessica X., Bamshad, Michael J., Nickerson, Deborah A., Mefford, Heather C., Doherty, Dan, Eichler, Evan E.

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Beare-Stevenson syndrome: Two new patients, including a novel finding of tracheal cartilaginous sleeve von Wenger, Tara L., Bhoj, Elizabeth J., Wetmore, Ralph F., Mennuti, Michael T., Bartlett, Scott P., Mollen, Thomas J., McDonald-McGinn, Donna M., Zackai, Elaine H.

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Delayed Subaponeurotic Fluid Collections of Infancy von Lee, Jonathan J., Wenger, Tara L.

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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants von Chawner, Samuel J.R.A, Doherty, Joanne L, Anney, Richard J. L, Antshel, Kevin M, Bearden, Carrie E, Bernier, Raphael, Chung, Wendy K, Clements, Caitlin C, Curran, Sarah R, Cuturilo, Goran, Fiksinski, Ania M, Gallagher, Louise, Goin-Kochel, Robin P, Gur, Raquel E, Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R, Kushan, Leila, Maillard, Anne M, McDonald-McGinn, Donna M, Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T, Green-Snyder, LeeAnne, Vorstman, Jacob A, Wenger, Tara L, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne B.M

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De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis von Timberlake, Andrew T., McGee, Stephen, Allington, Garrett, Kiziltug, Emre, Wolfe, Erin M., Stiegler, Amy L., Boggon, Titus J., Sanyoura, May, Morrow, Michelle, Wenger, Tara L., Fernandes, Erica M., Caluseriu, Oana, Persing, John A., Jin, Sheng Chih, Lifton, Richard P., Kahle, Kristopher T., Kruszka, Paul

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Alpelisib for the treatment of PIK3CA-related head and neck lymphatic malformations and overgrowth von Wenger, Tara L., Ganti, Sheila, Bull, Catherine, Lutsky, Erika, Bennett, James T., Zenner, Kaitlyn, Jensen, Dana M., Dmyterko, Victoria, Mercan, Ezgi, Shivaram, Giri M., Friedman, Seth D., Bindschadler, Michael, Drusin, Madeleine, Perkins, Jonathan N., Kong, Ada, Bly, Randall A., Dahl, John P., Bonilla-Velez, Juliana, Perkins, Jonathan A.

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Complex Airway Management in Patients with Tracheal Cartilaginous Sleeves von Noble, Anisha R., Cunningham, Michael L., Lam, Austin, Wenger, Tara L., Sie, Kathleen C., Perkins, Jonathan A., Dahl, John P.

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Spectrum of Disease in Hospitalized Newborns with Congenital Micrognathia: A Cohort of 3,236 Infants at North American Tertiary-Care Intensive Care Units von Padula, Michael A., Naing, Khatija, Wenger, Tara L., Ahmad, Irfan, Coghill, Carl H., Wild, K. Taylor, Rottgers, S. Alex, Resnick, Cory M., Goldstein, Jeffrey, Ehsan, Zarmina, Watkins, Donna, Deptula, Nicole, Lai, Kuan-Chi, Lioy, Janet, Gogcu, Semsa, Cielo, Christopher M.

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A genotype-specific surgical approach for patients with Pfeiffer syndrome due to W290C pathogenic variant in FGFR2 is associated with improved developmental outcomes and reduced mo... von Wenger, Tara L., Hopper, Richard A., Rosen, Anna, Tully, Hannah M., Cunningham, Michael L., Lee, Amy

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Perspectives on the future of dysmorphology von Solomon, Benjamin D., Adam, Margaret P., Fong, Chin‐To, Girisha, Katta M., Hall, Judith G., Hurst, Anna C. E., Krawitz, Peter M., Moosa, Shahida, Phadke, Shubha R., Tekendo‐Ngongang, Cedrik, Wenger, Tara L.

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41st Annual David W. Smith workshop on malformations and morphogenesis: Abstracts of the 2020 annual meeting von Gripp, Karen W., Jones, Kenneth Lyons, Wenger, Tara L., Adam, Margaret P.

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Phenotypes and genotypes in individuals with SMC1A variants von Huisman, Sylvia, Mulder, Paul A., Redeker, Egbert, Bader, Ingrid, Bisgaard, Anne‐Marie, Brooks, Alice, Cereda, Anna, Cinca, Constanza, Clark, Dinah, Cormier‐Daire, Valerie, Deardorff, Matthew A., Diderich, Karin, Elting, Mariet, van Essen, Anthonie, FitzPatrick, David, Gervasini, Cristina, Gillessen‐Kaesbach, Gabriele, Girisha, Katta M., Hilhorst‐Hofstee, Yvonne, Hopman, Saskia, Horn, Denise, Isrie, Mala, Jansen, Sandra, Jespersgaard, Cathrine, Kaiser, Frank J., Kaur, Maninder, Kleefstra, Tjitske, Krantz, Ian D., Lakeman, Phillis, Landlust, Annemiek, Lessel, Davor, Michot, Caroline, Moss, Jo, Noon, Sarah E., Oliver, Chris, Parenti, Ilaria, Pie, Juan, Ramos, Feliciano J., Rieubland, Claudine, Russo, Silvia, Selicorni, Angelo, Tümer, Zeynep, Vorstenbosch, Rieneke, Wenger, Tara L., van Balkom, Ingrid, Piening, Sigrid, Wierzba, Jolanta, Hennekam, Raoul C.

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Perspectives from the Society for Pediatric Research: advice on sustaining science and mentoring during COVID-19 von Forster, Catherine S., Nguyen, Suong T., Powell, Weston T., Moore, Daniel J., Ho, Jacqueline, Heyman, Melvin B., Wenger, Tara L., Gonzalez, Fernando, Hostetter, Margaret, Nowalk, Andrew, Rassbach, Caroline E., Boyer, Debra, Weiss, Pnina, Blankenburg, Rebecca L., Orange, Jordan S., Ackerman, Kate G., Burns, Audrea M.

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