Clinical application of whole-exome sequencing across clinical indications von Retterer, Kyle, Juusola, Jane, Cho, Megan T., Vitazka, Patrik, Millan, Francisca, Gibellini, Federica, Vertino-Bell, Annette, Smaoui, Nizar, Neidich, Julie, Monaghan, Kristin G., McKnight, Dianalee, Bai, Renkui, Suchy, Sharon, Friedman, Bethany, Tahiliani, Jackie, Pineda-Alvarez, Daniel, Richard, Gabriele, Brandt, Tracy, Haverfield, Eden, Chung, Wendy K., Bale, Sherri

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Clinical whole‐genome sequencing in cancer diagnosis von Hou, Ying‐Chen C., Neidich, Julie A., Duncavage, Eric J., Spencer, David H., Schroeder, Molly C.

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Diagnostic Utility of Next-Generation Sequencing for Disorders of Somatic Mosaicism: A Five-Year Cumulative Cohort von McNulty, Samantha N., Evenson, Michael J., Corliss, Meagan M., Love-Gregory, Latisha D., Schroeder, Molly C., Cao, Yang, Lee, Yi-Shan, Drolet, Beth A., Neidich, Julie A., Cottrell, Catherine E., Heusel, Jonathan W.

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Modified Rules for Classification of Variants Associated With Disorders of Somatic Mosaicism von Leon‐Quintero, Fernando Zazueta, Bowling, Kevin M., Dickson, Alexa, Corliss, Meagan M., Schroeder, Molly C., Neidich, Julie A., Heusel, Jonathan W., Krysiak, Kilannin, Polonis, Katarzyna, Parikh, Bijal A., Cao, Yang

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Comprehensive Analysis of TEK Variants in Patients With Vascular Malformations von Ghasemi, Reza, Corliss, Meagan M, Bowling, Kevin M, Krysiak, Kilannin, Walker, Jason, Dickson, Alexa M, Schroeder, Molly C, Parikh, Bijal A, Neidich, Julie A, Polonis, Katarzyna, Cao, Yang

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Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies von Vaseghi, Parisa, Habibi, Laleh, Neidich, Julie A., Cao, Yang, Fattahi, Neda, Rashidi-Nezhad, Ramin, Salehnezhad, Tayebeh, Dalili, Hossein, Rahimi Sharbaf, Fatemeh, Zarkesh, Mohammad Reza, Malekian, Mahtash, Mokhberdezfuli, Mahdieh, Mehrtash, Amirhosein, Ardeshirdavani, Amin, Kariminejad, Roxana, Ghorbansabagh, Vafa, Sadeghimoghadam, Parvane, Naddaf, Amir, Esmaeilnia Shirvany, Tahereh, Mosayebi, Ziba, Sahebdel, Behrokh, Golshahi, Fatemeh, Shirazi, Mahboobeh, Shamel, Shirin, Moeini, Roksana, Heidari, Abolfazl, Daneshmand, Mohammad Ali, Ghasemi, Reza, Akrami, Seyed Mohammad, Rashidi-Nezhad, Ali

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Homozygous, Intragenic Tandem Duplication of SFTPB Causes Neonatal Respiratory Failure von Wambach, Jennifer A, Wegner, Daniel J, Kitzmiller, Joseph, White, Frances V, Heins, Hillary B, Yang, Ping, Paul, Alexander J, Granadillo, Jorge L, Eghtesady, Pirooz, Kuklinski, Cadence, Turner, Tiffany, Fairman, Korre, Stone, Kristyne, Wilson, Theodore, Breman, Amy, Smith, Janice, Schroeder, Molly C, Neidich, Julie A, Whitsett, Jeffrey A, Cole, F Sessions

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Comparing Gene Panels for Non-Retinal Indications: A Systematic Review von Procopio, Rebecca, Pulido, Jose S, Gunton, Kammi B, Syed, Zeba A, Lee, Daniel, Moster, Mark L, Sergott, Robert, Neidich, Julie A, Reynolds, Margaret M

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High‐depth next‐generation sequencing panel testing in the evaluation of arteriovenous malformations von Hernandez, Patricia V., King, Katherine A., Evenson, Michael J., Corliss, Meagan M., Schroeder, Molly C., Heusel, Jonathan W., Neidich, Julie A., Cao, Yang

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A comparative analysis of RAS variants in patients with disorders of somatic mosaicism von Claire Hou, Ying-Chen, Evenson, Michael J., Corliss, Meagan M., Mahapatra, Lily, Aldawood, Ali, Carpentieri, David F., Chamlin, Sarah L., Kulungowski, Ann M., Madan-Khetarpal, Suneeta, Sebastian, Jessica, Pet, Mitchell A., Coughlin, Carrie C., Willing, Marcia C., Pearson, Gregory D., Setty, Bhuvana A., El-Haffaf, Zaki, Cottrell, Catherine E., Parikh, Bijal A., Krysiak, Kilannin, Schroeder, Molly C., Heusel, Jonathan W., Neidich, Julie A., Cao, Yang

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P515: A somatic pathogenic variant in PTPN11 in a patient with vascular malformation and hemihypertrophy von Mojarad, Bahareh, Fishman, Shelbie, King, Katherine, Sisk, Bryan, Neidich, Julie

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Acceptance of Saliva-Based Specimen Collection for SARS-CoV-2 Testing Among K-12 Students, Teachers, and Staff von McLaughlin, Heather P., Worrell, Mary Claire, Malone, Sara, Dawson, Patrick, Maricque, Brett, Halpin, Jessica L., Lee, Sooji, Fritz, Stephanie A., Tinker, Sarah C., Neidich, Julie A., Towns, Katie, Lee, Justin S., Barrios, Lisa C., Neatherlin, John C., Newland, Jason G., Salzer, Johanna S.

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Clinical whole-genome sequencing and FISH identify two different fusion partners for NUP98 in a patient with acute myeloid leukemia: A case report von Mojarad, Bahareh A, Crees, Zachary D, Schroeder, Molly C, Xiang, Zhifu, Vader, Justin, Sina, Jason, Jacoby, Meagan, Frater, John L, Duncavage, Eric J, Spencer, David H, Lavine, Kory, Neidich, Julie A, Amarillo, Ina

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Assessing COVID-19 testing strategies in K-12 schools in underserved populations: study protocol for a cluster-randomized trial von Hayes, Samantha, Malone, Sara, Bonty, Brittany, Mueller, Nancy, Reyes, Summer M, Reyes, Sydney A, Evans, Christina, Wilcher-Roberts, Myisha, Watterson, Tremayne, Akuse, Sewuese, Shelley, Jamee, Yuan, Grace, Lackey, Ian, Prater, Jasmine, Montgomery, Brock, Williams, Cynthia, Butler-Barnes, Sheretta T, Caburnay, Charlene, Dougherty, Nikole Lobb, Liu, Jingxia, Lai, Albert, Neidich, Julie, Fritz, Stephanie, Newland, Jason G

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SARS-CoV-2 screening testing in schools for children with intellectual and developmental disabilities von Sherby, Michael R, Walsh, Tyler J, Lai, Albert M, Neidich, Julie A, Balls-Berry, Joyce E, Morris, Stephanie M, Head, Richard, Prener, Christopher G, Newland, Jason G, Gurnett, Christina A

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Co-existence of 2 clinically significant variants causing disorders of somatic mosaicism von Cao, Yang, Evenson, Michael J., Corliss, Meagan M., Schroeder, Molly C., Heusel, Jonathan W., Neidich, Julie A.

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P697: Prenatal diagnosis and postnatal clinical course of a fetus with low-level mosaic trisomy 17q von Ghasemi, Reza, Trammel, Cassandra, Jensen, Nathaniel, Stanley, Amie, Smith, Sarah, Schroeder, Molly, Neidich, Julie, Shinawi, Marwan, Jackson, Sherri, Polonis, Katarzyna

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P673: Four cases of unbalanced (Xq28/Yq12): Autosome translocation identified by chromosomal microarray analysis von Krysiak, Kilannin, Stehl, Kate, Cao, Yang, Polonis, Katarzyna, Fritz, Joan, Amarillo, Ina, Neidich, Julie, Schroeder, Molly

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Correction: Assessing COVID-19 testing strategies in K-12 schools in underserved populations: study protocol for a cluster-randomized trial von Hayes, Samantha, Malone, Sara, Bonty, Brittany, Mueller, Nancy, Reyes, Summer M, Reyes, Sydney A, Evans, Christina, Wilcher-Roberts, Myisha, Watterson, Tremayne, Akuse, Sewuese, Shelley, Jamee, Yuan, Grace, Lackey, Ian, Prater, Jasmine, Montgomery, Brock, Williams, Cynthia, Butler-Barnes, Sheretta T, Harris, Kelly, Caburnay, Charlene, Dougherty, Nikole Lobb, Liu, Jingxia, Lai, Albert, Neidich, Julie, Fritz, Stephanie, Newland, Jason G

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Profiling PIK3CA variants in disorders of somatic mosaicism von Mojarad, Bahareh A., Hernandez, Patricia V., Evenson, Michael J., Corliss, Meagan M., Stein, Sarah L., Theos, Amy, Coughlin, Carrie C., Sisk, Bryan, Menezes, Maithilee, Schroeder, Molly C., Heusel, Jonathan W., Neidich, Julie A., Cao, Yang

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