Newborn Hearing Screening — A Silent Revolution von Morton, Cynthia C, Nance, Walter E

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Identification and function of long non-coding RNA von Ernst, Carl, Morton, Cynthia C

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Gene therapy for hearing loss von Omichi, Ryotaro, Shibata, Seiji B, Morton, Cynthia C, Smith, Richard J H

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Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries von Talkowski, Michael E., Rosenfeld, Jill A., Blumenthal, Ian, Pillalamarri, Vamsee, Chiang, Colby, Heilbut, Adrian, Ernst, Carl, Hanscom, Carrie, Rossin, Elizabeth, Lindgren, Amelia M., Pereira, Shahrin, Ruderfer, Douglas, Kirby, Andrew, Ripke, Stephan, Harris, David J., Lee, Ji-Hyun, Ha, Kyungsoo, Kim, Hyung-Goo, Solomon, Benjamin D., Gropman, Andrea L., Lucente, Diane, Sims, Katherine, Ohsumi, Toshiro K., Borowsky, Mark L., Loranger, Stephanie, Quade, Bradley, Lage, Kasper, Miles, Judith, Wu, Bai-Lin, Shen, Yiping, Neale, Benjamin, Shaffer, Lisa G., Daly, Mark J., Morton, Cynthia C., Gusella, James F.

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Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China von Wang, Qiuju, Xiang, Jiale, Sun, Jun, Yang, Yun, Guan, Jing, Wang, Dayong, Song, Cui, Guo, Ling, Wang, Hongyang, Chen, Yaqiu, Leng, Junhong, Wang, Xiaman, Zhang, Junqing, Han, Bing, Zou, Jing, Yan, Chengbin, Zhao, Lidong, Luo, Hongyu, Han, Yuan, Yuan, Wen, Zhang, Hongyun, Wang, Wei, Wang, Jian, Yang, Huanming, Xu, Xun, Yin, Ye, Morton, Cynthia C., Zhao, Lijian, Zhu, Shida, Shen, Jun, Peng, Zhiyu

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Clinical Diagnosis by Whole-Genome Sequencing of a Prenatal Sample von Talkowski, Michael E, Ordulu, Zehra, Pillalamarri, Vamsee, Benson, Carol B, Blumenthal, Ian, Connolly, Susan, Hanscom, Carrie, Hussain, Naveed, Pereira, Shahrin, Picker, Jonathan, Rosenfeld, Jill A, Shaffer, Lisa G, Wilkins-Haug, Louise E, Gusella, James F, Morton, Cynthia C

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Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration von Chiang, Colby, Jacobsen, Jessie C, Ernst, Carl, Hanscom, Carrie, Heilbut, Adrian, Blumenthal, Ian, Mills, Ryan E, Kirby, Andrew, Lindgren, Amelia M, Rudiger, Skye R, McLaughlan, Clive J, Bawden, C Simon, Reid, Suzanne J, Faull, Richard L M, Snell, Russell G, Hall, Ira M, Shen, Yiping, Ohsumi, Toshiro K, Borowsky, Mark L, Daly, Mark J, Lee, Charles, Morton, Cynthia C, MacDonald, Marcy E, Gusella, James F, Talkowski, Michael E

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Targeted insertion of conditional expression cassettes into the mouse genome using the modified i-PITT von Miura, Hiromi, Nakamura, Ayaka, Kurosaki, Aki, Kotani, Ai, Motojima, Masaru, Tanaka, Keiko, Kakuta, Shigeru, Ogiwara, Sanae, Ohmi, Yuhsuke, Komaba, Hirotaka, Schilit, Samantha L P, Morton, Cynthia C, Gurumurthy, Channabasavaiah B, Ohtsuka, Masato

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Next-Generation Sequencing Strategies Enable Routine Detection of Balanced Chromosome Rearrangements for Clinical Diagnostics and Genetic Research von Talkowski, Michael E., Ernst, Carl, Heilbut, Adrian, Chiang, Colby, Hanscom, Carrie, Lindgren, Amelia, Kirby, Andrew, Liu, Shangtao, Muddukrishna, Bhavana, Ohsumi, Toshiro K., Shen, Yiping, Borowsky, Mark, Daly, Mark J., Morton, Cynthia C., Gusella, James F.

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Intravenous leiomyomatosis: an unusual intermediate between benign and malignant uterine smooth muscle tumors von Ordulu, Zehra, Nucci, Marisa R, Dal Cin, Paola, Hollowell, Monica L, Otis, Christopher N, Hornick, Jason L, Park, Peter J, Kim, Tae-Min, Quade, Bradley J, Morton, Cynthia C

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A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndro... von Ben-Mahmoud, Afif, Kishikawa, Shotaro, Gupta, Vijay, Leach, Natalia T., Shen, Yiping, Moldovan, Oana, Goel, Himanshu, Hopper, Bruce, Ranguin, Kara, Gruchy, Nicolas, Maas, Saskia M, Lacassie, Yves, Kim, Soo-Hyun, Kim, Woo-Yang, Quade, Bradley J., Morton, Cynthia C., Kim, Cheol-Hee, Layman, Lawrence C., Kim, Hyung-Goo

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Derivation of Embryonic Stem-Cell Lines from Human Blastocysts von Cowan, Chad A, Klimanskaya, Irina, McMahon, Jill, McMahon, Andrew P, Atienza, Jocelyn, Witmyer, Jeannine, Zucker, Jacob P, Wang, Shunping, Morton, Cynthia C, Powers, Doug, Melton, Douglas A

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Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis von Ordulu, Zehra, Kammin, Tammy, Brand, Harrison, Pillalamarri, Vamsee, Redin, Claire E., Collins, Ryan L., Blumenthal, Ian, Hanscom, Carrie, Pereira, Shahrin, Bradley, India, Crandall, Barbara F., Gerrol, Pamela, Hayden, Mark A., Hussain, Naveed, Kanengisser-Pines, Bibi, Kantarci, Sibel, Levy, Brynn, Macera, Michael J., Quintero-Rivera, Fabiola, Spiegel, Erica, Stevens, Blair, Ulm, Janet E., Warburton, Dorothy, Wilkins-Haug, Louise E., Yachelevich, Naomi, Gusella, James F., Talkowski, Michael E., Morton, Cynthia C.

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Editorial: Chromosome structural variants: Epidemiology, identification and contribution to human diseases von Dong, Zirui, David, Dezso, Gonzaga-Jauregui, Claudia, Morton, Cynthia C., Zepeda-Mendoza, Cinthya J.

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A Comparative Analysis of Health-Related Quality of Life 1 Year Following Myomectomy or Uterine Artery Embolization: Findings from the COMPARE-UF Registry von Anchan, Raymond M, Wojdyla, Daniel, Bortoletto, Pietro, Terry, Kathryn, Disler, Emily, Milne, Ankrish, Gargiulo, Antonio, Petrozza, John, Brook, Olga, Srouji, Serene, Morton, Cynthia C, Greenberg, James, Wegienka, Ganesa, Stewart, Elizabeth A, Nicholson, Wanda K, Thomas, Laine, Venable, Sateria, Laughlin-Tommaso, Shannon, Diamond, Michael P, Maxwell, G Larry, Marsh, Erica E, Myers, Evan R, Vines, Anissa I, Wise, Lauren A, Wallace, Kedra, Jacoby, Vanessa L, Spies, James B

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Structural Genomic Variation and Personalized Medicine von Lee, Charles, Morton, Cynthia C

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ASHG 2020 Curt Stern Award introduction: Fowzan Sami Alkuraya von Morton, Cynthia C.

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Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial Clefting von Saadi, Irfan, Alkuraya, Fowzan S., Gisselbrecht, Stephen S., Goessling, Wolfram, Cavallesco, Resy, Turbe-Doan, Annick, Petrin, Aline L., Harris, James, Siddiqui, Ursela, Grix, Arthur W., Hove, Hanne D., Leboulch, Philippe, Glover, Thomas W., Morton, Cynthia C., Richieri-Costa, Antonio, Murray, Jeffrey C., Erickson, Robert P., Maas, Richard L.

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Describing Sequencing Results of Structural Chromosome Rearrangements with a Suggested Next-Generation Cytogenetic Nomenclature von Ordulu, Zehra, Wong, Kristen E., Currall, Benjamin B., Ivanov, Andrew R., Pereira, Shahrin, Althari, Sara, Gusella, James F., Talkowski, Michael E., Morton, Cynthia C.

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A multi-stage genome-wide association study of uterine fibroids in African Americans von Hellwege, Jacklyn N., Jeff, Janina M., Wise, Lauren A., Gallagher, C. Scott, Wellons, Melissa, Hartmann, Katherine E., Jones, Sarah F., Torstenson, Eric S., Dickinson, Scott, Ruiz-Narváez, Edward A., Rohland, Nadin, Allen, Alexander, Reich, David, Tandon, Arti, Pasaniuc, Bogdan, Mancuso, Nicholas, Im, Hae Kyung, Hinds, David A., Palmer, Julie R., Rosenberg, Lynn, Denny, Joshua C., Roden, Dan M., Stewart, Elizabeth A., Morton, Cynthia C., Kenny, Eimear E., Edwards, Todd L., Velez Edwards, Digna R.

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