Phylogenetic relationships of Vepris (Rutaceae) inferred from chloroplast, nuclear, and morphological data von Morton, Cynthia M

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

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

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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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The Iceberg under Water: Unexplored Complexity of Chromoanagenesis in Congenital Disorders von Zepeda-Mendoza, Cinthya J., Morton, Cynthia C.

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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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The Role of Regulatory Focus, Social Distance, and Involvement in Anti-High-Risk Drinking Advertising: A Construal-Level Theory Perspective von Park, Sun-Young, Morton, Cynthia R.

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Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarr... von David, Dezső, Fino, Joana, Oliveira, Renata, Dória, Sofia, Morton, Cynthia C.

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GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank von Wells, Helena R.R., Freidin, Maxim B., Zainul Abidin, Fatin N., Payton, Antony, Dawes, Piers, Munro, Kevin J., Morton, Cynthia C., Moore, David R., Dawson, Sally J., Williams, Frances M.K.

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SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility von Schilit, Samantha L.P., Menon, Shreya, Friedrich, Corinna, Kammin, Tammy, Wilch, Ellen, Hanscom, Carrie, Jiang, Sizun, Kliesch, Sabine, Talkowski, Michael E., Tüttelmann, Frank, MacQueen, Amy 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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New Subfamily Classification for the Rutaceae von Morton, Cynthia M, Telmer, Cheryl

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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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A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children von Shearer, A. Eliot, Shen, Jun, Amr, Sami, Morton, Cynthia C., Smith, Richard J.

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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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Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis von Wang, Huilin, Dong, Zirui, Zhang, Rui, Chau, Matthew Hoi Kin, Yang, Zhenjun, Tsang, Kathy Yin Ching, Wong, Hoi Kin, Gui, Baoheng, Meng, Zhuo, Xiao, Kelin, Zhu, Xiaofan, Wang, Yanfang, Chen, Shaoyun, Leung, Tak Yeung, Cheung, Sau Wai, Kwok, Yvonne K., Morton, Cynthia C., Zhu, Yuanfang, Choy, Kwong Wai

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Low-pass genome sequencing–based detection of absence of heterozygosity: validation in clinical cytogenetics von Dong, Zirui, Chau, Matthew Hoi Kin, Zhang, Yanyan, Yang, Zhenjun, Shi, Mengmeng, Wah, Yi Man, Kwok, Yvonne K., Leung, Tak Yeung, Morton, Cynthia C., Choy, Kwong Wai

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