CynthiaCassonMortonMD

PubMed

• 6 citations
  Investigating the shared genetic architecture of uterine leiomyoma and breast cancer: A genome-wide cross-trait analysis.
  Xueyao Wu, Chenghan Xiao, Zhitong Han, Li Zhang, Xunying Zhao, Yu Hao, Jinyu Xiao, C Scott Gallagher, Peter Kraft, Cynthia Casson Morton, Jiayuan Li, Xia Jiang> ;American Journal of Human Genetics. 2022 Jul 7
• 7 citations
  Genetics of Childhood Hearing Loss.
  Calli Ober Mitchell, Cynthia C. Morton> ;Otolaryngologic Clinics of North America. 2021 Dec 1
• 14 citations
  Low-pass genome sequencing–based detection of absence of heterozygosity: validation in clinical cytogenetics
  Zirui Dong, Matthew Hoi Kin Chau, Yanyan Zhang, Zhenjun Yang, Mengmeng Shi, Yi Man Wah, Yvonne K. Kwok, Tak Yeung Leung, Cynthia C. Morton, Kwong Wai Choy> ;Genetics in Medicine. 2021 Feb 1
• 2 citations
  First Report of Bilateral External Auditory Canal Cochlin Aggregates ("Cochlinomas") with Multifocal Amyloid-Like Deposits, Associated with Sensorineural Hearing Loss ...
  Atreyee Basu, Nicole J. Boczek, Nahid G. Robertson, Samih H. Nasr, Daniel Jethanamest, Ellen D. McPhail, Paul J. Kurtin, Surendra Dasari, Malinda L. Butz, Cynthia C. M...> ;Head and Neck Pathology. 2020 Sep 1
• 10 citations
  Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development
  Guney Bademci, Clemer Abad, Filiz Basak Cengiz, Serhat Seyhan, Armagan Incesulu, Shengru Guo, Suat Fitoz, Emine Ikbal Atli, Nicholas C. Gosstola, Selma Demir, Brett Co...> ;The Journal of Clinical Investigation. 2020 Aug 3
• 9 citations
  Comprehensive clinically oriented workflow for nucleotide level resolution and interpretation in prenatal diagnosis of de novo apparently balanced chromosomal transloc...
  Dezső David, João Freixo, Joana Fino, Inês Carvalho, Mariana Marques, Manuela Cardoso, Raul E. Piña-Aguilar, Cynthia C. Morton> ;Human Genetics. 2020 Feb 6
• 23 citations
  Generation of protective pneumococcal-specific nasal resident memory CD4+ T cells via parenteral immunization.
  Joanne M O'Hara, Naresh Singh Redhu, Elaine Cheung, Nahid G. Robertson, Izabel Patik, Shorouk El Sayed, Claudette M. Thompson, Muriel Herd, Katherine B Lucas, Evan Con...> ;Mucosal Immunology. 2020 Jan 1
• 54 citations
  SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility
  Samantha L.P. Schilit, Shreya Menon, Corinna Friedrich, Tammy Kammin, Ellen Wilch, Carrie Hanscom, Sizun Jiang, Sabine Kliesch, Michael E. Talkowski, Frank Tüttelmann,...> ;American Journal of Human Genetics. 2020 Jan 2
• 51 citations
  Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage
  Zirui Dong, Junhao Yan, Fengping Xu, Jianying Yuan, Hui Jiang, Huilin Wang, Haixiao Chen, Lei Zhang, Lingfei Ye, Jinjin Xu, Yuhua Shi, Zhenjun Yang, Ye Cao, Lingyun Ch...> ;American Journal of Human Genetics. 2019 Dec 5
• 30 citations
  A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children.
  A Eliot Shearer, Jun Shen, Sami Amr, Cynthia C Morton, Richard J Smith> ;Genetics in Medicine. 2019 Nov 1
• 58 citations
  Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China
  Pu Dai, Li Hui Huang, Guojian Wang, Xue Gao, Chun Yan Qu, Xiao Wei Chen, Fu Rong Ma, Jie Zhang, Wan Li Xing, Shu Yan Xi, Bin Rong Ma, Ying Pan, Xiao Hua Cheng, Hong Du...> ;American Journal of Human Genetics. 2019 Oct 3
• 88 citations
  GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank.
  Helena R R Wells, Maxim B. Freidin, Fatin N Zainul Abidin, Antony Payton, Piers Dawes, Kevin J. Munro, Cynthia C. Morton, David R. Moore, Sally J. Dawson, Frances M K ...> ;American Journal of Human Genetics. 2019 Oct 3
• 59 citations
  Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis.
  Huilin Wang, Zirui Dong, Rui Zhang, Matthew Hoi Kin Chau, Zhenjun Yang, Kathy Yin Ching Tsang, Hoi Kin Wong, Baoheng Gui, Zhuo Meng, Kelin Xiao, Xiaofan Zhu, Yanfang W...> ;Genetics in Medicine. 2020 Mar 1
• 60 citations
  Gene therapy for hearing loss
  Ryotaro Omichi, Seiji B. Shibata, Cynthia C. Morton, Richard J.H. Smith> ;Human Molecular Genetics. 2019 Oct 1
• 39 citations
  The Iceberg under Water: Unexplored Complexity of Chromoanagenesis in Congenital Disorders.
  Cinthya J. Zepeda-Mendoza, Cynthia C. Morton> ;American Journal of Human Genetics. 2019 Apr 4
• 38 citations
  Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China.
  Qiuju Wang, Jiale Xiang, Jun Sun, Yun Yang, Jing Guan, Dayong Wang, Cui Song, Ling Guo, Hongyang Wang, Yaqiu Chen, Junhong Leng, Xiaman Wang, Junqing Zhang, Bing Han, ...> ;Genetics in Medicine. 2019 Mar 20
• 12 citations
  Loss of LDAH associated with prostate cancer and hearing loss.
  Benjamin Currall, Ming Chen, Richard C Sallari, Maura Bríd Cotter, Kristen E Wong, Nahid G. Robertson, Kathryn L. Penney, Andrea Lunardi, Markus Reschke, Ann E. Hickox...> ;Human Molecular Genetics. 2018 Dec 15
• 40 citations
  Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource ...
  Darrel Waggoner, Karen E. Wain, Adrian M. Dubuc, Laura K. Conlin, Scott E. Hickey, Allen N. Lamb, Christa Lese Martin, Cynthia C. Morton, Kristen Rasmussen, Jane L. Sc...> ;Genetics in Medicine. 2018 Jun 18
• 2 citations
  Computational Prediction of Position Effects of Human Chromosome Rearrangements.
  Cinthya J. Zepeda-Mendoza, Shreya Menon, Cynthia C. Morton> ;Current Protocols in Human Genetics. 2018 Apr 1
• 10 citations
  Clinical, pathologic, cytogenetic, and molecular profiling in self-identified black women with uterine leiomyomata
  Mark A. Hayden, Zehra Ordulu, C. Scott Gallagher, Bradley J. Quade, Raymond M. Anchan, Nia Robinson Middleton, Serene S. Srouji, Elizabeth A. Stewart, Cynthia C. Morton> ;Cancer Genetics. 2018 Apr 1
• 7 citations
  Pelvic and pulmonary benign metastasizing leiomyoma: A case report.
  Jennifer B. Bakkensen, Wesley R Samore, Pietro Bortoletto, Cynthia C. Morton, Raymond M. Anchan> ;Case Reports in Women's Health. 2018 Mar 31
• 10 citations
  Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome Sequencing.
  Zirui Dong, Lingfei Ye, Yang Zhenjun, Haixiao Chen, Jianying Yuan, Huilin Wang, Xiaosen Guo, Yun Li, Jun Wang, Fang Chen, Sau Wai Cheung, Cynthia C. Morton, Hui Jiang,...> ;Current Protocols in Human Genetics. 2018 Jan 1
• 3 citations
  Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin.
  Cinthya J. Zepeda-Mendoza, Alexandra Bardon, Tammy Kammin, David J. Harris, Helen Cox, Claire Redin, Zehra Ordulu, Michael E. Talkowski, Cynthia C. Morton> ;European Journal of Human Genetics. 2018 Jan 10
• 2 citations
  3C-PCR: a novel proximity ligation-based approach to phase chromosomal rearrangement breakpoints with distal allelic variants.
  Samantha L.P. Schilit, Cynthia C. Morton> ;Human Genetics. 2018 Jan 1
• 42 citations
  Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural ...
  Zirui Dong, Huilin Wang, Haixiao Chen, Hui Jiang, Jianying Yuan, Zhenjun Yang, Wen-Jing Wang, Fengping Xu, Xiaosen Guo, Ye Cao, Zhenzhen Zhu, Chunyu Geng, Wan Chee Che...> ;Genetics in Medicine. 2018 Jul 1
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Journal Articles

• Yield of Additional Genetic Testing After Chromosomal Microarray for Diagnosis of Neurodevelopmental Disability and Congenital Anomalies: A Clinical Practice Resource ...  
  Scott E Hickey, Darrel Waggoner, David T Miller, Karen E Wain, Cynthia C Morton, Nature