Identification and function of long non-coding RNA

por Ernst, Carl, Morton, Cynthia C.
Publicado 2013

Training the Future Leaders in Personalized Medicine

por Mason-Suares, Heather, Sweetser, David A., Lindeman, Neal I., Morton, Cynthia C.
Publicado 2016

Pelvic and pulmonary benign metastasizing leiomyoma: A case report

por Bakkensen, Jennifer B., Samore, Wesley, Bortoletto, Pietro, Morton, Cynthia C., Anchan, Raymond M.
Publicado 2018

A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children

por Shearer, A. Eliot, Shen, Jun, Amr, Sami, Morton, Cynthia C., Smith, Richard J.
Publicado 2019

Correction: A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children

por Shearer, A. Eliot, Shen, Jun, Amr, Sami, Morton, Cynthia C., Smith, Richard J.
Publicado 2019

Experience of Low-Pass Whole-Genome Sequencing-Based Copy Number Variant Analysis: A Survey of Chinese Tertiary Hospitals

por Zheng, Yu, Zhu, Baosheng, Tan, Jichun, Guan, Yichun, Morton, Cynthia C., Lu, Guangxiu
Publicado 2022

Editorial: Chromosome structural variants: Epidemiology, identification and contribution to human diseases

por Dong, Zirui, David, Dezso, Gonzaga-Jauregui, Claudia, Morton, Cynthia C., Zepeda-Mendoza, Cinthya J.
Publicado 2022

Cochlin Deficiency Protects Against Noise-Induced Hearing Loss

por Seist, Richard, Landegger, Lukas D., Robertson, Nahid G., Vasilijic, Sasa, Morton, Cynthia C., Stankovic, Konstantina M.
Publicado 2021

Spectrum of genes involved in a unique case of Potocki Schaffer syndrome with a large chromosome 11 deletion

por Romeike, Bernd F.M., Shen, Yiping, Nishimoto, Hiromi Koso, Morton, Cynthia C., Layman, Lawrence C., Kim, Hyung-Goo
Publicado 2014

Hereditary leiomyomatosis and renal cell cancer: Cutaneous lesions & atypical fibroids

por Bortoletto, Pietro, Lindsey, Jennifer L., Yuan, Liping, Quade, Bradley J., Gargiulo, Antonio R., Morton, Cynthia C., Stewart, Elizabeth A., Anchan, Raymond M.
Publicado 2017

The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing

por Mitchell, Calli O., Rivera-Cruz, Greysha, Chau, Matthew Hoi Kin, Dong, Zirui, Choy, Kwong Wai, Shen, Jun, Amr, Sami, Giersch, Anne B. S., Morton, Cynthia C.
Publicado 2022

Complex cytogenetic rearrangements at the DURS1 locus in syndromic Duane retraction syndrome

por Baris, Hagit N, Chan, Wai-Man, Andrews, Caroline, Behar, Doron M, Donovan, Diana J, Morton, Cynthia C, Ranells, Judith, Pal, Tuya, Ligon, Azra H, Engle, Elizabeth C
Publicado 2013

Low-pass genome sequencing-based detection of absence of heterozygosity: validation in clinical cytogenetics

por 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
Publicado 2021

Intravenous Leiomyomatosis: An Unusual Intermediate between Benign and Malignant Uterine Smooth Muscle Tumors

por 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.
Publicado 2016

Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX Toolkit

por Morton, Cynthia C., Marazita, Mary L., Peter, Beate, Rice, Mabel L., Kraft, Shelly Jo, Barkmeier‐Kraemer, Julie, Balaban, Carey, Phillips, Michael, Schoden, Jennifer, Maiese, Deborah, Hendershot, Tabitha, Hamilton, Carol M.
Publicado 2021

Yield of Additional Genetic Testing after Chromosomal Microarray for Diagnosis of Neurodevelopmental Disability and Congenital Anomalies: a clinical practice resource of the Americ...

por Waggoner, Darrel, Wain, Karen E., Dubuc, Adrian M., Conlin, Laura, Hickey, Scott E., Lamb, Allen N, Lese Martin, Christa, Morton, Cynthia C., Rasmussen, Kristen, Schuette, Jane L, Schwartz, Stuart, Miller, David T.
Publicado 2018

Using population admixture to help complete maps of the human genome

por Genovese, Giulio, Handsaker, Robert E., Li, Heng, Altemose, Nicolas, Lindgren, Amelia M., Chambert, Kimberly, Pasaniuc, Bogdan, Price, Alkes L., Reich, David, Morton, Cynthia C., Pollak, Martin R., Wilson, James G., McCarroll, Steven A.
Publicado 2013

Generation of protective pneumococcal-specific nasal resident memory CD4(+) T cells via parenteral immunization

por O’Hara, Joanne M., Redhu, Naresh S, Cheung, Elaine, Robertson, Nahid G., Patik, Izabel, Sayed, Shorouk El, Thompson, Claudette M., Herd, Muriel, Lucas, Katherine B., Conaway, Evan, Morton, Cynthia C., Farber, Donna L., Malley, Richard, Horwitz, Bruce H.
Publicado 2019

Identification of Balanced Chromosomal Rearrangements Previously Unknown Among Participants in the 1000 Genomes Project: Implications for Interpretation of Structural Variation in...

por Dong, Zirui, Wang, Huilin, Chen, Haixiao, Jiang, Hui, Yuan, Jianying, Yang, Zhenjun, Wang, Wen-Jing, Xu, Fengping, Guo, Xiaosen, Cao, Ye, Zhu, Zhenzhen, Geng, Chunyu, Cheung, Wan Chee, Kwok, Yvonne K, Yang, Huangming, Leung, Tak Yeung, Morton, Cynthia C., Cheung, Sau Wai, Choy, Kwong Wai
Publicado 2017

Diagnosing and Preventing Hearing Loss in the Genomic Age

por McDermott, John H., Molina-Ramírez, Leslie P, Bruce, Iain A, Mahaveer, Ajit, Turner, Mark, Miele, Gino, Body, Richard, Mahood, Rachel, Ulph, Fiona, MacLeod, Rhona, Harvey, Karen, Booth, Nicola, Demain, Leigh A. M., Wilson, Paul, Black, Graeme C., Morton, Cynthia C., Newman, William G
Publicado 2019