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Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients.

• Authors : Mori, Kentaro; Moteki, Hideaki; Miyagawa, Maiko

• Source: PLoS ONE. September 14, 2016, Vol. 11 Issue 9, e0162230.

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Massively Parallel DNA Sequencing Successfully Identifies New Causative Mutations in Deafness Genes in Patients with Cochlear Implantation and EAS.

• Authors : Miyagawa, Maiko; Nishio, Shin-ya; Ikeda, Takuo

• Source: PLoS ONE. October 9, 2013, Vol. 8 Issue 10, e75793.

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Simultaneous Screening of Multiple Mutations by Invader Assay Improves Molecular Diagnosis of Hereditary Hearing Loss: A Multicenter Study.

• Authors : Usami, Shin-ichi; Nishio, Shin-ya; Nagano, Makoto

• Source: PLoS ONE. February 24, 2012, Vol. 7 Issue 2, e31276.

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Application of SNPscan in Genetic Screening for Common Hearing Loss Genes.

• Authors : Gao, Zixuan; Lu, Yu; Ke, Jia

• Source: PLoS ONE. October 28, 2016, Vol. 11 Issue 10, e0165650.

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Genetic hallmarks of recurrent/metastatic adenoid cystic carcinoma.

• Authors : Ho, Allen S.; Ochoa, Angelica; Jayakumaran, Gowtham

• Source: Journal of Clinical Investigation. October, 2019, Vol. 129 Issue 10, p4276, 14 p.

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Residual [beta] cell function and monogenic variants in long-duration type 1 diabetes patients.

• Authors : Yu, Marc Gregory; Keenan, Hillary A.; Shah, Hetal S.

• Source: Journal of Clinical Investigation. August, 2019, Vol. 129 Issue 8, p3252, 12 p.

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Hearing loss and tinnitus--are funders and industry listening?

• Authors : Cederroth, Christopher R; Canlon, Barbara; Langguth, Berthold

• Source: Nature Biotechnology. November, 2013, Vol. 31 Issue 11, p972, 3 p.

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An Efficient and Comprehensive Strategy for Genetic Diagnostics of Polycystic Kidney Disease.

• Authors : Eisenberger, Tobias; Decker, Christian; Hiersche, Milan

• Source: PLoS ONE. February 3, 2015, Vol. 10 Issue 2.

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Identification of Candidate Children for Maturity-Onset Diabetes of the Young Type 2 (MODY2) Gene Testing: A Seven-Item Clinical Flowchart (7-iF).

• Authors : Pinelli, Michele; Acquaviva, Fabio; Barbetti, Fabrizio

• Source: PLoS ONE. November 11, 2013, Vol. 8 Issue 11, e79933.

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Preface to 'What Causes Birth Defects?'

• Source: Opposing Viewpoints: Birth Defects. 2014.

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