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Author/Creator Guan, Qiaoning

2. AUDIOME: a tiered exome sequencing–based comprehensive gene panel for the diagnosis of heterogeneous nonsyndromic sensorineural hearing loss. (December 2018)

Authors:
Guan, Qiaoning; Balciuniene, Jorune; Cao, Kajia; Fan, Zhiqian; Biswas, Sawona; Wilkens, Alisha; Gallo, Daniel; Bedoukian, Emma; Tarpinian, Jennifer; Jayaraman, Pushkala; Sarmady, Mahdi; Dulik, Matthew; Santani, Avni; Spinner, Nancy; Abou Tayoun, Ahmad; Krantz, Ian; Conlin, Laura; Luo, Minjie
Journal:
Genetics in medicine
Issue:
Volume 20:Number 12(2018)
Page Start:
1600
Record Type:
Journal Article
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3. Correction: Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data. (November 2018)

Authors:
Gibson, Kristin McDonald; Nesbitt, Addie; Cao, Kajia; Yu, Zhenming; Denenberg, Elizabeth; DeChene, Elizabeth; Guan, Qiaoning; Bhoj, Elizabeth; Zhou, Xiangdong; Zhang, Bo; Wu, Chao; Dubbs, Holly; Wilkens, Alisha; Medne, Livija; Bedoukian, Emma; White, Peter S; Pennington, Jeffrey; Luo, Minjie; Con...
Journal:
Genetics in medicine
Issue:
Volume 20:Number 11(2018)
Page Start:
1486
Record Type:
Journal Article
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4. Correction: Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data. (October 2018)

Authors:
Gibson, Kristin McDonald; Nesbitt, Addie; Cao, Kajia; Yu, Zhenming; Denenberg, Elizabeth; DeChene, Elizabeth; Guan, Qiaoning; Bhoj, Elizabeth; Zhou, Xiangdong; Zhang, Bo; Wu, Chao; Dubbs, Holly; Wilkens, Alisha; Medne, Livija; Bedoukian, Emma; White, Peter S; Pennington, Jeffrey; Lou, Minjie; Con...
Journal:
Genetics in medicine
Issue:
Volume 20:Number 10(2018)
Page Start:
1298
Record Type:
Journal Article
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5. Prenatal diagnosis of Proteus syndrome: Diagnosis of an AKT1 mutation from amniocytes. Issue 19 (15th September 2020)

Authors:
Abell, Katherine; Tolusso, Leandra; Smith, Nicki; Hopkin, Robert; Vawter‐Lee, Marissa; Habli, Mounira; Riddle, Stefanie; Calvo‐Garcia, Maria A.; Guan, Qiaoning; Bierbrauer, Karin; Hwa, Vivian; Saal, Howard M.
Other Names:
Watanabe Michiko guestEditor.; Zhou Chengji J. guestEditor.
Journal:
Birth defects research
Issue:
Volume 112:Issue 19(2020)
Page Start:
1733
Record Type:
Journal Article
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6. The MAP3K7 gene: Further delineation of clinical characteristics and genotype/phenotype correlations. Issue 10 (29th July 2022)

Authors:
van Woerden, Geeske M.; Senden, Richelle; de Konink, Charlotte; Trezza, Rossella A.; Baban, Anwar; Bassetti, Jennifer A.; van Bever, Yolande; Bird, Lynne M.; van Bon, Bregje W.; Brooks, Alice S.; Guan, Qiaoning; Klee, Eric W.; Marcelis, Carlo; Rosado, Joel M.; Schimmenti, Lisa A.; Shikany, Amy R....
Journal:
Human mutation
Issue:
Volume 43:Issue 10(2022)
Page Start:
1377
Record Type:
Journal Article
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