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Author/Creator Shyr, Casper

3. Gain-of-function KCNJ6 Mutation in a Severe Hyperkinetic Movement Disorder Phenotype. (1st August 2018)

Authors:
Horvath, Gabriella A.; Zhao, Yulin; Tarailo-Graovac, Maja; Boelman, Cyrus; Gill, Harinder; Shyr, Casper; Lee, James; Blydt-Hansen, Ingrid; Drögemöller, Britt I.; Moreland, Jacqueline; Ross, Colin J.; Wasserman, Wyeth W.; Masotti, Andrea; Slesinger, Paul A.; van Karnebeek, Clara D.M.
Journal:
Neuroscience
Issue:
Volume 384(2018)
Page Start:
152
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. JASPAR 2016: a major expansion and update of the open-access database of transcription factor binding profiles. Issue Volume 44:Issue D1(2016) (3rd November 2015)

Authors:
Mathelier, Anthony; Fornes, Oriol; Arenillas, David J.; Chen, Chih-yu; Denay, Grégoire; Lee, Jessica; Shi, Wenqiang; Shyr, Casper; Tan, Ge; Worsley-Hunt, Rebecca; Zhang, Allen W.; Parcy, François; Lenhard, Boris; Sandelin, Albin; Wasserman, Wyeth W.
Journal:
Nucleic acids research
Issue:
Volume 44:Issue D1(2016)
Page Start:
D110
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region. Issue 1 (30th November 2020)

Authors:
Ye, Xin (Cynthia); Roslin, Nicole M; Paterson, Andrew D; Lyons, Christopher J; Pegado, Victor; Richmond, Phillip; Shyr, Casper; Fornes, Oriol; Han, XiaoHua; Higginson, Michelle; Ross, Colin J; Giaschi, Deborah; Gregory-Evans, Cheryl; Patel, Millan S; Wasserman, Wyeth W
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 1(2022)
Page Start:
46
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗