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Author/Creator Perrett, Daniel

1. DECIPHER: Supporting the interpretation and sharing of rare disease phenotype‐linked variant data to advance diagnosis and research. Issue 6 (21st February 2022)

Authors:
Foreman, Julia; Brent, Simon; Perrett, Daniel; Bevan, Andrew P.; Hunt, Sarah E.; Cunningham, Fiona; Hurles, Matthew E.; Firth, Helen V.
Other Names:
Boycott Kym guestEditor.; Hamosh Ada guestEditor.; Rehm Heidi guestEditor.
Journal:
Human mutation
Issue:
Volume 43:Issue 6(2022)
Page Start:
682
Record Type:
Journal Article
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2. Facilitating Collaboration in Rare Genetic Disorders Through Effective Matchmaking in DECIPHER. Issue 10 (20th August 2015)

Authors:
Chatzimichali, Eleni A.; Brent, Simon; Hutton, Benjamin; Perrett, Daniel; Wright, Caroline F.; Bevan, Andrew P.; Hurles, Matthew E.; Firth, Helen V.; Swaminathan, Ganesh J.
Journal:
Human mutation
Issue:
Volume 36:Issue 10(2015:Oct.)
Page Start:
941
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Registered access: authorizing data access. (December 2018)

Authors:
Dyke, Stephanie; Linden, Mikael; Lappalainen, Ilkka; Argila, Jordi; Carey, Knox; Lloyd, David; Spalding, J.; Cabili, Moran; Kerry, Giselle; Foreman, Julia; Cutts, Tim; Shabani, Mahsa; Rodriguez, Laura; Haeussler, Maximilian; Walsh, Brian; Jiang, Xiaoqian; Wang, Shuang; Perrett, Daniel; Boughtwood...
Journal:
European journal of human genetics
Issue:
Volume 26:Number 12(2018)
Page Start:
1721
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗