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Author/Creator Stroud, David A.

2. A patient with homozygous nonsense variants in two Leigh syndrome disease genes: Distinguishing a dual diagnosis from a hypomorphic protein‐truncating variant. Issue 7 (13th April 2019)

Authors:
Lake, Nicole J.; Formosa, Luke E.; Stroud, David A.; Ryan, Michael T.; Calvo, Sarah E.; Mootha, Vamsi K.; Morar, Bharti; Procopis, Peter G; Christodoulou, John; Compton, Alison G.; Thorburn, David R.
Journal:
Human mutation
Issue:
Volume 40:Issue 7(2019)
Page Start:
893
Record Type:
Journal Article
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6. Climate‐driven changes in winter abundance of a migratory waterbird in relation to EU protected areas. Issue 5 (15th January 2015)

Authors:
Pavón‐Jordán, Diego; Fox, Anthony D.; Clausen, Preben; Dagys, Mindaugas; Deceuninck, Bernard; Devos, Koen; Hearn, Richard D.; Holt, Chas A.; Hornman, Menno; Keller, Verena; Langendoen, Tom; Ławicki, Łukasz; Lorentsen, Svein H.; Luigujõe, Leho; Meissner, Włodzimierz; Musil, Petr; Nilsson, Leif; Pa...
Journal:
Diversity & distributions
Issue:
Volume 21:Issue 5(2015:May)
Page Start:
571
Record Type:
Journal Article
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8. FunRich: An open access standalone functional enrichment and interaction network analysis tool. Issue 15 (17th June 2015)

Authors:
Pathan, Mohashin; Keerthikumar, Shivakumar; Ang, Ching‐Seng; Gangoda, Lahiru; Quek, Camelia Y.J.; Williamson, Nicholas A.; Mouradov, Dmitri; Sieber, Oliver M.; Simpson, Richard J.; Salim, Agus; Bacic, Antony; Hill, Andrew F.; Stroud, David A.; Ryan, Michael T.; Agbinya, Johnson I.; Mariadason, Jo...
Journal:
Proteomics
Issue:
Volume 15:Issue 15(2015:Aug.)
Page Start:
2597
Record Type:
Journal Article
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10. Multiomic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10. Issue 1 (11th November 2020)

Authors:
Helman, Guy; Compton, Alison G.; Hock, Daniella H.; Walkiewicz, Marzena; Brett, Gemma R.; Pais, Lynn; Tan, Tiong Y.; De Paoli‐Iseppi, Ricardo; Clark, Michael B.; Christodoulou, John; White, Susan M.; Thorburn, David R.; Stroud, David A.; Stark, Zornitza; Simons, Cas
Journal:
Human mutation
Issue:
Volume 42:Issue 1(2021)
Page Start:
19
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗