Evan Reid - Concepedia

Author

Evan Reid

Also Known As

Detelina Grozeva, E REID, E Reid, E. Reid, Ernest Turro, Evan Reid, Geoff Woods, Irene Roberts, Julia Rankin, K. John. Pasi

109

Publications

7.5K

Citations

H-Index

Concepts

All Affiliations

University of Cambridge Addenbrooke's Hospital University College London Medical Research Council Great Ormond Street Hospital

About

Evan Reid is an author at University of Cambridge specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	26	3.4K
2	Health Sciences	3	3	105
3	Natural Sciences	3	3	561
4	Public Health	2	2	52
5	Engineering	1	1	19

Evan Reid

Publications

4.8K

Citations

H-Index

Page 1

	Year	Citations
A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10) Evan Reid, Mark Kloos, Allison E. Ashley‐Koch, The American Journal of Human Genetics BiologyMendelian DisorderGenetic DisorderMedicineGenetics	2002	533
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease Keren Carss, Gavin Arno, Marie Erwood, The American Journal of Human Genetics Whole-genome SequencingAllelic VariantGenetic DisorderMedicineGenetics	2016	463
The cargo-selective retromer complex is a recruiting hub for protein complexes that regulate endosomal tubule dynamics Michael E. Harbour, Sophia Y. Breusegem, Robin Antrobus, Journal of Cell Science Molecular BiologyMolecular GeneticsCytoskeletonCellular PhysiologyRetromer Complex	2010	248
Spastin Couples Microtubule Severing to Membrane Traffic in Completion of Cytokinesis and Secretion James W. Connell, Catherine Lindon, J. Paul Luzio, Traffic Protein SecretionImmunologyCytoskeletonCellular PhysiologyMembrane Transport	2008	239
The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B Evan Reid, James W. Connell, Thomas L. Edwards, Human Molecular Genetics	2004	198
Mutations in the KIAA0196 Gene at the SPG8 Locus Cause Hereditary Spastic Paraplegia Paul N. Valdmanis, Inge A. Meijer, Annie Reynolds, The American Journal of Human Genetics Genetic DisorderMedicineGeneticsKiaa0196 GeneMolecular Genetics	2006	191
Drosophila spichthyin inhibits BMP signaling and regulates synaptic growth and axonal microtubules Xinnan Wang, W. Robert Shaw, Hilda T.H. Tsang, Nature Neuroscience Inhibits BmpSynaptic GrowthDevelopmental BiologyMolecular NeuroscienceSynaptic Signaling	2007	174
Idiopathic Epilepsies with Seizures Precipitated by Fever and <i>SCN1A</i> Abnormalities Carla Marini, Davide Mei, Teresa Temudo, Epilepsia	2007	172
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12 Gladys Montenegro, Adriana Rebelo, James W. Connell, Journal of Clinical Investigation Neurodegenerative DiseasesMendelian DisorderEr LocalizationHereditary Spastic ParaplegiasMedicine	2012	168
Defects in ER–endosome contacts impact lysosome function in hereditary spastic paraplegia Rachel Allison, James R. Edgar, Guy Pearson, The Journal of Cell Biology	2017	166

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