Marian M. Humphries - Concepedia

Author

Marian M. Humphries

Also Known As

Humphries, M M, M M Humphries, M. Humphries, M. M. Humphries, M.M. Humphries, MARIAN M. HUMPHRIES, Marian Humphries, Marian M Humphries, Marian M. Humphries

106

Publications

5.1K

Citations

H-Index

Concepts

All Affiliations

Trinity College Dublin Royal Victoria Eye and Ear Hospital Imperial College London Tallaght University Hospital The University of Texas Health Science Center at Houston

About

Marian M. Humphries is an author at Trinity College Dublin specializing in medicine, cell biology, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	27	2.8K
2	Natural Sciences	3	3	415
3	Engineering	2	2	195
4	Health Sciences	2	2	35
5	Social Sciences	1	1	43

Marian M. Humphries

Publications

4.7K

Citations

H-Index

Page 1

	Year	Citations
Retinopathy induced in mice by targeted disruption of the rhodopsin gene Marian M. Humphries, Derrick E. Rancourt, G. Jane Farrar, Nature Genetics Ocular DiseaseSignal TransductionPhotoreceptor CellOphthalmologyRetina	1997	532
NLRP3 has a protective role in age-related macular degeneration through the induction of IL-18 by drusen components Sarah Doyle, Matthew Campbell, Ema Ozaki, Nature Medicine InflammationOcular DiseaseAutoimmune DiseaseOphthalmologyAge-related Diseases	2012	411
A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa G. Jane Farrar, Paul F. Kenna, Siobhán A. Jordan, Nature Protein FunctionPeripherin–rds GeneRetinitis PigmentosaGeneticsThree-base-pair Deletion	1991	388
Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3 Peter McWilliam, G. Jane Farrar, Paul F. Kenna, Genomics ChromatinChromosome DynamicsCytogeneticsGenetic DisorderGenetics	1989	244
Dose-dependent expression of claudin-5 is a modifying factor in schizophrenia Chris Greene, John Kealy, Marian M. Humphries, Molecular Psychiatry	2017	234
RNA Interference–Mediated Suppression and Replacement of Human Rhodopsin In Vivo Mary O’Reilly, Arpad Palfi, Naomi Chadderton, The American Journal of Human Genetics Systems BiologyMolecular PhysiologyEngineeringRna Binding ProteinsHuman Rhodopsin	2007	171
A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement Sara J. Bowne, Marian M. Humphries, Lori S. Sullivan, European Journal of Human Genetics Genome InstabilityMendelian DisorderGenetic DisorderMedicineGenetics	2011	152
Autoregulated paracellular clearance of amyloid-β across the blood-brain barrier James Keaney, Dominic M. Walsh, Tiernan T. O’Malley, Science Advances	2015	144
Suppression and Replacement Gene Therapy for Autosomal Dominant Disease in a Murine Model of Dominant Retinitis Pigmentosa Sophia Millington‐Ward, Naomi Chadderton, Mary O’Reilly, Molecular Therapy	2011	139
Blood–Brain Barrier Dysfunction as a Hallmark Pathology in Chronic Traumatic Encephalopathy Colin P. Doherty, Eoin O’Keefe, Eugene Wallace, Journal of Neuropathology & Experimental Neurology	2016	133

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