Manir Ali - Concepedia

Author

Manir Ali

Also Known As

Ali, Manir, Carmel Toomes, Graham E. Holder, M Ali, M. ALI, M. Ali, M.T. Al Ali, Manir ALI, Manir Ali, Marwa Ali Radi Ali

136

Publications

6.1K

Citations

H-Index

Concepts

All Affiliations

St James's University Hospital University of Leeds University College London Radboud University Nijmegen Radboud University Medical Center

About

Manir Ali is an author at St James's University Hospital specializing in medicine, genetics, and ophthalmology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	22	3.5K
2	Natural Sciences	2	2	42
3	Public Health	2	2	54
4	Biochemistry	2	2	42
5	Allergy	1	1	680

Manir Ali

Publications

5.2K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus Yanick J. Crow, Bruce E. Hayward, Rekha Parmar, Nature Genetics Ags1 LocusMendelian DisorderGenetic DisorderMedicineGenetics	2006	876
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response Gillian Rice, Jacquelyn Bond, Aruna Asipu, Nature Genetics AllergyAutoimmune DiseasePathogenesisImmunologyInnate Immune Response	2009	680
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection Yanick J. Crow, Andrea Leitch, Bruce E. Hayward, Nature Genetics Ribonuclease H2Viral EvolutionGenetic DisorderNeurovirologyGenetics	2006	666
Null Mutations in LTBP2 Cause Primary Congenital Glaucoma Manir Ali, Martin McKibbin, Adam Booth, The American Journal of Human Genetics Mendelian DisorderOphthalmologyNull MutationsGenetic DisorderGenetics	2009	322
<i>ZNF408</i> is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature Rob W.J. Collin, Konstantinos Nikopoulos, Margo Dona, Proceedings of the National Academy of Sciences Ocular DiseasePeripheral RetinaExome SequencingGeneticsPathology	2013	179
Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa Gavin Arno, Smriti A. Agrawal, Aiden Eblimit, The American Journal of Human Genetics	2016	129
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR Evangelia S. Panagiotou, Carla Sanjurjo Soriano, James A. Poulter, The American Journal of Human Genetics Ocular DiseaseSignal TransductionRetinaOphthalmologyPhotoreceptor Cell	2017	111
<i>CFH</i>,<i>VEGF</i>and<i>HTRA1</i>promoter genotype may influence the response to intravitreal ranibizumab therapy for neovascular age-related macular degeneration Martin McKibbin, Manir Ali, Shveta Bansal, British Journal of Ophthalmology	2011	100
Fcγ receptor type IIIA is associated with rheumatoid arthritis in two distinct ethnic groups Ann W Morgan, Bridget Griffiths, Frédérique Ponchel, Arthritis & Rheumatism	2000	97
Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects Kamron N. Khan, Clare V. Logan, Martin McKibbin, Human Molecular Genetics Ocular DiseaseGeneticsMolecular GeneticsDisease Gene IdentificationGenomics	2011	94

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