Naushin Waseem - UCL Institute of Ophthalmology, University College London

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论文共 75 篇作者统计合作学者相似作者

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Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration

Kiran Narta,Manoj Ramesh Teltumbade,Mansi Vishal,Samreen Sadaf,Mohd. Faruq, Hodan Jama,Naushin Waseem,Aparna Rao,Abhijit Sen,Kunal Ray,Arijit Mukhopadhyay

Genes（2023）

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Transcriptome Analysis Reveals Vimentin-Induced Disruption of Cell–Cell Associations Augments Breast Cancer Cell Migration

Saima Usman,Ahmad Jamal,Antesar Bushaala,Naushin H. H. Waseem,Hebah Al-Dehlawi,William Andrew Yeudall,Muy-Teck Teh,Hemanth Tummala,Ahmad Waseem

Cells（2022）

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Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in Its Development

Mark J. Simcoe,Ameet Shah,Baojian Fan,Helene Choquet,Nicole Weisschuh,Naushin H. Waseem,Chen Jiang,Ronald B. Melles,Robert Ritch,Omar A. Mahroo,Bernd Wissinger,Eric Jorgenson,Janey L. Wiggs,David F. Garway-Heath,Pirro G. Hysi,Christopher J. Hammond

Ophthalmologyno. 6 (2022): 626-636

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Dominant Cone Rod Dystrophy, Previously Assigned to a Missense Variant in RIMS1, is Fully Explained by Co-Inheritance of a Dominant Allele of PROM1

Maria Pilar Martin-Gutierrez,Elena R. Schiff,Genevieve Wright,Naushin Waseem,Omar A. Mahroo,Michel Michaelides,Anthony T. Moore,Andrew R. Webster,Gavin Arno

Investigative ophthalmology & visual scienceno. 9 (2022): 14-14

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Transcriptome analysis reveals vimentin-induced downregulation of cell-cell associations augments cancer cell migration

Saima Usman,Ahmad Jamal,Antesar Bushaala,Naushin H Waseem,Hebah Al-Dehlawi,Andrew Yeudall,Muy-Teck Teh,Hemanth Tummala,Ahmad Waseem

Research Square (Research Square) (2022)

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Genetic analyses identify the first two genetic loci associated with sporadic pigment dispersion syndrome and indicate myopia is a causal factor for disease onset

Mark James Simcoe,Baojian Fan,Naushin Waseem,Nicole Weisschuh,Omar Abdul Rahman Mahroo,Helene Choquet,Janey L. Wiggs,David F. Garway-Heath,Pirro G. Hysi,Christopher J. Hammond

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE（2021）

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Vimentin is at the Heart of Epithelial Mesenchymal Transition (EMT) Mediated Metastasis

Saima Usman,Naushin H. Waseem,Thuan Khanh Ngoc Nguyen,Sahar Mohsin,Ahmad Jamal,Muy-Teck Teh,Ahmad Waseem

Cancers（2021）

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Dominant cone rod dystrophy (CORD7) previously assigned to mutation of RIMS1, is fully explained by co-inheritance of a dominant allele of PROM1

G. Arno,E. Schiff,G. Wright,N. Waseem,M. Michaelides,A. T. Moore,A. R. Webster

EUROPEAN JOURNAL OF HUMAN GENETICS（2020）

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Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma

PLOS GENETICSno. 4 (2020)

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