Manir Ali

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 7

Top Topics

Optical Coherence Tomography

Dna Methylation

Age Related Macular Degeneration

Top Venues

Molecular genetics & genomic medicine

Molecular diagnosis & therapy

This page only lists publications with an associated author ORCID identifier.

Publications

Benjamin McClinton, Zelia Corradi, Martin McKibbin, Daan M Panneman, Susanne Roosing, Erica G M Boonen, Manir Ali, Christopher Mark Watson, David H Steel, Frans P M Cremers, Chris F Inglehearn, Rebekkah J Hitti-Malin, Carmel Toomes
Effective smMIPs-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UK. Genes 14 (1) (2023)
Samar Yahya, Christopher Mark Watson, Ian M Carr, Martin McKibbin, Laura A Crinnion, Morag Taylor, Hope Bonin, Tracy Fletcher, Mohammed E El-Asrag, Manir Ali, Carmel Toomes, Chris F Inglehearn
Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells. Molecular diagnosis & therapy (2023)
Benjamin McClinton, Zelia Corradi, Martin McKibbin, Daan M Panneman, Susanne Roosing, Erica G M Boonen, Manir Ali, Christopher Mark Watson, David H Steel, Frans P M Cremers, Chris F Inglehearn, Rebekkah J Hitti-Malin, Carmel Toomes
Effective smMIPs-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UK. Genes 14 (1) (2023)
Benjamin McClinton, Zelia Corradi, Martin McKibbin, Daan M Panneman, Susanne Roosing, Erica G M Boonen, Manir Ali, Christopher Mark Watson, David H Steel, Frans P M Cremers, Chris F Inglehearn, Rebekkah J Hitti-Malin, Carmel Toomes
Effective smMIPs-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UK. Genes 14 (1) (2023)
Benjamin McClinton, Laura A Crinnion, Martin McKibbin, Rajarshi Mukherjee, James A Poulter, Claire E L Smith, Manir Ali, Christopher Mark Watson, Chris F Inglehearn, Carmel Toomes
Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon-based short-read sequencing strategies. Molecular genetics & genomic medicine (2023)
Alison J Hardcastle, Petra Liskova, Yelena Bykhovskaya, Bennet J McComish, Alice E Davidson, Chris F Inglehearn, Xiaohui Li, Helene Choquet, Mahmoud Habeeb, Sionne E M Lucas, Srujana Sahebjada, Nikolas Pontikos, Karla E Rojas Lopez, Anthony P Khawaja, Manir Ali, Lubica Dudakova, Pavlina Skalicka, Bart T H Van Dooren, Annette J M Geerards, Christoph Walter Haudum, Valeria Lo Faro, Abi Tenen, Mark J Simcoe, Karina Patasova, Darioush Yarrand, Jie Yin, Salina Siddiqui, Aine Rice, Layal Abi Farraj, Yii-Der Ida Chen, Jugnoo S Rahi, Ronald M Krauss, Elisabeth Theusch, Jac C Charlesworth, Loretta Szczotka-Flynn, Carmel Toomes, Magda A Meester-Smoor, Andrea J Richardson, Paul A Mitchell, Kent D Taylor, Ronald B Melles, Anthony J Aldave, Richard A Mills, Ke Cao, Elsie Chan, Mark D Daniell, Jie Jing Wang, Jerome I Rotter, Alex W Hewitt, Stuart Macgregor, Caroline C W Klaver, Wishal D Ramdas, Jamie E Craig, Sudha K Iyengar, David O'Brart, Eric Jorgensen, Paul N Baird, Yaron S Rabinowitz, Kathryn P Burdon, Christopher J Hammond, Stephen J Tuft, Pirro G Hysi
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus. Communications biology 4 (1) (2021)
Julia Felden, Britta Baumann, Manir Ali, Isabelle Audo, Carmen Ayuso, Beatrice Bocquet, Ingele Casteels, Blanca Garcia-Sandoval, Samuel G Jacobson, Bernhard Jurklies, Ulrich Kellner, Line Kessel, Birgit Lorenz, Martin McKibbin, Isabelle Meunier, Thomy de Ravel, Thomas Rosenberg, Klaus Rüther, Maria Vadala, Bernd Wissinger, Katarina Stingl, Susanne Kohl
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene. Human mutation 40 (8) (2019)