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Igor Stevanovski

Igor Stevanovski

Role
Laboratory Research Assistant
Lab/Group
Genomic Technologies Lab

Selected publications

See all publications
  • 2024
    Nature Communications10.1038/s41467-024-53151-2

    Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

    Andrea Cortese, Sarah J Beecroft, Stefano Facchini, Riccardo Curro, Macarena Cabrera-Serrano, Igor Stevanovski, Sanjog R Chintalaphani, Hasindu Gamaarachchi, Ben Weisburd, Chiara Folland, Gavin Monahan, Carolin K Scriba, Lein Dofash, Mridul Johari, Bianca R Grosz, Melina Ellis, Liam G Fearnley, Rick Tankard, Justin Read, Ashirwad Merve, Natalia Dominik, Elisa Vegezzi, Ricardo P Schnekenberg, Gorka Fernandez-Eulate, Marion Masingue, Diane Giovannini, Martin B Delatycki, Elsdon Storey, Mac Gardner, David J Amor, Garth Nicholson, Steve Vucic, Robert D Henderson, Thomas Robertson, Jason Dyke, Vicki Fabian, Frank Mastaglia, Mark R Davis, Marina Kennerson, , Ros Quinlivan, Simon Hammans, Arianna Tucci, Melanie Bahlo, Catriona A McLean, Nigel G Laing, Tanya Stojkovic, Henry Houlden, Michael G Hanna, Ira W Deveson, Paul J Lockhart, Phillipa J Lamont, Michael C Fahey, Enrico Bugiardini, Gianina Ravenscroft
  • 2024
    Nature Communications10.1038/s41467-024-49950-2

    A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

    Andrea Cortese, Sarah J Beecroft, Stefano Facchini, Riccardo Curro, Macarena Cabrera-Serrano, Igor Stevanovski, Sanjog R Chintalaphani, Hasindu Gamaarachchi, Ben Weisburd, Chiara Folland, Gavin Monahan, Carolin K Scriba, Lein Dofash, Mridul Johari, Bianca R Grosz, Melina Ellis, Liam G Fearnley, Rick Tankard, Justin Read, Ashirwad Merve, Natalia Dominik, Elisa Vegezzi, Ricardo P Schnekenberg, Gorka Fernandez-Eulate, Marion Masingue, Diane Giovannini, Martin B Delatycki, Elsdon Storey, Mac Gardner, David J Amor, Garth Nicholson, Steve Vucic, Robert D Henderson, Thomas Robertson, Jason Dyke, Vicki Fabian, Frank Mastaglia, Mark R Davis, Marina Kennerson, , Ros Quinlivan, Simon Hammans, Arianna Tucci, Melanie Bahlo, Catriona A McLean, Nigel G Laing, Tanya Stojkovic, Henry Houlden, Michael G Hanna, Ira W Deveson, Paul J Lockhart, Phillipa J Lamont, Michael C Fahey, Enrico Bugiardini, Gianina Ravenscroft
  • 2024
    Nature Genetics10.1038/s41588-024-01808-5

    A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus.

    David Pellerin, Giulia F Del Gobbo, Madeline Couse, Egor Dolzhenko, Sathiji K Nageshwaran, Warren A Cheung, Isaac R L Xu, Marie-Josée Dicaire, Guinevere Spurdens, Gabriel Matos-Rodrigues, Igor Stevanovski, Carolin K Scriba, Adriana Rebelo, Virginie Roth, Marion Wandzel, Céline Bonnet, Catherine Ashton, Aman Agarwal, Cyril Peter, Dan Hasson, Nadejda M Tsankova, Ken Dewar, Phillipa J Lamont, Nigel G Laing, Mathilde Renaud, Henry Houlden, Matthis Synofzik, Karen Usdin, Andre Nussenzweig, Marek Napierala, Zhao Chen, Hong Jiang, Ira W Deveson, Gianina Ravenscroft, Schahram Akbarian, Michael A Eberle, Kym M Boycott, Tomi Pastinen, , Bernard Brais, Stephan Zuchner, Matt C Danzi
  • 2024
    Journal of the Peripheral Nervous System : JPNS10.1111/jns.12637

    A deep intronic variant in MME causes autosomal recessive Charcot-Marie-Tooth neuropathy through aberrant splicing.

    Bianca R Grosz, Jevin M Parmar, Melina Ellis, Samantha Bryen, Cas Simons, Andre L M Reis, Igor Stevanovski, Ira W Deveson, Garth Nicholson, Nigel Laing, Mathew Wallis, Gianina Ravenscroft, Kishore R Kumar, Steve Vucic, Marina L Kennerson
  • 2024
    Nature Communications10.1038/s41467-024-46456-9

    A universal molecular control for DNA, mRNA and protein expression.

    Helen M Gunter, Scott E Youlten, Andre L M Reis, Tim McCubbin, Bindu Swapna Madala, Ted Wong, Igor Stevanovski, Arcadi Cipponi, Ira W Deveson, Nadia S Santini, Sarah Kummerfeld, Peter I Croucher, Esteban Marcellin, Tim R Mercer