Martin Delatycki

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Bio

His research and clinical interests are neurogenetics and community genetics. Martin has over 250 publications and has obtained over $5 million in research funding.

Research Interests

Papers共 560 篇Author StatisticsCo-AuthorSimilar Experts

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Updating the Diagnosis and Management of Elevated Serum Ferritin Levels in the Era of Routine Ferritin Testing of Blood Donors by Australian Red Cross Lifeblood

Gary D Zhang,James Chen,Daniel M Johnstone,Martin B Delatycki,Katie Allen,John K Olynyk

The Medical journal of Australiano. 7 (2025): 334-336

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A Global Perspective on Research Advances and Future Challenges in Friedreich Ataxia

Elisabetta Indelicato,Martin B Delatycki,Jennifer Farmer,Marcondes C França,Susan Perlman,Myriam Rai,Sylvia Boesch

Nature reviews Neurologyno. 4 (2025): 204-215

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Bridging the Gap: a Prospective Trial Comparing Programmable Targeted Long-Read Sequencing and Short-Read Genome Sequencing for Genetic Diagnosis of Cerebellar Ataxia

Genome researchno. 4 (2025): 769-785

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Haemochromatosis Genotypes and Incident Dementia in a Prospective Study of Older Adults

Chenglong Yu,Martin Delatycki,Sultana Monira Hussain, John James McNeil,Paul Lacaze, John K Olynyk

Neurologyno. 12 (2025): e213743-e213743

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P675: Opportunities for Precision Medicine in Hereditary Disease Inferred from Large-Scale, Real-World Diagnostic Genetic Testing Results

Flavia M. Facio,Hillery Metz, Elaine Chen, Kathryn Hatchell, Adam Buchanan,Wendy Chung, Kristina Cusmano-Ozog,Martin Delatycki, Robert Green, Sulagna Saitta, Benjamin Solomon,Robert Nussbaum,Swaroop Aradhya

Genetics in Medicine Open (2025): 103044

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Neuroimaging Biomarkers for Friedreich Ataxia: A Cross-Sectional Analysis of the TRACK-FA Study

Nellie Georgiou-Karistianis,Louise A Corben, Eric F Lock, Helena Bujalka, Isaac Adanyeguh,Manuela Corti,Dinesh K Deelchand,Martin B Delatycki,Imis Dogan,Jennifer Farmer,Marcondes C França, Anthony S Gabay,William Gaetz,Ian H Harding, James Joers, Michelle A Lax, Jiakun Li,David R Lynch,Thomas H Mareci,Alberto R M Martinez,Massimo Pandolfo,Marina Papoutsi, Richard G Parker,Kathrin Reetz,Thiago J R Rezende, Timothy P Roberts,Sandro Romanzetti,David A Rudko, Susmita Saha, Jörg B Schulz, Sub H Subramony, Veena G Supramaniam,Christophe Lenglet, Pierre-Gilles Henry

Annals of neurology (2025)

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Pathogenic De Novo Variants in PPP2R5C Cause a Neurodevelopmental Disorder Within the Houge-Janssens Syndrome Spectrum

Iris Verbinnen,Sofia Douzgou Houge,Tzung-Chien Hsieh,Hellen Lesmann, Aron Kirchhoff,David Geneviève,Elise Brimble,Lisa Lenaerts,Dorien Haesen, Rebecca J Levy,Julien Thevenon,Laurence Faivre,Elysa Marco,Jessica X Chong,Mike Bamshad,Karynne Patterson,Ghayda M Mirzaa,Kimberly Foss,William Dobyns,Susan M White,Lynn Pais,Emily O'Heir,Raphaela Itzikowitz,Kirsten A Donald,Celia Van der Merwe,Alessandro Mussa, Raffaela Cervini,Elisa Giorgio,Tony Roscioli,Kerith-Rae Dias,Carey-Anne Evans,Natasha J Brown,Anna Ruiz,Juan Pablo Trujillo Quintero,Rachel Rabin,John Pappas, Hai Yuan,Katherine Lachlan,Simon Thomas, Anita Devlin,Michael Wright, Richard Martin, Joanna Karwowska,Renata Posmyk,Nicolas Chatron,Zornitza Stark, Oliver Heath,Martin Delatycki,Rebecca Buchert,Georg-Christoph Korenke,Keri Ramsey,Vinodh Narayanan,Dorothy K Grange,Judith L Weisenberg,Tobias B Haack,Stephanie Karch,Patricia Kipkemoi, Moses Mangi,Karen G C B Bindels de Heus,Marie-Claire Y de Wit,Tahsin Stefan Barakat,Derek Lim,Géraldine Van Winckel,Rebecca C Spillmann,Vandana Shashi,Maureen Jacob, Antonia M Stehr,Undiagnosed Diseases Network,Peter Krawitz,Gunnar Douzgos Houge,Veerle Janssens

American journal of human geneticsno. 3 (2025): 554-571

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The Australian Genomics Mitochondrial Flagship: A National Program Delivering Mitochondrial Diagnoses

Rocio Rius,Alison G. Compton,Naomi L. Baker,Shanti Balasubramaniam,Stephanie Best,Kaustuv Bhattacharya,Kirsten Boggs,Tiffany Boughtwood,Jeffrey Braithwaite,Drago Bratkovic,Alessandra Bray,Marie-Jo Brion,Jo Burke,Sarah Casauria,Belinda Chong,David Coman,Shannon Cowie,Mark Cowley,Michelle G. de Silva,Martin B. Delatycki,Samantha Edwards,Carolyn Ellaway,Michael C. Fahey,Keri Finlay,Janice Fletcher, Leah E. Frajman,Ann E. Frazier,Velimir Gayevskiy,Roula Ghaoui,Himanshu Goel,Ilias Goranitis,Matilda Haas,Daniella H. Hock,Denise Howting,Matilda R. Jackson,Maina P. Kava,Madonna Kemp,Sarah King-Smith,Nicole J. Lake,Phillipa J. Lamont, Joy Lee,Janet C. Long,Mandi Macshane,Evanthia O. Madelli,Ellenore M. Martin,Justine E. Marum,Tessa Mattiske,Jim Mcgill,Alejandro Metke,Sean Murray,Julie Panetta,Liza K. Phillips,Michael C. J. Quinn, Michael T. Ryan,Sarah Schenscher,Cas Simons, Nicholas Smith, David A. Stroud,Michel C. Tchan, Melanie Tom,Mathew Wallis,Tyson L. Ware,AnneMarie E. Welch,Christine Wools, You Wu,John Christodoulou,David R. Thorburn

GENETICS IN MEDICINE（2025）

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The MOXIe Trial of Omaveloxolone in Friedreich Ataxia: Exploring the Transient Nature of Treatment-emergent Adverse Events (P7-3.016)

David Lynch,Sylvia Boesch,Martin Delatycki,Paola Giunti,Angie Goldsberry,Chad Hoyle,Katherine Mathews, Seemi Khan,Colin Meyer, Masako Murai,Wolfgang Nachbauer,Susan Perlman,S Subramony,Theresa Zesiewicz

Neurology（2024）

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Papers共 560 篇Author StatisticsCo-AuthorSimilar Experts