Matt Danzi - Department of Human Genetics and Hussman Institute for Human Genomics, University of Miami

基本信息

Career Trajectory

Bio

Matt Danzi is a computational neurobiologist working at the University of Miami in the Hussman Institute for Human Genomics. Matt does research in Bioinformatics, Neuroscience, and Molecular Biology. He is currently an Assistant Scientist in the lab of Stephan Zuchner where he develops approaches to identify causal pathogenic variants in patients with Mendelian neuropathies. His PhD work focused on epigenetics and gene expression regulation in axon regeneration.

Research Interests

Papers共 123 篇Author StatisticsCo-AuthorSimilar Experts

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Late-onset Vestibulocerebellar Ataxia: Clinical and Genetic Studies in a Long Follow-Up Series of 50 Patients

David Genís, Berta Alemany,David Pellerin,Bernard Brais,Marie-Josée Dicaire,Víctor Volpini,Berta Campos,Jordi Corral, Josep Gardenyes,Laura de Jorge,Héctor San Nicolás, Maria Buxó, Joan Martínez Sancho,Maria Obon, Carles Roig,Laia Rodriguez-Revenga,María Isabel Alvarez-Mora,Matt C. Danzi,Henry Houlden,Stephan Zuchner,Fabián Márquez, Lluís Ramió i Torrentà

Journal of Neurologyno. 3 (2025): 1-8

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Recent Advances in the Genetics of Ataxias: an Update on Novel Autosomal Dominant Repeat Expansions

David Pellerin,Pablo Iruzubieta,Isaac R. L. Xu,Matt C. Danzi, Andrea Cortese,Matthis Synofzik,Henry Houlden,Stephan Zuchner,Bernard Brais

Current Neurology and Neuroscience Reportsno. 1 (2025): 1-15

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The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic Paraplegia

Luca Schierbaum,Vicente Quiroz,Kathryn Yang, Joshua Rong, Nicole Battaglia, Umar Zubair, Michelle Christie,Marie Davis, Daniel Calame,Matt C Danzi,Richard S Finkel,Joshua Burns,Donald L Gilbert, Dararat Mingbunjerdsuk, Greg Pruitt, Norma Pruitt, John Cobb,Reza Sadjadi, Christopher R Cashman,Craig Blackstone,John K Fink,Michael E Shy,Stephan Zuchner,Darius Ebrahimi-Fakhari

Neurology Geneticsno. 2 (2025): e200249-e200249

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Detailed Tandem Repeat Allele Profiling in 1,027 Long-Read Genomes Reveals Genome-Wide Patterns of Pathogenicity

Matt C Danzi,Isaac R L Xu,Sarah Fazal,Egor Dolzhenko,David Pellerin,Ben Weisburd,Chloe Reuter,Jacinda Sampson,Chiara Folland,Matthew Wheeler,Anne O'Donnell-Luria,Stefan Wuchty,Gianina Ravenscroft,Michael A Eberle, All of Us Research Program Long Read Working Group,Stephan Zuchner

bioRxiv the preprint server for biology (2025)

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FGF14 GAA Intronic Expansion in Unsolved Adult-Onset Ataxia in the Care4Rare Canada Consortium

Alexanne Cuillerier, Giulia F Del Gobbo, Layla Mackay, Erika Wall, Madeline Couse, Laura M McDonell, Mireille Cloutier,Matt C Danzi,Jodi Warman-Chardon,Pierre R Bourque,Oksana Suchowersky, Alan Mears, Luke Seldenthuis, Wendy Mears, Laura Larrigan, Alexandre White-Brown,Gerald Pfeffer,Dennis E Bulman, David Dyment, CareRare Canada Consortium, Kym M Boycott

Annals of clinical and translational neurology（2025）

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Diagnostic Yield and Limitations of Whole-Genome Sequencing for Hereditary Cerebellar Ataxia

Wai Yan Yau,Roisin Sullivan, Emer O'Connor,David Pellerin, Michael H Parkinson,Paola Giunti,Marie-Josée Dicaire,Matt C Danzi,Stephan Züchner,Bernard Brais, Nicholas W Wood,Henry Houlden,Jana Vandrovcova

Brain communicationsno. 3 (2025): fcaf188-fcaf188

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Involvement of the Superior Cerebellar Peduncles in GAA-FGF14 Ataxia

Shihan Chen,Catherine Ashton,Rawan Sakalla,Guillemette Clement,Sophie Planel,Céline Bonnet,Phillipa J Lamont,Karthik Kulanthaivelu,Atchayaram Nalini,Henry Houlden,Antoine Duquette,Marie-Josée Dicaire, Pablo Iruzubieta Agudo, Javier Ruiz-Martinez,Enrique Marco De Lucas, Rodrigo Sutil Berjon,Jon Infante Ceberio,Elisabetta Indelicato,Sylvia M Boesch,Matthis Synofzik,Benjamin Bender,Matt C Danzi,Stephan Zuchner,David Pellerin,Bernard Brais,Mathilde Renaud,Roberta La Piana

Neurology Geneticsno. 2 (2025): e200253-e200253

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Intronic FGF14 GAA Repeat Expansions Impact Progression and Survival in Multiple System Atrophy

Viorica Chelban,David Pellerin,Nirosen Vijiaratnam, Hamin Lee,Yen Yee Goh, Lauren Brown, Sara Sambin,Danielle Seilhean,Stephane Lehericy, Pablo Iruzubieta, Rahema Mohammad, Eleanor Self, Annarita Scardamaglia, Cameron Lee, Miriama Ostrozovicova,Marie-Josée Dicaire,Christine Girges,Emil K Gustavsson,David Murphy, Toby Curless, Joshua Laβ,Joanne Trinh,Timothy Rittman,James B Rowe,Marios Hadjivassiliou, Neil Archibald,Matt C Danzi,Catherine Ashton, Virginie Roth, Marion Wandzel, Warren A Cheung, Djordje O Gveric, Bart De Vil,Jordan Follett,P Nigel Leigh, Lukas Beichert, Tomi Pastinen,Céline Bonnet,Mathilde Renaud,Wassilios G Meissner, Anne Sieben,David Crosiers,Patrick Cras,Stephan Zuchner,Jean-Christophe Corvol, Matthew J Farrer,Matthis Synofzik,Bernard Brais,Tom Warner, Huw R Morris,Zane Jaunmuktane,Tom Foltynie,Henry Houlden

Brain a journal of neurology (2025)

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A Genome-Wide Approach for the Discovery of Novel Repeat Expansion Disorders in the Undiagnosed Diseases Network Cohort

Sarah Fazal,Harriet Dashnow,Maike F Dohrn, Jacquelyn Raposo, Laurel Hiatt,Matt C Danzi, Isaac R L Xu,Camilo Toro,David R Adams,Karen Usdin,Bruce Hayward,Shilpa Nadimpalli Kobren,Shamil R Sunyaev, Rebecca C Spillmann,Vandana Shashi,Adriana Rebelo,Guney Bademci, Undiagnosed Diseases Network,Mustafa Tekin,Aaron R Quinlan,Stephan Züchner

Genetics in medicine official journal of the American College of Medical Geneticspp.101462-101462, (2025)

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The Continued Promise of Genomic Technologies and Software in Neurogenetics

Isaac R L Xu,Matt C Danzi, Jacquelyn Raposo,Stephan Züchner

Journal of neuromuscular diseasespp.22143602251325345-22143602251325345, (2025)

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