Author

Marcondes C. França

Universidade Estadual de Campinas (UNICAMP)ORCID 0000-0003-0898-2419Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Research Focus:differential expression· 1 Organism:Drosophila· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:imaging· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

A. Nazlı BaşakiD· 1 shared Abigail D. WilsoniD· 1 shared Albena JordanovaiD· 1 shared Alberto MartíneziD· 1 shared Alexander Martin RossoriD· 1 shared Alexandra DürriD· 1 shared Ali CansuiD· 1 shared André Luiz Santos PessoaiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. Nazlı BaşakORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

NeurosciencebioRxivPreprintAug 8, 2025

A Core Pattern of Cerebellar and Brainstem Degeneration and Reduced Cerebrocerebellar Structural Covariance in Spinocerebellar Ataxia Type 3 (SCA3): MRI Volumetrics from ENIGMA-Ataxia

Jason W. Robertson, Isaac Mawusi Adanyeguh, David J. Arpin…·Carlos Roberto Hernandez-Castillo

This study uses MRI volumetrics to analyze cerebellar and brainstem degeneration in SCA3, finding consistent atrophy patterns and reduced cerebrocerebellar covariance.

1 citation

humanimaging

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Genetic & Genomic MedicinemedRxivPreprintMay 10, 2024

Biallelic variants in ARHGAP19 cause a motor-predominant neuropathy with asymmetry and conduction slowing

Natalia Dominik, Stéphanie Efthymiou, Christopher J. Record…·Henry Houlden

The paper identifies biallelic variants in ARHGAP19 as a cause of motor-predominant neuropathy with conduction slowing in multiple families.

2 citations

humanDrosophila

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GeneticsAgingPeer-reviewedMar 23, 2020

Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease

Fulya Akçimen, Sandra Martins, Calwing Liao…·Guy Armand Rouleau

This study identifies nine genetic loci associated with age at onset in Machado-Joseph disease, suggesting roles for DNA repair and synaptic pathways in disease progression.

28 citations

humanwhole-exome sequencing

𝕏 PostBluesky