Author

Daniel Sanchez

Florida Atlantic University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:Drosophila· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aashish R. JhaiD· 1 shared Abdelrahman Saad· 1 shared Ahmed Al Awadhi· 1 shared Albarah El-Khani· 1 shared Aleksander Medvedev· 1 shared Amna Alsuwaidi· 1 shared Andreas HenscheliD· 1 shared Antonio Milano· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aashish R. JhaORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

The Drosophila connectome reveals Axo-Axonic Synapses on Descending Neurons

César C. Ceballos, Juan Lopez, Ty Roachford, Daniel Sanchez, Sabrina D Jara, Kelli Robbins, Casey Spencer, Rodney K. Murphey, Rodrigo F. O. Pena

The paper maps axo-axonic synapses onto descending neurons in the Drosophila ventral nerve cord and identifies their functional roles in motor control.

iScience · Apr 7, 2026Peer-reviewedNeuroscience

Pathogenicity Reassessment and Novel Variant Discovery in Inherited Retinal Disease through Population-Scale Genomics in the United Arab Emirates

Budour Alkaf, Wadha Mohammed Abdulrahman, Sahar Al Marzooqi, Daniel Sanchez, Andreas Henschel, Aashish R. Jha, Abdelrahman Saad, Ahmed Al Awadhi, Albarah El-Khani, Aleksander Medvedev, Amna Alsuwaidi, Antonio Milano, Asma Al Mannaei, Ayesha Al Ali, Azza Attia, , Tiago R. Magalhães

The paper reassesses pathogenicity of variants in inherited retinal diseases using population-scale genomics in the UAE, identifying clinically relevant variants and highlighting discrepancies between clinical and population-based classifications.

medRxiv · Oct 14, 2025 · PreprintGenetic & Genomic Medicine