Author

Osvaldo Luis Podhajcer

Consejo Nacional de Investigaciones Científicas y TécnicasORCID 0000-0002-6512-8553Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adrian DockeryiD· 1 shared Alaa AlTalbishiiD· 1 shared Alexander HoischeniD· 1 shared Ana FakiniD· 1 shared Andrea Louise VincentiD· 1 shared Anna Maria TracewskaiD· 1 shared Anna MatyniaiD· 1 shared Aurore DevosiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Adrian DockeryORCID

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2 papers

Recent·Most cited

Development of novel high-affinity nanobodies against EGFR for cancer therapy

Mauro Heitrich, Marisa Mariel Fernández, Diana C. Aguilar-Cortes, Santiago Werbajh, Gabriela Canziani, Vanesa Zylberman, Luisina Belén Ripari, Guillermo A. Videla-Richardson, Emilio Luis Malchiodi, Osvaldo Luis Podhajcer, Sabrina E. Vinzón

This paper isolates and characterizes two high-affinity nanobodies against EGFR, showing their potent anti-tumor activity in vitro.

bioRxiv · Mar 16, 2025 · PreprintMolecular Biology

Resolving the dark matter of ABCA4 for 1,054 Stargardt disease probands through integrated genomics and transcriptomics

Mubeen Khan, Stéphanie S. Cornelis, Marta Del Pozo‐Valero, Laura Whelan, Esmee H. Runhart, Ketan Mishra, Femke Bults, Yahya AlSwaiti, Alaa AlTalbishi, Elfride De Baere, Sandro Banfi, Eyal Banin, Miriam Bauwens, Tamar Ben‐Yosef, Camiel J. F. Boon, , Frans P.M. Cremers

The paper identifies pathogenic deep-intronic and structural variants in 26% of unsolved Stargardt disease cases using integrated genomics and transcriptomics.

Genetics in Medicine · Apr 19, 2020Peer-reviewedGenetics