Jordi Maggi

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 13

Top Venues

Genes

International journal of molecular sciences

Cells

University of Zurich

University of Zurich (BSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Zurich Nov 01 2016

Switzerland

PhD student :: Institute of Medical Molecular Genetics

ProCrea Apr 01 2015 - Oct 31 2015

Switzerland

Scientific collaborator :: ProCrea genetic diagnostics lab

Genome Institute of Singapore Sep 09 2013 - Nov 07 2013

Singapore

Intern

ProCrea Jun 03 2013 - Jul 05 2013

Switzerland

Intern :: ProCrea genetic diagnostics lab

Education History

University of Zurich Sep 15 2010 - Nov 05 2013

Switzerland

BSC

Publications

David Atac, Kevin Maggi, Silke Feil, Jordi Maggi, Elisa Cuevas, Jane C Sowden, Samuel Koller, Wolfgang Berger
Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal Development. Cells 13 (13) (2024)
David Atac, Kevin Maggi, Silke Feil, Jordi Maggi, Elisa Cuevas, Jane C Sowden, Samuel Koller, Wolfgang Berger
Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal Development. Cells 13 (13) (2024)
Jordi Maggi, Silke Feil, Jiradet Gloggnitzer, Kevin Maggi, Ruxandra Bachmann-Gagescu, Christina Gerth-Kahlert, Samuel Koller, Wolfgang Berger
Nanopore Deep Sequencing as a Tool to Characterize and Quantify Aberrant Splicing Caused by Variants in Inherited Retinal Dystrophy Genes. International journal of molecular sciences 25 (17) (2024)
Jordi Maggi, Samuel Koller, Silke Feil, Ruxandra Bachmann-Gagescu, Christina Gerth-Kahlert, Wolfgang Berger
Limited Added Diagnostic Value of Whole Genome Sequencing in Genetic Testing of Inherited Retinal Diseases in a Swiss Patient Cohort. International journal of molecular sciences 25 (12) (2024)
Jordi Maggi, Samuel Koller, Silke Feil, Ruxandra Bachmann-Gagescu, Christina Gerth-Kahlert, Wolfgang Berger
Limited Added Diagnostic Value of Whole Genome Sequencing in Genetic Testing of Inherited Retinal Diseases in a Swiss Patient Cohort. International journal of molecular sciences 25 (12) (2024)
Samuel Koller, Tim Beltraminelli, Jordi Maggi, Agnès Wlodarczyk, Silke Feil, Luzy Baehr, Christina Gerth-Kahlert, Moreno Menghini, Wolfgang Berger
Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa. Genes 14 (4) (2023)
Samuel Koller, Tim Beltraminelli, Jordi Maggi, Agnès Wlodarczyk, Silke Feil, Luzy Baehr, Christina Gerth-Kahlert, Moreno Menghini, Wolfgang Berger
Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa. Genes 14 (4) (2023)
Samuel Koller, Tim Beltraminelli, Jordi Maggi, Agnès Wlodarczyk, Silke Feil, Luzy Baehr, Christina Gerth-Kahlert, Moreno Menghini, Wolfgang Berger
Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa. Genes 14 (4) (2023)
Samuel Koller, Tim Beltraminelli, Jordi Maggi, Agnès Wlodarczyk, Silke Feil, Luzy Baehr, Christina Gerth-Kahlert, Moreno Menghini, Wolfgang Berger
Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa. Genes 14 (4) (2023)
Florian Peters, Lynn J A Ebner, David Atac, Jordi Maggi, Wolfgang Berger, Anneke I den Hollander, Christian Grimm
Regulation of ABCA1 by AMD-Associated Genetic Variants and Hypoxia in iPSC-RPE. International journal of molecular sciences 23 (6) (2022)
Patricia Haug, Samuel Koller, Jordi Maggi, Elena Lang, Silke Feil, Agnès Wlodarczyk, Luzy Bähr, Katharina Steindl, Marianne Rohrbach, Christina Gerth-Kahlert, Wolfgang Berger
Whole Exome Sequencing in Coloboma/Microphthalmia: Identification of Novel and Recurrent Variants in Seven Genes. Genes 12 (1) (2021)
Jordi Maggi, Samuel Koller, Luzy Bähr, Silke Feil, Fatma Kivrak Pfiffner, James V M Hanson, Alessandro Maspoli, Christina Gerth-Kahlert, Wolfgang Berger
Long-Range PCR-Based NGS Applications to Diagnose Mendelian Retinal Diseases. International journal of molecular sciences 22 (4) (2021)
Jordi Maggi, Lisa Roberts, Samuel Koller, George Rebello, Wolfgang Berger, Rajkumar Ramesar
De Novo Assembly-Based Analysis of RPGR Exon ORF15 in an Indigenous African Cohort Overcomes Limitations of a Standard Next-Generation Sequencing (NGS) Data Analysis Pipeline. Genes 11 (7) (2020)

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Publication Activity (10 Years)

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Jordi Maggi