All papers authored by Isabelle Audo
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2022
Bernd Wissinger 
,
Britta Baumann,
Elena Buena-Atienza,
Zeinab Ravesh ,
Artur V. Cideciyan ,
Katarina Stingl ,
Isabelle Audo ,
Isabelle Meunier ,
Beatrice Bocquet ,
Elias I. Traboulsi ,
Alison J. Hardcastle ,
Jessica C. Gardner ,
Michel Michaelides,
Kari E. Branham,
Thomas Rosenberg
and 16 other authors
Download from doi.org
,
Britta Baumann,
Elena Buena-Atienza,
Zeinab Ravesh ,
Artur V. Cideciyan ,
Katarina Stingl ,
Isabelle Audo ,
Isabelle Meunier ,
Beatrice Bocquet ,
Elias I. Traboulsi ,
Alison J. Hardcastle ,
Jessica C. Gardner ,
Michel Michaelides,
Kari E. Branham,
Thomas Rosenberg
and 16 other authors
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Maria Solaki ,
Britta Baumann,
Peggy Reuter ,
Sten Andreasson,
Isabelle Audo ,
Carmen Ayuso,
Ghassan Balousha ,
Francesco Benedicenti ,
David Birch ,
Pierre Bitoun ,
Delphine Blain ,
Beatrice Bocquet,
Kari Branham,
Jaume Català‐Mora ,
Elfride De Baere
and 36 other authors
,
Britta Baumann,
Peggy Reuter ,
Sten Andreasson,
Isabelle Audo ,
Carmen Ayuso,
Ghassan Balousha ,
Francesco Benedicenti ,
David Birch ,
Pierre Bitoun ,
Delphine Blain ,
Beatrice Bocquet,
Kari Branham,
Jaume Català‐Mora ,
Elfride De Baere
and 36 other authors
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia
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2021
Ana Fakin ,
Crystel Bonnet,
Anne Kurtenbach,
Saddek Mohand-Said,
Ditta Zobor,
Katarina Stingl ,
Francesco Testa,
Francesca Simonelli,
José-Alain Sahel,
Isabelle Audo ,
Eberhart Zrenner,
Marko Hawlina,
Christine Petit
Download from doi.org
,
Crystel Bonnet,
Anne Kurtenbach,
Saddek Mohand-Said,
Ditta Zobor,
Katarina Stingl ,
Francesco Testa,
Francesca Simonelli,
José-Alain Sahel,
Isabelle Audo ,
Eberhart Zrenner,
Marko Hawlina,
Christine Petit
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Christina Zeitz ,
Cécile Méjécase ,
Christelle Michiels,
Christel Condroyer,
Juliette Wohlschlegel ,
Marine Foussard,
Aline Antonio,
Vanessa Démontant,
Lisa Emmenegger,
Audrey Schalk,
Marion Neuillé,
Elise Orhan ,
Sébastien Augustin,
Crystel Bonnet,
Amrit Estivalet
and 8 other authors
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,
Cécile Méjécase ,
Christelle Michiels,
Christel Condroyer,
Juliette Wohlschlegel ,
Marine Foussard,
Aline Antonio,
Vanessa Démontant,
Lisa Emmenegger,
Audrey Schalk,
Marion Neuillé,
Elise Orhan ,
Sébastien Augustin,
Crystel Bonnet,
Amrit Estivalet
and 8 other authors
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Vasily Smirnov,
Olivier Grunewald ,
Jean Muller ,
Christina Zeitz ,
Carolin D. Obermaier,
Aurore Devos,
Valérie Pelletier,
Béatrice Bocquet ,
Camille Andrieu,
Jean-Louis Bacquet,
Elodie Lebredonchel ,
Saddek Mohand-Saïd,
Sabine Defoort-Dhellemmes,
José-Alain Sahel,
Hélène Dollfus
and 5 other authors
,
Jean Muller ,
Christina Zeitz ,
Carolin D. Obermaier,
Aurore Devos,
Valérie Pelletier,
Béatrice Bocquet ,
Camille Andrieu,
Jean-Louis Bacquet,
Elodie Lebredonchel ,
Saddek Mohand-Saïd,
Sabine Defoort-Dhellemmes,
José-Alain Sahel,
Hélène Dollfus
and 5 other authors
Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy
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2020
Maria Solaguren‐Beascoa ,
Kinga M. Bujakowska ,
Cécile Méjécase ,
Lisa Emmenegger,
Elise Orhan ,
Marion Neuillé,
Saddek Mohand‐Saïd ,
Christel Condroyer,
Marie‐Elise Lancelot,
Christelle Michiels,
Vanessa Demontant,
Aline Antonio,
Mélanie Letexier,
Jean‐Paul Saraiva,
Christine Lonjou
and 8 other authors
,
Kinga M. Bujakowska ,
Cécile Méjécase ,
Lisa Emmenegger,
Elise Orhan ,
Marion Neuillé,
Saddek Mohand‐Saïd ,
Christel Condroyer,
Marie‐Elise Lancelot,
Christelle Michiels,
Vanessa Demontant,
Aline Antonio,
Mélanie Letexier,
Jean‐Paul Saraiva,
Christine Lonjou
and 8 other authors
WDR34 , a candidate gene for non‐syndromic rod‐cone dystrophy
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Maissa G. Bah ,
Diana Rodriguez ,
Cécile Cazeneuve,
Fanny Mochel ,
David Devos ,
Agnese Suppiej ,
Agathe Roubertie ,
Isabelle Meunier ,
Cyril Gitiaux ,
Aurore Curie ,
Frédéric Klapczynski,
Nouha Allani‐Essid,
Maryline Carneiro,
Rick Van Minkelen,
Anneke Kievit
and 19 other authors
,
Diana Rodriguez ,
Cécile Cazeneuve,
Fanny Mochel ,
David Devos ,
Agnese Suppiej ,
Agathe Roubertie ,
Isabelle Meunier ,
Cyril Gitiaux ,
Aurore Curie ,
Frédéric Klapczynski,
Nouha Allani‐Essid,
Maryline Carneiro,
Rick Van Minkelen,
Anneke Kievit
and 19 other authors
Deciphering the natural history of SCA7 in children
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Nicole Weisschuh ,
Marc Sturm ,
Britta Baumann,
Isabelle Audo ,
Carmen Ayuso,
Beatrice Bocquet,
Kari Branham,
Brian P. Brooks,
Jaume Catalá‐Mora,
Roberto Giorda,
John R. Heckenlively,
Robert B. Hufnagel,
Samuel G. Jacobson,
Ulrich Kellner,
Sofia Kitsiou‐Tzeli
and 11 other authors
,
Marc Sturm ,
Britta Baumann,
Isabelle Audo ,
Carmen Ayuso,
Beatrice Bocquet,
Kari Branham,
Brian P. Brooks,
Jaume Catalá‐Mora,
Roberto Giorda,
John R. Heckenlively,
Robert B. Hufnagel,
Samuel G. Jacobson,
Ulrich Kellner,
Sofia Kitsiou‐Tzeli
and 11 other authors
Deep‐intronic variants in CNGB3 cause achromatopsia by pseudoexon activation
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Julia Felden ,
Britta Baumann,
Manir Ali ,
Isabelle Audo ,
Carmen Ayuso,
Beatrice Bocquet,
Ingele Casteels,
Blanca Garcia‐Sandoval,
Samuel G. Jacobson,
Bernhard Jurklies,
Ulrich Kellner ,
Line Kessel,
Birgit Lorenz,
Martin McKibbin,
Isabelle Meunier
and 7 other authors
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,
Britta Baumann,
Manir Ali ,
Isabelle Audo ,
Carmen Ayuso,
Beatrice Bocquet,
Ingele Casteels,
Blanca Garcia‐Sandoval,
Samuel G. Jacobson,
Bernhard Jurklies,
Ulrich Kellner ,
Line Kessel,
Birgit Lorenz,
Martin McKibbin,
Isabelle Meunier
and 7 other authors
Upload
2018
Marco Nassisi,
Saddek Mohand-Saïd,
Claire-Marie Dhaenens,
Fiona Boyard,
Vanessa Démontant,
Camille Andrieu,
Aline Antonio,
Christel Condroyer,
Marine Foussard,
Cécile Méjécase,
Chiara Eandi,
José-Alain Sahel,
Christina Zeitz,
Isabelle Audo
Download from doi.org
Download from doi.org
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