All papers authored by Beatrice Bocquet
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2023
Béatrice Bocquet 
,
Caroline Borday,
Nejla Erkilic,
Daria Mamaeva ,
Alicia Donval,
Christel Masson,
Karine Parain,
Karolina Kaminska ,
Mathieu Quinodoz ,
Irene Perea-Romero ,
Gema Garcia-Garcia,
Carla Jimenez-Medina,
Hassan Boukhaddaoui,
Arthur Coget,
Nicolas Leboucq
and 15 other authors
,
Caroline Borday,
Nejla Erkilic,
Daria Mamaeva ,
Alicia Donval,
Christel Masson,
Karine Parain,
Karolina Kaminska ,
Mathieu Quinodoz ,
Irene Perea-Romero ,
Gema Garcia-Garcia,
Carla Jimenez-Medina,
Hassan Boukhaddaoui,
Arthur Coget,
Nicolas Leboucq
and 15 other authors
TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa
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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
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,
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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Anaïs F. Poncet,
Olivier Grunewald ,
Veronika Vaclavik,
Isabelle Meunier,
Isabelle Drumare,
Valérie Pelletier,
Béatrice Bocquet ,
Margarita G. Todorova,
Anne-Gaëlle Le Moing,
Aurore Devos,
Daniel F. Schorderet ,
Florence Jobic ,
Sabine Defoort-Dhellemmes,
Hélène Dollfus,
Vasily M. Smirnov
and 1 other authors
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,
Veronika Vaclavik,
Isabelle Meunier,
Isabelle Drumare,
Valérie Pelletier,
Béatrice Bocquet ,
Margarita G. Todorova,
Anne-Gaëlle Le Moing,
Aurore Devos,
Daniel F. Schorderet ,
Florence Jobic ,
Sabine Defoort-Dhellemmes,
Hélène Dollfus,
Vasily M. Smirnov
and 1 other authors
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2021
Kévin Mairot ,
Vasily Smirnov,
Béatrice Bocquet ,
Gilles Labesse ,
Carl Arndt,
Sabine Defoort-Dhellemmes,
Xavier Zanlonghi ,
Dalil Hamroun ,
Danièle Denis,
Marie-Christine Picot,
Thierry David ,
Olivier Grunewald ,
Mako Pégart,
Hélèna Huguet,
Anne-Françoise Roux
and 3 other authors
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,
Vasily Smirnov,
Béatrice Bocquet ,
Gilles Labesse ,
Carl Arndt,
Sabine Defoort-Dhellemmes,
Xavier Zanlonghi ,
Dalil Hamroun ,
Danièle Denis,
Marie-Christine Picot,
Thierry David ,
Olivier Grunewald ,
Mako Pégart,
Hélèna Huguet,
Anne-Françoise Roux
and 3 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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Isabelle Perrault ,
Sylvain Hanein ,
Xavier Gérard,
Nelson Mounguengue,
Ryme Bouyakoub,
Mohammed Zarhrate,
Cécile Fourrage,
Fabienne Jabot-Hanin,
Béatrice Bocquet ,
Isabelle Meunier,
Xavier Zanlonghi,
Josseline Kaplan,
Jean-Michel Rozet
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,
Sylvain Hanein ,
Xavier Gérard,
Nelson Mounguengue,
Ryme Bouyakoub,
Mohammed Zarhrate,
Cécile Fourrage,
Fabienne Jabot-Hanin,
Béatrice Bocquet ,
Isabelle Meunier,
Xavier Zanlonghi,
Josseline Kaplan,
Jean-Michel Rozet
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2019
Camille Piro-Mégy,
Emmanuelle Sarzi,
Aleix Tarrés-Solé ,
Marie Péquignot,
Fenna Hensen,
Mélanie Quilès,
Gaël Manes ,
Arka Chakraborty ,
Audrey Sénéchal,
Béatrice Bocquet ,
Chantal Cazevieille,
Agathe Roubertie,
Agnès Müller,
Majida Charif,
David Goudenège
and 10 other authors
,
Marie Péquignot,
Fenna Hensen,
Mélanie Quilès,
Gaël Manes ,
Arka Chakraborty ,
Audrey Sénéchal,
Béatrice Bocquet ,
Chantal Cazevieille,
Agathe Roubertie,
Agnès Müller,
Majida Charif,
David Goudenège
and 10 other authors
Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy
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