All papers authored by Andrea Superti-Furga
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2021
Sébastien Lebon 
,
Mathieu Quinodoz,
Virginie G. Peter,
Carole Gengler,
Gaëlle Blanchard,
Viviane Cina,
Belinda Campos-Xavier,
Carlo Rivolta ,
Andrea Superti-Furga
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,
Mathieu Quinodoz,
Virginie G. Peter,
Carole Gengler,
Gaëlle Blanchard,
Viviane Cina,
Belinda Campos-Xavier,
Carlo Rivolta ,
Andrea Superti-Furga
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Clara Velmans ,
Anne H. O'Donnell Luria,
Emanuela Argilli,
Frederic Tran Mau-Them,
Frederic Tran Mau-Them ,
Antonio Vitobello ,
Marcus Cy Chan,
Jasmine Lee-Fong Fung,
Megan Rech,
Angela Abicht,
Marion Aubert Mucca ,
Marion Aubert Mucca,
Jason Carmichael,
Nicolas Chassaing,
Robin Clark
and 26 other authors
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,
Anne H. O'Donnell Luria,
Emanuela Argilli,
Frederic Tran Mau-Them,
Frederic Tran Mau-Them ,
Antonio Vitobello ,
Marcus Cy Chan,
Jasmine Lee-Fong Fung,
Megan Rech,
Angela Abicht,
Marion Aubert Mucca ,
Marion Aubert Mucca,
Jason Carmichael,
Nicolas Chassaing,
Robin Clark
and 26 other authors
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Lila Allou,
Sara Balzano,
Andreas Magg ,
Mathieu Quinodoz,
Beryl Royer-Bertrand,
Robert Schöpflin,
Wing-Lee Chan,
Carlos E. Speck-Martins,
Daniel Rocha Carvalho,
Luciano Farage ,
Charles Marques Lourenço ,
Regina Albuquerque,
Srilakshmi Rajagopal,
Sheela Nampoothiri ,
Belinda Campos-Xavier
and 18 other authors
,
Mathieu Quinodoz,
Beryl Royer-Bertrand,
Robert Schöpflin,
Wing-Lee Chan,
Carlos E. Speck-Martins,
Daniel Rocha Carvalho,
Luciano Farage ,
Charles Marques Lourenço ,
Regina Albuquerque,
Srilakshmi Rajagopal,
Sheela Nampoothiri ,
Belinda Campos-Xavier
and 18 other authors
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator
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Maria Lisa Dentici ,
Viola Alesi,
Mathieu Quinodoz,
Barbara Robens,
Andrea Guerin,
Sébastien Lebon ,
Annapurna Poduri,
Lorena Travaglini,
Federica Graziola,
Alexandra Afenjar,
Boris Keren,
Valerio Licursi,
Alessandro Capuano,
Bruno Dallapiccola,
Andrea Superti-Furga
and 1 other authors
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,
Viola Alesi,
Mathieu Quinodoz,
Barbara Robens,
Andrea Guerin,
Sébastien Lebon ,
Annapurna Poduri,
Lorena Travaglini,
Federica Graziola,
Alexandra Afenjar,
Boris Keren,
Valerio Licursi,
Alessandro Capuano,
Bruno Dallapiccola,
Andrea Superti-Furga
and 1 other authors
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2020
Camille Kumps ,
Belinda Campos-Xavier,
Yvonne Hilhorst-Hofstee ,
Carlo Marcelis,
Marius Kraenzlin,
Nicole Fleischer,
Sheila Unger,
Andrea Superti-Furga
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,
Belinda Campos-Xavier,
Yvonne Hilhorst-Hofstee ,
Carlo Marcelis,
Marius Kraenzlin,
Nicole Fleischer,
Sheila Unger,
Andrea Superti-Furga
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2017
Stefano Volpi ,
Yasuhiro Yamazaki,
Patrick M. Brauer,
Ellen van Rooijen,
Atsuko Hayashida,
Anne Slavotinek,
Hye Sun Kuehn,
Maja Di Rocco,
Carlo Rivolta ,
Ileana Bortolomai,
Likun Du,
Kerstin Felgentreff,
Lisa Ott de Bruin,
Kazutaka Hayashida,
George Freedman
and 24 other authors
,
Yasuhiro Yamazaki,
Patrick M. Brauer,
Ellen van Rooijen,
Atsuko Hayashida,
Anne Slavotinek,
Hye Sun Kuehn,
Maja Di Rocco,
Carlo Rivolta ,
Ileana Bortolomai,
Likun Du,
Kerstin Felgentreff,
Lisa Ott de Bruin,
Kazutaka Hayashida,
George Freedman
and 24 other authors
EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay
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