Cristina Dias

VISITING SCIENTIST

Guillemot lab

Neural Stem Cell Biology Laboratory

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Generation of an iPSC line (CRICKi001-A) from an individual with a germline SMARCA4 missense mutation and autism spectrum disorder

Authors (5)

Stem Cell Research

Published 1 May 2021

Crick labs/ facilities

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De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome

Authors (48)

Gerarda Cappuccio
Camille Sayou
Pauline Le Tanno
Emilie Tisserant
Ange-Line Bruel
Sara El Kennani
[...]
Bekim Sadikovic
Julien Thevenon
Jérôme Govin
Antonio Vitobello
Nicola Brunetti-Pierri

Genetics in Medicine

Published 1 November 2020

Crick labs

Francois Guillemot

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Inflammatory arthritis as a possible feature of Coffin-Siris syndrome

Authors (7)

Sonia Melo Gomes
Cristina Dias
Ebun Omoyinmi
Sandrine Compeyrot-Lacassagne
Nigel Klein
Neil J Sebire
Paul Brogan

Pediatrics

Published 1 July 2019

Crick labs

Francois Guillemot

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Revealing the inner workings of organoids

Authors (2)

EMBO Journal

Published 24 April 2017

Crick labs

Francois Guillemot

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Coronavirus (COVID-19) response

Vacancies

Outwitting Cancer

Coronavirus (COVID-19) research

About us

Cristina Dias

VISITING SCIENTIST

Guillemot lab

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Year published

Research topics

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Journal

Crick Pre-Crick

Generation of an iPSC line (CRICKi001-A) from an individual with a germline SMARCA4 missense mutation and autism spectrum disorder

De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome

Inflammatory arthritis as a possible feature of Coffin-Siris syndrome

Revealing the inner workings of organoids

Francois Guillemot | BUILD clinical study

The Francis Crick Institute is a unique partnership between

Coronavirus (COVID-19) response

Vacancies

Outwitting Cancer

Coronavirus (COVID-19) research

About us

Guillemot lab

Links

Year published

Research topics

Publication type

Journal

Crick Pre-Crick

Generation of an iPSC line (CRICKi001-A) from an individual with a germline SMARCA4 missense mutation and autism spectrum disorder

De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome

Inflammatory arthritis as a possible feature of Coffin-Siris syndrome

Revealing the inner workings of organoids

Related content

Francois Guillemot | BUILD clinical study

The Francis Crick Institute is a unique partnership between