Rim Amouri

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 10

Top Topics

Intellectual Disability

Tyrosine Kinase

Top Venues

medRxiv : the preprint server for health sciences

Journal of neurogenetics

Clinical case reports

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

Publications

Emil Karl Gustavsson, Jordan Follett, Joanne Trinh, Sandeep Kumar Barodia, Raquel Real, Zhiyong Liu, Melissa Grant-Peters, Jesse D Fox, Silke Appel-Cresswell, A Jon Stoessl, Alex Rajput, Ali H Rajput, Roland Auer, Russel Tilney, Marc Sturm, Tobias B Haack, Suzanne Lesage, Christelle Tesson, Alexis Brice, Carles Vilariño-Güell, Mina Ryten, Matthew S Goldberg, Andrew B West, Michele Tao-Ming Hu, Huw R Morris, Manu Sharma, Ziv Gan Or, Bedia Samanci, Pawel Lis, Maria Teresa Periñán, Rim Amouri, Samia Ben Sassi, Faycel Hentati, null null, Francesca Tonelli, Dario R Alessi, Matthew J Farrer
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase . medRxiv : the preprint server for health sciences (2024)
Emil Karl Gustavsson, Jordan Follett, Joanne Trinh, Sandeep Kumar Barodia, Raquel Real, Zhiyong Liu, Melissa Grant-Peters, Jesse D Fox, Silke Appel-Cresswell, A Jon Stoessl, Alex Rajput, Ali H Rajput, Roland Auer, Russel Tilney, Marc Sturm, Tobias B Haack, Suzanne Lesage, Christelle Tesson, Alexis Brice, Carles Vilariño-Güell, Mina Ryten, Matthew S Goldberg, Andrew B West, Michele Tao-Ming Hu, Huw R Morris, Manu Sharma, Ziv Gan Or, Bedia Samanci, Pawel Lis, Maria Teresa Periñán, Rim Amouri, Samia Ben Sassi, Faycel Hentati, null null, Francesca Tonelli, Dario R Alessi, Matthew J Farrer
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase. medRxiv : the preprint server for health sciences (2024)
Emil Karl Gustavsson, Jordan Follett, Joanne Trinh, Sandeep Kumar Barodia, Raquel Real, Zhiyong Liu, Melissa Grant-Peters, Jesse D Fox, Silke Appel-Cresswell, A Jon Stoessl, Alex Rajput, Ali H Rajput, Roland Auer, Russel Tilney, Marc Sturm, Tobias B Haack, Suzanne Lesage, Christelle Tesson, Alexis Brice, Carles Vilariño-Güell, Mina Ryten, Matthew S Goldberg, Andrew B West, Michele Tao-Ming Hu, Huw R Morris, Manu Sharma, Ziv Gan Or, Bedia Samanci, Pawel Lis, Maria Teresa Periñán, Rim Amouri, Samia Ben Sassi, Faycel Hentati, null null, Francesca Tonelli, Dario R Alessi, Matthew J Farrer
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase. medRxiv : the preprint server for health sciences (2024)
Emil Karl Gustavsson, Jordan Follett, Joanne Trinh, Sandeep Kumar Barodia, Raquel Real, Zhiyong Liu, Melissa Grant-Peters, Jesse D Fox, Silke Appel-Cresswell, A Jon Stoessl, Alex Rajput, Ali H Rajput, Roland Auer, Russel Tilney, Marc Sturm, Tobias B Haack, Suzanne Lesage, Christelle Tesson, Alexis Brice, Carles Vilariño-Güell, Mina Ryten, Matthew S Goldberg, Andrew B West, Michele Tao-Ming Hu, Huw R Morris, Manu Sharma, Ziv Gan Or, Bedia Samanci, Pawel Lis, Maria Teresa Periñán, Rim Amouri, Samia Ben Sassi, Faycel Hentati, null null, Francesca Tonelli, Dario R Alessi, Matthew J Farrer
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase. medRxiv : the preprint server for health sciences (2024)
Emil Karl Gustavsson, Jordan Follett, Joanne Trinh, Sandeep Kumar Barodia, Raquel Real, Zhiyong Liu, Melissa Grant-Peters, Jesse D Fox, Silke Appel-Cresswell, A Jon Stoessl, Alex Rajput, Ali H Rajput, Roland Auer, Russel Tilney, Marc Sturm, Tobias B Haack, Suzanne Lesage, Christelle Tesson, Alexis Brice, Carles Vilariño-Güell, Mina Ryten, Matthew S Goldberg, Andrew B West, Michele Tao-Ming Hu, Huw R Morris, Manu Sharma, Ziv Gan Or, Bedia Samanci, Pawel Lis, Maria Teresa Periñán, Rim Amouri, Samia Ben Sassi, Faycel Hentati, null null, Francesca Tonelli, Dario R Alessi, Matthew J Farrer
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase. medRxiv : the preprint server for health sciences (2024)
Cyrine Jeridi, Amine Rachdi, Fatma Nabli, Zacharia Saied, Rania Zouari, Dina Ben Mohamed, Mariem Ben Said, Saber Masmoudi, Samia Ben Sassi, Rim Amouri
Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes. Journal of neurogenetics 37 (4) (2023)
Cyrine Jeridi, Amine Rachdi, Fatma Nabli, Zacharia Saied, Rania Zouari, Dina Ben Mohamed, Mariem Ben Said, Saber Masmoudi, Samia Ben Sassi, Rim Amouri
Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes. Journal of neurogenetics (2023)
Cyrine Jeridi, Amine Rachdi, Fatma Nabli, Zacharia Saied, Rania Zouari, Dina Ben Mohamed, Mariem Ben Said, Saber Masmoudi, Samia Ben Sassi, Rim Amouri
Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes. Journal of neurogenetics 37 (4) (2023)
Dina Ben Mohamed, Zacharia Saied, Samia Ben Sassi, Mariem Ben Said, Fatma Nabli, Afef Achouri, Cyrine Jeridi, Saber Masmoudi, Rim Amouri
A Tunisian patient with CLCN2-related leukoencephalopathy. Clinical case reports 10 (12) (2022)
Dina Ben Mohamed, Zacharia Saied, Samia Ben Sassi, Mariem Ben Said, Fatma Nabli, Afef Achouri, Cyrine Jeridi, Saber Masmoudi, Rim Amouri
A Tunisian patient with CLCN2-related leukoencephalopathy. Clinical case reports 10 (12) (2022)