Nael Nadif Kasri (Nael Nadif Khadri)

ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 24

Top Venues

European journal of human genetics : EJHG

The Journal of neuroscience : the official journal of the Society for Neuroscience

Brain structure & function

Molecular psychiatry

RadboudUMC

Katholieke Universiteit Leuven (MSC)

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

Affiliation History

RadboudUMC Jun 15 2010

Netherlands

assistant porfessor :: Cognitive Neurosciences

Cold Spring Harbor Laboratory Oct 15 2005 - Jun 14 2010

United States

Post doc

Katholieke Universiteit Leuven Aug 01 2000 - Oct 01 2005

Belgium

PhD student

Education History

Katholieke Universiteit Leuven Oct 01 1996 - Jun 01 2000

Belgium

MSC

Publications

Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibáñez-Mico, Laura Cuesta Herraiz, Irene Ferrer, Antonio Martínez Carrascal, Luis Alberto Pérez-Jurado, Gemma Aznar, Juan Dario Ortigoza-Escobar, Bert B A de Vries, David A Koolen, Rosanna Weksberg
A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. European journal of human genetics : EJHG (2024)
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibáñez-Mico, Laura Cuesta Herraiz, Irene Ferrer, Antonio Martínez Carrascal, Luis Alberto Pérez-Jurado, Gemma Aznar, Juan Dario Ortigoza-Escobar, Bert B A de Vries, David A Koolen, Rosanna Weksberg
Correction: A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. European journal of human genetics : EJHG (2024)
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibáñez-Mico, Laura Cuesta Herraiz, Irene Ferrer, Antonio Martínez Carrascal, Luis Alberto Pérez-Jurado, Gemma Aznar, Juan Dario Ortigoza-Escobar, Bert B A de Vries, David A Koolen, Rosanna Weksberg
A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. European journal of human genetics : EJHG 32 (3) (2024)
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibáñez-Mico, Laura Cuesta Herraiz, Irene Ferrer, Antonio Martínez Carrascal, Luis Alberto Pérez-Jurado, Gemma Aznar, Juan Dario Ortigoza-Escobar, Bert B A de Vries, David A Koolen, Rosanna Weksberg
A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. European journal of human genetics : EJHG (2024)
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibáñez-Mico, Laura Cuesta Herraiz, Irene Ferrer, Antonio Martínez Carrascal, Luis Alberto Pérez-Jurado, Gemma Aznar, Juan Dario Ortigoza-Escobar, Bert B A de Vries, David A Koolen, Rosanna Weksberg
A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. European journal of human genetics : EJHG (2024)
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibáñez-Mico, Laura Cuesta Herraiz, Irene Ferrer, Antonio Martínez Carrascal, Luis Alberto Pérez-Jurado, Gemma Aznar, Juan Dario Ortigoza-Escobar, Bert B A de Vries, David A Koolen, Rosanna Weksberg
Correction: A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. European journal of human genetics : EJHG (2024)
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibáñez-Mico, Laura Cuesta Herraiz, Irene Ferrer, Antonio Martínez Carrascal, Luis Alberto Pérez-Jurado, Gemma Aznar, Juan Dario Ortigoza-Escobar, Bert B A de Vries, David A Koolen, Rosanna Weksberg
A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. European journal of human genetics : EJHG (2024)
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibáñez-Mico, Laura Cuesta Herraiz, Irene Ferrer, Antonio Martínez Carrascal, Luis Alberto Pérez-Jurado, Gemma Aznar, Juan Dario Ortigoza-Escobar, Bert B A de Vries, David A Koolen, Rosanna Weksberg
A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. European journal of human genetics : EJHG 32 (3) (2024)
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibáñez-Mico, Laura Cuesta Herraiz, Irene Ferrer, Antonio Martínez Carrascal, Luis Alberto Pérez-Jurado, Gemma Aznar, Juan Dario Ortigoza-Escobar, Bert B A de Vries, David A Koolen, Rosanna Weksberg
A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. European journal of human genetics : EJHG 32 (3) (2024)
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibáñez-Mico, Laura Cuesta Herraiz, Irene Ferrer, Antonio Martínez Carrascal, Luis Alberto Pérez-Jurado, Gemma Aznar, Juan Dario Ortigoza-Escobar, Bert B A de Vries, David A Koolen, Rosanna Weksberg
A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. European journal of human genetics : EJHG 32 (3) (2024)
Zain Awamleh, Sanaa Choufani, Wendy Wu, Dmitrijs Rots, Alexander J M Dingemans, Nael Nadif Kasri, Susana Boronat, Salvador Ibáñez-Mico, Laura Cuesta Herraiz, Irene Ferrer, Antonio Martínez Carrascal, Luis Alberto Pérez-Jurado, Gemma Aznar, Juan Dario Ortigoza-Escobar, Bert B A de Vries, David A Koolen, Rosanna Weksberg
A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells. European journal of human genetics : EJHG 32 (3) (2024)
Maria W A Teunissen, Elly Lewerissa, Eline J H van Hugte, Shan Wang, Charlotte W Ockeloen, David A Koolen, Rolph Pfundt, Carlo L M Marcelis, Eva Brilstra, Jennifer L Howe, Stephen W Scherer, Xavier Le Guillou, Frédéric Bilan, Michelle Primiano, Jasmin Roohi, Amelie Piton, Anne de Saint Martin, Sarah Baer, Simone Seiffert, Konrad Platzer, Rami Abou Jamra, Steffen Syrbe, Jan Henje Doering, Shenela Lakhani, Srishti Nangia, Christian Gilissen, R Jeroen Vermeulen, Rob P W Rouhl, Han G Brunner, Marjolein H Willemsen, Nael Nadif Kasri
ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks. Human molecular genetics (2023)
Eline J H van Hugte, Dirk Schubert, Nael Nadif Kasri
E/I balance in epilepsies and neurodevelopmental disorders: depolarizing GABA as a common mechanism. Epilepsia (2023)
Nicky Scheefhals, Ummi Ciptasari, Eline J H van Hugte, Nael Nadif Kasri
The OTUD7A-Ankyrin pathway: a newly identified disease mechanism for the 15q13.3 microdeletion disorder. Molecular psychiatry (2023)
Rachel Mijdam, Chantal Bijnagte-Schoenmaker, Emma Dyke, Sam J Moons, Thomas J Boltje, Nael Nadif Kasri, Dirk J Lefeber
Sialic acid biosynthesis pathway blockade disturbs neuronal network formation in human iPSC-derived excitatory neurons. Journal of neurochemistry (2023)
Moritz Negwer, Bram Bosch, Maren Bormann, Rick Hesen, Lukas Lütje, Lynn Aarts, Carleen Rossing, Nael Nadif Kasri, Dirk Schubert
FriendlyClearMap: an optimized toolkit for mouse brain mapping and analysis. GigaScience 12 (2023)
Katrin Linda, Elly I Lewerissa, Anouk H A Verboven, Michele Gabriele, Monica Frega, Teun M Klein Gunnewiek, Lynn Devilee, Edda Ulferts, Marina Hommersom, Astrid Oudakker, Chantal Schoenmaker, Hans van Bokhoven, Dirk Schubert, Giuseppe Testa, David A Koolen, Bert B A de Vries, Nael Nadif Kasri
Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders. Autophagy (2021)
Britt Mossink, Jon-Ruben van Rhijn, Shan Wang, Katrin Linda, Maria R Vitale, Johanna E M Zöller, Eline J H van Hugte, Jitske Bak, Anouk H A Verboven, Martijn M Selten, Moritz Negwer, Brooke L Latour, Ilse M van der Werf, Jason M Keller, Teun M Klein Gunnewiek, Chantal Schoenmaker, Astrid Oudakker, Alessia Anania, Sophie Jansen, Klaus-Peter Lesch, Monica Frega, Hans van Bokhoven, Dirk Schubert, Nael Nadif Kasri
Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks. Molecular psychiatry (2021)
Britt Mossink, Moritz Negwer, Dirk Schubert, Nael Nadif Kasri
The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective. Cellular and molecular life sciences : CMLS 78 (6) (2020)
Moritz Negwer, Karol Piera, Rick Hesen, Lukas Lütje, Lynn Aarts, Dirk Schubert, Nael Nadif Kasri
EHMT1 regulates Parvalbumin-positive interneuron development and GABAergic input in sensory cortical areas. Brain structure & function 225 (9) (2020)
Monica Frega, Katrin Linda, Jason M Keller, Güvem Gümüş-Akay, Britt Mossink, Jon-Ruben van Rhijn, Moritz Negwer, Teun Klein Gunnewiek, Katharina Foreman, Nine Kompier, Chantal Schoenmaker, Willem van den Akker, Ilse M van der Werf, Astrid Oudakker, Huiqing Zhou, Tjitske Kleefstra, Dirk Schubert, Hans van Bokhoven, Nael Nadif Kasri
Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling. Nature communications 10 (1) (2019)
Jon-Ruben van Rhijn, Simon E Fisher, Sonja C Vernes, Nael Nadif Kasri
Foxp2 loss of function increases striatal direct pathway inhibition via increased GABA release. Brain structure & function 223 (9) (2018)
Shigeki Iwase, Nathalie G Bérubé, Zhaolan Zhou, Nael Nadif Kasri, Elena Battaglioli, Marilyn Scandaglia, Ángel Barco
Epigenetic Etiology of Intellectual Disability. The Journal of neuroscience : the official journal of the Society for Neuroscience 37 (45) (2017)
Thomas Arbogast, Giovanni Iacono, Claire Chevalier, Nurudeen O Afinowi, Xander Houbaert, Matthijs C van Eede, Christine Laliberte, Marie-Christine Birling, Katrin Linda, Hamid Meziane, Mohammed Selloum, Tania Sorg, Nael Nadif Kasri, David A Koolen, Henk G Stunnenberg, R Mark Henkelman, Maksym Kopanitsa, Yann Humeau, Bert B A De Vries, Yann Hérault
Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition. PLoS genetics 13 (7) (2017)
Li-Li Li, Raquel M Melero-Fernandez de Mera, Jia Chen, Wei Ba, Nael Nadif Kasri, Mingjie Zhang, Michael J Courtney
Unexpected Heterodivalent Recruitment of NOS1AP to nNOS Reveals Multiple Sites for Pharmacological Intervention in Neuronal Disease Models. The Journal of neuroscience : the official journal of the Society for Neuroscience 35 (19) (2015)

Nael Nadif Kasri.css-eqlu8i{font-size:small;padding-left:4px;} (Nael Nadif Khadri)

Publication Activity (10 Years)

Top Topics

Top Venues

Nael Nadif Kasri (Nael Nadif Khadri)