K. Linda

发表

Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition

B. D. de Vries, Y. Hérault, T. Sorg, 2017, PLoS genetics.

Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition

B. D. de Vries, Y. Hérault, T. Sorg, 2017, PLoS genetics.

Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling

Monica Frega, Huiqing Zhou, Moritz Negwer, 2019, Nature Communications.

Human neuronal networks on micro-electrode arrays are a highly robust tool to study disease-specific genotype-phenotype correlations in vitro

D. Schubert, T. Kleefstra, H. van Bokhoven, 2021, bioRxiv.

Added effects of dexamethasone and mesenchymal stem cells on early Natural Killer cell activation.

I. Joosten, A. van der Meer, B. van Cranenbroek, 2016, Transplant immunology.

Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders

B. D. de Vries, D. Schubert, H. van Bokhoven, 2021, Autophagy.

KANSL1 Deficiency Causes Neuronal Dysfunction by Oxidative Stress-Induced Autophagy

B. D. de Vries, D. Schubert, H. van Bokhoven, 2020 .

Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks

D. Schubert, H. van Bokhoven, N. N. Kasri, 2020, bioRxiv.

Rapid Neuronal Differentiation of Induced Pluripotent Stem Cells for Measuring Network Activity on Micro-electrode Arrays

Monica Frega, Cornelis A. Albers, Dirk Schubert, 2017, Journal of visualized experiments : JoVE.

The promise of induced pluripotent stem cells for neurodevelopmental disorders

N. N. Kasri, K. Linda, C. Fiuza, 2017, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant

Bradley P. Coe, Jessie H. Conta, B. Coe, 2015, European Journal of Human Genetics.

Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype.

D. Schubert, T. Kleefstra, H. van Bokhoven, 2020, Cell reports.

Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder

J. Schuurs-Hoeijmakers, S. Antonarakis, R. Płoski, 2021, Genetics in Medicine.

Distinct pathogenic genes causing intellectual disability and autism exhibit overlapping effects on neuronal network development

D. Schubert, H. Bokhoven, T. Kleefstra, 2018, bioRxiv.

Neuronal network dysfunction in a human model for Kleefstra syndrome mediated by enhanced NMDAR signaling

D. Schubert, T. Kleefstra, H. van Bokhoven, 2019, bioRxiv.

Brain-on-a chip technologies for investigating neuronal diseases: Toward precision medicine applications

J. Keller, M. Frega, B. Mossink, 2018, 2018 IEEE International Symposium on Circuits and Systems (ISCAS).

Mitochondrial dysfunction impairs human neuronal development and reduces neuronal network activity and synchronicity

D. Schubert, R. Rodenburg, D. Cassiman, 2019, bioRxiv.

Epigenetic regulation of autophagy-related genes: Implications for neurodevelopmental disorders

K. Linda, N. Nadif Kasri, Elly I. Lewerissa, 2023, Autophagy.

Integrative transcriptomics and electrophysiological profiling of hiPSC-derived neurons identifies novel druggable pathways in Koolen-de Vries Syndrome

N. N. Kasri, D. Koolen, K. Linda, 2024, bioRxiv.

m.3243A > G-Induced Mitochondrial Dysfunction Impairs Human Neuronal Development and Reduces Neuronal Network Activity and Synchronicity.

D. Oglesbee, K. Linda, N. Nadif Kasri, 2020, Cell reports.