Michaela Fenckova

发表

Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.

C. Webber, M. Huynen, Shivakumar Keerthikumar, 2016, American journal of human genetics.

A hundred genes implicated in intellectual disability and autism regulate habituation learning and reveal an opposing role for Ras-MAPK signaling in inhibitory and excitatory neurons

E. Eichler, C. R. Reyn, J. Glennon, 2019 .

Integrative cross-species analyses identify deficits in habituation learning as a widely affected mechanism in Autism

E. Eichler, J. Glennon, R. Bernier, 2018, bioRxiv.

Integrative Cross-species Analyses Suggest Deficits in Habituation Learning as a Widely Affected Mechanism in Intellectual Disability and Autism Spectrum Disorders

E. Eichler, J. Glennon, R. Bernier, 2018 .

Targeted sequencing identifies 91 neurodevelopmental disorder risk genes with autism and developmental disability biases

Bradley P. Coe, B. Coe, K. Friend, 2017, Nature Genetics.

De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila

L. Vissers, J. Schuurs-Hoeijmakers, A. Hoischen, 2016, European Journal of Human Genetics.

Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability.

Christian Gilissen, Annette Schenck, Koenraad Devriendt, 2012, American journal of human genetics.

Neuroinformatic analyses of common and distinct genetic components associated with major neuropsychiatric disorders

Robert W. Williams, J. Bralten, A. Alttoa, 2014, Front. Neurosci..

Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila

S. Fisher, A. Castells-Nobau, A. Schenck, 2019, PloS one.

O-GlcNAcase contributes to cognitive function in Drosophila

D. V. van Aalten, A. Schenck, Michaela Fenckova, 2020, The Journal of Biological Chemistry.

Intellectual disability-associated disruption of O-GlcNAc cycling impairs habituation learning in Drosophila

D. V. van Aalten, A. Schenck, Michaela Fenckova, 2022, PLoS genetics.

Genetics, molecular control and clinical relevance of habituation learning

A. Schenck, Michaela Fenckova, Laura E R Blok, 2022, Neuroscience & Biobehavioral Reviews.

From rare Copy Number Variations to biological processes in ADHD

B. Franke, M. Klein, A. Schenck, 2019 .

Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders.

Bradley P. Coe, B. Coe, J. Schuurs-Hoeijmakers, 2016, American journal of human genetics.

GATAD2B loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in Drosophila

B. V. van Bon, L. Vissers, B. D. de Vries, 2013, Journal of Medical Genetics.

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

B. Coe, K. Friend, P. Lockhart, 2017, Nature Genetics.

Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder

R. Pfundt, M. Reijnders, T. Kleefstra, 2017, PLoS genetics.

Habituation Learning Is a Widely Affected Mechanism in Drosophila Models of Intellectual Disability and Autism Spectrum Disorders

E. Eichler, J. Glennon, R. Bernier, 2019, Biological Psychiatry.

Intellectual disability-associated disruption of O-GlcNAcylation impairs neuronal development and cognitive function in Drosophila

D. V. van Aalten, A. Schenck, Michaela Fenckova, 2022, bioRxiv.

BOD1 Is Required for Cognitive Function in Humans and Drosophila

J. Swedlow, H. Scherthan, U. Felbor, 2016, PLoS genetics.

CEP89 is required for mitochondrial metabolism and neuronal function in man and fly.

B. V. van Bon, N. de Leeuw, B. D. de Vries, 2013, Human molecular genetics.

University of Dundee BOD 1 Is Required for Cognitive Function in Humans and Drosophila

Seyed, H. Scherthan, U. Felbor, 2016 .

Increased extracellular adenosine in Drosophila that are deficient in adenosine deaminase activates a release of energy stores leading to wasting and death

Michaela Fenckova, T. Doležal, P. Šimek, 2010, Disease Models & Mechanisms.

The epigenetic regulator G9a attenuates stress-induced resistance and metabolic transcriptional programs across different stressors and species

A. Schenck, Michaela Fenckova, Jamie M. Kramer, 2021, BMC Biology.

High-throughput Analysis of Locomotor Behavior in the Drosophila Island Assay

A. Schenck, Michaela Fenckova, Ilse Eidhof, 2017, Journal of visualized experiments : JoVE.

Functional characterization of ecto-5'-nucleotidases and apyrases in Drosophila melanogaster.

Z. Fric, Michaela Fenckova, T. Doležal, 2011, Insect biochemistry and molecular biology.

From Rare Copy Number Variants to Biological Processes in ADHD.

B. Franke, M. Klein, A. Schenck, 2020, The American journal of psychiatry.

A hundred genes implicated in intellectual disability and autism regulate habituation

Catherine R. von Reyn, C. R. Reyn, J. Glennon, 2019 .

Habituation Learning Is a Widely Affected Mechanism in Drosophila Models of Intellectual Disability and Autism Spectrum Disorders

E. Eichler, J. Glennon, R. Bernier, 2019, Biological Psychiatry.