Jamie M. Kramer

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.

Epigenetic mechanisms modulate differences in Drosophila foraging behavior

M. Sokolowski, Jamie M. Kramer, I. Anreiter, 2017, Proceedings of the National Academy of Sciences.

Epigenetic Regulation of Learning and Memory by Drosophila EHMT/G9a

Annette Schenck, Huiqing Zhou, Hendrik G. Stunnenberg, 2011, PLoS biology.

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

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

The histone methyltransferase G9a regulates tolerance to oxidative stress–induced energy consumption

P. Itskov, T. Kleefstra, A. Schenck, 2019, PLoS biology.

Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila

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

Identification of a novel synaptic protein, TMTC3, involved in periventricular nodular heterotopia with intellectual disability and epilepsy

John F. Robinson, R. Hegele, S. Mirsattari, 2017, Human molecular genetics.

Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome

R. Pfundt, M. Reijnders, D. Schubert, 2019, bioRxiv.

Drosophila equilibrative nucleoside transporter , a DmENT2 and functional characterization of Genomic analysis of nucleoside transporters in Diptera

M. Charlton, H. Bokhoven, T. Roscioli, 2015 .

Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome

L. Vissers, S. Cheung, J. Veltman, 2012, Nature Genetics.

A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder

E. Zackai, H. Hakonarson, H. Brunner, 2022, HGG advances.

Restoring polyamines protects from age-induced memory impairment in an autophagy-dependent manner

Annette Schenck, Stephan J Sigrist, Frank Sinner, 2013, Nature Neuroscience.

Conditioned courtship suppression in Drosophila melanogaster

Jamie M. Kramer, Spencer G Jones, Nicholas Raun, 2021, Journal of neurogenetics.

A Syndromic Neurodevelopmental Disorder Caused by Mutations in SMARCD1, a Core SWI/SNF Subunit Needed for Context-Dependent Neuronal Gene Regulation in Flies.

D. Baralle, C. Depienne, N. Matsumoto, 2019, American journal of human genetics.

Disruption of the epigenetic code: An emerging mechanism in mental retardation

H. Bokhoven, Jamie M. Kramer, 2010, Neurobiology of Disease.

Epigenetics in intellectual disability

N. Bérubé, Jamie M. Kramer, 2021, Epigenetics in Psychiatry.

The genetics of cognitive epigenetics

H. Bokhoven, T. Kleefstra, A. Schenck, 2014, Neuropharmacology.

Epigenetic regulation of memory: implications in human cognitive disorders

Jamie M. Kramer, 2013, Biomolecular concepts.

The Epigenetic Regulator G9a Mediates Tolerance to RNA Virus Infection in Drosophila

A. Schenck, Jamie M. Kramer, R. V. van Rij, 2015, PLoS pathogens.

Regulation of cell differentiation and function by the euchromatin histone methyltranserfases G9a and GLP.

Jamie M. Kramer, 2016, Biochemistry and cell biology = Biochimie et biologie cellulaire.

Mushroom Body Specific Transcriptome Analysis Reveals Dynamic Regulation of Learning and Memory Genes After Acquisition of Long-Term Courtship Memory in Drosophila

Jamie M. Kramer, Spencer G Jones, K. C. Nixon, 2018, G3: Genes, Genomes, 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.

Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.

Christian Gilissen, Bonnie Nijhof, Annette Schenck, 2013, Human molecular genetics.

neurodevelopmental and psychiatric disorders

L. Vissers, H. Peeters, J. Veltman, 2013 .

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.

Individual components of the SWI/SNF chromatin remodelling complex have distinct roles in memory neurons of the Drosophila mushroom body

Jamie M. Kramer, Max H Stone, Spencer G Jones, 2019, Disease Models & Mechanisms.

Genetic and epigenetic defects in mental retardation.

H. van Bokhoven, Jamie M. Kramer, 2009, The international journal of biochemistry & cell biology.

Optimal RNA isolation method and primer design to detect gene knockdown by qPCR when validating Drosophila transgenic RNAi lines

Jamie M. Kramer, Taylor A. Lyons, R. L. Mainland, 2017, BMC Research Notes.

Systematic functional characterization of the intellectual disability-associated SWI/SNF complex reveals distinct roles for the BAP and PBAP complexes in post-mitotic memory forming neurons of the Drosophila mushroom body

Jamie M. Kramer, Max H Stone, Spencer G Jones, 2018, bioRxiv.

Ubiquitin Ligase HUWE1 Regulates Axon Branching through the Wnt/β-Catenin Pathway in a Drosophila Model for Intellectual Disability

Bassem A. Hassan, Marion Langen, P. Verstreken, 2013, PloS one.

Drosophila Courtship Conditioning As a Measure of Learning and Memory

K. Keleman, H. van Bokhoven, R. Donders, 2017, Journal of visualized experiments : JoVE.

Altered GPM6A/M6 Dosage Impairs Cognition and Causes Phenotypes Responsive to Cholesterol in Human and Drosophila

A. Reis, R. Donders, C. Zweier, 2014, Human mutation.

CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation

F. Cremers, A. V. van Kessel, H. van Bokhoven, 2010, Human Genetics.

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.

Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration

Y. Hérault, Y. Humeau, P. Verstreken, 2015, Human molecular genetics.

CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation

F. Cremers, A. V. van Kessel, H. van Bokhoven, 2010, Human Genetics.

SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway.

R. Hennekam, T. Roscioli, R. Lindeman, 2009, Human molecular genetics.

The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.

Saskia M. J. Hopman, L. Vissers, R. Pfundt, 2023, American journal of human genetics.

Trithorax regulates long-term memory in Drosophila through epigenetic maintenance of mushroom body metabolic identity and translation capacity

Jamie M. Kramer, Deniz Top, Spencer G Jones, 2023, bioRxiv.

Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.

L. Vissers, H. Peeters, J. Veltman, 2013, Human molecular genetics.