Jamie M. Kramer
TitleCited byYear
Expressionof Drosophila FOXO regulates growth and can phenocopy starvation
JM Kramer, JT Davidge, JM Lockyer, BE Staveley
BMC developmental biology 3 (1), 5, 2003
Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability
T Kleefstra, JM Kramer, K Neveling, MH Willemsen, TS Koemans, ...
The American Journal of Human Genetics 91 (1), 73-82, 2012
Epigenetic regulation of learning and memory by Drosophila EHMT/G9a
JM Kramer, K Kochinke, MAW Oortveld, H Marks, D Kramer, EK de Jong, ...
PLoS biology 9 (1), 2011
Restoring polyamines protects from age-induced memory impairment in an autophagy-dependent manner
VK Gupta, L Scheunemann, T Eisenberg, S Mertel, A Bhukel, ...
Nature neuroscience 16 (10), 1453, 2013
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome
DA Koolen, JM Kramer, K Neveling, WM Nillesen, HL Moore-Barton, ...
Nature genetics 44 (6), 639, 2012
GAL4 causes developmental defects and apoptosis when expressed in the developing eye of Drosophila melanogaster
JM Kramer, BE Staveley
Genet Mol Res 2 (1), 43-47, 2003
Systematic phenomics analysis deconvolutes genes mutated in intellectual disability into biologically coherent modules
K Kochinke, C Zweier, B Nijhof, M Fenckova, P Cizek, F Honti, ...
The American Journal of Human Genetics 98 (1), 149-164, 2016
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders
Z Iqbal, G Vandeweyer, M van der Voet, AM Waryah, MY Zahoor, ...
Human molecular genetics 22 (10), 1960-1970, 2013
Genetic and epigenetic defects in mental retardation
JM Kramer, H van Bokhoven
The international journal of biochemistry & cell biology 41 (1), 96-107, 2009
SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway
ST Cliffe, JM Kramer, K Hussain, JH Robben, EK de Jong, AP de Brouwer, ...
Human molecular genetics 18 (12), 2257-2265, 2009
The genetics of cognitive epigenetics
T Kleefstra, A Schenck, JM Kramer, H van Bokhoven
Neuropharmacology 80, 83-94, 2014
Disruption of the epigenetic code: an emerging mechanism in mental retardation
H van Bokhoven, JM Kramer
Neurobiology of disease 39 (1), 3-12, 2010
CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation
A Mukhopadhyay, JM Kramer, G Merkx, D Lugtenberg, DF Smeets, ...
Human genetics 128 (3), 281-291, 2010
The epigenetic regulator G9a mediates tolerance to RNA virus infection in Drosophila
SH Merkling, AW Bronkhorst, JM Kramer, GJ Overheul, A Schenck, ...
PLoS pathogens 11 (4), 2015
Epigenetic mechanisms modulate differences in Drosophila foraging behavior
I Anreiter, JM Kramer, MB Sokolowski
Proceedings of the National Academy of Sciences 114 (47), 12518-12523, 2017
foxo is required for resistance to amino acid starvation in Drosophila
JM Kramer, JD Slade, BE Staveley
Genome 51 (8), 668-672, 2008
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder
TS Koemans, T Kleefstra, MC Chubak, MH Stone, MRF Reijnders, ...
PLoS genetics 13 (10), 2017
Regulation of cell differentiation and function by the euchromatin histone methyltranserfases G9a and GLP
JM Kramer
Biochemistry and Cell Biology 94 (1), 26-32, 2016
CEP89 is required for mitochondrial metabolism and neuronal function in man and fly
BWM van Bon, MAW Oortveld, LG Nijtmans, M Fenckova, B Nijhof, ...
Human molecular genetics 22 (15), 3138-3151, 2013
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration
A Dubos, A Castells-Nobau, H Meziane, MAW Oortveld, X Houbaert, ...
Human molecular genetics 24 (23), 6736-6755, 2015
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