Jamie M. Kramer
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Expressionof Drosophila FOXO regulates growth and can phenocopy starvation
JM Kramer, JT Davidge, JM Lockyer, BE Staveley
BMC developmental biology 3 (1), 1-14, 2003
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), 1453-1460, 2013
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 Biol 9 (1), e1000569, 2011
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), 639-641, 2012
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
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
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
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
Disruption of the epigenetic code: an emerging mechanism in mental retardation
H van Bokhoven, JM Kramer
Neurobiology of disease 39 (1), 3-12, 2010
The epigenetic regulator G9a mediates tolerance to RNA virus infection in Drosophila
SH Merkling, AW Bronkhorst, JM Kramer, GJ Overheul, A Schenck, ...
PLoS Pathog 11 (4), e1004692, 2015
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), e1006864, 2017
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
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
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
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