Contact and support
Need help, have a question, or want to contact the ResearchHub team?
© 2026 ResearchHub. Built for responsible scholarly connection.
Research graph
References from Behavioural effects of imprinted genes. Local targets link to admitted publications; unresolved targets remain external evidence.
Genomic imprinting in mammals: emerging themes and established theories
10.1371/journal.pgen.0020147 · 2006 · External reference
Genomic imprinting: recognition and marking of imprinted loci
10.1016/j.gde.2011.12.001 · 2012 · External reference
Genomic imprinting: the emergence of an epigenetic paradigm
10.1038/nrg3032 · 2011 · External reference
Imprinted genes in mouse placental development and the regulation of fetal energy stores
10.1530/rep-12-0511 · 2013 · External reference
Regulation of growth and metabolism by imprinted genes
10.1159/000090843 · 2006 · External reference
Genomic imprinting effects on brain development and function
10.1038/nrn2235 · 2007 · External reference
Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons
10.1038/nature10726 · 2012 · External reference
Dosage-sensitivity of imprinted genes expressed in the brain: 15q11-q13 and neuropsychiatric illness
10.1042/bst20130008 · 2013 · External reference
Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome
2014 · External reference
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism
10.1093/hmg/ddp263 · 2009 · External reference
Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome
10.1038/ejhg.2010.102 · 2010 · External reference
Prader–Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster
10.1038/ng.158 · 2008 · External reference
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
10.1371/journal.pone.0001709 · 2008 · External reference
Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation
10.1371/journal.pgen.0030235 · 2007 · External reference
Long noncoding RNAs with snoRNA ends
10.1016/j.molcel.2012.07.033 · 2012 · External reference
The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader–Willi syndrome
10.1038/ng.2968 · 2014 · External reference
R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensation
10.1073/pnas.1305426110 · 2013 · External reference
Truncating mutations of MAGEL2 cause Prader–Willi phenotypes and autism
10.1038/ng.2776 · 2013 · External reference
Clinical phenotypes of MAGEL2 mutations and deletions
10.1186/1750-1172-9-40 · 2014 · External reference
The imprinted gene Magel2 regulates normal circadian output
10.1038/ng2114 · 2007 · External reference
A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene
10.1093/hmg/ddq424 · 2010 · External reference
Distinct physiological and behavioural functions for parental alleles of imprinted Grb10
10.1038/nature09651 · 2011 · External reference
The Dalila effect: C57BL6 mice barber whiskers by plucking
10.1016/s0166-4328(99)00137-0 · 2000 · External reference
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark
10.1093/hmg/ddg110 · 2003 · External reference
Maternally-inherited Grb10 reduces placental size and efficiency
10.1016/j.ydbio.2009.10.011 · 2010 · External reference
Dual ablation of Grb10 and Grb14 in mice reveals their combined role in regulation of insulin signaling and glucose homeostasis
10.1210/me.2008-0386 · 2009 · External reference
Developmental programming mediated by complementary roles of imprinted Grb10 in mother and pup
10.1371/journal.pbio.1001799 · 2014 · External reference
Genomic imprinting of Grb10: coadaptation or conflict?
10.1371/journal.pbio.1001800 · 2014 · External reference
Adaptation of nutrient supply to fetal demand in the mouse involves interaction between the Igf2 gene and placental transporter systems
10.1073/pnas.0504468103 · 2005 · External reference
Placental programming of anxiety in adulthood revealed by Igf2-null models
10.1038/ncomms3311 · 2013 · External reference
How social experiences influence the brain
10.1016/j.conb.2005.10.001 · 2005 · External reference
DNA methylation at differentially methylated regions of imprinted genes is resistant to developmental programming by maternal nutrition
10.4161/epi.22141 · 2012 · External reference
An unbiased assessment of the role of imprinted genes in an intergenerational model of developmental programming
10.1371/journal.pgen.1002605 · 2012 · External reference
p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene
10.1101/gad.9.6.650 · 1995 · External reference
Dynamic temporal and spatial regulation of the cdk inhibitor p57(kip2) during embryo morphogenesis
10.1016/s0925-4773(01)00512-3 · 2001 · External reference
The cyclin-dependent kinase inhibitors p57 and p27 regulate neuronal migration in the developing mouse neocortex
10.1074/jbc.m609944200 · 2007 · External reference
Patterns of p57Kip2 expression in embryonic rat brain suggest roles in progenitor cell cycle exit and neuronal differentiation
10.1002/dneu.20680 · 2009 · External reference
p57(Kip2) regulates progenitor cell proliferation and amacrine interneuron development in the mouse retina
10.1242/dev.127.16.3593 · 2000 · External reference
ARX regulates cortical intermediate progenitor cell expansion and upper layer neuron formation through repression of Cdkn1c
2013 · External reference
The cyclin-dependent kinase inhibitor p57Kip2 regulates cell cycle exit, differentiation, and migration of embryonic cerebral cortical precursors
10.1093/cercor/bhq254 · 2011 · External reference
p57 controls adult neural stem cell quiescence and modulates the pace of lifelong neurogenesis
10.1038/emboj.2013.50 · 2013 · External reference
p57(Kip2) cooperates with Nurr1 in developing dopamine cells
10.1073/pnas.2635658100 · 2003 · External reference
Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome
10.1038/387151a0 · 1997 · External reference
Multigenerational programming in the glucocorticoid programmed rat is associated with generation-specific and parent of origin effects
10.4161/epi.6.11.17942 · 2011 · External reference
Effects of maternal care on the development of midbrain dopamine pathways and reward-directed behavior in female offspring
10.1111/ejn.12479 · 2014 · External reference
Early life protein restriction alters dopamine circuitry
10.1016/j.neuroscience.2010.04.010 · 2010 · External reference
Imprinted genes and mother–offspring interactions
10.1016/j.earlhumdev.2004.10.006 · 2005 · External reference
Genomic imprinting: the cost of mother's care
10.1002/bies.201100115 · 2011 · External reference
Loss of Gnas imprinting differentially affects REM/NREM sleep and cognition in mice
10.1371/journal.pgen.1002706 · 2012 · External reference