| scholarly article | Q13442814 |
| review article | Q7318358 |
| P6179 | Dimensions Publication ID | 1025064233 |
| P356 | DOI | 10.1038/NRG1062 |
| P698 | PubMed publication ID | 12728278 |
| P5875 | ResearchGate publication ID | 10777316 |
| P50 | author | Jon Wilkins | Q42843236 |
| P2093 | author name string | David Haig | |
| P2860 | cites work | Parental antagonism, relatedness asymmetries, and genomic imprinting | Q24673085 |
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| Physiological functions of imprinted genes. | Q34139655 | ||
| Structure and function of the mannose 6-phosphate/insulinlike growth factor II receptors | Q34236758 | ||
| The origins of genomic imprinting in mammals | Q34586399 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| P-type lectins | Q34838003 | ||
| Genomic imprinting, sibling solidairity and the logic of collective action | Q35212932 | ||
| Variable and tissue-specific hormone resistance in heterotrimeric Gs protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of the gsalpha gene | Q36214949 | ||
| Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality | Q36731073 | ||
| Genomic imprinting and the strange case of the insulin-like growth factor II receptor | Q37165552 | ||
| A rheostat model for a rapid and reversible form of imprinting-dependent evolution | Q37216954 | ||
| Characterization of mannose 6-phosphate receptors (MPRs) from opossum liver: opossum cation-independent MPR binds insulin-like growth factor-II. | Q38317253 | ||
| Growth effects of uniparental disomies and the conflict theory of genomic imprinting | Q41653858 | ||
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| Divergent evolution in M6P/IGF2R imprinting from the Jurassic to the Quaternary | Q43726417 | ||
| Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds | Q47645757 | ||
| Genomic imprinting is disrupted in interspecific Peromyscus hybrids | Q48003531 | ||
| Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest | Q48016474 | ||
| Maternal control of embryogenesis by MEDEA, a polycomb group gene in Arabidopsis | Q48038384 | ||
| Regulation of maternal behavior and offspring growth by paternally expressed Peg3. | Q48243147 | ||
| Genomic imprinting--defusing the ovarian time bomb | Q49110236 | ||
| Peromysci, promiscuity and imprinting. | Q50854130 | ||
| Inbreeding, maternal care and genomic imprinting. | Q52106256 | ||
| Genomic imprinting in ruminants: allele-specific gene expression in parthenogenetic sheep. | Q52184340 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Genomic imprinting of two antagonistic loci. | Q55424058 | ||
| The Kinship Theory of Genomic Imprinting | Q56049809 | ||
| Genetic Evidence for Long-Term Monogamy in a Small Rodent, Peromyscus polionotus | Q56533050 | ||
| Sex Specific X Chromosome Expression Caused by Genomic Imprinting | Q57065519 | ||
| Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote | Q58134572 | ||
| Parent-Specific Gene Expression and the Triploid Endosperm | Q58396544 | ||
| The Evolution of Genomic Imprinting: Two Modifier-Locus Models | Q61693875 | ||
| Did genomic imprinting and X chromosome inactivation arise from stochastic expression? | Q62059563 | ||
| Genetic conflicts in genomic imprinting | Q74602226 | ||
| Imprinting and monogamy | Q77883173 | ||
| Genetic conflicts and the private life of Peromyscus polionotus | Q77883178 | ||
| Do we understand the evolution of genomic imprinting? | Q77892020 | ||
| The kangaroo cation-independent mannose 6-phosphate receptor binds insulin-like growth factor II with low affinity | Q78239832 | ||
| Parental modifiers, antisense transcripts and loss of imprinting | Q78288697 | ||
| The nucleus and somatic cell variation | Q78600544 | ||
| Reproductive Isolation Mechanism Resulting from Resolution of Intragenomic Conflict | Q88192136 | ||
| Parent—offspring conflict: the full-sib—half-sib fallacy | Q93605568 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 359-368 | |
| P577 | publication date | 2003-05-01 | |
| P1433 | published in | Nature Reviews Genetics | Q1071824 |
| P1476 | title | What good is genomic imprinting: the function of parent-specific gene expression | |
| P478 | volume | 4 |
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| Q33263582 | A maternal-offspring coadaptation theory for the evolution of genomic imprinting |
| Q45303737 | A model for genomic imprinting in the social brain: adults |
| Q46324362 | A model for genomic imprinting in the social brain: elders |
| Q33996152 | A model for transgenerational imprinting variation in complex traits |
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| Q34230567 | Adaptation of nutrient supply to fetal demand in the mouse involves interaction between the Igf2 gene and placental transporter systems |
| Q79956169 | Affected-sib-pair test for linkage based on constraints for identical-by-descent distributions corresponding to disease models with imprinting |
| Q52060077 | Allelic expression of IGF2 in live-bearing, matrotrophic fishes. |
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| Q35102519 | Altered expression of the imprinted transcription factor PLAGL1 deregulates a network of genes in the human IUGR placenta |
| Q42855137 | An ICE pattern crystallizes |
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| Q41929351 | An imprinted IMAGe: insights into growth regulation through genomic analysis of a rare disease |
| Q37205763 | Analysis of the platypus genome suggests a transposon origin for mammalian imprinting |
| Q38952354 | Androgenesis: where males hijack eggs to clone themselves |
| Q33973417 | Anti‐cancer selection as a source of developmental and evolutionary constraints |
| Q36182585 | Assisted reproduction: the epigenetic perspective |
| Q33817092 | Asymmetric paternal effect on offspring size linked to parent-of-origin expression of an insulin-like growth factor |
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| Q36492692 | Changing images of the gene |
| Q34409829 | Co-evolution of X-chromosome inactivation and imprinting in mammals |
| Q27006276 | Coadaptation and conflict, misconception and muddle, in the evolution of genomic imprinting |
| Q47837471 | Coevolutionary feedbacks between family interactions and life history |
| Q39831972 | Comparative genomics of hormonal signaling in the chorioallantoic membrane of oviparous and viviparous amniotes |
| Q34790118 | Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians |
| Q50671001 | Conserved synteny of mammalian imprinted genes in chicken, frog, and fish genomes. |
| Q36436577 | Cross-species clues of an epigenetic imprinting regulatory code for the IGF2R gene |
| Q37893701 | DNA methylation in insects: on the brink of the epigenomic era. |
| Q36383223 | DNA methylation in the human placenta and fetal growth (review). |
| Q34071946 | Detecting disease variants in case-parent trio studies using the bioconductor software package trio |
| Q37777323 | Development of the eating behaviour in Prader-Willi Syndrome: advances in our understanding. |
| Q48098496 | Developmental biology. Which parental gene gets the upper hand? |
| Q34019927 | Different yet similar: evolution of imprinting in flowering plants and mammals |
| Q33902556 | Differential parental transmission of markers in BCL3 among Korean cleft case-parent trios |
| Q33740394 | Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations |
| Q34994085 | Dynamic expression of imprinted genes associates with maternally controlled nutrient allocation during maize endosperm development. |
| Q41812683 | Dynamic modeling of genes controlling cancer stem cell proliferation |
| Q58702354 | Effects of maternal nutrition on the expression of genomic imprinted genes in ovine fetuses |
| Q36804126 | Empirical testing of hypotheses about the evolution of genomic imprinting in mammals |
| Q38014083 | Endosperm: food for humankind and fodder for scientific discoveries. |
| Q29547452 | Environmental epigenomics and disease susceptibility |
| Q37049211 | Environmental epigenomics in human health and disease |
| Q37423792 | Epigenetic and genetic components of height regulation |
| Q36238483 | Epigenetic mechanisms in early mammalian development |
| Q35909876 | Epigenetic mechanisms of genomic imprinting: common themes in the regulation of imprinted regions in mammals, plants, and insects |
| Q34332425 | Epigenetic memory in plants |
| Q51878021 | Epigenetics and the brain: transcriptome sequencing reveals new depths to genomic imprinting. |
| Q37469995 | Epigenetics: definition, mechanisms and clinical perspective. |
| Q28469300 | Evidence for transgenerational transmission of epigenetic tumor susceptibility in Drosophila |
| Q33982925 | Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanisms |
| Q46538872 | Evolution and Function of the Insulin and Insulin-like Signaling Network in Ectothermic Reptiles: Some Answers and More Questions |
| Q26774995 | Evolution and function of genomic imprinting in plants |
| Q33364216 | Evolution of genomic imprinting with biparental care: implications for Prader-Willi and Angelman syndromes |
| Q35560450 | Evolutionary molecular medicine |
| Q60473642 | Evolutionary perspectives on psychoses and autism: Does genomic imprinting contribute to phenomenological antithesis? |
| Q35539621 | Evolutionary principles and their practical application |
| Q55116694 | Excess maternal transmission of markers in TCOF1 among cleft palate case-parent trios from three populations. |
| Q37154169 | Family-based association study between SLC2A1, HK1, and LEPR polymorphisms with myelomeningocele in Chile. |
| Q36930975 | Functional evolution of IGF2:IGF2R domain 11 binding generates novel structural interactions and a specific IGF2 antagonist |
| Q36572573 | Functional mapping imprinted quantitative trait loci underlying developmental characteristics |
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| Q33927893 | Gene interactions in the evolution of genomic imprinting. |
| Q35035641 | Generation of five human lactoferrin transgenic cloned goats using fibroblast cells and their methylation status of putative differential methylation regions of IGF2R and H19 imprinted genes |
| Q42424798 | Genes with monoallelic expression contribute disproportionately to genetic diversity in humans |
| Q41742513 | Genetic Regulation of Puberty Timing in Humans. |
| Q35554738 | Genetic conflict reflected in tissue-specific maps of genomic imprinting in human and mouse |
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| Q34579259 | Genetic differentiation of hypothalamus parentally biased transcripts in populations of the house mouse implicate the Prader-Willi syndrome imprinted region as a possible source of behavioral divergence |
| Q51647906 | Genetic modulation of energy metabolism in birds through mitochondrial function. |
| Q56903501 | Genetics of type 1 diabetes |
| Q33411083 | Genome-wide analysis of chicken snoRNAs provides unique implications for the evolution of vertebrate snoRNAs |
| Q37550517 | Genome-wide histone state profiling of fibroblasts from the opossum, Monodelphis domestica, identifies the first marsupial-specific imprinted gene. |
| Q38600407 | Genomic Imprinting Is Implicated in the Psychology of Music |
| Q49337089 | Genomic Imprinting was Evolutionarily Conserved during Wheat Polyploidization. |
| Q35533142 | Genomic conflicts and sexual antagonism in human health: insights from oxytocin and testosterone |
| Q50301666 | Genomic imprinting and conflict-induced decanalization |
| Q34385720 | Genomic imprinting and genetic effects on muscle traits in mice |
| Q37087594 | Genomic imprinting and imprinting defects in humans |
| Q35092426 | Genomic imprinting and the evolutionary psychology of human kinship |
| Q35575191 | Genomic imprinting and the social brain |
| Q43059479 | Genomic imprinting as a cause of disease |
| Q33691676 | Genomic imprinting does not reduce the dosage of UBE3A in neurons. |
| Q34699894 | Genomic imprinting effects on brain development and function |
| Q26828858 | Genomic imprinting in mammals |
| Q21145256 | Genomic imprinting in mammals: emerging themes and established theories |
| Q35105543 | Genomic imprinting of Grb10: coadaptation or conflict? |
| Q50787686 | Genomic imprinting; the cost of mother's care. |
| Q42778297 | Highly-interwoven communities of a gene regulatory network unveil topologically important genes for maize seed development. |
| Q92214845 | How conflict shapes evolution in poeciliid fishes |
| Q34340465 | How demography, life history, and kinship shape the evolution of genomic imprinting |
| Q92339946 | Human placental methylome in the interplay of adverse placental health, environmental exposure, and pregnancy outcome |
| Q35692856 | Humans as Superorganisms: How Microbes, Viruses, Imprinted Genes, and Other Selfish Entities Shape Our Behavior |
| Q34395064 | Hybrid mice reveal parent-of-origin and Cis- and trans-regulatory effects in the retina |
| Q36312103 | IGF2 DNA methylation is a modulator of newborn's fetal growth and development |
| Q24633385 | Imprint switch mutations at Rasgrf1 support conflict hypothesis of imprinting and define a growth control mechanism upstream of IGF1 |
| Q33724476 | Imprinted Nesp55 influences behavioral reactivity to novel environments |
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| Q52644142 | Impulsive Choice in Mice Lacking Paternal Expression of Grb10 Suggests Intragenomic Conflict in Behavior. |
| Q39504063 | Impulsive choices in mice lacking imprinted Nesp55. |
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| Q36524664 | Intracytoplasmic sperm injection--an assisted reproduction technique that should make us cautious about imprinting deregulation |
| Q92982560 | Intragenomic conflict over bet-hedging |
| Q33981079 | Intralocus sexual conflict can drive the evolution of genomic imprinting |
| Q37909236 | Is there a genomically imprinted social brain? |
| Q39631819 | Kin conflict in insect societies: a new epigenetic perspective. |
| Q35757642 | Kin recognition in Aleochara bilineata could support the kinship theory of genomic imprinting. |
| Q24324059 | LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia |
| Q51528127 | Male genotype influences female reproductive investment in Drosophila melanogaster. |
| Q33566637 | Maternal contributions to preterm delivery |
| Q36515731 | Maternal effects as the cause of parent-of-origin effects that mimic genomic imprinting |
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| Q34611930 | Maternal transmission of a humanised Igf2r allele results in an Igf2 dependent hypomorphic and non-viable growth phenotype |
| Q92461391 | Maternal transmission of an Igf2r domain 11: IGF2 binding mutant allele (Igf2rI1565A) results in partial lethality, overgrowth and intestinal adenoma progression |
| Q35152301 | Matrisibs, Patrisibs, and the Evolution of Imprinting on Autosomes and Sex Chromosomes |
| Q36854306 | Mechanisms of disease: the developmental origins of disease and the role of the epigenotype. |
| Q36783165 | Metastable epialleles, imprinting, and the fetal origins of adult diseases |
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| Q36336523 | Molecular features and functional constraints in the evolution of the mammalian X chromosome. |
| Q39695230 | Neocortical development as an evolutionary platform for intragenomic conflict |
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| Q47337053 | Reduced salivary gland size and increased presence of epithelial progenitor cells in DLK1-deficient mice. |
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