| scholarly article | Q13442814 |
| P50 | author | Christos Coutifaris | Q126595012 |
| P2093 | author name string | John P Gaughan | |
| Raffi Chalian | |||
| Carmen Sapienza | |||
| Nahid Turan | |||
| Sunita Katari | |||
| Leigh F Gerson | |||
| Michael W Foster | |||
| P2860 | cites work | Conservation of a maternal-specific methylation signal at the human IGF2R locus | Q41285894 |
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| Imprinted chromosomal regions of the human genome have unusually high recombination rates | Q42533261 | ||
| Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection | Q43202295 | ||
| GAPDH, 18S rRNA and YWHAZ are suitable endogenous reference genes for relative gene expression studies in placental tissues from human idiopathic fetal growth restriction | Q46442542 | ||
| IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch | Q46747937 | ||
| Size at birth and cord blood levels of insulin, insulin-like growth factor I (IGF-I), IGF-II, IGF-binding protein-1 (IGFBP-1), IGFBP-3, and the soluble IGF-II/mannose-6-phosphate receptor in term human infants. The ALSPAC Study Team. Avon Longitudin | Q47224724 | ||
| Selective loss of imprinting in the placenta following preimplantation development in culture | Q47232748 | ||
| Gene-specific timing and epigenetic memory in oocyte imprinting | Q48004990 | ||
| Dual effects of superovulation: loss of maternal and paternal imprinted methylation in a dose-dependent manner. | Q48712348 | ||
| Superovulation alters the expression of imprinted genes in the midgestation mouse placenta. | Q48764255 | ||
| Aberrant DNA methylation of imprinted loci in superovulated oocytes. | Q50645854 | ||
| Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome. | Q50936741 | ||
| Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development. | Q51976586 | ||
| Imprinting mechanisms. | Q52184196 | ||
| Genomic imprinting. Imprinting with and without methylation. | Q52218988 | ||
| Beckwith-Wiedemann syndrome and IVF: a case-control study | Q24533595 | ||
| Homeobox gene HLX1 expression is decreased in idiopathic human fetal growth restriction | Q24675020 | ||
| Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis | Q28144502 | ||
| CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus | Q28145756 | ||
| Monoallelic expression of the human H19 gene | Q28184725 | ||
| Epigenetic reprogramming in mammalian development | Q28212171 | ||
| Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight | Q28279818 | ||
| Insulin-like growth factors and their binding proteins: biological actions | Q28301853 | ||
| CTCF maintains differential methylation at the Igf2/H19 locus | Q28593901 | ||
| Human imprinted chromosomal regions are historical hot-spots of recombination. | Q33250071 | ||
| Time course analysis of RNA stability in human placenta | Q33417868 | ||
| Evolution in health and medicine Sackler colloquium: Stochastic epigenetic variation as a driving force of development, evolutionary adaptation, and disease | Q33844476 | ||
| Natural selection and the function of genome imprinting: beyond the silenced minority | Q33927035 | ||
| Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation | Q34206865 | ||
| Assisted reproductive technologies and the risk of birth defects--a systematic review | Q34371767 | ||
| A survey of assisted reproductive technology births and imprinting disorders. | Q34699309 | ||
| Imprinting disorders and assisted reproductive technology | Q34845922 | ||
| X chromosome-inactivation patterns of 1,005 phenotypically unaffected females | Q35015824 | ||
| Limited evolutionary conservation of imprinting in the human placenta | Q35025042 | ||
| H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19. | Q35194017 | ||
| Mammalian recombination hot spots: properties, control and evolution. | Q35311047 | ||
| Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples | Q35448168 | ||
| Mouse embryo culture induces changes in postnatal phenotype including raised systolic blood pressure | Q35720294 | ||
| Heritability of X chromosome--inactivation phenotype in a large family | Q35882786 | ||
| Genomic imprinting and reproduction | Q36267756 | ||
| Intracytoplasmic sperm injection may increase the risk of imprinting defects | Q37361933 | ||
| Interactions of IGF-II with the IGF2R/cation-independent mannose-6-phosphate receptor mechanism and biological outcomes. | Q37404002 | ||
| Long-term effect of in vitro culture of mouse embryos with serum on mRNA expression of imprinting genes, development, and behavior. | Q37645483 | ||
| Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer | Q40766020 | ||
| Numerology of development. | Q52967983 | ||
| Functional Polymorphism in the Parental Imprinting of the Human IGF2R Gene | Q57500167 | ||
| The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans | Q58061470 | ||
| Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies | Q58133996 | ||
| Placental IGF2 Expression in Normal and Intrauterine Growth Restricted (IUGR) Pregnancies | Q59504101 | ||
| IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome | Q70765937 | ||
| Parental genomic imprinting of the human IGF2 gene | Q72222239 | ||
| Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour | Q72703028 | ||
| Loss of imprinting of IGF2 and H19 in osteosarcoma is accompanied by reciprocal methylation changes of a CTCF-binding site | Q73006826 | ||
| Epigenetic change in IGF2R is associated with fetal overgrowth after sheep embryo culture | Q73435273 | ||
| Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes | Q73509793 | ||
| Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions | Q73543277 | ||
| Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo | Q73811130 | ||
| Hot-stop PCR: a simple and general assay for linear quantitation of allele ratios | Q74133538 | ||
| Loss of imprinting in normal tissue of colorectal cancer patients with microsatellite instability | Q77534962 | ||
| Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human | Q77790112 | ||
| A longitudinal study of X-inactivation ratio in human females | Q80509666 | ||
| Superovulation in mice alters the methylation pattern of imprinted genes in the sperm of the offspring | Q84114090 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 7 | |
| P921 | main subject | DNA methylation | Q874745 |
| P304 | page(s) | e1001033 | |
| P577 | publication date | 2010-07-22 | |
| P1433 | published in | PLOS Genetics | Q1893441 |
| P1476 | title | Inter- and intra-individual variation in allele-specific DNA methylation and gene expression in children conceived using assisted reproductive technology | |
| P478 | volume | 6 |
| Q38690993 | A Molecular Perspective on Procedures and Outcomes with Assisted Reproductive Technologies |
| Q34426327 | A systematic review and meta-analysis of DNA methylation levels and imprinting disorders in children conceived by IVF/ICSI compared with children conceived spontaneously |
| Q34196470 | Alteration of DNA demethylation dynamics by in vitro culture conditions in rabbit pre-implantation embryos |
| Q34807249 | Altered Methylation of IGF2 Locus 20 Years after Preterm Birth at Very Low Birth Weight |
| Q27990519 | Altered gene expression in human placentas after IVF/ICSI |
| Q26823852 | Are there subtle genome-wide epigenetic alterations in normal offspring conceived by assisted reproductive technologies? |
| Q53104592 | Assessing pre-implantation embryo development in mice provides a rationale for understanding potential adverse effects of ART and PGD procedures. |
| Q35766037 | Assisted reproduction treatment and epigenetic inheritance. |
| Q36586710 | Assisted reproductive technologies and perinatal morbidity: interrogating the association |
| Q93063992 | Assisted reproductive technologies are associated with limited epigenetic variation at birth that largely resolves by adulthood |
| Q35854896 | Association of cord blood methylation fractions at imprinted insulin-like growth factor 2 (IGF2), plasma IGF2, and birth weight |
| Q48204198 | Association of in vitro fertilization with global and IGF2/H19 methylation variation in newborn twins. |
| Q48248281 | Author’s response: Humans, fruit flies, and automatons. |
| Q51790505 | Combined Influence of Genetic Polymorphism and DNA Methylation on ABCB1 Expression and Function in Healthy Chinese Males. |
| Q90722510 | Comparison of DNA methylation patterns of parentally imprinted genes in placenta derived from IVF conceptions in two different culture media |
| Q36216309 | Comparison of genome-wide and gene-specific DNA methylation between ART and naturally conceived pregnancies |
| Q47867186 | Compromised oocyte quality and assisted reproduction contribute to sex-specific effects on offspring outcomes and epigenetic patterning |
| Q39127494 | Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors |
| Q38693782 | DNA methylation analysis in constitutional disorders: Clinical implications of the epigenome. |
| Q28729719 | DNA methylation differences at growth related genes correlate with birth weight: a molecular signature linked to developmental origins of adult disease? |
| Q35504751 | DNA methylation differences between in vitro- and in vivo-conceived children are associated with ART procedures rather than infertility |
| Q35841693 | DNA methylation of stress-related genes and LINE-1 repetitive elements across the healthy human placenta |
| Q37961785 | DNA methylation profiling highlights the unique nature of the human placental epigenome. |
| Q36557318 | Effect of sperm entry on blastocyst development after in vitro fertilization and intracytoplasmic sperm injection - mouse model |
| Q35242537 | Environmental and epigenetic effects upon preimplantation embryo metabolism and development |
| Q91619227 | Epigenetic changes in preterm birth placenta suggest a role for ADAMTS genes in spontaneous preterm birth |
| Q35803768 | Epigenetic differences in normal colon mucosa of cancer patients suggest altered dietary metabolic pathways |
| Q38667525 | Epigenetic imprinting during assisted reproductive technologies: The effect of temporal and cumulative fluctuations in methionine cycling on the DNA methylation state |
| Q26745950 | Epigenetics: A key paradigm in reproductive health |
| Q34059853 | Evidence for widespread changes in promoter methylation profile in human placenta in response to increasing gestational age and environmental/stochastic factors |
| Q35560450 | Evolutionary molecular medicine |
| Q56503296 | FETAL AND MATERNAL CONSEQUENCES OF PREGNANCIES CONCEIVED USING ART |
| Q37043802 | Frequency and characterization of DNA methylation defects in children born SGA. |
| Q34277727 | Imprinting methylation errors in ART. |
| Q33826326 | In vitro culture increases the frequency of stochastic epigenetic errors at imprinted genes in placental tissues from mouse concepti produced through assisted reproductive technologies. |
| Q36243658 | Interindividual epigenetic variation in ABCB1 promoter and its relationship with ABCB1 expression and function in healthy Chinese subjects |
| Q89394173 | Intracytoplasmic sperm injection for male infertility and consequences for offspring |
| Q92452836 | Locus-specific DNA methylation prediction in cord blood and placenta |
| Q36832799 | Long-term follow-up of children conceived through assisted reproductive technology |
| Q36625123 | Low birth weight: is it related to assisted reproductive technology or underlying infertility? |
| Q34050344 | Mapping personal functional data to personal genomes. |
| Q39400476 | Mechanistic Insight into Long Noncoding RNAs and the Placenta |
| Q38927386 | Morphologic and molecular changes in the placenta: what we can learn from environmental exposures |
| Q40184476 | Obstetrical and perinatal morbidity and mortality among in-vitro fertilization pregnancies: a population-based study |
| Q53691451 | Origins of lifetime health around the time of conception: causes and consequences. |
| Q36402581 | Outlier DNA methylation levels as an indicator of environmental exposure and risk of undesirable birth outcome |
| Q35976260 | Patterns of placental development evaluated by X chromosome inactivation profiling provide a basis to evaluate the origin of epigenetic variation. |
| Q40266942 | Peri-Implantation Hormonal Milieu: Elucidating Mechanisms of Adverse Neurodevelopmental Outcomes |
| Q30408297 | Peri-implantation hormonal milieu: elucidating mechanisms of abnormal placentation and fetal growth |
| Q50763500 | Placentas from pregnancies conceived by IVF/ICSI have a reduced DNA methylation level at the H19 and MEST differentially methylated regions. |
| Q48635946 | Post-implantation mortality of in vitro produced embryos is associated with DNA methyltransferase 1 dysfunction in sheep placenta. |
| Q35837193 | Primary epimutations introduced during intracytoplasmic sperm injection (ICSI) are corrected by germline-specific epigenetic reprogramming |
| Q33758127 | Pyrosequencing Evaluation of Widely Available Bisulfite Conversion Methods: Considerations for Application. |
| Q37636251 | Reshaping the transcriptional frontier: epigenetics and somatic cell nuclear transfer |
| Q28075554 | Risk of adverse pregnancy and perinatal outcomes after high technology infertility treatment: a comprehensive systematic review |
| Q34203901 | Similar DNA methylation levels in specific imprinting control regions in children conceived with and without assisted reproductive technology: a cross-sectional study |
| Q45813691 | Stability of genomic imprinting and gestational-age dynamic methylation in complicated pregnancies conceived following assisted reproductive technologies |
| Q35771472 | The effect of preconception paternal alcohol exposure on epigenetic remodeling of the h19 and rasgrf1 imprinting control regions in mouse offspring |
| Q47194086 | The epigenetic control of transposable elements and imprinted genes in newborns is affected by the mode of conception: ART versus spontaneous conception without underlying infertility. |
| Q38729483 | The health outcomes of human offspring conceived by assisted reproductive technologies (ART). |
| Q26795427 | The placenta: phenotypic and epigenetic modifications induced by Assisted Reproductive Technologies throughout pregnancy |
| Q88645051 | The placental gateway of maternal transgenerational epigenetic inheritance |
| Q36243244 | Transcriptional differences between rhesus embryonic stem cells generated from in vitro and in vivo derived embryos |
| Q33859385 | Validation of methylation biomarkers that distinguish normal colon mucosa of cancer patients from normal colon mucosa of patients without cancer |
| Q55376953 | What are the risks of the assisted reproductive technologies (ART) and how can they be minimized? |
| Q50535555 | [DOHaD and pre- or peri-conceptional programming]. |
| Q55354109 | rs10732516 polymorphism at the IGF2/H19 locus associates with genotype-specific effects on placental DNA methylation and birth weight of newborns conceived by assisted reproductive technology. |
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