| scholarly article | Q13442814 |
| P50 | author | Wolf Reik | Q15994704 |
| P2093 | author name string | E R Maher | |
| J R Sampson | |||
| T R Cole | |||
| M M Hawkins | |||
| F Macdonald | |||
| C L Barratt | |||
| W Cooper | |||
| L A Brueton | |||
| A Luharia | |||
| S C Bowdin | |||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Beckwith-Wiedemann syndrome | Q521863 |
| P304 | page(s) | 62-4 | |
| P577 | publication date | 2003-01-01 | |
| P1433 | published in | Journal of Medical Genetics | Q14640281 |
| P1476 | title | Beckwith-Wiedemann syndrome and assisted reproduction technology (ART) | |
| P478 | volume | 40 |
| Q38542163 | (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: a paradigm for genomic medicine. |
| Q37797961 | 6q24 transient neonatal diabetes. |
| Q38690993 | A Molecular Perspective on Procedures and Outcomes with Assisted Reproductive Technologies |
| Q35205842 | A potential use of embryonic stem cell medium for the in vitro culture of preimplantation embryos |
| Q34595528 | A review of known imprinting syndromes and their association with assisted reproduction technologies. |
| Q34699309 | A survey of assisted reproductive technology births and imprinting disorders. |
| Q43837126 | Aberrant DNA methylation of imprinted loci in human spontaneous abortions after assisted reproduction techniques and natural conception |
| Q51797620 | Abnormal development at early postimplantation stage in mouse embryos after preimplantation genetic diagnosis. |
| Q48719048 | Abnormal methylation at the KvDMR1 imprinting control region in clinically normal children conceived by assisted reproductive technologies. |
| Q34084829 | Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield. |
| Q41696623 | Altered methylations of H19, Snrpn, Mest and Peg3 are reversible by developmental reprogramming in kidney tissue of ICSI-derived mice |
| Q37312918 | An overview of studies on psychological well-being in children born following assisted reproductive technologies |
| Q41603973 | Analysis of DNA damage after human sperm cryopreservation in genes crucial for fertilization and early embryo development |
| Q35406359 | Analysis of H19 methylation in control and abnormal human embryos, sperm and oocytes |
| Q38672998 | Approach to the Diagnosis of Overgrowth Syndromes |
| Q35563779 | Are major defects in children conceived in vitro due to innate problems in patients or to induced genetic damage? |
| Q79803702 | As IVF becomes more common, some concerns remain |
| Q33303250 | Assisted Reproductive Technology affects developmental kinetics, H19 Imprinting Control Region methylation and H19 gene expression in individual mouse embryos |
| Q36321227 | Assisted reproduction technology and defects of genomic imprinting |
| Q35766037 | Assisted reproduction treatment and epigenetic inheritance. |
| Q35659475 | Assisted reproductive technologies do not alter mutation frequency or spectrum |
| Q34393122 | Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients. |
| Q24533595 | Beckwith-Wiedemann syndrome and IVF: a case-control study |
| Q84966064 | Beckwith–Wiedemann syndrome |
| Q36037545 | Benefits and challenges brought by improved results from in vitro fertilization |
| Q34433307 | Bringing epigenetics into the diagnostics of the andrology laboratory: challenges and perspectives |
| Q33285306 | Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7. |
| Q50718043 | Chapter 19 Cryopreservation Effect on Genetic Function: Neonatal Outcomes. |
| Q51528063 | Characterization of differentially methylated regions in 3 bovine imprinted genes: a model for studying human germ-cell and embryo development. |
| Q30466805 | Child health, developmental plasticity, and epigenetic programming |
| Q37897034 | Childhood outcomes of assisted reproductive technology |
| Q52984051 | Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques. |
| Q94460630 | Clinical and molecular features of children with Beckwith-Wiedemann syndrome in China: a single-center retrospective cohort study |
| Q40537300 | Clinical challenges in providing embryos for stem-cell initiatives. |
| Q24685607 | Comparative isoschizomer profiling of cytosine methylation: the HELP assay |
| Q35767738 | Comparison of elective single cleavage-embryo transfer to elective single blastocyst-embryo transfer in human IVF-ET |
| Q43884778 | Comparison of the clinical scoring systems in Silver-Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing. |
| Q62089503 | Comprehensive meta-analysis reveals association between multiple imprinting disorders and conception by assisted reproductive technology |
| Q36088644 | Compromised fertility disrupts Peg1 but not Snrpn and Peg3 imprinted methylation acquisition in mouse oocytes. |
| Q47867186 | Compromised oocyte quality and assisted reproduction contribute to sex-specific effects on offspring outcomes and epigenetic patterning |
| Q24792615 | Correlation of sperm penetration assay score with polyspermy rate in in-vitro fertilization |
| Q36783148 | Could epigenetics play a role in the developmental origins of health and disease? |
| Q37066438 | Current progress with primate embryonic stem cells |
| Q37719658 | DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation |
| Q35504751 | DNA methylation differences between in vitro- and in vivo-conceived children are associated with ART procedures rather than infertility |
| Q51380383 | DNA methylation errors in imprinting disorders and assisted reproductive technology. |
| Q39362648 | DNA methylation in spermatozoa as a prospective marker in andrology |
| Q33537490 | DNA methylation patterns in tissues from mid-gestation bovine foetuses produced by somatic cell nuclear transfer show subtle abnormalities in nuclear reprogramming |
| Q37961785 | DNA methylation profiling highlights the unique nature of the human placental epigenome. |
| Q38748339 | DNA methylation signatures in cord blood of ICSI children |
| Q88356800 | Detection of a case of Angelman syndrome caused by an imprinting error in 949 pregnancies analyzed for AS following IVF |
| Q48712348 | Dual effects of superovulation: loss of maternal and paternal imprinted methylation in a dose-dependent manner |
| Q28298817 | Dysmorphology demystified |
| Q34035548 | Effects of assisted reproduction technology on placental imprinted gene expression |
| Q38112247 | Effects of embryonic manipulation and epigenetics. |
| Q33586272 | Effects of ooplasm manipulation on DNA methylation and growth of progeny in mice |
| Q54942351 | Elective cryopreservation of all day 5 blastocysts is more effective than using day 6 blastocysts for improving pregnancy outcome in stimulated cycles. |
| Q36515828 | Embryo manipulation via assisted reproductive technology and epigenetic asymmetry in mammalian early development. |
| Q40339087 | Embryonic stem-cell gametes: the new frontier in human reproduction. |
| Q39659149 | Epigenetic Differences between Embryonic Stem Cells Generated from Blastocysts DevelopedIn VitroandIn Vivo |
| Q38554712 | Epigenetic alterations in sperm associated with male infertility |
| Q37196586 | Epigenetic consequences of assisted reproduction and infertility on the human preimplantation embryo |
| Q37961876 | Epigenetic discordance at imprinting control regions in twins |
| Q38667525 | Epigenetic imprinting during assisted reproductive technologies: The effect of temporal and cumulative fluctuations in methionine cycling on the DNA methylation state |
| Q50654192 | Epigenetic status of the H19 locus in human oocytes following in vitro maturation. |
| Q37919126 | Epigenetics and assisted reproductive technology |
| Q33909693 | Epigenetics and assisted reproductive technology: a call for investigation |
| Q37346204 | Epigenetics and obesity |
| Q37801493 | Epigenetics and the placenta |
| Q55010086 | Epigenetics in assisted reproductive technology. |
| Q33620204 | Epigenetics in the placenta |
| Q38681930 | Epigenetics of Autism Spectrum Disorder |
| Q48048199 | Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome |
| Q41825130 | Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology |
| Q48510862 | Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement |
| Q36499262 | Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine |
| Q34552072 | Familial molar tissues due to mutations in the inflammatory gene, NALP7, have normal postzygotic DNA methylation |
| Q36251483 | Gametes and embryo epigenetic reprogramming affect developmental outcome: implication for assisted reproductive technologies |
| Q38113238 | Genes, assisted reproductive technology and trans-illumination |
| Q51944781 | Genetic and epigenetic characteristics of ICSI children. |
| Q36856368 | Genetic aspects of birth defects: new understandings of old problems |
| Q34556925 | Genetic or epigenetic difference causing discordance between monozygotic twins as a clue to molecular basis of mental disorders |
| Q50683269 | Genetic variation in oocyte phenotype revealed through parthenogenesis and cloning: correlation with differences in pronuclear epigenetic modification. |
| Q36102997 | Genetics and assisted reproduction technology |
| Q36684104 | Genetics, epigenetics and gene silencing in differentiating mammalian embryos |
| Q37797697 | Genomic Imprinting Syndromes and Cancer |
| Q43059479 | Genomic imprinting as a cause of disease |
| Q24646016 | Genomic imprinting disorders in humans: a mini-review |
| Q91063421 | Genomic imprinting disorders: lessons on how genome, epigenome and environment interact |
| Q33419813 | Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome). |
| Q36340375 | High Frequency of Imprinted Methylation Errors in Human Preimplantation Embryos |
| Q37962006 | Human imprinting syndromes. |
| Q37339099 | Human teratogens: current controversies |
| Q46747937 | IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch |
| Q33328492 | Immature cryopreserved ovary restores puberty and fertility in mice without alteration of epigenetic marks |
| Q91618948 | Impact of assisted reproduction, infertility, sex and paternal factors on the placental DNA methylome |
| Q48110063 | Impairment of sperm DNA methylation in male infertility: a meta-analytic study. |
| Q34845922 | Imprinting disorders and assisted reproductive technology |
| Q84475523 | Imprinting disorders and assisted reproductive technology |
| Q64950830 | Imprinting disorders and assisted reproductive technology. |
| Q34277727 | Imprinting methylation errors in ART. |
| Q38619555 | In Vitro fertilization and adverse obstetric and perinatal outcomes |
| Q35919249 | In vitro fertilization (IVF): a review of 3 decades of clinical innovation and technological advancement |
| Q45833713 | In vitro fertilization alters growth and expression of Igf2/H19 and their epigenetic mechanisms in the liver and skeletal muscle of newborn and elder mice |
| Q33532631 | In vitro fertilization and embryo culture strongly impact the placental transcriptome in the mouse model |
| Q24532045 | In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene |
| Q36917079 | In vitro spermatogenesis as a method to bypass pre-meiotic or post-meiotic barriers blocking the spermatogenetic process: genetic and epigenetic implications in assisted reproductive technology |
| Q36854934 | Incidence and complications of multiple gestation in Canada: proceedings of an expert meeting |
| Q35448168 | Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples |
| Q33862981 | Infant leukemia and parental infertility or its treatment: a Children's Oncology Group report |
| Q36713717 | Intracytoplasmic sperm injection (ICSI)--what are the risks? |
| Q47107822 | Intracytoplasmic sperm injection: state of the art in humans |
| Q35558541 | Is intracytoplasmic sperm injection safe? |
| Q38098513 | Is there an increased risk of malformations after assisted reproductive technologies? |
| Q37378662 | Large offspring syndrome: a bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann. |
| Q36160389 | Long-term effects of culture of preimplantation mouse embryos on behavior. |
| Q35779087 | Loss of genomic imprinting in mouse embryos with fast rates of preimplantation development in culture. |
| Q34325361 | Low frequency of imprinting defects in ICSI children born small for gestational age. |
| Q50350055 | Maintenance of Mest imprinted methylation in blastocyst-stage mouse embryos is less stable than other imprinted loci following superovulation or embryo culture. |
| Q34108232 | Making the blastocyst: lessons from the mouse |
| Q51976586 | Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development. |
| Q34786920 | Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development |
| Q40123077 | Maternal fertility problems and risk for transient neonatal diabetes mellitus |
| Q35866635 | Meiotic and mitotic nondisjunction: lessons from preimplantation genetic diagnosis. |
| Q35151072 | Methodology matters: IVF versus ICSI and embryonic gene expression |
| Q50640391 | Methylation analysis of the intergenic differentially methylated region of DLK1-GTL2 in human. |
| Q37009895 | Mild diabetes models and their maternal-fetal repercussions. |
| Q36899210 | Modelling germ cell development in vitro. |
| Q54441687 | Modulation of imprinted gene network in placenta results in normal development of in vitro manipulated mouse embryos. |
| Q38099605 | Molecular findings in Beckwith-Wiedemann syndrome |
| Q101053728 | Mucopolysaccharidosis type I due to maternal uniparental disomy of chromosome 4 with partial isodisomy of 4p16.3p15.2. |
| Q81471510 | Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells |
| Q26822531 | New advances of preimplantation and prenatal genetic screening and noninvasive testing as a potential predictor of health status of babies |
| Q35990294 | Of light and mouse embryos: less is more |
| Q34581482 | Outcome of assisted reproduction. |
| Q36402581 | Outlier DNA methylation levels as an indicator of environmental exposure and risk of undesirable birth outcome |
| Q92179836 | Overgrowth syndromes - clinical and molecular aspects and tumour risk |
| Q89220348 | Overrepresentation of pregnancies conceived by artificial reproductive technology in prenatally identified fetuses with Beckwith-Wiedemann syndrome |
| Q35976292 | Parental infertility, infertility treatment and hepatoblastoma: a report from the Children's Oncology Group |
| Q30408297 | Peri-implantation hormonal milieu: elucidating mechanisms of abnormal placentation and fetal growth |
| Q46343342 | Perinatal outcome of ICSI pregnancies compared with a matched group of natural conception pregnancies in Flanders (Belgium): a cohort study |
| Q81390305 | Pregnancy and perinatal outcomes after assisted reproduction: a comparative study |
| Q50659795 | Preimplantation genetic diagnosis in assisted reproduction. |
| Q37693835 | Progenitor cells for regenerative medicine and consequences of ART and cloning-associated epimutations |
| Q37815537 | Prognostic markers for competent human spermatozoa: fertilizing capacity and contribution to the embryo |
| Q44926683 | Quality of human spermatozoa: relationship between high-magnification sperm morphology and DNA integrity. |
| Q34205147 | Rare congenital disorders, imprinted genes, and assisted reproductive technology |
| Q48801613 | Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndrome |
| Q64288870 | Risk of cancer in children and young adults conceived by assisted reproductive technology |
| Q37338436 | Role of ART in imprinting disorders |
| Q37078076 | Safety of assisted reproduction, assessed by risk of abnormalities in children born after use of in vitro fertilization techniques |
| Q35180365 | Scientific hazards of human reproductive 'cloning'. |
| Q59070520 | Seeds of doubt |
| Q36312101 | Semen samples showing an increased rate of spermatozoa with imprinting errors have a negligible effect in the outcome of assisted reproduction techniques |
| Q40544927 | Sequence of ejaculation affects the spermatozoon as a carrier and its message. |
| Q48829293 | Should non-patient volunteers donate eggs? |
| Q46490975 | Significance of large nuclear vacuoles in human spermatozoa: implications for ICSI. |
| Q36268899 | Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST |
| Q34203901 | Similar DNA methylation levels in specific imprinting control regions in children conceived with and without assisted reproductive technology: a cross-sectional study |
| Q30435048 | Skewed X inactivation and IVF-conceived infants |
| Q34328467 | Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men |
| Q33679414 | Sperm DNA damage in male infertility: etiologies, assays, and outcomes |
| Q34998961 | Sperm DNA damage: clinical significance in the era of assisted reproduction |
| Q50216717 | Sperm global DNA methylation level: association with semen parameters and genome integrity |
| Q57072718 | Stammzellforschung – Status, Ausblick und bioethischer Aspekt |
| Q35707619 | Stem cells today: A. Origin and potential of embryo stem cells |
| Q54663036 | Strategies for preimplantation genetic diagnosis of Angelman syndrome caused by mutations in the UBE3A gene. |
| Q36230633 | Study of DNA methylation patterns of imprinted genes in children born after assisted reproductive technologies reveals no imprinting errors: A pilot study |
| Q48764255 | Superovulation alters the expression of imprinted genes in the midgestation mouse placenta |
| Q48584147 | Superovulation induces alterations in the epigenome of zygotes, and results in differences in gene expression at the blastocyst stage in mice |
| Q36885699 | Syndromes and disorders associated with omphalocele (I): Beckwith-Wiedemann syndrome |
| Q36302091 | The cumulative effect of assisted reproduction procedures on placental development and epigenetic perturbations in a mouse model. |
| Q36268921 | The effects of age on DNA fragmentation, chromatin packaging and conventional semen parameters in spermatozoa of oligoasthenoteratozoospermic patients |
| Q50437193 | The epigenetic effects of assisted reproductive technologies: ethical considerations |
| Q36927144 | The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region |
| Q37186709 | The epigenetics of adult (somatic) stem cells |
| Q35960713 | The great opportunity: Evolutionary applications to medicine and public health |
| Q36594182 | The health risks of ART. |
| Q29617273 | The history of cancer epigenetics |
| Q34011361 | The impact of assisted reproductive technologies on genomic imprinting and imprinting disorders |
| Q43866478 | The impact of ovarian stimulation on the expression of candidate reprogramming genes in mouse preimplantation embryos |
| Q53247850 | The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues. |
| Q35227826 | The periconceptional environment and cardiovascular disease: does in vitro embryo culture and transfer influence cardiovascular development and health? |
| Q35647363 | The potential risks of abnormal transmission of mtDNA through assisted reproductive technologies. |
| Q30827441 | The primate embryo gene expression resource: a novel resource to facilitate rapid analysis of gene expression patterns in non-human primate oocytes and preimplantation stage embryos |
| Q81631750 | The problematic in-vitro embryo in the age of epigenetics |
| Q55029198 | The utility of alpha-fetoprotein screening in Beckwith-Wiedemann syndrome. |
| Q50679396 | Thirteen years' experience of preimplantation diagnosis: report of the Fifth International Symposium on Preimplantation Genetics. |
| Q38201989 | Totipotency and lineage segregation in the human embryo. |
| Q55376953 | What are the risks of the assisted reproductive technologies (ART) and how can they be minimized? |
| 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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