| scholarly article | Q13442814 |
| P356 | DOI | 10.1093/HMG/11.11.1317 |
| P698 | PubMed publication ID | 12019213 |
| P50 | author | Jeremy A. Squire | Q39802515 |
| Oana Caluseriu | Q113001000 | ||
| Adele Schneider | Q130279617 | ||
| P2093 | author name string | Elizabeth Ives | |
| David Chitayat | |||
| Rosanna Weksberg | |||
| Timothy H Bestor | |||
| Cheryl Shuman | |||
| Adam C Smith | |||
| Lyle Best | |||
| Paul Sadowski | |||
| Madeline Li | |||
| Tracy L Stockley | |||
| Ann Olney | |||
| Joy Nishikawa | |||
| Yan-Ling Fei | |||
| P433 | issue | 11 | |
| P921 | main subject | Beckwith-Wiedemann syndrome | Q521863 |
| P304 | page(s) | 1317-1325 | |
| P577 | publication date | 2002-05-01 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome | |
| P478 | volume | 11 |
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| Q34713637 | A twin approach to unraveling epigenetics |
| Q48182410 | Aberrant DNA methylation associated with bipolar disorder identified from discordant monozygotic twins |
| Q33745516 | Adult monozygotic twins discordant for intra-uterine growth have indistinguishable genome-wide DNA methylation profiles |
| Q28088478 | Advancements in the delivery of epigenetic drugs |
| 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? |
| Q34008019 | Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults |
| Q34463847 | Beckwith Wiedemann imprinting defect found in leucocyte but not buccal DNA in a child born small for gestational age |
| Q84116019 | Beckwith-Wiedemann syndrome |
| Q84966064 | Beckwith–Wiedemann syndrome |
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| Q34675182 | Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations |
| Q84061922 | DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins |
| Q37719658 | DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation |
| Q51646478 | DNA methylation in the IGF2 intragenic DMR is re-established in a sex-specific manner in bovine blastocysts after somatic cloning. |
| Q88356800 | Detection of a case of Angelman syndrome caused by an imprinting error in 949 pregnancies analyzed for AS following IVF |
| Q89623078 | Diagnosis and Management of Beckwith-Wiedemann Syndrome |
| Q34796061 | Dietary alleviation of maternal obesity and diabetes: increased resistance to diet-induced obesity transcriptional and epigenetic signatures |
| Q34710990 | Endogenous Voltage Potentials and the Microenvironment: Bioelectric Signals that Reveal, Induce and Normalize Cancer |
| Q38110380 | Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders |
| Q24531005 | Epigenetic differences arise during the lifetime of monozygotic twins |
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| Q37504694 | Epigenetic mechanisms that underpin metabolic and cardiovascular diseases |
| Q37242454 | Epigenetic regulation in mammalian preimplantation embryo development |
| Q47196130 | Epigenetic supersimilarity of monozygotic twin pairs |
| Q34995527 | Epigenetics lessons from twins: prospects for autoimmune disease. |
| Q34624829 | Epigenetics of discordant monozygotic twins: implications for disease |
| Q58224409 | Epimutation of the TNDM locus and the Beckwith–Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus |
| Q48126284 | Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome |
| Q50233680 | Esophageal atresia and Beckwith-Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first report. |
| Q35894474 | Expanding the 'central dogma': the regulatory role of nonprotein coding genes and implications for the genetic liability to schizophrenia |
| 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 |
| Q39409666 | GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association |
| Q36025711 | Genetic Determinants of Epigenetic Patterns: Providing Insight into Disease. |
| Q34556925 | Genetic or epigenetic difference causing discordance between monozygotic twins as a clue to molecular basis of mental disorders |
| Q34381971 | Genetic, environmental and stochastic factors in monozygotic twin discordance with a focus on epigenetic differences. |
| Q85927748 | Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromes |
| Q91063421 | Genomic imprinting disorders: lessons on how genome, epigenome and environment interact |
| Q42803489 | Global hypomethylation of the genome in XX embryonic stem cells. |
| Q64260073 | How Does Reprogramming to Pluripotency Affect Genomic Imprinting? |
| Q36669981 | Human metastable epiallele candidates link to common disorders |
| Q34507299 | Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype |
| Q91618948 | Impact of assisted reproduction, infertility, sex and paternal factors on the placental DNA methylome |
| Q84966055 | Imprinted genes and human disease |
| Q42738682 | Imprinting and Promoter Usage of Insulin-Like Growth Factor II in Twin Discordant Placenta |
| Q34845922 | Imprinting disorders and assisted reproductive technology |
| Q84475523 | Imprinting disorders and assisted reproductive technology |
| Q35213638 | Imprinting errors and developmental asymmetry |
| Q34277727 | Imprinting methylation errors in ART. |
| Q55520669 | Infants with Bochdalek diaphragmatic hernia: sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program. |
| Q36143199 | Inheritance pattern of familial moyamoya disease: autosomal dominant mode and genomic imprinting |
| Q36783409 | KCNQ1 and KCNE1 K+ channel components are involved in early left-right patterning in Xenopus laevis embryos |
| Q37378662 | Large offspring syndrome: a bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann. |
| Q34328129 | Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells |
| Q35228795 | Life or death? A physiogenomic approach to understand individual variation in responses to hemorrhagic shock |
| Q35747814 | Long noncoding RNAs in development and cancer: potential biomarkers and therapeutic targets |
| Q35752848 | Longitudinal weight differences, gene expression and blood biomarkers in BMI-discordant identical twins. |
| Q37573814 | Maternal Hypomethylation of KvDMR in a Monozygotic Male Twin Pair Discordant for Beckwith-Wiedemann Syndrome. |
| Q36371745 | Maternal gametic transmission of translocations or inversions of human chromosome 11p15.5 results in regional DNA hypermethylation and downregulation of CDKN1C expression |
| Q53426545 | Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring. |
| Q34075669 | Methyl donor-deficient diet during development can affect fear and anxiety in adulthood in C57BL/6J mice |
| Q34329150 | Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci |
| Q36786517 | Molecular studies of major depressive disorder: the epigenetic perspective |
| Q51688227 | Monozygotic female twins discordant for Silver-Russell syndrome and hypomethylation of the H19-DMR. |
| Q35897276 | Monozygotic twins discordant for constitutive BRCA1 promoter methylation, childhood cancer and secondary cancer |
| Q54661624 | Monozygous triplets discordant for transient neonatal diabetes mellitus and for imprinting of the TNDM differentially methylated region. |
| Q34701653 | Mutational analysis of steroidogenic factor 1 (NR5a1) in 24 boys with bilateral anorchia: a French collaborative study |
| Q61798296 | New insights into the pathogenicity of non-synonymous variants through multi-level analysis |
| 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 |
| Q92072874 | Pervasive Inter-Individual Variation in Allele-Specific Expression in Monozygotic Twins |
| Q48801613 | Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndrome |
| Q37344712 | Reprogramming cells and tissue patterning via bioelectrical pathways: molecular mechanisms and biomedical opportunities |
| Q36172165 | SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletions |
| Q33948170 | Search for genomic alterations in monozygotic twins discordant for cleft lip and/or palate |
| Q24678326 | Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome |
| Q21202882 | Silver-Russell syndrome: genetic basis and molecular genetic testing |
| Q35707619 | Stem cells today: A. Origin and potential of embryo stem cells |
| Q36885699 | Syndromes and disorders associated with omphalocele (I): Beckwith-Wiedemann syndrome |
| Q92932138 | Systemic signalling and local effectors in developmental stability, body symmetry, and size |
| Q36927144 | The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region |
| Q42739122 | Transmembrane voltage potential of somatic cells controls oncogene-mediated tumorigenesis at long-range |
| Q93192447 | Twin Registries Moving Forward and Meeting the Future: A Review |
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| Q54266930 | X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate. |
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