Wolf Reik

Q: What Schools Are Affiliated With Wolf Reik

Wolf Reik is affiliated with the following schools: Kyushu University, University of Cambridge

Wolf Reik's AcademicInfluence.com Rankings

Wolf Reik

Biology

#1224

World Rank

#2082

Historical Rank

Genetics

#263

World Rank

#313

Historical Rank

biology Degrees

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Biology

Why Is Wolf Reik Influential?

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According to Wikipedia, Wolf Reik FRS is a German molecular biologist and a group leader at the Babraham Institute, honorary professor of Epigenetics at the University of Cambridge and associate faculty at the Wellcome Trust Sanger Institute. He was announced as the director of Altos Labs Cambridge Institute when the company launched on 19 January 2022.

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Wolf Reik's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Evolution and Functions of Long Noncoding RNAs (2009) (4485)
Epigenetic Reprogramming in Mammalian Development (2001) (2921)
Genomic imprinting: parental influence on the genome (2001) (2255)
Stability and flexibility of epigenetic gene regulation in mammalian development (2007) (1953)
Epigenetic reprogramming in mammals. (2005) (1336)
The Human Cell Atlas (2017) (1285)
Dynamic reprogramming of DNA methylation in the early mouse embryo. (2002) (1218)
Epigenetic reprogramming in mouse primordial germ cells (2002) (1217)
Dynamic regulation of 5-hydroxymethylcytosine in mouse ES cells and during differentiation (2011) (1105)
Active genes dynamically colocalize to shared sites of ongoing transcription (2004) (1087)
Epigenetic Reprogramming in Plant and Animal Development (2010) (1071)
Active demethylation of the paternal genome in the mouse zygote (2000) (1045)
Placental-specific IGF-II is a major modulator of placental and fetal growth (2002) (1010)
SC3 - consensus clustering of single-cell RNA-Seq data (2016) (981)
Conservation of methylation reprogramming in mammalian development: Aberrant reprogramming in cloned embryos (2001) (977)
Genome-wide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency (2010) (876)
Single-Cell Genome-Wide Bisulfite Sequencing for Assessing Epigenetic Heterogeneity (2014) (840)
Quantitative Sequencing of 5-Methylcytosine and 5-Hydroxymethylcytosine at Single-Base Resolution (2012) (829)
The Dynamics of Genome-wide DNA Methylation Reprogramming in Mouse Primordial Germ Cells (2012) (810)
5-Hydroxymethylcytosine in the mammalian zygote is linked with epigenetic reprogramming. (2011) (752)
Uncovering the role of 5-hydroxymethylcytosine in the epigenome (2011) (710)
Resistance of IAPs to methylation reprogramming may provide a mechanism for epigenetic inheritance in the mouse (2003) (638)
The H19 lincRNA is a developmental reservoir of miR-675 which suppresses growth and Igf1r (2012) (607)
Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops (2004) (585)
Culture of Preimplantation Mouse Embryos Affects Fetal Development and the Expression of Imprinted Genes1 (2001) (579)
Beckwith-Wiedemann syndrome and assisted reproduction technology (ART) (2003) (576)
Resetting Transcription Factor Control Circuitry toward Ground-State Pluripotency in Human (2014) (559)
CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2. (2006) (551)
Parallel single-cell sequencing links transcriptional and epigenetic heterogeneity (2015) (531)
Epigenetic Marking Correlates with Developmental Potential in Cloned Bovine Preimplantation Embryos (2003) (524)
In utero undernourishment perturbs the adult sperm methylome and intergenerational metabolism (2014) (507)
Epigenetic dynamics of stem cells and cell lineage commitment: digging Waddington's canal (2009) (487)
Genomic imprinting determines methylation of parental alleles in transgenic mice (1987) (485)
A single-cell molecular map of mouse gastrulation and early organogenesis (2019) (481)
Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12 (2003) (472)
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. (1999) (455)
Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation (2004) (445)
scNMT-seq enables joint profiling of chromatin accessibility DNA methylation and transcription in single cells (2017) (436)
Dynamic chromatin modifications characterise the first cell cycle in mouse embryos. (2005) (417)
Reprogramming DNA methylation in the mammalian life cycle: building and breaking epigenetic barriers (2013) (409)
Regulation of supply and demand for maternal nutrients in mammals by imprinted genes (2003) (407)
Nanog-dependent function of Tet1 and Tet2 in establishment of pluripotency (2013) (398)
DNA methylation aging clocks: challenges and recommendations (2019) (393)
Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: association with aberrant phenotypes. (1998) (393)
Activation-induced Cytidine Deaminase Deaminates 5-Methylcytosine in DNA and Is Expressed in Pluripotent Tissues (2004) (385)
FGF Signaling Inhibition in ESCs Drives Rapid Genome-wide Demethylation to the Epigenetic Ground State of Pluripotency (2013) (378)
Global Mapping of DNA Methylation in Mouse Promoters Reveals Epigenetic Reprogramming of Pluripotency Genes (2008) (372)
The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery (2016) (360)
Cohesin Is Required for Higher-Order Chromatin Conformation at the Imprinted IGF2-H19 Locus (2009) (356)
DeepCpG: accurate prediction of single-cell DNA methylation states using deep learning (2017) (349)
Epigenetic restriction of embryonic cell lineage fate by methylation of Elf5 (2008) (336)
Transactivation of Igf2 in a mouse model of Beckwith–Wiedemann syndrome (1997) (335)
Methylation levels of maternal and paternal genomes during preimplantation development. (1991) (331)
BLUEPRINT to decode the epigenetic signature written in blood (2012) (320)
Adaptation of nutrient supply to fetal demand in the mouse involves interaction between the Igf2 gene and placental transporter systems. (2005) (310)
Beckwith-Wiedemann syndrome: imprinting in clusters revisited. (2000) (298)
Single-cell epigenomics: Recording the past and predicting the future (2017) (295)
Epigenetic reprogramming in early mammalian development and following somatic nuclear transfer. (2003) (292)
A screen for hydroxymethylcytosine and formylcytosine binding proteins suggests functions in transcription and chromatin regulation (2013) (291)
Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placenta. (2004) (291)
Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene. (1992) (290)
Naive Pluripotent Stem Cells Derived Directly from Isolated Cells of the Human Inner Cell Mass (2016) (289)
Imprinted Genes, Placental Development and Fetal Growth (2006) (288)
Oxidative bisulfite sequencing of 5-methylcytosine and 5-hydroxymethylcytosine (2013) (287)
Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome (2005) (286)
Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes. (1994) (285)
Reprogramming the Methylome: Erasing Memory and Creating Diversity (2014) (282)
Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2. (1997) (277)
Co-evolution of X-chromosome inactivation and imprinting in mammals (2005) (277)
Multi-tissue DNA methylation age predictor in mouse (2017) (270)
Multi-tissue DNA methylation age predictor in mouse (2017) (270)
DNA demethylation by DNA repair. (2009) (266)
Methylome analysis using MeDIP-seq with low DNA concentrations (2012) (258)
Culture of preimplantation embryos and its long-term effects on gene expression and phenotype. (2001) (255)
Single-cell epigenomics: powerful new methods for understanding gene regulation and cell identity (2016) (253)
Resetting Transcription Factor Control Circuitry toward Ground-State Pluripotency in Human (2014) (253)
Data Resource Profile: Accessible Resource for Integrated Epigenomic Studies (ARIES). (2015) (251)
Global Reorganization of the Nuclear Landscape in Senescent Cells (2015) (249)
Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote (2001) (247)
Transgenes as probes for active chromosomal domains in mouse development (1988) (240)
Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome) (2009) (233)
Single-Cell Landscape of Transcriptional Heterogeneity and Cell Fate Decisions during Mouse Early Gastrulation (2017) (232)
Retrovirus integration and chromatin structure: Moloney murine leukemia proviral integration sites map near DNase I-hypersensitive sites (1987) (231)
Epigenetic inheritance in the mouse (1997) (230)
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain. (1995) (230)
Dynamics of the epigenetic landscape during the maternal-to-zygotic transition (2018) (229)
Multi-omics profiling of mouse gastrulation at single cell resolution (2019) (224)
Tracking the embryonic stem cell transition from ground state pluripotency (2016) (221)
The long noncoding RNA Kcnq1ot1 organises a lineage-specific nuclear domain for epigenetic gene silencing (2009) (220)
Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19 (2000) (219)
Placental overgrowth in mice lacking the imprinted gene Ipl (2002) (219)
Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome. (1997) (219)
5-Formylcytosine can be a stable DNA modification in mammals. (2015) (218)
Genome-wide distribution of 5-formylcytosine in embryonic stem cells is associated with transcription and depends on thymine DNA glycosylase (2012) (216)
Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies. (2008) (211)
Dnmt2-dependent methylomes lack defined DNA methylation patterns (2013) (206)
How imprinting centres work (2006) (197)
Epigenetic resetting of human pluripotency (2017) (193)
Efficient targeted DNA methylation with chimeric dCas9–Dnmt3a–Dnmt3L methyltransferase (2016) (193)
Resourceful imprinting (2004) (191)
Establishment of porcine and human expanded potential stem cells (2019) (190)
Imprinting mechanisms. (1998) (189)
DNA methylation and mammalian epigenetics (2001) (188)
Imprinting mechanisms in mammals. (1998) (187)
Epigenetic modifications in an imprinting cluster are controlled by a hierarchy of DMRs suggesting long-range chromatin interactions. (2003) (187)
Adult phenotype in the mouse can be affected by epigenetic events in the early embryo. (1993) (186)
Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians (2008) (181)
Genomic imprinting and genetic disorders in man. (1989) (179)
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome (2000) (178)
Establishment of mouse expanded potential stem cells (2017) (178)
Redundant mechanisms to form silent chromatin at pericentromeric regions rely on BEND3 and DNA methylation. (2014) (173)
Regulation of placental efficiency for nutrient transport by imprinted genes. (2006) (173)
Molecular signatures of plastic phenotypes in two eusocial insect species with simple societies (2015) (172)
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation (1999) (169)
Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia. (2002) (164)
Genome-wide base-resolution mapping of DNA methylation in single cells using single-cell bisulfite sequencing (scBS-seq) (2017) (163)
An intragenic methylated region in the imprinted Igf2 gene augments transcription (2001) (160)
Comparison of whole-genome bisulfite sequencing library preparation strategies identifies sources of biases affecting DNA methylation data (2017) (155)
An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype. (2003) (155)
Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting. (2000) (154)
Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome (2003) (154)
Dietary restriction protects from age-associated DNA methylation and induces epigenetic reprogramming of lipid metabolism (2017) (153)
Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human. (2006) (151)
MERVL/Zscan4 Network Activation Results in Transient Genome-wide DNA Demethylation of mESCs (2016) (148)
Selective impairment of methylation maintenance is the major cause of DNA methylation reprogramming in the early embryo (2015) (146)
Structural differences in centromeric heterochromatin are spatially reconciled on fertilisation in the mouse zygote (2007) (145)
Overexpression of insulin-like growth factor-II in transgenic mice is associated with pancreatic islet cell hyperplasia. (1999) (144)
Impairment of DNA Methylation Maintenance Is the Main Cause of Global Demethylation in Naive Embryonic Stem Cells (2016) (143)
Promoter DNA methylation couples genome-defence mechanisms to epigenetic reprogramming in the mouse germline (2012) (141)
Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse. (2000) (141)
Mice Deficient in APOBEC2 and APOBEC3 (2005) (129)
Ageing affects DNA methylation drift and transcriptional cell-to-cell variability in mouse muscle stem cells (2018) (129)
Retinol and ascorbate drive erasure of epigenetic memory and enhance reprogramming to naïve pluripotency by complementary mechanisms (2016) (128)
Mammalian epigenomics: reprogramming the genome for development and therapy. (2003) (127)
Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. (1998) (125)
Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome. (1997) (121)
Dppa2 and Dppa4 directly regulate the Dux-driven zygotic transcriptional program (2018) (121)
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway. (1996) (120)
Single cell transcriptome analysis of human, marmoset and mouse embryos reveals common and divergent features of preimplantation development (2018) (118)
Impairment of DNA Methylation Maintenance Is the Main Cause of Global Demethylation in Naive Embryonic Stem Cells (2016) (113)
Conceptual links between DNA methylation reprogramming in the early embryo and primordial germ cells. (2013) (111)
Genome-wide Bisulfite Sequencing in Zygotes Identifies Demethylation Targets and Maps the Contribution of TET3 Oxidation (2014) (110)
Fetal growth restriction: a workshop report. (2004) (109)
Igf2 imprinting in development and disease. (2000) (108)
Transgenes as molecular probes for genomic imprinting. (1988) (108)
An upstream repressor element plays a role in Igf2 imprinting (2001) (107)
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans. (1997) (107)
Epigenetic asymmetry in the mammalian zygote and early embryo: relationship to lineage commitment? (2003) (106)
Maternal DNA Methylation Regulates Early Trophoblast Development (2016) (105)
Genomic imprinting: Silence across the border (2000) (105)
Active demethylation in mouse zygotes involves cytosine deamination and base excision repair (2013) (102)
Genetic conflict in early development: parental imprinting in normal and abnormal growth. (1996) (97)
Evaluation of epigenetic marks in human embryos derived from IVF and ICSI. (2010) (97)
Epigenetic dynamics of the Kcnq1 imprinted domain in the early embryo (2006) (97)
Frequent RASSF1A tumour suppressor gene promoter methylation in Wilms' tumour and colorectal cancer (2002) (97)
Instability of long inverted repeats within mouse transgenes. (1996) (94)
Comparative Principles of DNA Methylation Reprogramming during Human and Mouse In Vitro Primordial Germ Cell Specification (2016) (94)
Methylation analysis on individual chromosomes: improved protocol for bisulphite genomic sequencing. (1994) (92)
Transcriptional Heterogeneity in Naive and Primed Human Pluripotent Stem Cells at Single-Cell Resolution (2019) (92)
DNA methylation homeostasis in human and mouse development. (2017) (91)
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome. (1997) (91)
Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome. (1994) (89)
LifeTime and improving European healthcare through cell-based interceptive medicine (2020) (87)
Dynamic methylation adjustment and counting as part of imprinting mechanisms. (1996) (87)
Replication-competent Moloney murine leukemia virus carrying a bacterial suppressor tRNA gene: selective cloning of proviral and flanking host sequences. (1985) (84)
Genomic imprinting and embryonal tumours (1989) (83)
Imprinting by DNA methylation: from transgenes to endogenous gene sequences. (1990) (82)
Developmental consequences of imprinting of parental chromosomes by DNA methylation. (1990) (82)
Germline and Pluripotent Stem Cells. (2015) (81)
The H3K9 dimethyltransferases EHMT1/2 protect against pathological cardiac hypertrophy (2017) (81)
Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans (2005) (81)
Integration of spatial and single-cell transcriptomic data elucidates mouse organogenesis (2021) (78)
Cold-induced epigenetic programming of the sperm enhances brown adipose tissue activity in the offspring (2018) (77)
FGF signalling inhibition in ESCs drives rapid genome-wide demethylation to the epigenetic ground state of pluripotency (2013) (76)
Safeguarding parental identity: Dnmt1 maintains imprints during epigenetic reprogramming in early embryogenesis. (2008) (75)
Forget the Parents: Epigenetic Reprogramming in Human Germ Cells (2015) (74)
The non-canonical SMC protein SmcHD1 antagonises TAD formation and compartmentalisation on the inactive X chromosome (2019) (73)
Systematic elimination of parthenogenetic cells in mouse chimeras. (1989) (72)
Active turnover of DNA methylation during cell fate decisions (2020) (72)
Accurate prediction of single-cell DNA methylation states using deep learning (2016) (68)
Genome-Scale Oscillations in DNA Methylation during Exit from Pluripotency (2018) (67)
Incomplete methylation reprogramming in SCNT embryos (2012) (63)
In vivo genome-wide profiling reveals a tissue-specific role for 5-formylcytosine (2016) (62)
Genomic imprinting: a possible mechanism for the parental origin effect in Huntington's chorea. (1988) (62)
Direct sequencing of small genomes on the Pacific Biosciences RS without library preparation. (2012) (61)
Developmental adaptations to increased fetal nutrient demand in mouse genetic models of Igf2‐mediated overgrowth (2011) (61)
5-Formylcytosine organizes nucleosomes and forms Schiff base interactions with histones in mouse embryonic stem cells (2018) (60)
Influence of germline modifications of homologous chromosomes on mouse development. (1986) (60)
Imprinted genes and the coordination of fetal and postnatal growth in mammals. (2001) (60)
Proliferation Drives Aging-Related Functional Decline in a Subpopulation of the Hematopoietic Stem Cell Compartment (2017) (59)
Shifting behaviour: epigenetic reprogramming in eusocial insects. (2012) (59)
Epigenetic targeting in the mouse zygote marks DNA for later methylation: a mechanism for maternal effects in development (2001) (59)
Combined single-cell profiling of expression and DNA methylation reveals splicing regulation and heterogeneity (2018) (57)
The Human Cell Atlas White Paper (2018) (55)
Environmental effects on genomic imprinting in mammals. (2001) (55)
Screening for genes that accelerate the epigenetic aging clock in humans reveals a role for the H3K36 methyltransferase NSD1 (2019) (54)
An endosiRNA-Based Repression Mechanism Counteracts Transposon Activation during Global DNA Demethylation in Embryonic Stem Cells (2017) (53)
Epigenetic reprogramming: Back to the beginning (2002) (53)
Gender Differences in Global but Not Targeted Demethylation in iPSC Reprogramming (2017) (51)
Genomic imprinting and cancer; new paradigms in the genetics of neoplasia. (2001) (51)
Multi-omic rejuvenation of human cells by maturation phase transient reprogramming (2021) (47)
Genomic Imprinting Controls Matrix Attachment Regionsin the Igf2Gene (2003) (47)
Processive DNA Demethylation via DNA Deaminase-Induced Lesion Resolution (2014) (46)
Non‐coding transcripts in the H19 imprinting control region mediate gene silencing in transgenic Drosophila (2007) (45)
DNA demethylases: a new epigenetic frontier in drug discovery. (2011) (45)
Robust 3D DNA FISH Using Directly Labeled Probes (2013) (42)
Raised Late Pregnancy Glucose Concentrations in Mice Carrying Pups With Targeted Disruption of H19Δ13 (2009) (41)
Regulation of Lineage Specific DNA Hypomethylation in Mouse Trophectoderm (2013) (41)
A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA (2007) (40)
Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions (2020) (40)
Coupling shRNA screens with single-cell RNA-seq identifies a dual role for mTOR in reprogramming-induced senescence (2017) (40)
Disruption of mesodermal enhancers for Igf2 in the minute mutant. (2002) (39)
Genomic imprinting: Making sense or antisense? (1997) (38)
Dissecting de novo methylation (1999) (38)
A Hox-Embedded Long Noncoding RNA: Is It All Hot Air? (2016) (38)
Analysis of polysulfate-binding domains in porcine proacrosin, a putative zona adhesion protein from mammalian spermatozoa. (1995) (37)
Transgenerational transmission of hedonic behaviors and metabolic phenotypes induced by maternal overnutrition (2018) (36)
Age at onset in Huntington's disease and methylation at D4S95. (1993) (35)
A Single-Cell Transcriptomics CRISPR-Activation Screen Identifies Epigenetic Regulators of the Zygotic Genome Activation Program (2020) (35)
Silencing of CDKN 1 C ( p 57 KIP 2 ) is associated with hypomethylation at KvDMR 1 in Beckwith – Wiedemann syndrome (2003) (35)
Tandem Repeat Hypothesis in Imprinting: Deletion of a Conserved Direct Repeat Element Upstream of H19 Has No Effect on Imprinting in the Igf2-H19 Region (2004) (35)
Provision of the immunoglobulin heavy chain enhancer downstream of a test gene is sufficient to confer lymphoid‐specific expression in transgenic mice (1987) (34)
Analysis of germline CDKN 1 C ( p 57 KIP 2 ) mutations in familial and sporadic Beckwith-Wiedemann syndrome ( BWS ) provides a novel genotype-phenotype correlation (1999) (33)
Chromatin structure and imprinting: developmental control of DNase-I sensitivity in the mouse insulin-like growth factor 2 gene. (1995) (32)
DNA methylation repels binding of hypoxia-inducible transcription factors to maintain tumor immunotolerance (2020) (31)
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA. (2003) (30)
TET3 prevents terminal differentiation of adult NSCs by a non-catalytic action at Snrpn (2019) (28)
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster. (2000) (28)
Faculty Opinions recommendation of Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. (2006) (28)
The inheritance of germline-specific epigenetic modifications during development. (1993) (27)
Epigenetic priming by Dppa2 and 4 in pluripotency facilitates multi-lineage commitment (2020) (27)
Genetic conflict and evolution of mammalian X-chromosome inactivation. (1995) (26)
The Ageing Brain: Effects on DNA Repair and DNA Methylation in Mice (2017) (26)
The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster (2005) (26)
8C-like cells capture the human zygotic genome activation program in vitro (2022) (25)
Distinct Molecular Trajectories Converge to Induce Naive Pluripotency (2019) (25)
Chromosome loops, insulators, and histone methylation: new insights into regulation of imprinting in clusters. (2004) (25)
Pairing of Homologous Regions in the Mouse Genome Is Associated with Transcription but Not Imprinting Status (2012) (25)
Tet3 ablation in adult brain neurons increases anxiety-like behavior and regulates cognitive function in mice (2020) (25)
Multi‐omic rejuvenation of naturally aged tissues by a single cycle of transient reprogramming (2022) (24)
Defective germline reprogramming rewires the spermatogonial transcriptome (2018) (23)
Tet3 regulates cellular identity and DNA methylation in neural progenitor cells (2019) (23)
Analysis and identification of imprinted genes. (1998) (22)
Replication Timing Properties within the Mouse Distal Chromosome 7 Imprinting Cluster (2002) (22)
The Wellcome Prize Lecture. Genetic imprinting: the battle of the sexes rages on (1996) (21)
Highly multiplexed spatially resolved gene expression profiling of mouse organogenesis (2020) (20)
Amniogenesis occurs in two independent waves in primates (2022) (19)
Nucleotide sequence of a 28-kb mouse genomic region comprising the imprinted Igf2 gene. (1996) (18)
Gene expression: Silent clones speak up (2003) (18)
Erratum to: DeepCpG: accurate prediction of single-cell DNA methylation states using deep learning (2017) (18)
Developmental biology: The X-inactivation yo-yo (2005) (17)
A MILI-independent piRNA biogenesis pathway empowers partial germline reprogramming (2017) (16)
Imprinting in leukaemia (1992) (16)
Epigenetics: Cellular memory erased in human embryos (2014) (16)
Generation of monoparental embryos for investigation into genomic imprinting. (2001) (16)
Retrotransposons and germ cells: reproduction, death, and diversity (2010) (16)
Spatial profiling of early primate gastrulation in utero (2022) (14)
Genomic Imprinting: Imprinting with and without methylation (1994) (14)
Mutation analysis of H19 andNAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome (2000) (14)
Imprint switch mechanism indicated by mutations in Prader-Willi and Angelman syndromes. (1997) (14)
Silencing of CDKN1C ( p57 KIP2 ) is associated with hypomethylation at KvDMR1 in Beckwith–Wiedemann syndrome (2003) (14)
A single-cell molecular map of mouse gastrulation and early organogenesis (2019) (14)
Transcriptome and epigenome diversity and plasticity of muscle stem cells following transplantation (2020) (13)
Genomic imprinting and cancer. (1990) (13)
Enhancer-associated H3K4 methylation safeguards in vitro germline competence (2021) (13)
CpG methylation of an X-linked transgene is determined by somatic events postfertilization and not germline imprinting. (1988) (13)
Cancer genetics. Genomic imprinting and embryonal tumours. (1989) (13)
Single cell multi-omics profiling reveals a hierarchical epigenetic landscape during mammalian germ layer specification (2019) (13)
Decoding gene regulation in the mouse embryo using single-cell multi-omics (2022) (12)
A dominant modifier of transgene methylation is mapped by QTL analysis to mouse chromosome 13. (2001) (12)
The non-canonical SMC protein SmcHD1 antagonises TAD formation and compartmentalisation on the inactive X chromosome (2019) (11)
Chromosomal localization of human homologs of the Drosophila heterochromatin protein 1 (HP1) gene (2004) (11)
Regulation of Igf2 imprinting in development and disease. (1996) (10)
Mapping of a mouse homolog of a Heterochromatin protein gene to the X Chromosome (1991) (10)
Imprinting with and without methylation (1994) (10)
Genomic imprinting in the mouse. (1989) (10)
Author response: The Human Cell Atlas (2017) (10)
Maternal Dppa2 and Dppa4 are dispensable for zygotic genome activation but important for offspring survival (2021) (9)
Nucleus replacement in Mammalian oocytes. (2002) (9)
Retrovirus Integration andChromatin Structure: Moloney MurineLeukemia Proviral Integration Sites MapNear DNaseI-Hypersensitive Sites (1987) (8)
Placental-specific Igf-2 regulates the diffusional exchange characteristics of the mouse placenta (2004) (8)
cuRRBS: simple and robust evaluation of enzyme combinations for reduced representation approaches (2017) (8)
Genomic Imprinting and Modifier Genes in the Mouse (1996) (8)
Hepatic gene body hypermethylation is a shared epigenetic signature of murine longevity (2018) (8)
The need for Eed (2003) (8)
Prmt5: a guardian of the germline protects future generations (2015) (7)
Correction: Epigenetic resetting of human pluripotency (doi:10.1242/dev.146811) (2018) (7)
Enhancer priming by H3K4 methylation safeguards germline competence (2020) (7)
Single-cell multi-omics profiling links dynamic DNA methylation to cell fate decisions during mouse early organogenesis (2022) (7)
Integration of spatial and single-cell transcriptomic data elucidates mouse organogenesis (2021) (7)
Reprogramming by cell fusion: boosted by Tets. (2013) (7)
Publisher Correction: LifeTime and improving European healthcare through cell-based interceptive medicine (2021) (7)
A novel strategy to identify maternal and paternal inheritance in the mouse (1995) (7)
Histone modifications form a cell-type-specific chromosomal bar code that persists through the cell cycle (2021) (6)
Back to the beginning. (2002) (6)
Immunoglobulin Gene Expression (1988) (6)
Voices in methods development (2019) (6)
Artificial sperm and epigenetic reprogramming (2006) (6)
Genomic imprinting in mammals. (1992) (5)
Analysis of parent-specific gene expression in early mouse embryos and embryonic stem cells using high-resolution two-dimensional electrophoresis of proteins. (1996) (5)
Increased Placental Glucose Transport Rates in Pregnant Mice Carrying Fetuses with Targeted Disruption of Their Placental-Specific Igf2 Transcripts Are Not Associated with Raised Circulating Glucose Concentrations (2011) (5)
Early malnutrition and programming of adult degenerative diseases: experimental, epidemiological and preventive studies. (2001) (5)
Comparative Principles of DNA Methylation Reprogramming during Human and Mouse In Vitro Primordial Germ Cell Specification (2022) (4)
Cold-induced epigenetic programming of the sperm enhances brown adipose tissue activity in the offspring (2018) (4)
Genome-wide distribution of 5-formylcytosine in embryonic stem cells is associated with transcription and depends on thymine DNA glycosylase (2012) (4)
Etoposide Induces Nuclear Re-Localisation of AID (2013) (4)
5-Formylcytosine controls nucleosome positioning through covalent histone-DNA interaction (2017) (4)
DNA Methylation Repels Binding of HIF Transcription Factors to Maintain Tumour Immunotolerance (2020) (3)
The Epigenomic Landscape of Reprogramming in Mammals (2009) (3)
Modelling human zygotic genome activation in 8C-like cells in vitro (2021) (3)
lgf 2 imprinting 145 Igf 2 imprinting in development and disease (2000) (3)
Genomicimprinting: a possible mechanism forthe parental origin effect inHuntington's chorea (1988) (2)
The non-canonical SMC protein SmcHD1 antagonises TAD formation on the inactive X chromosome (2018) (2)
A single-cell transcriptomics CRISPR-activation screen identifies new epigenetic regulators of zygotic genome activation (2019) (2)
Conserved and divergent features of DNA methylation in embryonic stem cell-derived neurons (2020) (2)
Single-cell transcriptome analysis of human, marmoset and mouse embryos reveals common and divergent features of preimplantation development (2018) (2)
What the papers say. Imprintor or imprinted (1992) (2)
Publisher Correction: Cold-induced epigenetic programming of the sperm enhances brown adipose tissue activity in the offspring (2018) (2)
Establishment in Culture of Expanded Potential Stem Cells (2017) (2)
Mapping of two human homologs of a Drosophila heterochromatin protein gene to the X Chromosome (2004) (2)
Dppa2/4 target chromatin bivalency enabling multi-lineage commitment (2019) (2)
Selective impairment of methylation maintenance is the major cause of DNA methylation reprogramming in the early embryo (2015) (2)
Specialisation and plasticity in a primitively social insect (2020) (1)
Combined single-cell profiling of expression and DNA methylation reveals splicing regulation and heterogeneity (2019) (1)
Faculty Opinions recommendation of Epigenetic Variation between Human Induced Pluripotent Stem Cell Lines Is an Indicator of Differentiation Capacity. (2016) (1)
Comparison of whole-genome bisulfite sequencing library preparation strategies identifies sources of biases affecting DNA methylation data (2018) (1)
In vivo genome-wide profiling reveals a tissue-specific role for 5-formylcytosine (2016) (1)
Author ' s personal copy DNA demethylation by DNA repair (2009) (1)
scNMT-seq enables joint profiling of chromatin accessibility DNA methylation and transcription in single cells (2018) (1)
Cancer genetics. Imprinting in leukaemia. (1992) (1)
Self-organization of plasticity and specialization in a primitively social insect (2022) (1)
Correction to: Comparison of whole-genome bisulfite sequencing library preparation strategies identifies sources of biases affecting DNA methylation data (2019) (1)
Cbx-rs2 (M31), a mouse homolog of the Drosophila Heterochromatin protein 1 gene, maps to distal Chromosome 11 and is nonallelic to Om (1995) (1)
Dynamics of the epigenetic landscape during the maternal-to-zygotic transition (2018) (1)
1 2 3 DNA Demethylation by DNA Repair 4 5 (2011) (1)
LifeTime and improving European healthcare through cell-based interceptive medicine (2020) (1)
Single cell DNA methylation ageing in mouse blood (2023) (1)
Single-cell multi-omics of human preimplantation embryos shows susceptibility to glucocorticoids (2022) (1)
Inter-gastruloid heterogeneity revealed by single cell transcriptomics time course: implications for organoid based perturbation studies (2022) (1)
Author Correction: Cold-induced epigenetic programming of the sperm enhances brown adipose tissue activity in the offspring (2018) (1)
The Biology and Genomic Localization of Cytosine Modifications (2015) (1)
Inference of emergent spatio-temporal processes from single-cell sequencing reveals feedback between de novo DNA methylation and chromatin condensates (2021) (1)
Parental imprinting and epigenetic programming of the mouse genome: long lasting consequences for development and phenotype (1993) (1)
Correction to: Tet3 regulates cellular identity and DNA methylation in neural progenitor cells (2020) (1)
Active demethylation in mouse zygotes involves cytosine deamination and base excision repair (2013) (1)
A comprehensive approach for genome-wide efficiency profiling of DNA modifying enzymes (2022) (1)
O-107. Genomic imprinting in normal and abnormal development (1997) (1)
Multi-tissue DNA methylation age predictor in mouse (2017) (1)
A screen for hydroxymethylcytosine and formylcytosine binding proteins suggests functions in transcription and chromatin regulation (2013) (1)
Wolf Reik: Inheritance beyond DNA. Interview by Nicole Lebrasseur. (2010) (1)
Multi-tissue DNA methylation age predictor in mouse (2017) (1)
A non-catalytic role of TET3 promotes open chromatin and enhances global transcription (2017) (1)
IMPRINTING AND EPIGENETIC REPROGRAMMING IN MAMMALIAN DEVELOPMENT (2004) (1)
Mitigating age-related somatic mutation burden. (2023) (0)
Subject Index Vol. 65, Suppl. 3, 2006 (2006) (0)
Replication-competent Moloney mu bacterial suppressor tRNA gene: S and flanking host sequences (2016) (0)
Epigenetic regulation of imprinting, reprogramming, and lineage commitment in mammals (2010) (0)
Method for controlling an automated friction clutch acting between a drive motor and a transmission apparatus for implementing the method and regulation associated with a friction clutch (1990) (0)
Single-cell epigenomics: powerful new methods for understanding gene regulation and cell identity (2016) (0)
Michael John Owen Wakelam 1955–2020 (2020) (0)
Convergent phenotypes but non-convergent genomes in simple social insect societies (2014) (0)
University of Birmingham Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome) (2009) (0)
Faculty Opinions recommendation of Guidelines and techniques for the generation of induced pluripotent stem cells. (2009) (0)
Reduced hippocampal ten-eleven translocation 3 (Tet3) protein expression in Tet3 conditional knockout mice (2021) (0)
Driving train for a motor vehicle having an electric motor used as a motor and as a generator. (1999) (0)
mounting unit to compensate for jolts in the rotational movement of a motor (1996) (0)
TET3 prevents terminal differentiation of adult NSCs by a non-catalytic action at Snrpn (2019) (0)
Defective germline reprogramming rewires the spermatogonial transcriptome (2018) (0)
Clutch and gear actuator (1996) (0)
Dietary restriction protects from age-associated DNA methylation and induces epigenetic reprogramming of lipid metabolism (2017) (0)
Double-mass flywheel and clutch assembly (1994) (0)
The regulation mechanism of the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12 (2003) (0)
Genome wide efficiency profiling reveals modulation of maintenance and de novo methylation by Tets (2020) (0)
A method for cooling a liquid-cooled friction clutch, as well as liquid-cooled friction clutch (2006) (0)
mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation (1999) (0)
P.1.a.034 Role of Ten-Eleven Translocation 3 (TET3) in brain function (2017) (0)
NpgRj_ng_1423 1065..1071 (2004) (0)
Dispositif d'actionnement d'un embrayage et d'une transmission (1996) (0)
Methylation of H3K9 by G9a/GLP protects against pathological cardiac hypertrophy (2016) (0)
Electrical Motor in the Drive Train : Professional Article (2000) (0)
Erratum to: DeepCpG: accurate prediction of single-cell DNA methylation states using deep learning (2017) (0)
Mechanism to dampen oscillations in rotation, in particular in motor vehicles (1986) (0)
DNA methylation repels binding of hypoxia-inducible transcription factors to maintain tumor immunotolerance (2020) (0)
Split flywheel for internal combustion engines (1986) (0)
Means for compensating for drehstoessen (1984) (0)
Embryonic Stem Cell-Derived Neurons as a Model System for Epigenome Maturation during Development (2023) (0)
Control of fetal growth by genomic imprinting (1999) (0)
Erratum: Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans (Proceedings of the National Academy of Sciences of the USA (September 16, 1997) 19 (10243-10248)) (1997) (0)
Vibration damper door by an engine crankshaft piston (2003) (0)
Motor vehicle with a clutch mechanism and a box of automatic or manual transmission (2001) (0)
ROTOR FOR AN ELECTRIC MOTOR, ELECTRIC MOTOR AND METHOD FOR PRODUCING AN ELECTRIC MOTOR (2018) (0)
Active turnover of DNA methylation during cell fate decisions (2020) (0)
CTCF binding at the H19 ICR imparts maternally-inherited higher order chromatin conformations and regional epigenotype to restrict enhancer access to Igf2 (2006) (0)
Faculty Opinions recommendation of TET-mediated DNA demethylation controls gastrulation by regulating Lefty-Nodal signalling. (2016) (0)
Belt drive with translation switched by a lever actuator (2011) (0)
Publisher Correction: LifeTime and improving European healthcare through cell-based interceptive medicine (2021) (0)
Volume contents (2001) (0)
of reduction mechanism has smoothly rotated to internal combustion engines and method of manufacturing such a mechanism (1995) (0)
A Conversation with Wolf Reik. (2015) (0)
Dynamic reorganization of pericentromeric and centromeric satellite repeats in the early mouse embryo (2008) (0)
Single-cell bisulfite sequencing of spermatozoa from lean and obese humans reveals potential for the transmission of epimutations (2021) (0)
Device for compensating for jolts in the rotational movement of a motor (1984) (0)
Faculty Opinions recommendation of An interactive three-dimensional digital atlas and quantitative database of human development. (2016) (0)
Setting the epigenetic stage for differentiation: a collective phenomenon (2019) (0)
Device for compensating rotary impact (1994) (0)
Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions (2020) (0)
Flywheel divided for internal combustion engines. (1995) (0)
Means for hydraulic control of gas exchange valves of an internal combustion piston engine (2006) (0)
Development Epigenetic Reprogramming in Mammalian (2010) (0)
DeepCpG: accurate prediction of single-cell DNA methylation states using deep learning (2017) (0)
Genome-Scale Oscillation s in DNA Methylation during Exit from Pluripotency Graphical (2018) (0)
Correction to: Comparison of whole-genome bisulfite sequencing library preparation strategies identifies sources of biases affecting DNA methylation data (2019) (0)
Faculty Opinions recommendation of Human nuclear Dicer restricts the deleterious accumulation of endogenous double-stranded RNA. (2014) (0)
A method of controlling an effective between a drive engine and a transmission automated friction clutch (1990) (0)
A torque transmission (2002) (0)
Dynamic DNA methylation turnover at the exit of pluripotency epigenetically primes gene regulatory elements for hematopoietic lineage specification (2023) (0)
Maternal-Fetal Nutrition during Pregnancy and Lactation: Nutrition, environment, and epigenetics (2010) (0)
Genomic Imprinting at the Transcriptional Level (2006) (0)
Have you seen ? Prmt 5 : a guardian of the germline protects future generations (2015) (0)
Faculty Opinions recommendation of 5-hmC-mediated epigenetic dynamics during postnatal neurodevelopment and aging. (2012) (0)
Multi-omics profiling of mouse gastrulation at single-cell resolution (2019) (0)
Method for producing a damping device of angular oscillations (1987) (0)
Region Igf 2H 19 Imprinting in the Has No Effect on H 19 Element Upstream of Deletion of a Conserved Direct Repeat Tandem Repeat Hypothesis in Imprinting : (2004) (0)
Contents Vol. 113, 2006 (2006) (0)
A reduction of jolts torsional (1997) (0)
Coupling with a freewheeling clutch disc-containing (2013) (0)
Method and apparatus for controlling a motor vehicle crew of a gearbox (1999) (0)
Means for damping vibrations (1987) (0)
Document S1. Figure S1, Figure S2, Figure S3, Figure S4, Figure S5, Figure S6, Figure S7, Figure S8, Supplemental Experimental Procedures, and Supplemental References (2012) (0)
Establishment of porcine and human expanded potential stem cells (2019) (0)
Mechanisms of imprinting and epigenetic reprogramming in mammalian development (2008) (0)
Faculty Opinions recommendation of The obesity-associated FTO gene encodes a 2-oxoglutarate-dependent nucleic acid demethylase. (2008) (0)
Mechanism to compensate for jolts in rotation, particularly in internal combustion engines. (1986) (0)
The blueprint of primate preimplantation development (2017) (0)
Table S5. CGI Promoters with >25% Methylation in E11.5 PGC, Relates to Figure 3 (2012) (0)
Powertrain and method for controlling and / or regulating a powertrain (2003) (0)
Variation in behaviour plasticity by distinct regulation of the brain methylome (2014) (0)
Histone modifications form a cell-type-specific chromosomal bar code that modulates and maintains patterns of gene expression through the cell cycle (2020) (0)
Table S1. Details for all Illumina Sequencing Runs, Relates to Figure 1 (2012) (0)
Faculty Opinions recommendation of PGC7/Stella protects against DNA demethylation in early embryogenesis. (2007) (0)
Actuating device for vehicles including (1996) (0)
A variable valve drive of an internal combustion engine (2004) (0)
Rotational shock-reducing device (1986) (0)
Drive train with a vibration isolation device (2015) (0)
Imprintor or Imprinted? (1992) (0)
Pooled CRISPR-activation screening coupled with single-cell RNA-seq in mouse embryonic stem cells (2021) (0)
DNMT3A binds ubiquitinated histones to regulate bivalent genes (2022) (0)
Damper with centrifugal pendulum (2009) (0)
Publisher Correction: Cold-induced epigenetic programming of the sperm enhances brown adipose tissue activity in the offspring (2018) (0)
Author Correction: Cold-induced epigenetic programming of the sperm enhances brown adipose tissue activity in the offspring (2018) (0)
Piston engine torsional vibration damper as well as torsional vibration damper for a piston engine. (1998) (0)
Flywheel starter ring (2009) (0)
Method for controlling and / or setting up of a gearbox strategy and reporting changes to a gearbox (2003) (0)
DNA methylation aging clocks: challenges and recommendations (2019) (0)
The distinct effects of MEK and GSK3 inhibition upon the methylome and transcriptome of mouse embryonic stem cells (2021) (0)
World of hybrids – A difficult choice (2006) (0)
Epigenetic Reprogramming of 5-meC via DNA Deamination and DNA Repair (2008) (0)
Method for controlling an automatic friction clutch (1990) (0)
Actuator with a load torque lock (2008) (0)

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