Anne Ferguson-Smith

Anne Ferguson-Smith's AcademicInfluence.com Rankings

Anne Ferguson-Smith

Biology

#5377

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#7840

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Genetics

#636

World Rank

#720

Historical Rank

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Biology

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According to Wikipedia, Anne Carla Ferguson-Smith is a mammalian developmental geneticist. She is the Arthur Balfour Professor of Genetics and Pro-Vice Chancellor for Research and International Partnerships at the University of Cambridge. Formerly head of the Department of Genetics at the University of Cambridge, she is a Fellow of Darwin College, Cambridge and serves as President of the Genetics Society.

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Anne Ferguson-Smith'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

Placental-specific IGF-II is a major modulator of placental and fetal growth (2002) (1010)
The Air Noncoding RNA Epigenetically Silences Transcription by Targeting G9a to Chromatin (2008) (947)
Distinct fibroblast lineages determine dermal architecture in skin development and repair (2013) (829)
Genomic imprinting: the emergence of an epigenetic paradigm (2011) (598)
Comparative developmental anatomy of the murine and human definitive placentae. (2002) (595)
A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints. (2008) (592)
Parental origin of sequence variants associated with complex diseases (2009) (573)
A large imprinted microRNA gene cluster at the mouse Dlk1-Gtl2 domain. (2004) (513)
In utero undernourishment perturbs the adult sperm methylome and intergenerational metabolism (2014) (507)
Mammalian genomic imprinting. (2011) (474)
Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12 (2003) (472)
Parental-origin-specific epigenetic modification of the mouse H19 gene (1993) (437)
Mechanisms regulating imprinted genes in clusters. (2007) (420)
Regulation of supply and demand for maternal nutrients in mammals by imprinted genes (2003) (407)
Genomic imprinting at the mammalian Dlk1-Dio3 domain. (2008) (383)
Imprinting and the Epigenetic Asymmetry Between Parental Genomes (2001) (369)
The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery (2016) (360)
Imprinted microRNA genes transcribed antisense to a reciprocally imprinted retrotransposon-like gene (2003) (349)
RNAi-Mediated Allelic trans-Interaction at the Imprinted Rtl1/Peg11 Locus (2005) (335)
Embryological and molecular investigations of parental imprinting on mouse chromosome 7 (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)
Considerations when investigating lncRNA function in vivo (2014) (307)
Trim28 Is Required for Epigenetic Stability During Mouse Oocyte to Embryo Transition (2012) (298)
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)
Intergenerational Transmission of Glucose Intolerance and Obesity by In Utero Undernutrition in Mice (2009) (284)
Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes (2008) (283)
DNA methylation in genomic imprinting, development, and disease (2001) (282)
Transgenerational inheritance: Models and mechanisms of non–DNA sequence–based inheritance (2016) (269)
Transgenerational epigenetic inheritance: how important is it? (2013) (268)
Developmental Dynamics of the Definitive Mouse Placenta Assessed by Stereology1 (2004) (260)
Quantitative comparison of DNA methylation assays for biomarker development and clinical applications (2016) (251)
Genomic Imprinting and Physiological Processes in Mammals (2019) (250)
Postnatal loss of Dlk1 imprinting in stem cells and niche-astrocytes regulates neurogenesis (2011) (249)
Imprinted genes in the placenta--a review. (2005) (235)
Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2-H19. (2002) (231)
Mutation in Folate Metabolism Causes Epigenetic Instability and Transgenerational Effects on Development (2013) (228)
Delta-like and Gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12 (2000) (219)
Epigenetic regulation of the neural transcriptome: the meaning of the marks (2010) (218)
Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region. (2002) (213)
The IG-DMR and the MEG3-DMR at Human Chromosome 14q32.2: Hierarchical Interaction and Distinct Functional Properties as Imprinting Control Centers (2010) (202)
Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12. (2000) (173)
Epigenetic status of human embryonic stem cells (2005) (170)
The Evolution of the DLK1-DIO3 Imprinted Domain in Mammals (2008) (166)
Genome imprinting and development in the mouse. (1990) (165)
Temporal and spatial regulation of H19 imprinting in normal and uniparental mouse embryos. (1995) (159)
The mouse Gtl2 gene is differentially expressed during embryonic development, encodes multiple alternatively spliced transcripts, and may act as an RNA (1998) (158)
Uniparental disomy and human disease: An overview (2010) (154)
High-frequency generation of viable mice from engineered bi-maternal embryos (2007) (149)
Trim28 Haploinsufficiency Triggers Bi-stable Epigenetic Obesity (2016) (149)
Epigenetic Mechanisms of Transmission of Metabolic Disease across Generations. (2017) (149)
Genomic imprinting, growth control and the allocation of nutritional resources: consequences for postnatal life. (2007) (137)
Regional localization of the interferon-beta 2/B-cell stimulatory factor 2/hepatocyte stimulating factor gene to human chromosome 7p15-p21. (1988) (134)
The Dlk1-Gtl2 Locus Preserves LT-HSC Function by Inhibiting the PI3K-mTOR Pathway to Restrict Mitochondrial Metabolism. (2016) (133)
Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour (2005) (132)
Acclimatization of skeletal muscle mitochondria to high‐altitude hypoxia during an ascent of Everest (2012) (132)
Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expression (2015) (131)
Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region. (2001) (129)
Status of genomic imprinting in human embryonic stem cells as revealed by a large cohort of independently derived and maintained lines. (2007) (127)
Human chromosome 7 carries the beta 2 interferon gene. (1986) (126)
Roles for genomic imprinting and the zygotic genome in placental development (2001) (125)
An obesogenic diet during mouse pregnancy modifies maternal nutrient partitioning and the fetal growth trajectory (2013) (123)
Genomic Imprinting Contributes to Thyroid Hormone Metabolism in the Mouse Embryo (2002) (122)
Sixteen diverse laboratory mouse reference genomes define strain specific haplotypes and novel functional loci (2018) (122)
An Unbiased Assessment of the Role of Imprinted Genes in an Intergenerational Model of Developmental Programming (2012) (117)
High-resolution map and imprinting analysis of the Gtl2-Dnchc1 domain on mouse chromosome 12. (2006) (116)
Influence of paternally imprinted genes on development. (1991) (111)
ZNF445 is a primary regulator of genomic imprinting (2019) (105)
MicroRNA down‐regulated in human cholangiocarcinoma control cell cycle through multiple targets involved in the G1/S checkpoint (2011) (104)
Gene Dosage Effects of the Imprinted Delta-Like Homologue 1 (Dlk1/Pref1) in Development: Implications for the Evolution of Imprinting (2009) (102)
Differential regulation of imprinting in the murine embryo and placenta by the Dlk1-Dio3 imprinting control region (2007) (102)
Genomic imprinting: the emergence of an epigenetic paradigm (2011) (102)
A Small Family of Sushi-Class Retrotransposon-Derived Genes in Mammals and Their Relation to Genomic Imprinting (2005) (101)
Relationship between DNA methylation, histone H4 acetylation and gene expression in the mouse imprinted Igf2‐H19 domain (2001) (100)
The atypical mammalian ligand Delta-like homologue 1 (Dlk1) can regulate Notch signalling in Drosophila (2008) (98)
You are what your dad ate. (2011) (96)
Identification, Characterization, and Heritability of Murine Metastable Epialleles: Implications for Non-genetic Inheritance (2018) (93)
Ultrastructural changes in the interhaemal membrane and junctional zone of the murine chorioallantoic placenta across gestation (2005) (91)
Syncytial knots (Tenney-Parker changes) in the human placenta: evidence of loss of transcriptional activity and oxidative damage. (2013) (88)
CRISPR-Cas9-Mediated Genetic Screening in Mice with Haploid Embryonic Stem Cells Carrying a Guide RNA Library. (2015) (87)
Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome. (2000) (82)
Distinguishing epigenetic marks of developmental and imprinting regulation (2010) (79)
Two homoeo box loci mapped in evolutionarily related mouse and human chromosomes (1985) (78)
Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies. (2004) (78)
Epigenetic modifications on X chromosomes in marsupial and monotreme mammals and implications for evolution of dosage compensation (2010) (77)
Developing essential professional skills: a framework for teaching and learning about feedback (2005) (76)
Restricted co-expression of Dlk1 and the reciprocally imprinted non-coding RNA, Gtl2: implications for cis-acting control. (2007) (74)
Imprinted Gene Dosage Is Critical for the Transition to Independent Life (2012) (73)
Differential genomic imprinting regulates paracrine and autocrine roles of IGF2 in mouse adult neurogenesis (2015) (72)
Evidence for Transcriptional Activity in the Syncytiotrophoblast of the Human Placenta (2008) (69)
Phenotypic outcomes of imprinted gene models in mice: elucidation of pre- and postnatal functions of imprinted genes. (2014) (69)
Epigenetic Control of the Genome—Lessons from Genomic Imprinting (2014) (67)
Fetus-derived DLK1 is required for maternal metabolic adaptations to pregnancy and is associated with fetal growth restriction (2016) (66)
Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14 (2008) (65)
Genomic imprinting as an adaptative model of developmental plasticity (2011) (64)
Oxidative Stress and the Induction of Cyclooxygenase Enzymes and Apoptosis in the Murine Placenta (2007) (63)
A trans-homologue interaction between reciprocally imprinted miR-127 and Rtl1 regulates placenta development (2015) (62)
Activation of an imprinted Igf 2 gene in mouse somatic cell cultures (1993) (59)
The non-viability of uniparental mouse conceptuses correlates with the loss of the products of imprinted genes (1994) (57)
Homeo box genes in murine development. (1987) (55)
Imprinted X inactivation and reprogramming in the preimplantation mouse embryo. (2005) (55)
Interplay of cis and trans mechanisms driving transcription factor binding and gene expression evolution (2017) (55)
Epigenetic reprogramming: is deamination key to active DNA demethylation? (2011) (54)
Silencing of miR-370 in Human Cholangiocarcinoma by Allelic Loss and Interleukin-6 Induced Maternal to Paternal Epigenotype Switch (2012) (53)
DLK1/PREF1 regulates nutrient metabolism and protects from steatosis (2014) (51)
Genomic imprinting and cancer; new paradigms in the genetics of neoplasia. (2001) (51)
Cognate homeo-box loci mapped on homologous human and mouse chromosomes. (1986) (49)
The evolution of imprinting: chromosomal mapping of orthologues of mammalian imprinted domains in monotreme and marsupial mammals (2007) (49)
Dynamic temporal and spatial regulation of the cdk inhibitor p57kip2 during embryo morphogenesis (2001) (48)
Epigenetics: Perceptive enzymes (2007) (48)
Nonallelic Transcriptional Roles of CTCF and Cohesins at Imprinted Loci (2011) (47)
Genomic imprinting effects in a compromised in utero environment: implications for a healthy pregnancy. (2010) (45)
Epigenetic state and expression of imprinted genes in umbilical cord correlates with growth parameters in human pregnancy (2012) (44)
DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation (2013) (44)
Status of Genomic Imprinting in Epigenetically Distinct Pluripotent Stem Cells (2012) (44)
Insulin and insulin-like growth factor 1 receptors are required for normal expression of imprinted genes (2014) (44)
The discovery and importance of genomic imprinting (2018) (41)
Dlk1 is a negative regulator of emerging hematopoietic stem and progenitor cells (2013) (40)
Proteins involved in establishment and maintenance of imprinted methylation marks. (2012) (40)
Parental origin effects in human trisomy for chromosome 14q: implications for genomic imprinting. (1998) (40)
DNA sequence polymorphism within hominoid species exceeds the number of phylogenetically informative characters for a HOX2 locus. (1992) (39)
Different epigenetic states define syncytiotrophoblast and cytotrophoblast nuclei in the trophoblast of the human placenta. (2015) (39)
Identification, Characterization, and Heritability of Murine Metastable Epialleles: Implications for Non-genetic Inheritance (2018) (37)
Cooperativity of imprinted genes inactivated by acquired chromosome 20q deletions (2013) (37)
Genomic imprinting: Mother maintains methylation marks (2001) (37)
CG dinucleotide periodicities recognized by the Dnmt3a–Dnmt3L complex are distinctive at retroelements and imprinted domains (2009) (36)
Epigenetics and imprinting of the trophoblast -- a workshop report. (2006) (35)
Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13). (1989) (35)
ZFP57 regulation of transposable elements and gene expression within and beyond imprinted domains (2019) (35)
Non-CG DNA methylation is a biomarker for assessing endodermal differentiation capacity in pluripotent stem cells (2016) (34)
Genomic Matrix Attachment Region and Chromosome Conformation Capture Quantitative Real Time PCR Assays Identify Novel Putative Regulatory Elements at the Imprinted Dlk1/Gtl2 Locus* (2008) (33)
Visualizing Changes in Cdkn1c Expression Links Early-Life Adversity to Imprint Mis-regulation in Adults (2017) (32)
Genomic Imprinting Variations in the Mouse Type 3 Deiodinase Gene Between Tissues and Brain Regions (2014) (31)
Human Embryonic Stem Cells as a Model for Studying Epigenetic Regulation During Early Development (2005) (31)
Role of the BAHD1 Chromatin-Repressive Complex in Placental Development and Regulation of Steroid Metabolism (2016) (30)
TET3 prevents terminal differentiation of adult NSCs by a non-catalytic action at Snrpn (2019) (28)
ZFP57 and the Targeted Maintenance of Postfertilization Genomic Imprints. (2015) (28)
Analysis of mouse conceptuses with uniparental duplication/deficiency for distal chromosome 12: comparison with chromosome 12 uniparental disomy and implications for genomic imprinting (2006) (28)
Parental Imprinting on Mouse Chromosome 7 (1996) (27)
Genomic imprinting--insights from studies in mice. (2003) (27)
Imprinted small RNA genes (2004) (27)
Obstacles to detecting isoforms using full-length scRNA-seq data (2020) (27)
The inheritance of germline-specific epigenetic modifications during development. (1993) (27)
Novel Primate Model of Serotonin Transporter Genetic Polymorphisms Associated with Gene Expression, Anxiety and Sensitivity to Antidepressants (2016) (26)
Trim 28 Haploinsufficiency Triggers Bistable Epigenetic Obesity Graphical (2016) (24)
Imprinting moves to the centre (1996) (23)
Metastable epialleles and their contribution to epigenetic inheritance in mammals. (2019) (23)
L3mbtl, the mouse orthologue of the imprinted L3MBTL, displays a complex pattern of alternative splicing and escapes genomic imprinting. (2005) (21)
Germline and somatic imprinting in the nonhuman primate highlights species differences in oocyte methylation (2015) (21)
Coordinate regulation of Igf-2 and H19 in cultured cells. (1995) (21)
Mammalian homeo box genes. (1985) (20)
Genetic imprinting: Silencing elements have their say (2000) (20)
Simulation-based benchmarking of isoform quantification in single-cell RNA-seq (2018) (19)
Epigenetics: Monoallelic Expression in the Immune System (2002) (17)
Developmental biology: The X-inactivation yo-yo (2005) (17)
Complementary roles of genes regulated by two paternally methylated imprinted regions on chromosomes 7 and 12 in mouse placentation. (2006) (16)
KRAB zinc finger protein diversification drives mammalian interindividual methylation variability (2020) (16)
Parent-of-Origin Effects Implicate Epigenetic Regulation of Experimental Autoimmune Encephalomyelitis and Identify Imprinted Dlk1 as a Novel Risk Gene (2014) (16)
Appropriate expression of imprinted genes on mouse chromosome 12 extends development of bi‐maternal embryos to term (2007) (16)
Regulation of gene activity and repression: a consideration of unifying themes. (2004) (15)
Imprinting methylation in SNRPN and MEST1 in adult blood predicts cognitive ability (2019) (14)
Genomic imprinting and cancer. (1990) (13)
Erratum to “Epigenetics and Imprinting of the Trophoblast – A Workshop Report” [Placenta 27, supplement A, Trophoblast Research, Vol. 20 S122–S126] (2006) (13)
The imprinted gene Pw1/Peg3 regulates skeletal muscle growth, satellite cell metabolic state, and self-renewal (2018) (12)
Genomic properties of variably methylated retrotransposons in mouse (2020) (12)
Modeling methyl-sensitive transcription factor motifs with an expanded epigenetic alphabet (2016) (12)
Perturbations to the IGF1 growth pathway and adult energy homeostasis following disruption of mouse chromosome 12 imprinting (2013) (12)
MAMMOT - a set of tools for the design, management and visualization of genomic tiling arrays (2006) (12)
The mammalian LINC complex component SUN1 regulates muscle regeneration by modulating drosha activity (2019) (11)
Multiple laboratory mouse reference genomes define strain specific haplotypes and novel functional loci (2018) (11)
Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity (2020) (11)
Genomic Imprinting and the Regulation of Postnatal Neurogenesis (2017) (11)
X Inactivation: Pre- or Post-Fertilisation Turn-off? (2004) (11)
Strain-Specific Epigenetic Regulation of Endogenous Retroviruses: The Role of Trans-Acting Modifiers (2020) (11)
Targeted deletion of a 170-kb cluster of LINE-1 repeats and implications for regional control (2018) (10)
Life course epigenetics and healthy ageing (2013) (10)
Comparative Genetic Analysis of Homeobox Genes in Mouse and Man (1987) (10)
Genomic Imprinting – A Model for Roles of HistoneModifications in Epigenetic Control (2009) (10)
The genomics of human homeobox-containing loci. (1988) (10)
Isolation, chromosomal localization, and nucleotide sequence of the human HOX 1.4 homeobox. (1989) (9)
Variably methylated retrotransposons are refractory to a range of environmental perturbations (2021) (9)
Placental-specific Igf-2 regulates the diffusional exchange characteristics of the mouse placenta (2004) (8)
Defective folate metabolism causes germline epigenetic instability and distinguishes Hira as a phenotype inheritance biomarker (2020) (8)
Dlk1 dosage regulates hippocampal neurogenesis and cognition (2021) (8)
The need for Eed (2003) (8)
Monomorphism in humans and sequence differences among higher primates for a sequence tagged site (STS) in homeo box cluster 2 as assayed by denaturing gradient electrophoresis. (1990) (8)
Epigenetic Mechanisms of ART-Related Imprinting Disorders: Lessons From iPSC and Mouse Models (2021) (7)
The origins of genomic imprinting in mammals. (2019) (6)
A moderately frequent RFLP identified by both SacI and BanII with a probe from the HOX2 locus in man (17q11-17q22). (1987) (6)
Enhancer-dependent, locus-wide regulation of the imprinted mouse insulin-like growth factor II gene. (1998) (5)
Epigenetic changes induced by in utero dietary challenge result in phenotypic variability in successive generations of mice (2022) (5)
Cognate homeobox loci mapped on homologous human and mouse chromosomes ( gene mapping / developmental genetics / somatic cell hybrids / blot hybridization / in situ hybridization ) (5)
Imprinting methylation predicts hippocampal volumes and hyperintensities and the change with age in later life (2020) (4)
Balanced translocations for the analysis of imprinted regions of the mouse genome. (2001) (4)
Considerations when investigating lncRNA function (2014) (4)
Genomic imprinting (2004) (4)
Dinucleotide repeat polymorphism at the HOX 2B locus. (1992) (4)
Balanced gene dosage control rather than parental origin underpins genomic imprinting (2022) (3)
Genes and development--a workshop report. (2004) (3)
The evolution of genomic imprinting: Epigenetic control of mammary gland development and postnatal resource control (2019) (3)
Epigenetic Reprogramming in Mammalian Development (2001) (3)
Obstacles to detecting isoforms using full-length scRNA-seq data (2020) (2)
implications for genomic imprinting . trisomy for chromosome 14 q : Parental origin effects in human (2)
Epigenetic change induced by in utero dietary challenge provokes phenotypic variability across multiple generations of mice (2020) (2)
Germ line-specific programming of parental genomes for development (1993) (2)
DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation (2013) (2)
Mendel’s laws of heredity on his 200th birthday: What have we learned by considering exceptions? (2022) (2)
Obstacles to Studying Alternative Splicing Using scRNA-seq (2019) (2)
A spontaneous genetically induced epiallele at a retrotransposon shapes host genome function (2021) (2)
Genomic properties of variably methylated retrotransposons in mouse (2021) (2)
Simulation-based benchmarking of isoform quantification in single-cell RNA-seq (2018) (2)
Functional and Molecular Consequences of the Dnmt3aR882H Mutation in Acute Myeloid Leukaemia (2015) (2)
Deletion of paternal ventral prostate gland leads to aberrant methylation of embryonic genome in the golden hamster (2004) (1)
C. Thomas Caskey (1938–2022) (2022) (1)
Epigenetic regulation of unique genes and repetitive elements by the KRAB zinc finger protein ZFP57 (2019) (1)
'Imprinting and Growth Congress' 2002, London, UK. (2003) (1)
Erratum: Transgenerational epigenetic inheritance: how important is it? (2013) (1)
A spontaneous genetically-induced epiallele at a retrotransposon shapes host genome function (2020) (1)
Explorer Considerations when investigating lncRNA function in vivo (2014) (1)
Parental imprinting and epigenetic programming of the mouse genome: long lasting consequences for development and phenotype (1993) (1)
Weak parent-of-origin expression bias: Is this imprinting? (2022) (1)
Dad’s diet – smRNA methylation signatures in sperm pass on disease risk (2018) (1)
At the Controls: Genomic Imprinting and the Epigenetic Regulation of Gene Expression (2005) (1)
Interplay of cis and trans mechanisms driving transcription factor binding and gene expression evolution (2017) (1)
Parental Imprinting in Mammalian Development (1993) (1)
Interplay of cis and trans mechanisms driving transcription factor binding, chromatin, and gene expression evolution (2016) (1)
A review of genomic physical mapping. (1988) (1)
Epigenetics in Brain Development and Disease (2017) (1)
Cooperativity of imprinted genes inactivated by acquired chromosome 20q deletions (2013) (1)
RNA 2D/3D structure prediction with a consensus of covariance/contact methods (2019) (0)
Transgenerational effects of abnormal folate metabolism on fetal and placental development (2013) (0)
Visualizing Changes in Cd kn 1 c Expression Links Early-Life Adversity to Imprint Mis-regulation in Adults Graphical (0)
129 The CHR9P21 risk locus affects IL-1/TLR signalling in VSMC (2018) (0)
Genomic imprinting and its regulation (2007) (0)
Obituary: Denise Barlow (1950-2017) (2018) (0)
DLK1/PREF1 prevents hepatosteatosis by elevating pituitary GH secretion (2014) (0)
Imprinting methylation predicts hippocampal volumes and hyperintensities and the change with age in later life (2021) (0)
ANATOMY OPTION A: R ESEARCH IN DEVELOPMENTAL BIOLOGY AND NEUROSCIENCE (2006) (0)
Genomic imprinting and the epigenetic regulation of adult neurogenesis (2013) (0)
Genomic Imprinting: Its Role in Development and Disease (1999) (0)
Author response: Considerations when investigating lncRNA function in vivo (2014) (0)
Preimplantation genetic testing for a chr14q32 microdeletion in a family with Kagami-Ogata syndrome and Temple syndrome (2021) (0)
The cyclin-dependent kinase inhibitor P57kip2 exhibits a dynamic and temporally regulated expression pattern during embryonic morpho-genesis (2000) (0)
Reassessment of weak parent-of-origin expression bias shows it rarely exists outside of known imprinted regions (2023) (0)
Analysis ofFourMicrosatellite Markers on theLongArm ofChromosome9byMeiotic Recombination inFlow-sorted Single Sperm (1993) (0)
Correction for Li et al., Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies (2021) (0)
Signalling from fetus to mother; role of the Delta-like homologue 1 (2013) (0)
A potential role for male accessory sex gland secretions on the epigenetic regulation of embryo development in golden hamster (2003) (0)
The imprinted gene Pw1/Peg3 regulates skeletal muscle growth, satellite cell metabolic state, and self-renewal (2018) (0)
Mitotic heritability of DNA methylation at intermediately methylated sites is imprecise (2023) (0)
Physical Mapping Review (2014) (0)
Imprinted microRNA genes at the mouse Dlk1-GTl2 domain. (2004) (0)
Messerschmidt Embryo Transition Is Required for Epigenetic Stability During Mouse Oocyte to Trim 28 (2012) (0)
Abstract 100: An Altered Epigenomic Mark Predisposes to Dilated Cardiomyopathy Through Alternative Splicing of Sarcomeric Gene Expression in Mice (2012) (0)
Contents Vol. 113, 2006 (2006) (0)
in vivo and in vitro: Implications for Beckwith-Wiedemann syndrome (2000) (0)
Absence of accessory sex gland secretiion perturbs the active DNA demethylation of sperm genome in vivo in the fertilized oocytes of mouse and golden hamster (2005) (0)
Correction: Imprinting methylation in SNRPN and MEST1 in adult blood predicts cognitive ability (2019) (0)
Subnuclear localisation is associated with gene expression more than parental origin at the imprinted Dlk1-Dio3 locus (2022) (0)
ZFP57 regulation of transposable elements and gene expression within and beyond imprinted domains (2019) (0)
Human chromosome 7 carries the 182 interferon gene ( somatic cell genetics / genomic DNA blot-hybridization / restrictlon fragment length polymorphism ) (0)
TET3 prevents terminal differentiation of adult NSCs by a non-catalytic action at Snrpn (2019) (0)
Developmental effects of genomic imprinting on mouse chromosome 12 (1998) (0)
Sixteen diverse laboratory mouse reference genomes define strain-specific haplotypes and novel functional loci (2018) (0)
Mammary adipocyte flow cytometry as a tool to study mammary gland biology (2023) (0)
Author response: A spontaneous genetically induced epiallele at a retrotransposon shapes host genome function (2021) (0)
Elevated maternal plasma DLK1/PREF-1 in pregnancy is conceptus-derived and its abrogation affects maternal metabolic adaptations to pregnancy (2014) (0)
RNAi-Mediated Allelic trans-Interaction at the Imprinted Rtl1/Peg11 Locus (2005) (0)
The Placenta and Human Developmental Programming: Genomic imprinting (2010) (0)
Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expression (2015) (0)
Subnuclear localisation is associated with gene activation not repression or parental origin at the imprinted Dlk1-Dio3 locus (2021) (0)
Disruption of folate metabolism causes germline epigenetic instability and distinguishes HIRA as a biomarker of maternal transgenerational epigenetic inheritance (2020) (0)
A Conversation with Anne Ferguson-Smith. (2015) (0)

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