Published in PLoS Genet on November 11, 2016
Intergenerational Transmission of Maternal Childhood Maltreatment Exposure: Implications for Fetal Brain Development. J Am Acad Child Adolesc Psychiatry (2017) 0.77
Detection of Imprinted Genes by Single-Cell Allele-Specific Gene Expression. Am J Hum Genet (2017) 0.75
The Sequence Alignment/Map format and SAMtools. Bioinformatics (2009) 232.39
TopHat: discovering splice junctions with RNA-Seq. Bioinformatics (2009) 81.13
UHRF1 plays a role in maintaining DNA methylation in mammalian cells. Science (2007) 7.90
Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting. Nature (2004) 7.42
The role of Tet3 DNA dioxygenase in epigenetic reprogramming by oocytes. Nature (2011) 6.73
Epigenetic reprogramming in mouse primordial germ cells. Mech Dev (2002) 6.67
Single-cell RNA-Seq profiling of human preimplantation embryos and embryonic stem cells. Nat Struct Mol Biol (2013) 4.04
Dynamic CpG island methylation landscape in oocytes and preimplantation embryos. Nat Genet (2011) 3.99
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1. Nat Genet (2002) 3.88
Genomic imprinting--defusing the ovarian time bomb. Trends Genet (1994) 3.38
Genetic programs in human and mouse early embryos revealed by single-cell RNA sequencing. Nature (2013) 3.06
Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene. Cell (2001) 3.05
Contribution of intragenic DNA methylation in mouse gametic DNA methylomes to establish oocyte-specific heritable marks. PLoS Genet (2012) 2.89
Transcription is required for establishment of germline methylation marks at imprinted genes. Genes Dev (2009) 2.76
The DNA methylation landscape of human early embryos. Nature (2014) 2.67
Highly efficient vitrification for cryopreservation of human oocytes and embryos: the Cryotop method. Theriogenology (2006) 2.64
DNA methylation dynamics of the human preimplantation embryo. Nature (2014) 2.55
Genomic imprinting of Mash2, a mouse gene required for trophoblast development. Nat Genet (1995) 2.46
Resourceful imprinting. Nature (2004) 2.10
Limited evolutionary conservation of imprinting in the human placenta. Proc Natl Acad Sci U S A (2006) 2.08
Waves of early transcriptional activation and pluripotency program initiation during human preimplantation development. Development (2011) 1.88
A Unique Gene Regulatory Network Resets the Human Germline Epigenome for Development. Cell (2015) 1.86
The human placenta methylome. Proc Natl Acad Sci U S A (2013) 1.86
Functional polymorphism in the parental imprinting of the human IGF2R gene. Biochem Biophys Res Commun (1993) 1.79
The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta. Hum Mol Genet (2010) 1.73
Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib. Nat Genet (2004) 1.68
The Transcriptome and DNA Methylome Landscapes of Human Primordial Germ Cells. Cell (2015) 1.66
Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment. Genome Res (2014) 1.64
Protection against de novo methylation is instrumental in maintaining parent-of-origin methylation inherited from the gametes. Mol Cell (2012) 1.36
Genome-wide analysis of DNA methylation dynamics during early human development. PLoS Genet (2014) 1.26
Naive Human Pluripotent Cells Feature a Methylation Landscape Devoid of Blastocyst or Germline Memory. Cell Stem Cell (2016) 1.08
A genome-wide approach reveals novel imprinted genes expressed in the human placenta. Epigenetics (2012) 1.08
Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies. Epigenetics Chromatin (2011) 1.07
The genetics of gestational trophoblastic disease: a rare complication of pregnancy. Cancer Genet (2012) 1.00
Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment. Genome Biol (2015) 0.99
IGF2 is parentally imprinted in human preimplantation embryos. Nat Genet (1997) 0.98
Maternal DNA Methylation Regulates Early Trophoblast Development. Dev Cell (2016) 0.96
The Gpr1/Zdbf2 locus provides new paradigms for transient and dynamic genomic imprinting in mammals. Genes Dev (2014) 0.96
Early Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas. PLoS Genet (2015) 0.95
Stability of genomic imprinting and gestational-age dynamic methylation in complicated pregnancies conceived following assisted reproductive technologies. Biol Reprod (2013) 0.93
Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting. PLoS Genet (2015) 0.91
Epigenetic and transcriptional features of the novel human imprinted lncRNA GPR1AS suggest it is a functional ortholog to mouse Zdbf2linc. Epigenetics (2013) 0.89
Imprinted expression of SNRPN in human preimplantation embryos. Am J Hum Genet (1998) 0.88
Developmental differences in the expression of FGF receptors between human and mouse embryos. Placenta (2014) 0.87
Variable maternal methylation overlapping the nc886/vtRNA2-1 locus is locked between hypermethylated repeats and is frequently altered in cancer. Epigenetics (2014) 0.87
Pervasive polymorphic imprinted methylation in the human placenta. Genome Res (2016) 0.86
How has the study of the human placenta aided our understanding of partially methylated genes? Epigenomics (2013) 0.83
Germline-derived DNA methylation and early embryo epigenetic reprogramming: The selected survival of imprints. Int J Biochem Cell Biol (2015) 0.82
Variable imprinting of the MEST gene in human preimplantation embryos. Eur J Hum Genet (2012) 0.82
An earlier formulation of the genetic conflict hypothesis of genomic imprinting. Nat Genet (2006) 0.81
Expression pattern of JMJD1C in oocytes and its impact on early embryonic development. Genet Mol Res (2015) 0.76
Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism. Fertil Steril (2014) 1.43
Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell Syndrome-compatible phenotype. Eur J Hum Genet (2014) 1.11
Human genetic variation database, a reference database of genetic variations in the Japanese population. J Hum Genet (2016) 1.00
Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting. PLoS Genet (2015) 0.91
Targeted DNA demethylation in vivo using dCas9-peptide repeat and scFv-TET1 catalytic domain fusions. Nat Biotechnol (2016) 0.86
Identical NR5A1 Missense Mutations in Two Unrelated 46,XX Individuals with Testicular Tissues. Hum Mutat (2016) 0.84
Genome-wide multilocus imprinting disturbance analysis in Temple syndrome and Kagami-Ogata syndrome. Genet Med (2016) 0.82
Origins of De Novo Genes in Human and Chimpanzee. PLoS Genet (2015) 0.81
Identification of novel kinase fusion transcripts in paediatric B cell precursor acute lymphoblastic leukaemia with IKZF1 deletion. Br J Haematol (2015) 0.79
Repeated fecal microbiota transplantation in a child with ulcerative colitis. Pediatr Int (2016) 0.78
Compilation of copy number variants identified in phenotypically normal and parous Japanese women. J Hum Genet (2014) 0.77
Case of pachydermoperiostosis with solute carrier organic anion transporter family, member 2A1 (SLCO2A1) mutations. J Dermatol (2015) 0.77
Antifibrotic effect of pirfenidone in a mouse model of human nonalcoholic steatohepatitis. Sci Rep (2017) 0.75
DNA methyltransferase inhibitor zebularine induces human cholangiocarcinoma cell death through alteration of DNA methylation status. PLoS One (2015) 0.75
Nucleotide substitutions in CD101, the human homolog of a diabetes susceptibility gene in non-obese diabetic mouse, in patients with type 1 diabetes. J Diabetes Investig (2016) 0.75
Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with multilocus imprinting disturbance: a female-dominant phenomenon? J Hum Genet (2016) 0.75
A DNA methylation map of human cancer at single base-pair resolution. Oncogene (2017) 0.75
Direct platelet adhesion potentiates group 2 innate lymphoid cell functions. Allergy (2021) 0.75
Somatic HRAS p.G12S mosaic mutation causes unilaterally distributed epidermal nevi, woolly hair and palmoplantar keratosis. J Dermatol (2017) 0.75
Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early puberty. J Cell Mol Med (2017) 0.75
Changeability of the fully methylated status of the 15q11.2 region in induced pluripotent stem cells derived from a patient with Prader-Willi syndrome. Congenit Anom (Kyoto) (2016) 0.75
The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants. Gene (2016) 0.75
FOXP2 variation in great ape populations offers insight into the evolution of communication skills. Sci Rep (2017) 0.75
Human cytomegalovirus downregulates SLITRK6 expression through IE2. J Neurovirol (2016) 0.75
Comprehensive screening for monogenic diabetes in 89 Japanese children with insulin-requiring antibody-negative type 1 diabetes. Pediatr Diabetes (2017) 0.75
Copy number rather than epigenetic alterations are the major dictator of imprinted methylation in tumors. Nat Commun (2017) 0.75
Complete type of pachydermoperiostosis with a novel mutation c.510G>A of the SLCO2A1 gene. J Dermatol (2016) 0.75
Salvage of fetal karyotype information from SNP array data obtained from products of conception with maternal cell contamination. Prenat Diagn (2017) 0.75
Involvement of prostaglandin E2 in the first Japanese case of pachydermoperiostosis with HPGD mutation and recalcitrant leg ulcer. J Dermatol Sci (2015) 0.75
Genomic analysis of two rare cases of pediatric Ph-positive T-ALL. Pediatr Blood Cancer (2021) 0.75
Potential damaging mutation in LRP5 from genome sequencing of the first reported chimpanzee with the Chiari malformation. Sci Rep (2017) 0.75
An Alpha-kinase 2 Gene Variant Disrupts Filamentous Actin Localization in the Surface Cells of Colorectal Cancer Spheroids. Anticancer Res (2017) 0.75
Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum. Brain Dev (2017) 0.75
Infiltration of mast cells in pachydermia of pachydermoperiostosis. J Dermatol (2017) 0.75
CTCF deletion syndrome: clinical features and epigenetic delineation. J Med Genet (2017) 0.75
Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans. Trends Genet (2016) 0.75