Published in Mol Hum Reprod on December 09, 2009
The ontogeny of cKIT+ human primordial germ cells proves to be a resource for human germ line reprogramming, imprint erasure and in vitro differentiation. Nat Cell Biol (2012) 2.41
DNA methylation differences between in vitro- and in vivo-conceived children are associated with ART procedures rather than infertility. Clin Epigenetics (2015) 1.48
Are there subtle genome-wide epigenetic alterations in normal offspring conceived by assisted reproductive technologies? Fertil Steril (2011) 1.47
Evidence for widespread changes in promoter methylation profile in human placenta in response to increasing gestational age and environmental/stochastic factors. BMC Genomics (2011) 1.39
Genetics of recurrent miscarriage: challenges, current knowledge, future directions. Front Genet (2012) 1.16
DNA sequence polymorphisms in a panel of eight candidate bovine imprinted genes and their association with performance traits in Irish Holstein-Friesian cattle. BMC Genet (2010) 1.14
Assisted reproduction treatment and epigenetic inheritance. Hum Reprod Update (2012) 1.11
Endocrine disruptors, environmental oxygen, epigenetics and pregnancy. Front Biosci (Elite Ed) (2011) 1.07
DNA methylation at imprint regulatory regions in preterm birth and infection. Am J Obstet Gynecol (2013) 0.95
Methylation allelic polymorphism (MAP) in chorionic gonadotropin beta5 (CGB5) and its association with pregnancy success. J Clin Endocrinol Metab (2010) 0.88
Restoring fertility in sterile childhood cancer survivors by autotransplanting spermatogonial stem cells: are we there yet? Biomed Res Int (2013) 0.85
Imprinting methylation errors in ART. Reprod Med Biol (2014) 0.84
Similar DNA methylation levels in specific imprinting control regions in children conceived with and without assisted reproductive technology: a cross-sectional study. BMC Pediatr (2012) 0.81
The placenta: phenotypic and epigenetic modifications induced by Assisted Reproductive Technologies throughout pregnancy. Clin Epigenetics (2015) 0.77
Outlier DNA methylation levels as an indicator of environmental exposure and risk of undesirable birth outcome. Hum Mol Genet (2015) 0.76
DNA methyltransferase 3A promoter polymorphism is associated with the risk of human spontaneous abortion after assisted reproduction techniques and natural conception. J Assist Reprod Genet (2016) 0.75
Morphologic and molecular changes in the placenta: what we can learn from environmental exposures. Fertil Steril (2016) 0.75
Epigenetic reprogramming in mouse primordial germ cells. Mech Dev (2002) 6.67
A duplicated copy of DMRT1 in the sex-determining region of the Y chromosome of the medaka, Oryzias latipes. Proc Natl Acad Sci U S A (2002) 3.20
Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanisms. Cell Rep (2012) 2.67
Dynamic transcriptome analysis measures rates of mRNA synthesis and decay in yeast. Mol Syst Biol (2011) 2.37
In vitro-differentiated embryonic stem cells give rise to male gametes that can generate offspring mice. Dev Cell (2006) 2.30
Elevated levels of Rad51 recombination protein in tumor cells. Cancer Res (2002) 2.00
Comparative dynamic transcriptome analysis (cDTA) reveals mutual feedback between mRNA synthesis and degradation. Genome Res (2012) 1.77
Two patients with EP300 mutations and facial dysmorphism different from the classic Rubinstein-Taybi syndrome. Am J Med Genet A (2010) 1.68
Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder. Neurogenetics (2009) 1.58
A Bayesian network view on nested effects models. EURASIP J Bioinform Syst Biol (2009) 1.52
Identification of aberrant chromosomal regions from gene expression microarray studies applied to human breast cancer. Bioinformatics (2007) 1.50
Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns. Nucleic Acids Res (2010) 1.39
Comprehensive gene and microRNA expression profiling reveals a role for microRNAs in human liver development. PLoS One (2009) 1.37
Global analysis of eukaryotic mRNA degradation reveals Xrn1-dependent buffering of transcript levels. Mol Cell (2013) 1.35
Achalasia: will genetic studies provide insights? Hum Genet (2010) 1.30
Formation of higher-order nuclear Rad51 structures is functionally linked to p21 expression and protection from DNA damage-induced apoptosis. J Cell Sci (2002) 1.26
Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitus. Diabetes (2012) 1.25
Modeling the temporal interplay of molecular signaling and gene expression by using dynamic nested effects models. Proc Natl Acad Sci U S A (2009) 1.17
Pectus excavatum: history, hypotheses and treatment options. Interact Cardiovasc Thorac Surg (2012) 1.14
Epigenetic disturbances in in vitro cultured gametes and embryos: implications for human assisted reproduction. Fertil Steril (2013) 1.13
Analyzing gene perturbation screens with nested effects models in R and bioconductor. Bioinformatics (2008) 1.10
Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human. Hum Mol Genet (2007) 1.10
Periodic mRNA synthesis and degradation co-operate during cell cycle gene expression. Mol Syst Biol (2014) 1.10
Analyses of the extent of shared synteny and conserved gene orders between the genome of Fugu rubripes and human 20q. Genome Res (2002) 1.09
Methylation reprogramming and chromosomal aneuploidy in in vivo fertilized and cloned rabbit preimplantation embryos. Biol Reprod (2004) 1.08
Expression of BLIMP1/PRMT5 and concurrent histone H2A/H4 arginine 3 dimethylation in fetal germ cells, CIS/IGCNU and germ cell tumors. BMC Dev Biol (2008) 1.08
Epigenetics of gestational diabetes mellitus and offspring health: the time for action is in early stages of life. Mol Hum Reprod (2013) 1.07
Differences in DNA methylation patterns and expression of the CCRK gene in human and nonhuman primate cortices. Mol Biol Evol (2009) 1.07
Derivation of xeno-free and GMP-grade human embryonic stem cells--platforms for future clinical applications. PLoS One (2012) 1.03
Nested effects models for learning signaling networks from perturbation data. Biom J (2009) 1.01
A cascade of complex subtelomeric duplications during the evolution of the hominoid and Old World monkey genomes. Am J Hum Genet (2001) 1.01
Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes. Genomics (2006) 1.00
Limiting dilution bisulfite (pyro)sequencing reveals parent-specific methylation patterns in single early mouse embryos and bovine oocytes. Epigenetics (2011) 0.99
Human embryonic stem cells suppress T cell responses via arginase I-dependent mechanism. J Immunol (2009) 0.99
Starr: Simple Tiling ARRay analysis of Affymetrix ChIP-chip data. BMC Bioinformatics (2010) 0.99
Distribution of telomeric (TTAGGG)(n) sequences in avian chromosomes. Chromosoma (2002) 0.96
Monozygotic twins discordant for constitutive BRCA1 promoter methylation, childhood cancer and secondary cancer. Epigenetics (2012) 0.95
Four unrelated patients with Lubs X-linked mental retardation syndrome and different Xq28 duplications. Am J Med Genet A (2010) 0.94
Extreme methylation values of imprinted genes in human abortions and stillbirths. Am J Pathol (2010) 0.94
Intragenic deletions of IL1RAPL1: Report of two cases and review of the literature. Am J Med Genet A (2010) 0.94
Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein-Taybi syndrome. Hum Genet (2006) 0.94
The functional cancer map: a systems-level synopsis of genetic deregulation in cancer. BMC Med Genomics (2011) 0.93
Quantitative protein microarrays for time-resolved measurements of protein phosphorylation. Proteomics (2008) 0.93
Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment. Hum Mol Genet (2008) 0.93
Measurement of genome-wide RNA synthesis and decay rates with Dynamic Transcriptome Analysis (DTA). Bioinformatics (2012) 0.92
Comparative methylation profiles and telomerase biology of mouse multipotent adult germline stem cells and embryonic stem cells. Mol Hum Reprod (2009) 0.92
Quantitative analysis of processive RNA degradation by the archaeal RNA exosome. Nucleic Acids Res (2010) 0.91
Is the lung floating test a valuable tool or obsolete? A prospective autopsy study. Int J Legal Med (2012) 0.90
Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder. Am J Med Genet A (2009) 0.90
DNA integrity, growth pattern, spindle formation, chromosomal constitution and imprinting patterns of mouse oocytes from vitrified pre-antral follicles. Hum Reprod (2010) 0.90
Analysis of Affymetrix ChIP-chip data using starr and R/Bioconductor. Cold Spring Harb Protoc (2011) 0.90
Vascular endothelial cadherin expression in lung specimens of patients with sepsis-induced acute respiratory distress syndrome and endothelial cell cultures. Pathobiology (2013) 0.90
Inheritance and variable expression in Rubinstein-Taybi syndrome. Am J Med Genet A (2010) 0.90
Micro-array analyses decipher exceptional complex familial chromosomal rearrangement. Hum Genet (2006) 0.89
Automatic post-picking using MAPPOS improves particle image detection from cryo-EM micrographs. J Struct Biol (2013) 0.89
Drosophila miR-277 controls branched-chain amino acid catabolism and affects lifespan. RNA Biol (2013) 0.89
Fast and efficient dynamic nested effects models. Bioinformatics (2010) 0.89
Chronic exposure to a low concentration of bisphenol A during follicle culture affects the epigenetic status of germinal vesicles and metaphase II oocytes. Fertil Steril (2013) 0.89
Enterobacterial tumor colonization in mice depends on bacterial metabolism and macrophages but is independent of chemotaxis and motility. Int J Med Microbiol (2010) 0.88
Joint Bayesian inference of condition-specific miRNA and transcription factor activities from combined gene and microRNA expression data. Bioinformatics (2012) 0.88
Third Report on Chicken Genes and Chromosomes 2015. Cytogenet Genome Res (2015) 0.88
Transcriptional regulation of Nox4 by histone deacetylases in human endothelial cells. Basic Res Cardiol (2012) 0.88
Case report: Noonan syndrome with multiple giant cell lesions and review of the literature. Am J Med Genet A (2012) 0.88
Classification across gene expression microarray studies. BMC Bioinformatics (2009) 0.87
Multiplex rt-PCR expression analysis of developmentally important genes in individual mouse preimplantation embryos and blastomeres. Biol Reprod (2008) 0.87
MC EMiNEM maps the interaction landscape of the Mediator. PLoS Comput Biol (2012) 0.87
Human papilloma virus (HPV)-associated gynecological alteration in mothers of children with recurrent respiratory papillomatosis during long-term observation. Cancer Detect Prev (2007) 0.87
Plasticity of human chromosome 3 during primate evolution. Genomics (2004) 0.87
Constitutive promoter methylation of BRCA1 and RAD51C in patients with familial ovarian cancer and early-onset sporadic breast cancer. Hum Mol Genet (2012) 0.86
Isolation and differential expression of two isoforms of the ROBO2/Robo2 axon guidance receptor gene in humans and mice. Genomics (2006) 0.86
Medullary thyroid carcinoma in a 2-month-old male with multiple endocrine neoplasia 2B and symptoms of pseudo-Hirschsprung disease: a case report. J Pediatr Surg (2007) 0.85
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity. Am J Hum Genet (2013) 0.85
Mediator phosphorylation prevents stress response transcription during non-stress conditions. J Biol Chem (2012) 0.85
Chicken orthologues of mammalian imprinted genes are clustered on macrochromosomes and replicate asynchronously. Trends Genet (2005) 0.85
De novo t(7;10)(q33;q23) translocation and closely juxtaposed microdeletion in a patient with macrocephaly and developmental delay. Hum Genet (2005) 0.84
Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes. BMC Evol Biol (2009) 0.84
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association. Eur J Hum Genet (2013) 0.84
Semi-automated 3D leaf reconstruction and analysis of trichome patterning from light microscopic images. PLoS Comput Biol (2013) 0.84