| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S00439-007-0440-1 |
| P698 | PubMed publication ID | 17955261 |
| P50 | author | Thomas J. Hudson | Q3525236 |
| Kelly A. Frazer | Q72345870 | ||
| Katherine Pollard | Q90391163 | ||
| Elin Grundberg | Q109040416 | ||
| Xu Wang | Q57005325 | ||
| P2093 | author name string | Andrew G Clark | |
| David Serre | |||
| Heng Tao | |||
| P2860 | cites work | Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote | Q58134572 |
| Mapping common regulatory variants to human haplotypes | Q81511258 | ||
| Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes | Q82457009 | ||
| Genome-wide associations of gene expression variation in humans | Q21145274 | ||
| Common genetic variants account for differences in gene expression among ethnic groups | Q24626446 | ||
| The cell cycle control gene ZAC/PLAGL1 is imprinted--a strong candidate gene for transient neonatal diabetes | Q28143868 | ||
| The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted | Q28182925 | ||
| Whole-genome patterns of common DNA variation in three human populations | Q29616283 | ||
| Association of acetylated histones with paternally expressed genes in the Prader--Willi deletion region | Q32069478 | ||
| Allele-specific KRT1 expression is a complex trait | Q33247455 | ||
| Discovery of imprinted transcripts in the mouse transcriptome using large-scale expression profiling | Q33678359 | ||
| Allelic variation in gene expression is common in the human genome | Q33682674 | ||
| Genome-wide prediction of imprinted murine genes | Q33841575 | ||
| A census of mammalian imprinting. | Q34430259 | ||
| Analysis of allelic differential expression in human white blood cells | Q34483101 | ||
| Genetic conflicts, multiple paternity and the evolution of genomic imprinting. | Q34602685 | ||
| Limited evolutionary conservation of imprinting in the human placenta | Q35025042 | ||
| Imprinting evolution and the price of silence. | Q35136062 | ||
| Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies | Q35221453 | ||
| Gene-expression variation within and among human populations | Q35677775 | ||
| The quantitative genetics of transcription | Q36254231 | ||
| Survey of allelic expression using EST mining | Q39019455 | ||
| A survey of genetic and epigenetic variation affecting human gene expression | Q40621976 | ||
| In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit | Q40968079 | ||
| Tissue-specific imprinting of the ZAC/PLAGL1 tumour suppressor gene results from variable utilization of monoallelic and biallelic promoters. | Q51992629 | ||
| Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human | Q56982001 | ||
| Allelic Variation in Human Gene Expression | Q57293497 | ||
| P433 | issue | 6 | |
| P304 | page(s) | 625-634 | |
| P577 | publication date | 2007-10-23 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | A genome-wide approach to identifying novel-imprinted genes | |
| P478 | volume | 122 |
| Q36303309 | A genome-wide approach reveals novel imprinted genes expressed in the human placenta |
| Q34605643 | A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes |
| Q35221526 | A survey for novel imprinted genes in the mouse placenta by mRNA-seq |
| Q36815060 | A uniform survey of allele-specific binding and expression over 1000-Genomes-Project individuals |
| Q37210011 | Advances in the identification and analysis of allele-specific expression. |
| Q24655104 | Allele-specific gene expression patterns in primary leukemic cells reveal regulation of gene expression by CpG site methylation |
| Q50308058 | Allelic expression analysis in the brain suggests a role for heterogeneous insults affecting epigenetic processes in autism spectrum disorders |
| Q34138823 | Comparison of sequencing-based methods to profile DNA methylation and identification of monoallelic epigenetic modifications. |
| Q33632265 | Computational analysis of whole-genome differential allelic expression data in human |
| Q37231371 | DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome |
| Q35008254 | DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation. |
| Q35018646 | Deep bisulfite sequencing of aberrantly methylated loci in a patient with multiple methylation defects |
| Q34388626 | Detection of parent-of-origin specific expression quantitative trait loci by cis-association analysis of gene expression in trios |
| Q34329053 | Differential decay of parent-of-origin-specific genomic sharing in cystic fibrosis-affected sib pairs maps a paternally imprinted locus to 7q34. |
| Q35914852 | Effects of sequence variation on differential allelic transcription factor occupancy and gene expression |
| Q33735829 | Evaluation of allelic expression of imprinted genes in adult human blood. |
| Q35991193 | Genetic Variants in the Bone Morphogenic Protein Gene Family Modify the Association between Residential Exposure to Traffic and Peripheral Arterial Disease |
| Q28660776 | Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes |
| Q39573980 | Genome-wide assessment of imprinted expression in human cells |
| Q40001784 | Genome-wide mapping of allele-specific protein-DNA interactions in human cells. |
| Q46469126 | Genomic imprinting, disrupted placental expression, and speciation |
| Q35983120 | Genomic landscape of human allele-specific DNA methylation. |
| Q30981538 | High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta. |
| Q34832083 | Identification and resolution of artifacts in the interpretation of imprinted gene expression |
| Q35595321 | Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders |
| Q33959294 | Investigating parent of origin effects in studies of type 2 diabetes and obesity |
| Q54646491 | Involvement of parental imprinting in the antisense regulation of onco-miR-372-373. |
| Q33981739 | Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index |
| Q64066289 | Novel parent-of-origin-specific differentially methylated loci on chromosome 16 |
| Q28742324 | Novel retrotransposed imprinted locus identified at human 6p25 |
| Q36961278 | Overlapping euchromatin/heterochromatin- associated marks are enriched in imprinted gene regions and predict allele-specific modification |
| Q33759546 | Statistical inference of allelic imbalance from transcriptome data |
| Q33963896 | Successful computational prediction of novel imprinted genes from epigenomic features. |
| Q37034616 | Targeted screening of cis-regulatory variation in human haplotypes |
| Q38064462 | The impact of cis-acting polymorphisms on the human phenotype |
| Q33389173 | Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain |
| Q33927875 | Using next-generation RNA sequencing to identify imprinted genes. |
| Q39389232 | Zinc-finger protein 331, a novel putative tumor suppressor, suppresses growth and invasiveness of gastric cancer. |
Search more.