(Q37935869)

25 August 2017

1 reference

title

Parent of origin effects (English)

1 reference

25 August 2017

A Guilmatre

1

1 reference

PubMed ID

21933173

25 August 2017

A J Sharp

series ordinal

2

1 reference

25 August 2017

30 October 2011

1 reference

25 August 2017

1 reference

25 August 2017

81

1 reference

25 August 2017

3

1 reference

25 August 2017

201-209

1 reference

Genomic imprinting: parental influence on the genome

25 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

A survey for novel imprinted genes in the mouse placenta by mRNA-seq

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Role of paternal and maternal genomes in mouse development

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Molecular mechanisms of genomic imprinting and clinical implications for cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Genomic imprinting in mammalian development: a parental tug-of-war

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Imprinted genes in placental growth and obstetric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Imprinted gene expression in the brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

The importance of imprinting in the human placenta.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

The regulation and biological significance of genomic imprinting in mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Prader-Willi and Angelman syndromes. Disorders of genomic imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Parental origin of sequence variants associated with complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Linkage analysis of alcohol dependence using MOD scores

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

A genome scan for parent-of-origin linkage effects in alcoholism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Linkage analysis of alcoholism-related electrophysiological phenotypes: genome scans with microsatellites compared to single-nucleotide polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Genetic imprinting analysis for alcoholism genes using variance components approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Evidence for parent of origin effect in late-onset Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Genetic studies of autistic disorder and chromosome 7

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Preponderance of female sex in the transmission of seizure liability in idiopathic generalized epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Assessment of genetic linkage and parent-of-origin effects on obesity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Possible genomic imprinting of three human obesity-related genetic loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Analysis of HLA haplotypes in families with type 1 diabetes mellitus in La Réunion island.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

The analysis of parental origin of alleles may detect susceptibility loci for complex disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Increased trinucleotide repeat instability with advanced maternal age.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Slipping while sleeping? Trinucleotide repeat expansions in germ cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Maternal germline-specific effect of DNA ligase I on CTG/CAG instability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Molecular and phenotypic variation in patients with severe Hunter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Strong and weak male mutation bias at different sites in the primate genomes: insights from the human-chimpanzee comparison.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Variation in genome-wide mutation rates within and between human families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Maternal inheritance of human mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Intermale aggression tested in two procedures, using four inbred strains of mice and their reciprocal congenics: Y chromosomal implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Aggression in wild house mice: current state of affairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

It is not all hormones: alternative explanations for sexual differentiation of the brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

The parent-of-origin of the extra X chromosome may differentially affect psychopathology in Klinefelter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Identification of a cluster of X-linked imprinted genes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Ubiquitin tag for sperm mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Revealing the hidden complexities of mtDNA inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

wimp, a dominant maternal-effect mutation, reduces transcription of a specific subset of segmentation genes in Drosophila.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

The maternal-zygotic transition: death and birth of RNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Regulation of the oocyte-to-zygote transition

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

RNA-mediated non-mendelian inheritance of an epigenetic change in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Evidence for transgenerational transmission of epigenetic tumor susceptibility in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Folic acid, methylation and neural tube closure in humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Persistent epigenetic differences associated with prenatal exposure to famine in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Epigenetic gene promoter methylation at birth is associated with child's later adiposity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Epigenetic modification of the renin-angiotensin system in the fetal programming of hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Dietary protein restriction of pregnant rats in the F0 generation induces altered methylation of hepatic gene promoters in the adult male offspring in the F1 and F2 generations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Maternal protein restriction with or without folic acid supplementation during pregnancy alters the hepatic transcriptome in adult male rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Paternally induced transgenerational environmental reprogramming of metabolic gene expression in mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Chronic high-fat diet in fathers programs β-cell dysfunction in female rat offspring

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

RNA induction and inheritance of epigenetic cardiac hypertrophy in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Increased anxiety of mice lacking the serotonin1A receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

The serotonin1A receptor gene as a genetic and prenatal maternal environmental factor in anxiety

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Maternal programming of sexual behavior and hypothalamic-pituitary-gonadal function in the female rat

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Long-lasting changes in stress-induced corticosterone response and anxiety-like behaviors as a consequence of neonatal maternal separation in Long-Evans rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Epigenetic regulation of the glucocorticoid receptor in human brain associates with childhood abuse

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Maternal care and DNA methylation of a glutamic acid decarboxylase 1 promoter in rat hippocampus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Environmental regulation of the neural epigenome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Variants in nicotinic acetylcholine receptors alpha5 and alpha3 increase risks to nicotine dependence

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

A common genetic variant in the 15q24 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) is associated with a reduced ability of women to quit smoking in pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Hippocampal morphology in the inbred mouse strains NZB and CBA/H and their reciprocal congenics for the nonpseudoautosomal region of the Y chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Parent-of-origin effect in transthyretin related amyloid polyneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Excess of maternal HLA-DR3 antigens in HLA DR3,4 positive Type 1 (insulin-dependent) diabetic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

Genome-Wide Linkage Analysis Assessing Parent-of-Origin Effects in the Inheritance of Type 2 Diabetes and BMI in Pima Indians

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01790.X

10.1111/J.1399-0004.2011.01790.X

21 January 2018

Identifiers

DOI

1 reference

release_wxapkz5mgneqlarbzs6pfu3lqq

25 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/wxapkz5mgneqlarbzs6pfu3lqq

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

21933173

1 reference

PubMed ID

21933173