Parental origin of sequence variants associated with complex diseases - Wikidata - awgldk - TriplyDB

Parental origin of sequence variants associated with complex diseases

Parental origin of sequence variants associated with complex diseases

http://www.wikidata.org/entity/Q37102209

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Phased whole-genome genetic risk in a family quartet using a major allele reference sequence DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes Insights into the Genetic Susceptibility to Type 2 Diabetes from Genome-Wide Association Studies of Obesity-Related Traits Role of ZAC1 in transient neonatal diabetes mellitus and glucose metabolism Genomic imprinting effects on complex traits in domesticated animal species Genetic screening for the risk of type 2 diabetes: worthless or valuable?Genetics of impulsive behaviour Child development and molecular genetics: 14 years later Type 2 diabetes in East Asians: similarities and differences with populations in Europe and the United States Insights into the genetic basis of type 2 diabetes The quiescent cellular state is Arf/p53-dependent and associated with H2AX downregulation and genome stability Recent advances in the molecular genetics of type 2 diabetes mellitus Searching for the human genetic factors standing in the way of universally effective vaccines Maternal nutritional status, C(1) metabolism and offspring DNA methylation: a review of current evidence in human subjects Environmental Influences on Genomic Imprinting Epigenetic modifications: basic mechanisms and role in cardiovascular disease.Integrating Epigenomics into the Understanding of Biomedical Insight Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease Genetics of type 2 diabetes: pathophysiologic and clinical relevance A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway The emergence of human-evolutionary medical genomics Epigenetic and genetic variation at the IGF2/H19 imprinting control region on 11p15.5 is associated with cerebellum weight A role for coding functional variants in HNF4A in type 2 diabetes susceptibility Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility Individualized medicine from prewomb to tomb Missing heritability and strategies for finding the underlying causes of complex disease How Can Genetic Studies Help Us to Understand Links Between Birth Weight and Type 2 Diabetes?Bridging the gap between genetic associations and molecular mechanisms for type 2 diabetes.The architecture of risk for type 2 diabetes: understanding Asia in the context of global findings.Parent-of-origin effects on glucose homeostasis in polycystic ovary syndrome.Genome-wide mapping of methylated adenine residues in pathogenic Escherichia coli using single-molecule real-time sequencing.Maternal genetic mutations as gestational and early life influences in producing psychiatric disease-like phenotypes in mice.Review of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits.Nonparametric method for detecting imprinting effect using all members of general pedigrees with missing data.A genome-wide association study confirms previously reported loci for type 2 diabetes in Han Chinese

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Parental origin of sequence variants associated with complex diseases

http://www.wikidata.org/entity/Q37102209

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on December 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Parental origin of sequence variants associated with complex diseases

@en

Parental origin of sequence variants associated with complex diseases.

@nl

type

label

Parental origin of sequence variants associated with complex diseases

@en

Parental origin of sequence variants associated with complex diseases.

@nl

prefLabel

Parental origin of sequence variants associated with complex diseases

@en

Parental origin of sequence variants associated with complex diseases.

@nl

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P1476

Parental origin of sequence variants associated with complex diseases

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Anne C Ferguson-Smith

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Arnaldur Gylfason

http://www.w3.org/2001/XMLSchema#string

Asgeir Sigurdsson

http://www.w3.org/2001/XMLSchema#string

Astradur B Hreidarsson

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Bardur Sigurgeirsson

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Gisli Masson

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Gunnar Sigurdsson

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Helgi Sigurdsson

http://www.w3.org/2001/XMLSchema#string

Jon H Olafsson

http://www.w3.org/2001/XMLSchema#string

Kari Th Kristinsson

http://www.w3.org/2001/XMLSchema#string

P2860

Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution

New common variants affecting susceptibility to basal cell carcinoma

Genome-wide association study identifies novel breast cancer susceptibility loci

Analysis of the vertebrate insulator protein CTCF-binding sites in the human genome

Global analysis of the insulator binding protein CTCF in chromatin barrier regions reveals demarcation of active and repressive domains

Statistical significance for genomewide studies

Computational and experimental identification of novel human imprinted genes

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

Biallelic expression of HRAS and MUCDHL in human and mouse

Endosomal proteolysis of internalized insulin at the C-terminal region of the B chain by cathepsin D

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868-874

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scholarly article

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10.1038/NATURE08625

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7275

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462

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Gudmar Thorleifsson

Unnur Þorsteinsdóttir

Valgerdur Steinthorsdottir

Rafn Benediktsson

Daniel F Gudbjartsson

Aslaug Jonasdottir

Adalbjorg Jonasdottir

DIAGRAM Consortium

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2009-12-01T00:00:00Z

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40693969

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20016592

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3746295

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