(Q29417089)

21 June 2017

A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa (English)

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genome-wide association study

21 June 2017

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anorexia nervosa

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author name string

K Wang

1

1 reference

21 June 2017

H Zhang

2

1 reference

21 June 2017

C S Bloss

3

1 reference

21 June 2017

V Duvvuri

4

1 reference

21 June 2017

W Kaye

5

1 reference

21 June 2017

N J Schork

6

1 reference

21 June 2017

W Berrettini

7

1 reference

21 June 2017

H Hakonarson

8

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21 June 2017

Price Foundation Collaborative Group

9

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21 June 2017

language of work or name

English

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publication date

16 November 2010

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21 June 2017

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21 June 2017

16

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21 June 2017

949-959

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21 June 2017

9

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describes a project that uses

21 June 2017

genome-wide association study

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Evidence for the role of EPHX2 gene variants in anorexia nervosa

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

Genetic variants associated with disordered eating

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

A genome-wide association meta-analysis identifies new childhood obesity loci

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

A mega-analysis of genome-wide association studies for major depressive disorder

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

Five years of GWAS discovery

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

Genome-wide association study identifies five new schizophrenia loci

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

The prevalence and correlates of eating disorders in the National Comorbidity Survey Replication

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

Copy-number variations associated with neuropsychiatric conditions

18 April 2017

1 reference

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

22 April 2017

1 reference

PLINK: a tool set for whole-genome association and population-based linkage analyses

22 April 2017

1 reference

Identification of loci associated with schizophrenia by genome-wide association and follow-up

22 April 2017

1 reference

Common genetic variants on 5p14.1 associate with autism spectrum disorders

22 April 2017

1 reference

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

22 April 2017

1 reference

Large recurrent microdeletions associated with schizophrenia

22 April 2017

1 reference

Association between microdeletion and microduplication at 16p11.2 and autism

22 April 2017

1 reference

ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

22 April 2017

1 reference

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

22 April 2017

1 reference

Origins and functional impact of copy number variation in the human genome

22 April 2017

1 reference

GCTA: a tool for genome-wide complex trait analysis

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

Integrating common and rare genetic variation in diverse human populations

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

Genotype imputation for genome-wide association studies

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

GenABEL: an R library for genome-wide association analysis

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3859494

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

18 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Anorexia nervosa: current status and future directions

22 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Excess mortality, causes of death and prognostic factors in anorexia nervosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Controlled family study of anorexia nervosa and bulimia nervosa: evidence of shared liability and transmission of partial syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

A controlled family study of anorexia nervosa and bulimia nervosa: psychiatric disorders in first-degree relatives and effects of proband comorbidity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Prevalence, heritability, and prospective risk factors for anorexia nervosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

A preliminary population-based twin study of self-reported eating disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

The genetics of anorexia nervosa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Evidence for a susceptibility gene for anorexia nervosa on chromosome 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Candidate genes for anorexia nervosa in the 1p33-36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Further evidence of association of OPRD1 & HTR1D polymorphisms with susceptibility to anorexia nervosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Linkage analysis of anorexia nervosa incorporating behavioral covariates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Association of multiple DRD2 polymorphisms with anorexia nervosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

A search for susceptibility loci for anorexia nervosa: methods and sample description.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

The psychobiology and diagnostic significance of amenorrhea in patients with anorexia nervosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

The Yale-Brown Obsessive Compulsive Scale. I. Development, use, and reliability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

The dimensions of perfectionism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: a case-control study of female patients and several ethnic groups in the Israeli Jewish population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

A genome-wide investigation of SNPs and CNVs in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Singleton deletions throughout the genome increase risk of bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Disruption of contactin 4 in three subjects with autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Case???control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

Comorbidity between eating disorders and anxiety disorders: a review.

21 January 2018

1 reference

12 December 2020

The medical complications of anorexia nervosa

1 reference

12 December 2020

Patterns of menstrual disturbance in eating disorders.

1 reference

12 December 2020

Late onset eating disorders in Spain: clinical characteristics and therapeutic implications.

1 reference

12 December 2020

Using ancestry-informative markers to identify fine structure across 15 populations of European origin

1 reference

12 December 2020

Genetic findings in anorexia and bulimia nervosa

1 reference

12 December 2020

Mortality in anorexia nervosa

1 reference

12 December 2020

1 reference

12 December 2020

Review of the prevalence and incidence of eating disorders

1 reference

12 December 2020

Genome-wide association studies of obesity and metabolic syndrome

1 reference

12 December 2020

Long-term prognosis in anorexia nervosa: lessons from a 21-year follow-up study

1 reference

12 December 2020

Update on the treatment of anorexia nervosa: review of clinical trials, practice guidelines and emerging interventions

1 reference

12 December 2020

Childhood eating disorders: British national surveillance study.

1 reference

12 December 2020

Evoker: a visualization tool for genotype intensity data

1 reference

12 December 2020

Understanding the relation between anorexia nervosa and bulimia nervosa in a Swedish national twin sample

1 reference

12 December 2020

Candidate gene association analysis for a quantitative trait, using parent-offspring trios.

1 reference

12 December 2020

The Australian Burden of Disease Study: measuring the loss of health from diseases, injuries and risk factors.

1 reference

12 December 2020

Sample size requirements for association studies of gene-gene interaction

1 reference

12 December 2020

Fat mass and obesity-associated gene (FTO) in eating disorders: evidence for association of the rs9939609 obesity risk allele with bulimia nervosa and anorexia nervosa.

1 reference

12 December 2020

GWAMA: software for genome-wide association meta-analysis

1 reference

12 December 2020

Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers

1 reference

12 December 2020

Interspecies genetics of eating disorder traits

1 reference

12 December 2020

How high are the costs of eating disorders - anorexia nervosa and bulimia nervosa - for German society?

1 reference

12 December 2020

The mortality rate from anorexia nervosa.

1 reference

12 December 2020

Anorexia nervosa viewed as an extreme weight condition: genetic implications.

1 reference

12 December 2020

Medical complications in adolescents with anorexia nervosa: a review of the literature

1 reference

12 December 2020

Anorexia nervosa mortality in Northeast Scotland, 1965-1999.

1 reference

12 December 2020

Outcomes of eating disorders: a systematic review of the literature

1 reference

12 December 2020

Anorexia nervosa and major depression: shared genetic and environmental risk factors

1 reference

12 December 2020

Symptom profile of major depressive disorder in women with eating disorders.

1 reference

12 December 2020

Symptom fluctuation in eating disorders: correlates of diagnostic crossover.

1 reference

12 December 2020

Eating disorders: from twin studies to candidate genes and beyond

1 reference

12 December 2020

Comorbidity of anxiety disorders with anorexia and bulimia nervosa

1 reference

12 December 2020

Genetic and environmental influences on anorexia nervosa syndromes in a population-based twin sample

1 reference

12 December 2020

Mortality rates in patients with anorexia nervosa and other eating disorders. A meta-analysis of 36 studies

1 reference

12 December 2020

Academy for eating disorders position paper: eating disorders are serious mental illnesses

1 reference

12 December 2020

Anorexia nervosa treatment: a systematic review of randomized controlled trials

1 reference

12 December 2020

Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals

1 reference

12 December 2020

50-year trends in the incidence of anorexia nervosa in Rochester, Minn.: a population-based study

1 reference

12 December 2020

Risk factors for eating disorders

1 reference

12 December 2020

Genetic architectures of psychiatric disorders: the emerging picture and its implications

1 reference

12 December 2020

Genome-wide efficient mixed-model analysis for association studies

1 reference

12 December 2020

The 5-HT2A −1438G/A polymorphism in anorexia nervosa: a combined analysis of 316 trios from six European centres

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

7 January 2021

Use of percentiles for the body mass index in anorexia nervosa: diagnostic, epidemiological, and therapeutic considerations

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

7 January 2021

Structured Interview for Anorexic and Bulimic disorders for DSM-IV and ICD-10: updated (third) revision.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

7 January 2021

Disruption of the neurexin 1 gene is associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

7 January 2021

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FMP.2010.107

7 January 2021

Identifiers

DOI

10.1038/MP.2010.107

1 reference

Dimensions Publication ID

21 June 2017

1014189966

0 references

OpenCitations bibliographic resource ID

428960

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference