(Q29417097)

16 April 2017

title

Genome-wide association study in German patients with attention deficit/hyperactivity disorder (English)

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genome-wide association study

16 April 2017

main subject

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attention

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based on heuristic

inferred from title

attention deficit hyperactivity disorder

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6

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Karl-Heinz Jöckel

21

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André Scherag

2

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Johannes Hebebrand

36

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Anke Hinney

1

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Andreas Reif

34

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Klaus-Peter Lesch

33

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Barbara Franke

16

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Stephen Faraone

14

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Sven Cichon

17

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Anna-Lena Volckmar

12

Anna-Lena Volckmar

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Heike Weber

Heike Weber

9

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Maria R Dauvermann

Maria R Dauvermann

7

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Judith Sinzig

Judith Sinzig

28

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Per Hoffmann

Per Hoffmann

18

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Markus M Nöthen

Markus M Nöthen

19

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Beate Herpertz-Dahlmann

27

Beate Herpertz-Dahlmann

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22

H-Erich Wichmann

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20

Stefan Schreiber

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15

Benjamin M Neale

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31

Andreas Warnke

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23

Christine Freitag

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4

Özgür Albayrak

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30

Tobias J Renner

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Benno G. Schimmelmann

35

Benno G Schimmelmann

1 reference

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25

Jobst Meyer

1 reference

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10

Susann Scherag

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32

Marcel Romanos

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29

Gerd Lehmkuhl

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Ivonne Jarick

3

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Carolin Pütter

5

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Sebastian Beck

8

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Trang T Nguyen

11

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Nadja Knoll

13

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Thomas Lempp

24

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Susanne Gilsbach

26

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Psychiatric GWAS Consortium: ADHD subgroup

37

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language of work or name

English

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publication date

19 October 2011

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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

16 April 2017

published in

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16 April 2017

volume

156B

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16 April 2017

issue

8

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16 April 2017

page(s)

888-897

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describes a project that uses

16 April 2017

genome-wide association study

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based on heuristic

inferred from title

cites work

Molecular genetics of attention-deficit/hyperactivity disorder: an overview

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Genomic control for association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Molecular genetics of attention deficit hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Molecular genetics of attention-deficit/hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Genome-wide association studies in ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Phenotypic and measurement influences on heritability estimates in childhood ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Candidate gene studies of ADHD: a meta-analytic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Child and adolescent psychiatric genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Molecular genetic aspects of attention-deficit/hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

The IMAGE project: methodological issues for the molecular genetic analysis of ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Family-based designs in the age of large-scale gene-association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Mutation screening of two candidate genes from 13q32 in families affected with Bipolar disorder: human peptide transporter (SLC15A1) and human glypican5 (GPC5)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Family-based genome-wide association scan of attention-deficit/hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Genome-wide association scan of attention deficit hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Spoiling the whole bunch: quality control aimed at preserving the integrity of high-throughput genotyping

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

A framework for interpreting genome-wide association studies of psychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Allelic variants of SNAP25 in a family-based sample of ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Assessment of clinically silent atherosclerotic disease and established and novel risk factors for predicting myocardial infarction and cardiac death in healthy middle-aged subjects: rationale and design of the Heinz Nixdorf RECALL Study. Risk Facto

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Whole-genome association study of bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

A genetic risk factor for periodic limb movements in sleep

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Genomewide association for schizophrenia in the CATIE study: results of stage 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

GIT1 is associated with ADHD in humans and ADHD-like behaviors in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

Population differences in the International Multi-Centre ADHD Gene Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31246

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.31246

1 reference

16 April 2017

1 reference