(Q28943315)

1

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Susanne Walitza

object named as

Susanne Walitza

15

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Andreas Warnke

12

object named as

Andreas Warnke

1 reference

14 March 2017

11

Christine Freitag

1 reference

14 March 2017

3

Tobias J. Renner

1 reference

14 March 2017

5

Christoph Röser

1 reference

14 March 2017

8

Jasmin Romanos

1 reference

14 March 2017

9

Monika Heine

1 reference

14 March 2017

10

Jobst Meyer

1 reference

14 March 2017

14

Helmut Schäfer

1 reference

14 March 2017

13

Marcel Romanos

1 reference

14 March 2017

Nina Timmesfeld

2

1 reference

14 March 2017

Rebecca Halperin

4

1 reference

14 March 2017

T. Trang Nguyen

6

1 reference

14 March 2017

David W. Craig

7

1 reference

14 March 2017

Dietrich A. Stephan

17

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14 March 2017

Christian Jacob

Journal of Neural Transmission

18

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14 March 2017

language of work or name

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1 November 2008

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14 March 2017

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14 March 2017

115

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14 March 2017

11

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14 March 2017

1573–1585

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14 March 2017

https://scigraph.springernature.com/pub.10.1007/s00702-008-0119-3

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cites work

CSMD1 is a novel multiple domain complement-regulatory protein highly expressed in the central nervous system and epithelial tissues

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00702-008-0119-3

RhoA and Rac mediate endothelial cell polarization and detachment induced by T-cadherin

21 January 2018

1 reference

12 December 2020

Genome-wide association for methamphetamine dependence: convergent results from 2 samples

1 reference

12 December 2020

GRB10 binds to LRP6, the Wnt co-receptor and inhibits canonical Wnt signaling pathway

1 reference

12 December 2020

A whole genome association study of neuroticism using DNA pooling

1 reference

12 December 2020

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

1 reference

12 December 2020

Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.

1 reference

12 December 2020

Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays.

1 reference

12 December 2020

Mice that lack astrotactin have slowed neuronal migration

1 reference

12 December 2020

"Higher order" addiction molecular genetics: convergent data from genome-wide association in humans and mice

1 reference

12 December 2020

Kalirin-7 controls activity-dependent structural and functional plasticity of dendritic spines

1 reference

12 December 2020

Genome-wide association study identifies novel breast cancer susceptibility loci

1 reference

12 December 2020

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder

1 reference

12 December 2020

Co-morbidity of adult attention-deficit/hyperactivity disorder with focus on personality traits and related disorders in a tertiary referral center.

1 reference

12 December 2020

Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays

1 reference

12 December 2020

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

1 reference

12 December 2020

Applicability of DNA pools on 500 K SNP microarrays for cost-effective initial screens in genomewide association studies

1 reference

12 December 2020

Identification of proteins associating with glycosylphosphatidylinositol- anchored T-cadherin on the surface of vascular endothelial cells: role for Grp78/BiP in T-cadherin-dependent cell survival

1 reference

12 December 2020

Negative regulation of insulin-stimulated mitogen-activated protein kinase signaling by Grb10.

1 reference

12 December 2020

Cortical abnormalities in children and adolescents with attention-deficit hyperactivity disorder

1 reference

12 December 2020

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

Molecular genetics of attention-deficit/hyperactivity disorder

1 reference

12 December 2020

Deletion in Catna2, encoding alpha N-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation

1 reference

12 December 2020

Growth factor receptor-binding protein 10 (Grb10) as a partner of phosphatidylinositol 3-kinase in metabolic insulin action

1 reference

12 December 2020

Pooled DNA genotyping on Affymetrix SNP genotyping arrays

1 reference

12 December 2020

Specific inhibition by hGRB10zeta of insulin-induced glycogen synthase activation: evidence for a novel signaling pathway

1 reference

12 December 2020

Addiction molecular genetics: 639,401 SNP whole genome association identifies many "cell adhesion" genes

1 reference

12 December 2020

CNS gene encoding astrotactin, which supports neuronal migration along glial fibers

1 reference

12 December 2020

Common Kibra alleles are associated with human memory performance

1 reference

12 December 2020

Cell adhesion molecules: signalling functions at the synapse

1 reference

12 December 2020

Central nervous system neuronal migration

1 reference

12 December 2020

Pooled association genome scanning for alcohol dependence using 104,268 SNPs: validation and use to identify alcoholism vulnerability loci in unrelated individuals from the collaborative study on the genetics of alcoholism

1 reference

12 December 2020

Integrin-linked kinase is an essential mediator for T-cadherin-dependent signaling via Akt and GSK3beta in endothelial cells

1 reference

12 December 2020

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

1 reference

12 December 2020

Distinct roles for the two Rho GDP/GTP exchange factor domains of kalirin in regulation of neurite growth and neuronal morphology.

1 reference

12 December 2020

Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

1 reference

12 December 2020

The prevalence and correlates of adult ADHD in the United States: results from the National Comorbidity Survey Replication

1 reference

12 December 2020

Molecular genetics of nicotine dependence and abstinence: whole genome association using 520,000 SNPs

1 reference

12 December 2020

[Neurobiology of attention-deficit hyperactivity disorder].

1 reference

12 December 2020

Molecular genetics of successful smoking cessation: convergent genome-wide association study results

1 reference

12 December 2020

Algorithms for large-scale genotyping microarrays

1 reference

12 December 2020

A genome-wide association study in 574 schizophrenia trios using DNA pooling

1 reference

12 December 2020

Grb10: more than a simple adaptor protein

1 reference

12 December 2020

Identification of two new members of the CSMD gene family

1 reference

12 December 2020

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

1 reference

12 December 2020

SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays

1 reference

12 December 2020

Transcriptome analysis identifies pathways associated with enhanced maternal performance in QSi5 mice.

1 reference

12 December 2020

Lifetime prevalence and age-of-onset distributions of mental disorders in the World Health Organization's World Mental Health Survey Initiative

1 reference

12 December 2020

Neuropsychological endophenotype approach to genome-wide linkage analysis identifies susceptibility loci for ADHD on 2q21.1 and 13q12.11.

1 reference

12 December 2020

A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples

1 reference

12 December 2020

Dendritic spine dynamics--a key role for kalirin-7.

1 reference

12 December 2020

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

1 reference

12 December 2020

Isoforms of kalirin, a neuronal Dbl family member, generated through use of different 5'- and 3'-ends along with an internal translational initiation site

1 reference

12 December 2020

Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies

1 reference

12 December 2020

GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers

1 reference

12 December 2020

Novel genes identified in a high-density genome wide association study for nicotine dependence

1 reference

12 December 2020