(Q28245905)

DOI

10.1038/SJ.EJHG.5201794

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1038/SJ.EJHG.5201794

author

Doron Lancet

14

0 references

Edna Ben-Asher

7

0 references

Fabio Macciardi

object named as

Fabio Macciardi

12

0 references

Richard P. Ebstein

object named as

Richard P Ebstein

4

0 references

Jacques S Beckmann

object named as

Jacques S Beckmann

13

0 references

author name string

Daniela Amann-Zalcenstein

1

0 references

Nili Avidan

2

0 references

Kyra Kanyas

3

0 references

Yoav Kohn

5

0 references

Adnan Hamdan

6

0 references

Osnat Karni

8

0 references

Muhammed Mujaheed

9

0 references

Ronnen H Segman

10

0 references

Wolfgang Maier

11

0 references

Bernard Lerer

European Journal of Human Genetics

15

0 references

language of work or name

English

0 references

publication date

October 2006

0 references

published in

0 references

volume

14

0 references

issue

10

0 references

page(s)

1111-9

0 references

cites work

Implications of normal brain development for the pathogenesis of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

The neurodevelopmental model of schizophrenia: update 2005.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

The genetic epidemiology of schizophrenia and of schizophrenia spectrum disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Linkage and associated studies of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Genetics of schizophrenia and the new millennium: progress and pitfalls

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Disruption of two novel genes by a translocation co-segregating with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Genes for schizophrenia? Recent findings and their pathophysiological implications

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

The genes for schizophrenia: finally a breakthrough?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Genome scan for susceptibility loci for schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Excitement and confusion on chromosome 6q: the challenges of neuropsychiatric genetics in microcosm

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Research diagnostic criteria: rationale and reliability

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

The family history method using diagnostic criteria. Reliability and validity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Nosology of chronic mood disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

PBAT: tools for family-based association studies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

PBAT: a comprehensive software package for genome-wide association analysis of complex family-based studies.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

The structure of haplotype blocks in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

TFBS: Computational framework for transcription factor binding site analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Quantitative discrimination of MEF2 sites

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Genome annotation of a 1.5 Mb region of human chromosome 6q23 encompassing a quantitative trait locus for fetal hemoglobin expression in adults

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Consanguineous matings in an Israeli-Arab community

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Trends in the frequencies of consanguineous marriages in the Israeli Arab community

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Ahi-1, a novel gene encoding a modular protein with WD40-repeat and SH3 domains, is targeted by the Ahi-1 and Mis-2 provirus integrations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021

Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201675

7 January 2021