(Q80051194)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17389904%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

title

Dense SNP association study for bipolar I disorder on chromosome 18p11 suggests two loci with excess paternal transmission (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17389904%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

1 reference

Mulle JG

1

1 reference

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28 December 2019

Fallin MD

2

1 reference

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28 December 2019

Lasseter VK

3

1 reference

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28 December 2019

McGrath JA

4

1 reference

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28 December 2019

Wolyniec PS

5

1 reference

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28 December 2019

Pulver AE

6

1 reference

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28 December 2019

publication date

31 October 2006

1 reference

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28 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17389904%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

volume

12

1 reference

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28 December 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17389904%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

page(s)

367-375

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17389904%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.mp.4001916

28 December 2019

exact match

0 references

cites work

Costs of bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

The Heritability of Bipolar Affective Disorder and the Genetic Relationship to Unipolar Depression

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

The Wellcome trust UK–Irish bipolar affective disorder sibling-pair genome screen: first stage report

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Genomewide linkage scan for bipolar-disorder susceptibility loci among Ashkenazi Jewish families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

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.MP.4001916

7 January 2021

Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Linkage disequilibrium analysis of G-olf alpha (GNAL) in bipolar affective disorder.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Genomic structure and novel variants of myo-inositol monophosphatase 2 (IMPA2).

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Association analysis of the pituitary adenyl cyclase activating peptide gene (PACAP) on chromosome 18p11 with schizophrenia and bipolar disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder in Japanese and the National Institute of Mental Health pedigrees.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Lack of association between variations in the melanocortin 5 receptor gene and bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Analysis of variations in the NAPG gene on chromosome 18p11 in bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

A common variant associated with prostate cancer in European and African populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Sample size requirements for matched case-control studies of gene-environment interaction

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Haplotype and missing data inference in nuclear families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Haplotype inference in random population samples.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Assessment of the effect of age at onset on linkage to bipolar disorder: evidence on chromosomes 18p and 21q

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Methods for detection of parent-of-origin effects in genetic studies of case-parents triads

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Paternal transmission of the very common class I INS VNTR alleles predisposes to childhood obesity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Epigenetics and bipolar disorder: New opportunities and challenges

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

An integrated epigenetic and genetic approach to common human disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Epigenetics and human disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

The effects of human population structure on large genetic association studies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Demonstrating stratification in a European American population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

A census of mammalian imprinting.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Alternative transcripts and evidence of imprinting of GNAL on 18p11.2.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with schizophrenia in the Japanese population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001916

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001916

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17389904%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

1 reference