(Q36360605)

English

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

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10318931%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

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

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10318931%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

susceptibility locus

1 reference

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inferred from title

John I. Nurnberger

17

1 reference

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7 December 2019

author name string

S D Detera-Wadleigh

1

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7 December 2019

J A Badner

2

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7 December 2019

W H Berrettini

3

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7 December 2019

T Yoshikawa

4

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7 December 2019

L R Goldin

5

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7 December 2019

G Turner

6

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7 December 2019

D Y Rollins

7

1 reference

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7 December 2019

T Moses

8

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7 December 2019

A R Sanders

9

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7 December 2019

J D Karkera

10

1 reference

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7 December 2019

L E Esterling

11

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7 December 2019

J Zeng

12

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7 December 2019

T N Ferraro

13

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7 December 2019

J J Guroff

14

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7 December 2019

D Kazuba

15

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7 December 2019

M E Maxwell

16

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7 December 2019

E S Gershon

18

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7 December 2019

language of work or name

0 references

publication date

1 May 1999

1 reference

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7 December 2019

number of pages

6

1 reference

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inferred from page(s)

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

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7 December 2019

96

1 reference

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7 December 2019

5604-5609

1 reference

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7 December 2019

10

1 reference

Europe PubMed Central

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7 December 2019

Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

Optimal ascertainment strategies to detect linkage to common disease alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

Linkage of bipolar affective disorder to chromosome 18 markers in a new pedigree series.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

Allele-sharing models: LOD scores and accurate linkage tests

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

A metric map of humans: 23,500 loci in 850 bands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

The future of genetic studies of complex human diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

Parametric and nonparametric linkage analysis: a unified multipoint approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

The continuum of psychosis and its implication for the structure of the gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

Estimating the power of a proposed linkage study: a practical computer simulation approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

A controlled family study of chronic psychoses. Schizophrenia and schizoaffective disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

30 September 2017

Cytogenetic abnormalities on chromosome 18 associated with bipolar affective disorder or schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

28 June 2018

Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

28 June 2018

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

28 June 2018

Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

28 June 2018

A manic depressive history.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

28 June 2018

Type I bipolar disorder associated with a fragile site on chromosome 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

28 June 2018

Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

22 September 2018

The gene for Darier's disease maps to chromosome 12q23-q24.1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

22 September 2018

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

22 September 2018

Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=21907

22 September 2018

A locus for bipolar affective disorder on chromosome 4p

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.10.5604

21 January 2018

Continuity and discontinuity of affective disorders and schizophrenia. Results of a controlled family study

1 reference

https://pubmed.ncbi.nlm.nih.gov/10318931

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial cosegregation of major affective disorder and Darier's disease (keratosis follicularis)

1 reference

https://pubmed.ncbi.nlm.nih.gov/10318931

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations

1 reference

https://pubmed.ncbi.nlm.nih.gov/10318931

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal inheritance and chromosome 18 allele sharing in unilineal bipolar illness pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/10318931

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 3, 5, 15, 16, 17, and 22

1 reference

https://pubmed.ncbi.nlm.nih.gov/10318931

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An integrated physical map of 18p11.2: a susceptibility region for bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/10318931

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Affective disorder associated with a balanced translocation involving chromosome 14 and 18

1 reference

https://pubmed.ncbi.nlm.nih.gov/10318931

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significant linkage between bipolar affective disorder and chromosome 12q24

1 reference

https://pubmed.ncbi.nlm.nih.gov/10318931

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10318931

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.96.10.5604

1 reference

Europe PubMed Central

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7 December 2019

1999PNAS...96.5604D

0 references

1 reference

Europe PubMed Central

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7 December 2019

1 reference

Europe PubMed Central

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7 December 2019

ResearchGate publication ID

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