(Q36687516)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

0 references

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

author name string

L A McInnes

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

M A Escamilla

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

S K Service

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

P Leon

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

S Silva

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

E Rojas

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

M Spesny

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

S Baharloo

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

K Blankenship

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

A Peterson

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

D Tyler

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

N Shimayoshi

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

C Tobey

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

S Batki

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

S Vinogradov

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

L Meza

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

A Gallegos

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

E Fournier

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

L B Smith

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

S H Barondes

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

L A Sandkuijl

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

N B Freimer

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

language of work or name

English

0 references

publication date

1 November 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

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

21 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

93

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

page(s)

13060-13065

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

issue

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

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

21 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

A microsatellite genetic linkage map of human chromosome 13.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Mutational processes of simple-sequence repeat loci in human populations.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

A genome-wide search for human type 1 diabetes susceptibility genes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Sublocalization of an ataxia-telangiectasia gene distal to D11S384 by ancestral haplotyping in Costa Rican families

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Mapping genes for psychiatric disorders and behavioral traits

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

The 1993-94 Généthon human genetic linkage map

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Bipolar affective disorders linked to DNA markers on chromosome 11

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Allele frequency estimation from data on relatives

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

A second-generation linkage map of the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

The gene for an inherited form of deafness maps to chromosome 5q31

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

A diagnostic interview: the schedule for affective disorders and schizophrenia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Complex segregation analyses of old order Amish families ascertained through bipolar I individuals

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

A Danish Twin Study of Manic-Depressive Disorders

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

An approach to investigating linkage for bipolar disorder using large Costa Rican pedigrees

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Use of linkage disequilibrium approaches to map genes for bipolar disorder in the Costa Rican population

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Bipolar disorder: evidence for a major locus.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24046

Effects of flow patterns on the localization and expression of VE-cadherin at vascular endothelial cell junctions: in vivo and in vitro investigations

5 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.93.23.13060

Genetic linkage between X-chromosome markers and bipolar affective illness

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.93.23.13060

Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees

21 January 2018

1 reference

12 December 2020

Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree

1 reference

12 December 2020

Model misspecification and multipoint linkage analysis

1 reference

12 December 2020

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

1 reference

12 December 2020

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)

1 reference

12 December 2020

Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome llq

1 reference

12 December 2020

The analysis of X-linkage

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.93.23.13060

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8917544%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference