Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3. (Q84730497)

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scientific article published on 05 August 2012

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English	Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.	scientific article published on 05 August 2012

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instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

title

Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

main subject

periodic paralysis

1 reference

based on heuristic

inferred from title

Thyrotoxic periodic paralysis

1 reference

based on heuristic

inferred from title

genome-wide association study

1 reference

based on heuristic

inferred from title

author name string

Ching-Lung Cheung

series ordinal

1

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Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Kam-Shing Lau

series ordinal

2

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Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Andrew Y Y Ho

series ordinal

3

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Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Ka-Kui Lee

series ordinal

4

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Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Sau-Cheung Tiu

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Emmy Y F Lau

series ordinal

6

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stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

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9 February 2020

Jenny Leung

series ordinal

7

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PubMed publication ID

22863731

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Man-Wo Tsang

series ordinal

8

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Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Kin-Wah Chan

series ordinal

9

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stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

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9 February 2020

Chun-Yip Yeung

series ordinal

10

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Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Yu-Cho Woo

series ordinal

11

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Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Elaine Y N Cheung

series ordinal

12

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stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Victor H F Hung

series ordinal

13

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Ho-Kwong Pang

series ordinal

14

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Chi-Sang Hung

series ordinal

15

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Pak-Chung Sham

series ordinal

16

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

Annie W C Kung

series ordinal

17

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stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

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9 February 2020

publication date

5 August 2012

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Europe PubMed Central

PubMed publication ID

22863731

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

published in

Nature Genetics

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stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

volume

44

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Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

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9 February 2020

issue

9

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Europe PubMed Central

PubMed publication ID

22863731

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

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9 February 2020

page(s)

1026-1029

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22863731

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9 February 2020

describes a project that uses

genome-wide association study

1 reference

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cites work

Kir2.6 regulates the surface expression of Kir2.x inward rectifier potassium channels

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22863731

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical review: Thyrotoxic periodic paralysis: a diagnostic challenge

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22863731

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human inward rectifier K(+) channel subunit kir5.1 (KCNJ16) maps to chromosome 17q25 and is expressed in kidney and pancreas

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

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Measuring the accuracy of diagnostic systems

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

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The architecture of gene regulatory variation across multiple human tissues: the MuTHER study

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

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The meaning and use of the area under a receiver operating characteristic (ROC) curve

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

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Inwardly rectifying potassium channels: their structure, function, and physiological roles

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

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Genetic Inactivation of Kcnj16 Identifies Kir5.1 as an Important Determinant of Neuronal PCO2/pH Sensitivity

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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Genetic structure of the Han Chinese population revealed by genome-wide SNP variation

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

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Haploview: analysis and visualization of LD and haplotype maps

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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Dual-mode phospholipid regulation of human inward rectifying potassium channels

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

based on heuristic

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LocusZoom: regional visualization of genome-wide association scan results

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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based on heuristic

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22863731

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based on heuristic

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Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

based on heuristic

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A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome?

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

based on heuristic

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Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

based on heuristic

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KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/22863731

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12 December 2020

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Identifiers

DOI

10.1038/NG.2367

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

PubMed publication ID

22863731

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22863731

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22863731%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 February 2020

 

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