(Q84730497)

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

9 February 2020

title

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

1 reference

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9 February 2020

1 reference

Thyrotoxic periodic paralysis

1 reference

genome-wide association study

inferred from title

1 reference

Ching-Lung Cheung

1

1 reference

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

9 February 2020

Kam-Shing Lau

2

1 reference

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9 February 2020

Andrew Y Y Ho

3

1 reference

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9 February 2020

Ka-Kui Lee

4

1 reference

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9 February 2020

Sau-Cheung Tiu

5

1 reference

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9 February 2020

Emmy Y F Lau

6

1 reference

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9 February 2020

Jenny Leung

7

1 reference

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9 February 2020

Man-Wo Tsang

8

1 reference

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9 February 2020

Kin-Wah Chan

9

1 reference

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9 February 2020

Chun-Yip Yeung

10

1 reference

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9 February 2020

Yu-Cho Woo

11

1 reference

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9 February 2020

Elaine Y N Cheung

12

1 reference

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9 February 2020

Victor H F Hung

13

1 reference

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9 February 2020

Ho-Kwong Pang

14

1 reference

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9 February 2020

Chi-Sang Hung

15

1 reference

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9 February 2020

Pak-Chung Sham

16

1 reference

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9 February 2020

Annie W C Kung

17

1 reference

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9 February 2020

publication date

5 August 2012

1 reference

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9 February 2020

1 reference

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9 February 2020

volume

44

1 reference

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9 February 2020

issue

9

1 reference

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9 February 2020

page(s)

1026-1029

1 reference

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

describes a project that uses

9 February 2020

genome-wide association study

1 reference

https://scigraph.springernature.com/pub.10.1038/ng.2367

inferred from title

exact match

0 references

cites work

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

1 reference

12 December 2020

Clinical review: Thyrotoxic periodic paralysis: a diagnostic challenge

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Measuring the accuracy of diagnostic systems

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity

1 reference

12 December 2020

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

1 reference

12 December 2020

Haploview: analysis and visualization of LD and haplotype maps

1 reference

12 December 2020

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

1 reference

12 December 2020

Dual-mode phospholipid regulation of human inward rectifying potassium channels

1 reference

12 December 2020

LocusZoom: regional visualization of genome-wide association scan results

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.2367

1 reference

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

9 February 2020

1 reference