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

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9 February 2020

title

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

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9 February 2020

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Thyrotoxic periodic paralysis

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genome-wide association study

inferred from title

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Ching-Lung Cheung

1

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Kam-Shing Lau

2

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Andrew Y Y Ho

3

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Ka-Kui Lee

4

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Sau-Cheung Tiu

5

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Emmy Y F Lau

6

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Jenny Leung

7

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Man-Wo Tsang

8

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Kin-Wah Chan

9

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Chun-Yip Yeung

10

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Yu-Cho Woo

11

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Elaine Y N Cheung

12

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Victor H F Hung

13

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Ho-Kwong Pang

14

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Chi-Sang Hung

15

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Pak-Chung Sham

16

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Annie W C Kung

17

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publication date

5 August 2012

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volume

44

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issue

9

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page(s)

1026-1029

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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

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cites work

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

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12 December 2020

Clinical review: Thyrotoxic periodic paralysis: a diagnostic challenge

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12 December 2020

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

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12 December 2020

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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12 December 2020

Measuring the accuracy of diagnostic systems

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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12 December 2020

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

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12 December 2020

Dual-mode phospholipid regulation of human inward rectifying potassium channels

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12 December 2020

LocusZoom: regional visualization of genome-wide association scan results

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Identifiers

DOI

10.1038/NG.2367

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9 February 2020

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