(Q83593597)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22399142%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22399142%20AND%20SRC:MED&resulttype=core&format=json

hypokalemic periodic paralysis

25 January 2020

main subject

1 reference

genome-wide association study

inferred from title

1 reference

1 reference

16

Michiaki Kubo

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22399142%20AND%20SRC:MED&resulttype=core&format=json

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17

Yusuke Nakamura

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22399142%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

15

Naoyuki Kamatani

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22399142%20AND%20SRC:MED&resulttype=core&format=json

Surakameth Mahasirimongkol

25 January 2020

3

object named as

Surakameth Mahasirimongkol

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22399142%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

author name string

Wallaya Jongjaroenprasert

1

1 reference

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25 January 2020

Theerawut Phusantisampan

2

1 reference

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25 January 2020

Taisei Mushiroda

4

1 reference

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25 January 2020

Nattiya Hirankarn

5

1 reference

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25 January 2020

Thiti Snabboon

6

1 reference

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25 January 2020

Suwannee Chanprasertyotin

7

1 reference

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25 January 2020

Puntip Tantiwong

8

1 reference

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25 January 2020

Supamai Soonthornpun

9

1 reference

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25 January 2020

Paninee Rattanapichart

10

1 reference

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25 January 2020

Sunee Mamanasiri

11

1 reference

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25 January 2020

Thep Himathongkam

12

1 reference

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25 January 2020

Boonsong Ongphiphadhanakul

13

1 reference

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25 January 2020

Atsushi Takahashi

14

1 reference

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25 January 2020

publication date

8 March 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22399142%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

25 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22399142%20AND%20SRC:MED&resulttype=core&format=json

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volume

57

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22399142%20AND%20SRC:MED&resulttype=core&format=json

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issue

5

1 reference

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25 January 2020

page(s)

301-304

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22399142%20AND%20SRC:MED&resulttype=core&format=json

describes a project that uses

25 January 2020

genome-wide association study

1 reference

https://scigraph.springernature.com/pub.10.1038/jhg.2012.20

inferred from title

exact match

0 references

cites work

HLA and thyrotoxic periodic paralysis.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Association of novel single nucleotide polymorphisms in the calcium channel alpha 1 subunit gene (Ca(v)1.1) and thyrotoxic periodic paralysis.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Arg16Gly polymorphism in beta2-adrenergic receptor gene is not associated with thyrotoxic periodic paralysis in Korean male patients with Graves' disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

A novel sodium channel mutation in a family with hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Clinical and Molecular Analysis of Chinese Patients with Thyrotoxic Periodic Paralysis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Mutation screening in Chinese hypokalemic periodic paralysis patients

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Prospects for whole-genome linkage disequilibrium mapping of common disease genes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Population structure and eigenanalysis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

The International HapMap Project

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

A high-throughput SNP typing system for genome-wide association studies

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

SNPexp - A web tool for calculating and visualizing correlation between HapMap genotypes and gene expression levels

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Genetic and functional linkage of Kir5.1 and Kir2.1 channel subunits

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Long range chromatin interactions involved in gene regulation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.20

7 January 2021

Identifiers

DOI

10.1038/JHG.2012.20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22399142%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

1 reference