(Q43894399)

27 November 2017

A large-scale screen for coding variants predisposing to psoriasis (English)

1 reference

27 November 2017

Haojing Shao

19

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Jun Wang

object named as

Jun Wang

66

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author name string

Huayang Tang

1

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27 November 2017

Xin Jin

2

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27 November 2017

Yang Li

3

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27 November 2017

Hui Jiang

4

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27 November 2017

Xianfa Tang

5

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27 November 2017

Xu Yang

6

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27 November 2017

Hui Cheng

7

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27 November 2017

Ying Qiu

8

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27 November 2017

Gang Chen

9

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27 November 2017

Junpu Mei

10

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27 November 2017

Fusheng Zhou

11

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27 November 2017

Renhua Wu

12

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27 November 2017

Xianbo Zuo

13

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27 November 2017

Yong Zhang

14

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27 November 2017

Xiaodong Zheng

15

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27 November 2017

Qi Cai

16

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27 November 2017

Xianyong Yin

17

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27 November 2017

Cheng Quan

18

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27 November 2017

Yong Cui

20

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27 November 2017

Fangzhen Tian

21

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27 November 2017

Xia Zhao

22

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27 November 2017

Hong Liu

23

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27 November 2017

Fengli Xiao

24

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27 November 2017

Fengping Xu

25

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27 November 2017

Jianwen Han

26

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27 November 2017

Dongmei Shi

27

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27 November 2017

Anping Zhang

28

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27 November 2017

Cheng Zhou

29

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27 November 2017

Qibin Li

30

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27 November 2017

Xing Fan

31

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27 November 2017

Liya Lin

32

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27 November 2017

Hongqing Tian

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27 November 2017

Zaixing Wang

34

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27 November 2017

Huiling Fu

35

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27 November 2017

Fang Wang

36

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27 November 2017

Baoqi Yang

37

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27 November 2017

Shaowei Huang

38

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27 November 2017

Bo Liang

39

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27 November 2017

Xuefeng Xie

40

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27 November 2017

Yunqing Ren

41

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27 November 2017

Qingquan Gu

42

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27 November 2017

Guangdong Wen

43

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27 November 2017

Yulin Sun

44

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27 November 2017

Xueli Wu

45

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27 November 2017

Lin Dang

46

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27 November 2017

Min Xia

47

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27 November 2017

Junjun Shan

48

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27 November 2017

Tianhang Li

49

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27 November 2017

Lin Yang

50

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27 November 2017

Xiuyun Zhang

51

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27 November 2017

Yuzhen Li

52

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27 November 2017

Chundi He

53

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27 November 2017

Aie Xu

54

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27 November 2017

Liping Wei

55

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27 November 2017

Xiaohang Zhao

56

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27 November 2017

Xinghua Gao

57

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27 November 2017

Jinhua Xu

58

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27 November 2017

Furen Zhang

59

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27 November 2017

Jianzhong Zhang

60

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27 November 2017

Yingrui Li

61

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27 November 2017

Liangdan Sun

62

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27 November 2017

Runsheng Chen

64

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27 November 2017

Sen Yang

65

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27 November 2017

Xuejun Zhang

67

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27 November 2017

Jianjun Liu

63

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27 November 2017

language of work or name

English

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publication date

10 November 2013

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27 November 2017

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27 November 2017

46

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27 November 2017

1

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27 November 2017

45-50

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https://scigraph.springernature.com/pub.10.1038/ng.2827

27 November 2017

0 references

cites work

Genome-wide association study of skin complex diseases

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Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.

21 January 2018

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A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci

21 January 2018

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A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

21 January 2018

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Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways

21 January 2018

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Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2

21 January 2018

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Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL

21 January 2018

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Genome-wide association analysis identifies three psoriasis susceptibility loci

21 January 2018

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Association analyses identify six new psoriasis susceptibility loci in the Chinese population

21 January 2018

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Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis

21 January 2018

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Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene

21 January 2018

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Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci

21 January 2018

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Next-generation association studies for complex traits

21 January 2018

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Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

21 January 2018

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Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

21 January 2018

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Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

21 January 2018

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Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis

21 January 2018

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CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease

21 January 2018

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Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis

21 January 2018

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Exome sequencing identifies the cause of a mendelian disorder

21 January 2018

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Polymorphisms of the IL12B and IL23R genes are associated with psoriasis

21 January 2018

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Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

21 January 2018

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A method and server for predicting damaging missense mutations

21 January 2018

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Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

21 January 2018

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Structure of the connexin 26 gap junction channel at 3.5 A resolution

21 January 2018

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Structural basis for antigenic peptide precursor processing by the endoplasmic reticulum aminopeptidase ERAP1

21 January 2018

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Crystal structures of the endoplasmic reticulum aminopeptidase-1 (ERAP1) reveal the molecular basis for N-terminal peptide trimming

21 January 2018

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Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations

21 January 2018

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Common variants of FUT2 are associated with plasma vitamin B12 levels

21 January 2018

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PSORS2 is due to mutations in CARD14.

21 January 2018

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Systematic localization of common disease-associated variation in regulatory DNA

21 January 2018

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21 January 2018

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Architecture of the human regulatory network derived from ENCODE data

21 January 2018

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Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

21 January 2018

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Finding the missing heritability of complex diseases

21 January 2018

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Missing heritability and strategies for finding the underlying causes of complex disease

21 January 2018

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Direct selection of human genomic loci by microarray hybridization

21 January 2018

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Fast and accurate long-read alignment with Burrows-Wheeler transform

21 January 2018

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

21 January 2018

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SNP detection for massively parallel whole-genome resequencing

21 January 2018

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ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

21 January 2018

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

21 January 2018

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The power of the Mantel-Haenszel test for grouped failure time data

21 January 2018

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Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

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Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

21 January 2018

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A data-adaptive sum test for disease association with multiple common or rare variants

21 January 2018

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A groupwise association test for rare mutations using a weighted sum statistic

21 January 2018

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Statistical analysis of rare sequence variants: an overview of collapsing methods

21 January 2018

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Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

21 January 2018

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Rare-variant association testing for sequencing data with the sequence kernel association test

21 January 2018

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Pooled association tests for rare variants in exon-resequencing studies

21 January 2018

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Testing for an unusual distribution of rare variants

21 January 2018

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Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24212883

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.2827

1 reference

Dimensions Publication ID

27 November 2017

1018559551

0 references

Fatcat ID

release_ieocp7vznvbejgs5f24ye7kixm

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ieocp7vznvbejgs5f24ye7kixm

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference