(Q35677036)

9 August 2017

title

The support of human genetic evidence for approved drug indications (English)

1 reference

9 August 2017

Junwen Wang

10

0 references

John Whittaker

object named as

John C Whittaker

12

0 references

Philippe Sanseau

13

object named as

Philippe Sanseau

1 reference

9 August 2017

Matthew R Nelson

1

1 reference

9 August 2017

Hannah Tipney

2

1 reference

9 August 2017

Jeffery L Painter

3

1 reference

9 August 2017

Judong Shen

4

1 reference

9 August 2017

Paola Nicoletti

5

1 reference

9 August 2017

Yufeng Shen

6

1 reference

9 August 2017

Aris Floratos

7

1 reference

9 August 2017

Pak Chung Sham

8

1 reference

9 August 2017

Mulin Jun Li

9

1 reference

9 August 2017

Lon R Cardon

11

1 reference

9 August 2017

language of work or name

English

0 references

publication date

29 June 2015

1 reference

9 August 2017

1 reference

9 August 2017

volume

47

1 reference

9 August 2017

issue

8

1 reference

9 August 2017

page(s)

856-860

1 reference

https://scigraph.springernature.com/pub.10.1038/ng.3314

9 August 2017

exact match

0 references

cites work

Trends in risks associated with new drug development: success rates for investigational drugs

1 reference

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Lessons learned from the fate of AstraZeneca's drug pipeline: a five-dimensional framework

21 January 2018

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The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

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1 reference

Validating therapeutic targets through human genetics

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Common variants at 30 loci contribute to polygenic dyslipidemia

21 January 2018

1 reference

Genetics of rheumatoid arthritis contributes to biology and drug discovery

21 January 2018

1 reference

Use of genome-wide association studies for drug repositioning

21 January 2018

1 reference

GWASdb: a database for human genetic variants identified by genome-wide association studies

21 January 2018

1 reference

Rational drug repositioning by medical genetics.

21 January 2018

1 reference

21 January 2018

1 reference

Genic intolerance to functional variation and the interpretation of personal genomes

21 January 2018

1 reference

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

21 January 2018

1 reference

A map of human genome variation from population-scale sequencing

21 January 2018

1 reference

Mapping the genetic architecture of gene expression in human liver

21 January 2018

1 reference

Annotation of functional variation in personal genomes using RegulomeDB

21 January 2018

1 reference

Systematic localization of common disease-associated variation in regulatory DNA

21 January 2018

1 reference

The Comparative Toxicogenomics Database: update 2013.

21 January 2018

1 reference

Can the flow of medicines be improved? Fundamental pharmacokinetic and pharmacological principles toward improving Phase II survival

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26121088

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

UMLS-Interface and UMLS-Similarity : open source software for measuring paths and semantic similarity

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26121088

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.3314

1 reference

9 August 2017

1 reference