(Q33781077)

29 July 2017

title

Improving the prediction of the functional impact of cancer mutations by baseline tolerance transformation (English)

1 reference

29 July 2017

3

1 reference

29 July 2017

Abel Gonzalez-Perez

1

0 references

Jordi Deu-Pons

series ordinal

2

object named as

Jordi Deu-Pons

1 reference

29 July 2017

publication date

26 November 2012

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29 July 2017

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29 July 2017

volume

4

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29 July 2017

issue

11

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29 July 2017

page(s)

89

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The landscape of cancer genes and mutational processes in breast cancer

29 July 2017

cites work

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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Mutual exclusivity analysis identifies oncogenic network modules

4 July 2018

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Deep sequencing of gastric carcinoma reveals somatic mutations relevant to personalized medicine

4 July 2018

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Predicting the functional impact of protein mutations: application to cancer genomics

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

1 reference

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Prioritization of driver mutations in pancreatic cancer using cancer-specific high-throughput annotation of somatic mutations (CHASM).

4 July 2018

1 reference

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Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations

4 July 2018

1 reference

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

4 July 2018

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4 July 2018

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Somatic mutations affect key pathways in lung adenocarcinoma

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4064314

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4064314

Core signaling pathways in human pancreatic cancers revealed by global genomic analyses

4 July 2018

1 reference

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An integrated genomic analysis of human glioblastoma multiforme

4 July 2018

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4 July 2018

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The genomic landscapes of human breast and colorectal cancers

4 July 2018

1 reference

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A multidimensional analysis of genes mutated in breast and colorectal cancers

4 July 2018

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4 July 2018

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4 July 2018

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The consensus coding sequences of human breast and colorectal cancers

4 July 2018

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Differences in the evolutionary history of disease genes affected by dominant or recessive mutations

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4064314

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4 July 2018

1 reference

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Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4064314

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4064314

A census of human cancer genes

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4064314

SIFT: Predicting amino acid changes that affect protein function

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4064314

Human non-synonymous SNPs: server and survey

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4064314

Gene ontology: tool for the unification of biology

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4064314

SNPeffect v2.0: a new step in investigating the molecular phenotypic effects of human non-synonymous SNPs.

4 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FGM390

Highly consistent patterns for inherited human diseases at the molecular level.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FGM390

Distinct patterns in the regulation and evolution of human cancer genes

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4064314

Performance of mutation pathogenicity prediction methods on missense variants

30 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FGM390

Landscape of TET2 mutations in acute myeloid leukemia

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23181723

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/GM390

1 reference

Dimensions Publication ID

29 July 2017

0 references

1 reference

29 July 2017

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