(Q28729875)

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Functional impact of global rare copy number variation in autism spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

A small-cell lung cancer genome with complex signatures of tobacco exposure

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

A comprehensive catalogue of somatic mutations from a human cancer genome

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

Somatic mutations affect key pathways in lung adenocarcinoma

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

An integrated genomic analysis of human glioblastoma multiforme

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

The consensus coding sequences of human breast and colorectal cancers

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

KEGG for integration and interpretation of large-scale molecular data sets

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

Patterns of somatic mutation in human cancer genomes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

Diverse somatic mutation patterns and pathway alterations in human cancers

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

NGS catalog: A database of next generation sequencing studies in humans

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

Pathway analysis of genomic data: concepts, methods, and prospects for future development

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

PathScan: a tool for discerning mutational significance in groups of putative cancer genes

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

Enrichment map: a network-based method for gene-set enrichment visualization and interpretation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

The mutation spectrum revealed by paired genome sequences from a lung cancer patient

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

Gene ontology analysis for RNA-seq: accounting for selection bias

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

PIK3CA mutations and copy number gains in human lung cancers

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

Lung adenocarcinoma: guiding EGFR-targeted therapy and beyond

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3356304

Analysis of pathway mutation profiles highlights collaboration between cancer-associated superpathways.

3 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037595

Comment on "The consensus coding sequences of human breast and colorectal cancers".

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037595

Investigating single nucleotide polymorphism (SNP) density in the human genome and its implications for molecular evolution

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0037595

Comment on "The consensus coding sequences of human breast and colorectal cancers"

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22624051

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Comment on "The consensus coding sequences of human breast and colorectal cancers"

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22624051

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Patterns of nucleotide substitution in pseudogenes and functional genes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22624051

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0037595

1 reference

ADS bibcode

2012PLoSO...737595J

0 references

1 reference

1 reference

PubMed publication ID

22624051

1 reference