Genic intolerance to functional variation and the interpretation of personal genomes (Q31129974)

2 November 2017

Genic intolerance to functional variation and the interpretation of personal genomes (English)

1 reference

2 November 2017

Slavé Petrovski

1

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Erin L Heinzen

series ordinal

3

object named as

Erin L Heinzen

1 reference

2 November 2017

5

David B Goldstein

1 reference

2 November 2017

Quanli Wang

2

1 reference

PMC publication ID

3749936

2 November 2017

Andrew S Allen

series ordinal

4

1 reference

2 November 2017

22 August 2013

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2 November 2017

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2 November 2017

9

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2 November 2017

8

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2 November 2017

e1003709

1 reference

Creative Commons Attribution 4.0 International

2 November 2017

start time

22 August 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

21 June 2018

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De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

21 June 2018

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21 June 2018

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De Novo Gene Disruptions in Children on the Autistic Spectrum

21 June 2018

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Patterns and rates of exonic de novo mutations in autism spectrum disorders

21 June 2018

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

21 June 2018

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism

21 June 2018

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21 June 2018

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21 June 2018

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Prediction of missense mutation functionality depends on both the algorithm and sequence alignment employed

21 June 2018

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21 June 2018

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Identifying a high fraction of the human genome to be under selective constraint using GERP++.

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Analytical methods for inferring functional effects of single base pair substitutions in human cancers

21 June 2018

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The human disease network

21 June 2018

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A codon-based model of nucleotide substitution for protein-coding DNA sequences

21 June 2018

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A new method for estimating synonymous and nonsynonymous rates of nucleotide substitution considering the relative likelihood of nucleotide and codon changes

21 June 2018

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21 June 2018

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21 June 2018

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21 January 2018

Identifiers

DOI

1 reference

2 November 2017

1 reference

PMC publication ID

3749936

2 November 2017

PubMed publication ID

23990802

1 reference

PMC publication ID

3749936