(Q33354240)

26 July 2017

title

The next generation of complex lung genetic studies (English)

1 reference

26 July 2017

Ivana V Yang

1

1 reference

26 July 2017

David A Schwartz

series ordinal

2

1 reference

26 July 2017

language of work or name

English

0 references

publication date

30 August 2012

1 reference

American Journal of Respiratory and Critical Care Medicine

26 July 2017

published in

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26 July 2017

volume

186

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26 July 2017

issue

11

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26 July 2017

page(s)

1087-1094

1 reference

Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis

26 July 2017

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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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21 June 2018

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21 June 2018

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Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data

21 June 2018

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Rare and common regulatory variation in population-scale sequenced human genomes

21 June 2018

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The state of genome-wide association studies in pulmonary disease: a new perspective

21 June 2018

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Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms

21 June 2018

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21 June 2018

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

21 June 2018

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A common MUC5B promoter polymorphism and pulmonary fibrosis.

21 June 2018

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Efficient and cost effective population resequencing by pooling and in-solution hybridization

21 June 2018

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A framework for variation discovery and genotyping using next-generation DNA sequencing data

21 June 2018

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Genomic DNA pooling strategy for next-generation sequencing-based rare variant discovery in abdominal aortic aneurysm regions of interest-challenges and limitations

21 June 2018

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The properties and applications of single-molecule DNA sequencing.

21 June 2018

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Mapping copy number variation by population-scale genome sequencing

21 June 2018

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Rare Variant Association Analysis Methods for Complex Traits

21 June 2018

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A map of human genome variation from population-scale sequencing

21 June 2018

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Statistical analysis strategies for association studies involving rare variants

21 June 2018

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Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

21 June 2018

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

21 June 2018

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Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene

21 June 2018

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Next-generation genomics: an integrative approach

21 June 2018

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Challenges of sequencing human genomes

21 June 2018

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

21 June 2018

1 reference

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Uncovering the roles of rare variants in common disease through whole-genome sequencing

21 June 2018

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A method and server for predicting damaging missense mutations

21 June 2018

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Analysis of genetic inheritance in a family quartet by whole-genome sequencing

21 June 2018

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Target-enrichment strategies for next-generation sequencing

21 June 2018

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

21 June 2018

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Sequencing technologies - the next generation

21 June 2018

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Exome sequencing identifies the cause of a mendelian disorder

21 June 2018

1 reference

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An evaluation of statistical approaches to rare variant analysis in genetic association studies

21 June 2018

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

21 June 2018

1 reference

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

21 June 2018

1 reference

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Quantification of rare allelic variants from pooled genomic DNA

21 June 2018

1 reference

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

21 June 2018

1 reference

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DNA sequencing: bench to bedside and beyond

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530203

Distribution and intensity of constraint in mammalian genomic sequence

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530203

Initial sequencing and analysis of the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530203

The Sequence of the Human Genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3530203

De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1164%2FRCCM.201207-1178PP

10.1164/RCCM.201207-1178PP

21 January 2018

Identifiers

DOI

1 reference

26 July 2017

1 reference

26 July 2017

1 reference