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Genomics: In search of rare human variants

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Genomics: In search of rare human variants (English)

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Rasmus Nielsen

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language of work or name

English

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publication date

28 October 2010

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published in

Nature

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volume

467

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page(s)

1050-1

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issue

7319

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cites work

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20981085

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomewide association studies and human disease

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20981085

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The relationship between imputation error and statistical power in genetic association studies in diverse populations

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20981085

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Imputation-based analysis of association studies: candidate regions and quantitative traits

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20981085

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12 December 2020

based on heuristic

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Finding the missing heritability of complex diseases

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20981085

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Sequence of the Human Genome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20981085

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A map of human genome variation from population-scale sequencing

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20981085

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12 December 2020

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inferred from PubMed ID database lookup

Initial sequencing and analysis of the human genome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20981085

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12 December 2020

based on heuristic

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Identifiers

DOI

10.1038/4671050A

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1564897

Dimensions Publication ID

1011901631

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OpenCitations bibliographic resource ID

1564897

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stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1564897

ResearchGate publication ID

47567034

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Springer Nature article ID

10.1038/4671050a

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(Q28296883)

Genomics: In search of rare human variants

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