Rare variants in drug target genes contributing to complex diseases, phenome-wide

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Rare variants in drug target genes contributing to complex diseases, phenome-wide ; volume:8 ; number:1 ; day:15 ; month:3 ; year:2018 ; pages:1-16 ; date:12.2018
Scientific reports ; 8, Heft 1 (15.3.2018), 1-16, 12.2018

Creator: Verma, Shefali Setia

Contributor: Josyula, Navya
Verma, Anurag
Zhang, Xinyuan
Veturi, Yogasudha
Dewey, Frederick E.
Hartzel, Dustin N.
Lavage, Daniel R.
Leader, Joe
Ritchie, Marylyn D.
Pendergrass, Sarah A.
SpringerLink (Online service)

DOI: 10.1038/s41598-018-22834-4

URN: urn:nbn:de:1111-201805144202

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:55 AM CEST

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Verma, Shefali Setia
Josyula, Navya
Verma, Anurag
Zhang, Xinyuan
Veturi, Yogasudha
Dewey, Frederick E.
Hartzel, Dustin N.
Lavage, Daniel R.
Leader, Joe
Ritchie, Marylyn D.
Pendergrass, Sarah A.
SpringerLink (Online service)

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Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide

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Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide

Aufsatzsammlung

Analyzing rare variants in complex diseases

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Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide

Aufsatzsammlung

Analyzing rare variants in complex diseases

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A phenome-wide scan reveals convergence of common and rare variant associations

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Rare variants in drug target genes contributing to complex diseases, phenome-wide

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Other Objects (12)

Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide

Analyzing rare variants in complex diseases

The RD‐Connect Genome‐Phenome Analysis Platform: accelerating diagnosis, research, and gene discovery for rare diseases

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

A phenome-wide scan reveals convergence of common and rare variant associations

Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseases

Identifying pathogenic variants in rare pediatric neurological diseases using exome sequencing

Phenome-wide association study on miRNA-related sequence variants: the UK Biobank

Enhanced rare disease mapping for phenome-wide genetic association in the UK Biobank

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Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide

Analyzing rare variants in complex diseases

The RD‐Connect Genome‐Phenome Analysis Platform: accelerating diagnosis, research, and gene discovery for rare diseases

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

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Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseases

Identifying pathogenic variants in rare pediatric neurological diseases using exome sequencing

Phenome-wide association study on miRNA-related sequence variants: the UK Biobank

Enhanced rare disease mapping for phenome-wide genetic association in the UK Biobank

Pangenome graphs improve the analysis of structural variants in rare genetic diseases

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Rare Diseases Network

Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide

Analyzing rare variants in complex diseases

The RD‐Connect Genome‐Phenome Analysis Platform: accelerating diagnosis, research, and gene discovery for rare diseases

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

A phenome-wide scan reveals convergence of common and rare variant associations

Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseases

Identifying pathogenic variants in rare pediatric neurological diseases using exome sequencing

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Enhanced rare disease mapping for phenome-wide genetic association in the UK Biobank

Pangenome graphs improve the analysis of structural variants in rare genetic diseases

Phenome[n]on Corporis Lunaris

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