Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1473-1150

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes ; day:14 ; month:9 ; year:2018 ; pages:1-9
The pharmacogenomics journal ; (14.9.2018), 1-9

Creator: Choi, Jihoon

Contributor: Tantisira, Kelan G.
Duan, Qing Ling
SpringerLink (Online service)

DOI: 10.1038/s41397-018-0048-y

URN: urn:nbn:de:101:1-2018102900273655875056

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:58 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Choi, Jihoon
Tantisira, Kelan G.
Duan, Qing Ling
SpringerLink (Online service)

Other Objects (12)

In silico comparative characterization of pharmacogenomic missense variants

Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Genetic polymorphisms of pharmacogenomic VIP variants in the Mongol of Northwestern China

Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

Computational pharmacogenomic screen identifies drugs that potentiate the anti-breast cancer activity of statins

Genetic polymorphisms of pharmacogenomic VIP variants in the Uygur population from northwestern China

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants

In silico comparative characterization of pharmacogenomic missense variants

Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Genetic polymorphisms of pharmacogenomic VIP variants in the Mongol of Northwestern China

Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

Computational pharmacogenomic screen identifies drugs that potentiate the anti-breast cancer activity of statins

Genetic polymorphisms of pharmacogenomic VIP variants in the Uygur population from northwestern China

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants

In silico comparative characterization of pharmacogenomic missense variants

Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Genetic polymorphisms of pharmacogenomic VIP variants in the Mongol of Northwestern China

Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

Computational pharmacogenomic screen identifies drugs that potentiate the anti-breast cancer activity of statins

Genetic polymorphisms of pharmacogenomic VIP variants in the Uygur population from northwestern China

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

In silico comparative characterization of pharmacogenomic missense variants

Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Genetic polymorphisms of pharmacogenomic VIP variants in the Mongol of Northwestern China

Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

Computational pharmacogenomic screen identifies drugs that potentiate the anti-breast cancer activity of statins

Genetic polymorphisms of pharmacogenomic VIP variants in the Uygur population from northwestern China

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants

In silico comparative characterization of pharmacogenomic missense variants

Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Genetic polymorphisms of pharmacogenomic VIP variants in the Mongol of Northwestern China

Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

Computational pharmacogenomic screen identifies drugs that potentiate the anti-breast cancer activity of statins

Genetic polymorphisms of pharmacogenomic VIP variants in the Uygur population from northwestern China

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants

In silico comparative characterization of pharmacogenomic missense variants

Genetic analysis of osteopetrosis in Pakistani families identifies novel and known sequence variants

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility

Genetic polymorphisms of pharmacogenomic VIP variants in the Mongol of Northwestern China

Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

Computational pharmacogenomic screen identifies drugs that potentiate the anti-breast cancer activity of statins

Genetic polymorphisms of pharmacogenomic VIP variants in the Uygur population from northwestern China

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma

Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals

A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants

Related objects

Reset password