Erika Kvikstad

Erika Kvikstad

University of Oxford

H-index: 17

Europe-United Kingdom

About Erika Kvikstad

Erika Kvikstad, With an exceptional h-index of 17 and a recent h-index of 13 (since 2020), a distinguished researcher at University of Oxford, specializes in the field of genomics, bioinformatics, structural variation.

His recent articles reflect a diverse array of research interests and contributions to the field:

Proteomic Associations of Adverse Outcomes in Human Heart Failure

Plasma proteomic associations with genetics and health in the UK Biobank

Proteome-wide Mendelian randomization identifies candidate causal proteins for cardiovascular diseases

Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases

Proteomic analysis of effects of spironolactone in heart failure with preserved ejection fraction

Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis

016 Phenotypic effects of genetic loss of function in tyrosine kinase 2 (TYK2) using large-scale biobanks

274 Phenotypic Effects of Genetic Loss of Function in Tyrosine Kinase 2 Using Large-Scale Biobanks

Erika Kvikstad Information

University

Position

Research Associate

Citations(all)

1541

Citations(since 2020)

969

Cited By

754

hIndex(all)

17

hIndex(since 2020)

13

i10Index(all)

20

i10Index(since 2020)

15

Email

University Profile Page

Google Scholar

Erika Kvikstad Skills & Research Interests

genomics

bioinformatics

structural variation

Top articles of Erika Kvikstad

Title

Journal

Author(s)

Publication Date

Proteomic Associations of Adverse Outcomes in Human Heart Failure

Journal of the American Heart Association

Marie‐Joe Dib

Michael G Levin

Lei Zhao

Ahmed Diab

Zhaoqing Wang

...

2024/2/29

Plasma proteomic associations with genetics and health in the UK Biobank

Nature

Benjamin B Sun

Joshua Chiou

Matthew Traylor

Christian Benner

Yi-Hsiang Hsu

...

2023/10/12

Proteome-wide Mendelian randomization identifies candidate causal proteins for cardiovascular diseases

PLoS genetics

Alish B Palmos

Vincent Millischer

David K Menon

Timothy R Nicholson

Leonie S Taams

...

2022/3/3

Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases

Genome medicine

Alistair T Pagnamenta

Carme Camps

Edoardo Giacopuzzi

John M Taylor

Mona Hashim

...

2023/11/9

Proteomic analysis of effects of spironolactone in heart failure with preserved ejection fraction

Circulation: Heart Failure

Ali Javaheri

Ahmed Diab

Lei Zhao

Chenao Qian

Jordana B Cohen

...

2022/9

Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis

Communications biology

Sanni E Ruotsalainen

Ida Surakka

Nina Mars

Juha Karjalainen

Mitja Kurki

...

2022/8/17

016 Phenotypic effects of genetic loss of function in tyrosine kinase 2 (TYK2) using large-scale biobanks

Journal of Investigative Dermatology

N Raghupathy

E Kvikstad

E Holzinger

IM Catlett

J Maranville

2022/8/1

274 Phenotypic Effects of Genetic Loss of Function in Tyrosine Kinase 2 Using Large-Scale Biobanks

Journal of Investigative Dermatology

N Raghupathy

E Kvikstad

E Holzinger

I Catlett

J Maranville

2022/12/1

Genetic regulation of the human plasma proteome in 54,306 UK Biobank participants

BioRxiv

Benjamin B Sun

Joshua Chiou

Matthew Traylor

Christian Benner

Yi-Hsiang Hsu

...

2022/6/18

Dephospho-Uncarboxylated Matrix Gla-Protein and Adverse Outcomes in Heart Failure: A Mendelian Randomization Analysis

Circulation

Mahesh K Vidula

Leon J Schurgers

Chenao Qian

Oday Salman

Qasim Jehangir

...

2022/11/8

AB0003 PHENOTYPIC EFFECTS OF GENETIC LOSS OF FUNCTION IN TYROSINE KINASE 2 USING LARGE-SCALE BIOBANKS

N Raghupathy

E Kvikstad

E Holzinger

I Catlett

J Maranville

2022/6/1

Genetically Determined Levels of Apolipoprotein B and Low-Density Lipoprotein Are Not Associated With Increased Mortality in Heart Failure

Circulation

Preet Shaikh

Chenao Qian

Erika Kvikstad

Joseph Maranville

Lei Zhao

...

2022/11/8

Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals

The American Journal of Human Genetics

Jack A Kosmicki

Julie E Horowitz

Nilanjana Banerjee

Rouel Lanche

Anthony Marcketta

...

2021/7/1

Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank

Joseph D Szustakowski

Suganthi Balasubramanian

Erika Kvikstad

Shareef Khalid

Paola G Bronson

...

2021/7

A catalog of associations between rare coding variants and COVID-19 outcomes

medRxiv

JA Kosmicki

JE Horowitz

N Banerjee

R Lanche

A Marcketta

...

2021/2/27

Genetic association analysis of SARS-CoV-2 infection in 455,838 UK Biobank participants (preprint)

Jack A Kosmicki

Julie E Horowitz

Nilanjana Banerjee

Rouel Lanche

Anthony Marcketta

...

2020

The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United Kingdom

Genetics in Medicine

Katharina Schwarze

James Buchanan

Jilles M Fermont

Helene Dreau

Mark W Tilley

...

2020/1

See List of Professors in Erika Kvikstad University(University of Oxford)

Co-Authors

academic-engine