Concepedia

Author

Kaido Lepik

SIB Swiss Institute of BioinformaticsORCID

Also Known As

Kaido Lepik, Lepik, Kaido

29

Publications

1.3K

Citations

10

H-Index

34

Concepts

All Affiliations

SIB Swiss Institute of BioinformaticsUniversity of LausanneUniversity of TartuUniversitätsmedizin GreifswaldUniversity of Helsinki
KL

About

Kaido Lepik is an author at SIB Swiss Institute of Bioinformatics specializing in medicine, public health, and quantitative genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

2

2

101

2

Public Health

1

1

40

3

Biostatistics

1

1

40

4

Cell Biology

1

1

61

5

Epidemiology

1

1

61

Kaido Lepik

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9

Publications

660

Citations

9

H-Index

YearCitations

Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

Eleonora Porcu, Sina Rüeger, Kaido Lepik,

Nature Communications

2019

330

Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome

Eleonora Porcu, Marie C. Sadler, Kaido Lepik,

Nature Communications

2021

134

C-reactive protein upregulates the whole blood expression of CD59 - an integrative analysis

Kaido Lepik, Tarmo Annilo, Viktorija Kukuškina,

PLoS Computational Biology

2017

61

Quantifying the role of transcript levels in mediating DNA methylation effects on complex traits and diseases

Marie C. Sadler, Chiara Auwerx, Kaido Lepik,

Nature Communications

2022

42

Mendelian Randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

Eleonora Porcu, Sina Rüeger, Kaido Lepik,

2018

40

Limited evidence for blood eQTLs in human sexual dimorphism

Eleonora Porcu, Annique Claringbould, Antoine Weihs,

Genome Medicine

2022

18

The impact of 22q11.2 copy-number variants on human traits in the general population

Malú Zamariolli, Chiara Auwerx, Marie C. Sadler,

The American Journal of Human Genetics

2023

15

Stroke genetics informs drug discovery and risk prediction across ancestries

Stéphanie Debette, Aniket Mishra, Rainer Malik,

2022

10

Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations

Maarja Lepamets, Chiara Auwerx, Margit Nõukas,

Human Genetics and Genomics Advances

2022

10

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