Kaido Lepik

The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.

Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.

How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.

Assessed papers (1)

• Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome.
  2021 L1 100/100

1 assessed by us (1 reproduced) · 28 not yet assessed — every PubMed paper on record, linked below.

• LiMA: Robust inference of molecular mediation from summary statistics ↗

  The American Journal of Human Genetics · 2026 · PMID 41512839
  not yet assessed
• Genetic determinants of plasma protein levels in the Estonian population ↗

  Scientific Reports · 2024 · PMID 38565889
  not yet assessed
• pyTWMR: transcriptome-wide Mendelian randomization in python ↗

  Bioinformatics · 2024 · PMID 39128017
  not yet assessed
• Widespread natural selection on metabolite levels in humans ↗

  Genome Research · 2024 · PMID 39152035
  not yet assessed
• The impact of 22q11.2 copy-number variants on human traits in the general population ↗

  The American Journal of Human Genetics · 2023 · PMID 36706759
  not yet assessed
• Widespread natural selection on metabolite levels in humans ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2023
  not yet assessed
• Genetic determinants of plasma protein levels in the Estonian population ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2023
  not yet assessed
• Response to Bassett et al. ↗

  The American Journal of Human Genetics · 2023 · PMID 37419093
  not yet assessed
• Stroke genetics informs drug discovery and risk prediction across ancestries ↗

  Nature · 2022 · PMID 36180795
  not yet assessed
• Quantifying the role of transcript levels in mediating DNA methylation effects on complex traits and diseases ↗

  Nature Communications · 2022 · PMID 36477627
  not yet assessed
• Limited evidence for blood eQTLs in human sexual dimorphism ↗

  Genome Medicine · 2022 · PMID 35953856
  not yet assessed
• Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations ↗

  Human Genetics and Genomics Advances · 2022 · PMID 36035246
  not yet assessed
• Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries ↗

  Nature · 2022 · PMID 36376532
  not yet assessed
• Stroke genetics informs drug discovery and risk prediction across ancestries ↗

  Research Square · 2022
  not yet assessed
• Omics-informed CNV calls reduce false positive rate and improve power for CNV-trait associations ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2022
  not yet assessed
• The impact of 22q11.2 copy number variants on human traits in the general population ↗

  medRxiv · 2022
  not yet assessed
• Additional file 2 of Limited evidence for blood eQTLs in human sexual dimorphism ↗

  Open MIND · 2022
  not yet assessed
• Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome

  Nature Communications · 2021 · PMID 34561431
  L1 100/100
• Inferring causality between transcriptome and complex traits

  DSpace repository (University of Tartu) · 2021
  not yet assessed
• Causal Inference Methods to Integrate Omics and Complex Traits ↗

  Cold Spring Harbor Perspectives in Medicine · 2020 · PMID 32816877
  not yet assessed
• Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome ↗

  medRxiv · 2020
  not yet assessed
• The role of gene expression on human sexual dimorphism: too early to call ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2020
  not yet assessed
• Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ↗

  Nature Communications · 2019 · PMID 31341166
  not yet assessed
• An exploratory phenome wide association study linking asthma and liver disease genetic variants to electronic health records from the Estonian Biobank ↗

  PLoS ONE · 2019 · PMID 30978214
  not yet assessed
• Leveraging biobank-scale rare and common variant analyses to identify <i>ASPHD1</i> as the main driver of reproductive traits in the 16p11.2 locus ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2019
  not yet assessed
• Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

  Data Archiving and Networked Services (DANS) · 2019
  not yet assessed
• Mendelian Randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ↗

  bioRxiv (Cold Spring Harbor Laboratory) · 2018
  not yet assessed
• C-reactive protein upregulates the whole blood expression of CD59 - an integrative analysis ↗

  PLoS Computational Biology · 2017 · PMID 28922377
  not yet assessed
• New Quality Measure for CNV : A Multi-Omics Approach

  Data Archiving and Networked Services (DANS) · 2017
  not yet assessed