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Manuel Tardáguila

Wellcome Sanger Institute · GB
🔎 Find collaborators in Genetics · Molecular Biology →
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Area of research
Genetics · Molecular Biology
Research interest
Research interests include Genetic Associations and Epidemiology, RNA Research and Splicing, RNA modifications and cancer, and Genomics and Rare Diseases.
h-index
17
citations
2,121
works
42
NIH funding
primary concept
Biology
email

Recent publications

Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases
Nature Genetics 2022cited by 70position: middledoi
Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease
Nature Communications 2021cited by 74position: middledoi
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Cell 2020cited by 735position: middledoi
Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for twelve immune-mediated diseases
bioRxiv (Cold Spring Harbor Laboratory) 2020cited by 21position: middledoi
Variation in PU.1 binding and chromatin looping at neutrophil enhancers influences autoimmune disease susceptibility
bioRxiv (Cold Spring Harbor Laboratory) 2019cited by 1position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Hannes Ponstingl · Wellcome Sanger Institute2 papers (2020–2022)Oliver Stegle · Institut thématique Génétique, génomique et bioinformatique2 papers (2020–2022)Klaudia Walter · Wellcome Sanger Institute2 papers (2020–2022) · 2 papers (2020–2022)Carl A. Anderson · Wellcome Sanger Institute2 papers (2020–2022)Nicholas W. Morrell · Cambridge University Hospitals NHS Foundation Trust2 papers (2020–2022)Tomi Pastinen · McGill University Health Centre2 papers (2020–2022)Nicole Soranzo · University of Cambridge2 papers (2020–2022)Kousik Kundu · AstraZeneca (Spain)2 papers (2020–2022)Louella Vasquez · Lund University2 papers (2020–2022)Stephen Sawcer · University of Cambridge2 papers (2020–2022)Stephen M. Watt · University of Waterloo2 papers (2020–2022) · 1 papers (2022–2022)
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