Ioanna Tachmazidou
Target Sciences R&D
Stevenage, ENG, United Kingdom
Stevenage, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 38 publications
Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's disease.
Journal: Cell reports
Published: August 15, 2024
Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesis.
Journal: Nature genetics
Published: February 07, 2024
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.
Journal: Nature
Published: February 24, 2023
FinnGen provides genetic insights from a well-phenotyped isolated population.
Journal: Nature
Published: January 10, 2022
Rare variant contribution to human disease in 281,104 UK Biobank exomes.
Journal: Nature
Published: November 03, 2020
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
Journal: Addiction biology
Published: August 21, 2019
Exome sequencing and characterization of 49,960 individuals in the UK Biobank.
Journal: Nature
Published: March 14, 2019
The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA?
Journal: Clinical orthopaedics and related research
Published: February 23, 2019
Erratum to: The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA?
Journal: Clinical orthopaedics and related research
Published: February 15, 2019
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Journal: Cell
Published: September 13, 2018
Low-frequency variation in TP53 has large effects on head circumference and intracranial volume.
Journal: Nature communications
Published: June 06, 2018
Last Updated: 09/26/2026