Mihail Halachev

5PUBLICATIONS
38CO-AUTHORS
Gene mappingVision scienceGenetic immunologyGene expression (incl. microarray and other genome-wide approaches)
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Publications (5)

|Aug 05, 2026
Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

|Apr 29, 2025
Autophagy disruption and mitochondrial stress precede photoreceptor necroptosis in multiple mouse models of inherited retinal disorders.

Fay Newton, Mihail Halachev, Linda Nguyen

|Oct 02, 2024
Regionally enriched rare deleterious exonic variants in the UK and Ireland.

Mihail Halachev, Viktoria-Eleni Gountouna, Alison Meynert

|Aug 13, 2021
Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability.

Hemant Bengani, Detelina Grozeva, Lambert Moyon

|Nov 26, 2019
Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.

Mihail Halachev, Alison Meynert, Martin S Taylor

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Frequent Collaborators

3 joint publications

Alison Meynert

2 joint publications

Timothy J Aitman

2 joint publications

James G Prendergast

2 joint publications

James F Wilson