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- 2025
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Mark
A burden of rare copy number variants in obsessive-compulsive disorder
- Contribution to journal › Article
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Mark
Genetic associations of neuropathic pain and sensory profile in a deeply phenotyped neuropathy cohort
- Contribution to journal › Article
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Mark
Evaluation of a Mitochondrial Polygenic Score for Parkinson's Disease Across Ancestries
- Contribution to journal › Letter
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Mark
Capturing breast cancers’ copy-number landscape in routine pathology : Exploiting low-resolution, genome-wide sequencing to identify HRD and beyond
- Contribution to journal › Article
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Mark
Embryological cellular origins and hypoxia-mediated mechanisms in PIK3CA-driven refractory vascular malformations
- Contribution to journal › Article
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Mark
Epigenome-wide association study of objectively measured physical activity in peripheral blood leukocytes
- Contribution to journal › Article
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Mark
Feasibility of extracting usable DNA from blood samples stored up to 21 years in the DiPiS study
- Contribution to journal › Article
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Mark
Combined targeting of PRDX6 and GSTP1 as a potential differentiation strategy for neuroblastoma treatment
- Contribution to journal › Article
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Mark
Putative multiple myeloma susceptibility genes identified by exome sequencing of 347 familial and early-onset cases
(2025) In Leukemia
- Contribution to journal › Article
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Mark
The genomic landscape of relapsed infant and childhood KMT2A-rearranged acute leukemia
- Contribution to journal › Article
