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- 2022
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Mark
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
(
- Contribution to journal › Article
- 2021
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Mark
The genetics of sudden infant death syndrome—towards a gene reference resource
(
- Contribution to journal › Article
-
Mark
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk
(
- Contribution to journal › Article
- 2020
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Mark
Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene
(
- Contribution to journal › Article
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Mark
The CCND1 c.870G risk allele is enriched in individuals of African ancestry with plasma cell dyscrasias
(
- Contribution to journal › Letter