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- 2019
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Mark
Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia
(
- Contribution to journal › Article
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Mark
SVCurator: A Crowdsourcing app to visualize evidence of structural variants for the human genome
2019)(
- Working paper/Preprint › Preprint in preprint archive
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Mark
Mutations in the mitochondrial tryptophanyl-tRNA synthetase cause growth retardation and progressive leukoencephalopathy
(
- Contribution to journal › Article
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Mark
Upregulation of C1-inhibitor in pancreatic cancer
(
- Contribution to journal › Article
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Mark
Generation of two compound heterozygous HGSNAT-mutated lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo C syndrome
(
- Contribution to journal › Article
- 2018
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Mark
Heritability of End-Stage Renal Disease : A Swedish Adoption Study
(
- Contribution to journal › Article
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Mark
Inflammatory leiomyosarcoma is a distinct tumor characterized by near-haploidization, few somatic mutations, and a primitive myogenic gene expression signature
(
- Contribution to journal › Article
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Mark
Functional variants in the sucrase-isomaltase gene associate with increased risk of irritable bowel syndrome
(
- Contribution to journal › Article
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Mark
Bortezomib-induced peripheral neuropathy : A genome-wide association study on multiple myeloma patients
(
- Contribution to journal › Article
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Mark
Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia
(
- Contribution to journal › Article