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- 2020
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Mark
Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans
(
- Contribution to journal › Article
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Mark
Genomic imprinting analyses identify maternal effects as a cause of phenotypic variability in type 1 diabetes and rheumatoid arthritis
(
- Contribution to journal › Article
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Mark
Familial risks between Graves disease and Hashimoto thyroiditis and other autoimmune diseases in the population of Sweden
(
- Contribution to journal › Article
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Mark
Familial associations between autoimmune hepatitis and primary biliary cholangitis and other autoimmune diseases
(
- Contribution to journal › Article
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Mark
Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium
2020)(
- Working paper/Preprint › Preprint in preprint archive
- 2019
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Mark
Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS) : comparison with multiple myeloma
2019) In Leukemia(
- Contribution to journal › Letter
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Mark
Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma
(
- Contribution to journal › Article
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Mark
The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism : Association study and meta-analysis
(
- Contribution to journal › Article
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Mark
Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance
(
- Contribution to journal › Letter
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Mark
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
(
- Contribution to journal › Article