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- 2024
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Mark
Unraveling the metabolomic architecture of autism in a large Danish population-based cohort
(
- Contribution to journal › Article
- 2022
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Mark
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes
(
- Contribution to journal › Article
- 2021
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Mark
Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction
(
- Contribution to journal › Article
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Mark
Genetic regulation of spermine oxidase activity and cancer risk : a Mendelian randomization study
(
- Contribution to journal › Article
- 2020
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Mark
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth
(
- Contribution to journal › Article
- 2019
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Mark
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis
(
- Contribution to journal › Article
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Mark
Roadmap for a precision-medicine initiative in the Nordic region
2019) In Nature Genetics(
- Contribution to journal › Debate/Note/Editorial
- 2018
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Mark
Amniotic fluid INSL3 measured during the critical time window in human pregnancy relates to cryptorchidism, hypospadias, and phthalate load : A large case-control study
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- Contribution to journal › Article
- 2016
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Mark
Perfluorooctane Sulfonate Concentrations in Amniotic Fluid, Biomarkers of Fetal Leydig Cell Function, and Cryptorchidism and Hypospadias in Danish Boys (1980-1996)
(
- Contribution to journal › Article
- 2015
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Mark
Amniotic Fluid Phthalate Levels and Male Fetal Gonad Function.
(
- Contribution to journal › Article
- 2012
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Mark
Few differences in cytokines between patients newly diagnosed with type 1 diabetes and their healthy siblings
(
- Contribution to journal › Article
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Mark
Phthalates and Perfluorooctanesulfonic Acid in Human Amniotic Fluid: Temporal Trends and Timing of Amniocentesis in Pregnancy
(
- Contribution to journal › Article
- 2011
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Mark
Danish children born with glutamic acid decarboxylase-65 and islet antigen-2 autoantibodies at birth had an increased risk to develop type 1 diabetes
(
- Contribution to journal › Article
- 2010
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Mark
CAN GENETIC DIVERSITY EXPLAIN THE INCREASED RISK OF SCHIZOPHRENIA AMONG SECOND GENERATION IMMIGRANTS?
2010) 2nd Conference of the Schizophrenia-International-Research-Society (SIRS) In Schizophrenia Research 117(2-3). p.316-316(
- Contribution to journal › Published meeting abstract
- 2008
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Mark
A non-synonymous variant in SLC30A8 is not associated with type 1 diabetes in the Danish population
(
- Contribution to journal › Article
- 2007
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Mark
Type 1 diabetes risk analysis on dried blood spot samples from population-based newborns: design and feasibility of an unselected case-control study
(
- Contribution to journal › Article