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- 2024
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Mark
A genomic mutational constraint map using variation in 76,156 human genomes
(
- Contribution to journal › Article
- 2023
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Mark
A large meta-analysis identifies genes associated with anterior uveitis
(
- Contribution to journal › Article
- 2022
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Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
(
- Contribution to journal › Article
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Mark
Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis
(
- Contribution to journal › Article
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Mark
A saturated map of common genetic variants associated with human height
(
- Contribution to journal › Article
- 2021
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Mark
The trans-ancestral genomic architecture of glycemic traits
(
- Contribution to journal › Article
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Mark
The power of genetic diversity in genome-wide association studies of lipids
(
- Contribution to journal › Article
- 2020
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Mark
Protein-altering germline mutations implicate novel genes related to lung cancer development
(
- Contribution to journal › Article
- 2019
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Mark
PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional Outcome
(
- Contribution to journal › Article
- 2017
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Mark
A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
(
- Contribution to journal › Article
- 2016
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Mark
The genetic architecture of type 2 diabetes
(
- Contribution to journal › Article
- 2011
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Mark
Efficacy and safety of imatinib on top of BFM-like chemotherapy in pediatric patients with Ph+/BCR-ABL+ acute lymphoblastic leukemia (Ph+ALL). the EsPhALL study
(
- Contribution to journal › Published meeting abstract
- 2010
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Mark
Familial late-onset focal dystonia in an African American family
(
- Contribution to journal › Published meeting abstract
- 2009
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Mark
A rare blood group: p phenotype
(
- Contribution to journal › Article
- 2008
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Mark
Blood grouping discrepancies between ABO genotype and phenotype caused by O alleles
(
- Contribution to journal › Article
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Mark
The O2 allele : Questioning the phenotypic definition of an ABO allele
(
- Contribution to journal › Scientific review
- 2003
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Mark
A frequent allele codes for a truncated variant of semenogelin I, the major protein component of human semen coagulum
(
- Contribution to journal › Article
- 1999
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Mark
Allele-related variation in minisatellite repeats involved in the transcription of the blood group ABO gene
(
- Contribution to journal › Article
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Mark
Prevalence of IgA-antiendomysium and IgA-antigliadin autoantibodies at diagnosis of insulin-dependent diabetes mellitus in Swedish children and adolescents
(
- Contribution to journal › Article
- 1998
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Mark
Heterogeneity of the blood group Ax allele: genetic recombination of common alleles can result in the Ax phenotype
(
- Contribution to journal › Article
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Mark
Genomic typing of the Kidd blood group locus by a single-tube allele-specific primer PCR technique
(
- Contribution to journal › Article
-
Mark
The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein
(
- Contribution to journal › Article
-
Mark
A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency
(
- Contribution to journal › Article
-
Mark
The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families [3]
(
- Contribution to journal › Letter
- 1997
-
Mark
Molecular Genetic Studies of the Blood Group ABO Locus in Man
1997)(
- Thesis › Doctoral thesis (compilation)
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Mark
Evaluation of original and modified APC-resistance tests in unselected outpatients with clinically suspected thrombosis and in healthy controls
(
- Contribution to journal › Article
- 1996
-
Mark
HLA-DQB1*0201/0302 is associated with severe retinopathy in patients with IDDM
(
- Contribution to journal › Article
-
Mark
High prevalence of the FVR506Q mutation causing APC resistance in a region of southern Sweden with a high incidence of venous thrombosis.
(
- Contribution to journal › Letter