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- 2024
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Mark
A genomic mutational constraint map using variation in 76,156 human genomes
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- Contribution to journal › Article
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Mark
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
(
- Contribution to journal › Article
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Mark
Association of Body Mass Index and Parkinson Disease A Bidirectional Mendelian Randomization Study
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- Contribution to journal › Article
- 2023
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Mark
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
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- Contribution to journal › Article
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Mark
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci
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- Contribution to journal › Article
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Mark
A large meta-analysis identifies genes associated with anterior uveitis
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- Contribution to journal › Article
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Mark
Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases
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- Contribution to journal › Article
- 2022
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Mark
A saturated map of common genetic variants associated with human height
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- Contribution to journal › Article
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Mark
HLA analysis of immune checkpoint inhibitor-induced and idiopathic isolated ACTH deficiency
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- Contribution to journal › Article
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Mark
Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle-aged and older adults: A population-based cohort study
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- Contribution to journal › Letter
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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
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
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- Contribution to journal › Article
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Mark
Genetic Landscape of the ACE2 Coronavirus Receptor
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- Contribution to journal › Article
- 2020
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Mark
Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig
(
- Contribution to journal › Article
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Mark
Inferring structural variant cancer cell fraction
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- Contribution to journal › Article
- 2019
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Mark
Lack of gene flow : Narrow and dispersed differentiation islands in a triplet of Leptidea butterfly species
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- 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
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Mark
Polymorphisms in ADH1B and ALDH2 genes associated with the increased risk of gastric cancer in West Bengal, India
(
- Contribution to journal › Article
- 2016
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Mark
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
(
- Contribution to journal › Article
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Mark
Antiretroviral resistance at virological failure in the NEAT 001/ANRS 143 trial: Raltegravir plus darunavir/ritonavir or tenofovir/emtricitabine plus darunavir/ritonavir as first-line ART
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- Contribution to journal › Article
- 2014
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Mark
Mitochondrial D-loop and cytochrome oxidase C subunit I polymorphisms among the breast cancer patients of Mizoram, Northeast India
(
- Contribution to journal › Article
- 2013
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Mark
Rare allelic forms of PRDM9 associated with childhood leukemogenesis
(
- Contribution to journal › Article
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Mark
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders
(
- Contribution to journal › Article
- 2012
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Mark
IGHV3-21 Gene Frequency in a Swedish Cohort of Patients With Newly Diagnosed Chronic Lymphocytic Leukemia
(
- Contribution to journal › Article
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Mark
Empirical distributions of F(ST) from large-scale human polymorphism data
(
- Contribution to journal › Article
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Mark
Large-scale replication and heterogeneity in Parkinson disease genetic loci
(
- Contribution to journal › Article
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Mark
CRYAB-650 C>G (rs2234702) affects susceptibility to Type 1 diabetes and IAA-positivity in Swedish population
(
- Contribution to journal › Article
- 2011
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Mark
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
(
- Contribution to journal › Article
- 2010
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Mark
Association between vitamin D receptor gene polymorphisms, falls, balance and muscle power : results from two independent studies (APOSS and OPUS)
(
- Contribution to journal › Article
- 2008
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Mark
Genetic variation in the invasive avian parasite, Philornis downsi (Diptera, Muscidae) on the Galapagos archipelago
(
- Contribution to journal › Article
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Mark
Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis : the GENOMOS study
(
- Contribution to journal › Article
- 2005
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Mark
Association of oestrogen receptor alpha gene polymorphisms with postmenopausal bone loss, bone mass, and quantitative ultrasound properties of bone
(
- Contribution to journal › Article
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Mark
Polymorphisms of the CLCN7 gene are associated with BMD in women
(
- Contribution to journal › Article
- 2004
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Mark
Association of the Pro12Ala and C1431T variants of PPARG and their haplotypes with susceptibility to Type 2 diabetes
(
- Contribution to journal › Article
- 2002
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Mark
HLA-DQ genotypes in classic type 1 diabetes and in latent autoimmune diabetes of the adult.
(
- Contribution to journal › Article
- 2001
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Mark
Effect of a COL1A1 Sp1 binding site polymorphism on arterial pulse wave velocity : an index of compliance
(
- Contribution to journal › Article
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Mark
The NciI polymorphism in the cyclin D1 gene and sporadic primary hyperparathyroidism
(
- Contribution to journal › Article
- 2000
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Mark
Absence of cystatin C mutation in sporadic cerebral amyloid angiopathy-related hemorrhage
(
- Contribution to journal › Article
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Mark
Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion
(
- Contribution to journal › Article
- 1999
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Mark
Thrombophilia as a multigenic disease
(
- Contribution to journal › Article
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Mark
The Ala25-Thr mutation in the thrombomodulin gene is not frequent in Swedish patients suffering from ischemic heart disease [9]
(
- Contribution to journal › Letter
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Mark
The human BARX2 gene : genomic structure, chromosomal localization, and single nucleotide polymorphisms
(
- Contribution to journal › Article
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Mark
The prothrombin gene G20210A mutation and the platelet glycoprotein IIIa polymorphism PlA2 in patients with central retinal vein occlusion
(
- Contribution to journal › Article
- 1998
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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
(
- Contribution to journal › Letter
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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
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Mark
Geographic distribution of the 20210 G to A prothrombin variant
(
- Contribution to journal › Article
- 1997
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Mark
Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer
(
- Contribution to journal › Article
-
Mark
The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis
(
- Contribution to journal › Debate/Note/Editorial
- 1996
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Mark
Prevalence of factor V gene mutation amongst myocardial infarction patients and healthy controls is higher in Sweden than in other countries
(
- Contribution to journal › Article
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Mark
Resistance to activated protein C, the FV:Q506 allele, and venous thrombosis
(
- Contribution to journal › Scientific review