1 – 50 of 164
- show: 50
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2024
-
Mark
A genome-wide association study of social trust in 33,882 Danish blood donors
(
- Contribution to journal › Article
-
Mark
Reply to “Exploring the long-term effects of biologic initiation in severe asthma: Insights from the International Severe Asthma Registry”
(
- Contribution to journal › Article
-
Mark
Genetic correlations and causal relationships between cardio-metabolic traits and sepsis
(
- Contribution to journal › Article
-
Mark
CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods
(
- Contribution to journal › Article
-
Mark
Frailty and Cognitive Function in Middle-Aged and Older Adults With Congenital Heart Disease
(
- Contribution to journal › Article
-
Mark
Biomarkers and Proteomics in Sarcomeric Hypertrophic Cardiomyopathy in the Young—FGF-21 Highly Associated with Overt Disease
(
- Contribution to journal › Article
- 2023
-
Mark
Phenotype of Gambling Disorder Patients with Lotteries as a Preferred Form of Gambling
(
- Contribution to journal › Article
-
Mark
Inferring the genetic relationship between brain imaging-derived phenotypes and risk of complex diseases by Mendelian randomization and genome-wide colocalization
(
- Contribution to journal › Article
-
Mark
Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits
(
- Contribution to journal › Article
-
Mark
SID : A new carbohydrate blood group system based on a well-characterized but still mysterious antigen of great pathophysiologic interest
(
- Contribution to journal › Article
-
Mark
Elucidation of the low-expressing erythroid CR1 phenotype by bioinformatic mining of the GATA1-driven blood-group regulome
(
- Contribution to journal › Article
-
Mark
Is asthma's heterogeneity too vast to use traditional phenotyping for modern biologic therapies?
(
- Contribution to journal › Article
-
Mark
Early onset ataxia with comorbid myoclonus and epilepsy : A disease spectrum with shared molecular pathways and cortico-thalamo-cerebellar network involvement
(
- Contribution to journal › Article
-
Mark
Clusters based on immune markers in a Lithuanian asthma cohort study
(
- Contribution to journal › Article
-
Mark
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
(
- Contribution to journal › Article
- 2022
-
Mark
phenopype : A phenotyping pipeline for Python
(
- Contribution to journal › Article
-
Mark
A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B
w phenotype.
(
- Contribution to journal › Article
-
Mark
Computational phenotyping of obstructive airway diseases : protocol for a systematic review
(
- Contribution to journal › Article
-
Mark
Life histories as mosaics : Plastic and genetic components differ among traits that underpin life-history strategies
(
- Contribution to journal › Article
-
Mark
Multiple sclerosis diagnosis and phenotype identification by multivariate classification of in vivo frontal cortex metabolite profiles
(
- Contribution to journal › Article
-
Mark
The role of phenotypic plasticity in the establishment of range margins
2022) In Philosophical transactions of the Royal Society of London. Series B, Biological sciences 377(1846).(
- Contribution to journal › Article
-
Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
(
- Contribution to journal › Article
-
Mark
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
(
- Contribution to journal › Article
-
Mark
International stroke genetics consortium recommendations for studies of genetics of stroke outcome and recovery
(
- Contribution to journal › Article
- 2021
-
Mark
Congenital stationary night blindness : an update and review of the disease spectrum in Saudi Arabia
(
- Contribution to journal › Scientific review
-
Mark
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
(
- Contribution to journal › Article
-
Mark
Treatment outcomes in persons with severe haemophilia B in the Nordic region : The B-NORD study
(
- Contribution to journal › Article
-
Mark
Synovial fluid neutrophils in oligoarticular juvenile idiopathic arthritis have an altered phenotype and impaired effector functions
(
- Contribution to journal › Article
-
Mark
The European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)-clinical phenotypes and their predictors based on a cohort of 1000 patients
(
- Contribution to journal › Article
-
Mark
AXL Knock-Out in SNU475 Hepatocellular Carcinoma Cells Provides Evidence for Lethal Effect Associated with G2 Arrest and Polyploidization
(
- Contribution to journal › Article
- 2020
-
Mark
Diffusion-Weighted Imaging, MR Angiography, and Baseline Data in a Systematic Multicenter Analysis of 3,301 MRI Scans of Ischemic Stroke Patients—Neuroradiological Review Within the MRI-GENIE Study
(
- Contribution to journal › Article
-
Mark
Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma
(
- Contribution to journal › Article
-
Mark
Myoclonus-dystonia (DYT11, DYT-SGCE) - a channelopathy?
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Three-dimensional single-cell imaging for the analysis of RNA and protein expression in intact tumour biopsies
(
- Contribution to journal › Article
-
Mark
SSD1 modifies phenotypes of Elongator mutants
(
- Contribution to journal › Scientific review
-
Mark
A Functional Genomic Screen Identifies the Deubiquitinase USP11 as a Novel Transcriptional Regulator of ERα in Breast Cancer
(
- Contribution to journal › Article
- 2019
-
Mark
Gene transfer by interspecific hybridization in bryophytes
2019)(
- Thesis › Doctoral thesis (compilation)
-
Mark
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
(
- Contribution to journal › Article
-
Mark
Phenotype prediction accuracy – A Swedish perspective
(
- Contribution to journal › Article
-
Mark
Guidelines for the use of flow cytometry and cell sorting in immunological studies (second edition)
(
- Contribution to journal › Article
-
Mark
SSD1 suppresses phenotypes induced by the lack of Elongator-dependent tRNA modifications
(
- Contribution to journal › Article
- 2018
-
Mark
Towards precision medicine in severe asthma : Treatment algorithms based on treatable traits
(
- Contribution to journal › Scientific review
-
Mark
Contrasting results from GWAS and QTL mapping on wing length in great reed warblers
(
- Contribution to journal › Article
-
Mark
Molecular subtype profiling of urothelial carcinoma using a subtype-specific immunohistochemistry panel
(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Evaluating Sex and Age Differences in ADI-R and ADOS Scores in a Large European Multi-site Sample of Individuals with Autism Spectrum Disorder
(
- Contribution to journal › Article
-
Mark
Timing of onset affects arthritis presentation pattern in antisynthetase syndrome
(
- Contribution to journal › Article
-
Mark
A response to the forensic genetics policy initiative's report "Establishing Best Practice for Forensic DNA Databases"
(
- Contribution to journal › Letter
- 2017
-
Mark
Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12
(
- Contribution to journal › Article
-
Mark
Regulation of microRNA expression in vascular smooth muscle by MRTF-A and actin polymerization
(
- Contribution to journal › Article
-
Mark
Systemic frequencies of T helper 1 and T helper 17 cells in patients with age-related macular degeneration : A case-control study
(
- Contribution to journal › Article