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(25 - 48 of 125)

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The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia: design, results and future prospects
Another Brick in the Wall: the role of the actinobacterial cell wall in antibiotic resistance, phylogeny and development
Linking migraine frequency with family history of migraine
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP
The ApoE e4 Isoform: Can the Risk of Diseases be Reduced by Environmental Factors?
Novel hypotheses emerging from GWAS in migraine?
Longevity Around the Turn of the 20th Century: Life-Long Sustained Survival Advantage for Parents of Today's Nonagenarians
On the pathogenesis and clinical outcome of ANCA-associated vasculitis
Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2
PMS2-associated Lynch syndrome : the odd one out
Genetic determinants of cholesterol and energy metabolism : implications for cardiometabolic health
What's new in pontocerebellar hypoplasia? An update on genes and subtypes
Discovery of genetic defects in unexplained colorectal cancer syndromes
Expert consensus recommendations on the cardiogenetic care for patients with thoracic aortic disease and their first-degree relatives
Exploring the world of non-coding genes in stem cells and autoimmunity.
Brain Regions Showing White Matter Loss in Huntington's Disease Are Enriched for Synaptic and Metabolic Genes
Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis
Vulvar squamous cell carcinoma : genetics, morphology and clinical behaviour
Association of impaired renal function with venous thrombosis: A genetic risk score approach
Historical demography and longevity genetics: Back to the future
Genomic Influences on Susceptibility and Severity of Rheumatoid Arthritis
Implementing genetic education in primary care: the Gen-Equip programme
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects
White matter microstructure in a genetically defined group at increased risk of autism symptoms, and a comparison with idiopathic autism: an exploratory study

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