| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0049-3848(17)30077-4 |
| P698 | PubMed publication ID | 28262245 |
| P50 | author | Frank Rühle | Q84105295 |
| P2093 | author name string | Monika Stoll | |
| P2860 | cites work | Finding the missing heritability of complex diseases | Q22122198 |
| A global reference for human genetic variation | Q25909434 | ||
| A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke | Q28943400 | ||
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| A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1. | Q33772964 | ||
| Genetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis | Q35037432 | ||
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| Thrombophilia and first arterial ischaemic stroke: a systematic review | Q35283067 | ||
| Genetic Variation in Cardiomyopathy and Cardiovascular Disorders | Q36161328 | ||
| A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. | Q36166323 | ||
| Inherited risk factors for thrombotic diseases in children: the genome-wide perspective | Q37970331 | ||
| Venous thromboembolism in neonates and children | Q38041800 | ||
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| Rare Variants in the ADAMTS13 Von Willebrand Factor-Binding Domain Contribute to Pediatric Stroke | Q38842185 | ||
| Homocysteine, MTHFR 677C-->T polymorphism, and risk of ischemic stroke: results of a meta-analysis | Q44115099 | ||
| Risk of recurrent venous thrombosis in homozygous carriers and double heterozygous carriers of factor V Leiden and prothrombin G20210A. | Q44196663 | ||
| Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis. | Q44889703 | ||
| Venous thromboembolism in neonates and children--update 2013. | Q51207637 | ||
| Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. | Q51773327 | ||
| KNG1 Ile581Thr and susceptibility to venous thrombosis | Q57605719 | ||
| Genetics of Venous Thrombosis: update in 2015 | Q57611705 | ||
| Age- and Gender-Specific Familial Risks for Venous Thromboembolism | Q61634586 | ||
| Incidence and mortality of venous thrombosis: a population-based study | Q79969827 | ||
| Gene variants associated with deep vein thrombosis | Q80893876 | ||
| Fibrinogen alpha and gamma genes and factor VLeiden in children with thromboembolism: results from 2 family-based association studies | Q84041978 | ||
| P921 | main subject | venous thromboembolism | Q9397786 |
| P304 | page(s) | S97-S99 | |
| P577 | publication date | 2017-03-01 | |
| P1433 | published in | Thrombosis Research | Q15758741 |
| P1476 | title | Genetic factors in pediatric venous thromboembolism | |
| P478 | volume | 151 Suppl 1 |
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