scholarly article | Q13442814 |
P50 | author | Abdimajid Osman | Q57902212 |
P2093 | author name string | Abshir Ali Abdi | |
P2860 | cites work | Early back-to-Africa migration into the Horn of Africa | Q21144872 |
Causes of venous thrombosis | Q28080150 | ||
High frequencies of Y chromosome lineages characterized by E3b1, DYS19-11, DYS392-12 in Somali males | Q28238902 | ||
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm | Q29547194 | ||
A general framework for estimating the relative pathogenicity of human genetic variants | Q29615730 | ||
Human genetic selection on the MTHFR 677C>T polymorphism | Q33387977 | ||
A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1. | Q33772964 | ||
Prothrombin G20210A polymorphism and thrombophilia | Q33942201 | ||
Factor V Leiden thrombophilia | Q34152374 | ||
Mechanistic view of risk factors for venous thromboembolism | Q34255409 | ||
Non-O blood type is the commonest genetic risk factor for VTE: results from a meta-analysis of the literature | Q34284613 | ||
ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing | Q34320780 | ||
Resistance to activated protein C and factor V Leiden as risk factors for venous thrombosis | Q70943497 | ||
Single-nucleotide polymorphism analysis by pyrosequencing | Q73775865 | ||
Factor V Leiden G1691A and prothrombin G20210A mutations are common in Tunisia | Q79312648 | ||
ABO blood group genotypes and the risk of venous thrombosis: effect of factor V Leiden | Q81234402 | ||
Genetic variations associated with recurrent venous thrombosis | Q85290931 | ||
Hyperhomocysteinaemia and human reproduction | Q34395837 | ||
Frequency of APOE, MTHFR and ACE polymorphisms in the Zambian population | Q34503278 | ||
Genetics of venous thrombosis | Q34993966 | ||
G20210A is a functional mutation in the prothrombin gene; effect on protein levels and 3'-end formation | Q40600282 | ||
Factor V gene mutation causing inherited resistance to activated protein C as a basis for venous thromboembolism | Q40613029 | ||
Changes in frequencies of heterozygous thermolabile 5,10-methylenetetrahydrofolate reductase gene in fetuses with neural tube defects | Q43074789 | ||
Age Dependence of the Influence of Methylenetetrahydrofolate Reductase Genotype on Plasma Homocysteine Level | Q44636840 | ||
Distribution of blood groups in the East African Somali population | Q46596930 | ||
VKORC1 Asp36Tyr warfarin resistance marker is common in Ethiopian individuals | Q46686057 | ||
Absence of the factor V Leiden mutation in Ethiopians | Q46810813 | ||
Hyperhomocysteinemia as a risk factor for deep-vein thrombosis. | Q51037949 | ||
Hyperhomocysteinemia and venous thrombosis: a meta-analysis. | Q51565947 | ||
Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. | Q51773327 | ||
Factor V Leiden mutation and venous thrombosis | Q57089652 | ||
Multiple SNP testing improves risk prediction of first venous thrombosis | Q57788375 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 4 | |
P921 | main subject | Somalia | Q1045 |
thrombophilia | Q1570013 | ||
P304 | page(s) | 536-543 | |
P577 | publication date | 2017-09-09 | |
P1433 | published in | Journal of Thrombosis and Thrombolysis | Q15766541 |
P1476 | title | Prevalence of common hereditary risk factors for thrombophilia in Somalia and identification of a novel Gln544Arg mutation in coagulation factor V. | |
P478 | volume | 44 |