Associated Papers
Proteogenomic Profiling of Treatment-Naïve Metastatic Malignant Melanoma.
Kuras M et al.
Cancers, 2025
Computational analysis of congenital heart disease associated SNPs: unveiling their impact on the gene regulatory system.
Vashisht S et al.
Bmc Genomics, 2025
Heterozygosity in factor XIII genes and the manifestation of mild inherited factor XIII deficiency.
Singh S et al.
Journal of Thrombosis and Haemostasis : Jth, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Elife, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Biorxiv : the Preprint Server for Biology, 2023
Thrombophilic gene polymorphisms and recurrent pregnancy loss: a systematic review and meta-analysis.
Wen Y et al.
Journal of Assisted Reproduction and Genetics, 2023
An Exploratory Study Using Next-Generation Sequencing to Identify Prothrombotic Variants in Patients with Cerebral Vein Thrombosis.
Kramer RA et al.
International Journal of Molecular Sciences, 2023
Maternal Thrombophilic and Hypofibrinolytic Genetic Variants and Idiopathic Recurrent Pregnancy Loss: Correspondence.
Sookaromdee P et al.
Reproductive Sciences (thousand Oaks, Calif.), 2023
Maternal Thrombophilic and Hypofibrinolytic Genetic Variants in Idiopathic Recurrent Pregnancy Loss: a Continuing Mystery.
Younis M et al.
Reproductive Sciences (thousand Oaks, Calif.), 2023
Genetic markers for inherited thrombophilia related pregnancy loss and implantation failure in Indian population - implications for diagnosis and clinical management.
Udumudi A et al.
The Journal of Maternal-fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2022
The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options.
Jankovic M et al.
International Journal of Molecular Sciences, 2022
Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE).
Parsopoulou F et al.
Frontiers in Allergy, 2022
Combinations of fibrinolytic gene polymorphisms (plasminogen activator inhibitor type 1 4G/5G, factor XIII Val34Leu and angiotensin-converting enzyme I/D) in women with idiopathic infertility.
Velickovic J et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2021
Pharmacogenomics and Pharmacogenetics: In Silico Prediction of Drug Effects in Treatments for Novel Coronavirus SARS-CoV2 Disease.
Cafiero C et al.
Pharmacogenomics and Personalized Medicine, 2020
Population study of thrombophilic markers and pharmacogenetic markers of warfarin prevalence in Bosnia and Herzegovina.
Ašić A et al.
Croatian Medical Journal, 2019
Factor XIII polymorphism and risk of aneurysmal subarachnoid haemorrhage in a south Indian population.
Suvatha A et al.
Bmc Medical Genetics, 2018
Genetic and epigenetic variations associated with idiopathic recurrent pregnancy loss.
Arias-Sosa LA et al.
Journal of Assisted Reproduction and Genetics, 2018
Atherosclerotic and thrombotic genetic and environmental determinants in Egyptian coronary artery disease patients: a pilot study.
Fawzy MS et al.
Bmc Cardiovascular Disorders, 2017
Coagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII Action.
Thomas A et al.
Human Mutation, 2016
Factor XIII B subunit polymorphisms and the risk of coronary artery disease.
Mezei ZA et al.
International Journal of Molecular Sciences, 2015
Factor XIII Val34Leu polymorphism and recurrent myocardial infarction in patients with coronary artery disease.
Kreutz RP et al.
Journal of Thrombosis and Thrombolysis, 2014
Polymorphism of transglutaminase 2: unusually low frequency of genomic variants with deficient functions.
Király R et al.
Amino Acids, 2013
Activity and levels of factor XIII in a Venezuelan admixed population: association with rs5985 (Val35Leu) and STR F13A01 polymorphisms.
Vívenes M et al.
Thrombosis Research, 2012
Polymorphisms of genes encoding coagulation factors II, V, VII, and XIII in relation to pediatric ischemic stroke: family-based and case-control study.
Kopyta IA et al.
The Neurologist, 2012
Variation in 24 hemostatic genes and associations with non-fatal myocardial infarction and ischemic stroke.
Smith NL et al.
Journal of Thrombosis and Haemostasis : Jth, 2008
Joint linkage and association of six single-nucleotide polymorphisms in the factor XIII-A subunit gene point to V34L as the main functional locus.
de Lange M et al.
Arteriosclerosis, Thrombosis, and Vascular Biology, 2006