List of works - Ana I Anton

Antithrombin controls tumor migration, invasion and angiogenesis by inhibition of enteropeptidase

scientific article published on 8 June 2016

CALU A29809G polymorphism in coronary atherothrombosis: Implications for coronary calcification and prognosis.

scientific article published on September 2010

Chediak-Higashi syndrome: description of two novel homozygous missense mutations causing divergent clinical phenotype.

scientific article published on 24 October 2013

Compound heterozygosity involving Antithrombin Cambridge II (p.Ala416Ser) in antithrombin deficiency

scientific article published on 17 January 2013

Correction: Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency

scientific article published on 21 July 2016

Creating a genotype-based dosing algorithm for acenocoumarol steady dose.

scientific article published on 29 November 2012

Effect of VKORC1, CYP2C9 and CYP4F2 genetic variants in early outcomes during acenocoumarol treatment.

scientific article

Evaluation of Novel Platelet Polymorphisms in Stroke. Dichotomic Effect of rs5443 in GNB3.

scientific article

Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study.

scientific article

Functional consequences of the prothrombotic SERPINC1 rs2227589 polymorphism on antithrombin levels

scientific article published on 19 February 2009

Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation.

scientific article published on 18 August 2017

Genotype-guided therapy improves initial acenocoumarol dosing. Results from a prospective randomised study.

scientific article published on 5 November 2015

Genotype-phenotype relationship for six common polymorphisms in genes affecting platelet function from 286 healthy subjects and 160 patients with mucocutaneous bleeding of unknown cause.

scientific article published on 21 April 2009

Hermansky-Pudlak syndrome. Overview of clinical and molecular features and case report of a new HPS-1 variant.

scientific article published on 13 August 2014

Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency

scientific article

Identification of antithrombin-modulating genes. Role of LARGE, a gene encoding a bifunctional glycosyltransferase, in the secretion of proteins?

scientific article

Impaired leucocyte activation is underlining the lower thrombotic risk of essential thrombocythaemia patients with CALR mutations as compared with those with the JAK2 mutation.

scientific article

Influence of the F12 -4 C>T polymorphism on hemostatic tests

scientific article published on 01 October 2010

Novel cassette-based shuttle vector system for gram-positive bacteria

scientific article published on October 2004

Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children.

scientific article

Pharmacogenetics of acenocoumarol in patients with extreme dose requirements.

scientific article published on 9 February 2010

Prognostic signature and clonality pattern of recurrently mutated genes in inactive chronic lymphocytic leukemia

scientific article

Rare homozygous status of P43 β1-tubulin polymorphism causes alterations in platelet ultrastructure.

scientific article published on 8 March 2011

Regulatory regions of SERPINC1 gene: Identification of the first mutation associated with antithrombin deficiency

article

Study of 18 functional hemostatic polymorphisms in mucocutaneous bleeding disorders

scientific article published on 09 June 2010

The JAK2 46/1 haplotype does not predispose to CALR-mutated myeloproliferative neoplasms.

scientific article published on 9 December 2014

List of works by Ana I Anton

Antithrombin controls tumor migration, invasion and angiogenesis by inhibition of enteropeptidase

CALU A29809G polymorphism in coronary atherothrombosis: Implications for coronary calcification and prognosis.

Chediak-Higashi syndrome: description of two novel homozygous missense mutations causing divergent clinical phenotype.

Compound heterozygosity involving Antithrombin Cambridge II (p.Ala416Ser) in antithrombin deficiency

Correction: Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency

Creating a genotype-based dosing algorithm for acenocoumarol steady dose.

Effect of VKORC1, CYP2C9 and CYP4F2 genetic variants in early outcomes during acenocoumarol treatment.

Evaluation of Novel Platelet Polymorphisms in Stroke. Dichotomic Effect of rs5443 in GNB3.

Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study.

Functional consequences of the prothrombotic SERPINC1 rs2227589 polymorphism on antithrombin levels

Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation.

Genotype-guided therapy improves initial acenocoumarol dosing. Results from a prospective randomised study.

Genotype-phenotype relationship for six common polymorphisms in genes affecting platelet function from 286 healthy subjects and 160 patients with mucocutaneous bleeding of unknown cause.

Hermansky-Pudlak syndrome. Overview of clinical and molecular features and case report of a new HPS-1 variant.

Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency

Identification of antithrombin-modulating genes. Role of LARGE, a gene encoding a bifunctional glycosyltransferase, in the secretion of proteins?

Impaired leucocyte activation is underlining the lower thrombotic risk of essential thrombocythaemia patients with CALR mutations as compared with those with the JAK2 mutation.

Influence of the F12 -4 C>T polymorphism on hemostatic tests

Novel cassette-based shuttle vector system for gram-positive bacteria

Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children.

Pharmacogenetics of acenocoumarol in patients with extreme dose requirements.

Prognostic signature and clonality pattern of recurrently mutated genes in inactive chronic lymphocytic leukemia

Rare homozygous status of P43 β1-tubulin polymorphism causes alterations in platelet ultrastructure.

Regulatory regions of SERPINC1 gene: Identification of the first mutation associated with antithrombin deficiency

Study of 18 functional hemostatic polymorphisms in mucocutaneous bleeding disorders

The JAK2 46/1 haplotype does not predispose to CALR-mutated myeloproliferative neoplasms.