Rene Mulder

Groningen, GR, Netherlands

Last Updated: 09/26/2026

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Found 17 publications

Novel SERPINC1 variants in hereditary antithrombin deficiency: first pathogenic deep-intronic variant, revealed by multiple genomic and transcriptomic approaches.

Novel SERPINC1 variants in hereditary antithrombin deficiency: first pathogenic deep-intronic variant, revealed by multiple genomic and transcriptomic approaches.

Journal: Journal of thrombosis and haemostasis : JTH

Published: January 20, 2026

TEMPORARY REMOVAL: Direct oral anticoagulants in antithrombin deficiency: initial experience in a single center.

TEMPORARY REMOVAL: Direct oral anticoagulants in antithrombin deficiency: initial experience in a single center.

Journal: Thrombosis and haemostasis

Published: September 27, 2022

Clonal hematopoiesis in patients with stem cell mobilization failure: a nested case-control study.

Clonal hematopoiesis in patients with stem cell mobilization failure: a nested case-control study.

Journal: Blood advances

Published: March 07, 2022

Genetic testing of hereditary antithrombin deficiency in a large US pedigree using saliva samples.

Genetic testing of hereditary antithrombin deficiency in a large US pedigree using saliva samples.

Journal: International journal of laboratory hematology

Published: September 09, 2020

Erythrocytosis in the general population: clinical characteristics and association with clonal hematopoiesis.

Erythrocytosis in the general population: clinical characteristics and association with clonal hematopoiesis.

Journal: Blood advances

Published: September 01, 2020

Direct Oral Anticoagulants in Antithrombin Deficiency: Initial Experience in a Single Center.

Direct Oral Anticoagulants in Antithrombin Deficiency: Initial Experience in a Single Center.

Journal: Thrombosis and haemostasis

Published: August 31, 2020

Linkage analysis combined with whole-exome sequencing identifies a novel prothrombin (F2) gene mutation in a Dutch Caucasian family with unexplained thrombosis.

Linkage analysis combined with whole-exome sequencing identifies a novel prothrombin (F2) gene mutation in a Dutch Caucasian family with unexplained thrombosis.

Journal: Haematologica

Published: October 05, 2019

Monitoring of heparins in antithrombin-deficient patients.

Monitoring of heparins in antithrombin-deficient patients.

Journal: Thrombosis research

Published: August 30, 2018

Familial macrothrombocytopenia due to a double mutation in cis in the alpha-actinin 1 gene (ACTN1), previously considered to be chronic immune thrombocytopenic purpura.

Familial macrothrombocytopenia due to a double mutation in cis in the alpha-actinin 1 gene (ACTN1), previously considered to be chronic immune thrombocytopenic purpura.

Journal: Pediatric blood & cancer

Published: February 21, 2018

β-Antithrombin, subtype of antithrombin deficiency and the risk of venous thromboembolism in hereditary antithrombin deficiency: A family cohort study.

β-Antithrombin, subtype of antithrombin deficiency and the risk of venous thromboembolism in hereditary antithrombin deficiency: A family cohort study.

Journal: Thrombosis research

Published: December 18, 2017

High protein S activity due to C4b-binding protein deficiency in a 34-year-old Surinamese female with ischemic retinopathy.

High protein S activity due to C4b-binding protein deficiency in a 34-year-old Surinamese female with ischemic retinopathy.

Journal: Clinical case reports

Published: October 27, 2017

Factor 11 single-nucleotide variants in women with heavy menstrual bleeding.

Factor 11 single-nucleotide variants in women with heavy menstrual bleeding.

Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology

Published: June 14, 2017

Showing 1-12 of 17

Last Updated: 09/26/2026