A. Biswas

A. Biswas, R. Saxena, R. Ranjan, 2010, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

β2 Glycoprotein 1 in Indian Patients with SLE

A. Biswas, R. Saxena, Ashok Kumar, 2005, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

First report of a FVII-deficient Indian patient carrying double heterozygous mutations in the FVII gene.

E. Seifried, A. Biswas, J. Oldenburg, 2005, Thrombosis research.

The Relationship between Inflammatory Cytokines and Coagulopathy in Patients with COVID-19

A. Biswas, A. Dorgalaleh, A. Dabbagh, 2021, Journal of clinical medicine.

Coagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII Action

A. Biswas, J. Oldenburg, J. Dodt, 2016, Human mutation.

Exploring Diverse Coagulation Factor XIII Subunit Expression Datasets: A Bioinformatic Analysis

A. Biswas, M. Jamil, J. Oldenburg, 2022, International journal of molecular sciences.

Distinct 3-disulfide-bonded isomers of tridegin differentially inhibit coagulation factor XIIIa: The influence of structural stability on bioactivity.

A. Biswas, T. Steinmetzer, D. Imhof, 2020, European journal of medicinal chemistry.

Gene tracking in a family of novel identical twins affected by severe type-III von Willebrand Disease (vWD).

A. Biswas, R. Saxena, F. Ahmad, 2007, Thrombosis research.

An update of the mutation profile of Factor 13 A and B genes.

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2011, Blood reviews.

Exploring the structural similarity yet functional distinction between coagulation factor XIII-B and complement factor H sushi domains

A. Biswas, J. Oldenburg, Sneha Singh, 2019, Journal of Thrombosis and Thrombolysis.

Role of endothelial nitric oxide synthase gene in vascular diseases.

A. Biswas, R. Saxena, M. Akhter, 2009 .

Identification of Potential Novel Interacting Partners for Coagulation Factor XIII B (FXIII-B) Subunit, a Protein Associated with a Rare Bleeding Disorder

Christoph A. Krettler, P. Volkers, A. Biswas, 2019, International journal of molecular sciences.

Impact of interleukin 6 promoter polymorphisms (−174 G > C, −572 G > C and −597 G > A) on plasma IL-6 levels and their influence on the development of DVT: a study from India

A. Biswas, J. Oldenburg, Kanwaljeet Singh, 2018, Hematology.

Impact of Thrombogenic Mutations on Clinical Phenotypes of von Willebrand Disease

A. Biswas, R. Saxena, F. Ahmad, 2010, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Prothrombotic factors and the risk of acute onset non-cardioembolic stroke in young Asian Indians.

M. Behari, A. Biswas, R. Saxena, 2009, Thrombosis research.

NLRP7 inter-domain interactions: the NACHT-associated domain is the physical mediator for oligomeric assembly.

A. Biswas, H. Singer, J. Oldenburg, 2014, Molecular human reproduction.

Human VKORC1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces.

A. Biswas, J. Oldenburg, K. Czogalla, 2013, Blood.

interfaces 4-hydroxycoumarin resistance and affect putative warfarin binding Human VKORC1 mutations cause variable degrees of

A. Biswas, J. Oldenburg, K. Czogalla, 2013 .

THROMBOSIS AND HEMOSTASIS Human VKORC 1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces

A. Biswas, J. Oldenburg, K. Czogalla, 2013 .

Characterization of a novel large deletion caused by double-stranded breaks in 6-bp microhomologous sequences of intron 11 and 12 of the F13A1 gene

A. Biswas, J. Oldenburg, J. Goudemand, 2016, Human Genome Variation.

NMR-Based Structural Characterization of a Two-Disulfide-Bonded Analogue of the FXIIIa Inhibitor Tridegin: New Insights into Structure–Activity Relationships

A. Biswas, T. Steinmetzer, O. Ohlenschläger, 2021, International journal of molecular sciences.

Neoplasm-induced bleeding in inherited, heterozygous FXIII-A deficiency

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2015, Hämostaseologie.

Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2014, Annals of Hematology.

Coagulation factor XIII deficiency

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2014, Hämostaseologie.

Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2010, Haemophilia : the official journal of the World Federation of Hemophilia.

Evaluation of role of FV, FVIII and APLAs in the pathogenesis of APCR in FV Leiden negative DVT patients: a study in India

A. Biswas, Kanwaljeet Singh, R. Saxena, 2017, Journal of Thrombosis and Thrombolysis.

Prevalence of Factor V Genetic Variants Associated With Indian APCR Contributing to Thrombotic Risk

A. Biswas, K. Kishore, R. Saxena, 2017, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Identification and functional characterization of a novel F5 mutation (Ala512Val, FVBonn) associated with activated protein C resistance

A. Biswas, J. Oldenburg, A. Pavlova, 2016, Journal of thrombosis and haemostasis : JTH.

Genetic landscape in coagulation factor XIII associated defects - Advances in coagulation and beyond.

A. Biswas, J. Oldenburg, Sneha Singh, 2022, Blood reviews.

Novel insights into structure and function of factor XIIIa-inhibitor tridegin.

A. Biswas, Kornelia Hardes, T. Steinmetzer, 2014, Journal of medicinal chemistry.

A novel fibrinogen γ chain frameshift deletion (c.637delT) in a patient with hypodysfibrinogenemia associated with thrombosis.

A. Biswas, J. Oldenburg, A. Pavlova, 2015, Hamostaseologie.

Inhibitor in Congenital Factor VII Deficiency; a Rare but Serious Therapeutic Challenge—A Systematic Literature Review

A. Biswas, A. Dorgalaleh, F. Zaker, 2021, Journal of clinical medicine.

Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines

A. Biswas, A. Ichinose, H. Omura, 2014, Haemophilia : the official journal of the World Federation of Hemophilia.

Disruption of Structural Disulfides of Coagulation FXIII-B Subunit; Functional Implications for a Rare Bleeding Disorder

A. Biswas, J. Oldenburg, Sneha Singh, 2019, International journal of molecular sciences.

NLRP7, Involved in Hydatidiform Molar Pregnancy (HYDM1), Interacts with the Transcriptional Repressor ZBTB16

A. Biswas, H. Singer, J. Oldenburg, 2015, PloS one.

NLRP 7 , Involved in Hydatidiform Molar Pregnancy ( HYDM 1 ) , Interacts with the Transcriptional Repressor ZBTB 16

A. Biswas, H. Singer, J. Oldenburg, 2015 .

Clinicohematologic Spectrum in Patientswith Lupus Anticoagulant

A. Biswas, R. Saxena, M. Kannan, 2005, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Identification and characterization of a novel variant in C-terminal region of Antithrombin (Ala427Thr) associated with type II AT deficiency leading to polymer formation

A. Biswas, R. Saxena, Amit Sharma, 2020, Journal of Thrombosis and Thrombolysis.

Clinico-Hematologic Profile of Factor XIII-Deficient Patients

A. Biswas, R. Saxena, R. Ahmed, 2005, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Modulation of clinical phenotype of Glanzmann's thrombasthenia by thrombogenic mutations.

A. Biswas, R. Saxena, B. Yadav, 2009, Clinica chimica acta; international journal of clinical chemistry.

Use of Intron 1 and 22 inversions and linkage analysis in carrier detection of hemophilia A in Indians.

A. Biswas, R. Saxena, R. Ranjan, 2006, Clinica chimica acta; international journal of clinical chemistry.

Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients

A. Biswas, J. Oldenburg, A. Pavlova, 2012, Thrombosis and Haemostasis.

Type‐3 von Willebrand disease in India—Clinical spectrum and molecular profile

B. George, A. Viswabandya, A. Biswas, 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

Basal cell carcinomas developing independently from BAP1‐tumor predisposition syndrome in a patient with bilateral uveal melanoma

A. Biswas, Amit Sharma, F. Holz, 2019, Genes, chromosomes & cancer.

Warfarin and vitamin K compete for binding to Phe55 in human VKOR

V. Hornung, A. Biswas, J. Oldenburg, 2016, Nature Structural &Molecular Biology.

Mitochondria: Emerging Consequential in Sickle Cell Disease

A. Biswas, J. Oldenburg, A. Madkhali, 2023, Journal of clinical medicine.

Screening of the NOS3 gene identifies the variants 894G/T, 1998C/G and 2479G/A to be associated with acute onset ischemic stroke in young Asian Indians

M. Behari, A. Biswas, R. Saxena, 2014, Journal of the Neurological Sciences.

Inter-locus as well as intra-locus heterogeneity in LINE-1 promoter methylation in common human cancers suggests selective demethylation pressure at specific CpGs

R. Fimmers, H. Fröhlich, W. Schulz, 2015, Clinical Epigenetics.

Recurrent Abortions in Asian Indians: No Role of Factor V Leiden Hong Kong/Cambridge Mutation and MTHFR Polymorphism

A. Biswas, A. Mittal, R. Saxena, 2008, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Role of MTHFR C677T polymorphism in ischemic stroke.

M. Behari, A. Biswas, R. Saxena, 2006, Neurology India.

SARS-CoV-2 Infection: Modulator of Pulmonary Embolism Paradigm

A. Biswas, J. Oldenburg, Mohammad S Akhter, 2021, Journal of clinical medicine.

PPAR-Responsive Elements Enriched with Alu Repeats May Contribute to Distinctive PPARγ–DNMT1 Interactions in the Genome

O. Lichtarge, Hongde Liu, Panagiotis Katsonis, 2021, Cancers.

A novel missense mutation in the FGB gene (p.Gly302Arg) leading to afibrinogenemia

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2016, Hämostaseologie.

Protein C system defects in Indian children with thrombosis

A. Biswas, R. Saxena, V. Kalra, 2005, Annals of Hematology.

Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5' splice site.

A. Biswas, J. Oldenburg, J. Driesen, 2016, Blood.

Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII‐A2

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

A. Biswas, J. Oldenburg, T. Shamsi, 2017, Thrombosis Journal.

Structural and functional influences of coagulation factor XIII subunit B heterozygous missense mutants

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2015, Molecular genetics & genomic medicine.

Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function

A. Biswas, J. Oldenburg, P. Petrides, 2010, Haematologica.

Influence of Interleukin-6 (IL-6) Promoter Gene Polymorphisms (−174G>C, −572G>C, and −597G>A) on IL-6 Plasma Levels and Their Impact in the Development of Acute Ischemic Stroke in Young Indians

M. Behari, A. Biswas, R. Saxena, 2019, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Screening of the GPX3 gene identifies the "T" allele of the SNP -861A/T as a risk for ischemic stroke in young Asian Indians.

M. Behari, A. Biswas, R. Saxena, 2014, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Factor V Leiden: is it the chief contributor to activated protein C resistance in Asian-Indian patients with deep vein thrombosis?

A. Biswas, R. Saxena, R. Ranjan, 2008, Clinica chimica acta; international journal of clinical chemistry.

The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine-based ER retention motif.

A. Biswas, J. Oldenburg, K. Czogalla, 2014, Blood.

VKORC1 and VKORC1L1 have distinctly different oral anticoagulant dose-response characteristics and binding sites.

V. Hornung, A. Biswas, J. Oldenburg, 2018, Blood advances.

Structure functional insights into calcium binding during the activation of coagulation factor XIII A

P. Volkers, A. Biswas, J. Oldenburg, 2019, Scientific Reports.

Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

A. Biswas, J. Oldenburg, T. Shamsi, 2017, Thrombosis Journal.

Homocystine levels, polymorphisms and the risk of ischemic stroke in young Asian Indians.

M. Behari, A. Biswas, R. Saxena, 2009, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Coagulation Factor XIIIa Inhibitor Tridegin: On the Role of Disulfide Bonds for Folding, Stability, and Function.

A. Biswas, J. Oldenburg, Kornelia Hardes, 2019, Journal of medicinal chemistry.

In Vitro Secretion Deficits are Common Among Human Coagulation Factor XIII Subunit B Missense Mutants: Correlations with Patient Phenotypes and Molecular Models

A. Biswas, J. Oldenburg, C. Bevans, 2013, Human mutation.

The Role of PAI-1 4G/5G Promoter Polymorphism and Its Levels in the Development of Ischemic Stroke in Young Indian Population

M. Behari, A. Biswas, R. Saxena, 2017, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Insights into the Folding of Disulfide-Rich μ-Conotoxins

M. Hofmann-Apitius, J. Hamaekers, A. Biswas, 2018, ACS omega.

Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand disease

A. Biswas, J. Oldenburg, A. Pavlova, 2019, Haemophilia : the official journal of the World Federation of Hemophilia.

GGCX variants leading to biallelic deficiency to γ‐carboxylate GRP cause skin laxity in VKCFD1 patients

V. Hornung, A. Biswas, H. Singer, 2021, Human mutation.

Protein C and Protein S: Causative factor for developing a hemorrhagic infarct in a HbE/Beta thalassemia child

A. Biswas, R. Saxena, B. Kumar, 2010, Indian journal of pediatrics.

Thrombin activatable fibrinolysis inhibitor gene polymorphisms are associated with antigenic levels in the Asian‐Indian population but may not be a risk for stroke

M. Behari, A. Biswas, R. Saxena, 2008, British journal of haematology.

Combined coagulation factor VIII and factor IX deficiency (CDF8F9) in a patient from Lithuania

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2016, Hämostaseologie.

Inherited Warfarin Resistance in Indian Patients: Does It Occur?

A. Biswas, A. Mittal, R. Saxena, 2007, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Novel point mutation in fibrinogen (Innsbruck; BβArg44Gly)

A. Griesmacher, A. Biswas, J. Oldenburg, 2015, Hämostaseologie.

Human VKORC1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces.

A. Biswas, J. Oldenburg, K. Czogalla, 2013, Blood.