| Rare coagulation factor deficiencies: a countrywide screening data from India BKKG S. Shetty, T. Shelar, D. Mirgal, V. Nawadkar, P. Pinto, S. Shanbhag, A ... Haemophilia 20 (4), 575–581, 2014 | 45 | 2014 |
| The epidemiology of FVIII inhibitors in Indian haemophilia A patients P Pinto, T Shelar, V Nawadkar, D Mirgal, A Mukaddam, P Nair, P Kasatkar, ... Indian Journal of Hematology and Blood Transfusion 30, 356-363, 2014 | 27 | 2014 |
| Molecular pathology of rare bleeding disorders (RBDs) in India: a systematic review BP Kulkarni, SB Nair, M Vijapurkar, L Mota, S Shanbhag, S Ali, SD Shetty, ... PloS one 9 (10), e108683, 2014 | 19 | 2014 |
| Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: identification of fourteen novel mutations S Shanbhag, K Ghosh, S Shetty Blood Cells, Molecules, and Diseases 57, 81-84, 2016 | 13 | 2016 |
| Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected S Shanbhag, S Shetty, K Ghosh Haemophilia 17 (5), e843-e845, 2011 | 12 | 2011 |
| An improved, semi quantitative clot based assay for factor XIII S Shanbhag, S Shetty, B Kulkarni, K Ghosh Haemophilia 17 (4), 718-720, 2011 | 10 | 2011 |
| First trimester prenatal diagnosis of severe FXIII deficiency S Shanbhag, K Ghosh, S Shetty Haemophilia 5 (22), e443-e444, 2016 | 5 | 2016 |
| Antibody profile in post-vaccinated & SARS-CoV-2 infected individuals R Patil, S Shanbhag, A Shankarkumar, M Madkaikar Indian Journal of Medical Research 155 (5&6), 538-545, 2022 | 3 | 2022 |
| A de novo factor VIII mutation in a haemophilia B family leading to combined deficiency of factor VIII and IX. A Prabhudesai, S Shanbhag, D Mirgal, N Kawankar, S Shetty Haemophilia 23 (5), 2017 | 2 | 2017 |
| A rare case of Glanzmann's thrombasthenia and factor VII deficiency due to a combination of pathogenic and non‐pathogenic gene variants. R Deshpande, S Shanbhag, A Jadli, S Shetty Haemophilia 26 (1), 2020 | 1 | 2020 |
| Somatic mosaicism in a severe haemophilia B family detected by allele specific PCR: An alert to the genetic diagnostic laboratories S Shanbhag, K Ghosh, S Shetty Thrombosis Research 158, 138-139, 2017 | 1 | 2017 |
| Prenatal diagnosis in a family with purfura fulminans S Shanbhag, N Pai, K Ghosh, S Shetty Blood Coagulation & Fibrinolysis 26 (3), 350, 2015 | | 2015 |
| Prenatal diagnosis in a haemophilia carrier with triplet pregnancy. S Shanbhag, C Lulla, K Ghosh, S Shetty Haemophilia: the Official Journal of the World Federation of Hemophilia 21 …, 2015 | | 2015 |
| Molecular basis of 21 severe FXIIIA deficiency cases: 11 novel mutations detected SD Shanbhag, K Ghosh, S Shetty JOURNAL OF THROMBOSIS AND HAEMOSTASIS 11, 1018-1018, 2013 | | 2013 |
| A SEMIQUANTITAIVE ASSAY FOR DIAGNOSIS OF FACTOR XIII DEFICIENCY K Ghosh, S Shanbhag, S Shetty, B Kulkarni HAEMATOLOGICA-THE HEMATOLOGY JOURNAL 95, 754-754, 2010 | | 2010 |
kanjaksha ghoshFormer Director : National Institute of Immunohaematology , Indian Council of Medical Research.Verified email at hemophilia.in
