Pavithra M. Rallapalli

An interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia B

Pavithra M. Rallapalli, Geoffrey Kemball‐Cook, Edward G. D. Tuddenham et al. · Journal of Thrombosis and Haemostasis · 2013 · 171 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy

Amy J. Osborne, Matteo Breno, Nicolò Ghiringhelli Borsa et al. · The Journal of Immunology · 2018 · 168 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchers

John H. McVey, Pavithra M. Rallapalli, Geoffrey Kemball‐Cook et al. · Haemophilia · 2020 · 92 citations · Full text

Medicine, Genetics, Hematology +16

New functional and structural insights from updated mutational databases for complement factor H, Factor I, membrane cofactor protein and C3

Elizabeth Rodríguez, Pavithra M. Rallapalli, Amy J. Osborne et al. · Bioscience Reports · 2014 · 74 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

The EAHAD blood coagulation factor VII variant database

Muriel Giansily‐Blaizot, Pavithra M. Rallapalli, Stephen J. Perkins et al. · Human Mutation · 2020 · 46 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17