Miguel Martín Abelleyro

Assessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B

Liliana Carmen Rossetti, Miguel Martín Abelleyro, Miguel Candela et al. · Thrombosis and Haemostasis · 2012 · 38 citations · Full text

Genetics, Immunology, Genetic Epidemiology +22

Phenotype–genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X‐chromosome inactivation

Claudia Pamela Radic, Liliana Carmen Rossetti, Miguel Martín Abelleyro et al. · Journal of Thrombosis and Haemostasis · 2015 · 35 citations · Full text

Phenotype–genotype Correlations, Cytogenetics, Genetics +8

Factor <scp>VIII</scp> genotype characterization of haemophilia A affected patients with transient and permanent inhibitors: a comprehensive Argentine study of inhibitor risks

Liliana Carmen Rossetti, I. Szurkalo, Claudia Pamela Radic et al. · Haemophilia · 2013 · 14 citations · Full text

Curating the gnomAD database: Report of novel variants in the thyrogobulin gene using in silico bioinformatics algorithms

Mauricio Gomes Pio, Sofía Siffo, Karen G. Scheps et al. · Molecular and Cellular Endocrinology · 2021 · 14 citations

Engineering, Genetics, Molecular Biology +16

Inverse shifting PCR based prenatal diagnosis of hemophilia‐causative inversions involving <i>int22h</i> and <i>int1h</i> hotspots from chorionic villus samples

Claudia Pamela Radic, Liliana Carmen Rossetti, Johanna Romina Zuccoli et al. · Prenatal Diagnosis · 2009 · 11 citations · Full text