Laura Martin-Fernandez - Congenital Coagulopathies Lab, Blood & Tissue Bank

S. Marcellini-Antonio, I. Corrales-Insa, P. Bandini,N. Borrás,L. Martin-fernández, P. Galán-Álvarez, A. torres-Tienza, F. Vidal- Pérez, S. Valencia-Castillo, A. García-Mateo, C. Olivier-Cornacchia, J. Queizán-Hernández

Research and Practice in Thrombosis and Haemostasis (2023): 101280-101280

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First description of a bone marrow failure syndrome in Spain caused by compound heterozygous truncating mutations in ERCC6L2

Perla Bandini,Nina Borras,Laura Martin-Fernandez, Eugenia Fernandez-Mellid, Paula Melero-Valentin,Natalia Comes,Lorena Ramirez,Patricia Cadahia Fernandez, Matilde Rodriguez Ruiz,Manuel Mateo Perez Encinas,Francisco Vidal,Irene Corrales

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 438-438

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Key Genes of the Immune System and Predisposition to Acquired Hemophilia A: Evidence from a Spanish Cohort of 49 Patients Using Next-Generation Sequencing

Jose Pardos-Gea,Laura Martin-Fernandez,Laia Closa,Ainara Ferrero,Cristina Marzo,Manuel Rubio-Rivas,Francesca Mitjavila,Jose Ramon Gonzalez-Porras,Jose Maria Bastida,Jose Mateo,Marina Carrasco,Angel Bernardo,

International journal of molecular sciencesno. 22 (2023): 16372-16372

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Integrated GWAS and Gene Expression Suggest ORM1 As a Potential Regulator of Plasma Levels of Cell-Free DNA and Thrombosis Risk

Sonia Lopez,Angel Martinez-Perez,Alba Rodriguez-Rius,Ana Vinuela,Andrew A. Brown,Laura Martin-Fernandez,Noelia Vilalta,Marc Arus,Nikolaos Panousis,Alfonso Buil,Maria Sabater-Lleal,Juan Carlos Souto,

Thrombosis and haemostasis（2022）

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Molecular Study of a Large Cohort of 109 Haemophilia Patients from Cuba Using a Gene Panel with Next Generation Sequencing-Based Technology

Nina Borras,Dunia Castillo-Gonzalez,Natalia Comes,Laura Martin-Fernandez,Rene Antonio Rivero-Jimenez,Arturo Chang-Monteagudo, Vera Ruiz-Moleon, Heidys Garrote-Santana,Francisco Vidal,Consuelo Macias-Abraham

Haemophilia（2021）

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