Publications by authors named "Laura Tomas-Roca"

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Extranodal natural killer/T-cell lymphoma nasal type in a western population: Molecular profiling identifies new therapeutic targets.
Eva Gonzalez Barca, Laura Tomás-Roca, Anna Esteve, Marta Rodriguez, Lucía Gato

Am J Hematol· June 2023

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NanoString analysis of mycosis fungoides reveals individual molecular identity.
Ruth Alonso-Alonso, Marta Rodríguez, Nuria García-Díaz, Laura Tomás-Roca, Jennifer Borregón

Br J Dermatol· May 2023

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Developmental disruption and restoration of brain synaptome architecture in the murine Pax6 neurodevelopmental disease model.
Laura Tomas-Roca, Zhen Qiu, Erik Fransén, Ragini Gokhale, Edita Bulovaite

Nat Commun· November 2022

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An integrated prognostic model for diffuse large B-cell lymphoma treated with immunochemotherapy.
Marta Rodríguez, Ruth Alonso-Alonso, Ismael Fernández-Miranda, Rufino Mondéjar, Laura Cereceda

EJHaem· August 2022

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Peripheral T-cell lymphoma: molecular profiling recognizes subclasses and identifies prognostic markers.
Marta Rodríguez, Ruth Alonso-Alonso, Laura Tomás-Roca, Socorro M Rodríguez-Pinilla, Rebeca Manso-Alonso

Blood Adv· December 2021

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Estimation of the number of synapses in the hippocampus and brain-wide by volume electron microscopy and genetic labeling.
Andrea Santuy, Laura Tomás-Roca, José-Rodrigo Rodríguez, Juncal González-Soriano, Fei Zhu

Sci Rep· August 2020

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Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis.
Isabelle Schrauwen, Hanne Valgaeren, Laura Tomas-Roca, Manou Sommen, Umut Altunoglu

Genet Med· May 2019

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Crypto-rhombomeres of the mouse medulla oblongata, defined by molecular and morphological features.
Laura Tomás-Roca, Rubén Corral-San-Miguel, Pilar Aroca, Luis Puelles, Faustino Marín

Brain Struct Funct· March 2016

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De novo mutations in PLXND1 and REV3L cause Möbius syndrome.
Laura Tomas-Roca, Anastasia Tsaalbi-Shtylik, Jacob G Jansen, Manvendra K Singh, Jonathan A Epstein

Nat Commun· June 2015

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Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.
Zafar Iqbal, Geert Vandeweyer, Monique van der Voet, Ali Muhammad Waryah, Muhammad Yasir Zahoor

Hum Mol Genet· May 2013

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Developmental expression pattern of Hspb8 mRNA in the mouse brain: analysis through online databases.
Noelia García-Lax, Laura Tomás-Roca, Faustino Marín

Anat Rec (Hoboken)· March 2012

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In silico identification of new candidate genes for hereditary congenital facial paresis.
Laura Tomás-Roca, Antonio Pérez-Aytés, Luis Puelles, Faustino Marín

Int J Dev Neurosci· June 2011

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