Acceder Registro /

MARIA SABATER MOLINA

Buscador

Plaza-Zamora J, Sabater-Molina M, Rodríguez-Palmero M, Rivero M, Bosch V, Nadal JM, Zamora S, Larqué E. Polyamines in human breast milk for preterm and term infants. Br J Nutr. 2013 Aug 28;110(3):524-8. doi: 10.1017/S0007114512005284. PubMed PMID: 23286699.
AÑO: 2013; IF: 3.334
Pagán A, Sabater-Molina M, Olza J, Prieto-Sánchez MT, Blanco-Carnero JE, Parrilla JJ, Gil Á, Larqué E. A gene variant in the transcription factor 7-like 2 (TCF7L2) is associated with an increased risk of gestational diabetes mellitus. Eur J Obstet Gynecol Reprod Biol. 2014 Sep;180:77-82. doi: 10.1016/j.ejogrb.2014.06.024. PubMed PMID: 25048152.
AÑO: 2014; IF: 1.868
San Román I, Navarro M, Martínez F, Albert L, Polo L, Guardiola J, García-Molina E, Muñoz-Esparza C, López-Ayala JM, Sabater-Molina M, Gimeno JR. Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1. Clin Genet. 2016 Aug;90(2):171-6. doi: 10.1111/cge.12760. Epub 2016 Mar 23. PubMed PMID: 26857240.
AÑO: 2016; IF: 3.326
Sabater-Molina M, Saura D, García-Molina Sáez E, González-Carrillo J, Polo L, Pérez-Sánchez I, Olmo MDC, Oliva-Sandoval MJ, Barriales-Villa R, Carbonell P, Pascual-Figal D, Gimeno JR. A Novel Founder Mutation in MYBPC3: Phenotypic Comparison With the Most Prevalent MYBPC3 Mutation in Spain. Rev Esp Cardiol (Engl Ed). 2017 Feb;70(2):105-114. doi: 10.1016/j.rec.2016.06.020. Epub 2016 Oct 28. English, Spanish. PubMed PMID: 28029522.
AÑO: 2017; IF: 5.166
Sabater-Molina M, Navarro M, García-Molina Sáez E, Garrido I, Pascual-Figal D, González Carrillo J, Gimeno Blanes JR. Mutation in JPH2 cause dilated cardiomyopathy. Clin Genet. 2016 Nov;90(5):468-469. doi: 10.1111/cge.12825. Epub 2016 Jul 29. PubMed PMID: 27471098.
AÑO: 2016; IF: 3.326

Instituto de Investigación Sanitaria Acreditado

ISCII

Fondo Social Europeo "El FSE Invierte en tu futuro"

Fondo Social Europeo

Sello de Calidad Europeo "HR Excellence in Research"

HRS4R