Obesity and ischemic stroke modulate the methylation levels of KCNQ1 in white blood cells.
Gómez-Úriz AM, Milagro FI, Mansego ML, Cordero P, Abete I, De Arce A, Goyenechea E, Blázquez V, Martínez-Zabaleta M, Martínez JA, López De Munain A, Campión J.
Hum. Mol. Genet. 2015; 24: 1432-1440. FI: 6.393 (Q1).
Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2.
Lemmers RJLF, Goeman JJ, van der Vliet PJ, van Nieuwenhuizen MP, Balog J, Vos-Versteeg M, Camano P, Ramos MA, Jerico I, Rogers MT, Miller DG, Upadhyaya M, Verschuuren JJGM, Lopez de Munain A, van Engelen BGM, Padberg GW, Sacconi S, Tawil R, Tapscott SJ, Bakker B, van der Maarel SM.
Hum. Mol. Genet. 2015; 24: 659-669. FI: 6.393 (Q1).
Evaluating machine-learning techniques for recruitment forecasting of seven North East Atlantic fish species.
Fernandes JA, Irigoien X, Lozano JA, Inza I, Goikoetxea N, Perez A.
Ecol. Inform. 2015; 25: 35-42. FI: 1.727 (Q3).
Multidimensional Learning from Crowds: Usefulness and Application of Expertise Detection.
Hernandez-Gonzalez J, Inza I, Lozano JA.
Int. J. Intell. Syst. 2015; 30: 326-354. FI: 1.886 (Q2).
Clinical Correlations With Lewy Body Pathology in LRRK2-Related Parkinson Disease.
Kalia LV, Lang AE, Hazrati LN, Fujioka S, Wszolek ZK, Dickson DW, Ross OA, Van Deerlin VM, Trojanowski JQ, Hurtig HI, Alcalay RN, Marder KS, Clark LN, Gaig C, Tolosa E, Ruiz-Martinez J, Marti-Masso JF, Ferrer I, Lopez de Munain A, Goldman SM, Schuele B, Langston JW, Aasly JO, Giordana MT, Bonifati V, Puschmann A, Canesi M, Pezzoli G, De Paula AM, Hasegawa K, Duyckaerts C, Brice A, Stoessl AJ, Marras C.
JAMA Neurol. 2015; 72: 100-105. FI: 7.271 (Q1).
SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential Tremor.
Sánchez E, Bergareche A, Krebs CE, Gorostidi A, Makarov V, Ruiz-Martinez J, Chorny A, Lopez de Munain A, Marti-Masso JF, Paisán-Ruiz C.
ASN Neuro. 2015; 7. FI: 4.017 (Q1).
Maribel Forcadas Berdusan (1949-2012).
Lopez de Munain A.
Rev. Neurologia. 2013; 56: 448. FI: 1.179 (Q4).
Clinical experience of treatment with onabotulinumtoxin A in patients with refractory migraine.
Palma JA, Irimia P, Fernández-Torrón R, Ortega-Cubero S, Riverol M, Luquin MR, Martínez-Vila E.
Rev. Neurología. 2012; 54: 705-711. FI: 1.218 (Q3).
Conformation and Chiral Effects in alpha,beta,alpha-Tripeptides.
Saavedra CJ, Boto A, Hernández R, Miranda JI, Aizpurua JM.
J. Org. Chem. 2012; 77: 5907-5913. FI: 4.450 (Q1).
Grp Estudio Epilepsia Sociedad Esp. Consensus-recommended diagnostic and therapeutic guidelines for drug-resistant epilepsy in Spain (Consenso RATE-España).
Sánchez-Álvarez JC, Mauri-Llerda JA, Gil-Nagel A, Casas-Fernández C, Salas-Puig J, Lahuerta J, Sancho-Rieger J.
Neurología. 2012; 27: 481-490. FI: 0.790 (Q4).
Current mutation discovery approaches in Retinitis Pigmentosa.
Anasagasti A, Irigoyen C, Barandika O, López de Munain A, Ruiz-Ederra J.
Vision Res. 2012; 75: 117-129. FI: 2.414 (Q2).
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia.
Martí-Massó JF, Ruiz-Martínez J, Makarov V, López de Munain A, Gorostidi A, Bergareche A, Yoon S, Buxbaum JD, Paísan-Ruiz C.
Hum. Genet. 2012; 131: 435-442. FI: 5.069 (Q1).
HLA-DRB1*15:01 and multiple sclerosis: afemale association?.
Irizar H, Muñoz-Culla M, Zuriarrain O, Goyenechea E, Castillo-Treviño T, Prada A, Sáenz-Cuesta M, De Juan D, López de Munain A, Olascoaga J, Otaegui D.
Mult. Scler. J. 2012; 18: 569-577. FI: 4.255 (Q1).
Inactivation of CDK/pRb Pathway Normalizes Survival Pattern of Lymphoblasts Expressing the FTLD-Progranulin Mutation
Alquezar C, Esteras N, Alzualde A, Moreno F, Ayuso MS, López de Munain A, Martín-Requero A.
c.709-1G > A. PLoS One. 2012; 7: -0. FI: 4.092 (Q1).
