María Arnedo

Mutations in Cohesin Complex Members SMC3 and SMC1A Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation

Matthew A. Deardorff, Maninder Kaur, Dinah Yaeger et al. · The American Journal of Human Genetics · 2007 · 518 citations · Full text

Developmental Anomaly, Smc1a Cause, Mendelian Disorder +11

SAF-A Regulates Interphase Chromosome Structure through Oligomerization with Chromatin-Associated RNAs

Ryu-Suke Nozawa, Lora Boteva, Dinesh C. Soares et al. · Cell · 2017 · 229 citations · Full text

Mutations and variants in the cohesion factor genes <i>NIPBL</i>, <i>SMC1A</i>, and <i>SMC3</i> in a cohort of 30 unrelated patients with Cornelia de Lange syndrome

Juan Pié, María Concepción Gil‐Rodríguez, Milagros Ciero et al. · American Journal of Medical Genetics Part A · 2010 · 82 citations · Full text

Evaluating Face2Gene as a Tool to Identify Cornelia de Lange Syndrome by Facial Phenotypes

Ana Latorre, Ángela Ascaso, Laura Trujillano et al. · International Journal of Molecular Sciences · 2020 · 69 citations · Full text

Identify Cornelia, Biometrics, Genetic Epidemiology +23

The functional relevance of the lateral parabrachial nucleus in lithium chloride-induced aversion learning

María Arnedo, Milagros Gallo, Amadeo Puerto · Pharmacology Biochemistry and Behavior · 1993 · 65 citations

Lateral Parabrachial Nucleus, Neurobiological Mechanism, Cognitive Science +12