Centre National de la Recherche Scientifique-ko ikertzaileekin lankidetzan egindako argitalpenak (11)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

2022

  1. FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects

    Genetics in Medicine, Vol. 24, Núm. 12, pp. 2475-2486

2020

  1. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

  2. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

2017

  1. Building Bridges through Science

    Neuron

2015

  1. Serumuric acidandthe riskof cardiovascular and renal disease

    Journal of Hypertension, Vol. 33, Núm. 9, pp. 1729-1741

2014

  1. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

    Nature Genetics, Vol. 46, Núm. 9, pp. 989-993

2012

  1. Ovarian endometrioma but not deep infiltrating endometriosis is associated with increased serum levels of interleukin-8 and interleukin-6

    Journal of Reproductive Immunology, Vol. 95, Núm. 1-2, pp. 80-86

2010

  1. Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome

    Human Mutation, Vol. 31, Núm. 2, pp. 113-126

2007

  1. New ABCC8 mutations in relapsing neonatal diabetes and clinical features

    Diabetes, Vol. 56, Núm. 6, pp. 1737-1741

1989

  1. Normal insulin sensitivity during the phase of glucose intolerance but insulin resistance at the onset of diabetes in the spontaneously diabetic BB rat

    Diabetologia, Vol. 32, Núm. 12, pp. 839-844