Publicaciones en colaboración con investigadores/as de University of Michigan–Ann Arbor (20)

2023

  1. Discovery of AD258 as a Sigma Receptor Ligand with Potent Antiallodynic Activity

    Journal of Medicinal Chemistry, Vol. 66, Núm. 16, pp. 11447-11463

2022

  1. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

    Biological psychiatry, Vol. 91, Núm. 3, pp. 313-327

2021

  1. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

2020

  1. Cumulative Burden of Colorectal Cancer–Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset Cancer

    Gastroenterology, Vol. 158, Núm. 5, pp. 1274-1286.e12

2019

  1. A collaborative analysis of individual participant data from 19 prospective studies assesses circulating Vitamin D and prostate cancer risk

    Cancer Research, Vol. 79, Núm. 1, pp. 274-285

  2. Analysis of the genetic component of systemic sclerosis in Iranian and Turkish populations through a genome-wide association study

    Rheumatology (United Kingdom), Vol. 58, Núm. 2, pp. 289-298

  3. Genome-wide association study identifies 30 loci associated with bipolar disorder

    Nature Genetics, Vol. 51, Núm. 5, pp. 793-803

2018

  1. Analysis of shared heritability in common disorders of the brain

    Science, Vol. 360, Núm. 6395

  2. Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

    Communications Biology, Vol. 1, Núm. 1

  3. Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

    Nature Communications, Vol. 9, Núm. 1

  4. Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations

    PLoS ONE, Vol. 13, Núm. 1

  5. Improving genetic prediction by leveraging genetic correlations among human diseases and traits

    Nature Communications, Vol. 9, Núm. 1

2017

  1. An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

    Biological Psychiatry, Vol. 82, Núm. 5, pp. 322-329

  2. Interaction between the FTO gene, body mass index and depression: Meta-analysis of 13701 individuals

    British Journal of Psychiatry, Vol. 211, Núm. 2, pp. 70-76

2016

  1. A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease

    Science Translational Medicine, Vol. 8, Núm. 341

2015

  1. Associations between Potentially Modifiable Risk Factors and Alzheimer Disease: A Mendelian Randomization Study

    PLoS Medicine, Vol. 12, Núm. 6

  2. Rare coding variants and X-linked loci associated with age at menarche

    Nature Communications, Vol. 6

2014

  1. Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis

    American Journal of Human Genetics, Vol. 94, Núm. 1, pp. 47-61

2012

  1. Analysis of autosomal genes reveals gene-sex interactions and higher total genetic risk in men with systemic lupus erythematosus

    Annals of the Rheumatic Diseases, Vol. 71, Núm. 5, pp. 694-699

2008

  1. In vitro reduction of mutans streptococci by means of ozone gas application

    Quintessence International, Vol. 39, Núm. 10, pp. 827-831