Publicaciones en colaboración con investigadores/as de Albert Einstein College of Medicine (16)

2023

  1. 2-year outcomes of MitraClip as a bridge to heart transplantation: The international MitraBridge registry

    International Journal of Cardiology, Vol. 390

  2. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort

    Movement Disorders, Vol. 38, Núm. 2, pp. 286-303

  3. Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population

    Nature Communications, Vol. 14, Núm. 1

2020

  1. Coronary artery aneurysms, insights from the international coronary artery aneurysm registry (CAAR)

    International Journal of Cardiology, Vol. 299, pp. 49-55

2019

  1. Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (Nature Genetics, (2019), 51, 3, (414-430), 10.1038/s41588-019-0358-2)

    Nature Genetics

  2. Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

    Nature Genetics, Vol. 51, Núm. 3, pp. 414-430

2017

  1. Pleiotropy of genetic variants on obesity and smoking phenotypes: Results from the oncoarray project of the international lung cancer consortium

    PLoS ONE, Vol. 12, Núm. 9

2016

  1. MicroRNA profile in CD8+ T-lymphocytes from HIV-infected individuals: Relationship with antiviral immune response and disease progression

    PLoS ONE, Vol. 11, Núm. 5

2015

  1. Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types

    Journal of the National Cancer Institute, Vol. 107, Núm. 12

2014

  1. Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33

    Human Molecular Genetics, Vol. 23, Núm. 24, pp. 6616-6633

2011

  1. Physical illness in patients with severe mental disorders. I. Prevalence, impact of medications and disparities in health care

    World Psychiatry, Vol. 10, Núm. 1, pp. 52-77

  2. Physical illness in patients with severe mental disorders. II. Barriers to care, monitoring and treatment guidelines, plus recommendations at the system and individual level

    World Psychiatry, Vol. 10, Núm. 2, pp. 138-151

2010

  1. 8th international symposium on growth and nutrition in children with chronic renal disease: 2228-30 May 2009, Oviedo, Asturias, Spain

    Pediatric Nephrology

  2. The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: A meta-analysis study

    Journal of Alzheimer's Disease, Vol. 22, Núm. 1, pp. 247-255

1999

  1. Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease

    Journal of the American Society of Nephrology, Vol. 10, Núm. 11, pp. 2342-2351

1997

  1. A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2)

    American Journal of Human Genetics, Vol. 61, Núm. 3, pp. 547-555