Medicina
Departamento
Albert Einstein College of Medicine
Nueva York, Estados UnidosPublicaciones en colaboración con investigadores/as de Albert Einstein College of Medicine (16)
2023
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2-year outcomes of MitraClip as a bridge to heart transplantation: The international MitraBridge registry
International Journal of Cardiology, Vol. 390
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Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
Movement Disorders, Vol. 38, Núm. 2, pp. 286-303
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Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Nature Communications, Vol. 14, Núm. 1
2020
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Coronary artery aneurysms, insights from the international coronary artery aneurysm registry (CAAR)
International Journal of Cardiology, Vol. 299, pp. 49-55
2019
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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
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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
2016
2015
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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
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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
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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
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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
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8th international symposium on growth and nutrition in children with chronic renal disease: 2228-30 May 2009, Oviedo, Asturias, Spain
Pediatric Nephrology
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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
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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
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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