GRUPO ANDALUZ DE INVESTIGACION EN SALUD MENTAL
PsychInn
Queen Mary University of London
Londres, Reino UnidoPublicaciones en colaboración con investigadores/as de Queen Mary University of London (22)
2022
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Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Nature, Vol. 604, Núm. 7906, pp. 502-508
2021
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A multilayered post-GWAS assessment on genetic susceptibility to pancreatic cancer
Genome Medicine, Vol. 13, Núm. 1
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Deciphering the complex interplay between pancreatic cancer, diabetes mellitus subtypes and obesity/BMI through causal inference and mediation analyses
Gut, Vol. 70, Núm. 2, pp. 319-329
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Gallbladder disease and pancreatic cancer risk: a multicentric case-control European study
European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP), Vol. 30, Núm. 6, pp. 423-430
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Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Nature genetics, Vol. 53, Núm. 6, pp. 817-829
2020
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Pancreatic Cancer Risk in Relation to Lifetime Smoking Patterns, Tobacco Type, and Dose-Response Relationships
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, Vol. 29, Núm. 5, pp. 1009-1018
2019
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Genome-wide association study identifies 30 loci associated with bipolar disorder
Nature Genetics, Vol. 51, Núm. 5, pp. 793-803
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Pancreatic cancer and autoimmune diseases: An association sustained by computational and epidemiological case–control approaches
International Journal of Cancer, Vol. 144, Núm. 7, pp. 1540-1549
2018
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Analysis of shared heritability in common disorders of the brain
Science, Vol. 360, Núm. 6395
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Risk of pancreatic cancer associated with family history of cancer and other medical conditions by accounting for smoking among relatives
International Journal of Epidemiology, Vol. 47, Núm. 2, pp. 473-483
2017
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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
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Phenotypic association analyses with copy number variation in recurrent depressive disorder
Biological Psychiatry, Vol. 79, Núm. 4, pp. 329-336
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Polygenic interactions with environmental adversity in the aetiology of major depressive disorder
Psychological Medicine, Vol. 46, Núm. 4, pp. 759-770
2015
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A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder
BMC Medicine, Vol. 13, Núm. 1
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Familiality and SNP heritability of age at onset and episodicity in major depressive disorder
Psychological Medicine, Vol. 45, Núm. 10, pp. 2215-2225
2014
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Do patient and ward-related characteristics influence the use of coercive measures? Results from the EUNOMIA international study
Social Psychiatry and Psychiatric Epidemiology, Vol. 49, Núm. 10, pp. 1619-1629
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Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: A genome-wide association and polygenic scoring study
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 165, Núm. 5, pp. 428-437
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Investigating the genetic variation underlying episodicity in major depressive disorder: Suggestive evidence for a bipolar contribution
Journal of Affective Disorders, Vol. 155, Núm. 1, pp. 81-89
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Relationship between obesity and the risk of clinically significant depression: Mendelian randomisation study
British Journal of Psychiatry, Vol. 205, Núm. 1, pp. 24-28
2013
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Genome-wide association analysis of copy number variation in recurrent depressive disorder
Molecular Psychiatry, Vol. 18, Núm. 2, pp. 183-189