Complexo Hospitalario Universitario de Santiago
Centro de atención
University Hospital Bonn
Bonn, AlemaniaPublicacións en colaboración con investigadores/as de University Hospital Bonn (32)
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Corrigendum to “Dissecting the genetic heterogeneity of gastric cancer” (eBioMedicine (2023) 92, (S2352396423001810), (10.1016/j.ebiom.2023.104616))
eBioMedicine
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Dissecting the genetic heterogeneity of gastric cancer
eBioMedicine, Vol. 92
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Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database
eClinicalMedicine, Vol. 58
2022
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A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Communications Biology, Vol. 5, Núm. 1
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Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
PLoS genetics, Vol. 18, Núm. 11, pp. e1010367
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Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Nature, Vol. 604, Núm. 7906, pp. 502-508
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
2021
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Personalized medicine for allergy treatment: Allergen immunotherapy still a unique and unmatched model
Allergy: European Journal of Allergy and Clinical Immunology, Vol. 76, Núm. 4, pp. 1041-1052
2019
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Dolutegravir plus lamivudine versus dolutegravir plus tenofovir disoproxil fumarate and emtricitabine in antiretroviral-naive adults with HIV-1 infection (GEMINI-1 and GEMINI-2): week 48 results from two multicentre, double-blind, randomised, non-inferiority, phase 3 trials
The Lancet, Vol. 393, Núm. 10167, pp. 143-155
2018
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Perampanel in routine clinical use across Europe: Pooled, multicenter, observational data
Epilepsia, Vol. 59, Núm. 9, pp. 1727-1739
2017
2014
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Common variant at 16p11.2 conferring risk of psychosis
Molecular Psychiatry, Vol. 19, Núm. 1, pp. 108-114
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Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Nature Genetics, Vol. 46, Núm. 8, pp. 826-836
2011
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Common variants at VRK2 and TCF4 conferring risk of schizophrenia
Human Molecular Genetics, Vol. 20, Núm. 20, pp. 4076-4081
2009
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Common variants conferring risk of schizophrenia
Nature, Vol. 460, Núm. 7256, pp. 744-747
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Potential clinical utility of polymerase chain reaction in microbiological testing for sepsis
Critical Care Medicine, Vol. 37, Núm. 12, pp. 3085-3090
2004
2003
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Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin
Nature Genetics, Vol. 34, Núm. 2, pp. 151-153
2000
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A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3
American Journal of Human Genetics, Vol. 66, Núm. 6, pp. 1979-1983