Departamento de Ciencias Forenses, Anatomía Patolóxica, Xinecoloxía e Obstetricia e Pediatría
Fachbereich
University of Bonn
Bonn, AlemaniaPublikationen in Zusammenarbeit mit Forschern von University of Bonn (23)
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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Erratum: Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores (Nature communications (2021) 12 1 (3417))
Nature communications
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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New insights into the genetic etiology of Alzheimer's disease and related dementias
Nature genetics, Vol. 54, Núm. 4, pp. 412-436
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Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations
American Journal of Human Genetics, Vol. 109, Núm. 9, pp. 1680-1691
2021
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Common variants in Alzheimer's disease and risk stratification by polygenic risk scores
Nature communications, Vol. 12, Núm. 1, pp. 3417
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
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Identification of regulatory variants associated with genetic susceptibility to meningococcal disease
Scientific Reports, Vol. 9, Núm. 1
2017
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Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci
Nature Genetics, Vol. 49, Núm. 7, pp. 993-1004
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ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development
Scientific Reports, Vol. 7
2015
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RNA/DNA co-analysis from human skin and contact traces - Results of a sixth collaborative EDNAP exercise
Forensic Science International: Genetics, Vol. 16, pp. 139-147
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
2013
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RNA/DNA co-analysis from human saliva and semen stains-Results of a third collaborative EDNAP exercise
Forensic Science International: Genetics, Vol. 7, Núm. 2, pp. 230-239
2012
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Sarcomeric gene mutations in sudden infant death syndrome (SIDS)
Forensic Science International, Vol. 219, Núm. 1-3, pp. 278-281
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