Xenética
Servicio
University of Bonn
Bonn, AlemaniaPublicacións en colaboración con investigadores/as de University of Bonn (14)
2019
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Association analyses identify 31 new risk loci for colorectal cancer susceptibility
Nature Communications, Vol. 10, Núm. 1
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Erratum to: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (Nature Communications, (2018), 9, 1, (1340), 10.1038/s41467-018-03178-z)
Nature Communications
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Erratum to: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (Nature Communications, (2017), 8, 1, (1892), 10.1038/s41467-017-00320-1)
Nature Communications
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Erratum to: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (Nature Communications, (2018), 9, 1, (3707), 10.1038/s41467-018-04989-w)
Nature Communications
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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia
American Journal of Human Genetics, Vol. 104, Núm. 4, pp. 767-773
2018
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Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia
Nature Communications, Vol. 9, Núm. 1
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Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
Nature Communications, Vol. 9, Núm. 1
2017
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Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
Nature Communications, Vol. 8, Núm. 1
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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RNA/DNA co-analysis from human menstrual blood and vaginal secretion stains: Results of a fourth and fifth collaborative EDNAP exercise
Forensic Science International: Genetics, Vol. 8, Núm. 1, pp. 203-212
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
2009
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Involvement of hypertrophic cardiomyopathy genes in sudden infant death syndrome (SIDS)
Forensic Science International: Genetics Supplement Series, Vol. 2, Núm. 1, pp. 495-496