Genética de Enfermedades Complejas
GENOME
University of Groningen
Groninga, HolandaPublicaciones en colaboración con investigadores/as de University of Groningen (11)
2022
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
American Journal of Human Genetics, Vol. 109, Núm. 8, pp. 1366-1387
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A saturated map of common genetic variants associated with human height
Nature, Vol. 610, Núm. 7933, pp. 704-712
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Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome Biology, Vol. 23, Núm. 1
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Type 2 Diabetes-Related Variants Influence the Risk of Developing Prostate Cancer: A Population-Based Case-Control Study and Meta-Analysis
Cancers, Vol. 14, Núm. 10
2021
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Common gene variants within 3′-untranslated regions as modulators of multiple myeloma risk and survival
International Journal of Cancer, Vol. 148, Núm. 8, pp. 1887-1894
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The power of genetic diversity in genome-wide association studies of lipids
Nature, Vol. 600, Núm. 7890, pp. 675-679
2020
2019
2011
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Differential association of two PTPN22 coding variants with Crohn's disease and ulcerative colitis
Inflammatory Bowel Diseases, Vol. 17, Núm. 11, pp. 2287-2294
2010
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Association of FcgR2a, but not FcgR3a, with inflammatory bowel diseases across three Caucasian populations
Inflammatory Bowel Diseases, Vol. 16, Núm. 12, pp. 2080-2089