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DeepCNV: a deep learning approach for authenticating copy number variations., , , , , , , , , and . Briefings Bioinform., (2021)Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43, 870 individuals from the eMERGE network., , , , , , , , , and 14 other author(s). PSB, page 272-283. (2019)A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population, , , , , , , , , and 168 other author(s). Nature genetics, 42 (10): 885–892 (2010)Performance of model-based multifactor dimensionality reduction methods for epistasis detection by controlling population structure., , , , , , , , , and . BioData Min., 14 (1): 16 (2021)Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network., , , , , , , , , and 9 other author(s). J. Biomed. Informatics, (2019)Neuroimaging of the Philadelphia Neurodevelopmental Cohort., , , , , , , , , and 7 other author(s). NeuroImage, (2014)Heterogeneous impact of motion on fundamental patterns of developmental changes in functional connectivity during youth., , , , , , , , , and 5 other author(s). NeuroImage, (2013)High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications, , , , , , , , , and 27 other author(s). Genome Research, (2009)Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits, , , , , , , , , and 136 other author(s). PLOS Genetics, 16 (10): 1-26 (October 2020)137 ancient human genomes from across the Eurasian steppes, , , , , , , , , and 65 other author(s). Nature, 557 (7705): 369--374 (2018)