Publications
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Author Title [ Year
] Filters: Keyword is Genetic Diseases, Inborn [Clear All Filters]
Phenotype risk scores identify patients with unrecognized Mendelian disease patterns. Science 359, 1233-1239 (2018).
Improved methods for multi-trait fine mapping of pleiotropic risk loci. Bioinformatics 33, 248-255 (2017).
