Publications
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Filters: Author is Mangold, Elisabeth [Clear All Filters]
, “Whole exome association of rare deletions in multiplex oral cleft families.”, Genet Epidemiol, vol. 41, no. 1, pp. 61-69, 2017.
, “Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.”, Bioinformatics, vol. 30, no. 15, pp. 2189-96, 2014.
, “Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.”, Genetics, vol. 197, no. 3, pp. 1039-44, 2014.
