Publications
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Filtres: Author is Ruczinski, Ingo [Enlever les filtres]
, « Detection of rare disease variants in extended pedigrees using RVS. », Bioinformatics, 2018.
, « Whole exome association of rare deletions in multiplex oral cleft families. », Genet Epidemiol, vol. 41, nᵒ 1, p. 61-69, 2017.
, « Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. », Bioinformatics, vol. 30, nᵒ 15, p. 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, p. 1039-44, 2014.
