{"id":"W2037908858","doi":"10.1042/cs20070220","title":"Familial combined hyperlipidaemia: how can genetic disorders be common, complex and comprehensible?","year":2007,"lang":"en","type":"letter","venue":"Clinical Science","topic":"Lipid metabolism and disorders","field":"Medicine","cited_by":7,"is_retracted":false,"has_abstract":true,"ca_institutions":"McGill University","funders":"","keywords":"Phenotype; Disease; Complex disease; Clinical phenotype; Genetics; Biology; Gene; Underpinning; Bioinformatics; Computational biology; Medicine; Internal medicine","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":{"n_in":0,"stratum":"aff_core","weight":5595.2375,"opus":{"tier":"OUT","genre":"editorial/commentary","about_ca":false,"confidence":"high","reason":"Commentary proposing a disease model of familial combined hyperlipidaemia; a clinical-genetics topic."},"gpt":{"tier":"OUT","genre":"editorial/commentary","about_ca":false,"confidence":"high","reason":"It is a letter discussing familial hyperlipidaemia biology, not research itself."},"grok":{"tier":"OUT","genre":"editorial/commentary","about_ca":false,"confidence":"high","reason":"Letter proposing a multi-gene model of familial combined hyperlipidaemia; clinical commentary, not metaresearch."}}}