1. Cluster analysis of patterns generated from a web repository of HEPG2 transcriptomes. Genes of unknown functions coregulated in concert with cholesterol synthesis pathway. (August 2018) Authors: Altieri, G.I.; Noto, D.; Cefalu', A.B.; Giammanco, A.; Fayer, F.; Ingrassia, V.; Scrimali, C.; Spina, R.; Valenti, V.; Misiano, G.; Brucato, F.; Ganci, A.; Barbagallo, C.M.; Averna, M.R. Journal: Atherosclerosis Issue: Volume 275(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Coronary artery calcium is independently associated to pulse wave velocity and LDL cholesterol burden in patients with familial hypercholesterolemia. (August 2018) Authors: Mattina, A.; Noto, D.; Cefalù, A.B.; Barbagallo, C.M.; Giammanco, A.; Cardella, A.; Di Benedetto, C.; Fayer, F.; Spina, R.; Geraci, G.; D'Ignoto, F.; Smeraldi, T.; La Grutta, L.; Midiri, M.; Averna, M. Journal: Atherosclerosis Issue: Volume 275(2018) Page Start: e83 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Coronary artery calcium is strongly associated with pulse wave velocity and LDL-cholesterol burden in patients with familial hypercholesterolemia. (August 2022) Authors: Giammanco, A.; Mattina, A.; Cefalù, A.B.; Geraci, G.; Noto, D.; Nardi, E.; Barbagallo, C.M.; Fayer, F.; Spina, R.; D'Ignoto, F.; Cardella, A.; La Grutta, L.; Smeraldi, T.; Midiri, M.; Averna, M. Journal: Atherosclerosis Issue: Volume 355(2022) Page Start: 12 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Detection of copy number variations (CNVS) in LDLR gene by next generation sequencing in patients with familial hypercholesterolemia. (August 2018) Authors: Scrimali, C.; Spina, R.; Ingrassia, V.; Cefalu', A.B.; Valenti, V.; Altieri, G.I.; Noto, D.; Brucato, F.; Misiano, G.; Giammanco, A.; Barbagallo, C.M.; Ganci, A.; Fayer, F.; Averna, M.R. Journal: Atherosclerosis Issue: Volume 275(2018) Page Start: e154 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Familial hypobetalipoproteinemia: Analysis by next generation sequencing and identification of novel mutations in the APOB gene. (August 2018) Authors: Ingrassia, V.; Spina, R.; Cefalù, A.B.; Valenti, V.; Altieri, G.I.; Scrimali, C.; Noto, D.; Brucato, F.; Misiano, G.; Giammanco, A.; Ganci, A.; Fayer, F.; Barbagallo, C.M.; Averna, M.R. Journal: Atherosclerosis Issue: Volume 275(2018) Page Start: e154 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic epidemiology of ARH in Sicily. (September 2016) Authors: Spina, R.; Valenti, V.; Ingrassia, V.; La Spada, M.P.; Scrimali, C.; Misiano, G.; Noto, D.; Palesano, O.; Altieri, G.I.; Licata, V.; Fayer, F.; Barbagallo, C.M.; Cefalù, A.B.; Averna, M. Journal: Atherosclerosis Issue: Volume 252(2016) Page Start: e37 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Identification Of P.Leu167Del Apoe Gene Mutation By Next Generation Sequencing In A Large Hypercholesterolemic Family. (August 2019) Authors: Scrimali, C.; Spina, R.; Ingrassia, V.; Cefalù, A.B.; Brucato, F.; Misiano, G.; Valenti, V.; Noto, D.; Altieri, G.I.; Fayer, F.; Giammanco, A.; Barbagallo, C.; Averna, M. Journal: Atherosclerosis Issue: Volume 287(2019) Page Start: e213 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Metabolic disturbances and risk of cancer in the 25 years follow-up of the "Ventimiglia Heart Study" epidemiological project. (September 2016) Authors: Noto, D.; Cefalù, A.B.; Barbagallo, C.M.; Giammanco, A.; Fayer, F.; Palesano, O.; Altieri, G.I.; Spina, R.; Valenti, V.; Pagano, M.; Cavera, G.; Averna, M.R. Journal: Atherosclerosis Issue: Volume 252(2016) Page Start: e86 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Molecular characterization of patients with and without coronary artery disease with "extreme LDL-C phenotypes". (December 2020) Authors: Brucato, F.; Martinelli, N.; Spina, R.; Busti, F.; Ingrassia, V.; Scrimali, C.; Altieri, G.I.; Noto, D.; Misiano, G.; Giammanco, A.; Barbagallo, C.M.; Fayer, F.; Cefalù, A.B.; Olivieri, O.; Girelli, D.; Averna, M. Journal: Atherosclerosis Issue: Volume 315(2020) Page Start: e222 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mutation in candidate genes account for a small minority of hypobetalipoproteinemias and NGS analysis support polygenicity in mutation-negative patients. (December 2020) Authors: Giammanco, A.; Scrimali, C.; Spina, R.; Ingrassia, V.; Brucato, F.; Valenti, V.; Cefalù, A.B.; Misiano, G.; Altieri, G.I.; Noto, D.; Barbagallo, C.M.; Ganci, A.; Fayer, F.; Averna, M. Journal: Atherosclerosis Issue: Volume 315(2020) Page Start: e45 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗