1. A comment on "clinical experience with sex chromosome aneuploidies detected by noninvasive prenatal testing (NIPT): Accuracy and patient decision‐making". (20th November 2018) Authors: Ronzoni, Luisa; Silibello, Gaia; Quagliarini, Donatella; Lalatta, Faustina Journal: Prenatal diagnosis Issue: Volume 38:Number 13(2018) Page Start: 1129 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Adverse effect of PNPLA3 p.I148M genetic variant on kidney function in middle‐aged individuals with metabolic dysfunction. Issue 10 (22nd March 2023) Authors: Mantovani, Alessandro; Pelusi, Serena; Margarita, Sara; Malvestiti, Francesco; Dell'Alma, Michela; Bianco, Cristiana; Ronzoni, Luisa; Prati, Daniele; Targher, Giovanni; Valenti, Luca Journal: Alimentary pharmacology & therapeutics Issue: Volume 57:Issue 10(2023) Page Start: 1093 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical exome sequencing for diagnosing severe cryptogenic liver disease in adults: A case series. (15th February 2022) Authors: Pelusi, Serena; Ronzoni, Luisa; Malvestiti, Francesco; Bianco, Cristiana; Marini, Ilaria; D'Ambrosio, Roberta; Giannotta, Juri Alessandro; Soardo, Giorgio; Maggioni, Marco; Prati, Daniele; Valenti, Luca Journal: Liver international Issue: Volume 42:Number 4(2022) Page Start: 864 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetics: A new clinical tool for the hepatologist. (15th March 2022) Authors: Valenti, Luca; Ronzoni, Luisa Journal: Liver international Issue: Volume 42:Number 4(2022) Page Start: 724 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Incidence of chromosomal abnormalities in fetuses with first trimester ultrasound anomalies and a low‐risk cell‐free DNA test for common trisomies. (9th August 2020) Authors: Persico, Nicola; Boito, Simona; Volpe, Paolo; Ischia, Benedetta; Gentile, Mattia; Ronzoni, Luisa; De Robertis, Valentina; Fabietti, Isabella; Olivieri, Claudiana; Periti, Enrico; Ficarella, Romina; Silipigni, Rosamaria; Rembouskos, Georgios Journal: Prenatal diagnosis Issue: Volume 40:Number 11(2020) Page Start: 1474 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Increased RISK for 47, XXY on cell‐free DNA screen: Not always Klinefelter syndrome. (19th January 2021) Authors: Ronzoni, Luisa; Bedeschi, Maria Francesca; Silibello, Gaia; Accurti, Veronica; Di Segni, Marina; Nicotra, Valeria; Vizziello, Paola; Lalatta, Faustina Journal: Prenatal diagnosis Issue: Volume 41:Number 10(2021) Page Start: 1255 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Interstitial 6q25 microdeletion syndrome: ARID1B is the key gene. Issue 5 (11th January 2016) Authors: Ronzoni, Luisa; Tagliaferri, Francesco; Tucci, Arianna; Baccarin, Marco; Esposito, Susanna; Milani, Donatella Journal: American journal of medical genetics Issue: Volume 170:Issue 5(2016) Page Start: 1257 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Is cutis verticis Gyrata‐Intellectual Disability syndrome an underdiagnosed condition? A case report and review of 62 cases. Issue 3 (25th December 2016) Authors: Tucci, Arianna; Pezzani, Lidia; Scuvera, Giulietta; Ronzoni, Luisa; Scola, Elisa; Esposito, Susanna; Milani, Donatella Journal: American journal of medical genetics Issue: Volume 173:Issue 3(2017) Page Start: 638 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Modulation of gamma globin genes expression by histone deacetylase inhibitors: an in vitro study. (7th March 2014) Authors: Ronzoni, Luisa; Sonzogni, Laura; Fossati, Gianluca; Modena, Daniela; Trombetta, Elena; Porretti, Laura; Cappellini, Maria Domenica Journal: British journal of haematology Issue: Volume 165:Number 5(2014:Jun.) Page Start: 714 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Molecular cytogenetic characterization of a 2q35‐q37 duplication and a 4q35.1‐q35.2 deletion in two cousins: A genotype–phenotype analysis. (6th April 2015) Authors: Ronzoni, Luisa; Peron, Angela; Bianchi, Vera; Baccarin, Marco; Guerneri, Silvana; Silipigni, Rosamaria; Lalatta, Faustina; Bedeschi, Maria Francesca Journal: American journal of medical genetics Issue: Volume 167:Number 7(2015:Jul.) Page Start: 1551 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗