1. A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism. Issue 10 (7th August 2019) Authors: Diquigiovanni, Chiara; Bergamini, Christian; Diaz, Rebeca; Liparulo, Irene; Bianco, Francesca; Masin, Luca; Baldassarro, Vito Antonio; Rizzardi, Nicola; Tranchina, Antonia; Buscherini, Francesco; Wischmeijer, Anita; Pippucci, Tommaso; Scarano, Emanuela; Cordelli, Duccio Maria; Fato, Romana; Seri,... Journal: FASEB journal Issue: Volume 33:Issue 10(2019) Page Start: 11284 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures. Issue 12 (16th April 2021) Authors: Martinelli, Angela; Rice, Mabel L; Talcott, Joel B; Diaz, Rebeca; Smith, Shelley; Raza, Muhammad Hashim; Snowling, Margaret J; Hulme, Charles; Stein, John; Hayiou-Thomas, Marianna E; Hawi, Ziarih; Kent, Lindsey; Pitt, Samantha J; Newbury, Dianne F; Paracchini, Silvia Journal: Human molecular genetics Issue: Volume 30:Issue 12(2021) Page Start: 1160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Different laterality indexes are poorly correlated with one another but consistently show the tendency of males and females to be more left- and right-lateralized, respectively. Issue 4 (15th April 2020) Authors: Buenaventura Castillo, Carlos; Lynch, Andy G.; Paracchini, Silvia Journal: Royal Society open science Issue: Volume 7:Issue 4(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes. Issue 1 (December 2016) Authors: Pettigrew, Kerry; Frinton, Emily; Nudel, Ron; Chan, May; Thompson, Paul; Hayiou-Thomas, Marianna; Talcott, Joel; Stein, John; Monaco, Anthony; Hulme, Charles; Snowling, Margaret; Newbury, Dianne; Paracchini, Silvia Journal: Journal of neurodevelopmental disorders Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genome‐wide association study and polygenic risk score analysis for hearing measures in children. Issue 5 (3rd September 2021) Authors: Schmitz, Judith; Abbondanza, Filippo; Paracchini, Silvia Journal: American journal of medical genetics Issue: Volume 186:Issue 5(2021) Page Start: 318 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genomic Imprinting As a Window into Human Language Evolution. (27th May 2019) Authors: Hitchcock, Thomas J.; Paracchini, Silvia; Gardner, Andy Journal: BioEssays Issue: Volume 41:Number 6(2019:Jun.) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Hand preference and Mathematical Learning Difficulties: New data from Greece, the United Kingdom, and Germany and two meta-analyses of the literature. Issue 5 (3rd September 2021) Authors: Papadatou-Pastou, Marietta; Panagiotidou, Despoina-Athanasia; Abbondanza, Filippo; Fischer, Ursula; Paracchini, Silvia; Karagiannakis, Giannis Journal: Laterality Issue: Volume 26:Issue 5(2021) Page Start: 485 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. (9th October 2013) Authors: Simpson, Nuala H; Addis, Laura; Brandler, William M; Slonims, Vicky; Clark, Ann; Watson, Jocelynne; Scerri, Thomas S; Hennessy, Elizabeth R; Bolton, Patrick F; Conti‐Ramsden, Gina; Fairfax, Benjamin P; Knight, Julian C; Stein, John; Talcott, Joel B; O'Hare, Anne; Baird, Gillian; Paracchini, Silvi... Journal: Developmental medicine & child neurology Issue: Volume 56:Number 4(2014:Apr.) Page Start: 346 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration. Issue 16 (16th April 2019) Authors: Gostic, Monika; Martinelli, Angela; Tucker, Carl; Yang, Zhengyi; Gasparoli, Federico; Ewart, Jade‐Yi; Dholakia, Kishan; Sillar, Keith T.; Tello, Javier A.; Paracchini, Silvia Journal: Journal of comparative neurology Issue: Volume 527:Issue 16(2019) Page Start: 2634 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on. (6th October 2018) Authors: Guidi, Luiz G.; Velayos‐Baeza, Antonio; Martinez‐Garay, Isabel; Monaco, Anthony P.; Paracchini, Silvia; Bishop, Dorothy V. M.; Molnár, Zoltán Journal: European journal of neuroscience Issue: Volume 48:Number 10(2018) Page Start: 3212 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗