Search

Author/Creator Valente, Giulia

1. A novel approach to offering additional genomic findings—A protocol to test a two‐step approach in the healthcare system. Issue 2 (18th February 2019)

Authors:
Martyn, Melissa; Kanga‐Parabia, Anaita; Lynch, Elly; James, Paul A.; Macciocca, Ivan; Trainer, Alison H.; Halliday, Jane; Keogh, Louise; Wale, Janney; Winship, Ingrid; Bogwitz, Michael; Valente, Giulia; Walsh, Maie; Downie, Lilian; Amor, David; Wallis, Mathew; Cunningham, Fiona; Burgess, Matthew;...
Journal:
Journal of genetic counseling
Issue:
Volume 28:Issue 2(2019)
Page Start:
388
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Clinical impact of whole-genome sequencing in patients with early-onset dementia. Issue 11 (29th July 2022)

Authors:
Huq, Aamira J; Thompson, Bryony; Bennett, Mark F; Bournazos, Adam; Bommireddipalli, Shobhana; Gorelik, Alexandra; Schultz, Joshua; Sexton, Adrienne; Purvis, Rebecca; West, Kirsty; Cotter, Megan; Valente, Giulia; Hughes, Andrew; Riaz, Moeen; Walsh, Maie; Farrand, Sarah; Loi, Samantha M; Kilpatrick...
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 93:Issue 11(2022)
Page Start:
1181
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Mosaicism in tuberous sclerosis complex: Lowering the threshold for clinical reporting. Issue 12 (6th September 2022)

Authors:
Ye, Zimeng; Lin, Sufang; Zhao, Xia; Bennett, Mark F.; Brown, Natasha J.; Wallis, Mathew; Gao, Xinyi; Sun, Li; Wu, Jiarui; Vedururu, Ravikiran; Witkowski, Tom; Gardiner, Fiona; Stutterd, Chloe; Duan, Jing; Mullen, Saul A.; McGillivray, George; Bodek, Simon; Valente, Giulia; Reagan, Matthew; Yao, Yi
Journal:
Human mutation
Issue:
Volume 43:Issue 12(2022)
Page Start:
1956
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗