1. A case of neuroblastoma in DICER1 syndrome: Chance finding or noncanonical causation?. Issue 1 (2nd August 2017) Authors: Saskin, Avi; de Kock, Leanne; Sabbaghian, Nelly; Apellaniz‐Ruiz, Maria; Bozkurt, Ceyhun; Bouron‐Dal Soglio, Dorothée; Foulkes, William D. Journal: Pediatric blood & cancer Issue: Volume 65:Issue 1(2018) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Case Report of Syndromic Multinodular Goitre in Adolescence: Exploring the Phenotype Overlap between Cowden and DICER1 Syndromes. Issue 1 (21st January 2018) Authors: Bouron-Dal Soglio, Dorothée; de Kock, Leanne; Gauci, Richard; Sabbaghian, Nelly; Thomas, Elizabeth; Atkinson, Helen C.; Pachter, Nicholas; Ryan, Simon; Walsh, John P.; Kumarasinghe, M. Priyanthi; Carpenter, Karen; Aydoğan, Ayça; Stewart, Colin J.R.; Foulkes, William&... Journal: European thyroid journal Issue: Volume 7:Issue 1(2018) Page Start: 44 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A child with neuroblastoma and metachronous anaplastic sarcoma of the kidney: Underlying DICER1 syndrome?. Issue 12 (22nd June 2020) Authors: Apellaniz‐Ruiz, Maria; Colón‐González, Gloria; Perlman, Elizabeth J.; Bouron‐Dal Soglio, Dorothée; Sabbaghian, Nelly; Oehl‐Huber, Kathrin; Siebert, Reiner; Foulkes, William D. Journal: Pediatric blood & cancer Issue: Volume 67:Issue 12(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A novel DICER1 mutation in familial multinodular goitre. (4th May 2018) Authors: Caimari, Francisca; Kumar, Ajith V.; Kurzawinski, Thomas; Butler, Gary; Sabbaghian, Nelly; Foulkes, William D.; Korbonits, Márta Journal: Clinical endocrinology Issue: Volume 89:Number 1(2018) Page Start: 110 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Analysis of DICER1 in familial and sporadic cases of transposition of the great arteries. (5th February 2018) Authors: Sabbaghian, Nelly; Digilio, Maria C.; Blue, Gillian M.; Revil, Timothée; Winlaw, David S.; Foulkes, William D. Journal: Congenital heart disease Issue: Volume 13:Number 3(2018) Page Start: 401 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Analysis of the Novel Fanconi Anemia Gene SLX4/FANCP in Familial Breast Cancer Cases. Issue 1 (11th October 2012) Authors: Bakker, Janine L.; van Mil, Saskia E.; Crossan, Gerry; Sabbaghian, Nelly; De Leeneer, Kim; Poppe, Bruce; Adank, Muriel; Gille, Hans; Verheul, Henk; Meijers‐Heijboer, Hanne; de Winter, Johan P.; Claes, Kathleen; Tischkowitz, Marc; Waisfisz, Quinten Journal: Human mutation Issue: Volume 34:Issue 1(2013:Jan.) Page Start: 70 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Familial multinodular goiter and Sertoli-Leydig cell tumors associated with a large intragenic in-frame DICER1 deletion. Issue 2 (February 2018) Authors: Apellaniz-Ruiz, Maria; de Kock, Leanne; Sabbaghian, Nelly; Guaraldi, Federica; Ghizzoni, Lucia; Beccuti, Guglielmo; Foulkes, William D Journal: European journal of endocrinology Issue: Volume 178:Issue 2(2018) Page Start: K11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Further evidence that full gene deletions of DICER1 predispose to DICER1 syndrome. Issue 8 (28th January 2019) Authors: de Kock, Leanne; Hillmer, Morten; Wagener, Rabea; Soglio, Dorothée Bouron‐Dal; Sabbaghian, Nelly; Siebert, Reiner; Priest, John R.; Miller, Michal; Foulkes, William D. Journal: Genes, chromosomes & cancer Issue: Volume 58:Issue 8(2019) Page Start: 602 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Germline DICER1 mutation and associated loss of heterozygosity in a pineoblastoma. Issue 7 (20th June 2012) Authors: Sabbaghian, Nelly; Hamel, Nancy; Srivastava, Archana; Albrecht, Steffen; Priest, John R; Foulkes, William D Journal: Journal of medical genetics Issue: Volume 49:Issue 7(2012) Page Start: 417 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Germline PALB2 mutation analysis in breast–pancreas cancer families. Issue 8 (17th March 2011) Authors: Stadler, Zsofia K; Salo-Mullen, Erin; Sabbaghian, Nelly; Simon, Jennifer A; Zhang, Liying; Olson, Sara H; Kurtz, Robert; Offit, Kenneth; Foulkes, William D; Robson, Mark E; Tischkowitz, Marc Journal: Journal of medical genetics Issue: Volume 48:Issue 8(2011) Page Start: 523 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗