1. A germline mutation in PBRM1 predisposes to renal cell carcinoma. Issue 6 (24th April 2015) Authors: Benusiglio, Patrick R; Couvé, Sophie; Gilbert-Dussardier, Brigitte; Deveaux, Sophie; Le Jeune, Hélène; Da Costa, Mélanie; Fromont, Gaëlle; Memeteau, Françoise; Yacoub, Mokrane; Coupier, Isabelle; Leroux, Dominique; Méjean, Arnaud; Escudier, Bernard; Giraud, Sophie; Gimenez-Roqueplo, Anne-Paule; B... Journal: Journal of medical genetics Issue: Volume 52:Issue 6(2015) Page Start: 426 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers. Issue 1 (December 2015) Authors: Blein, Sophie; Bardel, Claire; Danjean, Vincent; McGuffog, Lesley; Healey, Sue; Barrowdale, Daniel; Lee, Andrew; Dennis, Joe; Kuchenbaecker, Karoline; Soucy, Penny; Terry, Mary; Chung, Wendy; Goldgar, David; Buys, Saundra; Janavicius, Ramunas; Tihomirova, Laima; Tung, Nadine; Dorfling, Cecilia; v... Journal: Breast cancer research Issue: Volume 17:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Endoscopic Phenotype of Monoallelic Carriers of MUTYH Gene Mutations in the Family of Polyposis Patients: A Prospective Study. Issue 4 (April 2019) Authors: El Hachem, Noha; Abadie, Caroline; Longy, Michel; Colas, Chrystelle; Fert-Ferrer, Sandra; Leroux, Dominique; Grandval, Philippe; Prieur, Fabienne; Collonge-Rame, MarieAgnes; Faivre, Laurence; Fricker, Jean-Pierre; Zerbib, Frank; Coupier, Isabelle; Cauchin, Estelle; Pinson, Stephane; Saurin, Jean ... Journal: Diseases of the colon & rectum Issue: Volume 62:Issue 4(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing. Issue 8 (13th November 2018) Authors: Girard, Elodie; Eon‐Marchais, Séverine; Olaso, Robert; Renault, Anne‐Laure; Damiola, Francesca; Dondon, Marie‐Gabrielle; Barjhoux, Laure; Goidin, Didier; Meyer, Vincent; Le Gal, Dorothée; Beauvallet, Juana; Mebirouk, Noura; Lonjou, Christine; Coignard, Juliette; Marcou, Morgane; Cavaciuti, Eve; B... Journal: International journal of cancer Issue: Volume 144:Issue 8(2019) Page Start: 1962 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. GENESIS: a French national resource to study the missing heritability of breast cancer. Issue 1 (December 2016) Authors: Sinilnikova, Olga; Dondon, Marie-Gabrielle; Eon-Marchais, Séverine; Damiola, Francesca; Barjhoux, Laure; Marcou, Morgane; Verny-Pierre, Carole; Sornin, Valérie; Toulemonde, Lucie; Beauvallet, Juana; Le Gal, Dorothée; Mebirouk, Noura; Belotti, Muriel; Caron, Olivier; Gauthier-Villars, Marion; Coup... Journal: BMC cancer Issue: Volume 16:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Identification of a novel BET bromodomain inhibitor‐sensitive, gene regulatory circuit that controls Rituximab response and tumour growth in aggressive lymphoid cancers. Issue 8 (4th July 2013) Authors: Emadali, Anouk; Rousseaux, Sophie; Bruder‐Costa, Juliana; Rome, Claire; Duley, Samuel; Hamaidia, Sieme; Betton, Patricia; Debernardi, Alexandra; Leroux, Dominique; Bernay, Benoit; Kieffer‐Jaquinod, Sylvie; Combes, Florence; Ferri, Elena; McKenna, Charles E.; Petosa, Carlo; Bruley, Christophe; Gar... Journal: EMBO molecular medicine Issue: Volume 5:Issue 8(2013:Aug.) Page Start: 1180 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma. Issue 4 (12th March 2011) Authors: Gardie, Betty; Remenieras, Audrey; Kattygnarath, Darouna; Bombled, Johny; Lefèvre, Sandrine; Perrier-Trudova, Victoria; Rustin, Pierre; Barrois, Michel; Slama, Abdelhamid; Avril, Marie-Françoise; Bessis, Didier; Caron, Olivier; Caux, Frédéric; Collignon, Patrick; Coupier, Isabelle; Cremin, Carol;... Journal: Journal of medical genetics Issue: Volume 48:Issue 4(2011) Page Start: 226 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Osteosarcoma without prior retinoblastoma related to RB1 low‐penetrance germline pathogenic variants: A novel type of RB1‐related hereditary predisposition syndrome?. Issue 12 (30th September 2019) Authors: Imbert‐Bouteille, Marion; Gauthier‐Villars, Marion; Leroux, Dominique; Meunier, Isabelle; Aerts, Isabelle; Lumbroso‐Le Rouic, Livia; Lejeune, Sophie; Delnatte, Capucine; Abadie, Caroline; Pujol, Pascal; Houdayer, Claude; Corsini, Carole Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 12(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Somatic MMR Gene Mutations as a Cause for MSI‐H Sebaceous Neoplasms in Muir–Torre Syndrome‐Like Patients. Issue 3 (13th March 2015) Authors: Joly, Marie‐Odile; Attignon, Valéry; Saurin, Jean‐Christophe; Desseigne, Françoise; Leroux, Dominique; Martin‐Denavit, Tanguy; Giraud, Sophie; Bonnet‐Dupeyron, Marie‐Noëlle; Faivre, Laurence; Auclair, Jessie; Grand‐Masson, Chloé; Audoynaud, Carole; Wang, Qing Journal: Human mutation Issue: Volume 36:Issue 3(2015:Mar.) Page Start: 292 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Somatic MMR Gene Mutations as a Cause for MSI‐H Sebaceous Neoplasms in Muir–Torre Syndrome‐Like Patients. Issue 3 (March 2015) Authors: Joly, Marie‐Odile; Attignon, Valéry; Saurin, Jean‐Christophe; Desseigne, Françoise; Leroux, Dominique; Martin‐Denavit, Tanguy; Giraud, Sophie; Bonnet‐Dupeyron, Marie‐Noëlle; Faivre, Laurence; Auclair, Jessie; Grand‐Masson, Chloé; Audoynaud, Carole; Wang, Qing Journal: Human mutation Issue: Volume 36:Issue 3(2015:Mar.) Page Start: 292 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗