1. 3081 Molecular Tumor Board (MTB) in non-small cell lung cancers (NSCLC) to optimize targeted therapies: 4 years' experience at Gustave Roussy. (September 2015) Authors: Planchard, D.; Faivre, L.; Sullivan, I.; Kahn-charpy, V.; Lacroix, L.; Auger, N.; Adam, J.; De Montpreville, V. Thomas; Dorfmuller, P.; Pechoux, C. Le; Chevalier, T. Le; Gazzah, A.; Remon, J.; Bescher, G.; Soria, J.C.; Pignon, J.P.; Besse, B. Journal: European journal of cancer Issue: Volume 51:(2015)Supplement 3 Page Start: S624 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 3127 Prognostic value of texture analysis in advanced non-small cell lung cancer (NSCLC). (September 2015) Authors: Bluthgen, M.V.; Caramella, C.; Faivre, L.; Rosellini, S.; Facchinetti, F.; Haspinger, E.; Ferte, C.; Ammari, S.; Michiels, S.; Soria, J.C.; Besse, B. Journal: European journal of cancer Issue: Volume 51:(2015)Supplement 3 Page Start: S645 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome. Issue 5 (3rd February 2016) Authors: Nizon, M.; Henry, M.; Michot, C.; Baumann, C.; Bazin, A.; Bessières, B.; Blesson, S.; Cordier‐Alex, M.‐P.; David, A.; Delahaye‐Duriez, A.; Delezoïde, A.‐L.; Dieux‐Coeslier, A.; Doco‐Fenzy, M.; Faivre, L.; Goldenberg, A.; Layet, V.; Loget, P.; Marlin, S.; Martinovic, J.; Odent, S. Journal: Clinical genetics Issue: Volume 89:Issue 5(2016) Page Start: 584 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral–facial–digital syndrome with short stature and brachymesophalangia. Issue 6 (29th April 2016) Authors: Thevenon, J.; Duplomb, L.; Phadke, S.; Eguether, T.; Saunier, A.; Avila, M.; Carmignac, V.; Bruel, A.‐L.; St‐Onge, J.; Duffourd, Y.; Pazour, G.J.; Franco, B.; Attie‐Bitach, T.; Masurel‐Paulet, A.; Rivière, J.‐B.; Cormier‐Daire, V.; Philippe, C.; Faivre, L.; Thauvin‐Robinet, C. Journal: Clinical genetics Issue: Volume 90:Issue 6(2016) Page Start: 509 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping. Issue 1 (24th May 2016) Authors: Amos, J.S.; Huang, L.; Thevenon, J.; Kariminedjad, A.; Beaulieu, C.L.; Masurel‐Paulet, A.; Najmabadi, H.; Fattahi, Z.; Beheshtian, M.; Tonekaboni, S.H.; Tang, S.; Helbig, K.L.; Alcaraz, W.; Rivière, J.‐B.; Faivre, L.; Innes, A.M.; Lebel, R.R.; Boycott, K.M. Journal: Clinical genetics Issue: Volume 91:Issue 1(2017) Page Start: 92 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis. Issue 2 (5th June 2016) Authors: Bruel, A.‐L.; Masurel‐Paulet, A.; Rivière, J.‐B.; Duffourd, Y.; Lehalle, D.; Bensignor, C.; Huet, F.; Borgnon, J.; Roucher, F.; Kuentz, P.; Deleuze, J.‐F.; Thauvin‐Robinet, C.; Faivre, L.; Thevenon, J. Journal: Clinical genetics Issue: Volume 91:Issue 2(2017) Page Start: 333 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Autosomal recessive variations of TBX6, from congenital scoliosis to spondylocostal dysostosis. Issue 6 (22nd February 2017) Authors: Lefebvre, M.; Duffourd, Y.; Jouan, T.; Poe, C.; Jean‐Marçais, N.; Verloes, A.; St‐Onge, J.; Riviere, J.‐B.; Petit, F.; Pierquin, G.; Demeer, B.; Callier, P.; Thauvin‐Robinet, C.; Faivre, L.; Thevenon, J. Journal: Clinical genetics Issue: Volume 91:Issue 6(2017) Page Start: 908 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutations. (22nd May 2021) Authors: Theiler, M.; Weibel, L.; Christen‐Zaech, S.; Carmignac, V.; Sorlin, A.; Neuhaus, K.; Chevarin, M.; Thauvin‐Robinet, C.; Philippe, C.; Faivre, L.; Vabres, P.; Kuentz, P. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 35:Number 10(2021) Page Start: 2085 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 cases. Issue 6 (23rd February 2017) Authors: Ranza, E.; Huber, C.; Levin, N.; Baujat, G.; Bole‐Feysot, C.; Nitschke, P.; Masson, C.; Alanay, Y.; Al‐Gazali, L.; Bitoun, P.; Boute, O.; Campeau, P.; Coubes, C.; McEntagart, M.; Elcioglu, N.; Faivre, L.; Gezdirici, A.; Johnson, D.; Mihci, E.; Nur, B.G. Journal: Clinical genetics Issue: Volume 91:Issue 6(2017) Page Start: 868 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Climbing for dummies: recommendation for multi‐specific fishways for the conservation of tropical eels and gobies. (6th May 2021) Authors: Lagarde, R.; Courret, D.; Grondin, H.; Faivre, L.; Ponton, D. Journal: Animal conservation Issue: Volume 24:Number 6(2021) Page Start: 970 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗