1. Atypical Aicardi‐Goutieres syndrome: Is the WRN locus a modifier?. Issue 10 (2nd July 2014) Authors: Lessel, Davor; Saha, Bidisha; Hisama, Fuki; Kaymakamzade, Bahar; Nurlu, Gulay; Gursoy‐Özdemir, Yasemin; Thiele, Holger; Nürnberg, Peter; Martin, George M.; Kubisch, Christian; Oshima, Junko Journal: American journal of medical genetics Issue: Volume 164:Issue 10(2014.) Page Start: 2510 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Atypical Aicardi‐Goutieres syndrome: Is the WRN locus a modifier?. Issue 10 (2nd July 2014) Authors: Lessel, Davor; Saha, Bidisha; Hisama, Fuki; Kaymakamzade, Bahar; Nurlu, Gulay; Gursoy‐Özdemir, Yasemin; Thiele, Holger; Nürnberg, Peter; Martin, George M.; Kubisch, Christian; Oshima, Junko Journal: American journal of medical genetics Issue: Volume 164:Issue 10(2014.) Page Start: 2510 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures. Issue 6 (4th November 2018) Authors: Sargolzaeiaval, Forough; Zhang, Jiaming; Schleit, Jennifer; Lessel, Davor; Kubisch, Christian; Precioso, Debora R.; Sillence, David; Hisama, Fuki M.; Dorschner, Michael; Martin, George M.; Oshima, Junko Journal: Molecular genetics & genomic medicine Issue: Volume 6:Issue 6(2018) Page Start: 1148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes. Issue 5 (1st July 2019) Authors: Maierhofer, Anna; Flunkert, Julia; Oshima, Junko; Martin, George M.; Poot, Martin; Nanda, Indrajit; Dittrich, Marcus; Müller, Tobias; Haaf, Thomas Journal: Aging cell Issue: Volume 18:Issue 5(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. ERCC4 variants identified in a cohort of patients with segmental progeroid syndromes. Issue 2 (17th November 2017) Authors: Mori, Takayasu; Yousefzadeh, Matthew J.; Faridounnia, Maryam; Chong, Jessica X.; Hisama, Fuki M.; Hudgins, Louanne; Mercado, Gabriela; Wade, Erin A.; Barghouthy, Amira S.; Lee, Lin; Martin, George M.; Nickerson, Deborah A.; Bamshad, Michael J.; Niedernhofer, Laura J.; Oshima, Junko Journal: Human mutation Issue: Volume 39:Issue 2(2018) Page Start: 255 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Ethnic‐specific WRN mutations in South Asian Werner syndrome patients: potential founder effect in patients with Indian or Pakistani ancestry. Issue 1 (28th March 2013) Authors: Saha, Bidisha; Lessel, Davor; Nampoothiri, Sheela; Rao, Anuradha S.; Hisama, Fuki M.; Peter, Dincy; Bennett, Chris; Nürnberg, Gudrun; Nürnberg, Peter; Martin, George M.; Kubisch, Christian; Oshima, Junko Journal: Molecular genetics & genomic medicine Issue: Volume 1:Issue 1(2013:May) Page Start: 7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. High incidence of BSCL2 intragenic recombinational mutation in Peruvian type 2 Berardinelli–Seip syndrome. Issue 2 (21st November 2016) Authors: Purizaca‐Rosillo, Nelson; Mori, Takayasu; Benites‐Cóndor, Yamali; Hisama, Fuki M.; Martin, George M.; Oshima, Junko Journal: American journal of medical genetics Issue: Volume 173:Issue 2(2017) Page Start: 471 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mitochondrial‐targeted catalase is good for the old mouse proteome, but not for the young: 'reverse' antagonistic pleiotropy?. Issue 4 (8th April 2016) Authors: Basisty, Nathan; Dai, Dao‐Fu; Gagnidze, Arni; Gitari, Lemuel; Fredrickson, Jeanne; Maina, Yvonne; Beyer, Richard P.; Emond, Mary J.; Hsieh, Edward J.; MacCoss, Michael J.; Martin, George M.; Rabinovitch, Peter S. Journal: Aging cell Issue: Volume 15:Issue 4(2016) Page Start: 634 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Photodynamic Therapy: A Clinical Consensus Guide. Issue 7 (July 2016) Authors: Ozog, David M.; Rkein, Ali M.; Fabi, Sabrina G.; Gold, Michael H.; Goldman, Mitchel P.; Lowe, Nicholas J.; Martin, George M.; Munavalli, Girish S. Journal: Dermatologic surgery Issue: Volume 42:Issue 7(2016:Jul.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome. Issue 11 (6th August 2015) Authors: Lessel, Davor; Hisama, Fuki M.; Szakszon, Katalin; Saha, Bidisha; Sanjuanelo, Alexander Barrios; Salbert, Bonnie A.; Steele, Pamela D.; Baldwin, Jennifer; Brown, W. Ted; Piussan, Charles; Plauchu, Henri; Szilvássy, Judit; Horkay, Edit; Högel, Josef; Martin, George M.; Herr, Alan J.; Oshima, Junko... Journal: Human mutation Issue: Volume 36:Issue 11(2015:Nov.) Page Start: 1070 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗