1. A Novel Variant of ATP5MC3 Associated with Both Dystonia and Spastic Paraplegia. Issue 2 (11th October 2021) Authors: Neilson, Derek E.; Zech, Michael; Hufnagel, Robert B.; Slone, Jesse; Wang, Xinjian; Homan, Shelli; Gutzwiller, Lisa M.; Leslie, Elizabeth J.; Leslie, Nancy D.; Xiao, Jianfeng; Hedera, Peter; LeDoux, Mark S.; Gebelein, Brian; Wilbert, Friederike; Eckenweiler, Matthias; Winkelmann, Juliane; Gilbert... Journal: Movement disorders Issue: Volume 37:Issue 2(2022) Page Start: 375 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Biallelic mutations in FDXR cause neurodegeneration associated with inflammation. Issue 12 (December 2018) Authors: Slone, Jesse; Peng, Yanyan; Chamberlin, Adam; Harris, Belinda; Kaylor, Julie; McDonald, Marie; Lemmon, Monica; El-Dairi, Mays; Tchapyjnikov, Dmitry; Gonzalez-Krellwitz, Laura; Sellars, Elizabeth; McConkie-Rosell, Allyn; Reinholdt, Laura; Huang, Taosheng Journal: Journal of human genetics Issue: Volume 63:Issue 12(2018) Page Start: 1211 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Biallelic mutations in FDXR cause neurodegeneration associated with inflammation. Issue 12 (December 2018) Authors: Slone, Jesse; Peng, Yanyan; Chamberlin, Adam; Harris, Belinda; Kaylor, Julie; McDonald, Marie; Lemmon, Monica; El-Dairi, Mays; Tchapyjnikov, Dmitry; Gonzalez-Krellwitz, Laura; Sellars, Elizabeth; McConkie-Rosell, Allyn; Reinholdt, Laura; Huang, Taosheng Journal: Journal of human genetics Issue: Volume 63:Issue 12(2018) Page Start: 1211 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Clinical utility of whole genome sequencing for the detection of mitochondrial genome mutations. (20th March 2020) Authors: Husami, Ammar; Slone, Jesse; Brown, Jenice; Bromwell, Meghan; Valencia, C. Alexander; Huang, Taosheng Journal: Journal of genetics and genomics Issue: Volume 47:Number 3(2020) Page Start: 167 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy. Issue 2 (1st December 2020) Authors: Campbell, Teresa; Lou, Xiaoting; Slone, Jesse; Brown, Jenice; Bromwell, Meghan; Liu, Jie; Bai, Renkui; Haude, Katrina; Balog, Amanda; Cui, Hong; Zou, Weiwei; Yang, Li; Al‐Beshri, Ali; Huang, Taosheng Journal: Human mutation Issue: Volume 42:Issue 2(2021) Page Start: 177 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy. Issue 2 (1st December 2020) Authors: Campbell, Teresa; Lou, Xiaoting; Slone, Jesse; Brown, Jenice; Bromwell, Meghan; Liu, Jie; Bai, Renkui; Haude, Katrina; Balog, Amanda; Cui, Hong; Zou, Weiwei; Yang, Li; Al‐Beshri, Ali; Huang, Taosheng Journal: Human mutation Issue: Volume 42:Issue 2(2021) Page Start: 177 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Mitochondrial replacement therapy: Genetic counselors' experiences, knowledge, and opinions. Issue 3 (19th January 2021) Authors: Aryamvally, Anjali; Myers, Melanie F.; Huang, Taosheng; Slone, Jesse; Pilipenko, Valentina; Hartmann, Julianne E. Journal: Journal of genetic counseling Issue: Volume 30:Issue 3(2021) Page Start: 828 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Next‐Generation Sequencing to Characterize Mitochondrial Genomic DNA Heteroplasmy. Issue 5 (9th May 2022) Authors: Yang, Zeyu; Slone, Jesse; Huang, Taosheng Journal: Current protocols Issue: Volume 2:Issue 5(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Premature aging is associated with higher levels of 8‐oxoguanine and increased DNA damage in the Polg mutator mouse. Issue 9 (22nd August 2022) Authors: Yu, Tenghui; Slone, Jesse; Liu, Wensheng; Barnes, Ryan; Opresko, Patricia L.; Wark, Landon; Mai, Sabine; Horvath, Steve; Huang, Taosheng Journal: Aging cell Issue: Volume 21:Issue 9(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Systemic administration of AAV-Slc25a46 mitigates mitochondrial neuropathy in Slc25a46−/− mice. (16th January 2020) Authors: Yang, Li; Slone, Jesse; Li, Zhuo; Lou, Xiaoting; Hu, Yueh-Chiang; Queme, Luis F; Jankowski, Michael P; Huang, Taosheng Journal: Human molecular genetics Issue: Volume 29:Number 4(2020) Page Start: 649 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗