1. Phenome-wide association studies across large population cohorts support drug target validation. Issue 1 (December 2018) Authors: Diogo, Dorothée; Tian, Chao; Franklin, Christopher; Alanne-Kinnunen, Mervi; March, Michael; Spencer, Chris; Vangjeli, Ciara; Weale, Michael; Mattsson, Hannele; Kilpeläinen, Elina; Sleiman, Patrick; Reilly, Dermot; McElwee, Joshua; Maranville, Joseph; Chatterjee, Arnaub; Bhandari, Aman; Nguyen, Kh... Journal: Nature communications Issue: Volume 9:Issue 1(2018) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Loss‐of‐Function Mutations in KIF15 Underlying a Braddock–Carey Genocopy. Issue 5 (10th March 2017) Authors: Sleiman, Patrick M.A.; March, Michael; Nguyen, Kenny; Tian, Lifeng; Pellegrino, Renata; Hou, Cuiping; Dridi, Walid; Sager, Mohamed; Housawi, Yousef H.; Hakonarson, Hakon Journal: Human mutation Issue: Volume 38:Issue 5(2017) Page Start: 507 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genetic analysis for type 1 diabetes genes in juvenile dermatomyositis unveils genetic disease overlap. (16th February 2022) Authors: Qu, Hui-Qi; Qu, Jingchun; Vaccaro, Courtney; Chang, Xiao; Mentch, Frank; Li, Jin; Mafra, Fernanda; Nguyen, Kenny; Gonzalez, Michael; March, Michael; Pellegrino, Renata; Glessner, Joseph; Sleiman, Patrick; Kao, Charlly; Hakonarson, Hakon Journal: Rheumatology Issue: Volume 61:Number 8(2022) Page Start: 3497 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Improved genetic risk scoring algorithm for type 1 diabetes prediction. Issue 3 (19th January 2022) Authors: Qu, Hui‐Qi; Qu, Jingchun; Glessner, Joseph; Liu, Yichuan; Mentch, Frank; Chang, Xiao; March, Michael; Li, Jin; Roizen, Jeffrey D.; Connolly, John J.; Sleiman, Patrick; Hakonarson, Hakon Journal: Pediatric diabetes Issue: Volume 23:Issue 3(2022) Page Start: 320 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments. Issue 1 (December 2016) Authors: Liu, Yichuan; Li, Yun; March, Michael; Nguyen, Kenny; Xu, Kexiang; Wang, Fengxiang; Guo, Yiran; Keating, Brendan; Glessner, Joseph; Li, Jiankang; Ganley, Theodore; Zhang, Jianguo; Deardorff, Matthew; Xu, Xun; Hakonarson, Hakon Journal: Human genomics Issue: Volume 10:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments. Issue 1 (December 2015) Authors: Liu, Yichuan; Li, Yun; March, Michael; Kenny, Nguyen; Xu, Kexiang; Wang, Fengxiang; Guo, Yiran; Keating, Brendan; Glessner, Joseph; Li, Jiankang; Ganley, Theodore; Zhang, Jianguo; Deardorff, Matthew; Xu, Xun; Hakonarson, Hakon Journal: Human genomics Issue: Volume 9:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments. Issue 1 (December 2015) Authors: Liu, Yichuan; Li, Yun; March, Michael; Nguyen, Kenny; Xu, Kexiang; Wang, Fengxiang; Guo, Yiran; Keating, Brendan; Glessner, Joseph; Li, Jiankang; Ganley, Theodore; Zhang, Jianguo; Deardorff, Matthew; Xu, Xun; Hakonarson, Hakon Journal: Human genomics Issue: Volume 9:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Common variants at 5q33.1 predispose to migraine in African-American children. Issue 12 (28th September 2018) Authors: Chang, Xiao; Pellegrino, Renata; Garifallou, James; March, Michael; Snyder, James; Mentch, Frank; Li, Jin; Hou, Cuiping; Liu, Yichuan; Sleiman, Patrick M A; Hakonarson, Hakon Journal: Journal of medical genetics Issue: Volume 55:Issue 12(2018) Page Start: 831 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Combined application of genetic and polygenic risk scores for type 1 diabetes risk prediction. Issue 8 (3rd June 2021) Authors: Qu, Hui‐Qi; Qu, Jingchun; Bradfield, Jonathan; Glessner, Joseph; Chang, Xiao; March, Michael; Mentch, Frank D.; Roizen, Jeffrey D.; Connolly, John J.; Sleiman, Patrick; Hakonarson, Hakon Journal: Diabetes, obesity & metabolism Issue: Volume 23:Issue 8(2021) Page Start: 2001 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The genetic basis of eosinophilic esophagitis. Issue 5 (October 2015) Authors: Sleiman, Patrick M.A.; March, Michael; Hakonarson, Hakon Journal: Best practice & research Issue: Volume 29:Issue 5(2015) Page Start: 701 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗