1. ALU transposition induces familial hypertrophic cardiomyopathy. Issue 1 (30th September 2019) Authors: Nfonsam, Landry; Huang, Lijia; Carson, Nancy; McGowan‐Jordan, Jean; Beaulieu Bergeron, Melanie; Goobie, Sharan; Conacher, Susan; McCarty, David; Benson, Lee; Hewson, Stacy; Zahavich, Laura; Sinclair‐Bourque, Elizabeth; Smith, Amanda; Potter, Ryan; Ghani, Mahdi; Bronicki, Lucas; Jarinova, Olga Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 1(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Characterizing familial corticobasal syndrome due to Alzheimer's disease pathology and PSEN1 mutations. Issue 5 (13th October 2016) Authors: Lam, Benjamin; Khan, Aun; Keith, Julia; Rogaeva, Ekaterina; Bilbao, Juan; St. George‐Hyslop, Peter; Ghani, Mahdi; Freedman, Morris; Stuss, Donald T.; Chow, Tiffany; Black, Sandra E.; Masellis, Mario Journal: Alzheimer's & dementia Issue: Volume 13:Issue 5(2017) Page Start: 520 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Coding mutations in SORL1 and Alzheimer disease. Issue 2 (February 2015) Authors: Vardarajan, Badri N.; Zhang, Yalun; Lee, Joseph H.; Cheng, Rong; Bohm, Christopher; Ghani, Mahdi; Reitz, Christiane; Reyes‐Dumeyer, Dolly; Shen, Yufeng; Rogaeva, Ekaterina; St George‐Hyslop, Peter; Mayeux, Richard Journal: Annals of neurology Issue: Volume 77:Issue 2(2015:Feb.) Page Start: 215 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetic and epigenetic study of ALS-discordant identical twins with double mutations in SOD1 and ARHGEF28. Issue 11 (6th May 2016) Authors: Zhang, Ming; Xi, Zhengrui; Ghani, Mahdi; Jia, Peixin; Pal, Mrinal; Werynska, Karolina; Moreno, Danielle; Sato, Christine; Liang, Yan; Robertson, Janice; Petronis, Arturas; Zinman, Lorne; Rogaeva, Ekaterina Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 87:Issue 11(2016) Page Start: 1268 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic Variation in the Ontario Neurodegenerative Disease Research Initiative. (15th August 2019) Authors: Dilliott, Allison A.; Evans, Emily C.; Farhan, Sali M.K.; Ghani, Mahdi; Sato, Christine; Zhang, Ming; McIntyre, Adam D.; Cao, Henian; Racacho, Lemuel; Robinson, John F.; Strong, Michael J.; Masellis, Mario; Bulman, Dennis E.; Rogaeva, Ekaterina; Black, Sandra E.; Finger, Elizabeth; Frank, Andrew;... Journal: Canadian journal of neurological sciences Issue: Volume 46:Number 5(2019) Page Start: 491 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Leveraging the power of new molecular technologies in the clinical setting requires unprecedented awareness of limitations and drawbacks: experience of one diagnostic laboratory. Issue 6 (21st September 2018) Authors: Nfonsam, Landry; Ordorica, Shelley; Ghani, Mahdi; Potter, Ryan; Schaffer, Audrey; Daoud, Hussein; Vasli, Nasim; Chisholm, Caitlin; Sinclair-Bourque, Elizabeth; McGowan-Jordan, Jean; Smith, Amanda C; Jarinova, Olga; Bronicki, Lucas Journal: Journal of medical genetics Issue: Volume 56:Issue 6(2019) Page Start: 408 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. O3‐05‐02: Genome wide analyses of runs of homozygosity among african americans revealed further evidence of recessive inheritance for Alzheimer's disease. (1st July 2015) Authors: Ghani, Mahdi; Reitz, Christiane; Cheng, Rong; Lee, Joseph H.; Vardarajan, Badri N.; Tosto, Giuseppe; St George-Hyslop, Peter; Mayeux, Richard; Rogaeva, Ekaterina Journal: Alzheimer's & dementia Issue: Volume 11(2015)Supplement 7:Part 5 Page Start: P228 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. O3‐13‐05: Rare coding mutations identified by targeted sequencing of Alzheimer's disease loci detected in genome‐wide association studies. (1st July 2015) Authors: Vardarajan, Badri N.; Ghani, Mahdi; Kahn, Amanda; Sheikh, Stephanie; Sato, Christine; Barral, Sandra; Lee, Joseph H.; Cheng, Rong; Reitz, Christiane; Lantigua, Rafael; Reyes-Dumeyer, Dolly; Medrano, Martin; Jimenez-Velazquez, Ivonne Z.; Rogaeva, Ekaterina; St George-Hyslop, Peter; Mayeux, Richard Journal: Alzheimer's & dementia Issue: Volume 11(2015)Supplement 7:Part 5 Page Start: P252 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. P1‐057: SEARCH FOR RECESSIVE ALZHEIMER DISEASE LOCI IN AFRICAN AMERICANS BY GENOME‐WIDE STUDY OF RUNS OF HOMOZYGOSITY. (1st July 2014) Authors: Rogaeva, Ekaterina; Ghani, Mahdi; Reitz, Christiane; Lee, Joseph H.; Vardarajan, Badri N.; Tosto, Giuseppe; St. George‐Hyslop, Peter; Mayeux, Richard Journal: Alzheimer's & dementia Issue: Volume 10:Supplement 4S(2014)Part 8 Page Start: P324 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. P2‐173: Mutation Analysis of the MS4A and TREM Gene‐Clusters in a Case‐Control Alzheimer's Disease Dataset. (1st July 2016) Authors: Ghani, Mahdi; Sato, Christine; Ghani kakhki, Erfan; Gibbs, J. Raphael; Traynor, Bryan; St George-Hyslop, Peter; Rogaeva, Ekaterina Journal: Alzheimer's & dementia Issue: Volume 12:Supplement 7S(2016)Part 14 Page Start: P682 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗