S. Mohsen Hosseini, M.D., Ph.D., FRCPC

Peer-Reviewed Articles

1. Manshaei R, DeLong S, Andric V, Joshi E, Okello JBA, Dhir P, Somerville C, Farncombe KM, Kalbfleisch K, Jobling RK, Scherer SW, Kim RH, Hosseini SM. GeneTerpret: a customizable multilayer approach to genomic variant prioritization and interpretation. BMC Med Genomics 15(1):31, 2022. e-Pub 2022. PMID: 35180879.
2. Hosseini SM, Khanafshar E, Seeley EJ, Ruiz-Cordero R. Molecular cytopathology diagnosis of a lung neoplasm: Case report of an unusual non-small cell carcinoma with MET exon 14 skipping mutation. Diagn Cytopathol 49(7):E258-E261, 2021. e-Pub 2021. PMID: 33433963.
3. Hosseini SM, Resta IT, Baloch ZW. Diagnostic performance of Milan system for reporting salivary gland cytopathology: A prospective study. Diagn Cytopathol 49(7):822-831, 2021. e-Pub 2021. PMID: 33823076.
4. Reuter MS, Chaturvedi RR, Liston E, Manshaei R, Aul RB, Bowdin S, Cohn I, Curtis M, Dhir P, Hayeems RZ, Hosseini SM, Khan R, Ly LG, Marshall CR, Mertens L, Okello JBA, Pereira SL, Raajkumar A, Seed M, Thiruvahindrapuram B, Scherer SW, Kim RH, Jobling RK. The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease. Genet Med 22(6):1015-1024, 2020. e-Pub 2020. PMID: 32037394.
5. Jalaly JB, Hosseini SM, Shafique K, Baloch ZW. Current Status of p16 Immunohistochemistry and HPV Testing in Fine Needle Aspiration Specimens of the Head and Neck. Acta Cytol 64(1-2):30-39, 2020. e-Pub 2019. PMID: 30783052.
6. Reuter MS, Jobling R, Chaturvedi RR, Manshaei R, Costain G, Heung T, Curtis M, Hosseini SM, Liston E, Lowther C, Oechslin E, Sticht H, Thiruvahindrapuram B, Mil SV, Wald RM, Walker S, Marshall CR, Silversides CK, Scherer SW, Kim RH, Bassett AS. Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot. Genet Med 21(4):1001-1007, 2019. e-Pub 2018. PMID: 30232381.
7. Pollack S, Igo RP, Jensen RA, Christiansen M, Li X, Cheng CY, Ng MCY, Smith AV, Rossin EJ, Segrè AV, Davoudi S, Tan GS, Chen YI, Kuo JZ, Dimitrov LM, Stanwyck LK, Meng W, Hosseini SM, Imamura M, Nousome D, Kim J, Hai Y, Jia Y, Ahn J, Leong A, Shah K, Park KH, Guo X, Ipp E, Taylor KD, Adler SG, Sedor JR, Freedman BI, Family Investigation of Nephropathy and Diabetes-Eye Research Group, DCCT/EDIC Research Group, Lee IT, Sheu WH, Kubo M, Takahashi A, Hadjadj S, Marre M, Tregouet DA, Mckean-Cowdin R, Varma R, McCarthy MI, Groop L, Ahlqvist E, Lyssenko V, Agardh E, Morris A, Doney ASF, Colhoun HM, Toppila I, Sandholm N, Groop PH, Maeda S, Hanis CL, Penman A, Chen CJ, Hancock H, Mitchell P, Craig JE, Chew EY, Paterson AD, Grassi MA, Palmer C, Bowden DW, Yaspan BL, Siscovick D, Cotch MF, Wang JJ, Burdon KP, Wong TY, Klein BEK, Klein R, Rotter JI, Iyengar SK, Price AL, Sobrin L. Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Diabetes 68(2):441-456, 2019. e-Pub 2018. PMID: 30487263.
8. Hosseini SM, Kim R, Udupa S, Costain G, Jobling R, Liston E, Jamal SM, Szybowska M, Morel CF, Bowdin S, Garcia J, Care M, Sturm AC, Novelli V, Ackerman MJ, Ware JS, Hershberger RE, Wilde AAM, Gollob MH, National Institutes of Health Clinical Genome Resource Consortium. Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome. Circulation 138(12):1195-1205, 2018. PMID: 29959160.
9. Tedja MS, Wojciechowski R, Hysi PG, Eriksson N, Furlotte NA, Verhoeven VJM, Iglesias AI, Meester-Smoor MA, Tompson SW, Fan Q, Khawaja AP, Cheng CY, Höhn R, Yamashiro K, Wenocur A, Grazal C, Haller T, Metspalu A, Wedenoja J, Jonas JB, Wang YX, Xie J, Mitchell P, Foster PJ, Klein BEK, Klein R, Paterson AD, Hosseini SM, Shah RL, Williams C, Teo YY, Tham YC, Gupta P, Zhao W, Shi Y, Saw WY, Tai ES, Sim XL, Huffman JE, Polašek O, Hayward C, Bencic G, Rudan I, Wilson JF, CREAM Consortium, 23andMe Research Team, UK Biobank Eye and Vision Consortium, Joshi PK, Tsujikawa A, Matsuda F, Whisenhunt KN, Zeller T, van der Spek PJ, Haak R, Meijers-Heijboer H, van Leeuwen EM, Iyengar SK, Lass JH, Hofman A, Rivadeneira F, Uitterlinden AG, Vingerling JR, Lehtimäki T, Raitakari OT, Biino G, Concas MP, Schwantes-An TH, Igo RP, Cuellar-Partida G, Martin NG, Craig JE, Gharahkhani P, Williams KM, Nag A, Rahi JS, Cumberland PM, Delcourt C, Bellenguez C, Ried JS, Bergen AA, Meitinger T, Gieger C, Wong TY, Hewitt AW, Mackey DA, Simpson CL, Pfeiffer N, Pärssinen O, Baird PN, Vitart V, Amin N, van Duijn CM, Bailey-Wilson JE, Young TL, Saw SM, Stambolian D, MacGregor S, Guggenheim JA, Tung JY, Hammond CJ, Klaver CCW. Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Nat Genet 50(6):834-848, 2018. e-Pub 2018. PMID: 29808027.
10. Lionel AC, Costain G, Monfared N, Walker S, Reuter MS, Hosseini SM, Thiruvahindrapuram B, Merico D, Jobling R, Nalpathamkalam T, Pellecchia G, Sung WWL, Wang Z, Bikangaga P, Boelman C, Carter MT, Cordeiro D, Cytrynbaum C, Dell SD, Dhir P, Dowling JJ, Heon E, Hewson S, Hiraki L, Inbar-Feigenberg M, Klatt R, Kronick J, Laxer RM, Licht C, MacDonald H, Mercimek-Andrews S, Mendoza-Londono R, Piscione T, Schneider R, Schulze A, Silverman E, Siriwardena K, Snead OC, Sondheimer N, Sutherland J, Vincent A, Wasserman JD, Weksberg R, Shuman C, Carew C, Szego MJ, Hayeems RZ, Basran R, Stavropoulos DJ, Ray PN, Bowdin S, Meyn MS, Cohn RD, Scherer SW, Marshall CR. Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test. Genet Med 20(4):435-443, 2018. e-Pub 2017. PMID: 28771251.
11. Reuter MS, Walker S, Thiruvahindrapuram B, Whitney J, Cohn I, Sondheimer N, Yuen RKC, Trost B, Paton TA, Pereira SL, Herbrick JA, Wintle RF, Merico D, Howe J, MacDonald JR, Lu C, Nalpathamkalam T, Sung WWL, Wang Z, Patel RV, Pellecchia G, Wei J, Strug LJ, Bell S, Kellam B, Mahtani MM, Bassett AS, Bombard Y, Weksberg R, Shuman C, Cohn RD, Stavropoulos DJ, Bowdin S, Hildebrandt MR, Wei W, Romm A, Pasceri P, Ellis J, Ray P, Meyn MS, Monfared N, Hosseini SM, Joseph-George AM, Keeley FW, Cook RA, Fiume M, Lee HC, Marshall CR, Davies J, Hazell A, Buchanan JA, Szego MJ, Scherer SW. The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants. CMAJ 190(5):E126-E136, 2018. PMID: 29431110.
12. Roshandel D, Klein R, Klein BE, Wolffenbuttel BH, van der Klauw MM, van Vliet-Ostaptchouk JV, Atzmon G, Ben-Avraham D, Crandall JP, Barzilai N, Bull SB, Canty AJ, Hosseini SM, Hiraki LT, Maynard J, Sell DR, Monnier VM, Cleary PA, Braffett BH, DCCT/EDIC Research Group, Paterson AD. New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins. Diabetes 65(7):2060-71, 2016. e-Pub 2016. PMID: 27207532.
13. Fan Q, Guo X, Tideman JW, Williams KM, Yazar S, Hosseini SM, Howe LD, Pourcain BS, Evans DM, Timpson NJ, McMahon G, Hysi PG, Krapohl E, Wang YX, Jonas JB, Baird PN, Wang JJ, Cheng CY, Teo YY, Wong TY, Ding X, Wojciechowski R, Young TL, Pärssinen O, Oexle K, Pfeiffer N, Bailey-Wilson JE, Paterson AD, Klaver CC, Plomin R, Hammond CJ, Mackey DA, He M, Saw SM, Williams C, Guggenheim JA, CREAM Consortium. Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium. Sci Rep 6:25853, 2016. e-Pub 2016. PMID: 27174397.
14. Porta M, Toppila I, Sandholm N, Hosseini SM, Forsblom C, Hietala K, Borio L, Harjutsalo V, Klein BE, Klein R, Paterson AD, DCCT/EDIC Research Group, Groop PH, FinnDiane Study Group. Variation in SLC19A3 and Protection From Microvascular Damage in Type 1 Diabetes. Diabetes 65(4):1022-30, 2016. e-Pub 2015. PMID: 26718501.
15. Fan Q, Verhoeven VJ, Wojciechowski R, Barathi VA, Hysi PG, Guggenheim JA, Höhn R, Vitart V, Khawaja AP, Yamashiro K, Hosseini SM, Lehtimäki T, Lu Y, Haller T, Xie J, Delcourt C, Pirastu M, Wedenoja J, Gharahkhani P, Venturini C, Miyake M, Hewitt AW, Guo X, Mazur J, Huffman JE, Williams KM, Polasek O, Campbell H, Rudan I, Vatavuk Z, Wilson JF, Joshi PK, McMahon G, St Pourcain B, Evans DM, Simpson CL, Schwantes-An TH, Igo RP, Mirshahi A, Cougnard-Gregoire A, Bellenguez C, Blettner M, Raitakari O, Kähönen M, Seppala I, Zeller T, Meitinger T, Consortium for Refractive Error and Myopia, Ried JS, Gieger C, Portas L, van Leeuwen EM, Amin N, Uitterlinden AG, Rivadeneira F, Hofman A, Vingerling JR, Wang YX, Wang X, Tai-Hui Boh E, Ikram MK, Sabanayagam C, Gupta P, Tan V, Zhou L, Ho CE, Lim W, Beuerman RW, Siantar R, Tai ES, Vithana E, Mihailov E, Khor CC, Hayward C, Luben RN, Foster PJ, Klein BE, Klein R, Wong HS, Mitchell P, Metspalu A, Aung T, Young TL, He M, Pärssinen O, van Duijn CM, Jin Wang J, Williams C, Jonas JB, Teo YY, Mackey DA, Oexle K, Yoshimura N, Paterson AD, Pfeiffer N, Wong TY, Baird PN, Stambolian D, Wilson JE, Cheng CY, Hammond CJ, Klaver CC, Saw SM, Rahi JS, Korobelnik JF, Kemp JP, Timpson NJ, Smith GD, Craig JE, Burdon KP, Fogarty RD, Iyengar SK, Chew E, Janmahasatian S, Martin NG, MacGregor S, Xu L, Schache M, Nangia V, Panda-Jonas S, Wright AF, Fondran JR, Lass JH, Feng S, Zhao JH, Khaw KT, Wareham NJ, Rantanen T, Kaprio J, Pang CP, Chen LJ, Tam PO, Jhanji V, Young AL, Döring A, Raffel LJ, Cotch MF, Li X, Yip SP, Yap MK, Biino G, Vaccargiu S, Fossarello M, Fleck B, Yazar S, Tideman JW, Tedja M, Deangelis MM, Morrison M, Farrer L, Zhou X, Chen W, Mizuki N, Meguro A, Mäkelä KM. Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error. Nat Commun 7:11008, 2016. e-Pub 2016. PMID: 27020472.
16. Hosseini SM, Boright AP, Sun L, Canty AJ, Bull SB, Klein BE, Klein R, DCCT/EDIC Research Group, Paterson AD. The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy. Hum Genet 134(2):247-57, 2015. e-Pub 2014. PMID: 25487307.
17. Li Q, Wojciechowski R, Simpson CL, Hysi PG, Verhoeven VJ, Ikram MK, Höhn R, Vitart V, Hewitt AW, Oexle K, Mäkelä KM, MacGregor S, Pirastu M, Fan Q, Cheng CY, St Pourcain B, McMahon G, Kemp JP, Northstone K, Rahi JS, Cumberland PM, Martin NG, Sanfilippo PG, Lu Y, Wang YX, Hayward C, Polašek O, Campbell H, Bencic G, Wright AF, Wedenoja J, Zeller T, Schillert A, Mirshahi A, Lackner K, Yip SP, Yap MK, Ried JS, Gieger C, Murgia F, Wilson JF, Fleck B, Yazar S, Vingerling JR, Hofman A, Uitterlinden A, Rivadeneira F, Amin N, Karssen L, Oostra BA, Zhou X, Teo YY, Tai ES, Vithana E, Barathi V, Zheng Y, Siantar RG, Neelam K, Shin Y, Lam J, Yonova-Doing E, Venturini C, Hosseini SM, Wong HS, Lehtimäki T, Kähönen M, Raitakari O, Timpson NJ, Evans DM, Khor CC, Aung T, Young TL, Mitchell P, Klein B, van Duijn CM, Meitinger T, Jonas JB, Baird PN, Mackey DA, Wong TY, Saw SM, Pärssinen O, Stambolian D, Hammond CJ, Klaver CC, Williams C, Paterson AD, Bailey-Wilson JE, Guggenheim JA, CREAM Consortium. Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium. Hum Genet 134(2):131-46, 2015. e-Pub 2014. PMID: 25367360.
18. Eny KM, Lutgers HL, Maynard J, Klein BE, Lee KE, Atzmon G, Monnier VM, van Vliet-Ostaptchouk JV, Graaff R, van der Harst P, Snieder H, van der Klauw MM, Sell DR, Hosseini SM, Cleary PA, Braffett BH, Orchard TJ, Lyons TJ, Howard K, Klein R, Crandall JP, Barzilai N, Milman S, Ben-Avraham D, LifeLines Cohort Study Group, DCCT/EDIC Research Group, Wolffenbuttel BH, Paterson AD. GWAS identifies an NAT2 acetylator status tag single nucleotide polymorphism to be a major locus for skin fluorescence. Diabetologia 57(8):1623-34, 2014. e-Pub 2014. PMID: 24934506.
19. Simpson CL, Wojciechowski R, Oexle K, Murgia F, Portas L, Li X, Verhoeven VJ, Vitart V, Schache M, Hosseini SM, Hysi PG, Raffel LJ, Cotch MF, Chew E, Klein BE, Klein R, Wong TY, van Duijn CM, Mitchell P, Saw SM, Fossarello M, Wang JJ, DCCT/EDIC Research Group, Polašek O, Campbell H, Rudan I, Oostra BA, Uitterlinden AG, Hofman A, Rivadeneira F, Amin N, Karssen LC, Vingerling JR, Döring A, Bettecken T, Bencic G, Gieger C, Wichmann HE, Wilson JF, Venturini C, Fleck B, Cumberland PM, Rahi JS, Hammond CJ, Hayward C, Wright AF, Paterson AD, Baird PN, Klaver CC, Rotter JI, Pirastu M, Meitinger T, Bailey-Wilson JE, Stambolian D. Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. PLoS One 9(9):e107110, 2014. e-Pub 2014. PMID: 25233373.
20. Cheng CY, Schache M, Ikram MK, Young TL, Guggenheim JA, Vitart V, MacGregor S, Verhoeven VJ, Barathi VA, Liao J, Hysi PG, Bailey-Wilson JE, St Pourcain B, Kemp JP, McMahon G, Timpson NJ, Evans DM, Montgomery GW, Mishra A, Wang YX, Wang JJ, Rochtchina E, Polasek O, Wright AF, Amin N, van Leeuwen EM, Wilson JF, Pennell CE, van Duijn CM, de Jong PT, Vingerling JR, Zhou X, Chen P, Li R, Tay WT, Zheng Y, Chew M, Consortium for Refractive Error and Myopia, Burdon KP, Craig JE, Iyengar SK, Igo RP, Lass JH, Fuchs' Genetics Multi-Center Study Group, Chew EY, Haller T, Mihailov E, Metspalu A, Wedenoja J, Simpson CL, Wojciechowski R, Höhn R, Mirshahi A, Zeller T, Pfeiffer N, Lackner KJ, Wellcome Trust Case Control Consortium 2, Bettecken T, Meitinger T, Oexle K, Pirastu M, Portas L, Nag A, Williams KM, Yonova-Doing E, Klein R, Klein BE, Hosseini SM, Paterson AD, Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions, and Complications Research Group, Makela KM, Lehtimaki T, Kahonen M, Raitakari O, Yoshimura N, Matsuda F, Chen LJ, Pang CP, Yip SP, Yap MK, Meguro A, Mizuki N, Inoko H, Foster PJ, Zhao JH, Vithana E, Tai ES, Fan Q, Xu L, Campbell H, Fleck B, Rudan I, Aung T, Hofman A, Uitterlinden AG, Bencic G, Khor CC, Forward H, Pärssinen O, Mitchell P, Rivadeneira F, Hewitt AW, Williams C, Oostra BA, Teo YY, Hammond CJ, Stambolian D, Mackey DA, Klaver CC, Wong TY, Saw SM, Baird PN. Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. Am J Hum Genet 93(2):264-77, 2013. PMID: 24144296.
21. Stambolian D, Wojciechowski R, Oexle K, Pirastu M, Li X, Raffel LJ, Cotch MF, Chew EY, Klein B, Klein R, Wong TY, Simpson CL, Klaver CC, van Duijn CM, Verhoeven VJ, Baird PN, Vitart V, Paterson AD, Mitchell P, Saw SM, Fossarello M, Kazmierkiewicz K, Murgia F, Portas L, Schache M, Richardson A, Xie J, Wang JJ, Rochtchina E, DCCT/EDIC Research Group, Viswanathan AC, Hayward C, Wright AF, Polasek O, Campbell H, Rudan I, Oostra BA, Uitterlinden AG, Hofman A, Rivadeneira F, Amin N, Karssen LC, Vingerling JR, Hosseini SM, Döring A, Bettecken T, Vatavuk Z, Gieger C, Wichmann HE, Wilson JF, Fleck B, Foster PJ, Topouzis F, McGuffin P, Sim X, Inouye M, Holliday EG, Attia J, Scott RJ, Rotter JI, Meitinger T, Bailey-Wilson JE. Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Hum Mol Genet 22(13):2754-64, 2013. e-Pub 2013. PMID: 23474815.
22. Lechner J, Dash DP, Muszynska D, Hosseini M, Segev F, George S, Frazer DG, Moore JE, Kaye SB, Young T, Simpson DA, Churchill AJ, Héon E, Willoughby CE. Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation. Invest Ophthalmol Vis Sci 54(5):3215-23, 2013. e-Pub 2013. PMID: 23599324.
23. Verhoeven VJ, Hysi PG, Wojciechowski R, Fan Q, Guggenheim JA, Höhn R, MacGregor S, Hewitt AW, Nag A, Cheng CY, Yonova-Doing E, Zhou X, Ikram MK, Buitendijk GH, McMahon G, Kemp JP, Pourcain BS, Simpson CL, Mäkelä KM, Lehtimäki T, Kähönen M, Paterson AD, Hosseini SM, Wong HS, Xu L, Jonas JB, Pärssinen O, Wedenoja J, Yip SP, Ho DW, Pang CP, Chen LJ, Burdon KP, Craig JE, Klein BE, Klein R, Haller T, Metspalu A, Khor CC, Tai ES, Aung T, Vithana E, Tay WT, Barathi VA, Consortium for Refractive Error and Myopia (CREAM), Chen P, Li R, Liao J, Zheng Y, Ong RT, Döring A, Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group, Evans DM, Timpson NJ, Verkerk AJ, Meitinger T, Raitakari O, Hawthorne F, Spector TD, Karssen LC, Pirastu M, Murgia F, Ang W, Wellcome Trust Case Control Consortium 2 (WTCCC2), Mishra A, Montgomery GW, Pennell CE, Cumberland PM, Cotlarciuc I, Mitchell P, Wang JJ, Schache M, Janmahasatian S, Janmahasathian S, Igo RP, Lass JH, Chew E, Iyengar SK, Fuchs' Genetics Multi-Center Study Group, Gorgels TG, Rudan I, Hayward C, Wright AF, Polasek O, Vatavuk Z, Wilson JF, Fleck B, Zeller T, Mirshahi A, Müller C, Uitterlinden AG, Rivadeneira F, Vingerling JR, Hofman A, Oostra BA, Amin N, Bergen AA, Teo YY, Rahi JS, Vitart V, Williams C, Baird PN, Wong TY, Oexle K, Pfeiffer N, Mackey DA, Young TL, van Duijn CM, Saw SM, Bailey-Wilson JE, Stambolian D, Klaver CC, Hammond CJ. Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat Genet 45(3):314-8, 2013. e-Pub 2013. PMID: 23396134.
24. Sandholm N, Salem RM, McKnight AJ, Brennan EP, Forsblom C, Isakova T, McKay GJ, Williams WW, Sadlier DM, Mäkinen VP, Swan EJ, Palmer C, Boright AP, Ahlqvist E, Deshmukh HA, Keller BJ, Huang H, Ahola AJ, Fagerholm E, Gordin D, Harjutsalo V, He B, Heikkilä O, Hietala K, Kytö J, Lahermo P, Lehto M, Lithovius R, Osterholm AM, Parkkonen M, Pitkäniemi J, Rosengård-Bärlund M, Saraheimo M, Sarti C, Söderlund J, Soro-Paavonen A, Syreeni A, Thorn LM, Tikkanen H, Tolonen N, Tryggvason K, Tuomilehto J, Wadén J, Gill GV, Prior S, Guiducci C, Mirel DB, Taylor A, Hosseini SM, DCCT/EDIC Research Group, Parving HH, Rossing P, Tarnow L, Ladenvall C, Alhenc-Gelas F, Lefebvre P, Rigalleau V, Roussel R, Tregouet DA, Maestroni A, Maestroni S, Falhammar H, Gu T, Möllsten A, Cimponeriu D, Ioana M, Mota M, Mota E, Serafinceanu C, Stavarachi M, Hanson RL, Nelson RG, Kretzler M, Colhoun HM, Panduru NM, Gu HF, Brismar K, Zerbini G, Hadjadj S, Marre M, Groop L, Lajer M, Bull SB, Waggott D, Paterson AD, Savage DA, Bain SC, Martin F, Hirschhorn JN, Godson C, Florez JC, Groop PH, Maxwell AP. New susceptibility loci associated with kidney disease in type 1 diabetes. PLoS Genet 8(9):e1002921, 2012. e-Pub 2012. PMID: 23028342.
25. Grassi MA, Tikhomirov A, Ramalingam S, Lee KE, Hosseini SM, Klein BE, Klein R, Lussier YA, Cox NJ, Nicolae DL. Replication analysis for severe diabetic retinopathy. Invest Ophthalmol Vis Sci 53(4):2377-81, 2012. e-Pub 2012. PMID: 22427569.
26. van Koolwijk LM, Ramdas WD, Ikram MK, Jansonius NM, Pasutto F, Hysi PG, Macgregor S, Janssen SF, Hewitt AW, Viswanathan AC, ten Brink JB, Hosseini SM, Amin N, Despriet DD, Willemse-Assink JJ, Kramer R, Rivadeneira F, Struchalin M, Aulchenko YS, Weisschuh N, Zenkel M, Mardin CY, Gramer E, Welge-Lüssen U, Montgomery GW, Carbonaro F, Young TL, DCCT/EDIC Research Group, Bellenguez C, McGuffin P, Foster PJ, Topouzis F, Mitchell P, Wang JJ, Wong TY, Czudowska MA, Hofman A, Uitterlinden AG, Wolfs RC, de Jong PT, Oostra BA, Paterson AD, Wellcome Trust Case Control Consortium 2, Mackey DA, Bergen AA, Reis A, Hammond CJ, Vingerling JR, Lemij HG, Klaver CC, van Duijn CM. Common genetic determinants of intraocular pressure and primary open-angle glaucoma. PLoS Genet 8(5):e1002611, 2012. e-Pub 2012. PMID: 22570627.
27. Nguyen DQ, Hosseini SM, Billingsley G, Héon E, Churchill AJ. Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutation. Acta Ophthalmol 88(6):695-9, 2010. PMID: 19432861.
28. Paterson AD, Waggott D, Boright AP, Hosseini SM, Shen E, Sylvestre MP, Wong I, Bharaj B, Cleary PA, Lachin JM, MAGIC (Meta-Analyses of Glucose and Insulin-related traits Consortium), Below JE, Nicolae D, Cox NJ, Canty AJ, Sun L, Bull SB, Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group. A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose. Diabetes 59(2):539-49, 2010. e-Pub 2009. PMID: 19875614.
29. Paterson AD, Lopes-Virella MF, Waggott D, Boright AP, Hosseini SM, Carter RE, Shen E, Mirea L, Bharaj B, Sun L, Bull SB, Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group. Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin. Arterioscler Thromb Vasc Biol 29(11):1958-67, 2009. e-Pub 2009. PMID: 19729612.
30. Hosseini SM, Herd S, Vincent AL, Héon E. Genetic analysis of chromosome 20-related posterior polymorphous corneal dystrophy: genetic heterogeneity and exclusion of three candidate genes. Mol Vis 14:71-80, 2008. e-Pub 2008. PMID: 18253095.
31. Billingsley G, Santhiya ST, Paterson AD, Ogata K, Wodak S, Hosseini SM, Manisastry SM, Vijayalakshmi P, Gopinath PM, Graw J, Héon E. CRYBA4, a novel human cataract gene, is also involved in microphthalmia. Am J Hum Genet 79(4):702-9, 2006. e-Pub 2006. PMID: 16960806.

Abstracts

1. Hosseini SM, Law G, Khanafshar E. Developing an Online Dashboard for Monitoring Cytopathology Workload. Poster Presentation. United States & Canadian Academy of Pathology 110th Annual Meeting-Virtual, 2021.
2. Hosseini SM, Tondi Resta I, Baloch ZW. Diagnostic performance of Milan system for reporting salivary gland cytopathology: an institutional experience. Poster Presentation. The 68th Annual Scientific Meeting of the American Society of Cytopathology-Virtual, 2020.
3. Hosseini SM, Tchou JC, Bleiweiss IJ, Nayak A. Diagnostic performance of sentinel node biopsy in node-positive breast cancer patients after neoadjuvant therapy. Poster Presentation. Canadian Association of Pathologists (CAP-ACP) Annual Meeting, 2019.
4. Hosseini SM, Saab J, Van Deelin VM, Haldar M. Molecular diagnosis of graft-versus-host disease after liver transplantation: an institutional experience. [AMP abstract G041]. The Journal of Molecular Diagnostics 20(6):907, 2018.
5. Hosseini SM, Manshaei R, Liston E, Chaturvedi RR, Kim RH, Bowdin S. A novel workflow for analysis of whole genome sequencing in cardiac disease using tissue-specific biological datasets. Poster Presentation. The 67th Annual Meeting of the American Society of Human Genetics, 2017.
6. Hosseini SM, Kim RH, Jobling RK, Liston E, Jamal SM, Costain G, Szybowska M, Morel CF, Bowdin S, Gollob MH. Gene curation for Brugada syndrome questions the clinical validity of some of the previously reported gene-disease associations. Poster Presentation. The Curating the Clinical Genome Meeting, 2017.
7. Hosseini, SM, Snell-Bergeon JK, Boright AP, Canty AJ, Sun L, Bull SB, Marcovina SM, Brunzell JD, the DCCT/EDIC Group Research. Identifying genetic variants for serum lipoprotein(a) independent of kringle repeat polymorphism. Poster Presentation. The 66th Annual Meeting of The American Society of Human Genetics, 2016.
8. Hiraki LT, Gallaugher M, de Boer IH, Canty AJ, Boright AP, Sun L, Klein R, Klein BEK, Maahs DM, Snell-Bergeon JK, Mauer SM, Caramori ML, Hosseini SM, Bull SB, Paterson AD. Genetic signal for renal function decline in type 1 diabetes identified by analysis of repeated longitudinal measures. (Abstract 80-OR) Oral Presentation. The American Diabetes Association's 75th Scientific Sessions, 2015.
9. Hosseini SM, Howard K, Sun L, Boright AP, Tregouet DA, Sandholm N, Hietala K, Toppila I, Lajer MS, Marre M, Rossing P, Groop PH, Canty AJ, Hadjadj S, Kleing BE, Bull SB, Klein R, Paterson AD, and the DCCT/EDIC Research Group. Polymorphism upstream of cryopyrin gene (NLRP3) is associated with severe retinopathy in type 1 diabetes. (Abstract 946S) Poster Presentation. The 64th Annual Meeting of the American Society of Human Genetics, 2014.
10. Hosseini SM, Howard K, Sun L, Boright AP, Tregouet DA, Sandholm N, Lajer MS, Hietala K, Forsblom C, Marre M, Rossing P, Groop PH, Canty AJ, Hadjadj S, Klein BE, Bull SB, Klein R, Paterson AD, The DCCT/EDIC Research Group. Dipeptidyl peptidase 10 is associated with severe retinopathy in type 1 diabetes. (Abstract 889T) Poster Presentation. The 63rd Annual Meeting of the American Society of Human Genetics, 2013.
11. Hosseini SM, Boright AP, Sun L, Howard K, Canty AJ, Bull SB, Klein BE, Klein R, Paterson AD, the DCCT/EDIC Research Group. Genome-wide association study of time-to diabetic retinopathy. (Abstract 2109 W) Poster Presentation. The 62nd Annual Meeting of the American Society of Human Genetics, 2012.
12. Hosseini SM, Howard K, Boright AP, Sun L, Canty AJ, Bull SB, Klein BE, Klein R, Paterson AD. Time-to-event analysis for genome-wide association study of diabetic retinopathy. Oral Presentation. The First Joint Canadian Human Genetics Conference and Canadian Genetic Epidemiology and Statistical Genetics Meeting, 2012.
13. Hosseini SM, Howard K, Boright AP, Sun L, Canty AJ, Bull SB, Klein BE, Klein R, Patterson AD. Using time-to-event analysis for genome wide association study in a long-term cohort of diabetic retinopathy. (Abstract 423W) Poster Presentation. The 12th International Congress of Human Genetics 2011/ 61st Annual Meeting of the American Society of Human Genetics, 2011.
14. Eny KM, Bull SB, Canty AJ, Sun L, Boright AP, Hosseini SM, Cleary PA, Lachin JM, Paterson AD, the DCCT/EDIC Research Group. Genome-wide association analysis of lactose consumption measured longitudinally identifies a novel variant 500kb downstream of the LCT gene region. (Abstract 882T) Poster Presentation. The 12th International Congress of Human Genetics 2011/61st Annual Meeting of the American Society of Human Genetics, 2011.
15. Hosseini SM, Waggott D, Shen E, Boright AP, Sylvestre MP, Sun W, Cleary PA, Canty AJ, Sun L, Bull SB, Paterson AD. Genome-wide association study of refractive error in 1304 individuals. Proceedings of the American Society of Human Genetics 2010; 60:348: Abstract 1114/T. Poster Presentation. The American Society of Human Genetics 60th Annual Meeting, 2010.
16. Paterson AD, Waggott D, Shen E, Boright AP, Hosseini, Cleary PA, Lachin JM, Sung L, Bull SB, the DCCT/EDIC Research Group. Genome-wide association study of risk for diabetic retinopathy in type 1 diabetes. Abstract 243-OR Oral Presentation. Diabetes 2010 The American Diabetes Association 70th Annual Scientific Sessions 59(1), 2010.
17. Hosseini SM, Waggott D, Boright AP, Shen E, Sylvestre MP, Cleary PA, Lachin JM, Below JE, Nicolae D, Cox NJ, Canty AJ, Sung L, Bull SB, Paterson AD, the DCCT/EDIC Research Group. Genetic variation at adenylate cyclase 5 (ADCY5) is associated with glycemic control in type 1 diabetes. Abstract 53-LB Poster Presentation. The American Diabetes Association 70th Annual Scientific Sessions 59(SA1:LB 15), 2010.
18. Hosseini SM, Shen E, Waggott D, Wood AR, Boright AP, Canty AJ, Sun L, Bull SB, Weedon MN, Frayling TM, Marcovina SM, Brunzell JD, Paterons AD, the DCCT?EDIC Research Group. Genome-wide association study of serum lipoprotein(a) concentration identifies multiple associated SNP's is addition to the kringle repeat. Oral Presentation. The Canadian Genetic Epidemiology & Statistical Genetics 5th Annual Meeting, 2010.
19. Paterson AD, Waggott D, Boright AP, Hosseini SM, Shen E, Sylvestre MP, Wong I, Bharaj B, Cleary PA, Lachin JM, Canty AJ, Sun L, Bull SB, DCCT/EDIC Research Group. A genome-wide association study identifies variation near SORCS1 as a major locus for glycemic control in type 1 diabetes, as measured by both HbA1c and glucose. Diabetes 2009; 58(S1): A16: Abstract 58-OR. Oral Presentation. The American Diabetes Association 69th Annual Scientific Sessions, 2009.
20. Hosseini SM, Shen E, Waggott D, Boright AP, Sun L, Bull SB, Marcovina SM, Brunzell JD, Paterson AD, DCCT/EDIC Research Group. Genome-wide association study of serum lipoprotein(a) concentration identifies multiple associated SNPs in addition to the kringle repeat. Proceedings of the American Society of Human Genetics 59th Annual Meeting. Poster Presentation. The American Society of Human Genetics 59th Annual Meeting 59:305, 2009.
21. Boright AP, Shen E, Waggott D, Hosseini SM, Cleary PA, Lachin JM, Canty AJ, Bull SB, Sun L, Paterson AD. Genome wide association analysis identifies genetic risk factors for coronary calcium in subjects with type 1 diabetes in the DCCT/EDIC genetics study. Diabetes 2009; 58(S1): A182: Abstract 677-P. Poster Presentation. The American Diabetes Association 69th Annual Scientific Sessions, 2009.
22. Hosseini SM, Waggott D, Boright AP, Bull SB, Sun W, Cleary PA, Patterson AD, DCCT/EDIC Research Group. Genome-wide association study of intraocular pressure in 1304 individuals. Proceedings of the American Society of Human Genetics. Poster Presentation. The American Society of Human Genetics 58th Annual Meeting 58:403, 2008.
23. Hosseini SM, Héon E. Identification of novel exons and different isoforms for VSX1. Proceedings of the American Society of Human Genetics. Poster Presentation. The American Society of Human Genetics 55th Annual Meeting 55:214, 2005.
24. Hosseini SM, Segev F, Héon E. Anticipation in Fuchs' endothelial corneal dystrophy. Poster Presentation. The 15th International Society for Genetic Eye Disease/12th International Retinoblastoma Symposium, 2005.
25. Hosseini SM, Segev F, Héon E. Anticipation like phenomenon in Fuschs' endothelial corneal dystrophy. Investigative Ophthalmology & Visual Science. Poster Presentation. The Association for Research in Vision and Ophthalmology 2005 Annual Meeting 46, 2005.
26. Hosseini SM, Billingsley G, Segev F, Héon E. COL8A2 mutation in a family with Fuchs' endothelial corneal dystrophy. Poster Presentation. The Canadian Genetic Disease Network 14th Annual Meeting, 2005.
27. Hosseini SM, Billingsley G, Levin AV, Kmoch S, Fillipec M, Stone EM, Héon E. Mutation analysis of COL8A2 gene in patients with posterior polymorphous corneal dystrophy. Poster Presentation. The American Society of Human Genetics 54th Annual Meeting, 2004.
28. Hosseini SM, Herd S, Noordeh N, Panton C, Westfall C, Héon E. Molecular Characterization of Bardet-Biedl Syndrome in a First Nation Dogrib Family. Poster Presentation. The Canadian Genetic Disease Network 13th Annual Meeting, 2004.