Sayed Mohsen Hosseini, MD, PhD, FRCPC

Peer-Reviewed Articles

1. Hamidi S, Dadu R, Iyer PC, Busaidy NL, Maniakas A, Wang JR, Banuchi VE, Hosseini SM, Williams MD, Zafereo ME, Cabanillas ME. Circulating Tumor DNA as a Biomarker for Disease Surveillance in Anaplastic Thyroid Cancer. JCO Precis Oncol 9, 2025. e-Pub 2025. PMID: 40570261.
2. Hamidi S, Maniakas A, Akhave NS, Banuchi VE, Busaidy NL, Dadu R, Ferrarotto R, Guise TA, Hofmann MC, Hosseini SM, Hu MI, Iyer PC, Mansour M, Marczyk VR, Roy-Chowdhuri S, Sherman SI, Sousa LG, Wang JR, Williams MD, Zafereo ME, Waguespack SG, Cabanillas ME. Characterization of advanced RAS-driven follicular-derived thyroid cancers and review of future therapeutic avenues. J Clin Endocrinol Metab, 2025. e-Pub 2025. PMID: 40568752.
3. Dagher SA, Learned KO, Dagher R, Wang JR, Zhao X, Hosseini SM, Maniakas A, Cabanillas ME, Busaidy NL, Dadu R, Iyer P, Zafereo ME, Khalaf AM. [18F]-Fluorodeoxyglucose Uptake as a Marker of Residual Anaplastic and Poorly Differentiated Thyroid Carcinoma Following BRAF-Targeted Therapy. AJNR Am J Neuroradiol, 2024. e-Pub 2024. PMID: 39572200.
4. Hamidi S, Dadu R, Zafereo ME, Ferrarotto R, Wang JR, Maniakas A, Gunn G, Lee A, Spiotto MT, Iyer PC, Sousa LG, Akhave NS, Ahmed S, Learned KO, Lu C, Lai SY, Williams M, Hosseini SM, Busaidy NL, Cabanillas ME. Initial Management of BRAF V600E-Variant Anaplastic Thyroid Cancer: The FAST Multidisciplinary Group Consensus Statement. JAMA Oncol, 2024. e-Pub 2024. PMID: 38990526.
5. Amin SE, Hosseini SM. Cytological Evaluation of a Neck Mass in a Patient with Advanced Breast and Lung Cancer. Diagn Cytopathol. e-Pub 2024.
6. Diks JEB, Najjar S, Geetha S, Hosseini SM. Quantitative Analysis of Diagnostic Features for Mucoepidermoid Carcinoma on Fine Needle Aspiration with Cyto-Histological Correlation. e-Pub 2024.
7. Allen DZ, Hosseini SM, Ratan R, Nair R, Lu C, Patel SR, Ravi V, Halperin DM, Busaidy NL, Iyer P, Grubbs EG, Diaz EM, Lango M, Wang RJ, Zafereo ME, Williams MD, Cabanillas ME, Maniakas A. Deceptive Thyroid Pathologies: Anaplastic Thyroid Carcinoma Mimics and Clinical Implications. Head & Neck. e-Pub 2024.
8. Ding Q, Somerville C, Manshaei R, Trost B, Reuter MS, Kalbfleisch K, Stanley K, Okello JBA, Hosseini SM, Liston E, Curtis M, Zarrei M, Higginbotham EJ, Chan AJS, Engchuan W, Thiruvahindrapuram B, Scherer SW, Kim RH, Jobling RK. SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing. Hum Genet 142(2):201-216, 2023. e-Pub 2023. PMID: 36376761.
9. 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.
10. 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.
11. 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.
12. 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.
13. 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 2019. PMID: 30232381.
14. 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 2019. PMID: 30487263.
15. 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. e-Pub 2018. PMID: 29959160.
16. 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, 23 and Me 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.
17. 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 2018. PMID: 28771251.
18. 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. e-Pub 2018. PMID: 29431110.
19. 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.
20. 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.
21. 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 2016. PMID: 26718501.
22. Fan Q, Verhoeven VJM, 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, Pourcain BS, Evans DM, Simpson CL, Schwantes-An T, Igo RP, Mirshahi A, Cougnard-Gregoire A, Bellenguez C, Blettner M, Raitakari O, Kähönen M, Seppälä I, Zeller T, Meitinger T, Ried JS, Gieger C, Portas L, van Leeuwen EM, Amin N, Uitterlinden AG, Rivadeneira F, Hofman A, Vingerling JR, Wang YX, Wang X, Boh ET, M Kamran Ikram M, Sabanayagam C, Gupta P, Tan V, Zhou L, Ho CEH, Lim W, Beuerman RW, Siantar R, Tai E, Vithana E, Mihailov E, Khor C, Hayward C, Luben RN, Foster PJ, Klein BEK, Klein R, Wong HS, Mitchell P, Metspalu A, Aung T, Young TL, He M, Pärssinen O, van Duijn CM, Wang JJ, Williams C, Jonas JB, Teo Y, Mackey DA, Oexle K, Yoshimura N, Paterson AD, Pfeiffer N, Wong T, Baird PN, Stambolian D, Bailey Wilson JE, Cheng C, Hammond CJ, W Klaver CC, Saw S, Consortium for Refractive Error and Myopia (CREAM). 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.
23. Shungin D, Winkler TW, Croteau-Chonka DC, Ferreira T, Locke AE, Mägi R, Strawbridge RJ, Pers TH, Fischer K, Justice AE, Workalemahu T, W Wu JM, Buchkovich ML, Heard-Costa NL, Roman TS, Drong AW, Song C, Gustafsson S, Day FR, Esko T, Fall T, Kutalik Z, Luan J, Randall JC, The ADIPOGen Consortium, The CARDIOGRAMplusC4D Consortium, The CKDGen Consortium, The GEFOS Consortium, The GENIE Consortium, The GLGC, The ICBP, The International Endogene Consortium, The LifeLines Cohort Study, The MAGIC Investigators, The MuTHER Consortium, The PAGE Consortium, The ReproGen Consortium, ..., Mohlke KL. New genetic loci link adipose and insulin biology to body fat distribution. Nature 518(7538):187-196, 2015. e-Pub 2015. PMID: 25673412.
24. Locke AE, Kahali B, Berndt SI, Justice AE, Pers TH, Day FR, Powell C, Vedantam S, Buchkovich ML, Yang J, Croteau-Chonka DC, Esko T, Fall T, Ferreira T, Gustafsson S, Kutalik Z, Luan J, Mägi R, Randall JC, Winkler TW, Wood AR, Workalemahu T, Faul JD, Smith JA, The LifeLines Cohort Study, The ADIPOGen Consortium, The AGEN-BMI Working Group, The CARDIOGRAMplusC4D Consortium, The CKDGen Consortium, The GLGC, The ICBP, The MAGIC Investigators, The MuTHER Consortium, The MIGen Consortium, The PAGE Consortium, The ReproGen Consortium, The GENIE Consortium, The International Endogene Consortium, ..., Speliotes EK. Genetic studies of body mass index yield new insights for obesity biology. Nature 518(7538):197-206, 2015. e-Pub 2015. PMID: 25673413.
25. 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 2015. PMID: 25367360.
26. 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 2015. PMID: 25487307.
27. 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.
28. 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.
29. Cheng C, Schache M, Ikram MK, Young TL, Guggenheim JA, Vitart V, MacGregor S, Verhoeven VJM, Barathi VA, Liao J, Hysi PG, Bailey-Wilson JE, Pourcain BS, 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 PTVM, 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, 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, DCCT/EDIC Research Group, Makela KM, Lehtimaki T, Kahonen M, Raitakari O, Yoshimura N, Matsuda F, Chen LJ, Pang CP, Yip SP, Yap MKH, 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 C, Forward H, Pärssinen O, Mitchell P, Rivadeneira F, Hewitt AW, Williams C, Oostra BA, Teo Y, Hammond CJ, Stambolian D, Mackey DA, W Klaver CC, Wong T, Saw S, 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. e-Pub 2013. PMID: 24144296.
30. 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.
31. 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.
32. Verhoeven VJM, Hysi PG, Wojciechowski R, Fan Q, Guggenheim JA, Höhn R, MacGregor S, Hewitt AW, Nag A, Cheng C, Yonova-Doing E, Zhou X, Ikram MK, Buitendijk GHS, McMahon G, Kemp JP, Pourcain BS, Simpson CL, Mäkelä KM, Lehtimäki T, Kähönen M, Paterson AD, Hosseini SM, Wong HS, Consortium for Refractive Error and Myopia (CREAM), DCCT/EDIC Research Group, Wellcome Trust Case Control Consortium 2 (WTCCC2), The Fuchs' Genetics Multi-Center Study Group, ..., 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.
33. 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.
34. 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.
35. van Koolwijk LME, 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.
36. Nguyen DQ, Hosseini M, 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. e-Pub 2010. PMID: 19432861.
37. 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, DCCT/EDIC 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 2010. PMID: 19875614.
38. Paterson AD, Lopes-Virella MF, Waggott D, Boright AP, Hosseini SM, Carter RE, Shen E, Mirea L, Bharaj B, Sun L, Bull SB, DCCT/EDIC 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.
39. 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.
40. 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.
41. Changiz T, Adibi P, Hosseini SM, Tootoonchi M. Viewpoints of supervisors about the problems in the process of dissertations for general medicine program Isfahan University of Medical Sciences. Ir J Med Educ 3(1):23-33, 2003. e-Pub 2003.

Review Articles

1. Cabanillas ME, Akhave N, Banuchi V, Busaidy N, Dadu R, Ferrarotto R, Gunn GB, Hamidi S, Hofmann MC, Hosseini SM, Iyer PC, Lai SY, Lee A, Maniakas A, Ning MS, Spiotto M, Wang JR, Williams MD, Zafereo M. Reimagining the Therapeutic Approach for Anaplastic Thyroid Cancer: The Roadmap to a Cure. Thyroid 35(5):462-470, 2025. e-Pub 2025. PMID: 40388579.
2. Hosseini SM, Stewart JM. Cytopathology assistance for optimizing interventional diagnostic procedures. Semin Diagn Pathol 39(6):389-393, 2022. e-Pub 2022. PMID: 35931593.
3. 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 2020. PMID: 30783052.

Abstracts

1. Cabanillas ME, Busaidy N, Iyer P, Wang JR, Hu MI, Zafereo M, Ferrarotto R, Lee A, Liu S, Gunn B, Spiotto M, Hamidi S, Akhave N, Sousa L, Maniakas A, Williams M, Banuchi V, Hosseini S, Dadu R. Lenvatinib (LEN) plus pembrolizumab (PEMBRO) in anaplastic thyroid cancer (ATC): a phase 2, single center trial. American Thyroid Association 2025 Annual Meeting 35(S1):e106, 2025. e-Pub 2025.
2. Hosseini SM. Utilizing ChatGPT to assign categories based on the Milan system for reporting salivary gland cytopathology. 22nd International Congress of Cytology 2025 69(suppl 1):84, 2025. e-Pub 2025.
3. Al-Attar M, Hosseini SM. Impact of Incorporating Clinical and Radiological Follow-Up Data on Risk of Malignancy Estimation in the Milan System for Reporting Salivary Gland Cytopathology. American Society of Cytopathology 72nd Annual Scientific Meeting 13(5):S33-S34, 2024. e-Pub 2024.
4. Hosseini SM, Zafereo ME, Cabanillas ME. Mutational Profiling of Anaplastic Thyroid Carcinoma Using Targeted Next-Generation Sequencing in a Large Cohort. AMP Europe 2024 Congress, 2024. e-Pub 2024.
5. Diks JEB, Najjar S, Hosseini SM. Morphological Spectrum of Mucoepidermoid Carcinoma on Fine Needle Aspiration with Histological Correlation. USCAP 113th Annual Meeting, 2024. e-Pub 2024.
6. Elzamly S, Amin SE, Hosseini SM. Clinicopathologic Features of Primary Thyroid Mucoepidermoid Carcinoma and Sclerosing Mucoepidermoid Carcinoma with Eosinophilia; A Series of 22 Rare Cases. USCAP 113th Annual Meeting, 2024. e-Pub 2024.
7. Allen D, Hosseini M, Ratan R, Nair R, Lu C, Patel S, Ravi V, Halperin D, Busaid N, Iyer P, Grubbs E, Diaz E, Lango M, Wang R, Zafereo M, Williams M, Cabanillas M, Maniakas A. Unusual Thyroid Pathologies: Presentation, Management, and Clinical Outcomes. Proceedings of the American Thyroid Association 2023 Annual Meeting 33(Suppl 1):A-167, 2023. e-Pub 2023.
8. Najjar S, Hosseini SM. Morphological Spectrum of Mucoepidermoid Carcinoma on Fine Needle Aspiration: A Retrospective Study. [Poster] In: Proceedings of the 21st International Congress of Cytology / American Society of Cytopathology 70th Annual Scientific Meeting. 2022; Baltimore, MD 11(6):S42-S43, 2022. e-Pub 2022.
9. Lee H, Khanafshar E, Ljung BM, Hosseini SM. Correlation of Cytologic and Radiologic Features with Molecular Finding in Indeterminate Thyroid Nodules. [Poster] In: Proceedings of the 21st International Congress of Cytology / American Society of Cytopathology 70th Annual Scientific Meeting. 2022; Baltimore, MD 11(6):S70, 2022. e-Pub 2022.
10. Lee H, Khanafshar E, Ljung BM, Hosseini SM. Cost-Analysis of ThyroSeq Molecular Testing: A Real-World Institutional Experience. [Poster] In: Proceedings of the United States & Canadian Academy of Pathology 111th Annual Meeting. 2022; Los Angeles, CA 102(Suppl 1):393, 2022. e-Pub 2022.
11. Hosseini SM, Law G, Khanafshar E. Developing an Online Dashboard for Monitoring Cytopathology Workload. United States & Canadian Academy of Pathology 110th Annual Meeting-Virtual, 2021. e-Pub 2021.
12. Hosseini SM, Law G, Khanafshar E. Developing an Online Dashboard for Monitoring Cytopathology Workload. [Poster] In: Proceedings of the United States & Canadian Academy of Pathology 110th Annual Meeting. 2021; Virtual 101(Suppl 1):937-938, 2021. e-Pub 2021.
13. Hosseini SM, Tondi Resta I, Baloch ZW. Diagnostic performance of Milan system for reporting salivary gland cytopathology: an institutional experience. The 68th Annual Scientific Meeting of the American Society of Cytopathology-Virtual, 2020. e-Pub 2020.
14. Hosseini SM, Baloch ZW. Diagnostic performance of Milan system for reporting salivary gland cytopathology: an institutional experience. [Poster] In: Proceedings of the 68th Annual Scientific Meeting of the American Society of Cytopathology. 2020; Virtual 9(6):S31, 2020. e-Pub 2020.
15. Hosseini SM, Tchou JC, Bleiweiss IJ, Nayak A. Diagnostic performance of sentinel node biopsy in node-positive breast cancer patients after neoadjuvant therapy. [Poster] In: Proceedings of the Canadian Association of Pathologists Annual Meeting. Niagara Falls, ON, Canada, 2019. e-Pub 2019.
16. Hosseini SM, Tchou JC, Bleiweiss IJ, Nayak A. Diagnostic performance of sentinel node biopsy in node-positive breast cancer patients after neoadjuvant therapy. Canadian Association of Pathologists (CAP-ACP) Annual Meeting, 2019. e-Pub 2019.
17. Hosseini SM, Saab J, Van Deelin VM, Haldar M. Molecular diagnosis of graft-versus-host disease after liver transplantation: an institutional experience. [Poster G041] In: Proceedings of the Association of Molecular Pathology 2018 Annual Meeting. 2018; San Antonio, TX 20(6):907, 2018. e-Pub 2018.
18. 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. e-Pub 2018.
19. 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] In: Proceedings of the 67th Annual Meeting of the American Society of Human Genetics. Orlando, FL, 2017. e-Pub 2017.
20. 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. The 67th Annual Meeting of the American Society of Human Genetics, 2017. e-Pub 2017.
21. 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. The Curating the Clinical Genome Meeting, 2017. e-Pub 2017.
22. 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] In: Proceedings of the Curating the Clinical Genome Meeting. Washington, DC, 2017. e-Pub 2017.
23. Hosseini SM, Snell-Bergeon JK, Boright AP, Canty AJ, Sun L, Bull SB, Marcovina SM, Brunzell JD, DCCT/EDIC Group Research, Paterson AD. Identifying genetic variants for serum lipoprotein(a) independent of kringle repeat polymorphism. [Poster] In: Proceedings of the 66th Annual Meeting of The American Society of Human Genetics. Vancouver, BC, 2016. e-Pub 2016.
24. Hosseini, SM, Snell-Bergeon JK, Boright AP, Canty AJ, Sun L, Bull SB, Marcovina SM, Brunzell JD, Group Research TD. Identifying genetic variants for serum lipoprotein(a) independent of kringle repeat polymorphism. The 66th Annual Meeting of The American Society of Human Genetics, 2016. e-Pub 2016.
25. 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, DCCT/EDIC research group, Paterson AD. Genetic signal for renal function decline in type 1 diabetes identified by analysis of repeated longitudinal measures. [Oral] In Proceedings of the American Diabetes Association's 75th Scientific Sessions. 2015; Boston, MA 64(Suppl 1):A21, 2015. e-Pub 2015.
26. 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). The American Diabetes Association's 75th Scientific Sessions, 2015. e-Pub 2015.
27. 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, Research Group ATD. Polymorphism upstream of cryopyrin gene (NLRP3) is associated with severe retinopathy in type 1 diabetes. (Abstract 946S). The 64th Annual Meeting of the American Society of Human Genetics, 2014. e-Pub 2014.
28. 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, DCCT/EDIC Research Group. Polymorphism upstream of cryopyrin gene (NLRP3) is associated with severe retinopathy in type 1 diabetes. [Poster] In: Proceedings of the 64th Annual Meeting of the American Society of Human Genetics. San Diego, CA, 2014. e-Pub 2014.
29. 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, DCCT/EDIC Research Group. Dipeptidyl peptidase 10 is associated with severe retinopathy in type 1 diabetes. [Poster] In: Proceedings of the 63rd Annual Meeting of the American Society of Human Genetics. Boston, MA, 2013. e-Pub 2013.
30. 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, Research Group TD. Dipeptidyl peptidase 10 is associated with severe retinopathy in type 1 diabetes. (Abstract 889T). The 63rd Annual Meeting of the American Society of Human Genetics, 2013. e-Pub 2013.
31. Hosseini SM, Boright AP, Sun L, Howard K, Canty AJ, Bull SB, Klein BE, Klein R, Paterson AD, Research Group TD. Genome-wide association study of time-to diabetic retinopathy. (Abstract 2109 W). The 62nd Annual Meeting of the American Society of Human Genetics, 2012. e-Pub 2012.
32. Hosseini SM, Boright AP, Sun L, Howard K, Canty AJ, Bull SB, Klein BE, Klein R, Paterson AD, DCCT/EDIC Research Group. Genome-wide association study of time-to diabetic retinopathy. [Poster] In: Proceedings of the 62nd Annual Meeting of the American Society of Human Genetics. San Francisco, CA, 2012. e-Pub 2012.
33. 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. The First Joint Canadian Human Genetics Conference and Canadian Genetic Epidemiology and Statistical Genetics Meeting, 2012. e-Pub 2012.
34. 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] In: Proceedings of the First Joint Canadian Human Genetics Conference and Canadian Genetic Epidemiology and Statistical Genetics Meeting. Niagara-on-the-Lake, ON, Canada, 2012. e-Pub 2012.
35. 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. [Poster] In: Proceedings of the 12th International Congress of Human Genetics 2011/ 61st Annual Meeting of the American Society of Human Genetics. Montreal, QC, Canada, 2011. e-Pub 2011.
36. Eny KM, Bull SB, Canty AJ, Sun L, Boright AP, Hosseini SM, Cleary PA, Lachin JM, Paterson AD, Research Group TD. Genome-wide association analysis of lactose consumption measured longitudinally identifies a novel variant 500kb downstream of the LCT gene region. The 12th International Congress of Human Genetics 2011/61st Annual Meeting of the American Society of Human Genetics, 2011. e-Pub 2011.
37. 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). The 12th International Congress of Human Genetics 2011/ 61st Annual Meeting of the American Society of Human Genetics, 2011. e-Pub 2011.
38. Eny KM, Bull SB, Canty AJ, Sun L, Boright AP, Hosseini SM, Cleary PA, Lachin JM, Paterson AD, DCCT/EDIC Research Group. Genome-wide association analysis of lactose consumption measured longitudinally identifies a novel variant 500kb downstream of the LCT gene region. [Poster] In: Proceedings of the 12th International Congress of Human Genetics 2011/61st Annual Meeting of the American Society of Human Genetics. Montreal, QC, Canada, 2011. e-Pub 2011.
39. 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. e-Pub 2010.
40. Hosseini SM, Waggott D, Shen E, Boright AP, Sylvestre MP, Sun W, Cleary PA, Canty AJ, Sun L, Bull SB, Paterson AD, DCCT/EDIC Research Group. Genome-wide association study of refractive error in 1304 individuals. [Poster] In: Proceedings of the American Society of Human Genetics 60th Annual Meeting. Washington, DC, 2010. e-Pub 2010.
41. Paterson AD, Waggott D, Shen E, Boright AP, Hosseini M, Cleary PA, Lachin JM, Sung L, Bull SB, DCCT/EDIC Research Group. Genome-wide association study of risk for diabetic retinopathy in type 1 diabetes. [Oral] In: Proceedings of the American Diabetes Association 70th Annual Scientific Sessions. 2010; Orlando, FL 59(S1):243-OR, 2010. e-Pub 2010.
42. Paterson AD, Waggott D, Shen E, Boright AP, Hosseini, Cleary PA, Lachin JM, Sung L, Bull SB, Research Group TD. 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. e-Pub 2010.
43. 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, Research Group TD. 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. e-Pub 2010.
44. 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, DCCT/EDIC Research Group. Genetic variation at adenylate cyclase 5 (ADCY5) is associated with glycemic control in type 1 diabetes. [Poster] In: Proceedings of the American Diabetes Association 70th Annual Scientific Sessions. 2010; Orlando, FL 59(S1A):LB15, 2010. e-Pub 2010.
45. 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, 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] In: Proceedings of the Canadian Genetic Epidemiology & Statistical Genetics 5th Annual Meeting. King City, ON, Canada, 2010. e-Pub 2010.
46. 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, Research Group TD. 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. e-Pub 2010.
47. 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. [Poster] In: Proceedings of the American Society of Human Genetics 59th Annual Meeting. Honolulu, HI, 2009. e-Pub 2009.
48. 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. [Oral] In: Proceedings of the American Diabetes Association 69th Annual Scientific Sessions. New Orleans, LA 58(S1):A16, 2009. e-Pub 2009.
49. 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. [Poster] In: Proceedings of the American Diabetes Association 69th Annual Scientific Sessions. New Orleans, LA 58(S1):A182, 2009. e-Pub 2009.
50. 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, Group DR. 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. e-Pub 2009.
51. Hosseini SM, Shen E, Waggott D, Boright AP, Sun L, Bull SB, Marcovina SM, Brunzell JD, Paterson AD, Group DR. 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. e-Pub 2009.
52. 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. The American Diabetes Association 69th Annual Scientific Sessions 58(S1):A182, 2009. e-Pub 2009.
53. Hosseini SM, Waggott D, Boright AP, Bull SB, Sun W, Cleary PA, Patterson AD, Group DR. Genome-wide association study of intraocular pressure in 1304 individuals. Proceedings of the American Society of Human Genetics. The American Society of Human Genetics 58th Annual Meeting 58:403, 2008. e-Pub 2008.
54. 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. [Poster] In: Proceedings of the American Society of Human Genetics 58th Annual Meeting. Philadelphia, PA, 2008. e-Pub 2008.
55. Hosseini SM, Héon E. Identification of novel exons and different isoforms for VSX1. Proceedings of the American Society of Human Genetics. The American Society of Human Genetics 55th Annual Meeting 55:214, 2005. e-Pub 2005.
56. Hosseini SM, Héon E. Identification of novel exons and different isoforms for VSX1. [Poster] In: Proceedings of the American Society of Human Genetics 55th Annual Meeting. Salt Lake City, UT, 2005. e-Pub 2005.
57. Hosseini SM, Segev F, Héon E. Anticipation in Fuchs' endothelial corneal dystrophy. [Poster] In: Proceedings of the 15th International Society for Genetic Eye Disease/12th International Retinoblastoma Symposium. Whistler, BC, Canada, 2005. e-Pub 2005.
58. Hosseini SM, Segev F, Héon E. Anticipation in Fuchs' endothelial corneal dystrophy. The 15th International Society for Genetic Eye Disease/12th International Retinoblastoma Symposium, 2005. e-Pub 2005.
59. Hosseini SM, Segev F, Héon E. Anticipation like phenomenon in Fuschs' endothelial corneal dystrophy. [Poster] In: Proceedings of the Association for Research in Vision and Ophthalmology 2005 Annual Meeting. Fort Lauderdale, FL 46(13):4938, 2005. e-Pub 2005.
60. Hosseini SM, Segev F, Héon E. Anticipation like phenomenon in Fuschs' endothelial corneal dystrophy. Investigative Ophthalmology & Visual Science. The Association for Research in Vision and Ophthalmology 2005 Annual Meeting 46, 2005. e-Pub 2005.
61. Hosseini SM, Billingsley G, Segev F, Héon E. COL8A2 mutation in a family with Fuchs' endothelial corneal dystrophy. The Canadian Genetic Disease Network 14th Annual Meeting, 2005. e-Pub 2005.
62. Hosseini SM, Billingsley G, Segev F, Héon E. COL8A2 mutation in a family with Fuchs' endothelial corneal dystrophy. [Poster] In: Proceedings of the Canadian Genetic Disease Network 14th Annual Meeting. Mt. Orford, QC, Canada, 2005. e-Pub 2005.
63. 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. The American Society of Human Genetics 54th Annual Meeting, 2004. e-Pub 2004.
64. Hosseini SM, Herd S, Noordeh N, Panton C, Westfall C, Héon E. Molecular Characterization of Bardet-Biedl Syndrome in a First Nation Dogrib Family. The Canadian Genetic Disease Network 13th Annual Meeting, 2004. e-Pub 2004.
65. Abubaker A, Fournier I, Gupta SK, Ahmed S, Kwon M, Williams MD, Hosseini SM, Zafereo M, Maniakas A. Isthmusectomy for papillary thyroid cancer: a single center experience. American Academy of Otolaryngology - Head and Neck Surgery Foundation 2025 Annual Meeting.
66. Fournier I, Zafereo ME, Wang JR, Banuchi VE, Gross ND, Lango MN, Goepfert RP, Sturgis EM, Graham PH, Grubbs EG, Gupta SK, Cabanillas ME, Busaidy NL, Hu MI, Dadu R, Iyer P, Hamidi S, Kwon M, Ahmed S, Williams MD, Hosseini SM, Maniakas A. Central and lateral lymph node metastasis in papillary thyroid cancer according to primary tumor location. American Academy of Otolaryngology - Head and Neck Surgery Foundation 2025 Annual Meeting.
67. Fournier I, Zafereo ME, Wang JR, Banuchi VE, Gross ND, Lango MN, Goepfert RP, Sturgis EM, Graham PH, Grubbs EG, Gupta SK, Cabanillas ME, Busaidy NL, Hu MI, Dadu R, Iyer P, Hamidi S, Kwon M, Ahmed S, Williams MD, Hosseini SM, Maniakas A. Gender and race disparity in patients undergoing surgery for papillary thyroid cancer. American Academy of Otolaryngology - Head and Neck Surgery Foundation 2025 Annual Meeting.

Books (edited and written)

1. Saboori M, Hadadgar A, Fatehi F, Okhovat H, Nasri P, Hosseini SM, Zandi S, Moeeny A, Assarzadegan M. Ward Book: A Guide to Clinical Learning for Medical Students. IUMS publications, 2003.