Sayed Mohsen Hosseini

Assistant Professor

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    20062023

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    • 2023

      SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing

      Ding, Q., Somerville, C., Manshaei, R., Trost, B., Reuter, M. S., Kalbfleisch, K., Stanley, K., Okello, J. B. A., Hosseini, S. M., Liston, E., Curtis, M., Zarrei, M., Higginbotham, E. J., Chan, A. J. S., Engchuan, W., Thiruvahindrapuram, B., Scherer, S. W., Kim, R. H. & Jobling, R. K., Feb 2023, In: Human genetics. 142, 2, p. 201-216 16 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      2 Scopus citations
    • 2022

      GeneTerpret: a customizable multilayer approach to genomic variant prioritization and interpretation

      Manshaei, R., DeLong, S., Andric, V., Joshi, E., Okello, J. B. A., Dhir, P., Somerville, C., Farncombe, K. M., Kalbfleisch, K., Jobling, R. K., Scherer, S. W., Kim, R. H. & Hosseini, S. M., Dec 2022, In: BMC medical genomics. 15, 1, 31.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      1 Scopus citations
    • 2021

      Diagnostic performance of Milan system for reporting salivary gland cytopathology: A prospective study

      Hosseini, S. M., Resta, I. T. & Baloch, Z. W., Jul 2021, In: Diagnostic Cytopathology. 49, 7, p. 822-831 10 p.

      Research output: Contribution to journalArticlepeer-review

      13 Scopus citations
    • Molecular cytopathology diagnosis of a lung neoplasm: Case report of an unusual non-small cell carcinoma with MET exon 14 skipping mutation

      Hosseini, S. M., Khanafshar, E., Seeley, E. J. & Ruiz-Cordero, R., Jul 2021, In: Diagnostic Cytopathology. 49, 7, p. E258-E261

      Research output: Contribution to journalArticlepeer-review

      1 Scopus citations
    • 2020

      The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease

      Reuter, M. S., Chaturvedi, R. R., Liston, E., Manshaei, R., Aul, R. B., Bowdin, S., Cohn, I., Curtis, M., Dhir, P., Hayeems, R. Z., Hosseini, S. M., Khan, R., Ly, L. G., Marshall, C. R., Mertens, L., Okello, J. B. A., Pereira, S. L., Raajkumar, A., Seed, M., Thiruvahindrapuram, B., & 3 othersScherer, S. W., Kim, R. H. & Jobling, R. K., Jun 1 2020, In: Genetics in Medicine. 22, 6, p. 1015-1024 10 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      48 Scopus citations
    • 2019

      Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot

      Reuter, M. S., Jobling, R., Chaturvedi, R. R., Manshaei, R., Costain, G., Heung, T., Curtis, M., Hosseini, S. M., Liston, E., Lowther, C., Oechslin, E., Sticht, H., Thiruvahindrapuram, B., Mil, S. V., Wald, R. M., Walker, S., Marshall, C. R., Silversides, C. K., Scherer, S. W., Kim, R. H., & 1 othersBassett, A. S., Apr 1 2019, In: Genetics in Medicine. 21, 4, p. 1001-1007 7 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      49 Scopus citations
    • Multiethnic genome-wide association study of diabetic retinopathy using liability threshold modeling of duration of diabetes and glycemic control

      Family Investigation of Nephropathy and Diabetes-Eye Research Group & DCCT/EDIC Research Group, Feb 1 2019, In: Diabetes. 68, 2, p. 441-456 16 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      50 Scopus citations
    • 2018

      Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

      CREAM, 23andMe Research Team & UK Biobank Eye and Vision Consortium, Jun 1 2018, In: Nature Genetics. 50, 6, p. 834-848 15 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      207 Scopus citations
    • Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

      Lionel, A. C., Costain, G., Monfared, N., Walker, S., Reuter, M. S., Hosseini, S. M., Thiruvahindrapuram, B., Merico, D., Jobling, R., Nalpathamkalam, T., Pellecchia, G., Sung, W. W. L., Wang, Z., Bikangaga, P., Boelman, C., Carter, M. T., Cordeiro, D., Cytrynbaum, C., Dell, S. D., Dhir, P., & 35 othersDowling, J. J., Heon, E., Hewson, S., Hiraki, L., Inbar-Feigenberg, M., Klatt, R., Kronick, J., Laxer, R. M., Licht, C., MacDonald, H., Mercimek-Andrews, S., Mendoza-Londono, R., Piscione, T., Schneider, R., Schulze, A., Silverman, E., Siriwardena, K., Snead, O. C., Sondheimer, N., Sutherland, J., Vincent, A., Wasserman, J. D., Weksberg, R., Shuman, C., Carew, C., Szego, M. J., Hayeems, R. Z., Basran, R., Stavropoulos, D. J., Ray, P. N., Bowdin, S., Meyn, M. S., Cohn, R. D., Scherer, S. W. & Marshall, C. R., Apr 1 2018, In: Genetics in Medicine. 20, 4, p. 435-443 9 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      367 Scopus citations
    • Reappraisal of reported genes for sudden arrhythmic death: Evidence-based evaluation of gene validity for brugada syndrome

      Hosseini, S. M., Kim, R., Udupa, S., Costain, G., Jobling, R., Liston, E., Jamal, S. M., Szybowska, M., Morel, C. F., Bowdin, S., Garcia, J., Care, M., Sturm, A. C., Novelli, V., Ackerman, M. J., Ware, J. S., Hershberger, R. E., Wilde, A. A. M. & Gollob, M. H., 2018, In: Circulation. 138, 12, p. 1195-1205 11 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      239 Scopus citations
    • The personal genome project Canada: Findings from whole genome sequences of the inaugural 56 participants

      Reuter, M. S., Walker, S., Thiruvahindrapuram, B., Whitney, J., Cohn, I., Sondheimer, N., Yuen, R. K. C., Trost, B., Paton, T. A., Pereira, S. L., Herbrick, J. A., Wintle, R. F., Merico, D., Howe, J., MacDonald, J. R., Lu, C., Nalpathamkalam, T., Sung, W. W. L., Wang, Z., Patel, R. V., & 33 othersPellecchia, G., Wei, J., Strug, L. J., Bell, S., Kellam, B., Mahtani, M. M., Bassett, A. S., Bombard, Y., Weksberg, R., Shuman, C., Cohn, R. D., Stavropoulos, D. J., Bowdin, S., Hildebrandt, M. R., Wei, W., Romm, A., Pasceri, P., Ellis, J., Ray, P., Meyn, M. S., Monfared, N., Hosseini, S. M., Joseph-George, A. M., Keeley, F. W., Cook, R. A., Fiume, M., Lee, H. C., Marshall, C. R., Davies, J., Hazell, A., Buchanan, J. A., Szego, M. J. & Scherer, S. W., Feb 5 2018, In: CMAJ. 190, 5, p. E126-E136

      Research output: Contribution to journalArticlepeer-review

      Open Access
      47 Scopus citations
    • 2016

      Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium

      The CREAM Consortium, May 13 2016, In: Scientific reports. 6, 25853.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      77 Scopus citations
    • Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

      Fan, Q., Verhoeven, V. J. M., Wojciechowski, R., Barathi, V. A., Hysi, P. G., Guggenheim, J. A., Hohn, R., Vitart, V., Khawaja, A. P., Yamashiro, K., Hosseini, S. M., Lehtimaki, T., Lu, Y., Haller, T., Xie, J., Delcourt, C., Pirastu, M., Wedenoja, J., Gharahkhani, P., Venturini, C., & 134 othersMiyake, M., Hewitt, A. W., Guo, X., Mazur, J., Huffman, J. E., Williams, K. M., Polasek, O., Campbell, H., Rudan, I., Vatavuk, Z., Wilson, J. F., Joshi, P. K., McMahon, G., St Pourcain, B., Evans, D. M., Simpson, C. L., Schwantes-An, T. H., Igo, R. P., Mirshahi, A., Cougnard-Gregoire, A., Bellenguez, C., Blettner, M., Raitakari, O., Kahonen, M., Seppala, I., Zeller, T., Meitinger, T., Ried, J. S., Gieger, C., Portas, L., Van Leeuwen, E. M., Amin, N., Uitterlinden, A. G., Rivadeneira, F., Hofman, A., Vingerling, J. R., Wang, Y. X., Wang, X., Tai-Hui Boh, E., Ikram, M. K., Sabanayagam, C., Gupta, P., Tan, V., Zhou, L., Ho, C. E. H., Lim, WE., Beuerman, R. W., Siantar, R., Tai, E. S., Vithana, E., Mihailov, E., Khor, C. C., Hayward, C., Luben, R. N., Foster, P. J., Klein, B. E. K., Klein, R., Wong, H. S., Mitchell, P., Metspalu, A., Aung, T., Young, T. L., He, M., Parssinen, O., Van Duijn, C. M., Jin Wang, J., Williams, C., Jonas, J. B., Teo, Y. Y., MacKey, D. A., Oexle, K., Yoshimura, N., Paterson, A. D., Pfeiffer, N., Wong, T. Y., Baird, P. N., Stambolian, D., Wilson, J. E. B., Cheng, C. Y., Hammond, C. J., Klaver, C. C. W., Saw, S. M., Rahi, J. S., Korobelnik, J. F., Kemp, J. P., Timpson, N. J., Smith, G. D., Craig, J. E., Burdon, K. P., Fogarty, R. D., Iyengar, S. K., Chew, E., Janmahasatian, S., Martin, N. G., MacGregor, S., Xu, L., Schache, M., Nangia, V., Panda-Jonas, S., Wright, A. F., Fondran, J. R., Lass, J. H., Feng, S., Zhao, J. H., Khaw, K. T., Wareham, N. J., Rantanen, T., Kaprio, J., Pang, C. P., Chen, L. J., Tam, P. O., Jhanji, V., Young, A. L., Doring, A., Raffel, L. J., Cotch, M. F., Li, X., Yip, S. P., Yap, M. K. H., Biino, G., Vaccargiu, S., Fossarello, M., Fleck, B., Yazar, S., Tideman, J. W. L., Tedja, M., Deangelis, M. M., Morrison, M., Farrer, L., Zhou, X., Chen, W., Mizuki, N., Meguro, A. & Makela, K. M., Mar 29 2016, In: Nature communications. 7, 11008.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      103 Scopus citations
    • New locus for skin intrinsic fluorescence in type 1 diabetes also associated with blood and skin glycated proteins

      Roshandel, D., Klein, R., Klein, B. E. K., Wolffenbuttel, B. H. R., Van Der Klauw, M. M., Van Vliet-Ostaptchouk, J. V., Atzmon, G., Ben-Avraham, D., Crandall, J. P., Barzilai, N., Bull, S. B., Canty, A. J., Hosseini, S. M., Hiraki, L. T., Maynard, J., Sell, D. R., Monnier, V. M., Cleary, P. A., Braffett, B. H. & Paterson, A. D., Jul 1 2016, In: Diabetes. 65, 7, p. 2060-2071 12 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      7 Scopus citations
    • Variation in SLC19A3 and protection from microvascular damage in type 1 diabetes

      Porta, M., Toppila, I., Sandholm, N., Hosseini, S. M., Forsblom, C., Hietala, K., Borio, L., Harjutsalo, V., Klein, B. E., Klein, R., Paterson, A. D. & Groop, P. H., Apr 2016, In: Diabetes. 65, 4, p. 1022-1030 9 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      34 Scopus citations
    • 2015

      Genetic studies of body mass index yield new insights for obesity biology

      Lifelines Cohort Study & ADIPOGen Consortium; AGEN-BMI Working Group; CARDIOGRAMplusC4D Consortium; CKDGen Consortium; GLGC; ICBP; MAGIC Investigators; MuTHER Consortium; MIGen Consortium; PAGE Consortium; ReproGen Consortium; GENIE Consortium; International Endogene Consortium, Feb 12 2015, In: Nature. 518, 7538, p. 197-206 10 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      3065 Scopus citations
    • Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

      The CREAM Consortium, Jan 13 2015, In: Human genetics. 134, 2, p. 131-146 16 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      20 Scopus citations
    • New genetic loci link adipose and insulin biology to body fat distribution

      ADIPOGen Consortium; CARDIOGRAMplusC4D Consortium; CKDGen Consortium; GEFOS Consortium; GENIE Consortium; GLGC; ICBP; International Endogene Consortium; LifeLines Cohort Study; MAGIC Investigators; MuTHER Consortium; PAGE Consortium; ReproGen Consortium, Feb 12 2015, In: Nature. 518, 7538, p. 187-196 10 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      1102 Scopus citations
    • The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy

      Hosseini, S. M., Boright, A. P., Sun, L., Canty, A. J., Bull, S. B., Klein, B. E. K., Klein, R. & Paterson, A. D., Jan 13 2015, In: Human genetics. 134, 2, p. 247-257 11 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      60 Scopus citations
    • 2014

      Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci

      Simpson, C. L., Wojciechowski, R., Oexle, K., Murgia, F., Portas, L., Li, X., Virginie, J. M. V., Vitart, V., Schache, M., Mohsen Hosseini, S., Hysi, P. G., Raffel, L. J., Cotch, M. F., Chew, E., Klein, B. E. K., Klein, R., Wong, T. Y., Van Duijn, C. M., Mitchell, P., Saw, S. M., & 397 othersFossarello, M., Wang, J. J., Polašek, O., Campbell, H., Rudan, I., Oostra, B. A., Uitterlinden, A. G., Hofman, A., Rivadeneira, F., Amin, N., Karssen, L. C., Vingerling, J. R., Döring, A., Bettecken, T., Bencic, G., Gieger, C., Wichmann, H. E., Wilson, J. F., Venturini, C., Fleck, B., Cumberland, P. M., Rahi, J. S., Hammond, C. J., Hayward, C., Wright, A. F., Paterson, A. D., Baird, P. N., Klaver, C. C. W., Rotter, J. I., Pirastu, M., Meitinger, T., Bailey-Wilson, J. E., Stambolian, D., Genuth, S., Nathan, D. M., Zinman, B., Crofford, O., Crandall, J., Reid, M., Brown-Friday, J., Engel, S., Sheindlin, J., Martinez, H., Shamoon, H., Engel, H., Phillips, M., Gubitosi-Klug, R., Mayer, L., Pendegast, S., Zegarra, H., Miller, D., Singerman, L., Smith-Brewer, S., Novak, M., Quin, J., Dahms, W., Genuth, S., Palmert, M., Brillon, D., Lackaye, M. E., Kiss, S., Chan, R., Reppucci, V., Lee, T., Heinemann, M., Whitehouse, F., Kruger, D., Jones, J. K., McLellan, M., Carey, J. D., Angus, E., Thomas, A., Galprin, A., Bergenstal, R., Johnson, M., Spencer, M., Morgan, K., Etzwiler, D., Kendall, D., Aiello, L. P., Golden, E., Jacobson, A., Beaser, R., Ganda, O., Hamdy, O., Wolpert, H., Sharuk, G., Arrigg, P., Schlossman, D., Rosenzwieg, J., Rand, L., Nathan, D. M., Larkin, M., Ong, M., Godine, J., Cagliero, E., Lou, P., Folino, K., Fritz, S., Crowell, S., Hansen, K., Gauthier-Kelly, C., Service, J., Ziegler, G., Luttrell, L., Caulder, S., Lopes-Virella, M., Colwell, J., Soule, J., Fernandes, J., Hermayer, K., Kwon, S., Brabham, M., Blevins, A., Parker, J., Lee, D., Patel, N., Pittman, C., Lindsey, P., Bracey, M., Lee, K., Nutaitis, M., Farr, A., Elsing, S., Thompson, T., Selby, J., Lyons, T., Yacoub-Wasef, S., Szpiech, M., Wood, D., Mayfield, R., Molitch, M., Schaefer, B., Jampol, L., Lyon, A., Gill, M., Strugula, Z., Kaminski, L., Mirza, R., Simjanoski, E., Ryan, D., Kolterman, O., Lorenzi, G., Goldbaum, M., Sivitz, W., Bayless, M., Counts, D., Johnsonbaugh, S., Hebdon, M., Salemi, P., Liss, R., Donner, T., Gordon, J., Hemady, R., Kowarski, A., Ostrowski, D., Steidl, S., Jones, B., Herman, W. H., Martin, C. L., Pop-Busui, R., Sarma, A., Albers, J., Feldman, E., Kim, K., Elner, S., Comer, G., Gardner, T., Hackel, R., Prusak, R., Goings, L., Smith, A., Gothrup, J., Titus, P., Lee, J., Brandle, M., Prosser, L., Greene, D. A., Stevens, M. J., Vine, A. K., Bantle, J., Wimmergren, N., Cochrane, A., Olsen, T., Steuer, E., Rath, P., Rogness, B., Hainsworth, D., Goldstein, D., Hitt, S., Giangiacomo, J., Schade, D. S., Ketai, L. H., Chapin, J. E., Braunstein, S., Bourne, P. A., Schwartz, S., Brucker, A., Maschak-Carey, B. J., Baker, L., Orchard, T., Silvers, N., Ryan, C., Songer, T., Doft, B., Olson, S., Bergren, R. L., Lobes, L., Rath, P. P., Becker, D., Rubinstein, D., Conrad, P. W., Yalamanchi, S., Drash, A., Morrison, A., Bernal, M. L., Vaccaro-Kish, J., Malone, J., Pavan, P. R., Grove, N., Iyer, M. N., Burrows, A. F., Tanaka, E. A., Gstalder, R., Dagogo-Jack, S., Wigley, C., Ricks, H., Kitabchi, A., Murphy, M. B., Moser, S., Meyer, D., Iannacone, A., Chaum, E., Yoser, S., Bryer-Ash, M., Schussler, S., Lambeth, H., Raskin, P., Strowig, S., Zinman, B., Barnie, A., Devenyi, R., Mandelcorn, M., Brent, M., Rogers, S., Gordon, A., Palmer, J., Catton, S., Brunzell, J., Wessells, H., de Boer, I. H., Hokanson, J., Purnell, J., Ginsberg, J., Kinyoun, J., Deeb, S., Weiss, M., Meekins, G., Distad, J., Van Ottingham, L., Dupre, J., Harth, J., Nicolle, D., Driscoll, M., Mahon, J., Canny, C., May, M., Lipps, J., Agarwal, A., Adkins, T., Survant, L., Pate, R. L., Munn, G. E., Lorenz, R., Feman, S., White, N., Levandoski, L., Boniuk, I., Grand, G., Thomas, M., Joseph, D. D., Blinder, K., Shah, G., Burgess, B., Santiago, J., Tamborlane, W., Gatcomb, P., Stoessel, K., Taylor, K., Goldstein, J., Novella, S., Mojibian, H., Cornfeld, D., Quin, J., Gaston, P., Palmert, M., Trail, R., Dahms, W., Lachin, J., Cleary, P., Backlund, J., Sun, W., Braffett, B., Klumpp, K., Chan, K., Diminick, L., Rosenberg, D., Petty, B., Determan, A., Kenny, D., Rutledge, B., Younes, N., Dews, W. L., Hawkins, M., Cowie, C., Fradkin, J., Siebert, C., Eastman, R., Danis, R., Gangaputra, S., Neill, S., Davis, M., Hubbard, L., Wabers, H., Burger, M., Dingledine, J., Gama, V., Sussman, R., Steffes, M., Bucksa, J., Nowicki, M., Chavers, B., Polak, J., Harrington, A., Funk, L., Crow, R., Gloeb, B., Thomas, S., O′Donnell, C., Soliman, E., Zhang, Z. M., Prineas, R., Campbell, C., Ryan, C., Sandstrom, D., Williams, T., Geckle, M., Cupelli, E., Thoma, F., Burzuk, B., Woodfill, T., Low, P., Sommer, C., Nickander, K., Budoff, M., Detrano, R., Wong, N., Fox, M., Kim, L., Oudiz, R., Lima, J., Bluemke, D., Turkbey, E., van der Geest, R. J., Liu, C., Malayeri, A., Jain, A., Miao, C., Chahal, H., Jarboe, R., Weir, G., Espeland, M., Manolio, T., Rand, L., Singer, D., Stern, M., Boulton, A. E., Clark, C., D′Agostino, R., Lopes-Virella, M., Garvey, W. T., Lyons, T. J., Jenkins, A., Virella, G., Jaffa, A., Carter, R., Lackland, D., Brabham, M., McGee, D., Zheng, D., Mayfield, R. K., Boright, A., Bull, S., Sun, L., Scherer, S., Zinman, B. & Maynard, J., Sep 18 2014, In: PloS one. 9, 9, e107110.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      38 Scopus citations
    • GWAS identifies an NAT2 acetylator status tag single nucleotide polymorphism to be a major locus for skin fluorescence

      Eny, K. M., Lutgers, H. L., Maynard, J., Klein, B. E. K., Lee, K. E., Atzmon, G., Monnier, V. M., Van Vliet-Ostaptchouk, J. V., Graaff, R., Van Der Harst, P., Snieder, H., Van Der Klauw, M. M., Sell, D. R., Hosseini, S. M., Cleary, P. A., Braffett, B. H., Orchard, T. J., Lyons, T. J., Howard, K., Klein, R., & 6 othersCrandall, J. P., Barzilai, N., Milman, S., Ben-Avraham, D., Wolffenbuttel, B. H. R. & Paterson, A. D., Aug 2014, In: Diabetologia. 57, 8, p. 1623-1634 12 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      30 Scopus citations
    • 2013

      Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

      Consortium for Refractive Error and Myopia (CREAM), The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group & Wellcome Trust Case Control Consortium 2 (WTCCC2), Mar 1 2013, In: Nature Genetics. 45, 3, p. 314-318 5 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      368 Scopus citations
    • 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

      Stambolian, D., Wojciechowski, R., Oexle, K., Pirastu, M., Li, X., Raffe, L. J., Cotch, M. F., Chew, E. Y., Klein, B., Klein, R., Wong, T. Y., Simpson, C. L., Klaver, C. C. W., van Duijn, C. M., Verhoeven, V. J. M., Baird, P. N., Vitart, V., Paterson, A. D., Mitchell, P., Saw, S. M., & 41 othersFossarello, M., Kazmierkiewicz, K., Murgia, F., Portas, L., Schache, M., Richardson, A., Xie, J., Wang, J. J., Rochtchina, E., Viswanathan, A. C., Hayward, C., Wright, A. F., Polašek, O., Campbell, H., Rudan, I., Oostra, B. A., Uitterlinden, A. G., Hofman, A., Rivadeneira, F., Amin, N., Karssen, L. C., Vingerling, J. R., Hosseini, S. M., Döring, A., Bettecken, T., Vatavuk, Z., Gieger, C., Wichmann, H. E., Wilson, J. F., Fleck, B., Foster, P. J., Topouzis, F., McGuffin, P., Sim, X., Inouye, M., Holliday, E. G., Attia, J., Scott, R. J., Rotter, J. I., Meitinger, T. & Bailey-Wilson, J. E., Jul 2013, In: Human molecular genetics. 22, 13, p. 2754-2764 11 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      52 Scopus citations
    • Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation

      Lechner, J., Dash, D. P., Muszynska, D., Hosseini, M., Segev, F., George, S., Frazer, D. G., Moore, J. E., Kaye, S. B., Young, T., Simpson, D. A., Churchill, A. J., Héon, E. & Willoughby, C. E., 2013, In: Investigative Ophthalmology and Visual Science. 54, 5, p. 3215-3223 9 p.

      Research output: Contribution to journalArticlepeer-review

      55 Scopus citations
    • Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

      Cheng, C. Y., Schache, M., Ikram, M. K., Young, T. L., Guggenheim, J. A., Vitart, V., MacGregor, S., Verhoeven, V. J. M., Barathi, V. A., Liao, J., Hysi, P. G., Bailey-Wilson, J. E., St. Pourcain, B., Kemp, J. P., McMahon, G., Timpson, N. J., Evans, D. M., Montgomery, G. W., Mishra, A., Wang, Y. X., & 88 othersWang, J. J., Rochtchina, E., Polasek, O., Wright, A. F., Amin, N., Van Leeuwen, E. M., Wilson, J. F., Pennell, C. E., Van Duijn, C. M., De Jong, P. T. V. M., Vingerling, J. R., Zhou, X., Chen, P., Li, R., Tay, W. T., Zheng, Y., Chew, M., Burdon, K. P., Craig, J. E., Iyengar, S. K., Igo, R. P., Lass, J. H., Chew, E. Y., Haller, T., Mihailov, E., Metspalu, A., Wedenoja, J., Simpson, C. L., Wojciechowski, R., Höhn, R., Mirshahi, A., Zeller, T., Pfeiffer, N., Lackner, K. J., Bettecken, T., Meitinger, T., Oexle, K., Pirastu, M., Portas, L., Nag, A., Williams, K. M., Yonova-Doing, E., Klein, R., Klein, B. E., Hosseini, S. M., Paterson, A. D., Makela, K. M., Lehtimaki, T., Kahonen, M., Raitakari, O., Yoshimura, N., Matsuda, F., Chen, L. J., Pang, C. P., Yip, S. P., Yap, M. K. H., Meguro, A., Mizuki, N., Inoko, H., Foster, P. J., Zhao, J. H., Vithana, E., Tai, E. S., Fan, Q., Xu, L., Campbell, H., Fleck, B., Rudan, I., Aung, T., Hofman, A., Uitterlinden, A. G., Bencic, G., Khor, C. C., Forward, H., Pärssinen, O., Mitchell, P., Rivadeneira, F., Hewitt, A. W., Williams, C., Oostra, B. A., Teo, Y. Y., Hammond, C. J., Stambolian, D., MacKey, D. A., Klaver, C. C. W., Wong, T. Y., Saw, S. M. & Baird, P. N., Aug 8 2013, In: American journal of human genetics. 93, 2, p. 264-277 14 p.

      Research output: Contribution to journalArticlepeer-review

      128 Scopus citations
    • 2012

      Common genetic determinants of intraocular pressure and primary open-angle Glaucoma

      van Koolwijk, L. M. E., Ramdas, W. D., Ikram, M. K., Jansonius, N. M., Pasutto, F., Hysi, P. G., Macgregor, S., Janssen, S. F., Hewitt, A. W., Viswanathan, A. C., ten Brink, J. B., Hosseini, S. M., Amin, N., Despriet, D. D. G., Willemse-Assink, J. J. M., Kramer, R., Rivadeneira, F., Struchalin, M., Aulchenko, Y. S., Weisschuh, N., & 29 othersZenkel, M., Mardin, C. Y., Gramer, E., Welge-Lüssen, U., Montgomery, G. W., Carbonaro, F., Young, T. L., Bellenguez, C., McGuffin, P., Foster, P. J., Topouzis, F., Mitchell, P., Wang, J. J., Wong, T. Y., Czudowska, M. A., Hofman, A., Uitterlinden, A. G., Wolfs, R. C. W., de Jong, P. T. V. M., Oostra, B. A., Paterson, A. D., Mackey, D. A., Bergen, A. A. B., Reis, A., Hammond, C. J., Vingerling, J. R., Lemij, H. G., Klaver, C. C. W. & van Duijn, C. M., May 2012, In: PLoS genetics. 8, 5, e1002611.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      144 Scopus citations
    • New Susceptibility Loci Associated with Kidney Disease in Type 1 Diabetes

      Sandholm, N., Salem, R. M., McKnight, A. J., Brennan, E. P., Forsblom, C., Isakova, T., McKay, G. J., Williams, W. W., Sadlier, D. M., Mäkinen, V. P., Swan, E. J., Palmer, C., Boright, A. P., Ahlqvist, E., Deshmukh, H. A., Keller, B. J., Huang, H., Ahola, A. J., Fagerholm, E., Gordin, D., & 73 othersHarjutsalo, V., He, B., Heikkilä, O., Hietala, K., Kytö, J., Lahermo, P., Lehto, M., Lithovius, R., Österholm, A. M., Parkkonen, M., Pitkäniemi, J., Rosengård-Bärlund, M., Saraheimo, M., Sarti, C., Söderlund, J., Soro-Paavonen, A., Syreeni, A., Thorn, L. M., Tikkanen, H., Tolonen, N., Tryggvason, K., Tuomilehto, J., Wadén, J., Gill, G. V., Prior, S., Guiducci, C., Mirel, D. B., Taylor, A., Hosseini, S. M., Parving, H. H., Rossing, P., Tarnow, L., Ladenvall, C., Alhenc-Gelas, F., Lefebvre, P., Rigalleau, V., Roussel, R., Tregouet, D. A., Maestroni, A., Maestroni, S., Falhammar, H., Gu, T., Möllsten, A., Cimponeriu, D., Ioana, M., Mota, M., Mota, E., Serafinceanu, C., Stavarachi, M., Hanson, R. L., Nelson, R. G., Kretzler, M., Colhoun, H. M., Panduru, N. M., Gu, H. F., Brismar, K., Zerbini, G., Hadjadj, S., Marre, M., Groop, L., Lajer, M., Bull, S. B., Waggott, D., Paterson, A. D., Savage, D. A., Bain, S. C., Martin, F., Hirschhorn, J. N., Godson, C., Florez, J. C., Groop, P. H., Maxwell, A. P. & Böger, C. A., Sep 2012, In: PLoS genetics. 8, 9, e1002921.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      193 Scopus citations
    • Replication analysis for severe diabetic retinopathy

      Grassi, M. A., Tikhomirov, A., Ramalingam, S., Lee, K. E., Mohsen Hosseini, S., Klein, B. E. K., Klein, R., Lussier, Y. A., Cox, N. J. & Nicolae, D. L., Apr 2012, In: Investigative Ophthalmology and Visual Science. 53, 4, p. 2377-2381 5 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      38 Scopus citations
    • 2010

      A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose

      Paterson, A. D., Waggott, D., Boright, A. P., Hosseini, S. M., Shen, E., Sylvestre, M. P., Wong, I., Bharaj, B., Cleary, P. A., Lachin, J. M., Below, J. E., Nicolae, D., Cox, N. J., Canty, A. J., Sun, L. & Bull, S. B., Feb 2010, In: Diabetes. 59, 2, p. 539-549 11 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      98 Scopus citations
    • Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutation

      Nguyen, D. Q., Hosseini, M., Billingsley, G., Héon, E. & Churchill, A. J., Sep 2010, In: Acta Ophthalmologica. 88, 6, p. 695-699 5 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      24 Scopus citations
    • 2009

      Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin

      Paterson, A. D., Lopes-Virella, M. F., Waggott, D., Boright, A. P., Hosseini, S. M., Carter, R. E., Shen, E., Mirea, L., Bharaj, B., Sun, L. & Bull, S. B., Nov 2009, In: Arteriosclerosis, thrombosis, and vascular biology. 29, 11, p. 1958-1967 10 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      165 Scopus citations
    • 2008

      Genetic analysis of chromosome 20-related posterior polymorphous corneal dystrophy: Genetic heterogeneity and exclusion of three candidate genes

      Hosseini, S. M., Herd, S., Vincent, A. L. & Héon, E., Jan 16 2008, In: Molecular Vision. 14, p. 71-80 10 p.

      Research output: Contribution to journalArticlepeer-review

      30 Scopus citations
    • 2006

      CRYBA4, a novel human cataract gene, is also involved in microphthalmia

      Billingsley, G., Santhiya, S. T., Paterson, A. D., Ogata, K., Wodak, S., Hosseini, S. M., Manisastry, S. M., Vijayalakshmi, P., Gopinath, P. M., Graw, J. & Héon, E., Oct 2006, In: American journal of human genetics. 79, 4, p. 702-709 8 p.

      Research output: Contribution to journalArticlepeer-review

      Open Access
      81 Scopus citations