91ɫƵ

header-logo
Ophthalmology_Hero Image 2
Elena Semina, PhD

Elena Semina, PhD

Marjorie and Joseph Heil Professor of Ophthalmology & Visual Sciences; Professor, Pediatrics; Professor, Cell Biology, Neurobiology and Anatomy

Contact Information

Education

PhD, National Center for Medical Genetics (Moscow, Russia), 1993
Postdoctoral, Research Centre for Medical Genetics of Russian Academy of Sciences, Moscow, Russia
Postdoctoral, The University of Iowa, Iowa City, Iowa

Research Areas of Interest

  • Animals
  • Aniridia
  • Cataract
  • Child
  • Coloboma
  • Eye Abnormalities
  • Eye Diseases, Hereditary
  • Glaucoma
  • Humans
  • Infant
  • Zebrafish

Research Experience

  • Adult
  • Animals
  • Cataract
  • Child
  • Child, Preschool
  • Eye Diseases, Hereditary
  • Glaucoma
  • Humans
  • Zebrafish

Research Interests

Genes involved in embryonic development, with particular focus on ocular and craniofacial development.

Our research focuses on a broad spectrum of developmental ocular conditions ranging from anophthalmia and microphthalmia to anterior segment dysgenesis, glaucoma, and cataract, both isolated and syndromic. We seek to better understand the mechanisms behind these potentially debilitating conditions through the identification of causative mutations/genes in affected human pedigrees and characterization of their function and molecular pathways in cell and animal models. Characterization of factors involved in human disease leads to better understanding of the processes required for normal embryonic development in humans as well as other species. For families and their clinicians, identification of the disease-causing mutation supplies important information by providing a specific diagnosis, enabling more precise determination of recurrence risks, and identifying associated health risks which may need to be monitored.

Publications

  • (Ceroni F, Cicekdal MB, Holt R, Sorokina E, Chassaing N, Clokie S, Naert T, Talbot LV, Muheisen S, Bax DA, Kesim Y, Kivuva EC, Vincent-Delorme C, Lienkamp SS, Plaisancié J, De Baere E, Calvas P, Vleminckx K, Semina EV, Ragge NK.) Nat Commun. 2024 Oct 26;15(1):9245 PMID: 39455595 PMCID: PMC11511899 SCOPUS ID: 2-s2.0-85207625328 10/26/2024

  • (Reis LM, Zaidman GW, Thompson S, Muheisen S, Glaser T, Semina EV.) Am J Med Genet A. 2024 Oct 25:e63911 PMID: 39450701 SCOPUS ID: 2-s2.0-85207538260 10/25/2024

  • (Reis LM, Seese SE, Costakos D, Semina EV.) Prog Retin Eye Res. 2024 Sep;102:101288 PMID: 39097141 PMCID: PMC11392650 SCOPUS ID: 2-s2.0-85200800135 08/04/2024

  • (Farris J, Khanna C, Smadbeck JB, Johnson SH, Bothun E, Kaplan T, Hoffman F, Polonis K, Oliver G, Reis LM, Semina EV, Rust L, Hoppman NL, Vasmatzis G, Marcou CA, Schimmenti LA, Klee EW.) Am J Med Genet A. 2024 May;194(5):e63542 PMID: 38234180 PMCID: PMC11003841 SCOPUS ID: 2-s2.0-85182427833 01/18/2024

  • (Untaroiu A, Reis LM, Higgins BP, Walesa A, Zacharias S, Nikezic D, Costakos DM, Carroll J, Semina EV.) Invest Ophthalmol Vis Sci. 2024 Apr 01;65(4):20 PMID: 38587439 PMCID: PMC11005067 SCOPUS ID: 2-s2.0-85190399640 04/08/2024

  • (.) . 12/20/2024

  • (Farris J, Khanna C, Smadbeck JB, Johnson SH, Bothun E, Kaplan T, Hoffman F, Polonis K, Oliver G, Reis LM, Semina EV, Rust L, Hoppman NL, Vasmatzis G, Marcou CA, Schimmenti LA, Klee EW.) American Journal of Medical Genetics, Part A. May 2024;194(5) SCOPUS ID: 2-s2.0-85182427833 05/01/2024

  • (Replogle MR, Thompson S, Reis LM, Semina EV.) Human Mutation. 2024;2024 SCOPUS ID: 2-s2.0-85185155859 01/01/2024

  • (Oppermann H, Marcos-Grañeda E, Weiss LA, Gurnett CA, Jelsig AM, Vineke SH, Isidor B, Mercier S, Magnussen K, Zacher P, Hashim M, Pagnamenta AT, Race S, Srivastava S, Frazier Z, Maiwald R, Pergande M, Milani D, Rinelli M, Levy J, Krey I, Fontana P, Lonardo F, Riley S, Kretzer J, Rankin J, Reis LM, Semina EV, Reuter MS, Scherer SW, Iascone M, Weis D, Fagerberg CR, Brasch-Andersen C, Hansen LK, Kuechler A, Noble N, Gardham A, Tenney J, Rathore G, Beck-Woedl S, Haack TB, Pavlidou DC, Atallah I, Vodopiutz J, Janecke AR, Hsieh TC, Lesmann H, Klinkhammer H, Krawitz PM, Lemke JR, Jamra RA, Nieto M, Tümer Z, Platzer K.) Eur J Hum Genet. 2023 Nov;31(11):1251-1260 PMID: 37644171 PMCID: PMC10620399 SCOPUS ID: 2-s2.0-85168862554 08/30/2023

  • (Reis LM, Amor DJ, Haddad RA, Nowak CB, Keppler-Noreuil KM, Chisholm SA, Semina EV.) Genes (Basel). 2023 Oct 17;14(10) PMID: 37895297 PMCID: PMC10606241 SCOPUS ID: 2-s2.0-85175276734 10/28/2023

  • (Reis LM, Atilla H, Kannu P, Schneider A, Thompson S, Bardakjian T, Semina EV.) Genes (Basel). 2023 Jan 14;14(1) PMID: 36672956 PMCID: PMC9859058 SCOPUS ID: 2-s2.0-85146756040 01/22/2023

  • (Oppermann H, Marcos-Grañeda E, Weiss LA, Gurnett CA, Jelsig AM, Vineke SH, Isidor B, Mercier S, Magnussen K, Zacher P, Hashim M, Pagnamenta AT, Race S, Srivastava S, Frazier Z, Maiwald R, Pergande M, Milani D, Rinelli M, Levy J, Krey I, Fontana P, Lonardo F, Riley S, Kretzer J, Rankin J, Reis LM, Semina EV, Reuter MS, Scherer SW, Iascone M, Weis D, Fagerberg CR, Brasch-Andersen C, Hansen LK, Kuechler A, Noble N, Gardham A, Tenney J, Rathore G, Beck-Woedl S, Haack TB, Pavlidou DC, Atallah I, Vodopiutz J, Janecke AR, Hsieh TC, Lesmann H, Klinkhammer H, Krawitz PM, Lemke JR, Jamra RA, Nieto M, Tümer Z, Platzer K.) European Journal of Human Genetics. November 2023;31(11):1251-1260 SCOPUS ID: 2-s2.0-85168862554 11/01/2023