[ sulge aken ]
| Elulookirjeldus (CV) | ||
| 1. | Eesnimi | Ruth |
| 2. | Perekonnanimi | Mikelsaar |
| 3. | Töökoht | TÜ üld- ja molekulaarpatoloogia instituut, inimese bioloogia ja geneetika õppetool (ÜMPI) |
| 4. | Ametikoht | dotsent |
| 5. | Sünniaeg | 11.04.1941 (päev.kuu.aasta) |
| 6. | Haridus | -1966 -lõpetanud Tartu Ülikooli arstiteaduskonna raviosakonna, arst Täiendused: -1974,1977 (4k.) -meditsiinigeneetika alal, Moskva Arstide Täiendusinstituudis -1984,1989 (4näd.)-Vilniuse Meditsiinigeneetika Keskus -1993 (3k.) -teadustöö, Lüübeki Meditsiini Ülikool -1998 (1näd.) -Dresdeni Ülikool, Tehnika Instituut, Kliinilise Geneetika osak. -2000 (3näd.) -koostöö-täiendus Helsingi Ühendlaboratooriumis, molekulaar- ja tsütogeneetika osak. |
| 7. | Teenistuskäik | -1966-1981 -Tartu Vabariiklik Psühhoneuroloogiahaigla, laborijuhataja -1981-1993 -TÜ ÜMPI nooremteadur, teadur -1993-1998 -TÜ ÜMPI vanemteadur, inimese geneetika labori juhataja -alates 1998-TÜ ÜMPI inimese bioloogia ja geneetika õppetooli dotsent, inimese geneetika labori juhataja |
| 8. | Teaduskraad | -1980 -meditsiinikandidaat, Moskva, NSVL MTA Meditsiinigeneetika Instituut(geneetika) eriala) |
| 9. | Teaduskraadi välja andnud asutus, aasta |
-1993 -meditsiinidoktor , Tartu Ülikool |
| 10. | Tunnustused | Ei ole |
| 11. | Teadusorganisatsiooniline ja –administratiivne tegevus |
Olen alljärgnevate rahvusvaheliste seltside liige: - European Society of Human Genetics - European Cytogenetic Association - International Society of Neonatal Screening - Estonian Society of Human Genetics 1996-1999 - TÜ arstiteaduskonna nõukogu liige |
| 12. | Juhendamisel kaitstud väitekirjad |
|
| 13. | Teadustöö põhisuunad | 1) dermatoglüüfika üldpopulatsioonis ja vaimsete haiguste puhul 2) inimese tsütogeneetika: vaimne alaareng, geneetilised sündroomid jt 3) inimese populatsioonigeneetika(vastsündinute skriining, kaasasündinud hüpotüreoos jt.) 4) inimese pärilikud haigused 5) meeste (naiste) infertiilsuse põhjuste uurimine |
| 14. | Jooksvad grandid | 1) Olen grandihoidja: ETF grant nr. 5486 "Vaimse alaarengu ja teiste patoloogiliste seisundite tekkepõhjuste uurimine molekulaarsete ja tsütogeneetiliste meetoditega", kestus 2003-2006. 2) Sihtfinantseeringu põhitäitja: TARMP0421 "Geneetilised ja rakulised haiguste põhjused, rakkude differentseerumine ja tüvirakud teraapias". 2003-2007. |
| 15. | Teaduspublikatsioonid |
Lissitsina Jelena, Punab Margus, Mikelsaar Ruth. Cytogenetic analyses in infertile men. Archives of Andrology 2006;52:91-95 Lissitsina J, Mikelsaar Ruth, Punab M. Kromosoomianomaaliad ja kromosoomivariandid infertiilsetel meestel. Eesti Arst (accepted). Mikelsaar Ruth, Pauklin M, Lissitsina J, Punab M. Reciprocal translocation t(7;16)(q21.2;p13.3) in an infertile man. Fertility and Sterility (accepted) Lissitsina J, Punab M, Mikelsaar Ruth V. Chromosomal analyses in males with azoo- and oligospermia. Abstract of the 5th European Cytogenetic Conference, Madrid, Spain. Chromosome Research 2005;13(Suppl.1):71-72. Mikelsaar Ruth, Lissitsina J, Pauklin M, Punab M. Cytogenetic analyses in infertile males: survey and a case with t(7;16)(q21.2;p13.3). Abstract of the 5th European Cytogenetic Conference, Madrid, Spain. Chromosome Research 2005;13(Suppl.1):57. Mikelsaar Ruth, Roomets E, Pihlau H. New syndrome – chromosome 19q distal deletion syndrome. Abstract of the European Human Genetics Conference 2004, Munich (Saksamaa). European J of Human Genetics 2004;12(Suppl.1):136. Varb K, Mikelsaar Ruth, Lissitsina J. Abielupaaride infertiilsuse tsütogeneetilised põhjused. Eesti Arst 2004;1:3-8. Lissitsina J, Mikelsaar Ruth, Varb K, Punab M. Cytogenetic study in infertile men. Abstract of the 4th European Cytogenetic Conference, Bologna (Italy). Annales De Génétique 2003;185 (P4.18). Mikelsaar Ruth, Vessel E, Mölder H, Punab M. Translocation t(10;15) in a man with pigment dispersion syndrome and infertility. Abstract of the European Human Genetics Conference, Birmingham (Inglismaa). European J of Human Genetics 2003:127 (P303). Lissitsina J, Mikelsaar Ruth, Varb K, Punab M. Chromosomal analyses in infertile men. Abstract of the European Human Genetics Conference 2002, Strasbourg (Prantsusmaa). European J of Human Genetics 2002;10(Suppl.1):160. Mikelsaar Ruth, Muru K, Kulla A, Suvari A. Psoriasis Vulgaris in a Male With Partial Deletion 18p. American J of Medical Genetics 2002;108:252-253. Mikelsaar Ruth, Muru K, Varb K, Kulla A, Suvari A. Partial Deletion 18p in a Patient with Psoriasis Vulgaris. Abstract of the European Human Genetics Conference 2002, Strasbourg (Prantsusmaa). European J of Human Genetics 2002;10(Suppl.1):151. Lissitsina J, Mikelsaar Ruth, Varb K, Timberg G, Punab M. Two cases of extra marker chromosome in infertile men. Abstract of the European Human Genetics Conference 2001, Vienna (Austria). European J of Human Genetics 2001;9(Suppl.1):148. Mikelsaar Ruth. Kromosoomihaigused. 2001,1-137. Mikelsaar Ruth, Salo A, Varb K, Suvari A, Muru K, Teek R. Chromosome analysis in mental retardation. Abstract of the European Human Genetics Conference 2001, Vienna (Austria). European J of Human Genetics 2001;9(Suppl.1):145. Mikelsaar Ruth, Varb K, Suvari A, Schinzel A. Mosaic terminal del(19)(q13.33:) in a girl with seizures and mental retardation. Journal of Medical Genetics 2001;38(1):e2. Mikelsaar Ruth, Varb K, Punab M, Lissitsina J. Extra marker chromosome in an infertile man. Abstract of the European Human Genetics Conference 2000, Amsterdam (The Netherlands). European J of Human Genetics 2000;8(Suppl.1):92. |
viimati muudetud: 10.10.2005
| Curriculum Vitae (CV) | ||
| 1. | First Name | Ruth |
| 2. | Surname | Mikelsaar |
| 3. | Institution | University of Tartu, Faculty of Medicine, Institute of General and Molecular Pathology (IGMP), Department of Human Biology and Genetics |
| 4. | Position | docent, head of Human Genetics Lab |
| 5. | Date of birth | 11.04.1941 (day.month.year) |
| 6. | Education | -1966 -graduated from the Faculty of Medicine of the University of Tartu, physician Studiums: -1974,1977 (4 months) -Institute of Advanced Training Courses, University of Moscow (medical genetics) -1984,1989 (4 weeks) -Vilnius Medical Genetics Centre -1993 (3 months) -scientific work, Medical University of Luebeck (Germany) -1998 (1week) -University of Dresden, Technical Institute, dept. of clinical genetics, -2000 (3weeks) -jointed work-studium, Jointed Laboratories, dept. of molecular and cytogenetics, Helsinki |
| 7. | Research and professional experience |
-1966-1981 -Tartu Republic Psychoneurological Hospital, head of laboratory -1981-1993 -University of Tartu, IGMP researcher -1993-1998 -University of Tartu, IGMP sen. researcher, head of Human Genetics Lab -since 1998 -University of Tartu, IGMP, Department of Human Biology and Genetics, docent, head of Human Genetics Lab |
| 8. | Academic degree | -1980 -Candidate of Medical Sciences, Academy of Medical Sciences U.S.S.R., Moscow (genetics) |
| 9. | Dates and sites of earning the degrees |
-1993 -Doctor of Medical Sciences, University of Tartu |
| 10. | Honours/awards | None |
| 11. | Research-administrative experience |
- Since 1993 head of Human Genetics Lab I am the member of the international societies: - European Society of Human Genetics - European Cytogenetic Association - International Society of Neonatal Screening - Estonian Society of Human Genetics 1996-1999 - the member of the Council of the Faculty of Medicine of the University of Tartu |
| 12. | Supervised dissertations | |
| 13. | Current research program | ) Studies of dermatoglyphics in general population and in mental disorders 2) Human cytogenetics: mental retardation, genetic syndromes etc. 3) Human population genetics (neonatal screening-congenital hypothyroidism etc.) 4) Inherited disorders in human 5) Causes of male (female) infertility |
| 14. | Current grant funding | 1) Principal investigator: ESF grant No 5486 "Studies of causes of mental retardation and other conditions using molecular and cytogenetic methods" 2003-2006 years. 2) Senior personnel of the target financing: TARMP0421 "Genetic and cellular causes of diseases, cell diferentiation and stem cells in therapy". 2003-2007. |
| 15. | List of most important publications |
Lissitsina Jelena, Punab Margus, Mikelsaar Ruth. Cytogenetic analyses in infertile men. Archives of Andrology 2006;52:91-95 Lissitsina J, Mikelsaar Ruth, Punab M. Kromosoomianomaaliad ja kromosoomivariandid infertiilsetel meestel. Eesti Arst (accepted). Mikelsaar Ruth, Pauklin M, Lissitsina J, Punab M. Reciprocal translocation t(7;16)(q21.2;p13.3) in an infertile man. Fertility and Sterility (accepted) Lissitsina J, Punab M, Mikelsaar Ruth V. Chromosomal analyses in males with azoo- and oligospermia. Abstract of the 5th European Cytogenetic Conference, Madrid, Spain. Chromosome Research 2005;13(Suppl.1):71-72. Mikelsaar Ruth, Lissitsina J, Pauklin M, Punab M. Cytogenetic analyses in infertile males: survey and a case with t(7;16)(q21.2;p13.3). Abstract of the 5th European Cytogenetic Conference, Madrid, Spain. Chromosome Research 2005;13(Suppl.1):57. Mikelsaar Ruth, Roomets E, Pihlau H. New syndrome – chromosome 19q distal deletion syndrome. Abstract of the European Human Genetics Conference 2004, Munich (Saksamaa). European J of Human Genetics 2004;12(Suppl.1):136. Varb K, Mikelsaar Ruth, Lissitsina J. Abielupaaride infertiilsuse tsütogeneetilised põhjused. Eesti Arst 2004;1:3-8. Lissitsina J, Mikelsaar Ruth, Varb K, Punab M. Cytogenetic study in infertile men. Abstract of the 4th European Cytogenetic Conference, Bologna (Italy). Annales De Génétique 2003;185 (P4.18). Mikelsaar Ruth, Vessel E, Mölder H, Punab M. Translocation t(10;15) in a man with pigment dispersion syndrome and infertility. Abstract of the European Human Genetics Conference, Birmingham (Inglismaa). European J of Human Genetics 2003:127 (P303). Lissitsina J, Mikelsaar Ruth, Varb K, Punab M. Chromosomal analyses in infertile men. Abstract of the European Human Genetics Conference 2002, Strasbourg (Prantsusmaa). European J of Human Genetics 2002;10(Suppl.1):160. Mikelsaar Ruth, Muru K, Kulla A, Suvari A. Psoriasis Vulgaris in a Male With Partial Deletion 18p. American J of Medical Genetics 2002;108:252-253. Mikelsaar Ruth, Muru K, Varb K, Kulla A, Suvari A. Partial Deletion 18p in a Patient with Psoriasis Vulgaris. Abstract of the European Human Genetics Conference 2002, Strasbourg (Prantsusmaa). European J of Human Genetics 2002;10(Suppl.1):151. Lissitsina J, Mikelsaar Ruth, Varb K, Timberg G, Punab M. Two cases of extra marker chromosome in infertile men. Abstract of the European Human Genetics Conference 2001, Vienna (Austria). European J of Human Genetics 2001;9(Suppl.1):148. Mikelsaar Ruth. Kromosoomihaigused. 2001,1-137. Mikelsaar Ruth, Salo A, Varb K, Suvari A, Muru K, Teek R. Chromosome analysis in mental retardation. Abstract of the European Human Genetics Conference 2001, Vienna (Austria). European J of Human Genetics 2001;9(Suppl.1):145. Mikelsaar Ruth, Varb K, Suvari A, Schinzel A. Mosaic terminal del(19)(q13.33:) in a girl with seizures and mental retardation. Journal of Medical Genetics 2001;38(1):e2. Mikelsaar Ruth, Varb K, Punab M, Lissitsina J. Extra marker chromosome in an infertile man. Abstract of the European Human Genetics Conference 2000, Amsterdam (The Netherlands). European J of Human Genetics 2000;8(Suppl.1):92. |
last updated: 10.10.2005
[ sulge aken ]