+3727319485
mari-liis.uudelepp@kliinikum.ee

Career

Institution(s) and position(s)
01.09.2012–...   
University of Tartu, Faculty of Medicine, Institute of Biomedicine, Chair of Human Biology and Genetics, resident in medical genetics (1,00)
01.09.2012–...   
Tartu University Hospital, United Laboratories of Tartu University Hospital, Department of Genetics, pediatrician (0,20)
01.09.2009–31.08.2012   
Tartu University Hospital, United Laboratories of Tartu University Hospital, Department of Genetics, pediatrician (1,00)
01.09.2005–31.08.2009   
University of Tartu, Faculty of Medicine, Department of Pediatrics, Chair of Paediatrics, resident in pediatrics (0,80)
 
 
Education
2013–2013   
Children's Hospital Colorado Metabolic University 101 - course on dietic treatment of inherited metabolic diseases, Denver, CO, U.S.A.
2011–2011   
Society for the Study of Inborn Errors of Metabolism (SSIEM) Academy 2011 on metabolic diseases, Amsterdam, Netherlands
2007–2007   
American Austrian Foundation and Open Medical Insitute, Pediatric Emergency Medicine and Pediatric Advanced Life Support Course, Salzburg, Austria
1999–2005   
University of Tartu, Faculty of Medicine
 
 
R&D related managerial and administrative work
2012−...   
Society for the Study of Inborn Errors of Metabolism (SSIEM) - member
2010−...   
Baltic Metabolic Group - member
2010−...   
European Union Network of Experts on Newborn Screening (EUNENBS) - member
2010−...   
International Society of Newborn Screening (ISNS) - member
2009−...   
Estonian Phenylketonuria Association - member
2005−...   
Estonian Doctors’ Association - member
2005−...   
Estonian Pediatric Association - member
 
 
Additional career information
Languages: Estonian- Native, English – Fluent, Russian, Finnish – Good, German – Basic;

Qualifications

Field of research
FIELD OF RESEARCH: 3. Health; 3.7. Clinical Medicine; CERCS SPECIALITY: B660 Pediatrics ; SPECIALITY: Medical genetics

Publications

Category
Year
Publication
 
1.1.
2012
1.3.
2012
5.2.
2012
1.1.
2011
5.2.
2011
3.5.
2010
5.2.
2010
5.2.
2010
5.2.
2010
1.3.
2009
5.2.
2008
1.3.
2006
22.04.2019
21.08.1981
+3727319485
mari-liis.uudelepp@kliinikum.ee

Teenistuskäik

Töökohad ja ametid
01.09.2012–...   
Tartu Ülikool, Arstiteaduskond, Biomeditsiini instituut, Inimese bioloogia ja geneetika õppetool, meditsiinigeneetika eriala arst-resident (1,00)
01.09.2012–...   
SA Tartu Ülikooli Kliinikum, Tartu Ülikooli Klliinikumi ühendlabor, Geneetikakeskuse pediaater (0,20)
01.09.2009–31.08.2012   
SA Tartu Ülikooli Kliinikum, Tartu Ülikooli Klliinikumi ühendlabor, Geneetikakakeskuse pediaater (1,00)
01.09.2005–31.08.2009   
Tartu Ülikool, Arstiteaduskond, Lastekliinik, Pediaatria õppetool, pediaatria eriala arst-resident (0,80)
 
 
Haridustee
2013–2013   
Colorado Lastehaigla harvaesinevate pärilike ainevahetushaiguste dieetravi alane täienduskursus Metabolic University 101, Denver, Colorado, Ameerika Ühendriigid
2011–2011   
Rahvusvahelise Ainevahetushaiguste Assotsiatsiooni harvaesinevate pärilike ainevahetushaiguste alane täienduskursus, Amsterdam, Holland
2007–2007   
American Austrian Foundation and Open Medical Insitute Laste erakorralise meditsiini alane täienduskursus, Salzburg, Austria
1999–2005   
Tartu Ülikool, Arstiteaduskond
 
 
Teadusorganisatsiooniline ja -administratiivne tegevus
2012−...   
Rahvusvaheline Ainevahetushaiguste Assotsiatsioon (SSIEM) - liige
2010−...   
Balti Metaboolsete Haiguste Grupp - liige
2010−...   
Euroopa Liidu vastsündinute skriiningu alane ekspertkomisjon (EUNENBS) - liige
2010−...   
Rahvusvaheline Vastsündinute Skriiningu Assotsiatsioon (ISNS) - liige
2009−...   
Eesti Fenüülketonuuria Ühing - liige
2005−...   
Eesti Arstide Liit - liige
2005−...   
Eesti Lastearstide Selts - liige
 
 
Teenistuskäigu lisainfo
Keelteoskus: eesti k - emakeel; inglise k - väga hea; vene k - suhtlustasandil; soome keel - hea; saksa keel - kesktase;

Kvalifikatsioon

Teadustöö põhisuunad
VALDKOND: 3. Terviseuuringud; 3.7. Kliiniline meditsiin; CERCS ERIALA: B660 Pediaatria ; PÕHISUUND: Kliiniline geneetika

Publikatsioonid

Klass
Aasta
Publikatsioon
 
1.1.
2012
1.3.
2012
5.2.
2012
1.1.
2011
5.2.
2011
3.5.
2010
5.2.
2010
5.2.
2010
5.2.
2010
1.3.
2009
5.2.
2008
1.3.
2006
22.04.2019
  • Found 13 results
PublicationAuthorsYearSource titleClassificationFileInstitutions
Smoking-Induced Expression of the GPR15 Gene Indicates Its Potential Role in the Chronic Inflammatory PathologiesKõks, Gea; Uudelepp, Mari-Liis; Limbach, Maia; Peterson, Pärt; Reimann, Ene; Kõks, Sulev2015The American journal of pathology1.1.Estonian University of Life Sciences, Institute of Veterinary Medicine and Animal Sciences;
University of Tartu, Faculty of Medicine, Institute of Biomedicine and Translational Medicine;
Competence Centre on Health Technologies
Prevalence of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency in EstoniaJoost, K.; Õunap, K.; Žordania, R.; Uudelepp, M.-L.; Olsen, R.K.; Kall, K.; Kilk, K.; Soomets, U.; Kahre, T.2012JIMD Reports1.1.University of Tartu, Faculty of Medicine, Department of Pediatrics, Chair of Paediatrics;
Solis BioDyne Ltd;
Tartu University Hospital, United Laboratories of Tartu University Hospital;
University of Tartu, Faculty of Medicine, Department of Biochemistry;
University of Tartu, Faculty of Medicine, Institute of Biomedicine, Chair of Human Biology and Genetics
Fenüülketonuuria Eesti ravijuhend Uudelepp, ML.; Joost, K.; Žordania, R.; Õunap, K.2012Eesti Arst1.3.Tartu University Hospital, United Laboratories of Tartu University Hospital
Dietic management of premature infant born at 30 gestational weeks with classical phenylketonuriaUudelepp, ML.; Vals, MA.; Kallas, E.; Päärson, K.; Joost, K.; Õunap, K.2012Journal of Inherited Metabolic Disease, 35 (Supplement 1)5.2.Tartu University Hospital, United Laboratories of Tartu University Hospital;
Tartu University Hospital;
Tartu University Hospital, Children's Clinic of Tartu University Hospital;
University of Tartu, Faculty of Medicine, Department of Pediatrics, Chair of Paediatrics
Long-term complications in Estonian galactosemia patients with a less strict lactose-free diet and metabolic control Krabbi, K.; Uudelepp, M.-L.; Joost, K.; Zordania, R.; Õunap, K.2011Molecular Genetics and Metabolism1.1.Health Board;
Tallinn University of Technology , Faculty of Science, Department of Chemistry, Chair of Biotechnology;
Tallinn Children Hospital;
University of Tartu, Faculty of Medicine, Department of Pediatrics;
Tartu University Hospital, United Laboratories of Tartu University Hospital;
University of Tartu, Faculty of Medicine, Centre of Molecular and Clinical Medicine
Infantile hypolactasia: a case with challenging diagnosisKrabbi, K.; Uudelepp, M.-L.; Rein, R.; Kahre, T.; Õunap, K.2011Journal of Inherited Metabolic Disease5.2.University of Tartu, Faculty of Medicine, Department of Pediatrics, Chair of Paediatrics;
Health Board;
Solis BioDyne Ltd;
Tartu University Hospital, United Laboratories of Tartu University Hospital;
University of Tartu, Faculty of Medicine, Institute of Biomedicine, Chair of Human Biology and Genetics
Eesti fenüülketonuuriaga patsientide potsensiaalne tetrahüdrobiopteriinitundlikkus genotüübi-fenotüübi analüüsi aluselUudelepp, ML.; Õunap, K.; Joost, K.; Kerna, I.; Tõnisson, N.2010Eesti Arst, 89 (Lisa1)3.5.Tartu University Hospital, United Laboratories of Tartu University Hospital;
Tartu University Hospital
Pika ahelaga hüdroksü-atsüül CoA dehüdrogenaasi defitsiidi esinemine EestisJoost, K; Kahre, T; Kilk, K; Uudelepp, M-L; Soomets, U; Õunap, K.2010Eesti Arst5.2.University of Tartu, Faculty of Medicine, Department of Pediatrics, Chair of Paediatrics;
University of Tartu, Faculty of Medicine, Department of Biochemistry;
University of Tartu, Faculty of Medicine, Department of Obstetrics and Gynecology, Chair of Obstetrics and Gynaecology;
Tartu University Hospital, United Laboratories of Tartu University Hospital;
University of Tartu, Faculty of Medicine, Institute of Biomedicine, Chair of Human Biology and Genetics
Pika ahelaga rasvhapete oksüdatsiooni defekt 1-aastasel lapsel. Haigusjuhu kirjeldusMüürsepp, P.; Tamm, E.; Joost, K.; Kahre, T.; Uudelepp, M.i-L.; Vainumäe, I.; Õunap, K.2010Eesti Arst5.2.University of Tartu, Faculty of Medicine, Department of Pediatrics, Chair of Paediatrics;
University of Tartu, Faculty of Medicine, Department of Obstetrics and Gynecology, Chair of Obstetrics and Gynaecology;
Tartu University Hospital, United Laboratories of Tartu University Hospital;
Tartu University Hospital, Children's Clinic of Tartu University Hospital;
University of Tartu;
University of Tartu, Faculty of Medicine, Institute of Biomedicine, Chair of Human Biology and Genetics
The analysis of genotype and phenotype of Estonian phenylketonuria patients for finding out potentially BH4-responsive formsUudelepp, ML.; Joost, K.; Kerna, I.; Tõnisson, N.; Õunap, K.2010European Journal of Human Genetics, 18 (Supplement 1)5.2.Tartu University Hospital, United Laboratories of Tartu University Hospital;
Tartu University Hospital
Kawasaki haigus Eestis aastatel 2002-2007Laan, M.; Plado, S.; Uudelepp, ML.; Jalas, T.; Tamm, E.2009Eesti Arst1.3.Tartu University Hospital, Children's Clinic of Tartu University Hospital;
University of Tartu
Bacterial meningitis in children in Estonia in 1980-1989 and 1998-2007Uudelepp, ML.; Tamm, E.; Torm, S.; Urbsoo, K.; Pruunsild, K.; Part, R.; Lutsar, I.20085.2.University of Tartu, Faculty of Medicine, Department of Microbiology, Chair of Medical Microbiology and Virology;
University of Tartu, Faculty of Medicine, Institute of Biomedicine, Chair of Human Biology and Genetics;
Tartu University Hospital, United Laboratories of Tartu University Hospital
Haigusjuht: haruldane suhkruhaigus MODY 2Uudelepp, M-L.; Kohtka, K.; Tillmann, V.2006Eesti Arst1.3.Tartu University Hospital;
Tartu University Hospital, Children's Clinic of Tartu University Hospital;
University of Tartu, Faculty of Medicine, Institute of Biomedicine, Chair of Human Biology and Genetics;
Tartu University Hospital, United Laboratories of Tartu University Hospital