Külliki Krabbi

https://www.etis.ee/CV/Külliki_Krabbi/est
17.01.1979
+372 5151857
+31 (0)104333095
kyllikrabbi@gmail.com

Teenistuskäik

Töökohad ja ametid
22.01.2001–31.07.2011   
Terviseamet, vanemspetsialist (1,00)
 
 
Haridustee
2003–2012   
Tallinna Tehnikaülikool, doktorantuur (keemia- ja geenitehnoloogia)
2001–2003   
Tallinna Tehnikaülikool, magistriõpe (keemia- ja materjaliteadus)
1997–2001   
Tallinna Tehnikaülikool, bakalaureuseõpe (bio- ja toiduainete tehnoloogia)
 
 
Teadusorganisatsiooniline ja -administratiivne tegevus
2007−...   
Baltic Metabolic Group liige

Kvalifikatsioon

Teaduskraadid
Külliki Krabbi, doktorikraad, 2012, (juh) Katrin Õunap; Tiiu-Maie Laht, Biochemical diagnosis of classical galactosemia and mucopolysaccharidoses in Estonia (Klassikalise galaktoseemia ja mukopolüsahharidooside biokeemiline diagnostika Eestis), Tallinna Tehnikaülikool, Matemaatika-loodusteaduskond, Keemiainstituut.
Külliki Krabbi, magistrikraad (teaduskraad), 2003, (juh) Mihkel Kaljurand; Tiiu-Maie Laht, Mõnede ainevahetushaiguste biomarkerite kromatograafiline identifitseerimine inimese kehavedelikes., Tallinna Tehnikaülikool, Matemaatika-loodusteaduskond, Keemiainstituut, Biotehnoloogia õppetool.
 
 
Teadustöö põhisuunad
VALDKOND: 3. Terviseuuringud; 3.11. Terviseuuringutega seotud uuringud, näiteks biokeemia, geneetika, mikrobioloogia, biotehnoloogia, molekulaarbioloogia, rakubioloogia, biofüüsika ja bioinformaatika; CERCS ERIALA: B190 Kliiniline keemia
VALDKOND: 4. Loodusteadused ja tehnika; 4.11. Keemia ja keemiatehnika; CERCS ERIALA: P300 Analüütiline keemia

Publikatsioonid

Klass
Aasta
Publikatsioon
 
1.1.
2012
Krabbi, K.; Joost, K.; Zordania, R.; Talvik, I.; Rein, R.; Huijmans, J. G. M.; Verheijen, F. V.; Õunap, K (2012). The live-birth prevalence of mucopolysaccharidoses in Estonia. Genetic Testing and Molecular Biomarkers, 16 (8), 846−849.10.1089/gtmb.2011.0307.
2.3.
2012
Krabbi, K.. (2012). Biochemical diagnosis of classical galactosemia and mucopolysaccharidoses in Estonia. (Doktoritöö). Tallinna Tehnikaülikooli Kirjastus.
1.1.
2011
Krabbi, K.; Uudelepp, M.-L.; Joost, K.; Zordania, R.; Õunap, K. (2011). Long-term complications in Estonian galactosemia patients with a less strict lactose-free diet and metabolic control. Molecular Genetics and Metabolism, 103 (3), 249−253.10.1016/j.ymgme.2011.03.023.
5.2.
2011
Kall, Kristina; Krabbi, Külliki; Laht, Tiiu-Maie; Joost, Kairit; Õunap, Katrin (2011). Biochemical changes in patients with pyruvate dehydrogenase deficiency. Journal of Inherited Metabolic Disease, 34: Society for the Study of Inborn Errors of Metabolism Annual Symposium, Geneva, Switzerland, 30.08.-02.09.2011. Toim. Brown, Garry; Hoffmann, Georg F. Springer, 167−167.
5.2.
2011
Krabbi, K.; Uudelepp, M.-L.; Rein, R.; Kahre, T.; Õunap, K. (2011). Infantile hypolactasia: a case with challenging diagnosis. Journal of Inherited Metabolic Disease, 34: SSIEM Annual symposium, Genf, Šveits, 30.08.-02.09.2011. x, x. (Supplement 1).
1.1.
2010
Õunap, K.; Joost, K.; Temberg, T.; Krabbi, K.; Tõnisson, N. (2010). Classical galactosemia in Estonia: selective neonatal screening, incidence, and genotype/phenotype data of diagnosed patients. Journal of Inherited Metabolic Disease, 33 (2), 175−176.10.1007/s10545-010-9045-2.
5.1.
2009
Kall, Kristina; Krabbi, Külliki; Laht, Tiiu-Maie; Joost, Kairit; Õunap, Katrin (2009). Laboratory diagnostics of mitochondrial disorders using GC/MS organic acid and LC amino acid profiles. MOLECULAR GENETICS AND METABOLISM, 98: 11th International Conference of Inborn Errors of Metabolism, San Diego, CA, AUG 29-SEP 02, 2009. SAN DIEGO: Elsevier, 97−97.10.1016/j.ymgme.2009.07.007.
5.2.
2008
Õunap, K.; Joost, K.; Kall, K.; Krabbi, K.; Laht, TM.; Zordania, R. (2008). The diagnostics of inherited metabolic diseases in Estonia. Laboratorine Medicina: 9th Baltic Congress of Laboratory Medicine; September 18-20 2008. 17−18. (10).
5.2.
2008
Krabbi, K.; Kall, K.; Laht, T.-M.; Õunap, K.; Joost, K.; Zordania, R. (2008). Galactosemia patients in Estonia, 15 years of selective screening. Journal of Inherited Metabolic Disease, 31 S1: SSIEM Annual Symposium; Lisboa, Portugal; 2-5 September 2008. Ed. Zschocke, J.; Hoffmann, G.; Brown, G.; Gibson, K.M. Springer, 45.
12.04.2019

Külliki Krabbi

https://www.etis.ee/CV/Külliki_Krabbi/eng
17.01.1979
+372 5151857
+31 (0)104333095
kyllikrabbi@gmail.com

Career

Institution(s) and position(s)
22.01.2001–31.07.2011   
Health Board, senior specialist (1,00)
 
 
Education
2003–2012   
Tallinn University of Technology, PhD student (chemistry-and geene technology)
2001–2003   
Tallinn University of Technology, MSc study (chemistry-and material science)
1997–2001   
Tallinn University of Technology, BSc study (bio-and food technology)
 
 
R&D related managerial and administrative work
2007−...   
Baltic Metabolic Group member

Qualifications

Academic degrees
Külliki Krabbi, Doctor's Degree, 2012, (sup) Katrin Õunap; Tiiu-Maie Laht, Biochemical diagnosis of classical galactosemia and mucopolysaccharidoses in Estonia, Tallinn University of Technology Faculty of Science, Department of Chemistry.
Külliki Krabbi, Master's Degree, 2003, (sup) Mihkel Kaljurand; Tiiu-Maie Laht, Mõnede ainevahetushaiguste biomarkerite kromatograafiline identifitseerimine inimese kehavedelikes. (Chromatographic identification of some biomarkers of metabolic diseases in human body fluids), Tallinn University of Technology Faculty of Science, Department of Chemistry, Chair of Biotechnology.
 
 
Field of research
FIELD OF RESEARCH: 3. Health; 3.11. Biochemistry, Genetics, Microbiology, Biotechnology, Molecular Biology, Cell Biology, Biophysics and Bioinformatics relating to Health Studies; CERCS SPECIALITY: B190 Clinical chemistry
FIELD OF RESEARCH: 4. Natural Sciences and Engineering; 4.11. Chemistry and Chemical Technology; CERCS SPECIALITY: P300 Analytical chemistry

Publications

Category
Year
Publication
 
1.1.
2012
Krabbi, K.; Joost, K.; Zordania, R.; Talvik, I.; Rein, R.; Huijmans, J. G. M.; Verheijen, F. V.; Õunap, K (2012). The live-birth prevalence of mucopolysaccharidoses in Estonia. Genetic Testing and Molecular Biomarkers, 16 (8), 846−849.10.1089/gtmb.2011.0307.
2.3.
2012
Krabbi, K.. (2012). Biochemical diagnosis of classical galactosemia and mucopolysaccharidoses in Estonia. (Doktoritöö). Tallinna Tehnikaülikooli Kirjastus.
1.1.
2011
Krabbi, K.; Uudelepp, M.-L.; Joost, K.; Zordania, R.; Õunap, K. (2011). Long-term complications in Estonian galactosemia patients with a less strict lactose-free diet and metabolic control. Molecular Genetics and Metabolism, 103 (3), 249−253.10.1016/j.ymgme.2011.03.023.
5.2.
2011
Kall, Kristina; Krabbi, Külliki; Laht, Tiiu-Maie; Joost, Kairit; Õunap, Katrin (2011). Biochemical changes in patients with pyruvate dehydrogenase deficiency. Journal of Inherited Metabolic Disease, 34: Society for the Study of Inborn Errors of Metabolism Annual Symposium, Geneva, Switzerland, 30.08.-02.09.2011. Toim. Brown, Garry; Hoffmann, Georg F. Springer, 167−167.
5.2.
2011
Krabbi, K.; Uudelepp, M.-L.; Rein, R.; Kahre, T.; Õunap, K. (2011). Infantile hypolactasia: a case with challenging diagnosis. Journal of Inherited Metabolic Disease, 34: SSIEM Annual symposium, Genf, Šveits, 30.08.-02.09.2011. x, x. (Supplement 1).
1.1.
2010
Õunap, K.; Joost, K.; Temberg, T.; Krabbi, K.; Tõnisson, N. (2010). Classical galactosemia in Estonia: selective neonatal screening, incidence, and genotype/phenotype data of diagnosed patients. Journal of Inherited Metabolic Disease, 33 (2), 175−176.10.1007/s10545-010-9045-2.
5.1.
2009
Kall, Kristina; Krabbi, Külliki; Laht, Tiiu-Maie; Joost, Kairit; Õunap, Katrin (2009). Laboratory diagnostics of mitochondrial disorders using GC/MS organic acid and LC amino acid profiles. MOLECULAR GENETICS AND METABOLISM, 98: 11th International Conference of Inborn Errors of Metabolism, San Diego, CA, AUG 29-SEP 02, 2009. SAN DIEGO: Elsevier, 97−97.10.1016/j.ymgme.2009.07.007.
5.2.
2008
Õunap, K.; Joost, K.; Kall, K.; Krabbi, K.; Laht, TM.; Zordania, R. (2008). The diagnostics of inherited metabolic diseases in Estonia. Laboratorine Medicina: 9th Baltic Congress of Laboratory Medicine; September 18-20 2008. 17−18. (10).
5.2.
2008
Krabbi, K.; Kall, K.; Laht, T.-M.; Õunap, K.; Joost, K.; Zordania, R. (2008). Galactosemia patients in Estonia, 15 years of selective screening. Journal of Inherited Metabolic Disease, 31 S1: SSIEM Annual Symposium; Lisboa, Portugal; 2-5 September 2008. Ed. Zschocke, J.; Hoffmann, G.; Brown, G.; Gibson, K.M. Springer, 45.
12.04.2019
Detailne otsing
  • Leitud 2 kirjet
ProgrammLiikNumberNimiProjekti algusProjekti lõppVastutav täitjaAsutusFinantseerijapoolne rahastamine
SFSF0142497s03Postgenoomne protsessidisain toidu- ja keskkonnabiotehnoloogias01.01.200331.12.2007Raivo ViluTallinna Tehnikaülikool, Matemaatika-loodusteaduskond348 925,64 EUR
SFSF0140090s08Toidu süsteemibioloogia ja füüsika01.01.200831.12.2013Toomas PaalmeTallinna Tehnikaülikool, Keemia ja materjalitehnoloogia teaduskond705 093,40 EUR