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Душан Кецкаревић — разлика између измена

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Ред 24: Ред 24:


'''M21- Рад у врхунском међународном часопису'''
'''M21- Рад у врхунском међународном часопису'''
# Kecmanović M, Jović N, Keckarević-Marković M, Keckarević D, Stevanović G, Ignjatović P, Romac S. (2016). Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin. {{cite journal|author=|title=|journal=|date=Clin Genet|volume=89 |issue=1 |pages=104–8|title= Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin|journal= Clinical Genetics|date= 2016|volume=89|issue=1|pages=104–108|doi=10.1111/cge.12570|last1= Kecmanović|first1= M.|last2= Jović|first2= N.|last3= Keckarević‐Marković|first3= M.|last4= Keckarević|first4= D.|last5= Stevanović|first5= G.|last6= Ignjatović|first6= P.|last7= Romac|first7= S.|pmid= 25683376|s2cid= 7451265}}
* {{cite journal|title= Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin|journal= Clinical Genetics|date= 2016|volume=89|issue=1|pages=104–108|doi=10.1111/cge.12570|last1= Kecmanović|first1= M.|last2= Jović|first2= N.|last3= Keckarević‐Marković|first3= M.|last4= Keckarević|first4= D.|last5= Stevanović|first5= G.|last6= Ignjatović|first6= P.|last7= Romac|first7= S.|pmid= 25683376|s2cid= 7451265}}
# Gagic M*, Keckarević Marković M* {{cite journal|last1= Gagic|first1= Milica|title= Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats|journal= Clinical Chemistry and Laboratory Medicine (CCLM)|date= 2016|volume=54|issue=5|pages=773–780|doi=10.1515/cclm-2015-0602|last2= Markovic|first2= Milica Keckarevic|last3= Kecmanovic|first3= Miljana|last4= Keckarevic|first4= Dusan|last5= Mladenovic|first5= Jelena|last6= Dackovic|first6= Jelena|last7= Milic-Rasic|first7= Vedrana|last8= Romac|first8= Stanka|pmid= 26479344|s2cid= 10092814|title= Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats|journal= Clinical Chemistry and Laboratory Medicine (CCLM)|date= 2016|volume=54|issue=5|pages=773–780|doi=10.1515/cclm-2015-0602|last1= Gagic|first1= Milica|last2= Markovic|first2= Milica Keckarevic|last3= Kecmanovic|first3= Miljana|last4= Keckarevic|first4= Dusan|last5= Mladenovic|first5= Jelena|last6= Dackovic|first6= Jelena|last7= Milic-Rasic|first7= Vedrana|last8= Romac|first8= Stanka|pmid= 26479344|s2cid= 10092814}}
* {{cite journal|title= Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats|journal= Clinical Chemistry and Laboratory Medicine (CCLM)|date= 2016|volume=54|issue=5|pages=773–780|doi=10.1515/cclm-2015-0602|last1= Gagic|first1= Milica|last2= Markovic|first2= Milica Keckarevic|last3= Kecmanovic|first3= Miljana|last4= Keckarevic|first4= Dusan|last5= Mladenovic|first5= Jelena|last6= Dackovic|first6= Jelena|last7= Milic-Rasic|first7= Vedrana|last8= Romac|first8= Stanka|pmid= 26479344|s2cid= 10092814}}
* {{cite journal|last1= Keckarević|first1= Dušan|title= A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression|journal= Amyotrophic Lateral Sclerosis|date= 2012|volume=13|issue=2|pages=237–240|doi=10.3109/17482968.2011.627588|last2= Stević|first2= Zorica|last3= Keckarević-Marković|first3= Milica|last4= Kecmanović|first4= Miljana|last5= Romac|first5= Stanka|pmid= 22214314|s2cid= 13341057}}
* {{cite journal|last1= Keckarević|first1= Dušan|title= A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression|journal= Amyotrophic Lateral Sclerosis|date= 2012|volume=13|issue=2|pages=237–240|doi=10.3109/17482968.2011.627588|last2= Stević|first2= Zorica|last3= Keckarević-Marković|first3= Milica|last4= Kecmanović|first4= Miljana|last5= Romac|first5= Stanka|pmid= 22214314|s2cid= 13341057}}
* {{cite journal|last1= Keckarevic-Markovic|first1= Milica|title= Mutational analysis of ''GJB1'' , ''MPZ'' , ''PMP22'' , ''EGR2'' , and ''LITAF/SIMPLE'' in Serbian Charcot-Marie-Tooth patients|journal= Journal of the Peripheral Nervous System|date= 2009|volume=14|issue=2|pages=125–136|doi=10.1111/j.1529-8027.2009.00222.x|last2= Milic-Rasic|first2= Vedrana|last3= Mladenovic|first3= Jelena|last4= Dackovic|first4= Jelena|last5= Kecmanovic|first5= Miljana|last6= Keckarevic|first6= Dusan|last7= Savic-Pavicevic|first7= Dusanka|last8= Romac|first8= Stanka|pmid= 19691535|s2cid= 28848763}}
* {{cite journal|last1= Keckarevic-Markovic|first1= Milica|title= Mutational analysis of ''GJB1'' , ''MPZ'' , ''PMP22'' , ''EGR2'' , and ''LITAF/SIMPLE'' in Serbian Charcot-Marie-Tooth patients|journal= Journal of the Peripheral Nervous System|date= 2009|volume=14|issue=2|pages=125–136|doi=10.1111/j.1529-8027.2009.00222.x|last2= Milic-Rasic|first2= Vedrana|last3= Mladenovic|first3= Jelena|last4= Dackovic|first4= Jelena|last5= Kecmanovic|first5= Miljana|last6= Keckarevic|first6= Dusan|last7= Savic-Pavicevic|first7= Dusanka|last8= Romac|first8= Stanka|pmid= 19691535|s2cid= 28848763}}
Ред 32: Ред 32:
* {{cite journal|last1= Keckarević|first1= Dušan|title= Population data on 14 STR loci from population of Serbia and Montenegro (New and renewed data)|journal= Forensic Science International|date= 2005|volume=151|issue=2–3|pages=315–316|doi=10.1016/j.forsciint.2005.01.009|last2= Savić|first2= Dušanka|last3= Keckarević|first3= Milica|last4= Stevanović|first4= Miljana|last5= Tarasjev|first5= Aleksej|last6= Čuljković|first6= Biljana|last7= Đarmati|first7= Ana|last8= Vukosavić|first8= Slobodanka|last9= Romac|first9= Stanka|pmid= 15939169}}
* {{cite journal|last1= Keckarević|first1= Dušan|title= Population data on 14 STR loci from population of Serbia and Montenegro (New and renewed data)|journal= Forensic Science International|date= 2005|volume=151|issue=2–3|pages=315–316|doi=10.1016/j.forsciint.2005.01.009|last2= Savić|first2= Dušanka|last3= Keckarević|first3= Milica|last4= Stevanović|first4= Miljana|last5= Tarasjev|first5= Aleksej|last6= Čuljković|first6= Biljana|last7= Đarmati|first7= Ana|last8= Vukosavić|first8= Slobodanka|last9= Romac|first9= Stanka|pmid= 15939169}}
* {{cite journal|last1= Savi?|first1= Du?Anka|title= 250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1|journal= Human Mutation|date= 2002|volume=19|issue=2|pages=131–139|doi=10.1002/humu.10027|last2= Rako?Vi?-Stojanovi?|first2= Vidosava|last3= Keckarevi?|first3= Du?an|last4= ?Uljkovi?|first4= Biljana|last5= Stojkovi?|first5= Oliver|last6= Mladenovi?|first6= Jelena|last7= Todorovi?|first7= Slobodanka|last8= Apostolski|first8= Slobodan|last9= Romac|first9= Stanka|pmid= 11793472|s2cid= 42660271}}
* {{cite journal|last1= Savi?|first1= Du?Anka|title= 250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1|journal= Human Mutation|date= 2002|volume=19|issue=2|pages=131–139|doi=10.1002/humu.10027|last2= Rako?Vi?-Stojanovi?|first2= Vidosava|last3= Keckarevi?|first3= Du?an|last4= ?Uljkovi?|first4= Biljana|last5= Stojkovi?|first5= Oliver|last6= Mladenovi?|first6= Jelena|last7= Todorovi?|first7= Slobodanka|last8= Apostolski|first8= Slobodan|last9= Romac|first9= Stanka|pmid= 11793472|s2cid= 42660271}}
* Culjkovic B, Stojkovic O, Savic D, Zamurovic N, Nesic M, Major T, Keckarevic D, Zamurovic B, Vukosavic S, Romac S. Comparison of the number of triplets in SCA1, MJD/SCA3, HD, SBMA, DRPLA, MD, FRAXA and FRDA genes in schizophrenic patients and a healthy population. Am. J. Med. Genet (Neuropsychiatry genetics). {{cite journal|author=|title=|journal=|date=|volume=96 |issue=6 |pages=884–887|author= |title= |journal= |date=2000 |volume=|issue=|pages=|doi=10.1002/1096-8628(20001204)96:6|doi-broken-date= 2023-09-16}}%3C884::AID-AJMG41%3E3.0.CO;2-M
* Culjkovic B, Stojkovic O, Savic D, Zamurovic N, Nesic M, Major T, Keckarevic D, Zamurovic B, Vukosavic S, Romac S. Comparison of the number of triplets in SCA1, MJD/SCA3, HD, SBMA, DRPLA, MD, FRAXA and FRDA genes in schizophrenic patients and a healthy population. Am. J. Med. Genet (Neuropsychiatry genetics). {{cite journal|issue=6 |pages=884–887|author= |title= |journal= |date=2000 |volume=96|doi=10.1002/1096-8628(20001204)96:6|doi-broken-date= 2023-09-16}}%3C884::AID-AJMG41%3E3.0.CO;2-M
# Keckarevic D, Culjkovic B, SavicD, Stojkovic O, Kostic V, Vukosavic S, Romac S. (2000). The status of SCA1, MJD/SCA3, FRDA, DRPLA and MD triplet containing genes in patients with Huntington disease and healthy controls. J Neurogenet. {{cite journal|author=|title=|journal=|date=Dec|volume=14 |issue=4 |pages=257–63|title= The Status of SCA1, MJD/SCA3, FRDA, DRPLA and MD Triplet Containing Genes in Patients with Huntington Disease and Healthy Controls|journal= Journal of Neurogenetics|date= 2000|volume=14|issue=4|pages=257–263|doi=10.3109/01677060009084502|last1= Keckarevic|first1= Dusan|last2= Culjkovic|first2= Biljana|last3= Savic|first3= Dusanka|last4= Stojkovic|first4= Oliver|last5= Kostic|first5= Vladimir|last6= Vukosavic|first6= Slobodanka|last7= Romac|first7= Stanka|pmid= 11342385|s2cid= 41845619}}
* {{cite journal|title= The Status of SCA1, MJD/SCA3, FRDA, DRPLA and MD Triplet Containing Genes in Patients with Huntington Disease and Healthy Controls|journal= Journal of Neurogenetics|date= 2000|volume=14|issue=4|pages=257–263|doi=10.3109/01677060009084502|last1= Keckarevic|first1= Dusan|last2= Culjkovic|first2= Biljana|last3= Savic|first3= Dusanka|last4= Stojkovic|first4= Oliver|last5= Kostic|first5= Vladimir|last6= Vukosavic|first6= Slobodanka|last7= Romac|first7= Stanka|pmid= 11342385|s2cid= 41845619}}


'''M22 - Рад у истакнутом међународном часопису'''
'''M22 - Рад у истакнутом међународном часопису'''
Ред 44: Ред 44:
'''М23 - Рад у међународном часопису M23'''
'''М23 - Рад у међународном часопису M23'''
# Kecmanović M, Ristic AJ, Ercegovac M, Keckarević-Marković M, Keckarević D, Sokic D, Romac S. : A Shared Haplotype Indicates a Founder Event in Unverricht-Lundborg Disease Patients from Serbia. {{cite journal|author=|date=2014 |title= |journal=Int J Neurosci |volume=24|issue=2|pages=102–9}}.
# Kecmanović M, Ristic AJ, Ercegovac M, Keckarević-Marković M, Keckarević D, Sokic D, Romac S. : A Shared Haplotype Indicates a Founder Event in Unverricht-Lundborg Disease Patients from Serbia. {{cite journal|author=|date=2014 |title= |journal=Int J Neurosci |volume=24|issue=2|pages=102–9}}.
# Keckarević Marković M, Dačković J, Mladenović J, Milić-Rašić V, Kecmanović M, Keckarević D, Romac S. : An algorithm for genetic testing of Serbian patients with demyelinating Charcot-Marie-Tooth. {{cite journal|author=|date=2013 |title= |journal=Genet Test Mol Biomarkers |volume=17|issue=1|pages=85–7}}.
# Keckarević Marković M, Dačković J, Mladenović J, Milić-Rašić V, Kecmanović M, Keckarević D, Romac S. : An algorithm for genetic testing of Serbian patients with demyelinating Charcot-Marie-Tooth. {{cite journal|date=2013 |title= An algorithm for genetic testing of Serbian patients with demyelinating Charcot-Marie-Tooth|journal=Genet Test Mol Biomarkers |volume=17|issue=1|pages=85–7|doi=10.1089/gtmb.2012.0238 |pmid=23163601 |last1=Keckarevic Markovic |first1=M. P. |last2=Dackovic |first2=J. |last3=Mladenovic |first3=J. |last4=Milic-Rasic |first4=V. |last5=Kecmanovic |first5=M. |last6=Keckarevic |first6=D. |last7=Romac |first7=S. |pmc=3525895 }}.
# Kecmanović M, Dobričić V, Dimitrijević R, Keckarević D, Savić Pavićević D, Keckarević-Marković M, Ivković M, Romac S. : Schizophrenia and apolipoprotein E gene polymorphisms in Serbian population. {{cite journal|author=|date=2010 |title= |journal=Int J Neurosci |volume=120|issue=7|pages=502–6}}.
# Kecmanović M, Dobričić V, Dimitrijević R, Keckarević D, Savić Pavićević D, Keckarević-Marković M, Ivković M, Romac S. : Schizophrenia and apolipoprotein E gene polymorphisms in Serbian population. {{cite journal|date=2010 |title= Schizophrenia and apolipoprotein e gene polymorphism in Serbian population|journal=Int J Neurosci |volume=120|issue=7|pages=502–6|doi=10.3109/00207451003765956 |pmid=20583903 |last1=Kecmanović |first1=M. |last2=Dobricić |first2=V. |last3=Dimitrijević |first3=R. |last4=Keckarević |first4=D. |last5=Savić-Pavićević |first5=D. |last6=Keckarević-Marković |first6=M. |last7=Ivkovic |first7=M. |last8=Romac |first8=S. |s2cid=33540118 }}.
# Dimitrijević R, Čadež I, Keckarević-Marković M, Keckarević D, Kecmanović M, Dobričić V, Savić Pavićević D, Brajušković G, Romac S. : Polymorphisms of the prion protein gene (PRNP) in a Serbian population. {{cite journal|author=|date=2010 |title= |journal=Int J Neurosci |volume=120|issue=7|pages=496–501}}.
# Dimitrijević R, Čadež I, Keckarević-Marković M, Keckarević D, Kecmanović M, Dobričić V, Savić Pavićević D, Brajušković G, Romac S. : Polymorphisms of the prion protein gene (PRNP) in a Serbian population. {{cite journal|date=2010 |title= Polymorphisms of the prion protein gene (PRNP) in a Serbian population|journal=Int J Neurosci |volume=120|issue=7|pages=496–501|doi=10.3109/00207451003765907 |pmid=20583902 |last1=Dimitrijević |first1=R. |last2=Cadez |first2=I. |last3=Keckarević-Marković |first3=M. |last4=Keckarević |first4=D. |last5=Kecmanović |first5=M. |last6=Dobricić |first6=V. |last7=Savić-Pavićević |first7=D. |last8=Brajusković |first8=G. |last9=Romac |first9=S. |s2cid=31055392 }}.
# Janković N, Kecmanović M, Dimitrijević R, Keckarević Marković M, Dobricić V, Keckarević D, Savić Pavicević D, Romac S. : HD phenocopies - possible role of Saitohin gene. {{cite journal|author=|date=2008 |title= |journal=Int J Neurosci |volume=118|issue=3|pages=391–7}}.
# Janković N, Kecmanović M, Dimitrijević R, Keckarević Marković M, Dobricić V, Keckarević D, Savić Pavicević D, Romac S. : HD phenocopies - possible role of Saitohin gene. {{cite journal|date=2008 |title= HD phenocopies--possible role of Saitohin gene|journal=Int J Neurosci |volume=118|issue=3|pages=391–7|doi=10.1080/00207450701593103 |pmid=18300012 |last1=Janković |first1=N. |last2=Kecmanović |first2=M. |last3=Dimitrijević |first3=R. |last4=Keckarević Marković |first4=M. |last5=Dobricić |first5=V. |last6=Keckarević |first6=D. |last7=Savić Pavicević |first7=D. |last8=Romac |first8=S. |s2cid=3281503 }}.
# Savić D, Keckarević D, Branković-Srećković V, Apostolski S, Todorović S, Romac S. : Clinical case report atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family history. {{cite journal|author=|date=2006 |title= |journal=Int J Neurosci |volume=116|issue=12|pages=1509–18}}.
# Savić D, Keckarević D, Branković-Srećković V, Apostolski S, Todorović S, Romac S. : Clinical case report atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family history. {{cite journal|date=2006 |title= Clinical case report atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family history|journal=Int J Neurosci |volume=116|issue=12|pages=1509–18|doi=10.1080/00207450600553182 |pmid=17145685 |last1=Savić |first1=D. |last2=Keckarević |first2=D. |last3=Branković-Srećković |first3=V. |last4=Apostolski |first4=S. |last5=Todorović |first5=S. |last6=Romac |first6=S. |s2cid=43474859 }}.
# Romac S, Čuljković B, Vukosavić S, Stojković O, Savić D, Keckarević D, Zamurović N, Major T, Keckarević M, Topisirović I. (2001). Dynamic mutations as a cause of hereditary neurological and psichiatric diseases. Yugoslav Med Biochem 10: 1-7.
# Romac S, Čuljković B, Vukosavić S, Stojković O, Savić D, Keckarević D, Zamurović N, Major T, Keckarević M, Topisirović I. (2001). Dynamic mutations as a cause of hereditary neurological and psichiatric diseases. Yugoslav Med Biochem 10: 1-7.


Верзија на датум 22. септембар 2023. у 21:34

Душан Кецкаревић
Лични подаци
Датум рођења(1971-09-12)12. септембар 1971. (52 год.)
Место рођењаБеоград, СФРЈ
Научни рад
Пољефорензичка и популациона генетика
ИнституцијаБиолошки факултет Универзитета у Београду

Душан Кецкаревић (12. септембар 1971, Београд) српски је молекуларни биолог-генетичар.[1] Дипломирaо је 1998. године на Универзитету у Београду-Биолошком факултету, одсјек Молекуларна биологија и физиологија, а докторат "Молекуларно генетичка основа амиотрофичне латералне склерозе код пацијената у популацији Србије" одбранио је 2011. године. Члан је Српског биолошког друштва, Друштва генетичара Србије, Српског друштва за молекуларну биологију и члан Интернационалног друштва за форензичку генетику, Друштва српских родословаца „Порекло”[2] гдје је предсједник научног савета Српског ДНК пројекта. Од 2008. године Кецкаревић је изабран за судског вјештака за ужу област форензичка генетика - ДНК анализе од стране Министарства правде Републике Србије. Обавља и дужност помоћника руководиоца Центра за примјену и развој ПЦР-а Биолошког факултета (сада Центра за хуману молекуларну генетику) за вјештачења у области кривично-правних процедура.

Научни рад

Аутор је бројних студија међу којима:[3]

M21- Рад у врхунском међународном часопису

  • Kecmanović, M.; Jović, N.; Keckarević‐Marković, M.; Keckarević, D.; Stevanović, G.; Ignjatović, P.; Romac, S. (2016). „Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin”. Clinical Genetics. 89 (1): 104—108. PMID 25683376. S2CID 7451265. doi:10.1111/cge.12570. 
  • Gagic, Milica; Markovic, Milica Keckarevic; Kecmanovic, Miljana; Keckarevic, Dusan; Mladenovic, Jelena; Dackovic, Jelena; Milic-Rasic, Vedrana; Romac, Stanka (2016). „Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats”. Clinical Chemistry and Laboratory Medicine (CCLM). 54 (5): 773—780. PMID 26479344. S2CID 10092814. doi:10.1515/cclm-2015-0602. 
  • Keckarević, Dušan; Stević, Zorica; Keckarević-Marković, Milica; Kecmanović, Miljana; Romac, Stanka (2012). „A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression”. Amyotrophic Lateral Sclerosis. 13 (2): 237—240. PMID 22214314. S2CID 13341057. doi:10.3109/17482968.2011.627588. 
  • Keckarevic-Markovic, Milica; Milic-Rasic, Vedrana; Mladenovic, Jelena; Dackovic, Jelena; Kecmanovic, Miljana; Keckarevic, Dusan; Savic-Pavicevic, Dusanka; Romac, Stanka (2009). „Mutational analysis of GJB1 , MPZ , PMP22 , EGR2 , and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients”. Journal of the Peripheral Nervous System. 14 (2): 125—136. PMID 19691535. S2CID 28848763. doi:10.1111/j.1529-8027.2009.00222.x. 
  • Kecmanović, Miljana; Ristić, Aleksandar J.; Sokić, Dragoslav; Keckarević-Marković, Milica; Vojvodić, Nikola; Ercegovac, Marko; Janković, Slavko; Keckarević, Dušan; Savić-Pavićević, Dušanka; Romac, Stanka (2009). „Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity”. Epilepsia. 50 (6): 1612—1615. PMID 19170735. S2CID 29486735. doi:10.1111/j.1528-1167.2008.01937.x. 
  • Stevanović, Miljana; Dobričić, Valerija; Keckarević, Dušan; Perović, Aleksandar; Savić-Pavićević, Dušanka; Keckarević-Marković, Milica; Jovanović, Aleksandar; Romac, Stanka (2007). „Human Y-specific STR haplotypes in population of Serbia and Montenegro”. Forensic Science International. 171 (2–3): 216—221. PMID 16806776. doi:10.1016/j.forsciint.2006.05.038. 
  • Keckarević, Dušan; Savić, Dušanka; Keckarević, Milica; Stevanović, Miljana; Tarasjev, Aleksej; Čuljković, Biljana; Đarmati, Ana; Vukosavić, Slobodanka; Romac, Stanka (2005). „Population data on 14 STR loci from population of Serbia and Montenegro (New and renewed data)”. Forensic Science International. 151 (2–3): 315—316. PMID 15939169. doi:10.1016/j.forsciint.2005.01.009. 
  • Savi?, Du?Anka; Rako?Vi?-Stojanovi?, Vidosava; Keckarevi?, Du?an; ?Uljkovi?, Biljana; Stojkovi?, Oliver; Mladenovi?, Jelena; Todorovi?, Slobodanka; Apostolski, Slobodan; Romac, Stanka (2002). „250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1”. Human Mutation. 19 (2): 131—139. PMID 11793472. S2CID 42660271. doi:10.1002/humu.10027. 
  • Culjkovic B, Stojkovic O, Savic D, Zamurovic N, Nesic M, Major T, Keckarevic D, Zamurovic B, Vukosavic S, Romac S. Comparison of the number of triplets in SCA1, MJD/SCA3, HD, SBMA, DRPLA, MD, FRAXA and FRDA genes in schizophrenic patients and a healthy population. Am. J. Med. Genet (Neuropsychiatry genetics). . 96 (6). 2000: 884—887. doi:10.1002/1096-8628(20001204)96:6 (неактивно 2023-09-16).  Недостаје или је празан параметар |title= (помоћ)%3C884::AID-AJMG41%3E3.0.CO;2-M
  • Keckarevic, Dusan; Culjkovic, Biljana; Savic, Dusanka; Stojkovic, Oliver; Kostic, Vladimir; Vukosavic, Slobodanka; Romac, Stanka (2000). „The Status of SCA1, MJD/SCA3, FRDA, DRPLA and MD Triplet Containing Genes in Patients with Huntington Disease and Healthy Controls”. Journal of Neurogenetics. 14 (4): 257—263. PMID 11342385. S2CID 41845619. doi:10.3109/01677060009084502. 

M22 - Рад у истакнутом међународном часопису

  • Kecmanović, Miljana; Jović, Nebojša; Čukić, Mirjana; Keckarević-Marković, Milica; Keckarević, Dušan; Stevanović, Galina; Romac, Stanka (2013). „Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene”. Journal of the Neurological Sciences. 325 (1–2): 170—173. PMID 23317923. S2CID 34474884. doi:10.1016/j.jns.2012.12.006. 
  • Šarić, M.; Zamurović, Lj; Keckarević-Marković, M.; Keckarević, D.; Stevanović, M.; Savić-Pavićević, D.; Jović, J.; Romac, S. (2006). „Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro”. Clinical Genetics. 70 (2): 170—172. PMID 16879202. S2CID 30037594. doi:10.1111/j.1399-0004.2006.00655.x. 
  • Topisirovic, I.; Dragaševic, N.; Savic, D.; Ristic, A.; Keckarevic, M.; Keckarevic, D.; Culjkovic, B.; Petrovic, I.; Romac, S.; Kostic, V. S. (2002). „Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia”. Clinical Genetics. 62 (4): 321—324. PMID 12372061. S2CID 39639412. doi:10.1034/j.1399-0004.2002.620412.x. 
  • Savić, Dušanka; Topisirović, Ivan; Keckarević, Milica; Keckarević, Dušan; Major, Tamara; Čuljković, Biljana; Stojković, Oliver; Rakočević-Stojanović, Vidosava; Mladenović, Jelena; Todorović, Slobodanka; Apostolski, Slobodan; Romac, Stanka (2001). „Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?”. Psychiatric Genetics. 11 (4): 201—205. PMID 11807410. S2CID 45461790. doi:10.1097/00041444-200112000-00004. 

М23 - Рад у међународном часопису M23

  1. Kecmanović M, Ristic AJ, Ercegovac M, Keckarević-Marković M, Keckarević D, Sokic D, Romac S. : A Shared Haplotype Indicates a Founder Event in Unverricht-Lundborg Disease Patients from Serbia. Int J Neurosci. 24 (2): 102—9. 2014.  Недостаје или је празан параметар |title= (помоћ).
  2. Keckarević Marković M, Dačković J, Mladenović J, Milić-Rašić V, Kecmanović M, Keckarević D, Romac S. : An algorithm for genetic testing of Serbian patients with demyelinating Charcot-Marie-Tooth. Keckarevic Markovic, M. P.; Dackovic, J.; Mladenovic, J.; Milic-Rasic, V.; Kecmanovic, M.; Keckarevic, D.; Romac, S. (2013). „An algorithm for genetic testing of Serbian patients with demyelinating Charcot-Marie-Tooth”. Genet Test Mol Biomarkers. 17 (1): 85—7. PMC 3525895 Слободан приступ. PMID 23163601. doi:10.1089/gtmb.2012.0238. .
  3. Kecmanović M, Dobričić V, Dimitrijević R, Keckarević D, Savić Pavićević D, Keckarević-Marković M, Ivković M, Romac S. : Schizophrenia and apolipoprotein E gene polymorphisms in Serbian population. Kecmanović, M.; Dobricić, V.; Dimitrijević, R.; Keckarević, D.; Savić-Pavićević, D.; Keckarević-Marković, M.; Ivkovic, M.; Romac, S. (2010). „Schizophrenia and apolipoprotein e gene polymorphism in Serbian population”. Int J Neurosci. 120 (7): 502—6. PMID 20583903. S2CID 33540118. doi:10.3109/00207451003765956. .
  4. Dimitrijević R, Čadež I, Keckarević-Marković M, Keckarević D, Kecmanović M, Dobričić V, Savić Pavićević D, Brajušković G, Romac S. : Polymorphisms of the prion protein gene (PRNP) in a Serbian population. Dimitrijević, R.; Cadez, I.; Keckarević-Marković, M.; Keckarević, D.; Kecmanović, M.; Dobricić, V.; Savić-Pavićević, D.; Brajusković, G.; Romac, S. (2010). „Polymorphisms of the prion protein gene (PRNP) in a Serbian population”. Int J Neurosci. 120 (7): 496—501. PMID 20583902. S2CID 31055392. doi:10.3109/00207451003765907. .
  5. Janković N, Kecmanović M, Dimitrijević R, Keckarević Marković M, Dobricić V, Keckarević D, Savić Pavicević D, Romac S. : HD phenocopies - possible role of Saitohin gene. Janković, N.; Kecmanović, M.; Dimitrijević, R.; Keckarević Marković, M.; Dobricić, V.; Keckarević, D.; Savić Pavicević, D.; Romac, S. (2008). „HD phenocopies--possible role of Saitohin gene”. Int J Neurosci. 118 (3): 391—7. PMID 18300012. S2CID 3281503. doi:10.1080/00207450701593103. .
  6. Savić D, Keckarević D, Branković-Srećković V, Apostolski S, Todorović S, Romac S. : Clinical case report atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family history. Savić, D.; Keckarević, D.; Branković-Srećković, V.; Apostolski, S.; Todorović, S.; Romac, S. (2006). „Clinical case report atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family history”. Int J Neurosci. 116 (12): 1509—18. PMID 17145685. S2CID 43474859. doi:10.1080/00207450600553182. .
  7. Romac S, Čuljković B, Vukosavić S, Stojković O, Savić D, Keckarević D, Zamurović N, Major T, Keckarević M, Topisirović I. (2001). Dynamic mutations as a cause of hereditary neurological and psichiatric diseases. Yugoslav Med Biochem 10: 1-7.

Види још

Референце

  1. ^ Професионалци: Доцент др Душан Кецкаревић
  2. ^ Основан Научни савет Српског ДНК пројекта
  3. ^ ИЗБОРНОМ ВЕЋУ УНИВЕРЗИТЕТА У БЕОГРАДУ-БИОЛОШКОГ ФАКУЛТЕТА - Извјештај Душан Кецкаревић

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