Цитати - 151 (Scopus - без автоцитатите на всички автори)

1. Slavena Atemin, Tihomir Todorov, Ivan Tourtourikov, Mariya B. Ivanova etal. Arginase deficiency in Bulgaria: first cases and potential endemic region for the disorder, Journal of Genetics,102, 2023, https://doi.org/10.1007/s12041-022-01399-2 (IF 1.508, Q2)
2. Ivanova, M., I. Sinigerska, D. Dimitrov, V. Jordanova, I. Kremensky: Inhereted Errors of Metabolim – Metabolomic Approuch for Diagnosis in Bulgaria, Pediatria, 4/ 2018, vol. LVIII , 6-10, ISSN0479-7876, (SJR=0.1, Q4)
3. М. Иванова, Ив. Синигерска, Д. Димитров, В. Йорданова, И. Кремнески Вроден грешки на обмяната. Метаболитна криза- метаболомен подход за диагностика в България; Практическа педиатрия, 9, 2018, ХХ, 10-13
4. Т. Делчев, Д. Авджиева, А. Кадъм, М. Иванова, Д. Илиев, Р. Тинчева. Орнитинтранскарбамилазен дефицит. Клиничен случай; Практическа педиатрия, 9, 2018, ХХ, 24-26
5. Angelina Mandadzhieva, Daniela Avdzhieva-Tzavella, Tihomir Todorov, Savina Tincheva, Vanya Sinigerska, Mariya Ivanova, Alexey Savov, Vanyo Mitev, Albena Todorova: Wolman Disease in Bulgarian Patients: Selective Genetic Screening in Two Presumable Endemic Regions(2017); American Journal of Molecular Biology, 2017, 7, 169-175 http://www.scirp.org/journal/ajmb
6. Penchev, V., Boueva, A., Kamenarova, K., Roussinov, D., Tzveova, R., Ivanova, M., Dimitrova, V., Kremensky, I., Mitev, V., Kaneva, R., Beltcheva, O. A familial case of severe infantile nephronophthisis explained by oligogenic inheritance (2017) European Journal of Medical Genetics, 60 (6), pp. 321-325. DOI: 10.1016/j.ejmg.2017.04.002 (IF= 2,004, Q3), цитирания 1
7. Pacheva, I., Ivanov, I., Penkov, M., Kancheva, D., Jordanova, A., Ivanova, M. Creatine deficiency syndrome could be missed easily: A case report of guanidinoacetate methyltransferase deficiency presented with neurodevelopmental delay, seizures, and behavioral changes, but normal structural MRI (2016) Annals of Clinical and Laboratory Science, 46 (5), pp. 557-561. (IF= 0.727, Q4), цитирания 1
8. Daniela Avdjieva-Tzavella, Albena Todorova, Hadil Kathom, Maria Ivanova, Iglika Yordanova, Tihomir Todorov, Ivan Litvinenko, Anna Dasheva-Dimitrova, Radka Tincheva: Barth syndrome in male and female siblings caused by a novel mutation in the TAZ gene. Genetic counseling (Geneva, Switzerland) (2016) 12/2016; 27(4). (IF= 0,236, Q4)
9. А. Кадъм, Д. Авджиева, И. Синигерска, Мария Иванова, М. Божидарова, Р. Тинчева, Клиничен случай на инфантилна форма на болест на Tay-Sachs (ганглиозидоза GM2), Pediatriya, 2016, 2:30-31, ISBN:954-649-199-3,
10. Kadam, A., Avdjieva-Tzavella, D, Andonova, S, M. Ivanova, Tincheva, R, Savov, A, Clinical and genetic characteristics of patients with phenylketonuria in Bulgaria, Pediatria, 2015, 4:28-31 (SJR=0.1, Q4)
11. Кадъм А., Д. Авджиева, И. Литвиненко, М. Иванова, Д. Илиев, Р. Тинчева, Клинични прояви при деца с алиментарен В12 дефицит., Практическа педиатрия, 2015, 1, 30-32
12. Zerjav Tansek, M., Groselj, U., Angelkova, N., Anton, D., Baric, I., Djordjevic, M., Grimci, L., Ivanova, M., Kadam, A., Kotori, V., Maksic, H., Marginean, O., Margineanu, O., Miljanovic, O., Moldovanu, F., Muresan, M., Nanu, M., Samardzic, M., Sarnavka, V., Savov, A., Stojiljkovic, M., Suzic, B., Tincheva, R., Tahirovic, H., Toromanovic, A., Usurelu, N., Battelino, T. Phenylketonuria screening and management in southeastern Europe - Survey results from 11 countries; (2015) Orphanet Journal of Rare Diseases, 10 (1), art. no. 68, . DOI: 10.1186/s13023-015-0283-0 MZ (IF=3.290, Q2) цитирания 8
13. Ivan S. Ivanov, Dimitar N. Azmanov, Mariya B. Ivanova, Teodora Chamova, Ilyana H. Pacheva, Margarita V. Panova, Sharon Song, Bharti Morar, Ralitsa V. Yordanova, Fani K. Galabova, Iglika G. Sotkova, Alexandar J. Linev, Stoyan Bitchev, Anne-Marie J. Shearwood, Dalia Kancheva, Dana Gabrikova, Veronika Karcagi, Velina Guergueltcheva, Ina E. Geneva, Veneta Bozhinova, Vili K. Stoyanova, Ivo Kremensky, Albena Jordanova, Aleksey Savov, Rita Horvath, Matthew A. Brown, Ivailo Tournev, Aleksandra Filipovska, Luba Kalaydjieva: Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children (2014). Molecular Genetics and Metabolism, 113(1-2 SI), 2014: 76-83, DOI:10.1016 (IF-2.625, Q2) цитирания – 8
14. Urh Groselj, Mojca Zerjav Tansek, Andraz Smon, Natalija Angelkova, Dana Anton, Ivo Baric, Maja Djordjevic, Lindita Grimci, Maria Ivanova, Adil Kadam, Vjosa Mulliqi Kotori, Hajrija Maksic, Oana Marginean, Otilia Margineanu, Olivera Milijanovic, Florentina Moldovanu, Mariana Muresan, Simona Murko, Michaela Nanu, Barbka Repic Lampret, Mira Samardzic, Vladimir Sarnavka, Aleksei Savov, Maja Stojiljkovic, Biljana Suzic, Radka Tincheva, Husref Tahirovic, Alma Toromanovic, Natalia Usurelu, Tadej Battelino: Newborn screening in southeastern Europe. Molecular Genetics and Metabolism 09/2014; 113(1-2), 42-45, DOI:10.1016/j.ymgme.2014.07.020 (IF=2.625, Q2) цитирания – 20,
15. D.M. AVDJIEVA-TZAVELLA, M.B. IVANOVA, T.P. TODOROV, A.P. TODOROVA, E.I. PANTELEEVA, S.S. TINCHEVA, E.A. LAZAROVA, H.M. KATHOM, P.G. YANEVA 5 AND R.S. TINCHEVA: First Bulgarian case of citrin deficiency caused by one novel and one recurrent mutation in the SLC25A13 gene. Genetic counseling (Geneva, Switzerland) 11/2014; 25(3), 271-276 (IF-0.444, Q4)
16. Stamenova Sv, Bojinova V., Stancheva M., Georgiev D., Milanov I., Shokova A., Ivanova M., Sinigerska I., Simeonov E. [Megalencephalic leukoecephalopathy with subcortical cysts: New clinical case from Bulgaria] Мегаленцефална левкодистрофия със субкортикални кисти: нов клиничен случаи от България. Българска неврология. Bulgarian Neurology, 14/3, 2013: 154-157
17. D. Tzoneva, V. Guergueltcheva, I. Litvinenko, M. Ivanova, S. Hinev: Sedation for magnetic resonance imaging study in paediatric patients with neurological disorders. Pediatriya 01/2012; 52(4).
18. David M S McHugh, Cynthia A Cameron, …, Maria Ivanova, et.al: Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative project. Genetics in medicine: official journal of the American College of Medical Genetics 02/2011; 13(3)., DOI:10.1097/GIM.0b013e31820d5e67 (IF =4.762, Q1) цитирания – 144,
19. I. Singerska, R. Vajarova, I. Bradinova, M. Ivanova, I. Hasanova, I. Kremenski: Laboratory approach to lysosomal storage diseases diagnostics. Pediatriya 01/2011; 51(1).
20. M. Ivanova, I. Bradinova, R. Vajarova, D. Dimitrov, I. Sinigerska, I. Kremenski: Hyperammonemia - Urea cycle disorders, diagnostic aproach. Pediatriya 01/2011; 51(1).
21. Kremenski, R. Vajarova, I. Brandinova, M. Ivanova, I. Sinigerska, D. Dimitrov, A. Savov, S. Bichev, S. Andonova: Current tools for screening and diagnosis of inborn errors of metabolism. Pediatriya 01/2010; 50.
22. R. Vajarova, I. Brandinova, A. Savov, S. Bichev, I. Singerska, M. Ivanova, I. Kremenski: Current tools for genetic diagnosis in idiopathic mental retardation. Pediatriya 01/2010; 50.
23. Stoyanka Slavcheva Atanassova, P Panchev, M Ivanova: Plasma levels and urinary excretion of amino acids by subjects with renal calculi. Amino Acids 09/2009; 38(5)., DOI:10.1007/s00726-009-0359 (IF=3.877, Q2) цитирания – 5,
24. M. Ivanova, I. Kremensky: Gas chromatography-mass spectrometry for diagnosis of X-linked adrenoleukodystrophy in Bulgaria. Pediatriya 01/2008; 48(1).
25. R. Tincheva, M. Ivanova, V. Konstantinova, R. Georgieva: Case with pyruvate dehydrogenase deficiency. Pediatriya 01/2005; 45(3).
26. Maria Ivanova, Ivanka Sinigerska, Irfet Hasanova and Ivo Kremensky, Selective Screening for Diagnostics of Inherited Metabolic Diseases in Bulgaria Advances in Bulgarian Science, 3-4, 2005: 56
27. Kremensky, A.Todorova, A. Jordanova, A. Savov, I. Tarnev, S. Iankova, B. Georgieva, B. Zaharova, R. Kaneva, R. Petkova, S. Andonova, M.Ivanova, N. Ivanova, R. Rainova and L. Kalaydjieva, Spectrum of Mutations of the most Common Genetic Disorders in Bulgaria. Journal for Quality of Life Research, 1(2), 2003: 172-185
28. L. Angelova, E.Michaylova, E. Stephanova, M.Ivanova, B. Molzer and I.Kremensky, X-linked Adrenoleokodystrophy: Unusual Clinical Manifestation. Journal of Endocrine Genetics, 4 (2), 2001:1-4 http://www.researchgate.net/journal/1565-012X_Journal_of_Endocrine_Genetics_The
29. V Mazneikova, V Dimitrova, Zh Karag'ozova, M Ivanova, E Mikhailova, A Stefanova, B Sl'ncheva, K Tsekova, S Lekova, Ts Furnadzhieva: [Pregnancy with Rh-isoimmunization. Results of a retrospective analysis in the maternity hospital "Maichin Dom"]. Akusherstvo i ginekologiia 02/2001; 40(3), 3-7
30. L. Angelova, E. Michaylova, E. Stephanova, M. Ivanova, B. Molzer, I. Kremensky: X-linked Adrenoleukodystrophy: Unusual Clinical Manifestation. International Journal on Disability and Human Development 01/2001; 2(4)., DOI:10.1515/IJDHD.2001.2.4.247
31. Kremensky I, Jordanova A, Michaylova E, Todorova A, Ivanova M, Petkova R, Andonova S, Savov A, Zaharova B, Iankova S, Kaneva R, Kalaydjieva L: Laboratory diagnosis of inherited disorders and congenital anomalies in Bulgaria. Balkan Journal of Medical Genetics 01/2000; 4 (Number Vol.3 (4), 2000). IF – 0.167 (2013)
32. Kremensky I, Jordanova A, Todorova A, Savov A, Iankova S, Georgieva B, Zaharova B, Kaneva R, Petkova R, Andonova S, Ivanova M, Michaylova E, Ivanova N, Kalaydjieva L.: Mutation profile of the most common genetic disorders in Bulgaria. Balkan Journal of Medical Genetics 01/2000; 4 (Number Vol.3 (4),3-12 IF – 0.167 (2013)
33. E. Paskalev, M. Ivanova, I. Kremenski: Plasma amino acid levels in patients on periodic hemodialysis treatment; Nephrology, hemodialysis and transplantasion, 5,1999 (3), 23-26
34. Dimitrova V, Ivanova M, Kremensky I., The impact of establishing local medians for biochemical markers on false positive rate in Down's syndrome serum screening. Balcan Journal of Medical Genetics, 1999
35. B. Radeva, M. Natcheva, W. Lehnert, I. Kremensky, E. Michaylova, M. Ivanova Canavan disease and erythrodermia ichthyosiformis. Clinical picture, diagnosis and treatment of Inherited metabolic diseases in infancy Part I, 1998; 113-116
36. Kremensky I, Ivanova M, Michajlova E.The Bulgarian programme for selective metabolic screening of inborn errors of metabolism. Balkan Journal of Medical Genetics, Vol 5(2), 160, 1998 IF=0.167
37. M. Ivanova, P.Yanakiev, E. Michaylova, I. Kremensky, Diagnosis of Organic Acidurias in Bulgaria,Balkan Journal of Medical Genetics, 1 (3), 1998: 128-131 IF – 0.167 (2013)
38. I.Kremensky, P. Janakiev, D. Grancharova, M. Ivanova, MCAD G985 mutation in Bulgarian population. Balkan Journal of Medical Genetics, 1(1), 1998: 18-20 IF – 0.167 (2013)
39. E. Michaylova, M. Ivanova, I. Kremensky, Identification of Organic acidurias by GC-MS. Balkan Journal of Clinical Laboratory, 5(2), 1997: