2019

• Korsunskiy I., Blyuss O., Gordukova M., Davydova N., Gordleeva S., Molchanov R., Asmanov A.. TREC and KREC Levels as a Predictors of Lymphocyte Subpopulations Measured by Flow Cytometry. Frontiers in Physiology. 01.2019; (9):1877. DOI: 10.3389/fphys.2018.01877
• Iourov I.Y., Vorsanova S.G., Yurov Y.B. Pathway-based classification of genetic diseases. Molecular Cytogenetics. 02.2019; (12):1-5. DOI:  10.1186/s13039-019-0418-4

2018

• Vorsanova S.G., Zelenova M.A., Yurov Y.B., Iourov I.Y. Behavioral Variability and Somatic Mosaicism: A Cytogenomic Hypothesis. Current Genomics. 01.2018; 19(3):158-162. DOI: 10.2174/1389202918666170719165339
• Goemans N., Mercuri E., Belousova E., Komaki H., Dubrovsky D., McDonald C.M., Kraus J.E., Lourbakos A., Lin Z., Campion G., Wang S.X., Campbell C. A randomized placebo-controlled phase 3 trial of an antisense oligonucleotide, drisapersen, in Duchenne muscular dystrophy. Neuromuscular Disorders. 02.2018; 28(1):4-15. DOI: 10.1016/j.nmd.2017.10.004
• Bissler J.J., Franz D.N., Frost M.D., Belousova E., Bebin E.M., Sparagana S., Berkowitz N., Ridolfi A., Kingswood J.C. The effect of everolimus on renal angiomyolipoma in pediatric patients with tuberous sclerosis being treated for subependymal giant cell astrocytoma. Pediatric Nephrology. 01.2018; 33(1):101-109. DOI: 10.1007/s00467-017-3806-1
• Morozov S.L., Guseva N.B., Dlin V.V., Korsunsky F. Treatment of Children with Overactive Bladder and Nocturnal Polyuria. Journal of Pediatrics and Infants. 01.2018; 1(1):9-11.
• Volynets G.V., Khavkin A.I., Skvortsova T.A., Panfilova V.N., Rogozina N.V., Komarova O.N. Chronic hepatitis C in children in the Russian Federation: a multicenter study. Journal of Gastroenterology and Metabolism. 02.2018; 1(1):1-5.
• Melnikov M., Rogovskii V., Boyko A., Pashenkov M. The influence of biogenic amines on Th17-mediated immune response in multiple sclerosis. Multiple Sclerosis and Related Disorders. 02.2018; (21):19-23. DOI: 10.1016/j.msard.2018.02.012
• Gorlishchev V.P., Kalinin L.A., Mikhalskii A.I., Shkolnikova M.A., Shkolnikov V.M. A Correction Method of Electrocardiographic Interval Subject to Heart Rate. Automation and Remote Control. 02.2018; 79(1):145-152.
• Voskoboeva E., Semyachkina A., Yablonskaya M., Nikolaeva E. Homocystinuria due to cystathionine beta-synthase (CBS) deficiency in Russia: Molecular and clinical characterization. Molecular Genetics and Metabolism Reports. 03.2018; (14):47-54. DOI: 10.1016/j.ymgmr.2017.11.001
• Suspitsin E.N., Yanus G.A., Dorofeeva M.Y., Ledashcheva T.A., Nikitina N.V., Buyanova G.V., Saifullina E.V., Sokolenko A.P., Imyanitov E.N. Pattern of TSC1 and TSC2 germline mutations in Russian patients with tuberous sclerosis. European Journal of Human Genetics. 02.2018; :597-605. DOI: 10.1038/s10038-018-0416-0
• Kingswood J.C., Belousova E., Benedik M.P., Carter T., Cottin V., Curatolo P., Dahlin M., D' Amato L., d'Augères G.B., de Vries P.J., Ferreira J.C., Feucht M., Fladrowski C., Hertzberg C., Jozwiak S. et al. Renal angiomyolipoma in patients with tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increase disease Awareness. Nephrology Dialysis Transplantation. 04.2018; (31):1-7. DOI: 10.1093/ndt/gfy063
• Volkov I.V., Volkova O.K., Tashkinova O.S., Belousova E.D. The short-term efficacy of combined hormone therapy in West syndrome. Journal of Epileptology. 02.2018; (26):15-21. DOI: 10.21307/jepil-2018-002
• Lozier E.R., Konovalov,F.A., Kanivets I.V., Pyankov D.V., Koshkin P.A., Baleva L.S., Sipyagina A.E., Yakusheva E.N., Kuchina A.E., Korostelev S.A. De novo nonsense mutation in WHSC1 (NSD2) in patient with intellectual disability and dysmorphic features. Journal of Human Genetics. 05.2018; 8(1):919-922. DOI: 10.1038/s10038-018-0464-5
• Burgmaier K., Kunzmann K., Ariceta G., Bergmann C., Buescher A., Burgmaier M., Dursun Ismail., Duzova A., Eid L., Erger F., Feldkoetter M., Galiano M., Geßner M., Goebel H., Gokce I. et al. Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease. The Journal of Pediatrics. 05.2018; (99):22-28. DOI: 10.1016/j.jpeds.2018.03.052
• Massella L., Mekahli D., Paripovic D., Prikhodina L., Godefroid N., Niemirska A., Agbasx A., Kalicka K., Jankauskiene A., Mizerska-Wasiak M., Caldas A.A., Salomon R., Deschenes G., Ariceta G. et al. Prevalence of Hypertension in Children with Early-Stage ADPKD. Clinical Journal of the American Society of Nephrology. 02.2018; 13(6):874-883.
• Marinich V., Mizernitski Y. Efficiency of prophylaxis of respiratory diseases in athletes-adolescents. Pedagogy and psychology of sport. 05.2018; 4(2):71-84. DOI: 10.12775/16940
• Kushnareva М.V., Markhulia Kh.М., Keshishyan E.S., Semenov A.V. Ventilator-Associated Pneumonia Caused by Klebsiella Pneumoniae in Preterm Newborn Infants. International Journal of Pediatric Research. 05.2018; 4(1):31-35. DOI: 10.23937/2469-5769/1510031
• Demikova N.S., Kakaulina V.S., Pechatnikova N.L., Polyakova N.A., Zakharova E.Y., Krylova T.D., Zubkova M.V. First report of microcephaly-capillary malformations syndrome in Russia. Egyptian Journal of Medical Human Genetics. 04.2018; 19(2):147-150. DOI: 10.1016/j.ejmhg.2017.08.011
• Semyachkina A., Voskoboeva E., Yablonskaya M., Nikolaeva Е. Clinical and Molecular Characteristics of Russian Patients with Homocystinuria due to Cystathionine Beta-Synthase Deficiency. Journal of Neurology and Neurophysiology. 02.2018; 9(1):459. DOI: 10.4172/2155-9562.1000458
• Zelenova M.A., Yurov Y.B., Vorsanova S.G., Iourov I.Y. Behavioral phenotypes in genetic syndromes associated with intellectual disability and autism. Clinical Neuroscience & Neurological Research International Journal (CNNRIJ). 05.2018; 1(1):180.
• Iourov I.Y., Vorsanova S.G., Yurov Y.B. Runs of homozygosity and epigenetic deregulation of genomic imprinting. OBM Genetics. 08.2018; 2:3.
• Yurieva E.A., Kushnareva M.V., Vozdvizhenskaya E.S. Transdermal therapy: tradition and innovation. Neurobiology of Aging. 02.2018; 7(12):424-430.
• Kozina A., Okuneva G.E., Baryshnikova V.N., Krasnenko Yu., Tsukanov K., Klimchuk I.O., Kondakova B.O., Larionova N., Batysheva T.T., Surkova I.E., Shatalov A., Ilinsky V.V. A novel MF9D8 mutation in a russian patient with neuronal ceroid lipofuscinicistype 7 a case report. BMC Genetics. 02.2018; 19:151-157. DOI: 10.1186/s12881-018-0669-7
• Savige J., Ariani F., Mari F., Bruttini M., Renieri A., Gross O., Deltas C., Flinter F., Ding J., Gale D.P., Nagel M., Yau M., Shagam L., Torra R., Ars E., Hoefele J., Garosi G., Storey H. Expert consensus guidelines for the genetic diagnosis of Alport syndrome. Pediatric Nephrology. 07.2018; (9):1-15. DOI: 10.1007/s00467-018-3985-4
• Munblit D., Abrol P., Sheth S., Yan Chow L., Asmanov A., Khaleva E. Levels of Growth Factors and IgA in the Colostrum of Women from Burundi and Italy. Nutrients. 05.2018; 10(9):1216. DOI: 10.3390/nu10091216
• Kozina A.A., Okuneva G.E., Baryshnikova V.N., Krasnenko Yu.A., Tsukanov Yu.K., Klimchuk I.O., Nikishina A.T., Fedoniuk D.I., Surkova I.E., Shatalov A.P., Ilinsky V.V. Atypical onset of nephropathic infantile cystinosis in a Russian patient with rare CTNS mutation. Clinical Case Reports. 06.2018; 6(9):1871-1876. DOI: 10.1002/ccr3.1678
• Yurov Y.B., Vorsanova S.G., Iourov I.Y. Human Molecular Neurocytogenetics. Current Genetic Medicine Reports. 09.2018; 6(4):155-164. DOI: 10.1007/s40142-018-0152-y
• Yurieva E.A., Dlin V.V., Kushnareva M.V., Novikova A.N., Vozdvizenskaya E.S., Morozov S.L. Pathogenetic Aspects of Urolithiasis Disease. Oxidative Stress. Journal of Pharmaceutical and Biomedical Sciences. 11.2018; 8(10):146-155. DOI: 10.20936/jpbms/08/10/01
• Bissler J.J., Nonomura N., Budde K., Zonnenberg  B.A., Fischereder M., Voi M., Louveau A.L., Herbst F., Bebin E.M., Curatolo P., Zonta A., Belousova E. Angiomyolipoma rebound tumor growth after discontinuation of everolimus in patients with tuberous sclerosis complex or sporadic lymphangioleiomyomatosis. Plos One. 09.2018; 13(9):e0201005. DOI: 10.1371/journal.pone.0201005
• Mau-Them F.T., Guibaud L., Duplomb L., Sharkov A., Vitobello A. De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy. Genetics in Medicine. 08.2018; :1-7. DOI: 10.1038/s41436-018-0143-0
• de Vries P.J., Belousova Е., Benedik M.P., Carter T., Cottin V., Curatolo P., Dahlin M., D’Amato L., d’Augères G.B., Ferreira J.C., Feucht M., Fladrowski C., Hertzberg C., Jozwiak S. et al. TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study. Orphanet Journal of Rare Diseases. 09.2018; (13):2-13. DOI: 10.1186/s13023-018-0901-8
• Nabbout R., Belousova E., Benedik M.P., Carter T., Cottin V., Curatolo P., Dahlin M. Epilepsy in Tuberous Sclerosis Complex: Findings from the TOSCA Study. Epilepsia Open. 12.2018; 4(1):73-84. DOI: 10.1186/s13023-018-0901-8

2017

• Vorsanova S.G., Yurov Y.B., Iourov I.Y. Neurogenomic Pathway of Autism Spectrum Disorders: Linking Germline and Somatic Mutations to Genetic-Environmental Interactions. Current Bioinformatics. 01.2017; 12(1):19-26.
• Giugliani R., Vieira T.A., Carvalho C.G., Muñoz-Rojas M.-V., Semyachkina A.N., Voinova V.Y., Richards S., Cox G.F., Yong Xue. Immune tolerance induction for laronidase treatment in mucopolysaccharidosis I. Molecular Genetics and Metabolism Reports. 04.2017; (10):61-66. DOI: 10.1016/j.ymgmr.2017.01.004
• Kushnareva M.V., Markhulia K.M., Dementyeva G.M., Keshishian E.S., Shaginyan I.A., Chernucha M.Y. Ventilator-associated pneumonia caused by Pseudomonas Aeroginosa in Preterm Newborn Infants. EC pediatrics. 04.2017; 3,4(207):390-397.
• Munblit D., Treneva M., Peroni D.G., Colicino S., Li Yan Chow , Dissanayeke S., Pampura A., Boner A.L., Geddes D.T., Boyle R.J., Warne J.O. Immune Components in Human Milk Are Associated with Early Infant Immunological Health Outcomes: A Prospective Three-Country Analysis. Nutrients. 04.2017; (9):532. DOI: 10.3390/nu9060532
• Treneva M., Varlamov E., Pampura A. A Third Year of Breastfeeding and Atopic Dermatitis Development: Data from a General Population Cohort of Full-Term Newborns. Research Journal of Clinical Pediatrics. 03.2017; (1):1-7.
• Deschênes G., Vivarelli M., Peruzzi L., Andersen R., Bald M., Benetti E., Berard E., Bockenhauer D., Boyer O., Brackman D., Dossier C., Ekinci Z., Emma F., Enneman B., Espinosa-Roman L. et al. Variability of diagnostic criteria and treatment of idiopathic nephrotic syndrome across European countries. European Journal Of Pediatrics. 05.2017; 176(5):647-654. DOI: 10.1007/s00431-017-2891-2
• Yurov Y.B. Meet Our Editorial Board Member. Current Aging Science. 06.2017; 10(2):79. DOI:    DOI:10.2174/187460981002170320205936
• Belousova Е., Sukhorukov V., Dorofeeva M., Shagam L., Vlodavetz D. Clinical report: a rare co-occurrence of tuberous sclerosis complex and Rett syndrome in a girl with mental retardation, epilepsy and autism. Journal of Epileptology. 08.2017; 25(1):1-5. DOI: 10.1515/joepi-2017-0002
• Bissler J.J., Kingswood J.C., Radzikowska E., Zonnenberg B.A., Belousova E., Frost M.D., Sauter M., Brakemeier S., de Vries P.J., Berkowitz N., Voi M., Peyrard S., Budde K. Everolimus long-term use in patients with tuberous sclerosis complex: four-year update of the EXIST-2 study. PLoS ONE. 08.2017; 12(8):1-16. DOI: 10.1371/journal.pone.0180939
• Iourov I.Y. Bioinformatics in Molecular Cytogenetics. Current Bioinformatics. 10.2017; 12(1):3. DOI: 10.2174/157489361201170105194100
• Khramova T.V., Kaysheva A.L., Ivanov Y.D., Pleshakova T.O., Iourov I.Y., Vorsanova S.G., Yurov Y.B., Schetkin A.A., Archakov A.I. Serologic Markers of Autism Spectrum Disorder. Journal of Molecular Neuroscience. 10.2017; 62:420-429. DOI: 10.1007/s12031-017-0950-9
• Munblit D., Treneva M., Korsunskiy I., Asmanov A., Pampura A., Warner J.O. A national survey of Russian physicians' knowledge of diagnosis and management of food-induced anaphylaxis. Bmj Open. 07.2017; 20(7)(7):1-7. DOI: 10.1136/bmjopen-2017-015901.
• Oksuzyan A., Demakakos P., Shkolnikova M.A., Thinggaard M., Vaupel Ja.W., Christensen K., Shkolnikov V.M. Handgrip strength and its prognostic value for mortality in moscow, denmark, and england. PLoS ONE. 08.2017; 12(9):1-16.
• Shkolnikova M., Yugay M., Pankevich V. Comparative Study of Physicians' Job Satisfaction Levels in the Public and the Private Sectors in Russia. Journal of Statistical Software. 08.2017; 5(8):101-113. DOI: 10.4236/jss.2017.58008
• Tasca G., Monforte M., Díaz-Manera J., Brisca G., Semplicini C., D'Amico A., Fattori F., Pichiecchio A., Berardinelli A., Maggi L., Maccagnano E., Løkken N., Marini-Bettolo C., Munell F., Sanchez A. et al. MRI in sarcoglycanopathies: a large international cohort study. Journal Of Neurology Neurosurgery And Psychiatry. 09.2017; 89(1):72-77. DOI: 10.1136/jnnp-2017-316736
• Kushnareva M.V., Gerasimov A.Y., Keshishyan E.S., Semenov A.V. The influence of vancomycin and linezolid on the phagocytic activity of blood neutrophils in vitro experiments in preterm newborns with "ventilator-associated" pneumonia. Journal of Pharmaceutical and Biomedical Sciences. 11.2017; 7(9):315-318.
• Nomura T., Baleva L.S., Ryo H., Adachi S., Sipyagina A.E., Karakhan N.M. Transgenerational effects of radiation on cancer and other disorders in mice and humans. Journal Of Radiation Research. 12.2017; 8(3):123-134. DOI: 10.4103/jrcr.jrcr _30_17
• Baleva L.S., Sukhorukov V.S., Marshall T., Sipyagina A.E., Abe H., Voronkova A.S., Karakhan N.M., Barach P., Sadykov A.R., Egorova N.I., Suchkov S.V. Higher risk for carcinogenesis for residents populatingthe isotope-contaminated territories as assessed by NanoString Gene Expression Profiling. Journal of Translational Science. 05.2017; 3(3):1-6.
• Yurieva E.А., Kushnareva M.V., Vozdvizhenskaya E.S. Transdermal pharmacotherapy: traditions and innovations (Review). Journal of Pharmaceutical and Biomedical Sciences. 12.2017; 7(12):424-430. DOI: 10.20936/jpbms/171204

2016

• Carlier P.G., Marty B., Scheidegger O., Loureiro de Sousa P., Baudin P.-Y., Snezhko E., Vlodavets D. Skeletal muscle quantitative nuclear magnetic resonance imaging and spectroscopy as an outcome measure for clinical trials. Journal of Neuromuscular Diseases. 01.2016; 3(1):1-28. DOI: 10.3233/JND-160145
• Fedenko E., Elisyutina O., Shtyrbul O., Pampura A., Valenta R., Lupinek C., Khaitov M. Microarray-based IgE-serology improves management of severe atopic dermatitis in two children. Pediatric Allergy And Immunology. 04.2016; (31):12572. DOI: 10.1111
• Franz D.N., Belousova E., Sparagana S., Bebin E.M., Frost M.D., Kuperman R., Witt O., Kohrman M.H., Flamini J.R., Wu J.Y., Curatolo P., de Vries P.J., Berkowitz N., Niolat J., Jóźwiak S. Long-Term Use of Everolimus in Patients with Tuberous Sclerosis Complex: Final Results from the EXIST-1 Study. PLoS ONE. 06.2016; 11(6):e0158476. DOI: 10.1371/journal.pone.0158476
• Mamedov I.S., Zolkina I.V., Glagovsky P.B., Sukhorukov V.S. Determining the Reference Intervals of Long-Chain Fatty Acids, Phytanic Acid and Pristanic Acid for Diagnostics of Peroxisome Disorders in Children. Journal of Life Science and Biomedicine. 07.2016; 6(4):83-89.
• Rinčić M., Iourov I.Y., Liehr T. Thoughts about SLC16A2, TSIX and XIST gene like sites in the human genome and a potential role in cellular chromosome counting. Molecular Cytogenetics. 08.2016; 56(9):-. DOI: 10.1186/s13039-016-0271-7
• Morozov S.L., Guseva N.B., Dlin V.V., Tonkikh E.V. THE CLINICAL SIGNIFICANCE OF THE COMBINATION OF PATHOGENIC THERAPY IN CHILDREN WITH OVERACTIVE BLADDER SYNDROME (OAB) AND NOCTURIA. Journal of Experimental Biology and Agricultural Sciences. 06.2016; 4(4):384-388. DOI: 10.18006/2016.4(4).384.388
• Savige J., Storey H., Cheong H.I, Kang H.G., Park E., Hilbert P., Persikov A., Torres-Fernandez G., Ars E., Torra R., Hertz J.M., Thomassen M., Shagam L. et al. X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations. PLoS ONE. 09.2016; 11(9):e0161802. DOI: 10.1371/journal.pone.0161802
• Munblit D., Treneva M., Peroni D.G., Colicino S., Chow L.Y., Dissanayeke S., Abrol P., Sheth S., Pampura A., Boner A.L., Geddes D.T., Boyle R.J., Warner J.O. Colostrum and Mature Human Milk of Women from London, Moscow, and Verona: Determinants of Immune Composition. Nutrients. 12.2016; (8(11)):695. DOI: 10.3390/nu8110695
• Yurieva E.A., Novikova N.N., Sukhorukov V.S., Kushnareva M.V., Vozdvizhenskaya E.S., Murashev A. Protective Effect of Bisphosphonates on the Pathological Changes in the Blood and Tissues in Case of Experimental Atherosclerosis. American Journal of Pharmacy and Pharmacology. 04.2016; 3(3):14-19.
• Yurieva E.A., Vozdvizhenskaya E.S., Kushnareva M.V., Novikova N.N. Endogenic Intoxication and Kidney. International Journal of Pediatric Research. 12.2016; 2(3):022-025.
• Carlier P.G., Marty B., Scheidegger O., Sousa P.L., Baudin P.Y., Snezhko E., Vlodavets D. Imagerie et spectroscopie par résonance magnétique nucléaire du muscle strié squelettique. Les Cahiers de Myologie. 12.2016; (13):34-67.
• Iourov I.Y. Meet Our Regional Editor. Current Bioinformatics. 12.2016; 11(5):501.
• Demikova N.S., Vydrych Yu.Y., Podolnaya M.A., Lapina A.S., Asanov A.Yu. Prevalence and descriptive epidemiology of esophageal atresia in the Russian Federation. Birth Defects Research Part A: Clinical and Molecular Teratology. 12.2016; 106(10):854-859. DOI: 10.1002/bdra.23553
• De Ferrari G.M., Dusi V., Spazzolini C., Schwartz P.J., Bos J.M., Ackerman M.J., Abrams D.J., Berul C.I., Crotti L., Eldar M., Khoury A., Krahn A.D., Odero A., Paul T., Rosés I., Noguer F., Shkolnikova M., Till J., Wilde A.A.M. RESPONSE TO LETTERS REGARDING ARTICLE, CLINICAL MANAGEMENT OF CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA: THE ROLE OF LEFT CARDIAC SYMPATHETIC DENERVATION. Circulation. 01.2016; 133(4):366-367. DOI: 10.1161/CIRCULATIONAHA.115.019465
• Sykhotukov V.S., Voronkova A.S., Litvinova N.A., Baranich T.I., Kharlamov D.A. Significance of mitochondrial individuality. Biology and Medicine. 12.2016; (8):27-45.

2015

• Aksenova M., Tsetlina V., Gutovskaya E., Mitrofanova A., Balashov D., Maschan A. BK virus nephropathy in a pediatric patient after hematopoietic stem cell transplantation. Pediatric Transplantation. 02.2015; 19(1):E29-E32. DOI: 10.1111/petr.12411
• Iourov I.Y., Vorsanova S.G., Zelenova M.A., Korostelev S.A., Yurov Y.B. Genomic copy number variation affecting genes involved in the cell cycle pathway: implications for somatic mosaicism. International Journal of Genomics. 06.2015; 2015(757680):1-7. DOI: 10.1155/2015/757680
• Mamedov I.S., Zolkina I.V., Glagovsky P.B., Sukhorukov V.S. Comparison of chromatographic mthods for determination of the major metabolites of catecholamines and serotonin. International Journal of BioMedicine. 06.2015; 5(2):87-90.
• Esakova N.V., Saakyan E.K., Kondratieva N.S., Kokaeva Z.G., Nesterova A.P., Golovatenko-Abramov P.K., Klimov E.A., Treneva M.S., Pampura A.N. Platelet-activating factor-acetylhydrolase gene (PLA2G7) expression in children with a history of food anaphylaxis. Journal of Allergy & Therapy. 06.2015; 6(2):1-5. DOI: 10.4172/2155-6121.1000211
• Groznova O., Shentseva D., Shagam L., Sukhorukov V., Dlin V. Russian family with X-linked alport syndrome and cardiovascular abnormalities. American Journal of Medical Sciences and Medicine. 06.2015; 3(2):20-23. DOI: 10.12691/ajmsm-3-2-3
• Iourov I.Yu., Vorsanova S.G., Korostelev S.A., Zelenova M.A., Yurov Yu.B. Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsy. Molecular Cytogenetics. 11.2015; 8(77):. 1-8. DOI: 10.1186/s13039-015-0182-z
• Treneva М., Pampura A., Munblit D. Аllergies in families of Moscow (Russia) newborns: suspected cases within three generations framework. American Journal of Public Health Research. 05.2015; 3(3):95-99. DOI: 10.12691/ajphr-3-3-3
• Novikova N., Kovalchuk M., Stepina N., Gaynutdinov R., Chukhrai E., Yurieva E. Distinct effect of xenobiotics on the metal-binding properties of protein molecules. Journal of Synchrotron Radiation. 11.2015; 22(4):1001-1007. DOI: 10.1107/S1600577515005627
• Esakova N.V., Treneva M.S., Okuneva T.S., Pampura A.N. Food anaphylaxis: reported cases in Russian Federation children. American Journal of Public Health Research. 11.2015; 3(5):187-191. DOI: 10.12691/ajphr-3-5-2
• Iourov I.Y., Vorsanova S.G., Demidova I.A., Aliamovskaia G.A., Keshishian E.S., Yurov Yu.B. 5p13.3p13.2 duplication associated with developmental delay, congenital malformations and chromosome instability manifested as low-level aneuploidy. SpringerPlus. 11.2015; 4(616):1-6. DOI: 10.1186/s40064-015-1399-3
• Iourov I.Y., Vorsanova S.G., Voinova V.Y., Yurov Yu.B. 3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances. Molecular Cytogenetics. 11.2015; 8(82):. 1-6.
• Mamedov I., Zolkina I., Nikolaeva E., Glagovsky P., Sukhorukov V. Carnitine insufficiency in children with inborn errors of metabolism: prevalence and treatment efficacy. Journal of Pediatric Endocrinology and Metabolism. 11.2015; 28(11-12):1299-1304. DOI: 10.1515/jpem-2015-0193
• Oksuzyan A., Shkolnikova M., Vaupel J.W., Christensen K., Shkolnikov V.M. Sex differences in biological markers of health in the study of stress, aging and health in Russia. PLoS ONE. 12.2015; 10(6):1-18. DOI: 10.1371/journal.pone.0131691
• De Ferrari G.M., Dusi V., Spazzolini C., Bos J.M., Abrams D.J., Berul C.I., Crotti L., Davis A.M., Eldar M., Kharlap M., Khoury A., Krahn A.D., Leenhardt A., Moir C.R., Odero A. et al. Clinical management of catecholaminergic polymorphic ventricular tachycardia the role of left cardiac sympathetic denervation. Circulation. 12.2015; 131(25):2185-2193. DOI: 10.1161/CIRCULATIONAHA.115.015731
• Baleva L.S., Sipyagina A.E., Zenker M., Kagan J.M., Danilycheva L.I., Sucalo M. Occurrence of the rare syndrome of Johanson-Blizzard in a child – longitudinal observations. International Journal of Developmental Disabilities. 12.2015; 21(2):119-121.
• Sipyagina А.Е., Baleva L.S., Karakhan N.M., Sukhorukov V.sS. Role of Postradiation genome instability in evaluating the development of radiation-determined pathology in children after Chernobyl accident and investigation perspectives. AASCIT Journal of Medicine. 06.2015; 1(2):18-22.