  | Petrov, V., Sharapov, S., Shagam, L., Nostaeva, A., Pezer, M., Li, D., Hanić, M., McGovern, D., LOUIS, E., Rahmouni, S., Lauc, G., Georges, M., & Aulchenko, Y. S. (29 April 2022). Association between human gut microbiome and N-glycan composition of total plasma proteome. Frontiers in Microbiology, 13:811922.  Peer Reviewed verified by ORBi Dataset: 10.3389/fmicb.2022.811922 |
 | Yang, H.* , Wu, J.* , Huang, X., Zhou, Y., Zhang, Y., Liu, M., Liu, Q., Ke, S., He, M., Fu, H., Fang, S., Xiong, X., Jiang, H., Chen, Z., Wu, Z., Gong, H., Tong, X., Huang, Y., Ma, J., ... Huang, L.*. (2022). ABO genotype alters the gut microbiota by regulating GalNAc levels in pigs. Nature. doi:10.1038/s41586-022-04769-z Peer Reviewed verified by ORBi Dataset: 10.1038/s41586-022-04769-z* These authors have contributed equally to this work. |
  | Latour, S., Shagam, L., Mariman, R., Momozawa, Y., Louis, E., Rahmouni, S., & Georges, M. (June 2021). Identification of novel loci associated with human microbiota composition [Poster presentation]. International Human Microbiome Consortium Congress 2021. |
 | Aksenova, M., & Shagam, L. (2018). Alport syndrome. In T. Rath (Ed.), Advances in nephrology. IntechOpen. Peer reviewed |
 | 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. (2018). Expert consensus guidelines for the genetic diagnosis of Alport syndrome. Pediatric nephrology (Berlin, Germany). doi:10.1007/s00467-018-3985-4 Peer reviewed |
 | Shagam, L., Gerasimov, A., Dlin, V., Sukhorukov, V., Aksenova, M., & Kuznetsova, T. (2018). A method of prognosing COL4A5 gene mutation in the patients with presumable diagnosis of Alport syndrome. |
 | Shagam, L., Sukhorukov, V., Kuznetsova, T., Aksenova, M., & Dlin, V. (2018). COL4A5 G624D: abundance of the Alport syndrome mutation in Russia along with Greek, Hungarian and Slovenian populations suggests it is a frequent mutation in Eastern Europe with mild phenotype. In COL4A5 G624D: abundance of the Alport syndrome mutation in Russia along with Greek, Hungarian and Slovenian populations suggests it is a frequent mutation in Eastern Europe with mild phenotype. Peer reviewed |
 | Shagam, L., Gerasimov, A., Kuznetsova, T., Aksenova, M., Akopova, T., & Dlin, V. (2017). Novel genotype-phenotype correlations in X-linked Alport syndrome: Serum albumin level, age at onset of hematuria and hypertension. In American Society of Human Genetics 67th Annual Meeting abstract book. October 17–21, 2017 in Orlando, Florida. Peer reviewed |
 | Ponomareva, N. V., Andreeva, T. V., Protasova, M. S., Shagam, L., Malina, D. D., Goltsov, A. Y., Fokin, V. F., Illarioshkin, S. N., & Rogaev, E. I. (2017). Quantitative EEG during normal aging: association with the Alzheimer's disease genetic risk variant in PICALM gene. Neurobiology of Aging, 51, 177.e1-177.e8. doi:10.1016/j.neurobiolaging.2016.12.010 Peer Reviewed verified by ORBi |
 | Andreeva, T., Protasova, M., Kunizheva, S., Shagam, L., Malina, D., Goltsov, A., Fokin, V., & Rogaev, E. (2017). DECLINE OF FUNCTIONAL INTERHEMISPHERIC CONNECTIVITY IN AGING: ASSOCIATION WITH PICALM GENOTYPE. Alzheimer's and Dementia: the Journal of the Alzheimer's Association. Peer Reviewed verified by ORBi |
 | Shagam, L., & Voinova, V. (2016). Next generation sequencing in the diagnosis of monogenic diseases: possibilities and restrictions. Rossijskij Vestnik Perinatologii i Pediatrii. Peer Reviewed verified by ORBi |
 | Savige, J., Storey, H., Il Cheong, H., Gyung Kang, H., Park, E., Hilbert, P., Persikov, A., Torres-Fernandez, C., Ars, E., Torra, R., Hertz, J. M., Thomassen, M., Shagam, L., Wang, D., Wang, Y., Flinter, F., & Nagel, M. (2016). X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations. PLoS ONE, 11 (9), 0161802. doi:10.1371/journal.pone.0161802 Peer Reviewed verified by ORBi |
Shagam, L., Polyakova, A., Kryganova, T., Shentseva, D., Sukhorukov, V., Konkova, N., & Dlin, V. (2015). Experience of Alport syndrome genetic testing by Ion Torrent panel in Russian patients [Paper presentation]. The 2015 international workshop on Alport syndrome (Goettingen, Germany). |
 | Groznova, O., Dlin, V., Shagam, L., Shentseva, D., & Konkova, N. (2015). The paper deals with the topical issues of using high-performance sequencing to diagnose monogenic diseases. The de facto method is widely used in clinical practice. The rapid development of high-performance sequencing requires that medical geneticists and pediatricians specializing in hereditary diseases should understand its possibilities and limitations, choose a strategy for diagnosis in each specific patient, and competently interpret the obtained results. Rossijskij Vestnik Perinatologii i Pediatrii. Peer Reviewed verified by ORBi |
 | Grigorenko, A., Gusev, F., Resgetov, D., Andreeva, T., Shagam, L., Goltsov, A., Kirgizova, V., Zolotareva, O., Protasova, M., van der Lee, S., Amin, N., Oostra, B., van Dujn, C., & Rogaev, E. (2015). Whole genome sequencing of late-onset Alzheimer's disease patients from genetic isolate. Alzheimer's and Dementia: the Journal of the Alzheimer's Association. Peer Reviewed verified by ORBi |
 | Shagam, L., Dorofeeva, M., Sadykov, A., Polyakova, A., Shatalova, D., & Sukhorukov, V. (2015). Identification of 4 novel mutations in a cohort of tuberous sclerosis patients from Russia. In American Society of Human Genetics annual meeting, 2015 abstract book. Peer reviewed |
 | Dorofeeva, M., Belousova, E., Pivovarova, A., Kobrinsky, Podolnaya, M., Shagam, L., Polyakova, A., Imyanitov, E., & Zakharova, E. (2015). The first results of tuberous sclerosis registry. Rossijskij Vestnik Perinatologii i Pediatrii. Peer Reviewed verified by ORBi |
Shagam, L., Gerasimov, A., Kryganova, T., Aksenova, M., Sukhorukov, V., Akopova, T., & Dlin, V. (17 September 2014). Features of blood and urine in Alport syndrome patients: novel genotype-phenotype correlations [Paper presentation]. The Seventh German- Russian Week of the Young Researcher. |
 | Ponomareva, N., Andreeva, T., Protasova, M., Shagam, L., Malina, D., Goltsov, A., Fokin, V., Mitrofanov, A., & Rogaev, E. (2013). Age-dependent effect of Alzheimer's risk variant of CLU on EEG alpha rhythm in non-demented adults. Frontiers in Aging Neuroscience, 5, 86. doi:10.3389/fnagi.2013.00086 Peer Reviewed verified by ORBi |
 | Shagam, L., & Shentseva, D. (2013). Molecular biological basis of Alport syndrome pathogenesis. Rossijskij Vestnik Perinatologii i Pediatrii. Peer Reviewed verified by ORBi |
 | Shagam, L., Terenin, I. M., Andreev, D. E., Dunaevsky, J. E., & Dmitriev, S. E. (2012). In vitro activity of human translation initiation factor eIF4B is not affected by phosphomimetic amino acid substitutions S422D and S422E. Biochimie, 94 (12), 2484-90. doi:10.1016/j.biochi.2012.06.021 Peer Reviewed verified by ORBi |
 | Golenkina, S. A., Gol'tsov, A. I., Kuznetsova, I. L., Grigorenko, A. P., Andreeva, T. V., Reshetov, D. A., Kunizheva, S. S., Shagam, L., Morozova, I. I., Goldenkova-Pavlova, I. V., Shimshilashvili, K., Viacheslavova, A. O., Faskhutdinova, G., Gareeva, A. E., Zainullina, A. G., Khusnutdinova, E. K., Puzyrev, V. P., Stepanov, V. A., Kolotvin, A. V., ... Rogaev, E. I. (2010). [Analysis of clusterin gene (CLU/APOJ) polymorphism in Alzheimer's disease patients and in normal cohorts from Russian populations]. Molekuliarnaia Biologiia, 44 (4), 620-6. Peer Reviewed verified by ORBi |