Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2006 | 1 |
2007 | 1 |
2009 | 1 |
2018 | 1 |
2019 | 1 |
2020 | 1 |
2023 | 2 |
2024 | 0 |
Search Results
7 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Clinical Presentation of the c.3844T>C (p.Trp1282Arg, W1282R) Variant in Russian Cystic Fibrosis Patients.
Genes (Basel). 2020 Sep 27;11(10):1137. doi: 10.3390/genes11101137.
Genes (Basel). 2020.
PMID: 32992607
Free PMC article.
Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report.
Vasilyeva TA, Marakhonov AV, Tebieva IS, Kadyshev VV, Borovikov AO, Markova ZG, Chukhrova AL, Ginter EK, Kutsev SI, Zinchenko RA.
Vasilyeva TA, et al. Among authors: ginter ek.
Int J Mol Sci. 2023 Feb 24;24(5):4515. doi: 10.3390/ijms24054515.
Int J Mol Sci. 2023.
PMID: 36901946
Free PMC article.
Item in Clipboard
Comprehensive genotyping reveals novel CFTR variants in cystic fibrosis patients from the Russian Federation.
Petrova NV, Marakhonov AV, Vasilyeva TA, Kashirskaya NY, Ginter EK, Kutsev SI, Zinchenko RA.
Petrova NV, et al. Among authors: ginter ek.
Clin Genet. 2019 Mar;95(3):444-447. doi: 10.1111/cge.13477. Epub 2018 Dec 12.
Clin Genet. 2019.
PMID: 30548586
Item in Clipboard
Epidemiology of PAX6 Gene Pathogenic Variants and Expected Prevalence of PAX6-Associated Congenital Aniridia across the Russian Federation: A Nationwide Study.
Vasilyeva TA, Marakhonov AV, Voskresenskaya AA, Kadyshev VV, Sukhanova NV, Minzhenkova ME, Shilova NV, Latyshova AA, Ginter EK, Kutsev SI, Zinchenko RA.
Vasilyeva TA, et al. Among authors: ginter ek.
Genes (Basel). 2023 Nov 4;14(11):2041. doi: 10.3390/genes14112041.
Genes (Basel). 2023.
PMID: 38002984
Free PMC article.
Item in Clipboard
Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH.
Kazantseva A, Goltsov A, Zinchenko R, Grigorenko AP, Abrukova AV, Moliaka YK, Kirillov AG, Guo Z, Lyle S, Ginter EK, Rogaev EI.
Kazantseva A, et al. Among authors: ginter ek.
Science. 2006 Nov 10;314(5801):982-5. doi: 10.1126/science.1133276.
Science. 2006.
PMID: 17095700
Item in Clipboard
Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state.
Plotnikova OV, Kondrashov FA, Vlasov PK, Grigorenko AP, Ginter EK, Rogaev EI.
Plotnikova OV, et al. Among authors: ginter ek.
Am J Hum Genet. 2007 Jul;81(1):32-43. doi: 10.1086/518616. Epub 2007 May 16.
Am J Hum Genet. 2007.
PMID: 17564961
Free PMC article.
Item in Clipboard
Genetic analysis of autosomal recessive osteopetrosis in Chuvashiya: the unique splice site mutation in TCIRG1 gene spread by the founder effect.
Bliznetz EA, Tverskaya SM, Zinchenko RA, Abrukova AV, Savaskina EN, Nikulin MV, Kirillov AG, Ginter EK, Polyakov AV.
Bliznetz EA, et al. Among authors: ginter ek.
Eur J Hum Genet. 2009 May;17(5):664-72. doi: 10.1038/ejhg.2008.234. Epub 2009 Jan 28.
Eur J Hum Genet. 2009.
PMID: 19172990
Free PMC article.
Item in Clipboard
Cite
Cite