Andrey Goltsov

533 total citations
19 papers, 314 citations indexed

About

Andrey Goltsov is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Andrey Goltsov has authored 19 papers receiving a total of 314 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Genetics. Recurrent topics in Andrey Goltsov's work include Prenatal Screening and Diagnostics (4 papers), Immune Cell Function and Interaction (4 papers) and T-cell and B-cell Immunology (4 papers). Andrey Goltsov is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Immune Cell Function and Interaction (4 papers) and T-cell and B-cell Immunology (4 papers). Andrey Goltsov collaborates with scholars based in Russia, United States and Italy. Andrey Goltsov's co-authors include Е. И. Рогаев, Anastasia P. Grigorenko, Yuri K. Moliaka, Р. А. Зинченко, А. В. Казанцева, E. K. Ginter, Zhiru Guo, Stephen Lyle, Т. В. Андреева and Fedor Gusev and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Scientific Reports.

In The Last Decade

Andrey Goltsov

19 papers receiving 307 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Andrey Goltsov Russia 9 168 84 78 65 36 19 314
Naveed Wasif Pakistan 11 202 1.2× 112 1.3× 101 1.3× 101 1.6× 9 0.3× 30 322
Akiko Iizuka‐Kogo Japan 11 297 1.8× 83 1.0× 30 0.4× 106 1.6× 21 0.6× 21 419
Amy R. Vandiver United States 7 250 1.5× 35 0.4× 25 0.3× 63 1.0× 43 1.2× 16 341
Jeppe Dyrberg Andersen Denmark 13 255 1.5× 148 1.8× 20 0.3× 142 2.2× 11 0.3× 57 509
Frédéric Torès France 13 260 1.5× 33 0.4× 16 0.2× 209 3.2× 35 1.0× 22 478
Wolfgang Hofmeister Sweden 12 194 1.2× 102 1.2× 22 0.3× 112 1.7× 7 0.2× 16 336
Ganka Douglas United States 10 228 1.4× 27 0.3× 31 0.4× 161 2.5× 6 0.2× 13 336
Saunders Ching United States 6 372 2.2× 22 0.3× 64 0.8× 284 4.4× 8 0.2× 7 501
Sher Alam Khan Pakistan 8 166 1.0× 38 0.5× 11 0.1× 139 2.1× 9 0.3× 27 252
Adam M. Coombs United States 4 159 0.9× 59 0.7× 26 0.3× 12 0.2× 241 6.7× 5 413

Countries citing papers authored by Andrey Goltsov

Since Specialization
Citations

This map shows the geographic impact of Andrey Goltsov's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Andrey Goltsov with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrey Goltsov more than expected).

Fields of papers citing papers by Andrey Goltsov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrey Goltsov. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Andrey Goltsov. The network helps show where Andrey Goltsov may publish in the future.

Co-authorship network of co-authors of Andrey Goltsov

This figure shows the co-authorship network connecting the top 25 collaborators of Andrey Goltsov. A scholar is included among the top collaborators of Andrey Goltsov based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Andrey Goltsov. Andrey Goltsov is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Loginova, Maria, et al.. (2025). Identification of the Novel HLA‐DQB1*06:02:65 Allele in a Russian Bone Marrow Donor. HLA. 105(3). e70111–e70111. 1 indexed citations
2.
Goltsov, Andrey, et al.. (2025). Novel STAG3 variant causes oligoasthenoteratozoospermia with high sperm aneuploidy rate. Journal of Assisted Reproduction and Genetics. 42(4). 1239–1245. 1 indexed citations
3.
Loginova, Maria, et al.. (2025). Description of the Novel Allele HLA‐C*03:702, Identified in a Bone Marrow Donor. HLA. 105(3). e70106–e70106. 1 indexed citations
4.
Loginova, Maria, et al.. (2025). Novel Synonymous HLA‐B*35:01:80 Allele Identified by Next‐Generation Sequencing. HLA. 105(1). e70023–e70023. 1 indexed citations
5.
Chaplin, Andrei V., V. A. Shcherbakova, Н. Е. Сузина, et al.. (2020). Hydrogeniiclostidium mannosilyticum gen. nov., sp. nov. isolated from human faeces. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 70(2). 1210–1216. 5 indexed citations
6.
Goltsov, Andrey, et al.. (2020). Prenatal diagnosis of Prader‐Willi syndrome due to uniparental disomy with NIPS: Case report and literature review. Molecular Genetics & Genomic Medicine. 8(10). e1448–e1448. 11 indexed citations
7.
Gusev, Fedor, Denis A. Reshetov, Amanda Mitchell, et al.. (2019). Epigenetic‐genetic chromatin footprinting identifies novel and subject‐specific genes active in prefrontal cortex neurons. The FASEB Journal. 33(7). 8161–8173. 8 indexed citations
8.
Chaplin, Andrei V., et al.. (2018). Noncontiguous finished genome sequence of Megasphaera sp. ASD88, isolated from faeces of a child with autism spectrum disorder. New Microbes and New Infections. 22. 13–16. 7 indexed citations
9.
Goltsov, Andrey, et al.. (2018). Quantification of fetal DNA in the plasma of pregnant women using next generation sequencing of frequent single nucleotide polymorphisms. Bulletin of Russian State Medical University. 29–33. 1 indexed citations
10.
Trofimov, D. Yu., et al.. (2017). In silico size selection is effective in reducing false positive NIPS cases of monosomy X that are due to maternal mosaic monosomy X. Prenatal Diagnosis. 37(13). 1305–1310. 9 indexed citations
11.
Loginova, Maria, et al.. (2017). Description of a new HLA‐A*02 allele, A*02:658, in a Russian individual. HLA. 89(4). 235–236. 3 indexed citations
12.
Grigorenko, Anastasia P., Olga Plotnikova, Smirnov Av, et al.. (2017). Mutational re-modeling of di-aspartyl intramembrane proteases: uncoupling physiologically-relevant activities from those associated with Alzheimer’s disease. Oncotarget. 8(47). 82006–82026. 1 indexed citations
13.
Пономарева, Н.В., et al.. (2016). 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. 14 indexed citations
14.
Grigorenko, Anastasia P., Т. В. Андреева, Fedor Gusev, et al.. (2016). Complete mitochondrial genome and evolutionary analysis of Turritopsis dohrnii, the “immortal” jellyfish with a reversible life-cycle. Molecular Phylogenetics and Evolution. 107. 232–238. 12 indexed citations
15.
Андреева, Т. В., Fedor Gusev, Andrey Goltsov, et al.. (2016). Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies. Scientific Reports. 6(1). 26440–26440. 25 indexed citations
16.
Grigorenko, Anastasia P., Т. В. Андреева, Denis A. Reshetov, et al.. (2015). Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry. European Journal of Human Genetics. 24(4). 550–555. 23 indexed citations
17.
Пономарева, Н.В., et al.. (2011). Age- and genotype-related neurophysiologic reactivity to oxidative stress in healthy adults. Neurobiology of Aging. 33(4). 839.e11–839.e21. 19 indexed citations
18.
Рогаев, Е. И., Anastasia P. Grigorenko, Yuri K. Moliaka, et al.. (2009). Genomic identification in the historical case of the Nicholas II royal family. Proceedings of the National Academy of Sciences. 106(13). 5258–5263. 38 indexed citations
19.
Казанцева, А. В., Andrey Goltsov, Р. А. Зинченко, et al.. (2006). Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene LIPH. Science. 314(5801). 982–985. 134 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Naveed Wasif Breakdown of academic impact, for papers by Akiko Iizuka‐Kogo Breakdown of academic impact, for papers by Amy R. Vandiver Breakdown of academic impact, for papers by Jeppe Dyrberg Andersen Breakdown of academic impact, for papers by Frédéric Torès Breakdown of academic impact, for papers by Wolfgang Hofmeister Breakdown of academic impact, for papers by Ganka Douglas Breakdown of academic impact, for papers by Saunders Ching Breakdown of academic impact, for papers by Sher Alam Khan Breakdown of academic impact, for papers by Adam M. Coombs
Rankless by CCL
2026