Larissa Savelyeva

2.5k citations

49 papers · 1.5k indexed · h-index 23

Impact in

Neurology top 5%
- Neuroblastoma Research and Treatments
Cancer Research top 5%
- Cancer, Hypoxia, and Metabolism
- MicroRNA in disease regulation

Papers in

Neurology 17
- Neuroblastoma Research and Treatments 17
Genetics 29
- Genomic variations and chromosomal abnormalities 17
- Genetics and Neurodevelopmental Disorders 12
- Virus-based gene therapy research 7
- BRCA gene mutations in cancer 6

Co-authors: Manfred Schwab Raffaella Corvi M. Schwab Andreas Claas Evgeny Sagulenko Frank Westermann Lukas C. Amler Christian Praml
Journals: Cancer Letters (11 papers)Genes Chromosomes and Cancer (6 papers)Human Molecular Genetics (2 papers)European Journal of Cancer (2 papers)Journal of Neuro-Oncology (2 papers)
Partner nations: Germany United Kingdom France

In The Last Decade

Larissa Savelyeva

49 papers receiving 1.5k citations

Peers

Countries citing papers authored by Larissa Savelyeva

Since Specialization

Citations

This map shows the geographic impact of Larissa Savelyeva'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 Larissa Savelyeva with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Larissa Savelyeva more than expected).

Fields of papers citing papers by Larissa Savelyeva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Larissa Savelyeva. 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 Larissa Savelyeva. The network helps show where Larissa Savelyeva may publish in the future.

Co-authors

The 25 scholars most cited alongside Larissa Savelyeva, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Larissa Savelyeva Line = papers co-authored together Larissa Savelyeva links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	CDK4 inhibition restores G₁-S arrest inMYCN-amplified neuroblastoma cells in the context of doxorubicin-induced DNA damage Cell Cycle ·Arnaud François, Volker Ehemann, Gabriele Becker, toran alizadeh, Daniel Dreidax, 许建柱, Ingo Nölte, Larissa Savelyeva, Emma Bell, Frank Westermann	2013	52
2	Low p14ARF expression in neuroblastoma cells is associated with repressed histone mark status, and enforced expression induces growth arrest and apoptosis Human Molecular Genetics ·Daniel Dreidax, Arnaud François, Christina I. Schroeder, Daniel Muth, toran alizadeh, Hyun-Ho Choi, Marc Zapatka, Jessica Theißen, Matthias Fischer, Volker Ehemann, Manfred Schwab, Larissa Savelyeva, Frank Westermann	2013	10
3	Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats Human Genetics ·toran alizadeh, Evgeny Sagulenko, Hyun-Ho Choi, 岡村敏宏, Roy Mael, Manfred Schwab, Larissa Savelyeva	2012	13
4	MicroRNA miR-885-5p targets CDK2 and MCM5, activates p53 and inhibits proliferation and survival Cell Death and Differentiation ·Elena Afanasyeva, Pieter Mestdagh, Candy Kumps, Jo Vandesompele, Volker Ehemann, Jessica Theißen, Matthias Fischer, Marc Zapatka, Benedikt Brors, Larissa Savelyeva, P. Marango, Frank Speleman, Matthias Schwab, Frank Westermann	2011	128
5	Generation and Characterization of Novel Local and Metastatic Human Neuroblastoma Variants Neoplasia ·Gary Singer, Orit Sagi‐Assif, W Van Velthoven, Jeff Tanner, Shelly Maman, N. Kariv, Leonor Leider–Trejo, Larissa Savelyeva, Manfred Schwab, Ilana Yron, Isaac P. Witz	2008	22
6	Novel aphidicolin‐inducible common fragile site FRA9G maps to 9p22.2, within the C9orf39 gene Genes Chromosomes and Cancer ·W. F. Wise, Karina Forte de Souza, Evgeny Sagulenko, Frank Westermann, Manfred Schwab, Larissa Savelyeva	2007	16
7	Suppression of polyploidy by the BRCA2 protein Cancer Letters ·Evgeny Sagulenko, Larissa Savelyeva, Volker Ehemann, Vitaliya Sagulenko, Wera Hofmann, Katrin Arnold, Andreas Claas, Siegfried Scherneck, Manfred Schwab	2007	10
8	Cloning of genetically tagged chromosome break sequences reveals new fragile sites at 6p21 and 13q22 International Journal of Cancer ·Juan Carlos Yelmo García, Temmuz Gönç Şavran, LAURA OLIVIERI CARNEIRO DE SOUZA, Manfred Schwab, Larissa Savelyeva	2007	18
9	Lower level of BRCA2 protein in heterozygous mutation carriers is correlated with an increase in DNA double strand breaks and an impaired DSB repair Cancer Letters ·Katrin Arnold, Minkyoung Kim, mohammed elghalmi, Lutz Edler, Larissa Savelyeva, Peter Schmezer, Ruprecht Wiedemeyer	2006	20
10	FRA1E common fragile site breaks map within a 370kilobase pair region and disrupt the dihydropyrimidine dehydrogenase gene (DPYD) Cancer Letters ·P. Einarsson, Karina Forte de Souza, Evgeny Sagulenko, Manfred Schwab, Larissa Savelyeva	2006	40
11	Low-frequency common fragile sites: Link to neuropsychiatric disorders? Cancer Letters ·Larissa Savelyeva, Evgeny Sagulenko, Karina Forte de Souza, Manfred Schwab	2005	15
12	Increased rates of spontaneous sister chromatid exchange in lymphocytes of BRCA2+/− carriers of familial breast cancer clusters Cancer Letters ·Min Kyoung Kim, Sabine Zitzmann, Frank Westermann, Katrin Arnold, Liu Lianhai, Manfred Schwab, Larissa Savelyeva	2004	18
13	Aflatoxin B1 aldehyde reductase (AFAR) genes cluster at 1p35–1p36.1 in a region frequently altered in human tumour cells Oncogene ·Christian Praml, Larissa Savelyeva, Manfred Schwab	2003	14
14	Preferential integration of a transfected marker gene into spontaneously expressed fragile sites of a breast cancer cell line Cancer Letters ·Marco Tulio Prado Gomes, Larissa Savelyeva, Manfred Schwab	2002	18
15	BRCA2: a genetic risk factor for breast cancer Cancer Letters ·Manfred Schwab, Andreas Claas, Larissa Savelyeva	2002	19
16	Amplification of oncogenes revisited: from expression profiling to clinical application Cancer Letters ·Larissa Savelyeva, Manfred Schwab	2001	86
17	Topology of double minutes (dmins) and homogeneously staining regions (HSRs) in nuclei of human neuroblastoma cell lines Genes Chromosomes and Cancer ·Irina Solovei, Dirk Kienle, Graham Little, Roland Eils, Larissa Savelyeva, Manfred Schwab, 范东君, Christoph Cremer, Thomas Cremer	2000	24
18	Patterns of oncogene activation in human neuroblastoma cells Journal of Neuro-Oncology ·Raffaella Corvi, Larissa Savelyeva, A. Didier	1997	17
19	Human homologue of a candidate for the Mom1 locus, the secretory type II phospholipase A2 (PLA2S-II), maps to 1p35-36.1/D1S199. PubMed ·Christian Praml, Larissa Savelyeva, Denis Le Paslier, Linda D. Siracusa, Arthur M. Buchberg, Manfred Schwab, Lukas C. Amler	1995	24
20	Reciprocal translocation at in a neuroblastoma cell line: Isolation of a YAC clone at the break European Journal of Cancer ·Lukas C. Amler, Raffaella Corvi, Christian Praml, Larissa Savelyeva, Denis Le Paslier, M. Schwab	1995	8

About Larissa Savelyeva

Larissa Savelyeva is a scholar working on Neurology, Genetics, Molecular Biology, Cancer Research and Cell Biology, having authored 49 papers that have together received 1.5k indexed citations. Recurring topics across this work include Neuroblastoma Research and Treatments (17 papers), Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (12 papers), DNA Repair Mechanisms (10 papers), Virus-based gene therapy research (7 papers), BRCA gene mutations in cancer (6 papers), Cancer-related Molecular Pathways (6 papers) and Microtubule and mitosis dynamics (5 papers). The work is most often cited by research in Neurology (382 citations), Cancer Research (357 citations), Genetics (461 citations), Molecular Biology (1.0k citations) and Immunology and Allergy (68 citations). Larissa Savelyeva has collaborated with scholars based in Germany, United Kingdom and France. Frequent co-authors include Manfred Schwab, Raffaella Corvi, M. Schwab, Manfred Schwab, Andreas Claas, Evgeny Sagulenko, Frank Westermann, Lukas C. Amler, Christian Praml and Volker Ehemann. Their work appears in journals such as Cancer Letters, Genes Chromosomes and Cancer, Human Molecular Genetics, European Journal of Cancer and Journal of Neuro-Oncology.

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.

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