Wiktor Borozdin

1.3k total citations
17 papers, 463 citations indexed

About

Wiktor Borozdin is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Wiktor Borozdin has authored 17 papers receiving a total of 463 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Surgery. Recurrent topics in Wiktor Borozdin's work include Renal and related cancers (5 papers), Epigenetics and DNA Methylation (3 papers) and Congenital heart defects research (3 papers). Wiktor Borozdin is often cited by papers focused on Renal and related cancers (5 papers), Epigenetics and DNA Methylation (3 papers) and Congenital heart defects research (3 papers). Wiktor Borozdin collaborates with scholars based in Germany, United States and United Kingdom. Wiktor Borozdin's co-authors include Jürgen Kohlhase, M. Leipoldt, Michael J. Bamshad, Johann Böhm, Elke Botzenhart, Wolfgang Wurst, Katharina Steinmann, Dimitra Kiritsi, Cristina Has and Johannes S. Kern and has published in prestigious journals such as Biochemical and Biophysical Research Communications, American Journal Of Pathology and British Journal of Dermatology.

In The Last Decade

Wiktor Borozdin

17 papers receiving 454 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wiktor Borozdin Germany 13 325 166 74 65 55 17 463
Axel Bohring Germany 13 361 1.1× 203 1.2× 58 0.8× 21 0.3× 44 0.8× 17 609
J. Kohlhase Germany 8 552 1.7× 211 1.3× 102 1.4× 41 0.6× 62 1.1× 9 761
Lynn Greenhalgh United Kingdom 8 226 0.7× 181 1.1× 80 1.1× 62 1.0× 14 0.3× 11 507
Nina Bögershausen Germany 11 280 0.9× 234 1.4× 46 0.6× 50 0.8× 34 0.6× 13 444
Véronica Cusin France 12 443 1.4× 309 1.9× 28 0.4× 86 1.3× 20 0.4× 13 721
Anne Destrèe Belgium 11 219 0.7× 253 1.5× 28 0.4× 68 1.0× 46 0.8× 13 458
Smita M. Purandare United States 11 323 1.0× 160 1.0× 35 0.5× 19 0.3× 114 2.1× 15 598
Maree Flaherty Australia 14 286 0.9× 257 1.5× 83 1.1× 62 1.0× 21 0.4× 30 566
Lucie Dupuis Canada 13 243 0.7× 335 2.0× 92 1.2× 19 0.3× 23 0.4× 28 554
Fernanda Sarquis Jehee Brazil 13 393 1.2× 521 3.1× 70 0.9× 40 0.6× 24 0.4× 26 691

Countries citing papers authored by Wiktor Borozdin

Since Specialization
Citations

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

Fields of papers citing papers by Wiktor Borozdin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wiktor Borozdin

This figure shows the co-authorship network connecting the top 25 collaborators of Wiktor Borozdin. A scholar is included among the top collaborators of Wiktor Borozdin 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 Wiktor Borozdin. Wiktor Borozdin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Lewczuk, Anna, et al.. (2012). Delayed diagnosis of adrenal hypoplasia congenita in a patient with a new mutation in the NR0B1 gene. Journal of Pediatric Endocrinology and Metabolism. 25(1-2). 147–8. 6 indexed citations
2.
Pauli, Silke, et al.. (2011). CHD7 mutations causing CHARGE syndrome are predominantly of paternal origin. Clinical Genetics. 81(3). 234–239. 19 indexed citations
3.
Stoevesandt, Johanna, Wiktor Borozdin, G Girschick, et al.. (2011). Lethal Junctional Epidermolysis Bullosa with Pyloric Atresia due to Compound Heterozygosity for Two Novel Mutations in the Integrin β4 Gene. Klinische Pädiatrie. 224(1). 8–11. 14 indexed citations
4.
Schlachetzki, Johannes C. M., Klaus Schmidtke, Jan Beckervordersandforth, et al.. (2009). Frequency of progranulin mutations in a German cohort of 79 frontotemporal dementia patients. Journal of Neurology. 256(12). 2043–2051. 6 indexed citations
5.
Kern, Johannes S., Marcel L. Müller, Hauke Schumann, et al.. (2009). Forty-two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large European dystrophic epidermolysis bullosa cohort. British Journal of Dermatology. 161(5). 1089–1097. 54 indexed citations
6.
Böhm, Johann, Wiktor Borozdin, Ashraf U. Mannan, et al.. (2008). Sall1, Sall2, and Sall4 Are Required for Neural Tube Closure in Mice. American Journal Of Pathology. 173(5). 1455–1463. 51 indexed citations
7.
Blaumeiser, Bettina, Barbara Oehl‐Jaschkowitz, Wiktor Borozdin, & Jürgen Kohlhase. (2008). Feingold syndrome associated with two novel MYCN mutations in sporadic and familial cases including monozygotic twins. American Journal of Medical Genetics Part A. 146A(17). 2304–2307. 10 indexed citations
8.
Sousa, Sérgio B., Lina Ramos, Wiktor Borozdin, et al.. (2008). Tetra‐amelia and lung hypo/aplasia syndrome: New case report and review. American Journal of Medical Genetics Part A. 146A(21). 2799–2803. 17 indexed citations
9.
Ala‐Mello, Sirpa, Carola Saloranta, Maila Penttinen, et al.. (2007). Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions. Genetics in Medicine. 9(10). 690–694. 38 indexed citations
10.
Borozdin, Wiktor, John M. Graham, Detlef Böhm, et al.. (2007). Multigene deletions on chromosome 20q13.13-q13.2 includingSALL4 result in an expanded phenotype of Okihiro syndrome plus developmental delay. Human Mutation. 28(8). 830–830. 42 indexed citations
11.
Böhm, Johann, Frank J. Kaiser, Wiktor Borozdin, Reinhard Depping, & Jürgen Kohlhase. (2007). Synergistic cooperation of Sall4 and Cyclin D1 in transcriptional repression. Biochemical and Biophysical Research Communications. 356(3). 773–779. 22 indexed citations
12.
Borozdin, Wiktor, E Seemanová, M. Leipoldt, et al.. (2006). Contiguous hemizygous deletion of TBX5, TBX3, and RBM19 resulting in a combined phenotype of Holt‐Oram and ulnar‐mammary syndromes. American Journal of Medical Genetics Part A. 140A(17). 1880–1886. 23 indexed citations
13.
Borozdin, Wiktor, Michael J. Bamshad, Elke Botzenhart, et al.. (2006). Expanding the spectrum ofTBX5 mutations in Holt-Oram syndrome: detection of two intragenic deletions by quantitative real time PCR, and report of eight novel point mutations. Human Mutation. 27(9). 975–976. 33 indexed citations
14.
Miertuš, Ján, Wiktor Borozdin, Vladimı́r Frecer, et al.. (2006). A SALL4 zinc finger missense mutation predicted to result in increased DNA binding affinity is associated with cranial midline defects and mild features of Okihiro syndrome. Human Genetics. 119(1-2). 154–161. 28 indexed citations
15.
Borozdin, Wiktor, Katharina Steinmann, Beate Albrecht, et al.. (2006). Detection of heterozygousSALL1 deletions by quantitative real time PCR proves the contribution of aSALL1 dosage effect in the pathogenesis of Townes-Brocks syndrome. Human Mutation. 27(2). 211–212. 38 indexed citations
16.
Borozdin, Wiktor, et al.. (2004). SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism. Journal of Medical Genetics. 41(9). e113–e113. 61 indexed citations
17.
Press, BioChem, Vladimı́r Frecer, Ján Miertuš, et al.. (2004). Molecular Modeling of c2h2 Zinc Finger Mutation of Putative Human Transcription Factor SALL4. 1 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.

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