Wiktor Borozdin

1.3k citations

17 papers · 463 · h-index 13

Impact in

Developmental Biology top 10%
Genetics
- Genomic variations and chromosomal abnormalities
- Congenital Ear and Nasal Anomalies

Papers in

Molecular Biology 9
- Renal and related cancers 5
- Epigenetics and DNA Methylation 3
- Congenital heart defects research 3
- Hedgehog Signaling Pathway Studies 2
Genetics 7
- Congenital Ear and Nasal Anomalies 3
- Genomic variations and chromosomal abnormalities 3

Co-authors: Jürgen Kohlhase (15 shared papers)M. Leipoldt (3 shared papers)Michael J. Bamshad (3 shared papers)Johann Böhm (2 shared papers)Elke Botzenhart (2 shared papers)Ibrahim M. Adham (1 shared paper)Beate Albrecht (1 shared paper)Wolfgang Wurst (1 shared paper)
Journals: Human Mutation (3 papers)American Journal Of Pathology (1 paper)Genetics in Medicine (1 paper)Clinical Genetics (1 paper)Journal of Medical Genetics (1 paper)
Partner nations: Germany United States United Kingdom

In The Last Decade

Wiktor Borozdin

17 papers receiving 454 citations

Peers

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-authors

The 25 scholars most cited alongside Wiktor Borozdin, 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 Wiktor Borozdin Line = papers co-authored together Wiktor Borozdin links everyone, so they are left out of the graph.

All Works

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17 of 17 papers shown

#	Work
1	SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism Journal of Medical Genetics ·Wiktor Borozdin, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2004	61
2	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 ·Johannes S. Kern, G. Grüninger, R. Imsak, Marcel L. Müller, Hauke Schumann, Dimitra Kiritsi, Steffen Emmert, Wiktor Borozdin, Jürgen Kohlhase, Leena Bruckner‐Tuderman, Cristina Has	2009	54
3	Sall1, Sall2, and Sall4 Are Required for Neural Tube Closure in Mice American Journal Of Pathology ·Johann Böhm, A. Buck, Wiktor Borozdin, Ashraf U. Mannan, Uta Matysiak‐Scholze, Ibrahim M. Adham, Walter Schulz‐Schaeffer, Thomas Floß, Wolfgang Wurst, Jürgen Kohlhase, Francisco J. Barrionuevo	2008	51
4	Multigene deletions on chromosome 20q13.13-q13.2 includingSALL4 result in an expanded phenotype of Okihiro syndrome plus developmental delay Human Mutation ·Wiktor Borozdin, John M. Graham, Detlef Böhm, Michael J. Bamshad, Stefanie Spranger, Leah W. Burke, M. Leipoldt, Jürgen Kohlhase	2007	42
5	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 ·Pia E. Vuorela, Sirpa Ala‐Mello, Carola Saloranta, Maila Penttinen, Minna Pöyhönen, Kirsi Huoponen, Wiktor Borozdin, Birke Bausch, Elke Botzenhart, Christian Wilhelm, Helena Kääriäinen, Jürgen Kohlhase	2007	38
6	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 ·Wiktor Borozdin, Katharina Steinmann, Beate Albrecht, Armand Bottani, Koenraad Devriendt, M. Leipoldt, Jürgen Kohlhase	2006	38
7	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 ·Wiktor Borozdin, Ana Maria Bravo Ferrer Acosta, Michael J. Bamshad, Elke Botzenhart, Ursula G. Froster, Johannes R. Lemke, Albert Schinzel, Stephanie Spranger, Julie McGaughran, Dorothea Wand, Krystyńa Chrzańowska, Jürgen Kohlhase	2006	33
8	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 ·Ján Miertuš, Wiktor Borozdin, Vladimı́r Frecer, Giuseppe Tonini, Sara Bertok, Antonio Amoroso, Stanislav Miertuš, Jürgen Kohlhase	2006	28
9	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 ·Wiktor Borozdin, Ana M. Bravo‐Ferrer Acosta, E Seemanová, M. Leipoldt, Michael J. Bamshad, Sheila Unger, Jürgen Kohlhase	2006	23
10	Synergistic cooperation of Sall4 and Cyclin D1 in transcriptional repression Biochemical and Biophysical Research Communications ·Johann Böhm, Frank J. Kaiser, Wiktor Borozdin, Reinhard Depping, Jürgen Kohlhase	2007	22
11	CHD7 mutations causing CHARGE syndrome are predominantly of paternal origin Clinical Genetics ·Silke Pauli, Nina von Velsen, Peter Burfeind, M Steckel, Johanna Mänz, Annick Buchholz, Wiktor Borozdin, Jürgen Kohlhase	2011	19
12	Tetra‐amelia and lung hypo/aplasia syndrome: New case report and review American Journal of Medical Genetics Part A ·Sérgio B. Sousa, Raquel Pina, Lina Ramos, Naigel Pereira, Martin Krahn, Wiktor Borozdin, Jürgen Kohlhase, Marta Amorim, Katia Gonnet, Nicolas Lévy, Isabel M. Carreira, Ana Bela Couceiro, Jorge Saraiva	2008	17
13	Lethal Junctional Epidermolysis Bullosa with Pyloric Atresia due to Compound Heterozygosity for Two Novel Mutations in the Integrin β4 Gene Klinische Pädiatrie ·Johanna Stoevesandt, Wiktor Borozdin, G Girschick, Henning Hamm, B. Höcht, Jürgen Kohlhase, A. Volz‐Thomas, B. Wiewrodt, Johannes Wirbelauer	2011	14
14	Feingold syndrome associated with two novel MYCN mutations in sporadic and familial cases including monozygotic twins American Journal of Medical Genetics Part A ·Bettina Blaumeiser, Barbara Oehl‐Jaschkowitz, Wiktor Borozdin, Jürgen Kohlhase	2008	10
15	Frequency of progranulin mutations in a German cohort of 79 frontotemporal dementia patients Journal of Neurology ·Johannes C. M. Schlachetzki, Klaus Schmidtke, Jan Beckervordersandforth, Wiktor Borozdin, Christian Wilhelm, Michael Hüll, Jürgen Kohlhase	2009	6
16	Delayed diagnosis of adrenal hypoplasia congenita in a patient with a new mutation in the NR0B1 gene Journal of Pediatric Endocrinology and Metabolism ·Zofia Esden-Tempska, Anna Lewczuk, Edward S. Tobias, Wiktor Borozdin, Juergen Kohlhase, Krzysztof Sworczak	2012	6
17	Molecular Modeling of c2h2 Zinc Finger Mutation of Putative Human Transcription Factor SALL4 BioChem Press, Vladimı́r Frecer, Ján Miertuš, Wiktor Borozdin, Jürgen Kohlhase, Stanislav Miertuš, Bratislava Sk	2004	1

About Wiktor Borozdin

Wiktor Borozdin is a scholar working on Molecular Biology, Genetics, Surgery, Genetics and Pulmonary and Respiratory Medicine, having authored 17 papers that have together received 463 indexed citations. Recurring topics across this work include Renal and related cancers (5 papers), Congenital Ear and Nasal Anomalies (3 papers), Epigenetics and DNA Methylation (3 papers), Tracheal and airway disorders (3 papers), Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Hedgehog Signaling Pathway Studies (2 papers) and Skin and Cellular Biology Research (2 papers). The work is most often cited by research in Developmental Biology (22 citations), Genetics (65 citations), Genetics (166 citations), Molecular Biology (325 citations) and Cell Biology (74 citations). Wiktor Borozdin has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Jürgen Kohlhase, M. Leipoldt, Michael J. Bamshad, Johann Böhm, Elke Botzenhart, Ibrahim M. Adham, Beate Albrecht, Wolfgang Wurst, Marcel L. Müller and Dimitra Kiritsi. Their work appears in journals such as Human Mutation, American Journal Of Pathology, Genetics in Medicine, Clinical Genetics and Journal of Medical Genetics.

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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