Bernd Dworniczak

4.7k total citations
38 papers, 1.5k citations indexed

About

Bernd Dworniczak is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Bernd Dworniczak has authored 38 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 23 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Bernd Dworniczak's work include Genetic and Kidney Cyst Diseases (18 papers), Genetic Syndromes and Imprinting (10 papers) and Renal and related cancers (10 papers). Bernd Dworniczak is often cited by papers focused on Genetic and Kidney Cyst Diseases (18 papers), Genetic Syndromes and Imprinting (10 papers) and Renal and related cancers (10 papers). Bernd Dworniczak collaborates with scholars based in Germany, United States and Bulgaria. Bernd Dworniczak's co-authors include Petra Pennekamp, Jürgen Horst, Boris V. Skryabin, Martin Blum, Anja Fischer, Axel Schweickert, Hiroshi Hamada, Manuela Simoni, Nadia Bogdanova and Arseni Markoff and has published in prestigious journals such as Science, Nucleic Acids Research and Journal of Clinical Oncology.

In The Last Decade

Bernd Dworniczak

37 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bernd Dworniczak Germany	18	1.2k	1.1k	206	122	108	38	1.5k
Sandrine Caburet France	23	1.3k 1.1×	686 0.6×	368 1.8×	63 0.5×	96 0.9×	39	1.9k
Howard Martin United Kingdom	16	727 0.6×	735 0.7×	52 0.3×	27 0.2×	47 0.4×	32	1.3k
Elena Klenova United Kingdom	31	2.8k 2.4×	937 0.9×	37 0.2×	106 0.9×	69 0.6×	47	3.3k
Judith Singer–Sam United States	24	1.5k 1.3×	918 0.8×	69 0.3×	29 0.2×	45 0.4×	38	1.9k
Matthieu Gérard France	22	1.7k 1.4×	542 0.5×	40 0.2×	37 0.3×	64 0.6×	35	1.9k
Virpi Töhönen Sweden	19	980 0.8×	445 0.4×	257 1.2×	26 0.2×	40 0.4×	32	1.4k
Anne‐Amandine Chassot France	23	1.1k 0.9×	910 0.8×	385 1.9×	19 0.2×	85 0.8×	32	1.6k
Sumiyo Morita Japan	25	1.7k 1.5×	501 0.5×	24 0.1×	42 0.3×	61 0.6×	48	2.2k
Michael J. Clarkson Australia	17	1.4k 1.2×	366 0.3×	74 0.4×	17 0.1×	157 1.5×	22	1.7k
E. Boyd United Kingdom	22	623 0.5×	804 0.7×	117 0.6×	35 0.3×	25 0.2×	55	1.3k

Countries citing papers authored by Bernd Dworniczak

Since Specialization

Citations

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

Fields of papers citing papers by Bernd Dworniczak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernd Dworniczak

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

All Works

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20 of 20 papers shown

Tüttelmann, Frank, Bernd Dworniczak, Albrecht Röpke, et al.. (2016). The humanRHOXgene cluster: target genes and functional analysis of gene variants in infertile men. Human Molecular Genetics. 25(22). ddw313–ddw313. 24 indexed citations

Saraga, Marijan, Katarina Vukojević, Vjekoslav Krželj, et al.. (2014). Mechanism of cystogenesis in nephrotic kidneys: a histopathological study. BMC Nephrology. 15(1). 3–3. 8 indexed citations

Yoshiba, Satoko, Hidetaka Shiratori, Ivana Y. Kuo, et al.. (2012). Cilia at the Node of Mouse Embryos Sense Fluid Flow for Left-Right Determination via Pkd2. Science. 338(6104). 226–231. 240 indexed citations

Tüttelmann, Frank, Manuela Simoni, Sabine Kliesch, et al.. (2011). Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only Syndrome. PLoS ONE. 6(4). e19426–e19426. 105 indexed citations

Burtey, Stéphane, Marta Riera, Judith Luciani, et al.. (2008). Centrosome overduplication and mitotic instability in PKD2 transgenic lines. Cell Biology International. 32(10). 1193–1198. 39 indexed citations

Kirsch, Stefan, Juan J. Pasantes, Andreas Wolf, et al.. (2008). Chromosomal evolution of the PKD1 gene family in primates. BMC Evolutionary Biology. 8(1). 263–263. 9 indexed citations

Romaker, Daniel, Sven Teschner, Johannes Donauer, et al.. (2008). Increased Expression of Secreted Frizzled-Related Protein 4 in Polycystic Kidneys. Journal of the American Society of Nephrology. 20(1). 48–56. 34 indexed citations

Burtey, Stéphane, Marta Riera, Petra Pennekamp, et al.. (2007). Overexpression of PKD2 in the mouse is associated with renal tubulopathy. Nephrology Dialysis Transplantation. 23(4). 1157–1165. 32 indexed citations

Stypmann, Jörg, Markus A. Engelen, Stefan Orwat, et al.. (2006). Cardiovascular characterization of Pkd2+/LacZ mice, an animal model for the autosomal dominant polycystic kidney disease type 2 (ADPKD2). International Journal of Cardiology. 120(2). 158–166. 12 indexed citations

10.

Preisler-Adams, Sabine, et al.. (2006). Gross rearrangements in BRCA1 but not BRCA2 play a notable role in predisposition to breast and ovarian cancer in high-risk families of German origin. Cancer Genetics and Cytogenetics. 168(1). 44–49. 48 indexed citations

11.

Hackmann, Karl, Arseni Markoff, Feng Qian, et al.. (2005). A splice form of polycystin-2, lacking exon 7, does not interact with polycystin-1. Human Molecular Genetics. 14(21). 3249–3262. 12 indexed citations

12.

Hunter, Michael, Janina Hantke, Dora Angelicheva, et al.. (2002). Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1-linked Australian families. Human Mutation. 19(3). 240–250. 6 indexed citations

13.

Bogdanova, Nadia, et al.. (2001). Homologues to the First Gene for Autosomal Dominant Polycystic Kidney Disease Are Pseudogenes. Genomics. 74(3). 333–341. 73 indexed citations

14.

Bogdanova, Nadja, et al.. (2000). Screening the 3? region of the polycystic kidney disease 1 (PKD1) gene in 41 Bulgarian and Australian kindreds reveals a prevalence of protein truncating mutations. Human Mutation. 16(2). 166–174. 8 indexed citations

15.

Bogdanova, Nadja, Bernd Dworniczak, Vladimir Todorov, et al.. (1995). Genetic heterogeneity of polycystic kidney disease in Bulgaria. Human Genetics. 95(6). 645–50. 55 indexed citations

16.

Dunnen, Johan T. den, et al.. (1995). Two polymorphic dinucleotide repeats in intron 44 of the dystrophin gene. Human Genetics. 95(4). 475–477. 12 indexed citations

17.

Dworniczak, Bernd, et al.. (1994). Clinical follow up of uniparental disomy 16: First data. The American Journal of Human Genetics. 55. 1 indexed citations

18.

Byck, Susan, Ken H. Morgan, Linda Tyfield, Bernd Dworniczak, & C R Scriver. (1994). Evidence for origin, by recurrent mutation, of the phenylalanine hydroxylase R408W mutation on two haplotypes in European and Quebec populations. Human Molecular Genetics. 3(9). 1675–1677. 28 indexed citations

19.

Kalaydjieva, Luba, et al.. (1991). Geographical distribution gradients of the major PKU mutations and the linked haplotypes. Human Genetics. 86(4). 411–3. 25 indexed citations

20.

Giebel, Lutz B., Bernd Dworniczak, & E. K. F. Bautz. (1987). Nucleotide sequence of a processed human hsc70 pseudogene. Nucleic Acids Research. 15(22). 9605–9605. 4 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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