Bernd Dworniczak

1.9k total citations
41 papers, 1.2k citations indexed

About

Bernd Dworniczak is a scholar working on Molecular Biology, Clinical Biochemistry and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Bernd Dworniczak has authored 41 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 13 papers in Clinical Biochemistry and 9 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Bernd Dworniczak's work include Metabolism and Genetic Disorders (13 papers), Amino Acid Enzymes and Metabolism (8 papers) and Cystic Fibrosis Research Advances (7 papers). Bernd Dworniczak is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Amino Acid Enzymes and Metabolism (8 papers) and Cystic Fibrosis Research Advances (7 papers). Bernd Dworniczak collaborates with scholars based in Germany, Bulgaria and United States. Bernd Dworniczak's co-authors include C. Aulehla‐Scholz, Jürgen Horst, Daniela M. Faust, Ekkehard K.F. Bautz, J. Horst, Luba Kalaydjieva, K. Bartholomé, Martin Konrad, Petra Pennekamp and Dieter Meschede and has published in prestigious journals such as Journal of Molecular Biology, The American Journal of Human Genetics and American Journal of Respiratory Cell and Molecular Biology.

In The Last Decade

Bernd Dworniczak

40 papers receiving 1.2k citations

Peers

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

#	Work	Indexed citations
1	Primary Ciliary Dyskinesia Associated Disease-Causing Variants in CCDC39 and CCDC40 Cause Axonemal Absence of Inner Dynein Arm Heavy Chains DNAH1, DNAH6, and DNAH7 2024 ·Cells ·(unknown), Inga M. Höben, Alexander Wolter, Niki T. Loges, Heike Olbrich, Isabella Aprea, Bernd Dworniczak, Johanna Raidt, Heymut Omran	2
2	Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal Ultrastructure 2022 ·Annals of the American Thoracic Society ·Johanna Raidt, Henrike Krenz, Johannes Tebbe, Jörg Große-Onnebrink, Heike Olbrich, Niki T. Loges, (unknown), (unknown), Christina Keßler, Julia Wallmeier, Bernd Dworniczak, Petra Pennekamp, Martin Dugas, Claudius Werner, Heymut Omran	21
3	SPEF2- and HYDIN -Mutant Cilia Lack the Central Pair–associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia Diagnostics 2019 ·American Journal of Respiratory Cell and Molecular Biology ·Sandra Cindrić, Gerard W. Dougherty, Heike Olbrich, Rim Hjeij, Niki T. Loges, Israel Amirav, (unknown), June K. Marthin, Kim G. Nielsen, Sivagurunathan Sutharsan, Johanna Raidt, Claudius Werner, Petra Pennekamp, Bernd Dworniczak, Heymut Omran	49
4	New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia 2013 ·European Journal of Human Genetics ·Sergio Laínez, Karl P. Schlingmann, Jenny van der Wijst, Bernd Dworniczak, Femke van Zeeland, Martin Konrad, René J.M. Bindels, Joost G.J. Hoenderop	52
5	Correction: Chromosomal evolution of the PKD1 gene family in primates (vol 8, pg 263, 2008) 2009 ·BMC Evolutionary Biology ·Stefan Kirsch, Juan J. Pasantes, (unknown), Nadja Bogdanova, Claudia Münch, Arseni Markoff, Petra Pennekamp, Michael Krawczak, Bernd Dworniczak, W. Schempp	2
6	11-P013 Gene expression in WT and Pkd2 mutant mouse embryos 2009 ·Mechanisms of Development ·Petra Pennekamp, (unknown), (unknown), (unknown), Peter Wieacker, Bernd Dworniczak	1
7	Sickle Cell Anemia: Conclusions from a Forensic Case Report of a Young African Woman Who Died After Anesthesia 2006 ·Ultrastructural Pathology ·(unknown), R. Wegener, Horst Nizze, (unknown), (unknown), Bernd Dworniczak, W. Nikolaus Kühn‐Velten, Gabriele Nöldge‐Schomburg, R. Hofmockel, Ludwig Jonas	2
8	Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A 2002 ·Human Mutation ·Nadja Bogdanova, Arseni Markoff, (unknown), Ulrike Nowak‐Göttl, Roswith Eisert, Bernd Dworniczak, (unknown), Jürgen Horst	13
9	Seven novel and four recurrent point mutations in the factor VIII (F8C) gene 2001 ·Human Mutation ·Nadja Bogdanova, Beate Lemcke, Arseni Markoff, (unknown), Bernd Dworniczak, (unknown), (unknown)	1
10	Seven novel and four recurrent point mutations in the factor VIII (F8C) gene 2001 ·Human Mutation ·Nadja Bogdanova, Beate Lemcke, Arseni Markoff, (unknown), Bernd Dworniczak, (unknown), (unknown)	4
11	A 28-kb Deletion Spanning D15S63 (PW71) in Five Families: A Rare Neutral Variant? 1999 ·The American Journal of Human Genetics ·Karin Buiting, Bärbel Dittrich, Bernd Dworniczak, Israela Lerer, Dvorah Abeliovich, Sally Cottrell, I. Karen Temple, John F. Harvey, Christina Lich, (unknown), Bernhard Horsthemke	7
12	Identification of four novel mutations in the factor VIII gene: Three missense mutations (E1875G, G2088S, I2185T) and a 2-bp deletion (1780delTC) 1998 ·Human Mutation ·(unknown), (unknown), Bernd Dworniczak, (unknown), Jürgen Horst	6
13	Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens 1997 ·Human Genetics ·Thilo Dörk, Bernd Dworniczak, C. Aulehla‐Scholz, Dagmar Wieczorek, (unknown), A Mayerová, H. H. Seydewitz, Eberhard Nieschlag, Dieter Meschede, Jürgen Horst, Hans-Jürgen Pander, H. Sperling, Félix Ratjen, Eberhard Passarge, (unknown), Manfred Stuhrmann	190
14	Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatally 1995 ·American Journal of Medical Genetics ·Peter Miny, (unknown), Bernd Dworniczak, Nadia Bogdanova, Wolfgang Holzgreve, Sevgi Tercanli, Seher Başaran, Helga Rehder, Rita Exeler, J. Horst	23
15	Heterogeneity of mutations in Bulgarian phenylketonuria haplotype 1 and 4 alleles 1992 ·Clinical Genetics ·Luba Kalaydjieva, Bernd Dworniczak, (unknown), (unknown), (unknown), (unknown), C. Aulehla‐Scholz, J. Horst	7
16	Recurrent nonsense mutation in exon 7 of the phenylalanine hydroxylase gene 1991 ·Human Genetics ·Bernd Dworniczak, Luba Kalaydjieva, C. Aulehla‐Scholz, Kurt Ullrich, Ivo Kremensky, (unknown), J. Horst	14
17	A frameshift mutation in exon 2 of the phenylalanine hydroxylase gene linked to RFLP haplotype 1 1991 ·Human Genetics ·A. Eigel, Bernd Dworniczak, Luba Kalaydjieva, J. Horst	11
18	Phenylalanine hydroxylase gene: Novel missense mutation in exon 7 causing severe phenylketonuria 1991 ·Genomics ·Bernd Dworniczak, (unknown), (unknown), K. Bartholomé, C. Aulehla‐Scholz, Jürgen Horst	40
19	Phenylketonuria: detection of a frequent haplotype 4 allele mutation 1989 ·Human Genetics ·Bernd Dworniczak, C. Aulehla‐Scholz, (unknown)	40
20	RNA polymerase II of Drosophila 1987 ·Journal of Molecular Biology ·(unknown), Bernd Dworniczak, Daniela M. Faust, Ekkehard K.F. Bautz	107

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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