B. Zabel

4.1k total citations
18 papers, 769 citations indexed

About

B. Zabel is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, B. Zabel has authored 18 papers receiving a total of 769 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Genetics and 2 papers in Pathology and Forensic Medicine. Recurrent topics in B. Zabel's work include Genetic Syndromes and Imprinting (3 papers), Genomics and Chromatin Dynamics (3 papers) and Metabolism and Genetic Disorders (2 papers). B. Zabel is often cited by papers focused on Genetic Syndromes and Imprinting (3 papers), Genomics and Chromatin Dynamics (3 papers) and Metabolism and Genetic Disorders (2 papers). B. Zabel collaborates with scholars based in Germany, United States and Czechia. B. Zabel's co-authors include Ernest M. Wright, E. Turk, Jane Dyer, Stefan Mundlos, Dirk Prawitt, Andreas Winterpacht, A.Y. Sakaguchi, Susan L. Naylor, P.A. Lalley and Elena Torban and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

B. Zabel

17 papers receiving 738 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B. Zabel Germany 13 467 249 174 166 87 18 769
Sachiko Ohmori Japan 17 430 0.9× 197 0.8× 217 1.2× 117 0.7× 75 0.9× 43 775
Joana Visa Spain 14 466 1.0× 307 1.2× 128 0.7× 197 1.2× 132 1.5× 16 936
Guido Verhoeven Belgium 7 439 0.9× 311 1.2× 227 1.3× 115 0.7× 50 0.6× 8 1.0k
David S. Loose‐Mitchell United States 14 326 0.7× 419 1.7× 112 0.6× 91 0.5× 114 1.3× 19 824
J. A. Rillema United States 16 509 1.1× 226 0.9× 341 2.0× 66 0.4× 231 2.7× 72 973
Hannah Cohen Israel 9 642 1.4× 112 0.4× 112 0.6× 155 0.9× 81 0.9× 14 934
Yuan-Yuan Ho Hong Kong 12 325 0.7× 275 1.1× 59 0.3× 83 0.5× 60 0.7× 18 785
Bhoom Suktitipat Thailand 18 273 0.6× 160 0.6× 96 0.6× 103 0.6× 78 0.9× 48 842
Tomoki Okazaki Japan 16 459 1.0× 141 0.6× 94 0.5× 129 0.8× 102 1.2× 39 844
Jean-Louis Danan France 22 559 1.2× 264 1.1× 96 0.6× 104 0.6× 97 1.1× 41 1.0k

Countries citing papers authored by B. Zabel

Since Specialization
Citations

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

Fields of papers citing papers by B. Zabel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Zabel

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

All Works

18 of 18 papers shown
1.
Schönberger, W, et al.. (2008). Verbesserung des Längenwachstums bei Ullrich-Turner-Syndrom durch Oxandrolon: Abhängigkeit von der Steroidhormonausscheidung im Urin. DMW - Deutsche Medizinische Wochenschrift. 107(26). 1008–1011.
2.
Melchior, Ralph, et al.. (2004). Effective parenteral clodronate treatment of a child with severe juvenile idiopathic osteoporosis. European Journal of Pediatrics. 164(1). 22–27. 18 indexed citations
3.
Amid, Clara, A. Bahr, Alejandro O. Mujica, et al.. (2001). Comparative genomic sequencing reveals a strikingly similar architecture of a conserved syntenic region on human chromosome 11p15.3 (including gene ST5) and mouse chromosome 7. Cytogenetic and Genome Research. 93(3-4). 284–290. 18 indexed citations
4.
Reutzel, Dirk, Meinhard Mende, Sabine Naumann, et al.. (2001). Genomic imbalances in 61 renal cancers from the proximal tubulus detected by comparative genomic hybridization. Cytogenetic and Genome Research. 93(3-4). 221–227. 32 indexed citations
5.
Häuser, H., Silke Schlaubitz, Dirk Prawitt, et al.. (2001). Comparative architectural aspects of regions of conserved synteny on human chromosome 11p15.3 and mouse chromosome 7 (including genes WEE1 and LMO1). Cytogenetic and Genome Research. 93(3-4). 277–283. 3 indexed citations
6.
Kim, Jungho, Dirk Prawitt, Nabeel Bardeesy, et al.. (1999). The Wilms’ Tumor Suppressor Gene (wt1) Product Regulates Dax-1 Gene Expression during Gonadal Differentiation. Molecular and Cellular Biology. 19(3). 2289–2299. 111 indexed citations
7.
Martı́n, Martı́n G., et al.. (1996). PRENATAL IDENTIFICATION OF A HETEROZYGOUS STATUS IN TWO FETUSES AT RISK FOR GLUCOSE–GALACTOSE MALABSORPTION. Prenatal Diagnosis. 16(5). 458–462. 6 indexed citations
8.
Wildhardt, G., et al.. (1996). Two different PAX3 gene mutations causing Waardenburg syndrome type I. Molecular and Cellular Probes. 10(3). 229–231. 9 indexed citations
9.
10.
Munroe, David J., Tess Whitton, Dirk Prawitt, et al.. (1995). Systematic screening of an arrayed cDNA library by PCR.. Proceedings of the National Academy of Sciences. 92(6). 2209–2213. 44 indexed citations
11.
Pohlenz, Joachim, et al.. (1995). Phenotypic variability in patients with generalised resistance to thyroid hormone.. Journal of Medical Genetics. 32(5). 393–395. 12 indexed citations
12.
Buiting, Karin, Valerie Greger, Bernard H. Brownstein, et al.. (1992). A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes.. Proceedings of the National Academy of Sciences. 89(12). 5457–5461. 39 indexed citations
13.
Schneider, Rainer, E. Schneider-Scherzer, Monica Hirsch‐Kauffmann, et al.. (1992). The human ribonuclease/angiogenin inhibitor is encoded by a gene mapped to chromosome 11p15.5, within 90 kb of the HRAS protooncogene. Cytogenetic and Genome Research. 59(4). 264–267. 4 indexed citations
14.
Wright, Ernest M., E. Turk, B. Zabel, Stefan Mundlos, & Jane Dyer. (1991). Molecular genetics of intestinal glucose transport.. Journal of Clinical Investigation. 88(5). 1435–1440. 69 indexed citations
15.
Turk, E., B. Zabel, Stefan Mundlos, Jane Dyer, & Ernest M. Wright. (1991). Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter. Nature. 350(6316). 354–356. 292 indexed citations
16.
Zabel, B., Susan L. Naylor, A.Y. Sakaguchi, & James F. Gusella. (1986). Mapping of the DNA locus D4S10 and the linked Huntington’s disease gene to 4p16→p15. Cytogenetic and Genome Research. 42(4). 187–190. 12 indexed citations
17.
Sakaguchi, A.Y., P.A. Lalley, B. Zabel, et al.. (1984). Chromosome assignments of four mouse cellular homologs of sarcoma and leukemia virus oncogenes.. Proceedings of the National Academy of Sciences. 81(2). 525–529. 53 indexed citations
18.
Zabel, B., R. E. K. Fournier, P.A. Lalley, Susan L. Naylor, & A.Y. Sakaguchi. (1984). Cellular homologs of the avian erythroblastosis virus erb-A and erb-B genes are syntenic in mouse but asyntenic in man.. Proceedings of the National Academy of Sciences. 81(15). 4874–4878. 29 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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