Bettina Bochow

827 total citations
12 papers, 574 citations indexed

About

Bettina Bochow is a scholar working on Nutrition and Dietetics, Health, Toxicology and Mutagenesis and Hematology. According to data from OpenAlex, Bettina Bochow has authored 12 papers receiving a total of 574 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Nutrition and Dietetics, 7 papers in Health, Toxicology and Mutagenesis and 6 papers in Hematology. Recurrent topics in Bettina Bochow's work include Trace Elements in Health (9 papers), Heavy Metal Exposure and Toxicity (7 papers) and Iron Metabolism and Disorders (6 papers). Bettina Bochow is often cited by papers focused on Trace Elements in Health (9 papers), Heavy Metal Exposure and Toxicity (7 papers) and Iron Metabolism and Disorders (6 papers). Bettina Bochow collaborates with scholars based in Germany, Poland and Greece. Bettina Bochow's co-authors include Janine Genschel, Hartmut Schmidt, Herbert Lochs, Anna Członkowska, Grzegorz Chabik, Grażyna Gromadzka, Beata Tarnacka, M. Rodo, Tomasz Litwin and George Dedoussis and has published in prestigious journals such as Movement Disorders, Alimentary Pharmacology & Therapeutics and Human Mutation.

In The Last Decade

Bettina Bochow

12 papers receiving 569 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bettina Bochow Germany	11	364	285	187	126	107	12	574
Koshi MORI Japan	8	209 0.6×	121 0.4×	77 0.4×	45 0.4×	20 0.2×	8	359
Tomohiro Miyai Japan	6	254 0.7×	137 0.5×	71 0.4×	53 0.4×	29 0.3×	9	383
Masatoshi Ohtake Japan	9	87 0.2×	45 0.2×	125 0.7×	14 0.1×	64 0.6×	13	365
Yvonne Mark United States	7	136 0.4×	45 0.2×	61 0.3×	30 0.2×	51 0.5×	11	293
Ernest Beutler United States	12	207 0.6×	18 0.1×	310 1.7×	15 0.1×	37 0.3×	13	550
Dunja Ferring–Appel Germany	7	238 0.7×	21 0.1×	366 2.0×	24 0.2×	12 0.1×	7	581
Masami Kawamura Japan	8	148 0.4×	82 0.3×	36 0.2×	32 0.3×	22 0.2×	13	337
Kuerbanjiang Abuduxikuer China	12	47 0.1×	36 0.1×	15 0.1×	19 0.2×	60 0.6×	33	295
Chang Liao United States	9	115 0.3×	33 0.1×	59 0.3×	6 0.0×	15 0.1×	11	391
Horst Oexle Austria	4	81 0.2×	16 0.1×	168 0.9×	17 0.1×	10 0.1×	5	358

Countries citing papers authored by Bettina Bochow

Since Specialization

Citations

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

Fields of papers citing papers by Bettina Bochow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bettina Bochow

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

All Works

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12 of 12 papers shown

Elsayed, Solaf M., et al.. (2008). Mutational analysis of ATP7B gene in Egyptian children with Wilson disease: 12 novel mutations. Journal of Human Genetics. 53(8). 681–687. 33 indexed citations

Deguti, Marta Mitiko, Janine Genschel, Eduardo Luiz Rachid Cançado, et al.. (2007). Neurological manifestations and ATP7B mutations in Wilson's disease. Parkinsonism & Related Disorders. 14(3). 246–249. 15 indexed citations

Gromadzka, Grażyna, Janine Genschel, Bettina Bochow, et al.. (2005). p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease. Movement Disorders. 21(2). 245–248. 60 indexed citations

Dedoussis, George, Janine Genschel, Bettina Bochow, et al.. (2005). Wilson Disease: High Prevalence in a Mountaineous Area of Crete. Annals of Human Genetics. 69(3). 268–274. 35 indexed citations

Gromadzka, Grażyna, Hartmut Schmidt, Janine Genschel, et al.. (2005). Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease. Clinical Genetics. 68(6). 524–532. 110 indexed citations

Dedoussis, George, Janine Genschel, Bettina Bochow, et al.. (2005). Wilson Disease: High Prevalence in a Mountaineous Area of Crete. Annals of Human Genetics. 69(3). 268–274. 37 indexed citations

Büning, Carsten, Janine Genschel, Sabine Bühner, et al.. (2004). Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperation. Alimentary Pharmacology & Therapeutics. 19(10). 1073–1078. 104 indexed citations

Dedoussis, George, Janine Genschel, Bettina Bochow, et al.. (2004). Molecular characterization of familial hypercholesterolemia in German and Greek patients. Human Mutation. 23(3). 285–286. 36 indexed citations

Deguti, Marta Mitiko, Janine Genschel, Eduardo Luiz Rachid Cançado, et al.. (2004). Wilson disease: Novel mutations in theATP7B gene and clinical correlation in Brazilian patients. Human Mutation. 23(4). 398–398. 82 indexed citations

10.

Genschel, Janine, Bettina Bochow, Ralf Ewert, et al.. (2001). A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy. Human Mutation. 17(2). 154–154. 38 indexed citations

11.

Genschel, Janine, Anna Członkowska, Grit Sommer, et al.. (2001). Three novel mutations (P760L, L1305P, Q1351Stop) causing Wilson disease. Human Mutation. 17(2). 156–156. 7 indexed citations

12.

Genschel, Janine, et al.. (2000). Three novel mutations, c314C>A, C778insC, and c1285+2T>A, in exon 2 of the Wilson disease gene. Human Mutation. 16(3). 278–278. 17 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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