B. Halliger–Keller

456 total citations
8 papers, 324 citations indexed

About

B. Halliger–Keller is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, B. Halliger–Keller has authored 8 papers receiving a total of 324 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Clinical Biochemistry and 2 papers in Physiology. Recurrent topics in B. Halliger–Keller's work include Muscle Physiology and Disorders (3 papers), Amino Acid Enzymes and Metabolism (2 papers) and Ion channel regulation and function (2 papers). B. Halliger–Keller is often cited by papers focused on Muscle Physiology and Disorders (3 papers), Amino Acid Enzymes and Metabolism (2 papers) and Ion channel regulation and function (2 papers). B. Halliger–Keller collaborates with scholars based in Germany, United Kingdom and Slovakia. B. Halliger–Keller's co-authors include C. R. Müller, Caroline A. Sewry, Graeme M. Bydder, Ana Ferreiro, Martin Brockington, Heinz Jungbluth, H. Collmann, Francesco Muntoni, Victor Dubowitz and A. Manzur and has published in prestigious journals such as Neurology, European Journal of Human Genetics and Cytogenetic and Genome Research.

In The Last Decade

B. Halliger–Keller

8 papers receiving 319 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
B. Halliger–Keller Germany	6	249	127	70	58	51	8	324
Satu Sandell Finland	10	232 0.9×	114 0.9×	89 1.3×	18 0.3×	56 1.1×	21	313
Nicolas Chrestian Canada	10	195 0.8×	62 0.5×	142 2.0×	26 0.4×	34 0.7×	24	272
Jens Schallner Germany	11	182 0.7×	34 0.3×	50 0.7×	120 2.1×	55 1.1×	15	324
Devon Lamb Thrush United States	10	218 0.9×	27 0.2×	54 0.8×	141 2.4×	25 0.5×	19	334
Hervé Testard France	7	186 0.7×	34 0.3×	96 1.4×	34 0.6×	16 0.3×	9	289
Michele Rana Italy	9	301 1.2×	54 0.4×	50 0.7×	25 0.4×	21 0.4×	11	376
Irene Colombo Italy	7	155 0.6×	63 0.5×	30 0.4×	14 0.2×	53 1.0×	14	198
Simone Spinozzi United States	9	213 0.9×	118 0.9×	50 0.7×	14 0.2×	20 0.4×	12	314
Jenni Jonasson Sweden	10	242 1.0×	73 0.6×	93 1.3×	44 0.8×	4 0.1×	14	307
Xavière Lornage France	10	186 0.7×	105 0.8×	54 0.8×	43 0.7×	40 0.8×	19	243

Countries citing papers authored by B. Halliger–Keller

Since Specialization

Citations

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

Fields of papers citing papers by B. Halliger–Keller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Halliger–Keller

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

All Works

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8 of 8 papers shown

1.

Halliger–Keller, B., et al.. (2018). Distribution and Structure of DM2 Repeat Tract Alleles in the German Population. Frontiers in Neurology. 9. 463–463. 15 indexed citations

2.

Stahl, Sonja, Oǧuzkan Sürücü, B. Halliger–Keller, et al.. (2006). CCM1 gene deletion identified by MLPA in cerebral cavernous malformation. Neurosurgical Review. 30(2). 155–160. 24 indexed citations

3.

Jungbluth, Heinz, Haiyan Zhou, Louise Hartley, et al.. (2005). Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene. Neurology. 65(12). 1930–1935. 100 indexed citations

4.

Jungbluth, Heinz, C. R. Müller, B. Halliger–Keller, et al.. (2002). Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores. Neurology. 59(2). 284–287. 114 indexed citations

5.

Collmann, H., et al.. (2000). Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses). Cytogenetic and Genome Research. 91(1-4). 134–137. 41 indexed citations

6.

Müller, C R, et al.. (1999). Allelic heterogeneity of alkaptonuria in Central Europe. European Journal of Human Genetics. 7(6). 645–651. 24 indexed citations

7.

Schmidt, Stefan, et al.. (1999). The genetic defect of the alkaptonuric mouse ( aku ). Mammalian Genome. 10(1). 68–70. 5 indexed citations

8.

Halliger–Keller, B., et al.. (1996). Genetic heterogeneity of oculopharyngeal muscular dystrophy (OPMD). Neuromuscular Disorders. 6(2). S30–S30. 1 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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