A. Eigel

681 total citations
25 papers, 475 citations indexed

About

A. Eigel is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, A. Eigel has authored 25 papers receiving a total of 475 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Hematology. Recurrent topics in A. Eigel's work include Hemoglobinopathies and Related Disorders (10 papers), Iron Metabolism and Disorders (5 papers) and Cystic Fibrosis Research Advances (4 papers). A. Eigel is often cited by papers focused on Hemoglobinopathies and Related Disorders (10 papers), Iron Metabolism and Disorders (5 papers) and Cystic Fibrosis Research Advances (4 papers). A. Eigel collaborates with scholars based in Germany, Bulgaria and Thailand. A. Eigel's co-authors include J. Horst, Horst Feldmann, Torpong Sanguansermsri, G. Flatz, Luba Kalaydjieva, B Helbig, Michael Ludwig, May F. Sadiq, Klaus Olek and Andreas Fregin and has published in prestigious journals such as Nucleic Acids Research, The EMBO Journal and Blood.

In The Last Decade

A. Eigel

25 papers receiving 454 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Eigel Germany 12 203 193 188 78 65 25 475
F E Cash United States 12 189 0.9× 468 2.4× 274 1.5× 99 1.3× 61 0.9× 12 683
Shi‐Ping Cai United States 11 422 2.1× 287 1.5× 614 3.3× 99 1.3× 175 2.7× 19 835
Surinder Safaya United States 12 260 1.3× 208 1.1× 316 1.7× 73 0.9× 92 1.4× 22 539
PH Chen Taiwan 9 128 0.6× 94 0.5× 125 0.7× 42 0.5× 82 1.3× 16 337
B Josephson United States 14 316 1.6× 525 2.7× 423 2.3× 178 2.3× 110 1.7× 23 894
C Natta United States 13 222 1.1× 143 0.7× 350 1.9× 20 0.3× 56 0.9× 18 489
S. Murphy United States 8 121 0.6× 80 0.4× 129 0.7× 20 0.3× 33 0.5× 13 341
Manoussos N. Papadakis Greece 10 139 0.7× 105 0.5× 203 1.1× 85 1.1× 76 1.2× 22 301
Nisha Vasavda United Kingdom 13 290 1.4× 130 0.7× 319 1.7× 120 1.5× 102 1.6× 19 575
VK Kalra India 10 113 0.6× 80 0.4× 160 0.9× 37 0.5× 17 0.3× 32 390

Countries citing papers authored by A. Eigel

Since Specialization
Citations

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

Fields of papers citing papers by A. Eigel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Eigel

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

All Works

20 of 20 papers shown
1.
Meschede, Dieter, Christoph Keck, Christian De Geyter, et al.. (2008). Mutation im Zystische-Fibrose-Transmembran-Regulator-Gen bei beiderseitiger kongenitaler Ductus-deferens-Aplasie*. DMW - Deutsche Medizinische Wochenschrift. 118(18). 661–664. 1 indexed citations
2.
Oldenburg, Johannes, Jean‐Maurice Lavergne, Michael Ludwig, et al.. (2001). Somatic Mosaicism in Hemophilia A: A Fairly Common Event. The American Journal of Human Genetics. 69(1). 75–87. 97 indexed citations
3.
Sadiq, May F., A. Eigel, & J. Horst. (2001). Spectrum of β‐thalassemia in Jordan: Identification of two novel mutations. American Journal of Hematology. 68(1). 16–22. 32 indexed citations
4.
Horst, Basil A., A. Eigel, Torpong Sanguansermsri, & B. Brinkmann. (1999). Human Y-chromosomal STR types in north Thailand. International Journal of Legal Medicine. 112(3). 211–212. 2 indexed citations
5.
Dame, Christof, Norbert Albers, Carola Hasan, et al.. (1999). Homozygous α-thalassaemia and hypospadias - common aetiology or incidental association?. European Journal of Pediatrics. 158(3). 217–220. 28 indexed citations
6.
Bissé, E., Nathalie Zorn, A. Eigel, et al.. (1998). Hemoglobin Rambam (beta69[E13]Gly-->Asp), a pitfall in the assessment of diabetic control: characterization by electrospray mass spectrometry and HPLC.. PubMed. 44(10). 2172–7. 13 indexed citations
7.
Horst, Basil A., A. Eigel, Torpong Sanguansermsri, & Burkhard Rolf. (1997). Analysis of the short tandem repeat systems HumVWA and HumF13B in a population sample from northern Thailand. International Journal of Legal Medicine. 110(4). 235–237. 4 indexed citations
8.
Eigel, A., et al.. (1996). Prevalence of α-thalassemias in northern Thailand. Human Genetics. 98(3). 345–347. 72 indexed citations
9.
Eigel, A., et al.. (1994). Nonisotopic detection of mutations using a modified single-strand conformation polymorphism analysis. Human Mutation. 4(1). 55–56. 4 indexed citations
10.
Steger, Heinrich, A. Eigel, G. Flatz, & J. Horst. (1993). Hemoglobin E and codon 17 nonsense: Two β-globin gene mutations common in Southeast Asia detected by the use of ARMS. Annals of Hematology. 67(3). 119–120. 2 indexed citations
11.
Savov, Alexey, Dora Angelicheva, Albena Jordanova, A. Eigel, & Luba Kalaydjieva. (1992). High percentage acrylamide gels improve resolution in SSCP analysis. Nucleic Acids Research. 20(24). 6741–6742. 38 indexed citations
12.
Eigel, A., Bernd Dworniczak, Luba Kalaydjieva, & J. Horst. (1991). A frameshift mutation in exon 2 of the phenylalanine hydroxylase gene linked to RFLP haplotype 1. Human Genetics. 87(6). 739–41. 11 indexed citations
13.
Aulehla‐Scholz, C., R. Kaiser, John Weber, et al.. (1990). The frequency of the CF ΔF508 deletion in CF chromosomes of different ethnic origin. Human Genetics. 85(4). 392–393. 4 indexed citations
14.
Schnee, Janet, C. Aulehla‐Scholz, A. Eigel, & J. Horst. (1990). Hb D Los Angeles (D-Punjab) and Hb Presbyterian: analysis of the defect at the DNA level. Human Genetics. 84(4). 365–7. 11 indexed citations
15.
Kalaydjieva, Luba, Bernd Dworniczak, C. Aulehla‐Scholz, et al.. (1990). Classical phenylketonuria in Bulgaria: RFLP haplotypes and frequency of the major mutations.. Journal of Medical Genetics. 27(12). 742–745. 14 indexed citations
16.
Schnee, Janet, A. Eigel, & J. Horst. (1989). Direct mutation analysis of ?-thalassemia genes in families of various ethnic origins residing in Germany. Annals of Hematology. 59(3). 237–239. 1 indexed citations
17.
Eigel, A., et al.. (1989). Mutation analysis of β-thalassemia genes in a German family reveals a rare transversion in the first intron. Human Genetics. 81(4). 371–372. 9 indexed citations
18.
Kalaydjieva, Luba, A. Eigel, & J. Horst. (1989). The molecular basis of beta thalassaemia in Bulgaria.. Journal of Medical Genetics. 26(10). 614–618. 15 indexed citations
19.
Schnee, Janet, et al.. (1989). Beta-thalassemia gene analysis in a Turkish family reveals a 7 BP deletion in the coding region [letter]. Blood. 73(8). 2224–2225. 20 indexed citations
20.
Weber, John, C. Aulehla‐Scholz, R. Kaiser, et al.. (1988). Cystic fibrosis: typing 89 German families with linked DNA probes. Human Genetics. 81(1). 54–56. 11 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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