A Meindl

3.4k total citations
33 papers, 1.4k citations indexed

About

A Meindl is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, A Meindl has authored 33 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 17 papers in Molecular Biology and 7 papers in Immunology. Recurrent topics in A Meindl's work include BRCA gene mutations in cancer (8 papers), Immunodeficiency and Autoimmune Disorders (6 papers) and DNA Repair Mechanisms (4 papers). A Meindl is often cited by papers focused on BRCA gene mutations in cancer (8 papers), Immunodeficiency and Autoimmune Disorders (6 papers) and DNA Repair Mechanisms (4 papers). A Meindl collaborates with scholars based in Germany, United Kingdom and United States. A Meindl's co-authors include B. H. Belohradsky, Viktoria Atanassova, Heide Hellebrand, Miroslav Habán, Volkmar Jansson, Veit Grote, Allen Mayer, Juliane Ramser, K. Schneider and J Diébold and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

A Meindl

31 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A Meindl Germany	13	769	375	313	256	166	33	1.4k
J. Merregaert Belgium	24	1.2k 1.5×	386 1.0×	191 0.6×	229 0.9×	166 1.0×	55	1.9k
C. Ring United Kingdom	21	579 0.8×	404 1.1×	55 0.2×	61 0.2×	98 0.6×	35	1.3k
Benjamin Yu United States	17	2.0k 2.6×	305 0.8×	78 0.2×	84 0.3×	328 2.0×	27	2.6k
John F. Klement United States	23	965 1.3×	509 1.4×	147 0.5×	112 0.4×	534 3.2×	32	2.1k
C. Halbert United States	12	736 1.0×	556 1.5×	38 0.1×	121 0.5×	201 1.2×	25	1.6k
Ailsa Webster United Kingdom	18	1.0k 1.4×	496 1.3×	58 0.2×	72 0.3×	149 0.9×	22	2.0k
Annahita Keravala United States	18	868 1.1×	324 0.9×	57 0.2×	56 0.2×	135 0.8×	27	1.1k
Nanette Mittereder United States	10	905 1.2×	669 1.8×	67 0.2×	68 0.3×	437 2.6×	11	1.6k
Robert Kokenyesi United States	13	858 1.1×	209 0.6×	110 0.4×	76 0.3×	99 0.6×	14	1.6k
Joseph W. Foley United States	18	794 1.0×	236 0.6×	42 0.1×	48 0.2×	98 0.6×	29	1.4k

Countries citing papers authored by A Meindl

Since Specialization

Citations

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

Fields of papers citing papers by A Meindl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A Meindl

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Meindl, A, Juliane Ramser, Jan Hauke, & Eric Hahnen. (2015). Genetic aspects of hereditary breast and ovarian cancer: options and limits. Kölner Universitäts PublikationsServer (Universität zu Köln). 1 indexed citations

Meindl, A, Kerstin Rhiem, Christoph Engel, et al.. (2013). Clinical course and genetics of hereditary breast and ovarian cancer. mediaTUM (Technical University of Munich).

Avril, Stefanie, Michaela Aubele, Tibor Schuster, et al.. (2013). Somatic copy number changes in DPYD are associated with lower risk of recurrence in triple-negative breast cancers. British Journal of Cancer. 109(9). 2347–2355. 10 indexed citations

Fischer, Christine, Christoph Engel, Christian Sutter, et al.. (2011). BRCA1/2 testing: uptake, phenocopies, and strategies to improve detection rates in initially negative families. Clinical Genetics. 82(5). 478–483. 12 indexed citations

Wappenschmidt, Barbara, Rolf Fimmers, Kerstin Rhiem, et al.. (2005). Strong evidence that the common variant S384F in BRCA2has no pathogenic relevance in hereditary breast cancer. Breast Cancer Research. 7(5). R775–9. 5 indexed citations

Ahearn, Mary Ellen, Devin Dressman, Kemal O. Yariz, et al.. (2004). X-linked lethal infantile (XL)-SMA: new clinical information, variant phenotypes, and candidate disease gene studies.. mediaTUM (Technical University of Munich). 1 indexed citations

Hügle, Boris, Heide Hellebrand, Brian K. Adler, et al.. (2004). Persistent Hypogammaglobulinemia Following Mononucleosis in Boys Is Highly Suggestive of X-Linked Lymphoproliferative Disease—Report of Three Cases. Journal of Clinical Immunology. 24(5). 515–522. 9 indexed citations

Atanassova, Viktoria, et al.. (2001). Prevalence of Staphylococcus aureus and staphylococcal enterotoxins in raw pork and uncooked smoked ham—a comparison of classical culturing detection and RFLP-PCR. International Journal of Food Microbiology. 68(1-2). 105–113. 134 indexed citations

Brandau, Oliver, Volker Schuster, Michael Weiss, et al.. (1999). Epstein--Barr Virus-Negative Boys With Non-Hodgkin Lymphoma Are Mutated in the Sh2D1A Gene, as Are Patients With X-Linked Lymphoproliferative Disease (XLP). Human Molecular Genetics. 8(13). 2407–2413. 81 indexed citations

10.

Wappenschmidt, Barbara, Yutaka Hayashi, A Meindl, et al.. (1999). Exclusion of a major role for the PTEN tumour-suppressor gene in breast carcinomas. British Journal of Cancer. 79(5-6). 754–758. 60 indexed citations

11.

Klopstock, Thomas, Elke Holinski‐Feder, A Meindl, et al.. (1999). Markedly different course of Friedreich's ataxia in sib pairs with similar GAA repeat expansions in the frataxin gene. Acta Neuropathologica. 97(2). 139–142. 17 indexed citations

12.

Vihinen, Mauno, Robert N. Haire, Elke Holinski‐Feder, et al.. (1997). BTKbase, mutation database for X-linked agammaglobulinemia (XLA). Nucleic Acids Research. 25(1). 166–171. 37 indexed citations

13.

Schindelhauer, Dirk, Heide Hellebrand, Ingrid Bader, et al.. (1996). Long-range map of a 3.5-Mb region in Xp11.23-22 with a sequence-ready map from a 1.1-Mb gene-rich interval.. Genome Research. 6(11). 1056–1069. 24 indexed citations

14.

Meindl, A, Katherine L. Dry, Karin A. Herrmann, et al.. (1996). A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3). Nature Genetics. 13(1). 35–42. 391 indexed citations

15.

Schindelhauer, Dirk, Michael Weiss, Heide Hellebrand, et al.. (1996). Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene product. Human Genetics. 98(1). 68–76. 75 indexed citations

16.

Holinski‐Feder, Elke, Astrid Golla, Imma Rost, et al.. (1996). Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33). American Journal of Medical Genetics. 64(1). 125–130. 18 indexed citations

17.

Schäble, Karlheinz F., R. Thiebe, Alexander Flügel, A Meindl, & Hans G. Zachau. (1994). The Human Immunoglobulin ϰ Locus: Pseudogenes, Unique and Repetitive Sequences. Biological Chemistry Hoppe-Seyler. 375(3). 189–200. 19 indexed citations

18.

Schindelhauer, Dirk, Helene Achatz, Tim M. Strom, et al.. (1994). Isolation and fine mapping of (CA)_n repeats from the Xp11.23 and Xp11.4 region. Human Molecular Genetics. 3(6). 1027–1027. 1 indexed citations

19.

Berger, Wolfgang, A Meindl, B. de Leeuw, et al.. (1992). Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosome. Human Genetics. 90(3). 243–246. 8 indexed citations

20.

Meindl, A, et al.. (1990). Polymorphisms in the VK gene patterns of rheumatoid arthritis patients and control individuals.. PubMed. 7(1). 20–5. 5 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.

Explore authors with similar magnitude of impact