Alfons Meindl

1.3k total citations
14 papers, 490 citations indexed

About

Alfons Meindl is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Alfons Meindl has authored 14 papers receiving a total of 490 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Oncology. Recurrent topics in Alfons Meindl's work include DNA Repair Mechanisms (2 papers), BRCA gene mutations in cancer (2 papers) and Cell death mechanisms and regulation (2 papers). Alfons Meindl is often cited by papers focused on DNA Repair Mechanisms (2 papers), BRCA gene mutations in cancer (2 papers) and Cell death mechanisms and regulation (2 papers). Alfons Meindl collaborates with scholars based in Germany, United States and Netherlands. Alfons Meindl's co-authors include Heide Hellebrand, Rita K. Schmutzler, Thomas Meitinger, Juliane Ramser, Peter Lichtner, C Lenski, Robin D. Clark, Nina Ditsch, Michael von Rhein and Marion Kiechle and has published in prestigious journals such as Nature Genetics, PLoS ONE and Journal of Allergy and Clinical Immunology.

In The Last Decade

Alfons Meindl

14 papers receiving 483 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alfons Meindl Germany	11	332	121	102	65	41	14	490
Suna Önengüt United States	11	396 1.2×	120 1.0×	71 0.7×	47 0.7×	31 0.8×	11	551
Annette Düwel Spain	10	397 1.2×	92 0.8×	68 0.7×	29 0.4×	43 1.0×	13	575
Luke C. Gandolfo Australia	12	267 0.8×	83 0.7×	87 0.9×	32 0.5×	10 0.2×	13	573
Marta Albajar Spain	11	481 1.4×	110 0.9×	90 0.9×	53 0.8×	46 1.1×	22	698
Qing Yan United States	11	340 1.0×	74 0.6×	103 1.0×	37 0.6×	14 0.3×	19	583
Juliane S. Müller Germany	16	394 1.2×	74 0.6×	66 0.6×	91 1.4×	41 1.0×	20	843
Rachel Soemedi United States	9	405 1.2×	108 0.9×	44 0.4×	61 0.9×	116 2.8×	11	523
Anna Abramowicz Poland	6	440 1.3×	149 1.2×	52 0.5×	25 0.4×	21 0.5×	8	636
Haruka Hirose Japan	12	305 0.9×	37 0.3×	112 1.1×	69 1.1×	24 0.6×	35	579
Sigve Nakken Norway	14	354 1.1×	89 0.7×	115 1.1×	20 0.3×	16 0.4×	40	640

Countries citing papers authored by Alfons Meindl

Since Specialization

Citations

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

Fields of papers citing papers by Alfons Meindl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alfons Meindl

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

All Works

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14 of 14 papers shown

Heublein, Sabine, et al.. (2017). Vitamin D receptor, Retinoid X receptor and peroxisome proliferator-activated receptor γ are overexpressed in BRCA1 mutated breast cancer and predict prognosis. Journal of Experimental & Clinical Cancer Research. 36(1). 57–57. 28 indexed citations

Groß, Eva, Harm van Tinteren, Stefanie Avril, et al.. (2016). Identification of BRCA1-like triple-negative breast cancers by quantitative multiplex-ligation-dependent probe amplification (MLPA) analysis of BRCA1-associated chromosomal regions: a validation study. BMC Cancer. 16(1). 811–811. 11 indexed citations

Heublein, Sabine, Doris Mayr, Alfons Meindl, et al.. (2015). Thyroid Hormone Receptors Predict Prognosis in BRCA1 Associated Breast Cancer in Opposing Ways. PLoS ONE. 10(6). e0127072–e0127072. 36 indexed citations

Magdolen, Viktor, Tibor Schuster, Matthias Kotzsch, et al.. (2013). Downregulation of Serine Protease HTRA1 Is Associated with Poor Survival in Breast Cancer. PLoS ONE. 8(4). e60359–e60359. 34 indexed citations

Meindl, Alfons, Katharina Eirich, Stefanie Engert, et al.. (2012). Germline RAD51C mutations confer susceptibility to ovarian cancer. Nature Genetics. 44(5). 476–476. 5 indexed citations

Belohradsky, Bernd H., et al.. (2011). Two new families with X-linked inhibitor of apoptosis deficiency and a review of all 26 published cases. Journal of Allergy and Clinical Immunology. 127(2). 544–546. 11 indexed citations

Ramser, Juliane, Mary Ellen Ahearn, C Lenski, et al.. (2008). Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy. The American Journal of Human Genetics. 82(1). 188–193. 124 indexed citations

Martínez‐Garay, Isabel, Miguel Tomás Vila, Silvestre Oltra, et al.. (2006). A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation. European Journal of Human Genetics. 15(1). 29–34. 28 indexed citations

Hügle, Boris, Itziar Astigarraga, Jan‐Inge Henter, et al.. (2006). Simultaneous manifestation of fulminant infectious mononucleosis with haemophagocytic syndrome and B-cell lymphoma in X-linked lymphoproliferative disease. European Journal of Pediatrics. 166(6). 589–593. 8 indexed citations

10.

Frank, Bernd, Kari Hemminki, Barbara Wappenschmidt, et al.. (2005). Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant. Carcinogenesis. 27(3). 606–609. 42 indexed citations

11.

Groß, Eva, Katharina Seck, Volkmar Mueller, et al.. (2003). Detailed analysis of five mutations in dihydropyrimidine dehydrogenase detected in cancer patients with 5-fluorouracil-related side effects. Human Mutation. 22(6). 498–498. 49 indexed citations

12.

Linari, Marco, Forbes Manson, Alan J. Wright, et al.. (1998). The delta subunit of rod phosphodiesterase interacts with the RCC1 homologous domain of RPGR. MPG.PuRe (Max Planck Society). 1 indexed citations

13.

Meindl, Alfons, et al.. (1995). Missense mutations in the NDP gene in patients with a less severe course of Norrie disease. Human Molecular Genetics. 4(3). 489–490. 53 indexed citations

14.

Deufel, Thomas, Astrid Golla, David Iles, et al.. (1992). Evidence for genetic heterogeneity of malignant hyperthermia susceptibility.. PubMed. 50(6). 1151–61. 60 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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