Marion Mandl

771 total citations
8 papers, 572 citations indexed

About

Marion Mandl is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Marion Mandl has authored 8 papers receiving a total of 572 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pathology and Forensic Medicine, 2 papers in Molecular Biology and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Marion Mandl's work include Genetic factors in colorectal cancer (7 papers), Colorectal Cancer Treatments and Studies (2 papers) and Cancer Genomics and Diagnostics (2 papers). Marion Mandl is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Colorectal Cancer Treatments and Studies (2 papers) and Cancer Genomics and Diagnostics (2 papers). Marion Mandl collaborates with scholars based in Germany and France. Marion Mandl's co-authors include Waltraut Friedl, Reiner Caspari, Peter Propping, Martina Kadmon, Gabriela Möslein, Albert J. Augustin, T. Böker, Cécile Boisson, Gilles Thomas and K. W. Ecker and has published in prestigious journals such as The Lancet, Human Molecular Genetics and Human Genetics.

In The Last Decade

Marion Mandl

8 papers receiving 542 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marion Mandl Germany	8	502	299	118	112	103	8	572
P Mondini Italy	14	290 0.6×	186 0.6×	110 0.9×	110 1.0×	205 2.0×	28	568
Sandra Birdsall United Kingdom	12	168 0.3×	119 0.4×	93 0.8×	240 2.1×	173 1.7×	15	488
Ella Barclay United Kingdom	13	408 0.8×	288 1.0×	40 0.3×	200 1.8×	400 3.9×	18	800
Kazuhisa Shitoh Japan	11	439 0.9×	378 1.3×	29 0.2×	54 0.5×	285 2.8×	19	669
G Michils Belgium	9	211 0.4×	129 0.4×	237 2.0×	136 1.2×	152 1.5×	13	525
Kevin Pack United Kingdom	11	560 1.1×	594 2.0×	31 0.3×	273 2.4×	273 2.7×	18	928
W. Weybora Austria	6	72 0.1×	149 0.5×	70 0.6×	113 1.0×	83 0.8×	13	354
Bénédicte Thuille France	5	345 0.7×	272 0.9×	50 0.4×	275 2.5×	271 2.6×	8	668
Iwona Wlodarska Belgium	11	250 0.5×	137 0.5×	48 0.4×	31 0.3×	96 0.9×	14	441
Dietlinde Stienen Germany	9	514 1.0×	230 0.8×	18 0.2×	92 0.8×	198 1.9×	11	715

Countries citing papers authored by Marion Mandl

Since Specialization

Citations

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

Fields of papers citing papers by Marion Mandl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marion Mandl

This figure shows the co-authorship network connecting the top 25 collaborators of Marion Mandl. A scholar is included among the top collaborators of Marion Mandl 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 Marion Mandl. Marion Mandl 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.

Mandl, Marion, Reiner Caspari, Anna Jauch, et al.. (1996). Familial adenomatous polyposis: A submicroscopic deletion at the APC locus in a family with mentally normal patients. Human Genetics. 97(2). 204–208. 19 indexed citations

2.

Caspari, Reiner, Waltraut Friedl, Marion Mandl, et al.. (1995). Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444. Human Molecular Genetics. 4(3). 337–340. 283 indexed citations

3.

Caspari, Reiner, Waltraut Friedl, Marion Mandl, et al.. (1994). Familial adenomatous polyposis: mutation at codon 1309 and early onset of colon cancer. The Lancet. 343(8898). 629–632. 158 indexed citations

4.

Mandl, Marion, et al.. (1994). A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells — implications for predictive diagnosis. Human Molecular Genetics. 3(6). 1009–1011. 13 indexed citations

5.

Mandl, Marion, et al.. (1994). Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis. Human Molecular Genetics. 3(1). 181–184. 50 indexed citations

6.

Mandl, Marion, et al.. (1994). Eleven novel germline mutations in the adenomatous polyposis coli (APC) gene. Human Molecular Genetics. 3(9). 1703–1704. 17 indexed citations

7.

Friedl, Waltraut, et al.. (1993). Single-step screening method for the most common mutations in familial adenomatous polyposis. Human Molecular Genetics. 2(9). 1481–1482. 16 indexed citations

8.

Caspari, Reiner, Waltraut Friedl, Albert J. Augustin, et al.. (1993). Predictive diagnosis in familial adenomatous polyposis: evaluation of molecular genetic and ophthalmologic methods.. PubMed. 31(11). 646–52. 16 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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