Marco Mächler

1.0k total citations
16 papers, 841 citations indexed

About

Marco Mächler is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Marco Mächler has authored 16 papers receiving a total of 841 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 4 papers in Immunology. Recurrent topics in Marco Mächler's work include Neutrophil, Myeloperoxidase and Oxidative Mechanisms (2 papers), Neuroblastoma Research and Treatments (2 papers) and Prenatal Screening and Diagnostics (2 papers). Marco Mächler is often cited by papers focused on Neutrophil, Myeloperoxidase and Oxidative Mechanisms (2 papers), Neuroblastoma Research and Treatments (2 papers) and Prenatal Screening and Diagnostics (2 papers). Marco Mächler collaborates with scholars based in Switzerland, Germany and United Kingdom. Marco Mächler's co-authors include Max L. Birnstiel, Paul Boseley, Rudolf Portmann, Tom Moss, W. Bär, Adelgunde Kratzer, Werner Schmid, Wendy P. Robinson, A. Prader and Yan‐Xin Xie and has published in prestigious journals such as Cell, Nucleic Acids Research and Blood.

In The Last Decade

Marco Mächler

16 papers receiving 783 citations

Peers

Marco Mächler
Emmelien Aten Netherlands
Andreas Ohlenbusch Germany
Panayiotis A. Ioannou Australia
Marja E. Jakobs Netherlands
R. Curtis Rogers United States
John Melnyk United States
Andrew Collick United Kingdom
Katsuhiro FUKUTA Japan
Chiara Rasi Sweden
R Hubert India
Emmelien Aten Netherlands
Marco Mächler
Citations per year, relative to Marco Mächler Marco Mächler (= 1×) peers Emmelien Aten

Countries citing papers authored by Marco Mächler

Since Specialization
Citations

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

Fields of papers citing papers by Marco Mächler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Mächler

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

All Works

16 of 16 papers shown
1.
Castro-Giner, Francesc, Manolis Kogevinas, Medea Imboden, et al.. (2009). Joint effect of obesity andTNFAvariability on asthma: two international cohort studies. European Respiratory Journal. 33(5). 1003–1009. 39 indexed citations
2.
Mächler, Marco, Toni M Glaus, & Claudia E Reusch. (2004). Lebensbedrohliche intestinale Blutungen bei einem Bearded Collie im Zusammenhang mit einem Futterzusatz für Pferde. Schweizer Archiv für Tierheilkunde. 146(10). 479–482. 3 indexed citations
3.
Lorenz, Peter, R Bollmann, Marco Mächler, et al.. (1991). False‐negative prenatal exclusion of Wiskott‐Aldrich syndrome by measurement of fetal platelet count and size. Prenatal Diagnosis. 11(11). 819–825. 4 indexed citations
4.
Spiegel, Roland, et al.. (1991). [Neurofibromatosis Type 1: genetic studies with DNA markers in 38 families].. PubMed. 121(40). 1445–52. 3 indexed citations
5.
Robinson, Wendy P., Armand Bottani, Yan‐Xin Xie, et al.. (1991). Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients. PubMed. 49(6). 1219–34. 229 indexed citations
6.
Liechti‐Gallati, Sabina, Volker Schneider, Marco Mächler, et al.. (1990). Haplotype analysis for CF‐linked DNA polymorphisms in Switzerland. Clinical Genetics. 37(6). 442–449. 3 indexed citations
7.
Robinson, Wendy P., et al.. (1990). A second Nsil RFLP at the CYBB locus. Nucleic Acids Research. 18(16). 4966–4966. 13 indexed citations
8.
Orth, Ulrike, Albert Schinzel, Marco Mächler, & A. Gal. (1990). X-chromosomal erbliche Nachtblindheit: Erkennen von Überträgerinnen durch Segregationsanalyse mit gekoppelten DNA-Markern. Klinische Monatsblätter für Augenheilkunde. 196(5). 269–272. 3 indexed citations
9.
Gal, Andreas, A. Schinzel, Ulrike Orth, et al.. (1989). Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp. Human Genetics. 81(4). 315–318. 35 indexed citations
10.
Boltshauser, Eugen, et al.. (1989). Neurofibromatosis type 1 in a child of a parent with segmental neurofibromatosis (NF-5).. PubMed. 2(4). 244–5. 36 indexed citations
11.
Bär, W., Adelgunde Kratzer, Marco Mächler, & Werner Schmid. (1988). Postmortem stability of DNA. Forensic Science International. 39(1). 59–70. 154 indexed citations
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14.
Hammer, Jürg, Marco Mächler, & Werner Schmid. (1987). [DNA diagnosis of Huntington's chorea. Application and genetic counseling in 4 involved families].. PubMed. 117(51). 2074–80. 1 indexed citations
15.
Grosschedl, Rudolf, Marco Mächler, Urs Hoffmann Rohrer, & Max L. Birnstiel. (1983). A functional component of the sea urchin H2A gene modulator contains an extended sequence homology to a viral enhancer. Nucleic Acids Research. 11(23). 8123–8136. 23 indexed citations
16.
Boseley, Paul, Tom Moss, Marco Mächler, Rudolf Portmann, & Max L. Birnstiel. (1979). Sequence organization of the spacer DNA in a ribosomal gene unit of Xenopus laevis. Cell. 17(1). 19–31. 208 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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