M Doss

46 papers receiving 511 citations

Peers

M Doss
Comparison fields: 5 of 68
  • Pediatrics, Perinatology and Child Health 210
  • Clinical Biochemistry 63
  • Molecular Biology 453
  • Rheumatology 91
  • Pulmonary and Respiratory Medicine 107
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Countries citing papers authored by M Doss

Since Specialization
Citations

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

Fields of papers citing papers by M Doss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside M Doss, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M Doss Line = papers co-authored together M Doss links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 53 papers — load more, or switch the sort, to bring in the rest.

#Work
1 197145
2 197444
3 200440
4 198740
5
Diagnostic and pathogenetic implications of urinary coproporphyrin excretion in the Dubin-Johnson syndrome.
199031
6 198128
7
Hepatic porphyrias: pathobiochemical, diagnostic, and therapeutic implications.
198228
8 198027
9 197224
10 198523
11 198522
12
Hexachlorobenzene porphyria in rats as a model for human chronic hepatic porphyrias.
197621
13 197117
14 196917
15 197915
16 197813
17 199911
18 197110
19
[Influence of diet, glycine and alcohol on porphyrinuria in chronic hepatitic porphyria].
19719
20 19857

About M Doss

M Doss is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Clinical Biochemistry, Pulmonary and Respiratory Medicine and Rheumatology, having authored 53 papers that have together received 564 indexed citations. Recurring topics across this work include Porphyrin Metabolism and Disorders (42 papers), Neonatal Health and Biochemistry (30 papers), Heme Oxygenase-1 and Carbon Monoxide (23 papers), Metabolism and Genetic Disorders (13 papers), Folate and B Vitamins Research (4 papers), Methemoglobinemia and Tumor Lysis Syndrome (4 papers), Biomedical Research and Pathophysiology (2 papers) and Porphyrin and Phthalocyanine Chemistry (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (210 citations), Clinical Biochemistry (63 citations), Molecular Biology (453 citations), Rheumatology (91 citations) and Pulmonary and Respiratory Medicine (107 citations). M Doss has collaborated with scholars based in Germany, France and United States. Frequent co-authors include Axel J. Schmidt, M. Frank, W Meinhof, R. v. Tiepermann, U. Groß, G. Koss, H Henning, H. P. Seelig, Shigeru Sassa and G Strohmeyer. Their work appears in journals such as Journal of Molecular Medicine, Journal of Inherited Metabolic Disease, Clinical Chemistry and Laboratory Medicine (CCLM), Hormone and Metabolic Research and Annals of Clinical Biochemistry International Journal of Laboratory Medicine.

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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