Tuula Manninen

2.0k citations
16 papers · 1.4k · 1 hit paper · h-index 14

Impact in

Papers in

    • Glycosylation and Glycoproteins Research 5
    • Mitochondrial Function and Pathology 5
    • ATP Synthase and ATPases Research 2
    • RNA Research and Splicing 1
    • Lysosomal Storage Disorders Research 8

Tuula Manninen

16 papers receiving 1.3k citations

Tuula Manninen's Hit Papers

Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype 2002 · 530 citations
5300+8+16Years since publication100200300400500

Peers

Tuula Manninen
Comparison fields: 5 of 79
  • Neurology 389
  • Clinical Biochemistry 142
  • Immunology 343
  • Physiology 399
  • Cell Biology 167
Replace Bettina Brunner with:
Bettina Brunner Germany
Nicoleta Moisoi United Kingdom
Xavier Guillonneau France
Outi Kopra Finland
Alexander Reuter Germany
Kristina Klupsch United Kingdom
Julien Couthouis United States
Julia S. Schlehe United States
Yun-Zheng Le United States
Aleksandar Raković Germany
Tuula Manninen relative to Bettina Brunner Germany Bettina Brunner's profile →
Citations per field
00.5×1.5×2.1×
Bettina Brunner · 1×
Citations per year

Countries citing papers authored by Tuula Manninen

Since Specialization
Citations

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

Fields of papers citing papers by Tuula Manninen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Tuula Manninen, 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 Tuula Manninen Line = papers co-authored together Tuula Manninen links everyone, so they are left out of the graph.

All Works

16 of 16 papers shown
#Work
1
Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype
Hit paper breakdown →
2002530
2 2013149
3 1992113
4 1991105
5 200472
6 201271
7 200468
8 199154
9 201053
10 201234
11 199234
12 199529
13 199524
14 202415
15 19907
16 20245

About Tuula Manninen

Tuula Manninen is a scholar working on Molecular Biology, Physiology, Cell Biology, Rheumatology and Immunology, having authored 16 papers that have together received 1.4k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (8 papers), Glycosylation and Glycoproteins Research (5 papers), Mitochondrial Function and Pathology (5 papers), Cellular transport and secretion (4 papers), Glycogen Storage Diseases and Myoclonus (3 papers), ATP Synthase and ATPases Research (2 papers), RNA Research and Splicing (1 paper) and Trypanosoma species research and implications (1 paper). The work is most often cited by research in Neurology (389 citations), Clinical Biochemistry (142 citations), Immunology (343 citations), Physiology (399 citations) and Cell Biology (167 citations). Tuula Manninen has collaborated with scholars based in Finland, United States and Netherlands. Frequent co-authors include Leena Peltonen, Marino Muxfeldt Bianchin, Juha Paloneva, Grant P. Christman, Rolf Adolfsson, Karine Hovanes, Lisbeth Tranebjærg, Andrea Salmaggi, Yrjö T. Konttinen and Jami Mandelin. Their work appears in journals such as Genomics, Proceedings of the National Academy of Sciences, Human Molecular Genetics, Neurobiology of Disease and Pediatric Research.

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