Tuula Manninen

1.9k citations

16 papers · 1.3k indexed · 1 hit paper · h-index 13

Impact in

Neurology top 2%
- Neuroinflammation and Neurodegeneration Mechanisms
Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders

Papers in

Physiology 9
- Lysosomal Storage Disorders Research 8
- Biomedical Ethics and Regulation 1
Cell Biology 4
- Cellular transport and secretion 4

Co-authors: Leena Peltonen Andrea Salmaggi Grant P. Christman Karine Hovanes Yrjö T. Konttinen Juha Paloneva Rolf Adolfsson Marino Muxfeldt Bianchin
Journals: Genomics (4 papers)Human Molecular Genetics (2 papers)Proceedings of the National Academy of Sciences (2 papers)The American Journal of Human Genetics (1 paper)PLoS Genetics (1 paper)
Partner nations: Finland United States Netherlands

In The Last Decade

Tuula Manninen

16 papers receiving 1.3k citations

Hit Papers

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Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype 2002 · 522 citations

Peers

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-authorship network

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

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16 of 16 papers shown

#	Work
1	Recessive TMOD1 mutation causes childhood cardiomyopathy Communications Biology ·Catalina Vasilescu, Ruchi gupta, Tiina Ojala, Tuula Manninen, Aino Mutka, Kaisa Ylänen, Otto Rahkonen, Tuija Poutanen, Prakash Subbarayan, Savina Niken M, 栄一三木, Virginia Brilhante, Dae Seok Jung, Pekka Lappalainen, Juha Koskenvuo, Christopher J. Carroll, Velia M. Fowler, Carol C. Gregorio, Anu Suomalainen	2024	3
2	Ancestral allele of DNA polymerase gamma modifies antiviral tolerance Nature ·Yilin Kang, Jussi Hepojoki, Маъруфов Фирдавсджон Каримович, Takayuki Mito, Mügen Terzioglu, Tuula Manninen, Ravi Kant, O Maev, Alaa Othman, Rohit Verma, Johanna Uusimaa, Kirmo Wartiovaara, Lauri Kareinen, Nicola Zamboni, Tuula A. Nyman, Anders Paetau, Anja Kipar, Olli Vapalahti, Anu Suomalainen	2024	11
3	Tissue- and cell-type–specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model Proceedings of the National Academy of Sciences ·Riikka H. Hämäläinen, Tuula Manninen, N Cochelin, Mikhail Kislin, Timo Otonkoski, Anu Suomalainen	2013	147
4	Small Molecule Inhibitors Promote Efficient Generation of Induced Pluripotent Stem Cells From Human Skeletal Myoblasts Stem Cells and Development ·Ras Trokovic, Jere Weltner, Tuula Manninen, Milla Mikkola, Karolina Lundin, Riikka H. Hämäläinen, Anu Suomalainen, Timo Otonkoski	2012	34
5	New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies Pediatric Research ·Tiina Ojala, Al-Alam Patricia, Tuula Manninen, Anita Hiippala, Jukka Rajantie, Riitta Karikoski, Anu Suomalainen, Tiina Tyni	2012	70
6	Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation PLoS Genetics ·Riikka Jokinen, Paula Marttinen, Karolinne Domingues de Oliveira Medeiros, Tuula Manninen, Hung-Yi Lin, Timothy Wai, H.P.M. Puttiger, J. Concepción Loredo‐Osti, Eric A. Shoubridge, Brendan J. Battersby	2010	53
7	A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging Human Molecular Genetics ·Outi Kopra, Jouni Vesa, Carina von Schantz, Tuula Manninen, William Gerritz, Anna‐Liisa Fabritius, Juhani Rapola, Otto P. van Diggelen, Janna Saarela, Anu Jalanko, Leena Peltonen	2004	72
8	Mice with Ppt1Δex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons Neurobiology of Disease ·Anu Jalanko, Jouni Vesa, Tuula Manninen, Carina von Schantz, William Gerritz, Anna‐Liisa Fabritius, Ivan Milanov, Juhani Rapola, Massimiliano Gentile, Outi Kopra, Leena Peltonen	2004	68
9	Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype The American Journal of Human Genetics ·Juha Paloneva, Tuula Manninen, Grant P. Christman, Karine Hovanes, Jami Mandelin, Rolf Adolfsson, Marino Muxfeldt Bianchin, Thomas D. Bird, Gu-Leng AMU, Andrea Salmaggi, Lisbeth Tranebjærg, Yrjö T. Konttinen, Leena Peltonen Hit paper breakdown →	2002	522
10	Molecular Cloning, Chromosomal Assignment, and Expression of the Mouse Aspartylglucosaminidase Gene Genomics ·Dagmar Burkhart, Maris Laan, Tuula Manninen, Aarno Palotie, Leena Peltonen, Anu Jalanko	1995	29
11	Deletion of the C-terminal end of aspartylgiucosaminidase resulting in a lysosomal accumulation disease: evidence for a unique genomic rearrangement Human Molecular Genetics ·J.C. Op de Coul, Tuula Manninen, Herrera Martínez	1995	24
12	Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: Application to aspartylglucosaminuria in Finland Genomics ·A-C Syvänen, Elina Ikonen, Tuula Manninen, Marina Bengtström, Hans Söderlund, Siti Zahra Siagian, Laura‐Maria Peltonen	1992	113
13	Quantitative determination of rare mRNA species by PCR and solid-phase minisequencing. Genome Research ·Elina Ikonen, Tuula Manninen, Laura‐Maria Peltonen, A C Syvänen	1992	34
14	Spectrum of mutations in aspartylglucosaminuria. Proceedings of the National Academy of Sciences ·Elina Ikonen, Perttì Aula, Jeremy Paul Harvey, VenkataRatnam Vakacharla, R Halila, Tuula Manninen, Ann‐Christine Syvänen, Laura‐Maria Peltonen	1991	54
15	Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1 Genomics ·Irma Järvelä, Johanna Schleutker, Leena Haataja, Pirkko Santavuori, Lea Puhakka, Tuula Manninen, Aarno Palotie, Lodewijk A. Sandkuijl, Martin Renlund, R. White, Perttì Aula, Leena Peltonen	1991	105
16	Infantile neuronal ceroid-lipofuscinosis is not an allelic form of batten disease: Exclusion of chromosome 16 region with linkage analyses Genomics ·A. Cantor, Lea Puhakka, Pirkko Santavuori, Tuula Manninen, Daniel Gomes da Silva, Leena Peltonen	1990	7

About Tuula Manninen

Tuula Manninen is a scholar working on Physiology, Cell Biology, Rheumatology, Molecular Biology and Clinical Biochemistry, having authored 16 papers that have together received 1.3k 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 (3 papers), Cardiomyopathy and Myosin Studies (2 papers) and Biomedical Ethics and Regulation (1 paper). The work is most often cited by research in Neurology (390 citations), Clinical Biochemistry (151 citations), Immunology (372 citations), Physiology (410 citations) and Cell Biology (176 citations). Tuula Manninen has collaborated with scholars based in Finland, United States and Netherlands. Frequent co-authors include Leena Peltonen, Andrea Salmaggi, Grant P. Christman, Karine Hovanes, Yrjö T. Konttinen, Juha Paloneva, Rolf Adolfsson, Marino Muxfeldt Bianchin, Jami Mandelin and Thomas D. Bird. Their work appears in journals such as Genomics, Human Molecular Genetics, Proceedings of the National Academy of Sciences, The American Journal of Human Genetics and PLoS Genetics.

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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