Paula Jalonen

487 total citations
8 papers, 286 citations indexed

About

Paula Jalonen is a scholar working on Molecular Biology, Clinical Biochemistry and Sensory Systems. According to data from OpenAlex, Paula Jalonen has authored 8 papers receiving a total of 286 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 2 papers in Sensory Systems. Recurrent topics in Paula Jalonen's work include Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (4 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Paula Jalonen is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (4 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Paula Jalonen collaborates with scholars based in Sweden, United Kingdom and Belgium. Paula Jalonen's co-authors include Elena Jazin, Ulf Gyllensten, Lucia Cavelier, Eva Lindholm, Rolf Adolfsson, Ulf Pettersson, Robin Sherrington, Sarah H. Shaw, Birgit Ekholm and Guy Van Camp and has published in prestigious journals such as The American Journal of Human Genetics, Human Genetics and European Journal of Human Genetics.

In The Last Decade

Paula Jalonen

8 papers receiving 276 citations

Peers

Paula Jalonen

MB

GENET

CB

SS

NEURO

M. Maheshwari United States

Ernest C. Steele United States

Nadia Bahi France

Mohammad Saharul Islam Japan

Emily Moon United States

Haitian Nan China

Estelle Fédirko France

María T. Lázaro United States

Fabrice D. Heitz Switzerland

Kiyonobu Mizuno Japan

M. Maheshwari United States

Paula Jalonen

202 ×1.1

MB

139 ×1.3

GENET

8 ×0.2

CB

50 ×1.1

SS

13 ×0.4

NEURO

Citations per year, relative to Paula Jalonen Paula Jalonen (= 1×) peers M. Maheshwari

Countries citing papers authored by Paula Jalonen

Since Specialization

Citations

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

Fields of papers citing papers by Paula Jalonen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paula Jalonen

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

Cavelier, Lucia, Martti T. Tammi, Paula Jalonen, et al.. (2004). MtDNA Mutations in Maternally Inherited Diabetes: Presence of the 3397 ND1 Mutation Previously Associated with Alzheimer's and Parkinson's Disease. Hereditas. 135(1). 65–70. 20 indexed citations

2.

Lindholm, Eva, Birgit Ekholm, Sarah H. Shaw, et al.. (2001). A Schizophrenia-Susceptibility Locus at 6q25, in One of the World's Largest Reported Pedigrees. The American Journal of Human Genetics. 69(1). 96–105. 111 indexed citations

3.

Cavelier, Lucia, Elena Jazin, Paula Jalonen, & Ulf Gyllensten. (2000). MtDNA substitution rate and segregation of heteroplasmy in coding and noncoding regions. Human Genetics. 107(1). 45–50. 43 indexed citations

4.

Cavelier, Lucia, Elena Jazin, Paula Jalonen, & Ulf Gyllensten. (2000). MtDNA substitution rate and segregation of heteroplasmy in coding and noncoding regions. Human Genetics. 107(1). 45–50. 19 indexed citations

5.

Balciuniene, Jorune, Niklas Dahl, Paula Jalonen, et al.. (1999). Alpha-tectorin involvement in hearing disabilities: one gene - two phenotypes. Human Genetics. 105(3). 211–216. 49 indexed citations

6.

Balciuniene, Jorune, Niklas Dahl, Paula Jalonen, et al.. (1999). Alpha-tectorin involvement in hearing disabilities: one gene – two phenotypes. Human Genetics. 105(3). 211–216. 2 indexed citations

7.

Lindholm, Eva, Lucia Cavelier, W. Mathias Howell, et al.. (1998). Mitochondrial sequence variants in patients with schizophrenia.. PubMed. 5(6). 406–12. 23 indexed citations

8.

Lindholm, Eva, Lucia Cavelier, W. Mathias Howell, et al.. (1997). Mitochondrial Sequence Variants in Patients with Schizophrenia. European Journal of Human Genetics. 5(6). 406–412. 19 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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