Eva Lindholm

2.3k total citations
14 papers, 625 citations indexed

About

Eva Lindholm is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Eva Lindholm has authored 14 papers receiving a total of 625 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Eva Lindholm's work include Genetic Associations and Epidemiology (7 papers), Mitochondrial Function and Pathology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Eva Lindholm is often cited by papers focused on Genetic Associations and Epidemiology (7 papers), Mitochondrial Function and Pathology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Eva Lindholm collaborates with scholars based in Sweden, United States and United Kingdom. Eva Lindholm's co-authors include Elena Jazin, Peter Saetre, Elin Axelsson, Johan Kreuger, Lina Emilsson, Rolf Adolfsson, Ulf Pettersson, Birgit Ekholm, Paula Jalonen and Karolina A. Åberg and has published in prestigious journals such as Genome Research, The American Journal of Human Genetics and BMC Psychiatry.

In The Last Decade

Eva Lindholm

14 papers receiving 611 citations

Peers

Eva Lindholm
Kaori Sudo Japan
Janet Harwood United Kingdom
Rodrigo R. R. Duarte United Kingdom
Sharon Mexal United States
Adam R. Smith United Kingdom
Hae‐Chul Park South Korea
Romana Tomasoni Italy
William S. Ulrich United States
Kyungdeok Kim South Korea
Annie Kathuria United States
Kaori Sudo Japan
Eva Lindholm
Citations per year, relative to Eva Lindholm Eva Lindholm (= 1×) peers Kaori Sudo

Countries citing papers authored by Eva Lindholm

Since Specialization
Citations

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

Fields of papers citing papers by Eva Lindholm

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eva Lindholm

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

All Works

14 of 14 papers shown
1.
Kawecki, Maciej, Philipp Gutfreund, Eva Lindholm, et al.. (2016). Probing the dynamics of high-viscosity entangled polymers under shear using Neutron Spin Echo spectroscopy. Journal of Physics Conference Series. 746. 12014–12014. 5 indexed citations
2.
Åberg, Karolina A., Elin Axelsson, Peter Saetre, et al.. (2008). Support for schizophrenia susceptibility locus on chromosome 2q detected in a Swedish isolate using a dense map of microsatellites and SNPs. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(7). 1238–1244. 10 indexed citations
3.
Saetre, Peter, Lina Emilsson, Elin Axelsson, et al.. (2007). Inflammation-related genes up-regulated in schizophrenia brains. BMC Psychiatry. 7(1). 46–46. 230 indexed citations
4.
Åberg, Karolina A., Peter Saetre, Eva Lindholm, et al.. (2005). Human QKI, a new candidate gene for schizophrenia involved in myelination. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(1). 84–90. 90 indexed citations
5.
Lindholm, Eva, Junying Zhang, Susan E. Hodge, & David A. Greenberg. (2004). The Reliability of Haplotyping Inference in Nuclear Families: Misassignment Rates for SNPs and Microsatellites. Human Heredity. 57(3). 117–127. 4 indexed citations
6.
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
7.
Lindholm, Eva, Susan E. Hodge, & David A. Greenberg. (2004). Comparative Informativeness for Linkage of Multiple SNPs and Single Microsatellites. Human Heredity. 58(3-4). 164–170. 8 indexed citations
8.
Lindholm, Eva, et al.. (2004). Reconstruction of ancestral haplotypes in a 12-generation schizophrenia pedigree. Psychiatric Genetics. 14(1). 1–8. 19 indexed citations
9.
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
10.
Lindholm, Eva, Birgit Ekholm, Jorune Balciuniene, et al.. (1999). Linkage analysis of a large swedish kindred provides further support for a susceptibility locus for schizophrenia on chromosome 6p23. American Journal of Medical Genetics. 88(4). 369–377. 40 indexed citations
11.
Lindholm, Eva, Birgit Ekholm, Jorune Balciuniene, et al.. (1999). Linkage analysis of a large swedish kindred provides further support for a susceptibility locus for schizophrenia on chromosome 6p23. American Journal of Medical Genetics. 88(4). 369–377. 5 indexed citations
12.
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
13.
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
14.
Magnusson, Patrik K. E., Jorune Balciuniene, Claes Wadelius, et al.. (1996). Chromosome-specific panels of tri- and tetranucleotide microsatellite markers for multiplex fluorescent detection and automated genotyping: evaluation of their utility in pathology and forensics.. Genome Research. 6(12). 1170–1176. 41 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Kaori Sudo Breakdown of academic impact, for papers by Janet Harwood Breakdown of academic impact, for papers by Rodrigo R. R. Duarte Breakdown of academic impact, for papers by Sharon Mexal Breakdown of academic impact, for papers by Adam R. Smith Breakdown of academic impact, for papers by Hae‐Chul Park Breakdown of academic impact, for papers by Romana Tomasoni Breakdown of academic impact, for papers by William S. Ulrich Breakdown of academic impact, for papers by Kyungdeok Kim Breakdown of academic impact, for papers by Annie Kathuria
Rankless by CCL
2026