Ilga Porth

4.1k total citations
81 papers, 2.1k citations indexed

About

Ilga Porth is a scholar working on Molecular Biology, Genetics and Nature and Landscape Conservation. According to data from OpenAlex, Ilga Porth has authored 81 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 27 papers in Genetics and 20 papers in Nature and Landscape Conservation. Recurrent topics in Ilga Porth's work include Plant biochemistry and biosynthesis (17 papers), Plant Gene Expression Analysis (16 papers) and Forest ecology and management (16 papers). Ilga Porth is often cited by papers focused on Plant biochemistry and biosynthesis (17 papers), Plant Gene Expression Analysis (16 papers) and Forest ecology and management (16 papers). Ilga Porth collaborates with scholars based in Canada, China and United States. Ilga Porth's co-authors include Yousry A. El‐Kassaby, Jaroslav Klápště, Blaise Ratcliffe, Shawn D. Mansfield, Carl J. Douglas, Charles Chen, Omnia Gamal El‐Dien, Antoine Kremer, Kornél Burg and Caroline Scotti‐Saintagne and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and PLANT PHYSIOLOGY.

In The Last Decade

Ilga Porth

79 papers receiving 2.1k citations

Peers

Ilga Porth

GENET

NLC

ECOLO

Filippos A. Aravanopoulos Greece

Paul Arens Netherlands

Peter Breyne Belgium

Marco Cosimo Simeone Italy

Craig S. Echt United States

Josquin Tibbits Australia

M. Ángeles Guevara Spain

Scott E. Schlarbaum United States

Matthias Fladung Germany

J. H. A. Barker United Kingdom

Filippos A. Aravanopoulos Greece

Ilga Porth

664 ×0.7

418 ×0.5

GENET

349 ×0.4

230 ×0.5

NLC

244 ×1.0

ECOLO

Citations per year, relative to Ilga Porth Ilga Porth (= 1×) peers Filippos A. Aravanopoulos

Countries citing papers authored by Ilga Porth

Since Specialization

Citations

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

Fields of papers citing papers by Ilga Porth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilga Porth

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

All Works

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20 of 20 papers shown

Wang, Siqin, Miao Yu, Chang Liu, et al.. (2025). Integrating mitoflash, energy substrate, and hormone analyses to advance understanding of Magnolia endodormancy mechanisms. International Journal of Biological Macromolecules. 315(Pt 1). 144333–144333. 1 indexed citations

Fijarczyk, Anna, Ilga Porth, Piotr Robakowski, et al.. (2025). Genomic investigations of successful invasions: the picture emerging from recent studies. Biological reviews/Biological reviews of the Cambridge Philosophical Society. 100(3). 1396–1418. 6 indexed citations

Hernández‐Díaz, José Ciro, Juan Pablo Jaramillo‐Correa, David S. Gernandt, et al.. (2024). Causes of heterozygosity excess: The case of Mexican populations of Populus tremuloides. Plant Diversity. 47(3). 415–428.

Godbout, Julie, et al.. (2024). A cryptic syngameon withinBetulashrubs revealed: Implications for conservation in changing subarctic environments. Evolutionary Applications. 17(4). e13689–e13689. 2 indexed citations

DeMerchant, Ian, et al.. (2024). Oak genomics for nature-based solutions: shaping future forests and resilient landscapes in Canada. Tree Genetics & Genomes. 20(3). 2 indexed citations

Nie, Shuai, Tian‐Le Shi, Xue-Chan Tian, et al.. (2024). Progress in phylogenetics, multi-omics and flower coloration studies in <i>Rhododendron</i>. SHILAP Revista de lepidopterología. 4(1). 0–0. 2 indexed citations

Roe, Amanda D., Brian Boyle, Melody A. Keena, et al.. (2024). Tracking the North American Asian Longhorned Beetle Invasion With Genomics. Evolutionary Applications. 17(11). e70036–e70036. 2 indexed citations

El‐Kassaby, Yousry A., Eduardo P. Cappa, Charles Chen, Blaise Ratcliffe, & Ilga Porth. (2024). Efficient genomics-based ‘end-to-end’ selective tree breeding framework. Heredity. 132(2). 98–105. 7 indexed citations

Yu, Miao, Siqin Wang, Tian‐Le Shi, et al.. (2024). Integration of Mitoflash and Time‐Series Transcriptomics Facilitates Energy Dynamics Tracking and Substrate Supply Analysis of Floral Thermogenesis in Lotus. Plant Cell & Environment. 48(1). 893–906. 8 indexed citations

10.

He, Xiangfeng, Xuemei Yan, Cunfu Lu, et al.. (2023). Chromosome‐scale genome assembly and insights into the metabolome and gene regulation of leaf color transition in an important oak species, Quercus dentata. New Phytologist. 238(5). 2016–2032. 30 indexed citations

11.

Javal, Marion, Isabelle Giguère, Géraldine Roux, et al.. (2022). Genome‐scale phylogeography resolves the native population structure of the Asian longhorned beetle, Anoplophora glabripennis (Motschulsky). Evolutionary Applications. 15(6). 934–953. 12 indexed citations

12.

Jiao, Si‐Qian, Meiyu Li, Shanshan Zhou, et al.. (2021). Variation in Platycladus orientalis (Cupressaceae) Reproductive Output and Its Effect on Seed Orchard Crops’ Genetic Diversity. Forests. 12(11). 1429–1429. 2 indexed citations

13.

Klápště, Jaroslav, Antoine Kremer, Kornél Burg, et al.. (2020). Quercus species divergence is driven by natural selection on evolutionarily less integrated traits. Heredity. 126(2). 366–382. 6 indexed citations

14.

Torre, Amanda R. De La, et al.. (2019). Functional and morphological evolution in gymnosperms: A portrait of implicated gene families. Evolutionary Applications. 13(1). 210–227. 34 indexed citations

15.

Zhou, Shanshan, Zhen Xing, Hui Liu, et al.. (2019). In-depth transcriptome characterization uncovers distinct gene family expansions for Cupressus gigantea important to this long-lived species’ adaptability to environmental cues. BMC Genomics. 20(1). 213–213. 13 indexed citations

16.

Prunier, Julien, Audrey Lemaçon, Alexandre Bastien, et al.. (2019). LD-annot: A Bioinformatics Tool to Automatically Provide Candidate SNPs With Annotations for Genetically Linked Genes. Frontiers in Genetics. 10. 1192–1192. 8 indexed citations

17.

Porth, Ilga, Richard White, Barry Jaquish, & Kermit Ritland. (2018). Partial correlation analysis of transcriptomes helps detangle the growth and defense network in spruce. New Phytologist. 218(4). 1349–1359. 18 indexed citations

18.

McKown, Athena D., Jaroslav Klápště, Robert D. Guy, et al.. (2017). Sexual homomorphism in dioecious trees: extensive tests fail to detect sexual dimorphism in Populus. Scientific Reports. 7(1). 49 indexed citations

19.

Porth, Ilga, Jaroslav Klápště, Athena D. McKown, et al.. (2015). Evolutionary Quantitative Genomics of Populus trichocarpa. PLoS ONE. 10(11). e0142864–e0142864. 20 indexed citations

20.

McKown, Athena D., Jaroslav Klápště, Robert D. Guy, et al.. (2014). Genome-wide association implicates numerous genes and pleiotropy underlying ecological trait variation in natural populations of Populus trichocarpa. New Phytologist. 1 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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