Märt Möls

801 total citations
18 papers, 298 citations indexed

About

Märt Möls is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Märt Möls has authored 18 papers receiving a total of 298 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in Märt Möls's work include Genomics and Phylogenetic Studies (5 papers), Genetic Associations and Epidemiology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Märt Möls is often cited by papers focused on Genomics and Phylogenetic Studies (5 papers), Genetic Associations and Epidemiology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Märt Möls collaborates with scholars based in Estonia, Finland and Australia. Märt Möls's co-authors include Maido Remm, Lauris Kaplinski, Maarja Lepamets, Kristiina Rull, Sulev Kõks, Jaana Männik, Kärt Tomberg, Tarmo Puurand, Maris Laan and Gyaneshwer Chaubey and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Märt Möls

17 papers receiving 296 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Märt Möls Estonia	8	136	75	62	38	35	18	298
Huaming Xu China	11	277 2.0×	32 0.4×	18 0.3×	26 0.7×	50 1.4×	33	420
Honghong He China	14	230 1.7×	78 1.0×	26 0.4×	3 0.1×	64 1.8×	52	489
Xiefang Yuan China	12	117 0.9×	16 0.2×	25 0.4×	22 0.6×	70 2.0×	19	334
Michiyo Sugiyama Japan	11	70 0.5×	39 0.5×	18 0.3×	79 2.1×	15 0.4×	38	333
Alise J. Ponsero United States	14	276 2.0×	27 0.4×	74 1.2×	3 0.1×	17 0.5×	29	493
Benedikt Hild Germany	6	186 1.4×	20 0.3×	17 0.3×	9 0.2×	44 1.3×	12	309
Wonsuck Yoon South Korea	15	148 1.1×	136 1.8×	6 0.1×	10 0.3×	61 1.7×	39	549
Ikuko Watanabe Japan	9	82 0.6×	22 0.3×	16 0.3×	6 0.2×	158 4.5×	10	427
Tamara Ćiković Germany	3	362 2.7×	73 1.0×	12 0.2×	10 0.3×	111 3.2×	3	448
Azra Khanum Pakistan	14	161 1.2×	71 0.9×	16 0.3×	6 0.2×	52 1.5×	29	444

Countries citing papers authored by Märt Möls

Since Specialization

Citations

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

Fields of papers citing papers by Märt Möls

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Märt Möls

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

All Works

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18 of 18 papers shown

Kasela, Silva, et al.. (2025). Polygenic and pharmacogenomic contributions to medication dosing: a real-world longitudinal biobank study. Journal of Translational Medicine. 23(1). 727–727. 1 indexed citations

Puurand, Tarmo, Märt Möls, Lauris Kaplinski, et al.. (2025). Y-mer: a k-mer based method for determining human Y chromosome haplogroups from ultra-low sequencing depth data. Genome biology. 26(1). 243–243.

Alver, Maris, Silva Kasela, Liina Haring, et al.. (2024). Genetic predisposition and antipsychotic treatment effect on metabolic syndrome in schizophrenia: a ten-year follow-up study using the Estonian Biobank. The Lancet Regional Health - Europe. 41. 100914–100914. 7 indexed citations

Kaplinski, Lauris, Märt Möls, Tarmo Puurand, & Maido Remm. (2023). DOCEST—fast and accurate estimator of human NGS sequencing depth and error rate. Bioinformatics Advances. 3(1). vbad084–vbad084. 1 indexed citations

Mändul, Merli, et al.. (2023). Analysis of follow-up data in large biobank cohorts: a review of methodology. bioRxiv (Cold Spring Harbor Laboratory). 1 indexed citations

Kaplinski, Lauris, et al.. (2021). KATK: Fast genotyping of rare variants directly from unmapped sequencing reads. Human Mutation. 42(6). 777–786. 2 indexed citations

Örd, Tiit, Tarmo Puurand, Daima Örd, et al.. (2020). A human-specific VNTR in the TRIB3 promoter causes gene expression variation between individuals. PLoS Genetics. 16(8). e1008981–e1008981. 10 indexed citations

Lang, Mait, et al.. (2020). Remote-sensing support for the Estonian National Forest Inventory, facilitating the construction of maps for forest height, standing-wood volume, and tree species composition. Forestry Studies / Metsanduslikud Uurimused. 73(1). 77–97. 3 indexed citations

Möls, Märt, et al.. (2018). PlasmidSeeker: identification of known plasmids from bacterial whole genome sequencing reads. PeerJ. 6. e4588–e4588. 61 indexed citations

10.

Kaplinski, Lauris, et al.. (2017). FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads. Scientific Reports. 7(1). 2537–2537. 26 indexed citations

11.

Kaplinski, Lauris, Märt Möls, Reidar Andreson, et al.. (2017). StrainSeeker: fast identification of bacterial strains from raw sequencing reads using user-provided guide trees. PeerJ. 5. e3353–e3353. 37 indexed citations

12.

Palta, Priit, Lauris Kaplinski, Liina Nagirnaja, et al.. (2015). Haplotype Phasing and Inheritance of Copy Number Variants in Nuclear Families. PLoS ONE. 10(4). e0122713–e0122713. 7 indexed citations

13.

Lilleväli, Kersti, Hendrik Luuk, Silva Sütt, et al.. (2014). Initiation and developmental dynamics of Wfs1 expression in the context of neural differentiation and ER stress in mouse forebrain. International Journal of Developmental Neuroscience. 35(1). 80–88. 18 indexed citations

14.

Mallick, Chandana Basu, Märt Möls, Sarah C. Hill, et al.. (2013). The Light Skin Allele of SLC24A5 in South Asians and Europeans Shares Identity by Descent. PLoS Genetics. 9(11). e1003912–e1003912. 75 indexed citations

15.

Rull, Kristiina, Kärt Tomberg, Sulev Kõks, et al.. (2013). Increased placental expression and maternal serum levels of apoptosis-inducing TRAIL in recurrent miscarriage. Placenta. 34(2). 141–148. 43 indexed citations

16.

Rull, Kristiina, Kärt Tomberg, Sulev Kõks, et al.. (2012). WITHDRAWN: TNF-Related Apoptosis-Inducing Ligand TRAIL as a Potential Biomarker for Early Pregnancy Complications. The Journal of Clinical Endocrinology & Metabolism. 2 indexed citations

17.

Isotalo, Jarkko, Märt Möls, & Simo Puntanen. (2006). Invariance of the BLUE under the linear fixed and mixed effects models. Acta et Commentationes Universitatis Tartuensis de Mathematica. 10. 69–76. 1 indexed citations

18.

Möls, Märt. (2003). Constraints on Random Effects and Mixed Linear Model Predictions. Acta Applicandae Mathematicae. 79(1-2). 17–23. 3 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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