Mateja Smogavec

407 total citations
16 papers, 149 citations indexed

About

Mateja Smogavec is a scholar working on Genetics, Molecular Biology and Health. According to data from OpenAlex, Mateja Smogavec has authored 16 papers receiving a total of 149 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Health. Recurrent topics in Mateja Smogavec's work include Genomic variations and chromosomal abnormalities (5 papers), Health disparities and outcomes (3 papers) and Genomics and Rare Diseases (2 papers). Mateja Smogavec is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Health disparities and outcomes (3 papers) and Genomics and Rare Diseases (2 papers). Mateja Smogavec collaborates with scholars based in Austria, Germany and Poland. Mateja Smogavec's co-authors include Zalika Klemenc–Ketiš, Janko Kersnik, Knut Brockmann, Silke Pauli, Peter Burfeind, Florian M. Pauler, Elizabeth E. Palmer, Daniel Malzl, Barbara Zoll and Iris Bartels and has published in prestigious journals such as Cell, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Mateja Smogavec

15 papers receiving 147 citations

Peers

Mateja Smogavec

GENET

GHP

PPCH

Kelly L. Jones United States

María Teresa Flores-Dorantes Mexico

Laura G. Hendon United States

Elisenda Cortès‐Saladelafont Spain

Sheila P. Gregório Brazil

Maria Antonietta Pisanti Italy

Ross Thomson United Kingdom

Mathias Gorski Germany

Lesley Turner Canada

Anthony F. Kirkpatrick United States

Kelly L. Jones United States

Mateja Smogavec

81 ×1.4

90 ×1.7

GENET

7 ×0.4

GHP

23 ×1.5

PPCH

19 ×1.4

Citations per year, relative to Mateja Smogavec Mateja Smogavec (= 1×) peers Kelly L. Jones

Countries citing papers authored by Mateja Smogavec

Since Specialization

Citations

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

Fields of papers citing papers by Mateja Smogavec

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mateja Smogavec

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

All Works

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16 of 16 papers shown

Basilico, Bernadette, Daniel Malzl, Mateja Smogavec, et al.. (2023). Large neutral amino acid levels tune perinatal neuronal excitability and survival. Cell. 186(9). 1950–1967.e25. 37 indexed citations

Rehder, Helga, Susanne Gerit Kircher, Katharina Schoner, et al.. (2023). Brain malformations in diprosopia observed in clinical cases, museum specimens and artistic representations. Orphanet Journal of Rare Diseases. 18(1). 57–57. 2 indexed citations

Ponleitner, Markus, Manfred Hecking, Senta Graf, et al.. (2023). Phenotyping of a novel COL4A4 and novel GLA variant in a patient presenting with microhematuria and mildly impaired kidney function: a case report. Frontiers in Genetics. 14. 1211858–1211858.

Pradère, Benjamin, Paweł Rajwa, Gero Kramer, et al.. (2023). Performance of clinical risk scores and prediction models to identify pathogenic germline variants in patients with advanced prostate cancer. World Journal of Urology. 41(8). 2091–2097. 1 indexed citations

Kratzer, Bernhard, Katharina Grabmeier‐Pfistershammer, Doris Trapin, et al.. (2023). Mycobacterium avium Complex Infections: Detailed Phenotypic and Functional Immunological Work-Up Is Required despite Genetic Analyses. International Archives of Allergy and Immunology. 184(9). 914–931. 1 indexed citations

Smogavec, Mateja, Reinhard Lehner, Jürgen Neesen, et al.. (2022). Singleton exome sequencing of 90 fetuses with ultrasound anomalies revealing novel disease-causing variants and genotype–phenotype correlations. European Journal of Human Genetics. 30(4). 428–438. 8 indexed citations

Smogavec, Mateja, Jürgen Neesen, & Franco Laccone. (2019). Genetische Diagnostik. 14(1-4). 29–47. 1 indexed citations

Smogavec, Mateja, et al.. (2018). Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22. Molecular Cytogenetics. 11(1). 62–62. 9 indexed citations

Smogavec, Mateja, et al.. (2017). An overview of self-treatment and selfmedication practices among Slovenian citizens. SHILAP Revista de lepidopterología. 12 indexed citations

10.

Smogavec, Mateja, Jana Zschüntzsch, Wolfram Kreß, et al.. (2017). Novel fukutin mutations in limb-girdle muscular dystrophy type 2M with childhood onset. Neurology Genetics. 3(4). e167–e167. 2 indexed citations

11.

Pohl, Esther, Jan Hauke, Judit Horváth, et al.. (2017). NGS-based multi-gene panel analysis in BRCA1/2-negative breast and ovarian cancer families.. Journal of Clinical Oncology. 35(15_suppl). 1526–1526. 1 indexed citations

12.

Smogavec, Mateja, Juliane Hoyer, Damien Lederer, et al.. (2016). Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum. Journal of Medical Genetics. 53(12). 820–827. 41 indexed citations

13.

Schwaibold, Eva Maria Christina, Mateja Smogavec, Elke Hobbiebrunken, et al.. (2014). Intragenic duplication of EHMT1 gene results in Kleefstra syndrome. Molecular Cytogenetics. 7(1). 10 indexed citations

14.

Klemenc–Ketiš, Zalika, et al.. (2011). Health-Related Quality of Life: a Population Based Study from Slovenia. Central European Journal of Public Health. 19(1). 7–12. 12 indexed citations

15.

Smogavec, Mateja, et al.. (2011). Prevalence of chronic diseases among adult Slovene population. Slovenian Journal of Public Health. 50(3). 11 indexed citations

16.

Klemenc–Ketiš, Zalika, Mateja Smogavec, & Janko Kersnik. (2011). Healt H-related quality of life: a population based study from s lovenia. 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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