Marta Smyk

801 total citations
25 papers, 486 citations indexed

About

Marta Smyk is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marta Smyk has authored 25 papers receiving a total of 486 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 15 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marta Smyk's work include Genomic variations and chromosomal abnormalities (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Sexual Differentiation and Disorders (5 papers). Marta Smyk is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Sexual Differentiation and Disorders (5 papers). Marta Smyk collaborates with scholars based in Poland, United States and United Kingdom. Marta Smyk's co-authors include Paweł Stankiewicz, Sau Wai Cheung, Beata Nowakowska, Ewa Bocian, Ewa Obersztyn, Katarzyna Derwińska, Barbara Wiśniowiecka‐Kowalnik, Martin Erdel, Milan Theurl and J.R. Lupski and has published in prestigious journals such as Human Molecular Genetics, Cells and Advances in experimental medicine and biology.

In The Last Decade

Marta Smyk

23 papers receiving 469 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marta Smyk Poland	11	373	312	83	76	29	25	486
Hayk Barseghyan United States	14	326 0.9×	315 1.0×	35 0.4×	65 0.9×	76 2.6×	22	527
Tatjana Adamović Sweden	11	218 0.6×	224 0.7×	100 1.2×	37 0.5×	13 0.4×	30	420
Simone Schiller Germany	6	393 1.1×	307 1.0×	65 0.8×	34 0.4×	25 0.9×	8	507
T. Lukusa Belgium	10	287 0.8×	214 0.7×	89 1.1×	70 0.9×	9 0.3×	32	397
Rudolf A. Pfeiffer Germany	13	383 1.0×	438 1.4×	97 1.2×	75 1.0×	22 0.8×	18	672
Marsha Speevak Canada	17	420 1.1×	302 1.0×	96 1.2×	141 1.9×	6 0.2×	37	636
M. Mullarkey Ireland	9	170 0.5×	197 0.6×	16 0.2×	28 0.4×	30 1.0×	15	298
M. Winkelmann Germany	7	739 2.0×	638 2.0×	162 2.0×	49 0.6×	88 3.0×	7	923
Elke Back Germany	15	576 1.5×	456 1.5×	247 3.0×	138 1.8×	58 2.0×	36	829
Chansonette Harvard Canada	17	417 1.1×	294 0.9×	85 1.0×	185 2.4×	12 0.4×	19	681

Countries citing papers authored by Marta Smyk

Since Specialization

Citations

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

Fields of papers citing papers by Marta Smyk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Smyk

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

Bekiesińska‐Figatowska, Monika, et al.. (2025). Reversed cortico-medullary differentiation in kidneys on fetal magnetic resonance imaging — a case series. Pediatric Nephrology. 41(1). 77–79.

Rzońca, Sylwia, et al.. (2023). The Generation of Human iPSC Lines from Three Individuals with Dravet Syndrome and Characterization of Neural Differentiation Markers in iPSC-Derived Ventral Forebrain Organoid Model. Cells. 12(2). 339–339. 6 indexed citations

Kutkowska‐Kaźmierczak, Anna, Gail Deutsch, Marta Smyk, et al.. (2023). Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis. Genes. 14(3). 563–563.

Smyk, Marta, Magdalena Bartnik, Barbara Wiśniowiecka‐Kowalnik, et al.. (2022). Application of array comparative genomic hybridization (aCGH) for identification of chromosomal aberrations in the recurrent pregnancy loss. Journal of Assisted Reproduction and Genetics. 39(2). 357–367. 7 indexed citations

Figura, Monika, Maciej Geremek, Stanisław Szlufik, et al.. (2021). Movement disorders associated with chromosomal aberrations diagnosed in adult patients. Neurologia i Neurochirurgia Polska. 55(3). 300–305. 5 indexed citations

Geremek, Maciej, et al.. (2019). Null variants in AGRN cause lethal fetal akinesia deformation sequence. Clinical Genetics. 97(4). 634–638. 3 indexed citations

Jurkiewicz, Dorota, Agata Skórka, Robert Śmigiel, et al.. (2016). A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith–Wiedemann or Silver–Russell syndrome in a single family. American Journal of Medical Genetics Part A. 173(1). 72–78. 24 indexed citations

Smyk, Marta, et al.. (2016). Novel 14q11.2 microduplication including the CHD8 and SUPT16H genes associated with developmental delay. American Journal of Medical Genetics Part A. 170(5). 1325–1329. 11 indexed citations

Szczałuba, Krzysztof, Beata Nowakowska, Marta Smyk, et al.. (2016). Application of Array Comparative Genomic Hybridization in Newborns with Multiple Congenital Anomalies. Advances in experimental medicine and biology. 912. 1–9. 4 indexed citations

10.

Smyk, Marta, Elizabeth Roeder, Sau Wai Cheung, Przemysław Szafrański, & Paweł Stankiewicz. (2015). A de novo 1.58 Mb deletion, including MAP2K6 and mapping 1.28 Mb upstream to SOX9, identified in a patient with Pierre Robin sequence and osteopenia with multiple fractures. American Journal of Medical Genetics Part A. 167(8). 1842–1850. 9 indexed citations

11.

Szczałuba, Krzysztof, Beata Nowakowska, Marta Smyk, et al.. (2015). High-Resolution Array Comparative Genomic Hybridization Utility in Polish Newborns with Isolated Cleft Lip and Palate. Neonatology. 107(3). 173–178. 7 indexed citations

12.

Smyk, Marta, Przemysław Szafrański, Michał Startek, Anna Gambin, & Paweł Stankiewicz. (2013). Chromosome conformation capture-on-chip analysis of long-range cis-interactions of the SOX9 promoter. Chromosome Research. 21(8). 781–788. 19 indexed citations

13.

Vissers, Lisenka E.L.M., Samarth Bhatt, Irene M. Janssen, et al.. (2009). Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture. Human Molecular Genetics. 18(19). 3579–3593. 114 indexed citations

14.

Jamsheer, Aleksander, Marta Smyk, Jolanta Wierzba, et al.. (2008). Subtle familial translocation t(11;22)(q24.2;q13.33) resulting in Jacobsen syndrome and distal trisomy 22q13.3: further details of genotype—phenotype maps. Journal of Applied Genetics. 49(4). 397–405. 4 indexed citations

15.

Nowakowska, Beata, Paweł Stankiewicz, Ewa Obersztyn, et al.. (2008). Application of metaphase HR‐CGH and targeted chromosomal microarray analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features. American Journal of Medical Genetics Part A. 146A(18). 2361–2369. 12 indexed citations

16.

Derwińska, Katarzyna, Marta Smyk, M. Lance Cooper, et al.. (2008). PTCH1 duplication in a family with microcephaly and mild developmental delay. European Journal of Human Genetics. 17(2). 267–271. 32 indexed citations

17.

Smyk, Marta, Ewa Obersztyn, Beata Nowakowska, et al.. (2007). Different‐sized duplications of Xq28, including MECP2, in three males with mental retardation, absent or delayed speech, and recurrent infections. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(6). 799–806. 47 indexed citations

18.

Smyk, Marta, Ewa Obersztyn, Beata Nowakowska, et al.. (2007). Recurrent SOX9 deletion campomelic dysplasia due to somatic mosaicism in the father. American Journal of Medical Genetics Part A. 143A(8). 866–870. 25 indexed citations

19.

Smyk, Marta, Jonathan S. Berg, Amber N. Pursley, et al.. (2007). Male-to-female sex reversal associated with an ∼250 kb deletion upstream of NR0B1 (DAX1). Human Genetics. 122(1). 63–70. 49 indexed citations

20.

Leipoldt, M., Martin Erdel, Marta Smyk, et al.. (2006). Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia. Clinical Genetics. 71(1). 67–75. 82 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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