Magdalena Socha

528 total citations
24 papers, 260 citations indexed

About

Magdalena Socha is a scholar working on Molecular Biology, Genetics and Developmental Biology. According to data from OpenAlex, Magdalena Socha has authored 24 papers receiving a total of 260 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 4 papers in Developmental Biology. Recurrent topics in Magdalena Socha's work include Congenital limb and hand anomalies (4 papers), Genomics and Chromatin Dynamics (4 papers) and Genetic Syndromes and Imprinting (3 papers). Magdalena Socha is often cited by papers focused on Congenital limb and hand anomalies (4 papers), Genomics and Chromatin Dynamics (4 papers) and Genetic Syndromes and Imprinting (3 papers). Magdalena Socha collaborates with scholars based in Poland, Germany and Australia. Magdalena Socha's co-authors include Aleksander Jamsheer, Anna Sowińska‐Seidler, Anna Latos‐Bieleńska, Ewelina Bukowska‐Olech, Tomasz Trzeciak, Joanna Didkowska, Renata Glazar, Paulina Wieszczy, Jarosław Reguła and Michał F. Kamiński and has published in prestigious journals such as Nature Communications, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Magdalena Socha

22 papers receiving 247 citations

Peers

Magdalena Socha

GENET

ONCOL

PRM

Anna Sowińska‐Seidler Poland

Randi Koll Germany

Maha Faden Saudi Arabia

Wim Brussel Netherlands

Ellen Moran United States

Angeline Lai Singapore

Clémentine Mahaut France

Kristen L. Sund United States

Emiel Baten Belgium

Philip N. Mowrey United States

Anna Sowińska‐Seidler Poland

Magdalena Socha

254 ×1.8

237 ×2.1

GENET

98 ×2.1

31 ×0.7

ONCOL

12 ×0.3

PRM

Citations per year, relative to Magdalena Socha Magdalena Socha (= 1×) peers Anna Sowińska‐Seidler

Countries citing papers authored by Magdalena Socha

Since Specialization

Citations

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

Fields of papers citing papers by Magdalena Socha

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Magdalena Socha

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

Bukowska‐Olech, Ewelina, et al.. (2025). Fibrodysplasia ossificans progressiva: genetic and clinical characterization in a cohort of Polish patients and review of potential therapies. Journal of Applied Genetics. 67(1). 193–203.

Socha, Magdalena, Guerra Mc, Katarzyna Błaszczyk, et al.. (2025). ETVs dictate hPSC differentiation by tuning biophysical properties. Nature Communications. 16(1). 1999–1999. 1 indexed citations

Wawrocka, Anna, et al.. (2023). Molecular Re-Diagnosis with Whole-Exome Sequencing Increases the Diagnostic Yield in Patients with Non-Syndromic Retinitis Pigmentosa. Diagnostics. 13(4). 730–730. 3 indexed citations

Sowińska‐Seidler, Anna, et al.. (2023). A genotype–phenotype correlation in split-hand/foot malformation type 1: further refinement of the phenotypic subregions within the 7q21.3 locus. Frontiers in Molecular Biosciences. 10. 1250714–1250714. 1 indexed citations

Socha, Magdalena, et al.. (2022). A pure de novo 16p13.3 duplication and amplification in a patient with femoral hypoplasia, psychomotor retardation, heart defect, and facial dysmorphism—a case report and literature review of the partial 16p13.3 trisomy syndrome. Journal of Applied Genetics. 64(1). 125–134.

Januszewicz, Władysław, Paulina Wieszczy, Magdalena Socha, et al.. (2021). Prevalence and risk factors of upper gastrointestinal cancers missed during endoscopy: a nationwide registry-based study. Endoscopy. 54(7). 653–660. 35 indexed citations

Socha, Magdalena, Anna Sowińska‐Seidler, Uirá Souto Melo, et al.. (2021). Position effects at the FGF8 locus are associated with femoral hypoplasia. The American Journal of Human Genetics. 108(9). 1725–1734. 7 indexed citations

Wawrocka, Anna, Joanna Walczak‐Sztulpa, Magdalena Socha, et al.. (2021). Homozygous microdeletion in the 11p13 region in the patient with isolated form of aniridia: New challenges in the genetic diagnostics of aniridia. American Journal of Medical Genetics Part A. 188(2). 642–647. 2 indexed citations

Bukowska‐Olech, Ewelina, Delfina Popiel, Grzegorz Koczyk, et al.. (2020). Adapting SureSelect enrichment protocol to the Ion Torrent S5 platform in molecular diagnostics of craniosynostosis. Scientific Reports. 10(1). 4159–4159. 4 indexed citations

10.

Sowińska‐Seidler, Anna, Ewelina Bukowska‐Olech, Magdalena Socha, et al.. (2019). Functional analysis of novel RUNX2 mutations identified in patients with cleidocranial dysplasia. Clinical Genetics. 96(5). 429–438. 16 indexed citations

11.

Sowińska‐Seidler, Anna, Ewelina Bukowska‐Olech, Magdalena Socha, Dawid Larysz, & Aleksander Jamsheer. (2018). Novel 1q22-q23.1 duplication in a patient with lambdoid and metopic craniosynostosis, muscular hypotonia, and psychomotor retardation. Journal of Applied Genetics. 59(3). 281–289. 5 indexed citations

12.

Walczak‐Sztulpa, Joanna, Anna Wawrocka, Anna Świąder-Leśniak, et al.. (2017). Clinical and molecular genetic characterization of a male patient with Sensenbrenner syndrome (cranioectodermal dysplasia) and biallelic WDR35 mutations. Birth Defects Research. 110(4). 376–381. 6 indexed citations

13.

Jamsheer, Aleksander, Aleksandra Jezela‐Stanek, Andrzej Witek, et al.. (2016). Clinical expression of Holt-Oram syndrome on the basis of own clinical experience considering prenatal diagnosis. Ginekologia Polska. 87(10). 706–710. 1 indexed citations

14.

Iwanicka‐Pronicka, Katarzyna, Magdalena Socha, Maria Jędrzejowska, Małgorzata Krajewska‐Walasek, & Aleksander Jamsheer. (2016). Life-threatening cardiac episode in a Polish patient carrying contiguous gene microdeletion of the TBX5 and the TBX3 genes. SpringerPlus. 5(1). 1638–1638. 6 indexed citations

15.

Jamsheer, Aleksander, Anna Sowińska‐Seidler, Ewelina Bukowska‐Olech, et al.. (2016). Variable expressivity of the phenotype in two families with brachydactyly type E, craniofacial dysmorphism, short stature and delayed bone age caused by novel heterozygous mutations in the PTHLH gene. Journal of Human Genetics. 61(5). 457–461. 12 indexed citations

16.

Jamsheer, Aleksander, et al.. (2014). Mutational screening of EXT1 and EXT2 genes in Polish patients with hereditary multiple exostoses. Journal of Applied Genetics. 55(2). 183–188. 22 indexed citations

17.

Jamsheer, Aleksander, Anna Sowińska‐Seidler, Magdalena Socha, et al.. (2014). Three novel GJA1 missense substitutions resulting in oculo-dento-digital dysplasia (ODDD) — Further extension of the mutational spectrum. Gene. 539(1). 157–161. 16 indexed citations

18.

Sowińska‐Seidler, Anna, Monika Piwecka, Ewelina Bukowska‐Olech, et al.. (2014). Hyperosmia, ectrodactyly, mild intellectual disability, and other defects in a male patient with an X-linked partial microduplication and overexpression of the KAL1 gene. Journal of Applied Genetics. 56(2). 177–184. 12 indexed citations

19.

Sowińska‐Seidler, Anna, Magdalena Socha, & Aleksander Jamsheer. (2013). Split-hand/foot malformation - molecular cause and implications in genetic counseling. Journal of Applied Genetics. 55(1). 105–115. 60 indexed citations

20.

Jamsheer, Aleksander, Tomasz Żemojtel, Mateusz Kolanczyk, et al.. (2013). Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusion. Journal of Medical Genetics. 50(9). 579–584. 25 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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