Mark Screen

6.6k total citations
7 papers, 252 citations indexed

About

Mark Screen is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Mark Screen has authored 7 papers receiving a total of 252 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 2 papers in Genetics. Recurrent topics in Mark Screen's work include Muscle Physiology and Disorders (4 papers), Genetic Neurodegenerative Diseases (3 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Mark Screen is often cited by papers focused on Muscle Physiology and Disorders (4 papers), Genetic Neurodegenerative Diseases (3 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Mark Screen collaborates with scholars based in Finland, United Kingdom and United States. Mark Screen's co-authors include Bjarne Udd, Peter Hackman, Anna Vihola, Per Harald Jonson, Anni Evilä, J. Sarparanta, Juha Kere, Myriam Hemberger, Sara Lehtinen and Gabrielle Åhlberg and has published in prestigious journals such as PLoS ONE, Development and Annals of Neurology.

In The Last Decade

Mark Screen

7 papers receiving 251 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mark Screen Finland	6	199	83	52	49	38	7	252
Giovanni Marrosu Italy	12	227 1.1×	50 0.6×	57 1.1×	28 0.6×	24 0.6×	19	349
Simone Pizzi Italy	11	185 0.9×	18 0.2×	53 1.0×	45 0.9×	12 0.3×	31	313
Mridul Johari Finland	9	133 0.7×	63 0.8×	54 1.0×	39 0.8×	16 0.4×	28	194
A. Maerkens Germany	5	202 1.0×	83 1.0×	69 1.3×	33 0.7×	11 0.3×	8	275
Sonisha Warren United States	7	341 1.7×	166 2.0×	107 2.1×	19 0.4×	28 0.7×	11	402
Rosamaria Silipigni Italy	10	144 0.7×	12 0.1×	16 0.3×	50 1.0×	26 0.7×	35	264
Teresa Giugliano Italy	12	189 0.9×	54 0.7×	26 0.5×	51 1.0×	110 2.9×	21	339
Thomas Smol France	10	129 0.6×	18 0.2×	17 0.3×	36 0.7×	6 0.2×	34	224
Marius Kuhn Germany	10	107 0.5×	37 0.4×	50 1.0×	37 0.8×	14 0.4×	16	207

Countries citing papers authored by Mark Screen

Since Specialization

Citations

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

Fields of papers citing papers by Mark Screen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Screen

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Screen, Mark, Per Harald Jonson, Olayinka Raheem, et al.. (2014). Abnormal Splicing of NEDD4 in Myotonic Dystrophy Type 2. American Journal Of Pathology. 184(8). 2322–2332. 16 indexed citations

2.

Screen, Mark, Olayinka Raheem, Per Harald Jonson, et al.. (2014). Gene Expression Profiling in Tibial Muscular Dystrophy Reveals Unfolded Protein Response and Altered Autophagy. PLoS ONE. 9(3). e90819–e90819. 14 indexed citations

3.

Evilä, Anni, Anna Vihola, J. Sarparanta, et al.. (2014). Atypical phenotypes in titinopathies explained by second titin mutations. Annals of Neurology. 75(2). 230–240. 63 indexed citations

4.

Evilä, Anni, Anna Vihola, J. Sarparanta, et al.. (2013). P.3.11 Atypical phenotypes in titinopathies explained by second titin mutations and compound heterozygosity. Neuromuscular Disorders. 23(9-10). 758–759. 2 indexed citations

5.

Vihola, Anna, Mario Sirito, Linda L. Bachinski, et al.. (2012). Altered expression and splicing of Ca²⁺ metabolism genes in myotonic dystrophies DM1 and DM2. Neuropathology and Applied Neurobiology. 39(4). 390–405. 22 indexed citations

6.

Hackman, Peter, J. Sarparanta, Sara Lehtinen, et al.. (2012). Welander distal myopathy is caused by a mutation in the RNA‐binding protein TIA1. Annals of Neurology. 73(4). 500–509. 103 indexed citations

7.

Screen, Mark, Wendy Dean, James C. Cross, & Myriam Hemberger. (2008). Cathepsin proteases have distinct roles in trophoblast function and vascular remodelling. Development. 135(19). 3311–3320. 32 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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