Martin Schalling

40.0k total citations · 3 hit papers
314 papers, 18.2k citations indexed

About

Martin Schalling is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Martin Schalling has authored 314 papers receiving a total of 18.2k indexed citations (citations by other indexed papers that have themselves been cited), including 115 papers in Molecular Biology, 104 papers in Cellular and Molecular Neuroscience and 55 papers in Genetics. Recurrent topics in Martin Schalling's work include Neuropeptides and Animal Physiology (46 papers), Genetic Neurodegenerative Diseases (30 papers) and Genetics and Neurodevelopmental Disorders (29 papers). Martin Schalling is often cited by papers focused on Neuropeptides and Animal Physiology (46 papers), Genetic Neurodegenerative Diseases (30 papers) and Genetics and Neurodevelopmental Disorders (29 papers). Martin Schalling collaborates with scholars based in Sweden, United States and Germany. Martin Schalling's co-authors include Tomas Hökfelt, Louise Nordfors, David E. Housman, Catharina Lavebratt, Fredrik Lönnqvist, Peter Arner, Carolina Johansson, Jeanette E. Johansen, Christian Broberger and Roser Cortés and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Martin Schalling

311 papers receiving 17.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

PDGF-A Signaling Is a Critical Event in Lung Alveolar Myofibroblast Development and Alveogenesis

1996 667 citations Martin Schalling et al. profile →
The neuropeptide Y/agouti gene-related protein (AGRP) brain circuitry in normal, anorectic, and monosodium glutamate-treated mice

1998 647 citations Carolina Johansson, Martin Schalling et al. profile →
Overexpression of the obese (ob) gene in adipose tissue of human obese subjects

1995 598 citations Louise Nordfors, Martin Schalling et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Martin Schalling Sweden	71	6.7k	5.0k	3.1k	3.0k	2.2k	314	18.2k
Catherine Rivier United States	90	6.4k 1.0×	7.7k 1.5×	4.5k 1.4×	5.5k 1.8×	1.4k 0.6×	348	36.7k
Frank R. Sharp United States	87	12.3k 1.8×	7.3k 1.5×	1.5k 0.5×	3.9k 1.3×	1.5k 0.7×	376	27.7k
Pierre Gressèns France	75	5.1k 0.8×	3.3k 0.7×	1.6k 0.5×	1.4k 0.5×	876 0.4×	464	21.1k
Joseph B. Martin United States	67	5.8k 0.9×	8.2k 1.6×	2.3k 0.7×	2.4k 0.8×	1.1k 0.5×	246	16.8k
Helgi B. Schiöth Sweden	69	6.6k 1.0×	3.2k 0.6×	5.3k 1.7×	3.2k 1.1×	804 0.4×	443	19.9k
Norio Ozaki Japan	59	4.6k 0.7×	4.4k 0.9×	1.1k 0.4×	2.3k 0.8×	2.3k 1.0×	748	16.2k
Michael V. Johnston United States	73	5.0k 0.8×	5.9k 1.2×	1.2k 0.4×	1.1k 0.4×	1.6k 0.7×	301	17.7k
Scott J. Russo United States	70	6.0k 0.9×	6.9k 1.4×	1.5k 0.5×	2.4k 0.8×	1.7k 0.7×	195	21.4k
Kwok‐Fai So Hong Kong	73	7.7k 1.2×	5.7k 1.1×	880 0.3×	2.5k 0.9×	661 0.3×	636	21.7k
Paul A. Kelly France	81	7.8k 1.2×	2.4k 0.5×	1.2k 0.4×	2.0k 0.7×	4.7k 2.1×	404	23.2k

Countries citing papers authored by Martin Schalling

Since Specialization

Citations

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

Fields of papers citing papers by Martin Schalling

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Schalling

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Schalling. A scholar is included among the top collaborators of Martin Schalling 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 Martin Schalling. Martin Schalling 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:

20 of 20 papers shown

1.

Koskuvi, Marja, Sohvi Ohtonen, Eszter Molnár, et al.. (2025). Human oligodendrocyte progenitor cells mediate synapse elimination through TAM receptor activation. Nature Communications. 16(1). 10612–10612.

2.

Koskuvi, Marja, Anniella Isgren, Helena Fatouros‐Bergman, et al.. (2024). Lower complement C1q levels in first-episode psychosis and in schizophrenia. Brain Behavior and Immunity. 117. 313–319. 2 indexed citations

3.

Veldić, Marin, Vincent Millischer, John D. Port, et al.. (2019). Genetic variant in SLC1A2 is associated with elevated anterior cingulate cortex glutamate and lifetime history of rapid cycling. Translational Psychiatry. 9(1). 149–149. 20 indexed citations

4.

Gisslinger, Heinz, Bettina Gisslinger, Martin Schalling, et al.. (2018). Effect of Ropeginterferon Alfa-2b in Prefibrotic Primary Myelofibrosis. Blood. 132(Supplement 1). 3029–3029. 7 indexed citations

5.

Efstathopoulos, Paschalis, Vincent Millischer, Eric Olsson, et al.. (2018). Mitochondrial DNA copy number is associated with psychosis severity and anti-psychotic treatment. Scientific Reports. 8(1). 12743–12743. 37 indexed citations

6.

Lavebratt, Catharina, Eric Olsson, Claes‐Göran Östenson, et al.. (2017). Troponin T levels associated with genetic variants in NOTCH2 and MTNR1B in women with psychosis. Psychiatry Research. 250. 217–220. 3 indexed citations

7.

Forsell, Yvonne, et al.. (2015). Depression-associatedARNTLandPER2genetic variants in psychotic disorders. Chronobiology International. 32(4). 579–584. 12 indexed citations

8.

Wei, Ya Bin, Lina Martinsson, Jia Jia Liu, et al.. (2015). hTERT genetic variation in depression. Journal of Affective Disorders. 189. 62–69. 29 indexed citations

9.

Lonsdorf, Tina B., et al.. (2013). Attention biases and habituation of attention biases are associated with 5-HTTLPR and COMTval158met. Cognitive Affective & Behavioral Neuroscience. 14(1). 354–363. 11 indexed citations

10.

Witasp, Anna, Tomas J. Ekström, Bengt Lindholm, et al.. (2013). Novel insights from genetic and epigenetic studies in understanding the complex uraemic phenotype. Nephrology Dialysis Transplantation. 29(5). 964–971. 8 indexed citations

11.

Lavebratt, Catharina, Louise K. Sjöholm, Timo Partonen, Martin Schalling, & Yvonne Forsell. (2010). PER2 Variantion Is Associated With Depression Vulnerability. STM:n Hallinnonalan avoin julkaisuarkisto (Julkari). 6 indexed citations

12.

Lavebratt, Catharina, Louise K. Sjöholm, Pia Soronen, et al.. (2010). CRY2 Is Associated with Depression. eScholarship (California Digital Library). 2 indexed citations

13.

Partonen, Timo, Jens Treutlein, Asude Alpman, et al.. (2007). Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression. Annals of Medicine. 39(3). 229–238. 209 indexed citations

14.

Lichtenstein, Paul, Patrick F. Sullivan, Sven Cnattingius, et al.. (2006). The Swedish Twin Registry in the Third Millennium: An Update. Twin Research and Human Genetics. 9(6). 875–882. 275 indexed citations

15.

Lichtenstein, Paul, Patrick F. Sullivan, Sven Cnattingius, et al.. (2006). The Swedish Twin Registry in the Third Millennium: An Update. Twin Research and Human Genetics. 9(6). 875–882. 313 indexed citations

16.

Kumar, Rajiv, Somali Sanyal, Bengt Lindholm, et al.. (2005). Basal cell carcinoma and variants in genes coding for immune response, DNA repair, folate and iron metabolism. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 574(1-2). 105–111. 64 indexed citations

17.

Loehlin, John C., Erik G. Jönsson, Petter Gustavsson, et al.. (2004). Gender Diagnosticity and Androgen Receptor Gene CAG Repeat Sequence. Twin Research. 7(5). 456–461. 3 indexed citations

18.

Johansson, Carolina, Matthäus Willeit, Jenny Ekholm, et al.. (2004). Seasonal affective disorder and the G-protein β-3-subunit C825T polymorphism. Biological Psychiatry. 55(3). 317–319. 20 indexed citations

19.

Lindblad, K, Haydeh Payami, William G. Johnson, et al.. (1995). No evidence for association of familial Parkinson's disease with CAG repeat expansion. Neurology. 45(9). 1760–1763. 22 indexed citations

20.

Schalling, Martin, Håkan Persson, Markku Pelto‐Huikko, et al.. (1990). Expression and localization of gastrin messenger RNA and peptide in spermatogenic cells.. Journal of Clinical Investigation. 86(2). 660–669. 52 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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