Malin Melin

1.2k total citations
20 papers, 799 citations indexed

About

Malin Melin is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Malin Melin has authored 20 papers receiving a total of 799 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Malin Melin's work include Veterinary Oncology Research (6 papers), Immunodeficiency and Autoimmune Disorders (5 papers) and Blood disorders and treatments (4 papers). Malin Melin is often cited by papers focused on Veterinary Oncology Research (6 papers), Immunodeficiency and Autoimmune Disorders (5 papers) and Blood disorders and treatments (4 papers). Malin Melin collaborates with scholars based in Sweden, United States and United Kingdom. Malin Melin's co-authors include Niklas Dahl, Göran Carlsson, Jan Palmblad, Bengt Fadeel, Jan‐Inge Henter, Kerstin Lindblad‐Toh, Patricio Rivera, Jens Häggström, Henrik von Euler and Christoph Klein and has published in prestigious journals such as Nature Genetics, Cancer Research and Scientific Reports.

In The Last Decade

Malin Melin

19 papers receiving 780 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Malin Melin Sweden 13 514 306 236 165 155 20 799
Jumpei Yamazaki Japan 16 184 0.4× 104 0.3× 526 2.2× 36 0.2× 200 1.3× 57 939
Mario Cervone Italy 8 84 0.2× 160 0.5× 214 0.9× 79 0.5× 47 0.3× 24 571
Long Vien United States 9 139 0.3× 330 1.1× 374 1.6× 24 0.1× 40 0.3× 11 778
Anne Polvi Finland 17 203 0.4× 184 0.6× 293 1.2× 145 0.9× 19 0.1× 23 906
Roberta Zuntini Italy 14 145 0.3× 278 0.9× 235 1.0× 21 0.1× 54 0.3× 39 669
Nathan D. Montgomery United States 17 201 0.4× 80 0.3× 613 2.6× 47 0.3× 70 0.5× 53 1.1k
Alisha M. Gruntman United States 14 259 0.5× 35 0.1× 360 1.5× 34 0.2× 189 1.2× 34 699
Francesca Pala Italy 13 142 0.3× 240 0.8× 270 1.1× 74 0.4× 22 0.1× 39 614
Michael Ehrhardt United States 13 166 0.3× 295 1.0× 211 0.9× 13 0.1× 38 0.2× 20 702
Nuria Perez‐Reyes United States 13 73 0.1× 109 0.4× 253 1.1× 51 0.3× 62 0.4× 16 792

Countries citing papers authored by Malin Melin

Since Specialization
Citations

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

Fields of papers citing papers by Malin Melin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Malin Melin

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

All Works

20 of 20 papers shown
1.
Coster, Wouter De, Ida Höijer, Inge Bruggeman, et al.. (2024). Visualization and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR. Genome Research. 34(11). 2074–2080. 5 indexed citations
2.
Arendt, Maja L., Sharadha Sakthikumar, Malin Melin, et al.. (2023). PIK3CA is recurrently mutated in canine mammary tumors, similarly to in human mammary neoplasia. Scientific Reports. 13(1). 632–632. 12 indexed citations
3.
Ljungström, Viktor, Malin Melin, Maja L. Arendt, et al.. (2020). Targeted sequencing reveals the somatic mutation landscape in a Swedish breast cancer cohort. Scientific Reports. 10(1). 19304–19304. 14 indexed citations
4.
Körberg, Izabella Baranowska, Daniel Nowinski, Marie-Louise Bondeson, et al.. (2020). A progressive and complex clinical course in two family members with ERF-related craniosynostosis: a case report. BMC Medical Genetics. 21(1). 90–90. 10 indexed citations
5.
Biasoli, Deborah, Sally L. Ricketts, Céline Courtay-Cahen, et al.. (2019). A synonymous germline variant in a gene encoding a cell adhesion molecule is associated with cutaneous mast cell tumour development in Labrador and Golden Retrievers. PLoS Genetics. 15(3). e1007967–e1007967. 11 indexed citations
6.
Gudmundsson, Sanna, Göran Annerén, Íñigo Marcos‐Alcalde, et al.. (2018). A novel RAD21 p.(Gln592del) variant expands the clinical description of Cornelia de Lange syndrome type 4 – Review of the literature. European Journal of Medical Genetics. 62(6). 103526–103526. 12 indexed citations
7.
Melin, Malin, Patricio Rivera, Maja L. Arendt, et al.. (2016). Genome-Wide Analysis Identifies Germ-Line Risk Factors Associated with Canine Mammary Tumours. PLoS Genetics. 12(5). e1006029–e1006029. 21 indexed citations
8.
Arendt, Maja L., Malin Melin, Noriko Tonomura, et al.. (2015). Genome-Wide Association Study of Golden Retrievers Identifies Germ-Line Risk Factors Predisposing to Mast Cell Tumours. PLoS Genetics. 11(11). e1005647–e1005647. 37 indexed citations
9.
Tullis, J. L. & Malin Melin. (2015). Management of Christmas Disease and Stuart-Prower Deficiency with a Prothrombin-Complex Concentrate (Factors II, VII, IX, X). Proceedings of the International Society of Blood Transfusion. 29. 1134–1139. 1 indexed citations
10.
Borge, Kaja Sverdrup, Malin Melin, Patricio Rivera, et al.. (2013). The ESR1 gene is associated with risk for canine mammary tumours. BMC Veterinary Research. 9(1). 69–69. 15 indexed citations
11.
Rivera, Patricio, Malin Melin, Tara Biagi, et al.. (2009). Mammary Tumor Development in Dogs Is Associated with BRCA1 and BRCA2. Cancer Research. 69(22). 8770–8774. 113 indexed citations
12.
Carlsson, Göran, Ingrid van’t Hooft, Malin Melin, et al.. (2008). Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutations. Journal of Internal Medicine. 264(4). 388–400. 66 indexed citations
13.
Carlsson, Göran, Malin Melin, Niklas Dahl, et al.. (2007). Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia. Acta Paediatrica. 96(6). 813–819. 36 indexed citations
14.
Melin, Malin, Miriam Entesarian, Göran Carlsson, et al.. (2006). Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern Sweden. Biochemical and Biophysical Research Communications. 353(3). 571–575. 12 indexed citations
15.
Marklund, Lena, Malin Melin, Atle Melberg, Vilmantas Giedraitis, & Niklas Dahl. (2006). Adult‐onset autosomal dominant leukodystrophy with autonomic symptoms restricted to 1.5 Mbp on chromosome 5q23. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(6). 608–614. 26 indexed citations
16.
Melin, Malin, Birgit Carlsson, Henrik Anckarsäter, et al.. (2006). Constitutional Downregulation of <i>SEMA5A</i> Expression in Autism. Neuropsychobiology. 54(1). 64–69. 63 indexed citations
17.
Melin, Malin, Joakim Klar, Robert Fredriksson, et al.. (2006). A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype association. Journal of Human Genetics. 51(10). 864–871. 15 indexed citations
18.
Klein, Christoph, Giridharan Appaswamy, Manuela Germeshausen, et al.. (2006). HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Nature Genetics. 39(1). 86–92. 322 indexed citations
19.
Melin, Malin, et al.. (1994). Gastrointestinal hemorrhage complicating systemic neurofibromatosis.. PubMed. 89(10). 1888–90. 8 indexed citations
20.
Giles, Graham G., et al.. (1969). Effect of auxiliary liver transplantation on haptoglobin synthesis in the dog.. PubMed. 20. 367–9.

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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