Miriam Entesarian

1.2k total citations
15 papers, 626 citations indexed

About

Miriam Entesarian is a scholar working on Immunology, Genetics and Molecular Biology. According to data from OpenAlex, Miriam Entesarian has authored 15 papers receiving a total of 626 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Immunology, 6 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Miriam Entesarian's work include Immune Cell Function and Interaction (4 papers), Autoimmune and Inflammatory Disorders Research (4 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Miriam Entesarian is often cited by papers focused on Immune Cell Function and Interaction (4 papers), Autoimmune and Inflammatory Disorders Research (4 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Miriam Entesarian collaborates with scholars based in Sweden, Norway and Pakistan. Miriam Entesarian's co-authors include Niklas Dahl, Joakim Klar, Jan‐Inge Henter, Magnus Nordenskjöld, Maria Sobol, Yoshio Hayashi, Rieko Arakaki, Anne Isine Bolstad, Roland Jonsson and Hideyo Ohuchi and has published in prestigious journals such as Nature Genetics, Blood and Biochemical and Biophysical Research Communications.

In The Last Decade

Miriam Entesarian

15 papers receiving 616 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Miriam Entesarian Sweden 12 295 168 161 99 97 15 626
Jan F. Meilof Netherlands 19 195 0.7× 80 0.5× 296 1.8× 62 0.6× 92 0.9× 45 1.0k
Wenke Seifert Germany 11 184 0.6× 256 1.5× 313 1.9× 81 0.8× 254 2.6× 16 716
Sofia Grigoriadou United Kingdom 13 243 0.8× 356 2.1× 359 2.2× 70 0.7× 205 2.1× 29 1.0k
Alessandra Iaconcig Italy 14 486 1.6× 98 0.6× 73 0.5× 45 0.5× 27 0.3× 21 834
Carolyn Applegate United States 17 328 1.1× 270 1.6× 84 0.5× 237 2.4× 35 0.4× 24 821
Andreas Sjöberg Sweden 9 199 0.7× 36 0.2× 493 3.1× 101 1.0× 149 1.5× 16 882
Joel Schneider United States 15 396 1.3× 124 0.7× 111 0.7× 78 0.8× 47 0.5× 47 657
Mickaël Ménager France 9 209 0.7× 40 0.2× 234 1.5× 79 0.8× 106 1.1× 13 613
Alan M. Roth United States 20 433 1.5× 99 0.6× 72 0.4× 30 0.3× 36 0.4× 52 1.5k
Lara Wine Lee United States 11 459 1.6× 111 0.7× 90 0.6× 34 0.3× 22 0.2× 66 860

Countries citing papers authored by Miriam Entesarian

Since Specialization
Citations

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

Fields of papers citing papers by Miriam Entesarian

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miriam Entesarian

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

All Works

15 of 15 papers shown
1.
Khandagale, Avinash, Miriam Entesarian, Daniel Nilsson, et al.. (2020). Severe congenital neutropenia‐associated JAGN1 mutations unleash a calpain‐dependent cell death programme in myeloid cells. British Journal of Haematology. 192(1). 200–211. 11 indexed citations
2.
Kapoor, Seema, Nita Khurana, Miriam Entesarian, et al.. (2014). An Indian boy with griscelli syndrome type 2: Case report and review of literature. Indian Journal of Dermatology. 59(4). 394–394. 10 indexed citations
3.
Chiang, Samuel C. C., Marie Meeths, Bianca Tesi, et al.. (2014). An N-Terminal Missense Mutation in STX11 Causative of FHL4 Abrogates Syntaxin-11 Binding to Munc18-2. Frontiers in Immunology. 4. 515–515. 17 indexed citations
4.
Klar, Joakim, Maria Sobol, Atle Melberg, et al.. (2013). Welander Distal Myopathy Caused by an Ancient Founder Mutation inTIA1Associated with Perturbed Splicing. Human Mutation. 34(4). n/a–n/a. 81 indexed citations
5.
Mougiakakos, Dimitrios, Maciej Machaczka, Regina Jitschin, et al.. (2012). Treatment of Familial Hemophagocytic Lymphohistiocytosis with Third-Party Mesenchymal Stromal Cells. Stem Cells and Development. 21(17). 3147–3151. 15 indexed citations
6.
Fröjmark, Anne-Sophie, Jens Schuster, Maria Sobol, et al.. (2011). Mutations in Frizzled 6 Cause Isolated Autosomal-Recessive Nail Dysplasia. The American Journal of Human Genetics. 88(6). 852–860. 49 indexed citations
7.
Gabriková, Dana, Carina Frykholm, Ulla Friberg, et al.. (2010). Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association. Journal of Human Genetics. 55(12). 834–837. 22 indexed citations
8.
Meeths, Marie, Miriam Entesarian, Waleed Al–Herz, et al.. (2010). Spectrum of clinical presentations in familial hemophagocytic lymphohistiocytosis type 5 patients with mutations in STXBP2. Blood. 116(15). 2635–2643. 89 indexed citations
9.
Melberg, Atle, Raili Raininko, Eva Kumlien, et al.. (2009). SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(7). 984–992. 40 indexed citations
10.
Entesarian, Miriam, Birgit Carlsson, Mahmoud Mansouri, et al.. (2009). A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish population. American Journal of Medical Genetics Part A. 149A(3). 380–386. 11 indexed citations
11.
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
12.
Rasool, Mahmood, Jens Schuster, Muhammad Aslam, et al.. (2008). A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia. Journal of Human Genetics. 53(10). 894–898. 26 indexed citations
13.
Entesarian, Miriam, et al.. (2007). FGF10 missense mutations in aplasia of lacrimal and salivary glands (ALSG). European Journal of Human Genetics. 15(3). 379–382. 53 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.
Entesarian, Miriam, Hans Matsson, Joakim Klar, et al.. (2005). Mutations in the gene encoding fibroblast growth factor 10 are associated with aplasia of lacrimal and salivary glands. Nature Genetics. 37(2). 125–128. 124 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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