Marta Morell

499 total citations
20 papers, 383 citations indexed

About

Marta Morell is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Marta Morell has authored 20 papers receiving a total of 383 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Hematology, 6 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Marta Morell's work include Blood Coagulation and Thrombosis Mechanisms (11 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (3 papers) and Complement system in diseases (3 papers). Marta Morell is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (11 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (3 papers) and Complement system in diseases (3 papers). Marta Morell collaborates with scholars based in Spain, United Kingdom and United States. Marta Morell's co-authors include Xavier Estivill, Núria Sala, Xavier Navarro, Yolanda Espinosa‐Parrilla, Juan Carlos Souto, J. Fontcuberta, Isabel Tirado, Rosario Osta, Renzo Mancuso and Albert Alé and has published in prestigious journals such as Blood, PLoS ONE and Scientific Reports.

In The Last Decade

Marta Morell

19 papers receiving 375 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marta Morell Spain	13	135	88	75	54	51	20	383
Kiandokht Keyhanian United States	11	15 0.1×	81 0.9×	27 0.4×	199 3.7×	30 0.6×	19	398
Ajay Ashok United States	10	39 0.3×	143 1.6×	23 0.3×	20 0.4×	4 0.1×	22	323
I. Desguerre France	12	20 0.1×	194 2.2×	13 0.2×	33 0.6×	26 0.5×	37	400
Reeteka Sud United States	10	27 0.2×	159 1.8×	32 0.4×	34 0.6×	8 0.2×	19	409
J J van de Kamp Netherlands	8	17 0.1×	109 1.2×	22 0.3×	34 0.6×	7 0.1×	13	279
Eduardo López‐Laso Spain	12	25 0.2×	224 2.5×	29 0.4×	54 1.0×	3 0.1×	40	453
R. Kálmánchey Hungary	10	8 0.1×	206 2.3×	20 0.3×	41 0.8×	12 0.2×	27	422
Tjalf Ziemssen Germany	9	10 0.1×	66 0.8×	32 0.4×	53 1.0×	3 0.1×	26	237
Michaël W. Pankhurst New Zealand	16	12 0.1×	144 1.6×	8 0.1×	15 0.3×	9 0.2×	36	643
Seema Kapoor India	11	17 0.1×	157 1.8×	14 0.2×	7 0.1×	3 0.1×	40	283

Countries citing papers authored by Marta Morell

Since Specialization

Citations

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

Fields of papers citing papers by Marta Morell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Morell

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

1.

Roldán, Mónica, Lluı́s Armengol, Marcos Frías, et al.. (2023). Advanced Optical Microscopy: Unveiling Functional Insights Regarding a Novel PPP2R1A Variant and Its Unreported Phenotype. International Journal of Molecular Sciences. 24(18). 13699–13699.

2.

Willis, Jesse R., Marta Morell, Eva Real, et al.. (2022). Changes in the stool and oropharyngeal microbiome in obsessive-compulsive disorder. Scientific Reports. 12(1). 1448–1448. 30 indexed citations

3.

Mancuso, Renzo, Anna Martínez‐Muriana, David I. Gregorio, et al.. (2016). Neuregulin-1 promotes functional improvement by enhancing collateral sprouting in SOD1G93A ALS mice and after partial muscle denervation. Neurobiology of Disease. 95. 168–178. 45 indexed citations

4.

Costas, Javier, Noa Carrera, Pino Alonso, et al.. (2016). Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia. Translational Psychiatry. 6(3). e768–e768. 45 indexed citations

5.

Alé, Albert, Jordi Bruna, Marta Morell, et al.. (2014). Treatment with anti-TNF alpha protects against the neuropathy induced by the proteasome inhibitor bortezomib in a mouse model. Experimental Neurology. 253. 165–173. 42 indexed citations

6.

Mancuso, Renzo, Jaume del Valle, Marta Morell, et al.. (2014). Lack of synergistic effect of resveratrol and sigma-1 receptor agonist (PRE-084) in SOD1G93A ALS mice: overlapping effects or limited therapeutic opportunity?. Orphanet Journal of Rare Diseases. 9(1). 78–78. 21 indexed citations

7.

Morell, Marta, et al.. (2009). Nucleotide, Cytogenetic and Expression Impact of the Human Chromosome 8p23.1 Inversion Polymorphism. PLoS ONE. 4(12). e8269–e8269. 18 indexed citations

8.

Ponsa, Immaculada, Josep Antoni Ramos‐Quiroga, Marta Ribasès, et al.. (2009). Absence of cytogenetic effects in children and adults with attention-deficit/hyperactivity disorder treated with methylphenidate. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 666(1-2). 44–49. 13 indexed citations

9.

Espinosa‐Parrilla, Yolanda, Marta Morell, Montserrat Borrell, et al.. (2000). Optimization of a simple and rapid single-strand conformation analysis for detection of mutations in thePROS1 gene: Identification of seven novel mutations and three novel, apparently neutral, variants. Human Mutation. 15(5). 463–473. 22 indexed citations

10.

Espinosa‐Parrilla, Yolanda, et al.. (2000). Homozygosity for the Protein S Heerlen Allele Is Associated with Type I PS Deficiency in a Thrombophilic Pedigree with Multiple Risk Factors. Thrombosis and Haemostasis. 83(1). 102–106. 19 indexed citations

11.

Espinosa‐Parrilla, Yolanda, Marta Morell, Montserrat Borrell, et al.. (2000). Optimization of a simple and rapid single-strand conformation analysis for detection of mutations in the PROS1 gene: Identification of seven novel mutations and three novel, apparently neutral, variants. Human Mutation. 15(5). 463–463. 1 indexed citations

12.

Espinosa‐Parrilla, Yolanda, Marta Morell, Juan Carlos Souto, et al.. (1999). Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiency. Human Mutation. 14(1). 30–30. 1 indexed citations

13.

Espinosa‐Parrilla, Yolanda, Marta Morell, Juan Carlos Souto, et al.. (1999). Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiency. Human Mutation. 14(1). 30–39. 28 indexed citations

14.

Rahman, Sadequr, et al.. (1997). A complex arrangement of genes at a starch branching enzyme I locus in the D-genome donor of wheat. Genome. 40(4). 465–474. 44 indexed citations

15.

Espinosa‐Parrilla, Yolanda, Marta Morell, Juan Carlos Souto, et al.. (1997). Absence of Linkage Between Type III Protein S Deficiency and the PROS1 and C4BP Genes in Families Carrying the Protein S Heerlen Allele. Blood. 89(8). 2799–2806. 22 indexed citations

16.

Soria, José Manuel, Marta Morell, Xavier Estivill, & Núria Sala. (1996). Recurrence of thePROC gene mutation R178Q: Independent origins in Spanish protein C deficiency patients. Human Mutation. 8(1). 71–73. 2 indexed citations

17.

Soria, José Manuel, Caroline J. Formstone, Marta Morell, et al.. (1996). Aberrant RNA splicing of the protein C and protein S genes in healthy individuals. Blood Coagulation & Fibrinolysis. 7(6). 625–631. 4 indexed citations

18.

Soria, José Manuel, Marta Morell, Ioana Nicolau, Xavier Estivill, & Núria Sala. (1996). Homozygosity for R87H missense mutation and for a rare intron 7 DNA variant (7054G???A) in the PROC genes of three siblings initially classified as heterozygotes for protein C deficiency. Blood Coagulation & Fibrinolysis. 7(1). 15–23. 18 indexed citations

19.

Morell, Marta, et al.. (1995). A novel polymorphism (6376 G/T) in intron 7 of the human protein C gene. Human Genetics. 96(2). 243–244. 1 indexed citations

20.

Soria, José Manuel, et al.. (1995). Severe Type I Protein C Deficiency in a Compound Heterozygote for Y124C and Q132X Mutations in Exon 6 of the PROC Gene. Thrombosis and Haemostasis. 74(5). 1215–1220. 7 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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