Marta Morell

499 citations

20 papers · 383 · h-index 13

Impact in

Hematology top 10%
- Blood Coagulation and Thrombosis Mechanisms
- Hemophilia Treatment and Research
Biological Psychiatry

Papers in

Hematology 12
- Blood Coagulation and Thrombosis Mechanisms 11
- Hemophilia Treatment and Research 2
Molecular Biology 6

Co-authors: Xavier Estivill (15 shared papers)Núria Sala (11 shared papers)Xavier Navarro (3 shared papers)Yolanda Espinosa‐Parrilla (6 shared papers)Juan Carlos Souto (5 shared papers)Renzo Mancuso (2 shared papers)Isabel Tirado (3 shared papers)Rosario Osta (2 shared papers)
Journals: Human Mutation (5 papers)Blood Coagulation & Fibrinolysis (2 papers)Thrombosis and Haemostasis (2 papers)Experimental Neurology (1 paper)Scientific Reports (1 paper)
Partner nations: Spain United Kingdom United States

In The Last Decade

Marta Morell

19 papers receiving 375 citations

Peers

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-authors

The 25 scholars most cited alongside Marta Morell, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Marta Morell Line = papers co-authored together Marta Morell links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Neuregulin-1 promotes functional improvement by enhancing collateral sprouting in SOD1G93A ALS mice and after partial muscle denervation Neurobiology of Disease ·Renzo Mancuso, Anna Martínez‐Muriana, Tatiana Leiva-Rodríguez, David I. Gregorio, Lorena Ariza, Marta Morell, Jesús Esteban‐Pérez, Alberto García‐Redondo, Ana Cristina Calvo, Gabriela Atencia-Cibreiro, Gabriel Corfas, Rosario Osta, Assumpció Bosch, Xavier Navarro	2016	45
2	Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia Translational Psychiatry ·Javier Costas, Noa Carrera, Pino Alonso, Xaquín Gurriarán, Cinto Segalàs, Eva Real, Clara López‐Solà, Sergi Mas, Patricia Gassó, Laura Domènech, Marta Morell, Inés Quintela, Luisa Lázaro, José M. Menchón, Xavier Estivill, Ãngel Carracedo	2016	45
3	A complex arrangement of genes at a starch branching enzyme I locus in the D-genome donor of wheat Genome ·Sadequr Rahman, Marta Morell, R. Appels, S. Abrahams, D. Abbott, Michael S. Samuel, Y. Mukai	1997	44
4	Treatment with anti-TNF alpha protects against the neuropathy induced by the proteasome inhibitor bortezomib in a mouse model Experimental Neurology ·Albert Alé, Jordi Bruna, Marta Morell, Helgi van de Velde, Johan Monbaliu, Xavier Navarro, Esther Udina	2014	42
5	Changes in the stool and oropharyngeal microbiome in obsessive-compulsive disorder Scientific Reports ·Laura Domènech, Jesse R. Willis, María Alemany-Navarro, Marta Morell, Eva Real, Geòrgia Escaramís, Sara Bertolín, Daniel Sánchez Chinchilla, Susana Balcells, Cinto Segalàs, Xavier Estivill, José M. Menchón, Toni Gabaldón, Pino Alonso, Raquel Rabionet	2022	30
6	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 ·Yolanda Espinosa‐Parrilla, Marta Morell, Juan Carlos Souto, Isabel Tirado, J. Fontcuberta, Xavier Estivill, Núria Sala	1999	28
7	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 ·Yolanda Espinosa‐Parrilla, Marta Morell, Montserrat Borrell, Juan Carlos Souto, J. Fontcuberta, Xavier Estivill, Núria Sala	2000	22
8	Absence of Linkage Between Type III Protein S Deficiency and the PROS1 and C4BP Genes in Families Carrying the Protein S Heerlen Allele Blood ·Yolanda Espinosa‐Parrilla, Marta Morell, Juan Carlos Souto, Montserrat Borrell, Damián Heine‐Suñer, Isabel Tirado, Vı́ctor Volpini, Xavier Estivill, Núria Sala	1997	22
9	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 ·Renzo Mancuso, Jaume del Valle, Marta Morell, Mercè Pallàs, Rosario Osta, Xavier Navarro	2014	21
10	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 ·Yolanda Espinosa‐Parrilla, G Navarro, Marta Morell, Eugènia Abella, Xavier Estivill, Núria Sala	2000	19
11	Nucleotide, Cytogenetic and Expression Impact of the Human Chromosome 8p23.1 Inversion Polymorphism PLoS ONE ·Nina Bosch, Marta Morell, Immaculada Ponsa, Josep M. Mercader, Lluı́s Armengol, Xavier Estivill	2009	18
12	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 ·José Manuel Soria, Marta Morell, Ioana Nicolau, Xavier Estivill, Núria Sala	1996	18
13	Absence of cytogenetic effects in children and adults with attention-deficit/hyperactivity disorder treated with methylphenidate Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Immaculada Ponsa, Josep Antoni Ramos‐Quiroga, Marta Ribasès, Rosa Bosch, Anna Bielsa, Maria Teresa Ordeig, Marta Morell, Rosa Miró, Rafael de Cid, Xavier Estivill, Miguel Casas, Mónica Bayés, Bru Cormand, Amaia Hervás	2009	13
14	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 ·José Manuel Soria, Marta Morell, Carmen Jimeénez-Astorga, Xavier Estivill, Núria Sala	1995	7
15	Aberrant RNA splicing of the protein C and protein S genes in healthy individuals Blood Coagulation & Fibrinolysis ·L-P. Berg, José Manuel Soria, Caroline J. Formstone, Marta Morell, V V Kakkar, Xavier Estivill, Núria Sala, D.N. Cooper	1996	4
16	Recurrence of thePROC gene mutation R178Q: Independent origins in Spanish protein C deficiency patients Human Mutation ·José Manuel Soria, Marta Morell, Xavier Estivill, Núria Sala	1996	2
17	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 ·Yolanda Espinosa‐Parrilla, Marta Morell, Juan Carlos Souto, Isabel Tirado, J. Fontcuberta, Xavier Estivill, Núria Sala	1999	1
18	A novel polymorphism (6376 G/T) in intron 7 of the human protein C gene Human Genetics ·Jos�Manuel Soria, Marta Morell, Xavier Estivill, Núria Sala	1995	1
19	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 ·Yolanda Espinosa‐Parrilla, Marta Morell, Montserrat Borrell, Juan Carlos Souto, J. Fontcuberta, Xavier Estivill, Núria Sala	2000	1
20	Advanced Optical Microscopy: Unveiling Functional Insights Regarding a Novel PPP2R1A Variant and Its Unreported Phenotype International Journal of Molecular Sciences ·Mónica Roldán, Gregorio Nolasco, Lluı́s Armengol, Marcos Frías, Marta Morell, Manel García‐Aragonés, Florencia Epifani, Jordi Muchart, María Luisa Ramírez-Almaraz, Loreto Martorell, Cristina Hernando‐Davalillo, Roser Urreizti, Mercedes Serrano	2023	0

About Marta Morell

Marta Morell is a scholar working on Hematology, Molecular Biology, Genetics, Genetics and Immunology, having authored 20 papers that have together received 383 indexed citations. Recurring topics across this work include Blood Coagulation and Thrombosis Mechanisms (11 papers), Complement system in diseases (3 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (3 papers), Hemophilia Treatment and Research (2 papers), Obsessive-Compulsive Spectrum Disorders (2 papers), Protease and Inhibitor Mechanisms (2 papers), Cellular transport and secretion (2 papers) and Wheat and Barley Genetics and Pathology (1 paper). The work is most often cited by research in Hematology (135 citations), Biological Psychiatry (19 citations), Genetics (75 citations), Internal Medicine (22 citations) and Neurology (54 citations). Marta Morell has collaborated with scholars based in Spain, United Kingdom and United States. Frequent co-authors include Xavier Estivill, Núria Sala, Xavier Navarro, Yolanda Espinosa‐Parrilla, Juan Carlos Souto, Renzo Mancuso, Isabel Tirado, Rosario Osta, J. Fontcuberta and Helgi van de Velde. Their work appears in journals such as Human Mutation, Blood Coagulation & Fibrinolysis, Thrombosis and Haemostasis, Experimental Neurology and Scientific Reports.

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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