Marisa I. Mendes

881 total citations
16 papers, 237 citations indexed

About

Marisa I. Mendes is a scholar working on Molecular Biology, Rheumatology and Biochemistry. According to data from OpenAlex, Marisa I. Mendes has authored 16 papers receiving a total of 237 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 4 papers in Rheumatology and 3 papers in Biochemistry. Recurrent topics in Marisa I. Mendes's work include RNA modifications and cancer (7 papers), RNA and protein synthesis mechanisms (7 papers) and RNA Research and Splicing (6 papers). Marisa I. Mendes is often cited by papers focused on RNA modifications and cancer (7 papers), RNA and protein synthesis mechanisms (7 papers) and RNA Research and Splicing (6 papers). Marisa I. Mendes collaborates with scholars based in Netherlands, United States and Germany. Marisa I. Mendes's co-authors include Gajja S. Salomons, Desirée E.C. Smith, Paula Leandro, Henk J. Blom, Alan R. Lehmann, Joseph G. Gleeson, Anja Raams, Donata Orioli, Arjan F. Theil and Majdi Kara and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Marisa I. Mendes

14 papers receiving 236 citations

Peers

Countries citing papers authored by Marisa I. Mendes

Since Specialization

Citations

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

Fields of papers citing papers by Marisa I. Mendes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marisa I. Mendes. 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 Marisa I. Mendes. The network helps show where Marisa I. Mendes may publish in the future.

Co-authorship network of co-authors of Marisa I. Mendes

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Loss‐of‐Function CARS1 Variants in a Patient With Microcephaly, Developmental Delay, and a Brittle Hair Phenotype 2025 ·Molecular Genetics & Genomic Medicine ·(unknown), (unknown), Desirée E.C. Smith, Marisa I. Mendes, (unknown), (unknown), (unknown), Sergej Šesták, (unknown), Anthony Antonellis	0
2	Dominant-negative NARS1 R534∗ mutation causes wild-type subunit poisoning and heterodimer predominance in cells 2025 ·Journal of Biological Chemistry ·(unknown), Ryan Shapiro, (unknown), Marisa I. Mendes, Desirée E.C. Smith, Qian Zhang, Taisuke Kanaji, Bernhard Kuhle, Xiang‐Lei Yang	0
3	Isoleucine-to-valine substitutions support cellular physiology during isoleucine deprivation 2024 ·Nucleic Acids Research ·(unknown), Imre F. Schene, (unknown), (unknown), Marisa I. Mendes, Desirée E.C. Smith, Gajja S. Salomons, (unknown), Judith Jans, (unknown), Tim A. Hoek, (unknown), Holger Rehmann, Edward E. S. Nieuwenhuis, Harmjan R. Vos, Sabine A. Fuchs	1
4	Simultaneous determination of cytosolic aminoacyl-tRNA synthetase activities by LC–MS/MS 2024 ·Nucleic Acids Research ·Marisa I. Mendes, Nicole I. Wolf, Joëlle Rudinger‐Thirion, Dominic Lenz, Magali Frugier, Patrick Verloo, Hanna Mandel, (unknown), Rachel Kassel, Willemijn E. Corpeleijn, (unknown), (unknown), Silvy J.M. van Dooren, Christian Staufner, Gajja S. Salomons, Desirée E.C. Smith	1
5	A bi‐allelic loss‐of‐function SARS1 variant in children with neurodevelopmental delay, deafness, cardiomyopathy, and decompensation during fever 2021 ·Human Mutation ·Jean‐Marie Ravel, Natacha Dreumont, (unknown), Desirée E.C. Smith, Marisa I. Mendes, Arnaud Wiedemann, David Coelho, Emmanuelle Schmitt, Jean‐Baptiste Rivière, Frédéric Tran Mau‐Them, Julien Thévenon, Paul Kuentz, Marc Polivka, Sabine A. Fuchs, (unknown), Christel Thauvin‐Robinet, Jean‐Louis Guéant, Gajja S. Salomons, Laurence Faivre, François Feillet	6
6	A Hypomorphic Dars1D367Y Model Recapitulates Key Aspects of the Leukodystrophy HBSL 2021 ·Frontiers in Cellular Neuroscience ·Dominik Fröhlich, Marisa I. Mendes, Andrew J. Kueh, André Bongers, Marco J. Herold, Gajja S. Salomons, Gary D. Housley, Matthias Klugmann	7
7	Protein instability associated with AARS1 and MARS1 mutations causes trichothiodystrophy 2021 ·Human Molecular Genetics ·Elena Botta, Arjan F. Theil, Anja Raams, Giuseppina Caligiuri, (unknown), Silvia Bione, Maria Accadia, (unknown), Desirée E.C. Smith, Marisa I. Mendes, Sigrid Swagemakers, Peter J. van der Spek, Gajja S. Salomons, Jan H.J. Hoeijmakers, (unknown), Sheela Nampoothiri, Tomoo Ogi, Alan R. Lehmann, Donata Orioli, Wim Vermeulen	29
8	Rescue of respiratory failure in pulmonary alveolar proteinosis due to pathogenic MARS1 variants 2020 ·Pediatric Pulmonology ·Dominic Lenz, Mirjam Stahl, Elias Seidl, (unknown), Heiko Brennenstuhl, (unknown), (unknown), Thomas Longerich, Marisa I. Mendes, Holger Prokisch, Gajja S. Salomons, (unknown), Desirée E.C. Smith, Olaf Sommerburg, Matias Wagner, Jens H. Westhoff, Karl Reiter, Christian Staufner, Matthias Griese	19
9	Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly 2020 ·Nature Communications ·Lu Wang, Zhen Li, (unknown), Desirée E.C. Smith, Marisa I. Mendes, Dillon Y. Chen, Valentina Stanley, (unknown), Yulu Wang, Majdi Kara, Ayça Dilruba Aslanger, Rasim Özgür Rosti, Henry Houlden, Gajja S. Salomons, Joseph G. Gleeson	55
10	Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype 2019 ·The American Journal of Human Genetics ·Arjan F. Theil, Elena Botta, Anja Raams, Desirée E.C. Smith, Marisa I. Mendes, Giuseppina Caligiuri, (unknown), Silvia Bione, Roberta Carriero, Giordano Liberi, (unknown), Sigrid Swagemakers, Gajja S. Salomons, Alain Sarasin, Alan R. Lehmann, Peter J. van der Spek, Tomoo Ogi, Jan H.J. Hoeijmakers, Wim Vermeulen, Donata Orioli	42
11	Clinically Distinct Phenotypes of Canavan Disease Correlate with Residual Aspartoacylase Enzyme Activity 2017 ·Human Mutation ·Marisa I. Mendes, Desirée E.C. Smith, Ana Pop, (unknown), (unknown), Warsha A. Kanhai, (unknown), Yair Anikster, (unknown), (unknown), Jaime Campistol, Lonneke de Boer, Ariana Kariminejad, Hülya Kayserili, Agathe Roubertie, K. T. Verbruggen, Christine Vianey‐Saban, Monique J. Williams, Gajja S. Salomons	21
12	Small aminothiol compounds improve the function of Arg to Cys variant proteins: effect on the human cystathionine β-synthase p.R336C 2015 ·Human Molecular Genetics ·Marisa I. Mendes, Desirée E.C. Smith, João B. Vicente, Isabel Tavares de Almeida, Tawfeg Ben‐Omran, Gajja S. Salomons, Isabel Rivera, Paula Leandro, Henk J. Blom	10
13	Cystathionine β-synthase and the interplay between the bioenergetically relevant gasotransmitters NO, CO and H2S 2014 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Alessandro Giuffrè, Henrique G. Colaço, Daniela Mastronicola, Marisa I. Mendes, Paolo Sarti, Paula Leandro, João B. Vicente	2
14	Insights into the Regulatory Domain of Cystathionine Beta-Synthase: Characterization of Six Variant Proteins 2014 ·Human Mutation ·Marisa I. Mendes, (unknown), Desirée E.C. Smith, (unknown), Henrique G. Colaço, Isabel Tavares de Almeida, João B. Vicente, Gajja S. Salomons, Isabel Rivera, Henk J. Blom, Paula Leandro	14
15	Reduced response of Cystathionine Beta‐Synthase (CBS) to S‐Adenosylmethionine (SAM): Identification and functional analysis of CBS gene mutations in Homocystinuria patients 2013 ·Journal of Inherited Metabolic Disease ·Marisa I. Mendes, Henrique G. Colaço, Desirée E.C. Smith, Rúben J. Ramos, Ana Pop, Silvy J.M. van Dooren, Isabel Tavares de Almeida, Leo A. J. Kluijtmans, Mirian C. H. Janssen, Isabel Rivera, Gajja S. Salomons, Paula Leandro, Henk J. Blom	24
16	A liquid chromatography mass spectrometry method for the measurement of cystathionine β-synthase activity in cell extracts 2012 ·Journal of Chromatography B ·Desirée E.C. Smith, Marisa I. Mendes, Leo A. J. Kluijtmans, Mirian C. H. Janssen, Yvo M. Smulders, Henk J. Blom	6

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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