Sabrina Martín

1.7k total citations
33 papers, 1.2k citations indexed

About

Sabrina Martín is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Sabrina Martín has authored 33 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 7 papers in Hematology. Recurrent topics in Sabrina Martín's work include Vascular Anomalies and Treatments (6 papers), Chronic Lymphocytic Leukemia Research (3 papers) and Tracheal and airway disorders (3 papers). Sabrina Martín is often cited by papers focused on Vascular Anomalies and Treatments (6 papers), Chronic Lymphocytic Leukemia Research (3 papers) and Tracheal and airway disorders (3 papers). Sabrina Martín collaborates with scholars based in United States, France and Netherlands. Sabrina Martín's co-authors include Franck Lebrin, Christine L. Mummery, Helen M. Arthur, Karine Raymond, F. J. M. Disch, Repke J. Snijder, Johannes J. Mager, Carlo M. Croce, Florent Soubrier and Jean‐Léon Thomas and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Circulation.

In The Last Decade

Sabrina Martín

26 papers receiving 1.2k citations

Peers

Countries citing papers authored by Sabrina Martín

Since Specialization

Citations

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

Fields of papers citing papers by Sabrina Martín

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabrina Martín

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

#	Work	Indexed citations
1	Characterization of congenital hyperinsulinism in Argentina: Clinical features, genetic findings, and treatment outcomes 2025 ·PLoS ONE ·(unknown), (unknown), Juan Cáceres, Guillermo Alonso, (unknown), (unknown), Adriana Flores, (unknown), (unknown), Jayne Houghton, (unknown), Sabrina Martín, Sarah E. Flanagan, (unknown)	0
2	X-ray Radiotherapy Impacts Cardiac Dysfunction by Modulating the Sympathetic Nervous System and Calcium Transients 2024 ·International Journal of Molecular Sciences ·(unknown), Nadine Suffee, Florence Bachelot, Morgane Dos Santos, Nathalie Mougenot, Elise Delage, (unknown), Sabrina Martín, Isabelle Brunet, Pierre Sicard, Virginie Monceau	0
3	Vascular dysfunction is at the onset of oxaliplatin-induced peripheral neuropathy symptoms in mice 2024 ·Life Science Alliance ·(unknown), (unknown), (unknown), Anne Boulay, Sabrina Martín, Corinne Blugeon, Laurent Jourdren, Rémi Freydier, Martine Cohen‐Salmon, Jamïlé Hazan, Isabelle Brunet	0
4	Eritroqueratodermia variable y progresiva: comunicación de una serie de casos con variantes en dos genes 2022 ·Sabrina Martín, Daniela Espósito, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	0
5	A New Wnt1-CRE Tomato ^Rosa Embryonic Stem Cell Line: A Tool for Studying Neural Crest Cell Integration Capacity 2017 ·Stem Cells and Development ·(unknown), Sabrina Martín, Sabine Kuchler‐Bopp, Sandy Ribes, (unknown), Catherine Chaussain, Sophie Creuzet, Hervé Lesot, Franck Lebrin, Anne Poliard	0
6	The TGFβ pathway is a key player for the endothelial-to-hematopoietic transition in the embryonic aorta 2017 ·Developmental Biology ·(unknown), (unknown), (unknown), Sabrina Martín, (unknown), Karine Raymond, Franck Lebrin, C. Drevon, Thierry Jaffredo	13
7	Interaction Between ALK1 Signaling and Connexin40 in the Development of Arteriovenous Malformations 2016 ·Arteriosclerosis Thrombosis and Vascular Biology ·Konstantinos Gkatzis, (unknown), (unknown), Sabrina Martín, Noël Lamandé, M.F. Carette, F. J. M. Disch, Repke J. Snijder, Cornelius J.J. Westermann, Johannes J. Mager, S. Paul Oh, Lucile Miquerol, Helen M. Arthur, Christine L. Mummery, Franck Lebrin	19
8	Rituximab Extended Schedule or Re-Treatment Trial for Low–Tumor Burden Follicular Lymphoma: Eastern Cooperative Oncology Group Protocol E4402 2014 ·Journal of Clinical Oncology ·Brad S. Kahl, Fangxin Hong, Michael E. Williams, Randy D. Gascoyne, Lynne I. Wagner, John C. Krauss, Thomas M. Habermann, Lode J. Swinnen, Stephen J. Schuster, Christopher G. Peterson, Mark D. Sborov, Sabrina Martín, Matthias Weiss, W. Christopher Ehmann, Sandra J. Horning	138
9	Aminoglycosides Restore Full-length Type VII Collagen by Overcoming Premature Termination Codons: Therapeutic Implications for Dystrophic Epidermolysis Bullosa 2014 ·Molecular Therapy ·Jon Cogan, (unknown), Xinyi Wang, Yingping Hou, Sabrina Martín, Andrew P. South, David T. Woodley, Mei Chen	49
10	ENDOGLIN Is Dispensable for Vasculogenesis, but Required for Vascular Endothelial Growth Factor-Induced Angiogenesis 2014 ·PLoS ONE ·Zhen Liu, Franck Lebrin, Janita A. Maring, Sander van den Driesche, (unknown), Maarten van Dinther, Midory Thorikay, Sabrina Martín, Kazuki Kobayashi, Lukas J.A.C. Hawinkels, Laurens A. van Meeteren, Evangelia Pardali, Jeroen Korving, Michelle Letarte, Helen M. Arthur, Charles P. Theuer, Marie‐José Goumans, Christine L. Mummery, Peter ten Dijke	61
11	A phase 2 trial of extended induction epratuzumab and rituximab for previously untreated follicular lymphoma: CALGB 50701 2013 ·Cancer ·Barbara Grant, Sin‐Ho Jung, Jeffrey L. Johnson, Lale Kostakoğlu, Eric D. Hsi, John C. Byrd, Jeffrey A. Jones, John P. Leonard, Sabrina Martín, Bruce D. Cheson	42
12	A One-Step Prescreening for Point Mutations and Large Rearrangement in BRCA1 and BRCA2 Genes Using Quantitative Polymerase Chain Reaction and High-Resolution Melting Curve Analysis 2010 ·Genetic Testing and Molecular Biomarkers ·Florence Coulet, (unknown), Étienne Rouleau, Cédrick Lefol, Sabrina Martín, Chrystelle Colas, Odile Cohen‐Haguenauer, Irina Giurgea, Anne Fajac, Catherine Noguès, Liliane Demange, Agnès Hardouin, Rosette Lidereau, Florent Soubrier	16
13	Thalidomide stimulates vessel maturation and reduces epistaxis in individuals with hereditary hemorrhagic telangiectasia 2010 ·Nature Medicine ·Franck Lebrin, (unknown), Karine Raymond, Sabrina Martín, Stieneke van den Brink, Catarina Freitas, Christiane Bréant, Thomas Mathivet, Bruno Larrivée, Jean‐Léon Thomas, Helen M. Arthur, Cornelis J.J. Westermann, F. J. M. Disch, Johannes J. Mager, Repke J. Snijder, Anne Eichmann, Christine L. Mummery	267
14	BRCA1 E1644X: a deleterious mutation in an African American individual with early onset breast cancer 2008 ·Breast Cancer Research and Treatment ·Sabrina Martín, Mark Sausen, Abraham Joseph, David D. Biggs, Brewster F. Kingham, Eric S. Martin	3
15	Altered endothelial gene expression associated with hereditary haemorrhagic telangiectasia 2007 ·European Journal of Clinical Investigation ·(unknown), Mélanie Eyries, Kévin Montagne, Sabrina Martín, Monique Agrapart, (unknown), Michelle Letarte, Florent Soubrier	23
16	Risk Factors for Buruli Ulcer Disease (Mycobacterium ulcerans Infection): Results from a Case-Control Study in Ghana 2005 ·Clinical Infectious Diseases ·Pratima L. Raghunathan, Ellen A. Spotts Whitney, Kwame Asamoa, Ymkje Stienstra, Thomas H. Taylor, George Amofah, David Ofori‐Adjei, Karen M. Dobos, Jeannette Guarner, Sabrina Martín, Surya Prakash Pathak, Erasmus Klutse, Samuel Etuaful, Winette T.A. van der Graaf, Tjip S. van der Werf, Charles H. King, Jordan W. Tappero, David A. Ashford	118
17	High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity 2002 ·European Journal of Human Genetics ·Florent Soubrier, Sabrina Martín, (unknown), Sophie Visvikis‐Siest, Laurence Tiret, Fumihiko Matsuda, G.M. Lathrop, Martin Farrall	73
18	Bernard-Soulier syndrome: Common ancestry in two African American families with the GP Ib? Leu129Pro mutation 2000 ·American Journal of Hematology ·(unknown), Eric S. Martin, Peter J. Hulick, Abraham Joseph, Sabrina Martín	9
19	Studies in a Large Family with Late-Onset Alzheimer Disease (LOAD) 1997 ·Alzheimer Disease & Associated Disorders ·Eric S. Martin, Sabrina Martín, (unknown), Digamber S. Borgaonkar	3
20	Complex chromosome 4, 9, and 22 rearrangement in a patient presenting with AML-FAB M2 1997 ·Cancer Genetics and Cytogenetics ·Eric S. Martin, A Joseph, Munirah Ahmad, D. S. Borgaonkar, Sabrina Martín	2

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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