Sabina Domené

1.0k total citations
19 papers, 436 citations indexed

About

Sabina Domené is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Sabina Domené has authored 19 papers receiving a total of 436 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Endocrinology, Diabetes and Metabolism, 11 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Sabina Domené's work include Growth Hormone and Insulin-like Growth Factors (9 papers), Hedgehog Signaling Pathway Studies (3 papers) and Genetic Syndromes and Imprinting (3 papers). Sabina Domené is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (9 papers), Hedgehog Signaling Pathway Studies (3 papers) and Genetic Syndromes and Imprinting (3 papers). Sabina Domené collaborates with scholars based in Argentina, United States and Brazil. Sabina Domené's co-authors include Erich Roessler, Maximilian Muenke, Horacio M. Domené, Jong‐Sun Kang, Robert S. Krauss, Gyu‐Un Bae, Karen A. Schachter, Viviana Varela, Héctor M. Targovnik and Christian M. Moya and has published in prestigious journals such as Journal of Neuroscience, The Journal of Clinical Endocrinology & Metabolism and Philosophical Transactions of the Royal Society B Biological Sciences.

In The Last Decade

Sabina Domené

19 papers receiving 431 citations

Peers

Countries citing papers authored by Sabina Domené

Since Specialization

Citations

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

Fields of papers citing papers by Sabina Domené

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabina Domené

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	An in vivo functional assay to characterize human STAT5B genetic variants during zebrafish development 2023 ·Human Molecular Genetics ·(unknown), Liliana Karabatas, Tomás Gómez, (unknown), Paula Scaglia, Laura Ramírez, Ana Keselman, Débora Braslavsky, (unknown), P. Pennisi, Rodolfo A. Rey, Ignacio Bergadá, Héctor Jasper, Horacio M. Domené, Paola V. Plazas, Sabina Domené	1
2	Applying Bioinformatic Platforms, In Vitro, and In Vivo Functional Assays in the Characterization of Genetic Variants in the GH/IGF Pathway Affecting Growth and Development 2021 ·Cells ·Sabina Domené, Paula Scaglia, Mariana Gutiérrez, Horacio M. Domené	7
3	Unraveling the Molecular Players at the Cholinergic Efferent Synapse of the Zebrafish Lateral Line 2020 ·Journal of Neuroscience ·(unknown), (unknown), (unknown), (unknown), Sabina Domené, (unknown), (unknown), Carolina Wedemeyer, Juan D. Goutman, Paola V. Plazas, Ana Belén Elgoyhen	11
4	The role of acid-labile subunit (ALS) in the modulation of GH-IGF-I action 2020 ·Molecular and Cellular Endocrinology ·Sabina Domené, Horacio M. Domené	23
5	Expression of acid-labile subunit (ALS) in developing and adult zebrafish and its role in dorso-ventral patterning during development 2020 ·General and Comparative Endocrinology ·(unknown), Liliana Karabatas, Paula Scaglia, (unknown), Mariana Gutiérrez, Laura Ramírez, Ignacio Bergadá, Rodolfo A. Rey, Héctor Jasper, Horacio M. Domené, Paola V. Plazas, Sabina Domené	7
6	A novel heterozygous STAT5B variant in a patient with short stature and partial growth hormone insensitivity (GHI) 2019 ·Growth Hormone & IGF Research ·Laura Ramírez, (unknown), Paula Scaglia, Ana Keselman, Marı́a Gabriela Ballerini, Liliana Karabatas, (unknown), (unknown), Sabina Domené, P. Pennisi, Héctor Jasper, Rodolfo A. Rey, Martı́n Vázquez, Horacio M. Domené, Ignacio Bergadá, Mariana Gutiérrez	8
7	Genetic Mutations in the GH/IGF Axis. 2018 ·PubMed ·Sabina Domené, Horacio M. Domené	14
8	Characterization of four Latin American families confirms previous findings and reveals novel features of acid‐labile subunit deficiency 2017 ·Clinical Endocrinology ·Paula Scaglia, Ana Keselman, Débora Braslavsky, (unknown), Liliana Karabatas, Sabina Domené, Mariana Gutiérrez, Marı́a Gabriela Ballerini, María Gabriela Ropelato, Angela Maria Spinola‐Castro, (unknown), (unknown), (unknown), Rodolfo A. Rey, Héctor Jasper, Ignacio Bergadá, Horacio M. Domené	7
9	Assessment of pathogenicity of natural IGFALS gene variants by in silico bioinformatics tools and in vitro functional studies 2016 ·Molecular and Cellular Endocrinology ·(unknown), Mariana Gutiérrez, Liliana Karabatas, Paula Scaglia, Rodolfo A. Rey, Horacio M. Domené, Héctor Jasper, Sabina Domené	9
10	Recurrent IGFALS Gene Mutations p.E35Gfs*17 and p.(L409F; A475V): Hot Spot or Founder Effect? 2015 ·Paula Scaglia, Andrea Sala, Ignacio Bergadá, Débora Braslavsky, Ana Keselman, (unknown), Sabina Domené, Héctor Jasper, Daniel Corach, Horacio M. Domené	1
11	ALS Deficiency due to a Novel and Two Already Described IGFALS Gene Mutations in an Unusual Non Consanguineous Family: Two Compound Heterozygous (Father and Son) and Two Heterozygous Carriers (Brother and Mother) 2014 ·Paula Scaglia, Ana Keselman, (unknown), Liliana Karabatas, Marı́a Gabriela Ballerini, Sabina Domené, (unknown), Héctor Jasper, Horacio M. Domené	1
12	Enhancer turnover and conserved regulatory function in vertebrate evolution 2013 ·Philosophical Transactions of the Royal Society B Biological Sciences ·Sabina Domené, Viviana F Bumaschny, Flávio S. J. de Souza, Lucía F. Franchini, Sofía Nasif, Malcolm J. Low, Marcelo Rubinstein	32
13	Mutations in CDON, Encoding a Hedgehog Receptor, Result in Holoprosencephaly and Defective Interactions with Other Hedgehog Receptors 2011 ·The American Journal of Human Genetics ·Gyu‐Un Bae, Sabina Domené, Erich Roessler, Karen A. Schachter, Jong‐Sun Kang, Maximilian Muenke, Robert S. Krauss	100
14	Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility 2010 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Sabina Domené, Horia Stanescu, Deeann Wallis, (unknown), (unknown), Robert Kleta, Mauricio Arcos‐Burgos, Erich Roessler, Maximilian Muenke	48
15	Association of the TGrI29 microsatellite in thyroglobulin gene with autoimmune thyroiditis in a Argentinian population: a case–control study 2010 ·Endocrine ·Viviana Varela, Leonardo Rizzo, Sabina Domené, Oscar D. Bruno, Mariana L. Tellechea, (unknown), Héctor M. Targovnik	5
16	A novel SIX3 mutation segregates with holoprosencephaly in a large family 2009 ·American Journal of Medical Genetics Part A ·Benjamin D. Solomon, Felicitas Lacbawan, Mahim Jain, Sabina Domené, Erich Roessler, Cynthia A. Moore, William B. Dobyns, Maximilian Muenke	32
17	Mutations in the human SIX3 gene in holoprosencephaly are loss of function 2008 ·Human Molecular Genetics ·Sabina Domené, Erich Roessler, Kênia Balbi El-Jaick, Mirit Snir, (unknown), Jorge I. Vélez, Sherri J. Bale, Felicitas Lacbawan, Maximilian Muenke, Benjamin Feldman	42
18	Two Distinct Compound Heterozygous Constellations (R277X/IVS34–1G>C and R277X/R1511X) in the Thyroglobulin (TG) Gene in Affected Individuals of a Brazilian Kindred with Congenital Goiter and Defective TG Synthesis 2004 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Christian M. Moya, (unknown), Sabina Domené, Viviana Varela, (unknown), Geraldo Medeiros‐Neto, Héctor M. Targovnik	49
19	Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect 2003 ·Human Mutation ·(unknown), Sebastián Esperante, Laura Gruñeiro‐Papendieck, Ana Chiesa, Christian M. Moya, Sabina Domené, Viviana Varela, Héctor M. Targovnik	39

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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