Fernando Scaglia

15.1k total citations · 2 hit papers
168 papers, 7.1k citations indexed

About

Fernando Scaglia is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Fernando Scaglia has authored 168 papers receiving a total of 7.1k indexed citations (citations by other indexed papers that have themselves been cited), including 124 papers in Molecular Biology, 86 papers in Clinical Biochemistry and 32 papers in Genetics. Recurrent topics in Fernando Scaglia's work include Metabolism and Genetic Disorders (86 papers), Mitochondrial Function and Pathology (82 papers) and ATP Synthase and ATPases Research (25 papers). Fernando Scaglia is often cited by papers focused on Metabolism and Genetic Disorders (86 papers), Mitochondrial Function and Pathology (82 papers) and ATP Synthase and ATPases Research (25 papers). Fernando Scaglia collaborates with scholars based in United States, Hong Kong and China. Fernando Scaglia's co-authors include Ayman W. El‐Hattab, Lee‐Jun C. Wong, Adekunle M. Adesina, Nicola Brunetti‐Pierri, William J. Craigen, Mohammed Almannai, Jeremy Jones, William J. Craigen, Brendan Lee and Lisa Emrick and has published in prestigious journals such as SHILAP Revista de lepidopterología, The EMBO Journal and Molecular and Cellular Biology.

In The Last Decade

Fernando Scaglia

159 papers receiving 7.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options

2015 389 citations Ayman W. El‐Hattab, Fernando Scaglia et al. Molecular Genetics and Metabolism profile →
Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

2014 372 citations Sumit Parikh, Amy Goldstein et al. Genetics in Medicine profile →

Peers

Countries citing papers authored by Fernando Scaglia

Since Specialization

Citations

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

Fields of papers citing papers by Fernando Scaglia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fernando Scaglia

This figure shows the co-authorship network connecting the top 25 collaborators of Fernando Scaglia. A scholar is included among the top collaborators of Fernando Scaglia 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 Fernando Scaglia. Fernando Scaglia 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	Paleoecology and diversity of Pliocene to Pleistocene fossorial mammals in the Pampean region of Argentina based on a quantitative analysis of fossil burrows 2024 ·Palaeogeography Palaeoclimatology Palaeoecology ·Néstor Toledo, (unknown), M. Susana Bargo, Verónica Krapovickas, Matías L. Taglioretti, Laura M. Pérez, Marcelo Zárate, Sergio F. Vizcaı́no, (unknown), Adriano Boscaini, Federico Ignacio Isla, Aldo Iván Vassallo, Fernando Scaglia	1
2	Hyperkinetic Movement Disorder Caused by the Recurrent c. 892C >T NACC1 Variant 2024 ·Movement Disorders Clinical Practice ·(unknown), Salla M. Kangas, Estrella López‐Martín, Timothy Feyma, Fernando Scaglia, Beatriz Martı́nez-Delgado, Outi Kuismin, Maria Suo‐Palosaari, Lucinda Carr, Reetta Hinttala, Manju A. Kurian, Johanna Uusimaa	1
3	Intracranial calcifications simulating Aicardi‐Goutières syndrome in PARS2‐related mitochondrial disease 2024 ·American Journal of Medical Genetics Part A ·Amanda Gerard, (unknown), Carrie Mohila, (unknown), Jill V. Hunter, Debra L. Kearney, Seema R. Lalani, Fernando Scaglia	1
4	Cardiomyopathy, an uncommon phenotype of congenital disorders of glycosylation: Recommendations for baseline screening and follow-up evaluation 2024 ·Molecular Genetics and Metabolism ·Roni Zemet, (unknown), Andrew C. Edmondson, (unknown), (unknown), (unknown), Justin H. Berger, Kyriakie Sarafoglou, Austin Larson, Christina Lam, Éva Morava, Fernando Scaglia	4
5	Expansion of the clinical and molecular spectrum of WWOX‐related epileptic encephalopathy 2022 ·American Journal of Medical Genetics Part A ·(unknown), Ye Cao, Eva Fung, Soledad Kleppe, Karen W. Gripp, Jozef Hertecant, Ayman W. El‐Hattab, Jehan Suleiman, Gary Clark, Gretchen Von Allmen, (unknown), Richard A. Lewis, Jill A. Rosenfeld, Jie Dong, (unknown), Xia Wang, Marcus J. Miller, Weimin Bi, Pengfei Liu, Fernando Scaglia	2
6	Expansion of the clinical phenotype of GALE deficiency 2021 ·American Journal of Medical Genetics Part A ·(unknown), Nichole Owen, Lisa Forbes Satter, Susan E. Kirk, Donald H. Mahoney, Alison A. Bertuch, Fernando Scaglia	7
7	Severe Generalized Epidermolysis Bullosa Simplex in Two Hong Kong Children due to De Novo Variants in KRT14 and KRT5 2020 ·SHILAP Revista de lepidopterología ·(unknown), Kam‐Lun Ellis Hon, Fernando Scaglia, Chung Mo Chow, (unknown), Tor Chiu, Alexander K. C. Leung	3
8	Clinical trials in mitochondrial disorders, an update 2020 ·Molecular Genetics and Metabolism ·Mohammed Almannai, Ayman W. El‐Hattab, (unknown), Claudia Soler‐Alfonso, Fernando Scaglia	50
9	GNA11 brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis 2019 ·Neurology Genetics ·(unknown), (unknown), (unknown), Peyman Bizargity, Haley Streff, Yi-Shan Lee, Hongzheng Dai, Satyamaanasa Polubothu, Grace Lee, Vicky Ren, Jill V. Hunter, Daniel J. Curry, Fernando Scaglia, Adekunle M. Adesina, Imran Ali, Veronica A. Kinsler, Lindsay C. Burrage, Dana Marafi	2
10	TANGO2-Related Metabolic Encephalopathy and Arrhythmias 2018 ·Seema R. Lalani, Brett H. Graham, Lindsay C. Burrage, Yi‐Chen Lai, Fernando Scaglia, Claudia Soler‐Alfonso, Christina Y. Miyake, Yaping Yang	7
11	Mitochondrial Cardiomyopathies 2016 ·Frontiers in Cardiovascular Medicine ·Ayman W. El‐Hattab, Fernando Scaglia	130
12	Early onset and severe clinical course associated with the m.5540G>A mutation in MT-TW 2014 ·Molecular Genetics and Metabolism Reports ·Jorge L. Granadillo, (unknown), Richard A. Lewis, (unknown), (unknown), Jing Wang, Lee-Jun Wong, Fernando Scaglia	3
13	Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society breakdown → 2014 ·Genetics in Medicine ·Sumit Parikh, Amy Goldstein, Mary Kay Koenig, Fernando Scaglia, Gregory M. Enns, Russell P. Saneto, Irina Anselm, Bruce H. Cohen, Marni J. Falk, Carol L. Greene, Andrea Gropman, Richard Haas, Michio Hirano, Philip G. Morgan, Katherine B. Sims, Mark A. Tarnopolsky, Johan L.K. Van Hove, Lynne A. Wolfe, Salvatore DiMauro	372
14	Titaniferous magnetite and barite from the San Gregorio de Polanco dike swarm, Paraná Magmatic Province, Uruguay 2013 ·SHILAP Revista de lepidopterología ·(unknown), Fernando Scaglia, Henri Masquelin	2
15	Dilation of the aortic root in mitochondrial disease patients 2011 ·Molecular Genetics and Metabolism ·Nicola Brunetti‐Pierri, Ricardo H. Pignatelli, (unknown), Jeffrey A. Towbin, John W. Belmont, William J. Craigen, Lee‐Jun Wong, John L. Jefferies, Fernando Scaglia	19
16	Deletion and duplication of 15q24: Molecular mechanisms and potential modification by additional copy number variants 2010 ·Genetics in Medicine ·Ayman W. El‐Hattab, Feng Zhang, Rolanda Maxim, Katherine Christensen, Jewell C. Ward, Stacy J. Hines‐Dowell, Fernando Scaglia, James R. Lupski, Sau Wai Cheung	27
17	Case-control study in an integrated treatment of gonarthrosis using magnetotherapy and therapeutic exercise VS the same treatment in association with endo-articular injections. 2010 ·European Journal of Physical and Rehabilitation Medicine ·(unknown), (unknown), (unknown), Fernando Scaglia, (unknown), Giulia Letizia Mauro	1
18	Ménage-à-Trois 1 Is Critical for the Transcriptional Function of PPARγ Coactivator 1 2007 ·Cell Metabolism ·Motoaki Sano, Yasukatsu Izumi, Katja Helenius, Masanori Asakura, Derrick J. Rossi, Min Xie, George Taffet, Lingyun Hu, Robia G. Pautler, Christopher R. Wilson, Sihem Boudina, E. Dale Abel, Heinrich Taegtmeyer, Fernando Scaglia, Brett H. Graham, Anastasia Kralli, Noriaki Shimizu, Hirotoshi Tanaka, Tomi P. Mäkelä, Michael Schneider	50
19	Clinical Consequences of Urea Cycle Enzyme Deficiencies and Potential Links to Arginine and Nitric Oxide Metabolism 2004 ·Journal of Nutrition ·Fernando Scaglia, Nicola Brunetti‐Pierri, Soledad Kleppe, Juan C. Marini, Susan Carter, Peter J. Garlick, Farook Jahoor, William E. O’Brien, Brendan Lee	69
20	Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency 1998 ·Genetics in Medicine ·Fernando Scaglia, Yuhuan Wang, Rani H. Singh, Philip P. Dembure, Marzia Pasquali, Paul M. Fernhoff, Nicola Longo	54

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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