Lucía Schottlaender

1.3k total citations
15 papers, 437 citations indexed

About

Lucía Schottlaender is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Lucía Schottlaender has authored 15 papers receiving a total of 437 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Neurology, 6 papers in Molecular Biology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Lucía Schottlaender's work include Parkinson's Disease Mechanisms and Treatments (6 papers), Neurological diseases and metabolism (4 papers) and Genetic Neurodegenerative Diseases (3 papers). Lucía Schottlaender is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (6 papers), Neurological diseases and metabolism (4 papers) and Genetic Neurodegenerative Diseases (3 papers). Lucía Schottlaender collaborates with scholars based in United Kingdom, United States and Argentina. Lucía Schottlaender's co-authors include Henry Houlden, Sebastián F. Ameriso, Eelco F. M. Wijdicks, Kelly D. Flemming, Gustavo Ortiz, Alejandro A. Rabinstein, Kailash P. Bhatia, Jennifer E. Fugate, Janice L. Holton and Xin You Tai and has published in prestigious journals such as PLoS ONE, Stroke and The American Journal of Human Genetics.

In The Last Decade

Lucía Schottlaender

14 papers receiving 424 citations

Peers

Countries citing papers authored by Lucía Schottlaender

Since Specialization

Citations

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

Fields of papers citing papers by Lucía Schottlaender

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucía Schottlaender

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Feeding difficulties in children and adolescents with spinal muscular atrophy type 2 2020 ·Neuromuscular Disorders ·Renske I. Wadman, Ramona De Amicis, (unknown), Alberto Battezzati, Simona Bertoli, (unknown), Marion Main, (unknown), Chiara Mastella, Pinki Munot, (unknown), Lucía Schottlaender, Anna Sárközy, Federica Trucco, Giovanni Baranello, Mariacristina Scoto, Francesco Muntoni	16
2	Investigation of somatic CNVs in brains of synucleinopathy cases using targeted SNCA analysis and single cell sequencing 2019 ·Acta Neuropathologica Communications ·Diego Pérez‐Rodríguez, (unknown), (unknown), Tammaryn Lashley, Maxime Tarabichi, Viorica Chelban, Steve Gentleman, Lucía Schottlaender, (unknown), George Vasmatzis, Henry Houlden, Anthony H.V. Schapira, Thomas T. Warner, Janice L. Holton, Zane Jaunmuktane, Christos Proukakis	32
3	LRP10 in alpha-synucleinopathies 2018 ·UCL Discovery (University College London) ·Lasse Pihlstrøm, Lucía Schottlaender, (unknown), Henry Houlden	4
4	Nutritional status of a large cohort of children with spinal muscular atrophy type 2 (SMA2) 2017 ·Neuromuscular Disorders ·Lucía Schottlaender, Mariacristina Scoto, (unknown), (unknown), (unknown), Pinki Munot, Anna Sárközy, (unknown), Francesco Muntoni	1
5	Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients 2016 ·PLoS ONE ·Lucía Schottlaender, Conceição Bettencourt, Aoife P. Kiely, Annapurna Chalasani, Viruna Neergheen, Janice L. Holton, Iain P. Hargreaves, Henry Houlden	44
6	Analysis of the prion protein gene in multiple system atrophy 2016 ·Neurobiology of Aging ·Viorica Chelban, Andreea Manole, Lasse Pihlstrøm, Lucía Schottlaender, Stéphanie Efthymiou, Emer O’Connor, Wassilios G. Meissner, Janice L. Holton, Henry Houlden	7
7	Deconstructing Fahr's disease/syndrome of brain calcification in the era of new genes 2016 ·Parkinsonism & Related Disorders ·Amit Batla, Xin You Tai, Lucía Schottlaender, Roberto Erro, Bettina Balint, Kailash P. Bhatia	59
8	Multiple system atrophy: the application of genetics in understanding etiology 2015 ·Clinical Autonomic Research ·Monica Federoff, Lucía Schottlaender, Henry Houlden, Andrew Singleton	11
9	The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism 2014 ·Neurobiology of Aging ·Lucía Schottlaender, James M. Polke, Helen Ling, (unknown), Arianna Tucci, Tina Nanji, Alan Pittman, Rohan de Silva, Janice L. Holton, Tamás Révész, Mary G. Sweeney, Andy Singleton, Andrew J. Lees, Kailash P. Bhatia, Henry Houlden	34
10	Diagnostic clues and manifesting carriers in fukutin-related protein (FKRP) limb-girdle muscular dystrophy 2014 ·Journal of the Neurological Sciences ·Lucía Schottlaender, Axel Petzold, Nicholas Wood, Henry Houlden	6
11	White matter relapsing remitting disease: “Susac’s syndrome”—An underdiagnosed entity 2013 ·Multiple Sclerosis and Related Disorders ·Lucía Schottlaender, Jorge Correale, Sebastián F. Ameriso, (unknown), Lucía Crivelli, Francisco Meli, Marcela Fiol	4
12	Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity 2013 ·The American Journal of Human Genetics ·Monia Hammer, (unknown), Lucía Schottlaender, (unknown), J. Raphael Gibbs, (unknown), Sean Chong, Dena Hernández, Anna Sailer, Guoxiang Liu, Pramod K. Mistry, Huaibin Cai, (unknown), Celeste Sassi, Yosr Bouhlal, Henry Houlden, Fayçal Hentati, Rim Amouri, Andrew B. Singleton	93
13	The frequency of spinocerebellar ataxia type 23 in a UK population 2012 ·Journal of Neurology ·Katherine A. Fawcett, Mohadeseh Mehrabian, Yo‐Tsen Liu, Sherifa A. Hamed, Elahe Elahi, Tamás Révész, Georgios Koutsis, (unknown), Lucía Schottlaender, Mark Wardle, Patrick J. Morrison, Huw R. Morris, Paola Giunti, Nicholas Wood, Henry Houlden	9
14	High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients 2012 ·Neurobiology of Aging ·Kin Y. Mok, Georgios Koutsis, Lucía Schottlaender, James M. Polke, Μάριος Πάνας, Henry Houlden	33
15	Variable Presentations of Postpartum Angiopathy 2012 ·Stroke ·Jennifer E. Fugate, Sebastián F. Ameriso, Gustavo Ortiz, Lucía Schottlaender, Eelco F. M. Wijdicks, Kelly D. Flemming, Alejandro A. Rabinstein	84

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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