D. de Leon

1.4k total citations
18 papers, 941 citations indexed

About

D. de Leon is a scholar working on Neurology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, D. de Leon has authored 18 papers receiving a total of 941 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Neurology, 11 papers in Cellular and Molecular Neuroscience and 4 papers in Genetics. Recurrent topics in D. de Leon's work include Neurological disorders and treatments (14 papers), Genetic Neurodegenerative Diseases (9 papers) and Hereditary Neurological Disorders (5 papers). D. de Leon is often cited by papers focused on Neurological disorders and treatments (14 papers), Genetic Neurodegenerative Diseases (9 papers) and Hereditary Neurological Disorders (5 papers). D. de Leon collaborates with scholars based in United States, Russia and Poland. D. de Leon's co-authors include Neil Risch, Mitchell F. Brin, Susan Bressman, P. L. Kramer, Laurie J. Ozelius, Deborah Raymond, Stanley Fahn, Xandra O. Breakefield, Christine Klein and Robert E. Burke and has published in prestigious journals such as Neurology, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

D. de Leon

17 papers receiving 909 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
D. de Leon United States	14	845	733	81	65	61	18	941
Jennifer Garrels United States	6	416 0.5×	280 0.4×	92 1.1×	88 1.4×	76 1.2×	7	482
J.J. Zarranz Spain	4	542 0.6×	294 0.4×	48 0.6×	63 1.0×	99 1.6×	7	622
Ignacio Rubio‐Agusti United Kingdom	11	347 0.4×	197 0.3×	63 0.8×	110 1.7×	97 1.6×	13	591
Nathaniel R. Whaley United States	11	545 0.6×	342 0.5×	37 0.5×	103 1.6×	75 1.2×	12	670
Susen Winkler Germany	15	559 0.7×	342 0.5×	86 1.1×	204 3.1×	124 2.0×	19	750
Christian Kabus Germany	8	423 0.5×	265 0.4×	45 0.6×	41 0.6×	83 1.4×	11	510
Robert S. Raike United States	15	401 0.5×	500 0.7×	29 0.4×	225 3.5×	96 1.6×	28	659
Michele L. Rajput Canada	13	716 0.8×	238 0.3×	24 0.3×	72 1.1×	124 2.0×	15	793
José Miguel Laffita‐Mesa Sweden	14	324 0.4×	490 0.7×	54 0.7×	432 6.6×	79 1.3×	38	658
Humberto Moreno United States	5	343 0.4×	483 0.7×	74 0.9×	369 5.7×	19 0.3×	8	605

Countries citing papers authored by D. de Leon

Since Specialization

Citations

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

Fields of papers citing papers by D. de Leon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. de Leon. 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 D. de Leon. The network helps show where D. de Leon may publish in the future.

Co-authorship network of co-authors of D. de Leon

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

All Works

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18 of 18 papers shown

Leon, D. de, et al.. (2023). Academic Stress in the Psychological Well-being of Higher Education Students. 1 indexed citations

Weedon, Michael N., TJ Wilkin, L D Voss, et al.. (2003). A Common haplotype in the glucokinase gene is associated with increased fasting glucose and altered birth weight. LSHTM Research Online (London School of Hygiene and Tropical Medicine).

Doheny, Dana, Fabio Danisi, Christopher J. Smith, et al.. (2002). Clinical findings of a myoclonus-dystonia family with two distinct mutations. Neurology. 59(8). 1244–1246. 44 indexed citations

Bressman, Susan, Deborah Raymond, Kristin J. Wendt, et al.. (2002). Diagnostic criteria for dystonia in DYT1 families. Neurology. 59(11). 1780–1782. 54 indexed citations

Bressman, Susan, Chiara Sabatti, Deborah Raymond, et al.. (2000). The DYT1 phenotype and guidelines for diagnostic testing. Neurology. 54(9). 1746–1753. 242 indexed citations

Klein, Christine, Peter A. LeWitt, D. de Leon, et al.. (1999). Genetic analysis of three patients with an 18p− syndrome and dystonia. Neurology. 52(3). 649–649. 30 indexed citations

Brin, Mitchell F., D. de Leon, Limborskaia Sa, et al.. (1998). De Novo Mutations (GAG Deletion) in the DYT1 Gene in Two Non-Jewish Patients with Early-onset Dystonia. Human Molecular Genetics. 7(7). 1133–1136. 47 indexed citations

Bressman, S. B., D. de Leon, Deborah Raymond, et al.. (1998). Clinical-genetic spectrum of primary dystonia.. PubMed. 78. 79–91. 36 indexed citations

Bressman, Susan, D. de Leon, Deborah Raymond, et al.. (1998). The role of the DYT1 gene in secondary dystonia.. PubMed. 78. 107–15. 9 indexed citations

10.

Ozelius, L. J., Jeffrey Hewett, S. B. Bressman, et al.. (1998). The gene (DYT1) for early-onset torsion dystonia encodes a novel protein related to the Clp protease/heat shock family.. PubMed. 78. 93–105. 41 indexed citations

11.

Almasy, Laura, Susan Bressman, Deborah Raymond, et al.. (1997). Idiopathic torsion dystonia linked to chromosome 8 in two mennonite families. Annals of Neurology. 42(4). 670–673. 116 indexed citations

12.

Bressman, Susan, D. de Leon, Deborah Raymond, et al.. (1997). Secondary dystonia and the DYTI gene. Neurology. 48(6). 1571–1577. 17 indexed citations

13.

Bressman, Susan, P. Greene, Deborah Raymond, et al.. (1996). Exclusion of the DYT1 locus in familial torticollis. Annals of Neurology. 40(4). 681–684. 47 indexed citations

14.

Bressman, Susan, Gary A. Heiman, Torbjoern G. Nygaard, et al.. (1994). A study of idiopathic torsion dystonia in a non‐Jewish family. Neurology. 44(2). 283–283. 54 indexed citations

15.

Kramer, P. L., Gary A. Heiman, Thomas Gasser, et al.. (1994). The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews.. PubMed. 55(3). 468–75. 89 indexed citations

16.

Ozelius, Laurie J., P. L. Kramer, D. de Leon, et al.. (1992). Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews.. PubMed. 50(3). 619–28. 97 indexed citations

17.

Ozelius, Laurie J., P. L. Kramer, D. de Leon, et al.. (1992). Principles of molecular genetics/Dystonia. Movement Disorders. 7(S1). 2–2. 1 indexed citations

18.

Bressman, Susan, D. de Leon, Neil Risch, et al.. (1988). Inheritance of idiopathic torsion dystonia among Ashkenazi Jews.. PubMed. 50. 45–56. 16 indexed citations

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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