L. J. Ozelius

698 total citations
13 papers, 537 citations indexed

About

L. J. Ozelius is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, L. J. Ozelius has authored 13 papers receiving a total of 537 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Neurology, 8 papers in Cellular and Molecular Neuroscience and 2 papers in Molecular Biology. Recurrent topics in L. J. Ozelius's work include Neurological disorders and treatments (9 papers), Genetic Neurodegenerative Diseases (7 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). L. J. Ozelius is often cited by papers focused on Neurological disorders and treatments (9 papers), Genetic Neurodegenerative Diseases (7 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). L. J. Ozelius collaborates with scholars based in United States, Australia and United Kingdom. L. J. Ozelius's co-authors include X. O. Breakefield, Christine Klein, Christine Konradi, S. B. Bressman, Deborah Raymond, Xandra O. Breakefield, D. de Leon, J. H. Edwards, Brian P. Chadwick and Lynda J. Campbell and has published in prestigious journals such as Neuron, Neurology and Genomics.

In The Last Decade

L. J. Ozelius

13 papers receiving 527 citations

Peers

Countries citing papers authored by L. J. Ozelius

Since Specialization

Citations

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

Fields of papers citing papers by L. J. Ozelius

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L. J. Ozelius. 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 L. J. Ozelius. The network helps show where L. J. Ozelius may publish in the future.

Co-authorship network of co-authors of L. J. Ozelius

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

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	High mutation rate in dopa-responsive dystonia: Detection with comprehensive GCHI screening 2005 ·Neurology ·J. Hagenah, Rachel Saunders‐Pullman, Katja Hedrich, Kemal Kabakci, (unknown), Karin Wiegers, (unknown), Thora Lohnau, Deborah Raymond, P. Vieregge, (unknown), L. J. Ozelius, S. B. Bressman, Christine Klein	65
2	Mutations in DYT1 2004 ·Neurology ·Kemal Kabakci, Katja Hedrich, Joanne Leung, Manfred Mitterer, P. Vieregge, Rebekka Lencer, J. Hagenah, Jennifer Garrels, Karsten Witt, Fabian Klostermann, Marina Svetel, Jennifer Friedman, Vladimir Kostić, S. B. Bressman, X. O. Breakefield, L. J. Ozelius, Peter P. Pramstaller, Christine Klein	55
3	Exon deletions in the GCHI gene in two of four Turkish families with dopa-responsive dystonia 2002 ·Neurology ·Christine Klein, Katja Hedrich, Kemal Kabakci, (unknown), Karin Wiegers, Olfert Landt, J. Hagenah, E. Schwinger, Peter P. Pramstaller, L. J. Ozelius, Kıvılcım Gücüyener, Sabiha Aysun, Eşref Demir	22
4	The GAG deletion of the DYT1 gene is infrequent in musicians with focal dystonia 2000 ·Neurology ·Jennifer Friedman, Christine Klein, Joanne Leung, (unknown), L. J. Ozelius, X. O. Breakefield, Michael E. Charness	13
5	REPORT on the Sixth International Workshop on Chromosome 9 held at Denver, Colorado, U.S.A., 27 October 1998 1999 ·Annals of Human Genetics ·Brian P. Chadwick, Lynda J. Campbell, Cynthia L. Jackson, L. J. Ozelius, Susan Slaugenhaupt, Dennis A. Stephenson, J. H. Edwards, Jonathan S. Wiest, Sue Povey	97
6	Genetic analysis of three patients with an 18p− syndrome and dystonia 1999 ·Neurology ·Christine Klein, (unknown), Peter A. LeWitt, (unknown), D. de Leon, Yasser M. Awaad, X. O. Breakefield, Mitchell F. Brin, L. J. Ozelius	30
7	Clinical-genetic spectrum of primary dystonia. 1998 ·PubMed ·S. B. Bressman, D. de Leon, Deborah Raymond, L. J. Ozelius, X. O. Breakefield, Torbjoern G. Nygaard, Laura Almasy, Neil Risch, P. L. Kramer	36
8	The role of the DYT1 gene in secondary dystonia. 1998 ·PubMed ·Susan Bressman, D. de Leon, Deborah Raymond, P. Greene, Mitchell F. Brin, Stanley Fahn, L. J. Ozelius, X. O. Breakefield, P. L. Kramer, Neil Risch	9
9	The gene (DYT1) for early-onset torsion dystonia encodes a novel protein related to the Clp protease/heat shock family. 1998 ·PubMed ·L. J. Ozelius, Jeffrey Hewett, (unknown), S. B. Bressman, P. L. Kramer, Christo Shalish, D. de Leon, Mitchell F. Brin, Deborah Raymond, Daniel Jacoby, John B. Penney, Neil Risch, Stanley Fahn, James F. Gusella, X. O. Breakefield	41
10	Rapid-onset dystonia-parkinsonism: a report of clinical, biochemical, and genetic studies in two families. 1998 ·PubMed ·Allison Brashear, I. Butler, L. J. Ozelius, (unknown), Martin R. Farlow, X. O. Breakefield, William B. Dobyns	19
11	Secondary dystonia and the DYTI gene 1997 ·Neurology ·Susan Bressman, D. de Leon, Deborah Raymond, P. Greene, (unknown), Stanley Fahn, L. J. Ozelius, X. O. Breakefield, P. L. Kramer, Neil Risch	17
12	Highly polymorphic (GT)n repeat sequence in intron II of the human MAOB gene 1992 ·Genomics ·Christine Konradi, L. J. Ozelius, Xandra O. Breakefield	43
13	Monoamine oxidase deficiency in males with an X chromosome deletion 1989 ·Neuron ·Katherine B. Sims, Albert de la Chapelle, Reijo Norio, (unknown), Yun‐Pung P. Hsu, William B. Rinehart, (unknown), L. J. Ozelius, John Powell, G Bruns, James F. Gusella, Dennis L. Murphy, Xandra O. Breakefield	90

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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