Ebba Lohmann

10.0k total citations · 1 hit paper
73 papers, 3.3k citations indexed

About

Ebba Lohmann is a scholar working on Neurology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ebba Lohmann has authored 73 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Neurology, 25 papers in Neurology and 22 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ebba Lohmann's work include Parkinson's Disease Mechanisms and Treatments (34 papers), Neurological diseases and metabolism (16 papers) and Neurological disorders and treatments (14 papers). Ebba Lohmann is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (34 papers), Neurological diseases and metabolism (16 papers) and Neurological disorders and treatments (14 papers). Ebba Lohmann collaborates with scholars based in Türkiye, Germany and France. Ebba Lohmann's co-authors include Alexis Brice, Alexandra Dürr, Yves Agid, Pierre Pollak, Pablo Ibáñez, François Tison, Başar Bılgıç, Hakan Gürvıt, Suzanne Lesage and Murat Emre and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Ebba Lohmann

73 papers receiving 3.3k 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.

Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease

2004 818 citations Pablo Ibáñez, Ebba Lohmann et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ebba Lohmann Türkiye	26	2.1k	1.2k	1.0k	826	801	73	3.3k
Pau Pástor Spain	36	2.2k 1.0×	819 0.7×	790 0.8×	952 1.2×	1.2k 1.5×	123	3.6k
Pingyi Xu China	32	1.0k 0.5×	1.3k 1.0×	774 0.7×	1.2k 1.4×	510 0.6×	133	3.2k
Marina Romero‐Ramos Denmark	32	1.8k 0.9×	1.3k 1.0×	1.2k 1.1×	829 1.0×	605 0.8×	56	3.0k
Daniel Alvarez‐Fischer Germany	24	1.3k 0.6×	989 0.8×	1.1k 1.0×	904 1.1×	478 0.6×	44	3.1k
Derya R. Shimshek Switzerland	30	683 0.3×	924 0.7×	572 0.6×	1.0k 1.2×	949 1.2×	54	3.0k
James B. Koprich Canada	33	1.9k 0.9×	1.6k 1.3×	545 0.5×	820 1.0×	537 0.7×	63	3.2k
Michael Mante United States	42	2.0k 1.0×	1.7k 1.4×	1.3k 1.2×	1.1k 1.4×	1.8k 2.2×	69	4.3k
Nadia Stefanova Austria	36	3.4k 1.6×	2.1k 1.7×	2.0k 1.9×	1.1k 1.3×	1.2k 1.5×	112	4.9k
Caryl E. Sortwell United States	35	2.0k 1.0×	2.2k 1.8×	696 0.7×	1.2k 1.5×	530 0.7×	105	3.9k
Nicola Vanacore Italy	18	2.6k 1.3×	1.4k 1.1×	802 0.8×	1.1k 1.4×	681 0.9×	31	3.7k

Countries citing papers authored by Ebba Lohmann

Since Specialization

Citations

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

Fields of papers citing papers by Ebba Lohmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ebba Lohmann

This figure shows the co-authorship network connecting the top 25 collaborators of Ebba Lohmann. A scholar is included among the top collaborators of Ebba Lohmann 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 Ebba Lohmann. Ebba Lohmann 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

Güven, Gamze, Ebba Lohmann, Bedia Samancı, et al.. (2023). Association of Estrogen Receptor 1 PvuII and XbaI Polymorphisms and Peripheral Estrogen Receptor 1 mRNA Levels with Alzheimer’s Disease in Turkish Patients. SHILAP Revista de lepidopterología. 29(3). 195–203. 1 indexed citations

Güven, Gamze, Ebba Lohmann, Başar Bılgıç, et al.. (2021). EXPRESSION OF SELECTED miRNAs IN CIRCULATING BLOOD OF EARLY AND LATE-ONSET ALZHEIMER DISEASE PATIENTS. SHILAP Revista de lepidopterología. 84(2). 165–174. 3 indexed citations

Park, Yangshin, Ebba Lohmann, Anneke J.A. Kievit, et al.. (2021). A new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson's disease. Parkinsonism & Related Disorders. 89. 63–72. 20 indexed citations

Brownjohn, Philip W., James Smith, Ebba Lohmann, et al.. (2018). Functional Studies of Missense TREM2 Mutations in Human Stem Cell-Derived Microglia. Stem Cell Reports. 10(4). 1294–1307. 124 indexed citations

Lohmann, Ebba, Thomas Gasser, & Kathrin Grundmann. (2017). Needs and Requirements of Modern Biobanks on the Example of Dystonia Syndromes. Frontiers in Neurology. 8. 9–9. 4 indexed citations

Keßler, Christoph, Haşmet Hanağası, Javier Simón‐Sánchez, et al.. (2017). Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey. Parkinsonism & Related Disorders. 48. 34–39. 9 indexed citations

Darwent, Lee, Susana Carmona, Ebba Lohmann, et al.. (2017). Mutations in TYROBP are not a common cause of dementia in a Turkish cohort. Neurobiology of Aging. 58. 240.e1–240.e3. 9 indexed citations

Guerreiro, Rita, Ebba Lohmann, José Brás, et al.. (2013). Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement. JAMA Neurology. 70(1). 78–78. 262 indexed citations

Weißbach, Anne, Norbert Brüggemann, Alexander Schmidt, et al.. (2012). Exome sequencing in a family with restless legs syndrome. Movement Disorders. 27(13). 1686–1689. 17 indexed citations

10.

Lohmann, Ebba, et al.. (2012). Clinical and polysomnographic features of a large Turkish pedigree with restless leg syndrome and periodic limb movements. Sleep And Breathing. 17(2). 741–746. 3 indexed citations

11.

Bılgıç, Başar, Ali Bayram, Ali Bilgin Arslan, et al.. (2012). Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson’s disease: Contribution of automated segmentation neuroimaging method. Parkinsonism & Related Disorders. 18(5). 562–566. 11 indexed citations

12.

Lohmann, Ebba, Suzanne Lesage, Haşmet Hanağası, et al.. (2012). Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population. European Journal of Neurology. 19(5). 769–775. 12 indexed citations

13.

Ribeiro, Maria-João, Stéphane Thobois, Ebba Lohmann, et al.. (2009). A Multitracer Dopaminergic PET Study of Young-Onset Parkinsonian Patients With and Without Parkin Gene Mutations. Journal of Nuclear Medicine. 50(8). 1244–1250. 29 indexed citations

14.

Lohmann, Ebba, Marie‐Laure Welter, Valérie Fraix, et al.. (2008). Are parkin patients particularly suited for deep‐brain stimulation?. Movement Disorders. 23(5). 740–743. 29 indexed citations

15.

Lohmann, Ebba, Laurence Leclere, Suzanne Lesage, et al.. (2008). A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations. Parkinsonism & Related Disorders. 15(4). 273–276. 21 indexed citations

16.

Arnulf, Isabelle, Jørgen E. Nielsen, Ebba Lohmann, et al.. (2008). Rapid Eye Movement Sleep Disturbances in Huntington Disease. Archives of Neurology. 65(4). 482–482. 164 indexed citations

17.

Lesage, Suzanne, Laurence Leclere, Ebba Lohmann, et al.. (2007). Frequency of the <i>LRRK2 </i>G2019S Mutation in Siblings with Parkinson’s Disease. Neurodegenerative Diseases. 4(2-3). 195–198. 10 indexed citations

18.

Ibáñez, Pablo, Suzanne Lesage, Ebba Lohmann, et al.. (2006). Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. Brain. 129(3). 686–694. 123 indexed citations

19.

West, Andrew B., Magali Periquet, Sarah Lincoln, et al.. (2002). Complex relationship between Parkin mutations and Parkinson disease. American Journal of Medical Genetics. 114(5). 584–591. 164 indexed citations

20.

Engelhardt, P, et al.. (1979). [Meningeosis leucaemica. Diagnosis and therapy (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 50(4). 245–53. 1 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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