Ann Löfgren

1.4k total citations
16 papers, 1.1k citations indexed

About

Ann Löfgren is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Ann Löfgren has authored 16 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cellular and Molecular Neuroscience, 9 papers in Molecular Biology and 4 papers in Neurology. Recurrent topics in Ann Löfgren's work include Hereditary Neurological Disorders (7 papers), Mitochondrial Function and Pathology (6 papers) and Genetic Neurodegenerative Diseases (6 papers). Ann Löfgren is often cited by papers focused on Hereditary Neurological Disorders (7 papers), Mitochondrial Function and Pathology (6 papers) and Genetic Neurodegenerative Diseases (6 papers). Ann Löfgren collaborates with scholars based in Belgium, France and Austria. Ann Löfgren's co-authors include Christine Van Broeckhoven, Peter De Jonghe, Berten Ceulemans, Dominique Audenaert, Bart Dermaut, J.J. Martin, G. Van Goethem, Jurgen Del‐Favero, Laurence Claes and Gert Van Goethem and has published in prestigious journals such as Neurology, Human Molecular Genetics and Journal of the Neurological Sciences.

In The Last Decade

Ann Löfgren

16 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ann Löfgren Belgium	13	722	502	325	227	189	16	1.1k
M L Savontaus Finland	15	1.2k 1.6×	218 0.4×	495 1.5×	32 0.1×	158 0.8×	18	1.4k
Claude Mignard France	5	690 1.0×	688 1.4×	41 0.1×	51 0.2×	49 0.3×	7	865
Dorota Hoffman‐Zacharska Poland	14	216 0.3×	169 0.3×	31 0.1×	64 0.3×	126 0.7×	53	541
Farzad Sina Iran	11	231 0.3×	242 0.5×	48 0.1×	75 0.3×	57 0.3×	24	706
Saadet Mercimek‐Andrews Canada	13	276 0.4×	77 0.2×	189 0.6×	63 0.3×	226 1.2×	52	623
Pierre Cacciagli France	15	410 0.6×	100 0.2×	49 0.2×	104 0.5×	391 2.1×	25	739
Marie Coutelier France	13	341 0.5×	255 0.5×	39 0.1×	20 0.1×	107 0.6×	15	537
A.-E. Lehesjoki Finland	12	241 0.3×	128 0.3×	33 0.1×	133 0.6×	310 1.6×	16	610
Saeko Ishida Japan	12	402 0.6×	191 0.4×	24 0.1×	195 0.9×	337 1.8×	20	719
Rebecca Buchert Germany	13	333 0.5×	136 0.3×	58 0.2×	23 0.1×	154 0.8×	26	645

Countries citing papers authored by Ann Löfgren

Since Specialization

Citations

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

Fields of papers citing papers by Ann Löfgren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ann Löfgren

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

All Works

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16 of 16 papers shown

Schoonjans, An‐Sofie, Sarah Weckhuysen, Kristof Van Schil, et al.. (2023). From diagnosis to treatment in genetic epilepsies: Implementation of precision medicine in real-world clinical practice. European Journal of Paediatric Neurology. 48. 46–60. 5 indexed citations

Quaegebeur, Annelies, Gert Van Goethem, Ann Löfgren, et al.. (2015). The spectrum of epilepsy caused by POLG mutations. Acta Neurologica Belgica. 116(1). 17–25. 16 indexed citations

Löfgren, Ann, Albena Jordanova, Tine Deconinck, et al.. (2006). Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegia. Clinical Genetics. 70(6). 490–495. 6 indexed citations

Goethem, G. Van, Petri Luoma, Maria Rantamäki, et al.. (2004). POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement. Neurology. 63(7). 1251–1257. 205 indexed citations

Claes, Lieve, Berten Ceulemans, Dominique Audenaert, et al.. (2003). De novoSCN1Amutations are a major cause of severe myoclonic epilepsy of infancy. Human Mutation. 21(6). 615–621. 152 indexed citations

Goethem, Gert Van, Marianne Schwartz, Ann Löfgren, et al.. (2003). Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy. European Journal of Human Genetics. 11(7). 547–549. 114 indexed citations

Goethem, G. Van, J.J. Martin, Bart Dermaut, et al.. (2003). Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia. Neuromuscular Disorders. 13(2). 133–142. 181 indexed citations

Audenaert, Dominique, Laurence Claes, Berten Ceulemans, et al.. (2003). A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy. Neurology. 61(6). 854–856. 139 indexed citations

Nelis, Eva, Sevim Erdem‐Özdamar, Eng M. Tan, et al.. (2002). A novel homozygous missense mutation in the myotubularin-related protein 2 gene associated with recessive Charcot–Marie–Tooth disease with irregularly folded myelin sheaths. Neuromuscular Disorders. 12(9). 869–873. 18 indexed citations

10.

Michalik, Andrej, Jurgen Del‐Favero, C. Mauger, Ann Löfgren, & Christine Van Broeckhoven. (1999). Genomic organisation of the spinocerebellar ataxia type 7 ( SCA7 ) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration. Human Genetics. 105(5). 410–417. 15 indexed citations

11.

Jonghe, Peter De, Vincent Timmerman, Eva Nelis, et al.. (1999). A Novel Type of Hereditary Motor and Sensory Neuropathy Characterized by a Mild Phenotype. Archives of Neurology. 56(10). 1283–1283. 7 indexed citations

12.

Martin, Jean‐Jacques, Nicole Van Regemorter, Jurgen Del‐Favero, Ann Löfgren, & Christine Van Broeckhoven. (1999). Spinocerebellar ataxia type 7 (SCA7) – correlations between phenotype and genotype in one large Belgian family. Journal of the Neurological Sciences. 168(1). 37–46. 51 indexed citations

13.

Nelis, Eva, Vincent Timmerman, Ann Löfgren, et al.. (1997). Mutation analysis of the connexin 32 (Cx32) gene in charcot-marie-tooth neuropathy type 1: Identification of five new mutations. Human Mutation. 9(1). 47–52. 30 indexed citations

14.

Timmerman, Vincent, Ann Löfgren, E. Le Guern, et al.. (1996). Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP). Human Genetics. 97(1). 26–34. 23 indexed citations

15.

Jonghe, Peter De, Andrej Michalik, Jamïlé Hazan, et al.. (1996). Pure Familial Spastic Paraplegia:Clinical and Genetic Analysis ofNine Belgian Pedigrees. European Journal of Human Genetics. 4(5). 260–266. 13 indexed citations

16.

Palau, Francesc, Ann Löfgren, Peter De Jonghe, et al.. (1993). Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis. Human Molecular Genetics. 2(12). 2031–2035. 102 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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