Ann Löfgren

1.4k citations

16 papers · 1.1k · h-index 13

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Neuroscience and Neuropharmacology Research

Papers in

Cellular and Molecular Neuroscience 10
- Hereditary Neurological Disorders 7
- Genetic Neurodegenerative Diseases 6
Molecular Biology 9
- Mitochondrial Function and Pathology 6
- ATP Synthase and ATPases Research 2

Co-authors: Christine Van Broeckhoven (13 shared papers)Peter De Jonghe (9 shared papers)Berten Ceulemans (3 shared papers)Dominique Audenaert (2 shared papers)Bart Dermaut (2 shared papers)G. Van Goethem (2 shared papers)J.J. Martin (2 shared papers)Jurgen Del‐Favero (3 shared papers)
Journals: Human Mutation (2 papers)European Journal of Human Genetics (2 papers)Neurology (2 papers)Neuromuscular Disorders (2 papers)Human Genetics (2 papers)
Partner nations: Belgium France Spain

In The Last Decade

Ann Löfgren

16 papers receiving 1.0k citations

Peers

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-authors

The 25 scholars most cited alongside Ann Löfgren, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ann Löfgren Line = papers co-authored together Ann Löfgren links everyone, so they are left out of the graph.

All Works

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16 of 16 papers shown

#	Work
1	POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement Neurology ·G. Van Goethem, Petri Luoma, Maria Rantamäki, A. Al Memar, Seppo Kaakkola, Peter Hackman, Ralf Krahe, Ann Löfgren, J.J. Martin, Peter De Jonghe, Anu Suomalainen, Bjarne Udd, Christine Van Broeckhoven	2004	205
2	Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia Neuromuscular Disorders ·G. Van Goethem, J.J. Martin, Bart Dermaut, Ann Löfgren, Alain Wibail, D Ververken, Peter I. Tack, I. Dehaene, Michel Van Zandijcke, M Moonen, C. Ceuterick, Peter De Jonghe, Christine Van Broeckhoven	2003	181
3	De novoSCN1Amutations are a major cause of severe myoclonic epilepsy of infancy Human Mutation ·Lieve Claes, Berten Ceulemans, Dominique Audenaert, Katrien Smets, Ann Löfgren, Jurgen Del‐Favero, Sirpa Ala‐Mello, Lina Basel‐Vanagaite, Barbara Plecko, Salmo Raskin, Paul Thiry, Nicole I. Wolf, Christine Van Broeckhoven, Peter De Jonghe	2003	152
4	A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy Neurology ·Dominique Audenaert, Laurence Claes, Berten Ceulemans, Ann Löfgren, Christine Van Broeckhoven, Peter De Jonghe	2003	139
5	Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy European Journal of Human Genetics ·Gert Van Goethem, Marianne Schwartz, Ann Löfgren, Bart Dermaut, Christine Van Broeckhoven, John Vissing	2003	114
6	Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis Human Molecular Genetics ·Francesc Palau, Ann Löfgren, Peter De Jonghe, S Bort, Eva Nelis, Teresa Sevilla, Jean‐Jacques Martin, Juan J. Vílchez, Félix Prieto, Christine Van Broeckhoven	1993	102
7	Spinocerebellar ataxia type 7 (SCA7) – correlations between phenotype and genotype in one large Belgian family Journal of the Neurological Sciences ·Jean‐Jacques Martin, Nicole Van Regemorter, Jurgen Del‐Favero, Ann Löfgren, Christine Van Broeckhoven	1999	51
8	Mutation analysis of the connexin 32 (Cx32) gene in charcot-marie-tooth neuropathy type 1: Identification of five new mutations Human Mutation ·Eva Nelis, Sandra Simokovic, Vincent Timmerman, Ann Löfgren, H. Backhovens, Peter De Jonghe, Jean-Jacques Martin, Christine Van Broeckhoven	1997	30
9	Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP) Human Genetics ·Vincent Timmerman, Ann Löfgren, E. Le Guern, Ping Liang, Peter De Jonghe, Jean-Jacques Martin, Damienne Verhalle, Wim Robberecht, Riadh Gouider, Alexis Brice, Christine Van Broeckhoven	1996	23
10	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 ·Eva Nelis, Sevim Erdem‐Özdamar, Eng M. Tan, Ann Löfgren, C. Ceuterick, Peter DeJonghe, Christine Van Broeckhoven, Vincent Timmerman, Haluk Topaloğlu	2002	18
11	The spectrum of epilepsy caused by POLG mutations Acta Neurologica Belgica ·Wouter Janssen, Annelies Quaegebeur, Gert Van Goethem, Ann Löfgren, Katrien Smets, Rik Vandenberghe, Wim Van Paesschen	2015	16
12	Genomic organisation of the spinocerebellar ataxia type 7 ( SCA7 ) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration Human Genetics ·Andrej Michalik, Jurgen Del‐Favero, C. Mauger, Ann Löfgren, Christine Van Broeckhoven	1999	15
13	Pure Familial Spastic Paraplegia:Clinical and Genetic Analysis ofNine Belgian Pedigrees European Journal of Human Genetics ·Peter De Jonghe, Luc Krols, Andrej Michalik, Jamïlé Hazan, Gisèle Smeyers, Ann Löfgren, Jean Weissenbach, Jean‐Jacques Martin, Christine Van Broeckhoven	1996	13
14	A Novel Type of Hereditary Motor and Sensory Neuropathy Characterized by a Mild Phenotype Archives of Neurology ·Peter De Jonghe, Vincent Timmerman, Eva Nelis, Els De Vriendt, Ann Löfgren, C. Ceuterick, Jean-Jacques Martin, Christine Van Broeckhoven	1999	7
15	Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegia Clinical Genetics ·Н. В. Иванова, Ann Löfgren, I. Tournev, R Rousev, A. S. Andreevа, Albena Jordanova, V. Georgieva, Tine Deconinck, Vincent Timmerman, Ivo Kremensky, Peter De Jonghe, Vanio Mitev	2006	6
16	From diagnosis to treatment in genetic epilepsies: Implementation of precision medicine in real-world clinical practice European Journal of Paediatric Neurology ·Matthias De Wachter, An‐Sofie Schoonjans, Sarah Weckhuysen, Kristof Van Schil, Ann Löfgren, Marije Meuwissen, Anna Jansen, Berten Ceulemans	2023	5

About Ann Löfgren

Ann Löfgren is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Psychiatry and Mental health and Genetics, having authored 16 papers that have together received 1.1k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (7 papers), Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (6 papers), Neurological diseases and metabolism (4 papers), Epilepsy research and treatment (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Metabolism and Genetic Disorders (2 papers) and ATP Synthase and ATPases Research (2 papers). The work is most often cited by research in Clinical Biochemistry (325 citations), Cellular and Molecular Neuroscience (502 citations), Psychiatry and Mental health (227 citations), Neurology (112 citations) and Molecular Biology (722 citations). Ann Löfgren has collaborated with scholars based in Belgium, France and Spain. Frequent co-authors include Christine Van Broeckhoven, Peter De Jonghe, Berten Ceulemans, Dominique Audenaert, Bart Dermaut, G. Van Goethem, J.J. Martin, Jurgen Del‐Favero, Laurence Claes and Gert Van Goethem. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, Neurology, Neuromuscular Disorders and Human Genetics.

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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