A. Löfgren

2.6k citations

37 papers · 1.8k · 1 hit paper · h-index 18

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases

Papers in

Cellular and Molecular Neuroscience 26
- Hereditary Neurological Disorders 23
- Genetic Neurodegenerative Diseases 15
Molecular Biology 17
- Mitochondrial Function and Pathology 10
- ATP Synthase and ATPases Research 5

Co-authors: Christine Van Broeckhoven (27 shared papers)Gert Van Goethem (4 shared papers)Bart Dermaut (1 shared paper)Jean‐Jacques Martin (1 shared paper)Vincent Timmerman (22 shared papers)Eva Nelis (12 shared papers)Peter De Jonghe (13 shared papers)C. Ceuterick (6 shared papers)
Journals: Neurology (5 papers)Neuromuscular Disorders (4 papers)Human Mutation (3 papers)Prenatal Diagnosis (2 papers)Pflügers Archiv - European Journal of Physiology (2 papers)
Partner nations: Belgium United States Germany

In The Last Decade

A. Löfgren

36 papers receiving 1.8k citations

A. Löfgren's Hit Papers

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Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions 2001 · 610 citations

Peers

Countries citing papers authored by A. Löfgren

Since Specialization

Citations

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Fields of papers citing papers by A. Löfgren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside A. 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 A. Löfgren Line = papers co-authored together A. Löfgren links everyone, so they are left out of the graph.

All Works

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#	Work
1	Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions Nature Genetics ·Gert Van Goethem, Bart Dermaut, A. Löfgren, Jean‐Jacques Martin, Christine Van Broeckhoven Hit paper breakdown →	2001	610
2	Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin The American Journal of Human Genetics ·Anna H. Hakonen, Silja Heiskanen, Vesa Juvonen, Ilse Lappalainen, Petri Luoma, Maria Rantamäki, Gert Van Goethem, A. Löfgren, Peter Hackman, Anders Paetau, Seppo Kaakkola, Kari Majamaa, Teppo Varilo, Bjarne Udd, Helena Kääriäinen, Laurence A. Bindoff, Anu Suomalainen	2005	227
3	The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotype Brain ·Peter De Jonghe, Vincent Timmerman, C. Ceuterick, Eva Nelis, Els De Vriendt, A. Löfgren, Anina Vercruyssen, Christine Verellen, Lionel Van Maldergem, J. J. Martin, Christine Van Broeckhoven	1999	175
4	Novel missense mutation in the early growth response 2 gene associated with Dejerine–Sottas syndrome phenotype Neurology ·Vincent Timmerman, Peter De Jonghe, C. Ceuterick, Els De Vriendt, A. Löfgren, Eva Nelis, Laura E. Warner, James R. Lupski, J. J. Martin, Christine Van Broeckhoven	1999	121
5	Charcot‐Marie‐Tooth Disease: A Clinico‐genetic Confrontation Annals of Human Genetics ·Nina Barišić, Kristl G. Claeys, Maja Sirotković-Skerlev, A. Löfgren, Eva Nelis, Peter De Jonghe, Vincent Timmerman	2008	119
6	Linkage and mutation analysis of Charcot‐Marie‐Tooth neuropathy type 2 families with chromosomes 1p35‐p36 and Xq13 Neurology ·Vincent Timmerman, Peter De Jonghe, Petra Spoelders, Sandra Simokovic, A. Löfgren, Eva Nelis, Jeffery M. Vance, Jean‐Jacques Martin, Christine Van Broeckhoven	1996	66
7	Patient homozygous for a recessive POLG mutation presents with features of MERRF Neurology ·G. Van Goethem, R. Mercelis, A. Löfgren, Sara Seneca, C. Ceuterick, Jean‐Jacques Martin, Christine Van Broeckhoven	2003	63
8	Normal pregnancy after preimplantation DNA diagnosis of a dystrophin gene deletion Prenatal Diagnosis ·Jiaen Liu, Willy Lissens, Christine Van Broeckhoven, A. Löfgren, Michel Camus, Ingeborg Liebaers, André Van Steirteghem	1995	45
9	Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent. Journal of Medical Genetics ·Vincent Timmerman, Bernd Rautenstrauß, Lawrence T. Reiter, Thearith Koeuth, A. Löfgren, Thomas Liehr, Eva Nelis, K D Bathke, Peter De Jonghe, H. Grehl, Jean‐Jacques Martin, James R. Lupski, Christine Van Broeckhoven	1997	44
10	Novel PCR-based diagnostic tools for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsies. PubMed ·Stronach Ea, Catherine K. Clark, Callum J. Bell, A. Löfgren, McKay Ng, Vincent Timmerman, Christine Van Broeckhoven, Haites Ne	1999	35
11	Gene dosage imbalances in patients with 46,XY gonadal DSD detected by an in‐house‐designed synthetic probe set for multiplex ligation‐dependent probe amplification analysis Clinical Genetics ·Michela Barbaro, Alessandro Cicognani, Antonio Balsamo, A. Löfgren, Lilia Baldazzi, Anna Wedell, Mikael Oscarson	2008	33
12	Prenatal diagnosis of charcot‐marie‐tooth disease type 1a (CMT1A) using molecular genetic techniques Prenatal Diagnosis ·Ruth Navon, Vincent Timmerman, A. Löfgren, Ping Liang, Eva Nelis, Móshe Zeitune, Christine Van Broeckhoven	1995	30
13	Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsies Annals of Neurology ·Damienne Verhalle, A. Löfgren, Eva Nelis, I. Dehaene, P. Theys, Martin Lammens, R. Dom, Christine Van Broeckhoven, Wim Robberecht	1994	27
14	A Novel POLG Gene Mutation in 4 Children With Alpers-like Hepatocerebral Syndromes Archives of Neurology ·Bülent Kurt, Jaak Jaeken, Johan Van Hove, Lieven Lagae, A. Löfgren, David B. Everman, Parul Jayakar, Ali Naini, Klaas J. Wierenga, Gert Van Goethem, William C. Copeland, Salvatore DiMauro	2010	23
15	Charcot–Marie–Tooth disease with giant axons Neurology ·Giacomo Lus, Eva Nelis, Albena Jordanova, A. Löfgren, Tiziana Cavallaro, A. Ammendola, Mariarosa Anna Beatrice Melone, N. Rizzuto, Vincent Timmerman, Roberto Cotrufo, Peter De Jonghe	2003	22
16	PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1A Neurology ·Peter Young, Fabian Stögbauer, Heiko Wiebusch, A. Löfgren, Vincent Timmerman, Christine Van Broeckhoven, E B Ringelstein, G. Aßmann, Harald Funke	1998	20
17	A novel 3′-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies Neuromuscular Disorders ·Jan Meuleman, A Pou-Serradell, A. Löfgren, C. Ceuterick, J. J. Martin, Vincent Timmerman, Christine Van Broeckhoven, Peter De Jonghe	2001	19
18	Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family Pflügers Archiv - European Journal of Physiology ·Lea Leonardis, Janez Zidar, Mara Popović, Vincent Timmerman, A. Löfgren, Christine Van Broeckhoven, Duśan Butinar	2000	18
19	Polymerase gamma deficiency (POLG): Clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh’s encephalopathy European Journal of Paediatric Neurology ·Emmanuel Scalais, Baudouin François, Patrick Schlesser, René Stevens, C. Nuttin, Jean‐Jacques Martin, Rudy Van Coster, Sara Seneca, Frank Roels, Gert Van Goethem, A. Löfgren, Linda De Meırleır	2012	16
20	Associations of leptin with body fat distribution and metabolic parameters in non—insulin-dependent diabetic patients: No effect of apolipoprotein E polymorphism Metabolism ·M. Wauters, Robert V. Considine, A. Löfgren, Christine Van Broeckhoven, J.-C. van der Auwera, I. De Leeuw, L. Van Gaal	2000	15

About A. Löfgren

A. Löfgren is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Cell Biology and Neurology, having authored 37 papers that have together received 1.8k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (23 papers), Genetic Neurodegenerative Diseases (15 papers), Neurological diseases and metabolism (10 papers), Mitochondrial Function and Pathology (10 papers), ATP Synthase and ATPases Research (5 papers), Metabolism and Genetic Disorders (4 papers), Botulinum Toxin and Related Neurological Disorders (4 papers) and Cellular Mechanics and Interactions (4 papers). The work is most often cited by research in Clinical Biochemistry (558 citations), Cellular and Molecular Neuroscience (878 citations), Neurology (308 citations), Neurology (304 citations) and Molecular Biology (1.1k citations). A. Löfgren has collaborated with scholars based in Belgium, United States and Germany. Frequent co-authors include Christine Van Broeckhoven, Gert Van Goethem, Bart Dermaut, Jean‐Jacques Martin, Vincent Timmerman, Eva Nelis, Peter De Jonghe, C. Ceuterick, J. J. Martin and Els De Vriendt. Their work appears in journals such as Neurology, Neuromuscular Disorders, Human Mutation, Prenatal Diagnosis and Pflügers Archiv - European Journal of Physiology.

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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