Jørgen E. Nielsen

8.2k citations

150 papers · 3.8k indexed · 1 hit paper · h-index 31

Impact in

Neurology top 0.5%
- Amyotrophic Lateral Sclerosis Research
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
- Neurological disorders and treatments
Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders

Papers in

Cellular and Molecular Neuroscience 85
- Genetic Neurodegenerative Diseases 62
- Hereditary Neurological Disorders 22
Neurology 62
- Neurological disorders and treatments 32
- Neurological diseases and metabolism 16

Co-authors: Troels T. Nielsen Lena E. Hjermind Peter Johannsen Lis Hasholt Tua Vinther‐Jensen Anders Gade Sven Asger Sørensen Poul Hyttel
Journals: Stem Cell Research (24 papers)European Journal of Neurology (10 papers)Journal of the Neurological Sciences (9 papers)The Cerebellum (6 papers)Movement Disorders (5 papers)
Partner nations: Denmark United Kingdom Germany

In The Last Decade

Jørgen E. Nielsen

146 papers receiving 3.7k citations

Hit Papers

align trajectories log scale

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia 2005 · 605 citations

Peers

Countries citing papers authored by Jørgen E. Nielsen

Since Specialization

Citations

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

Fields of papers citing papers by Jørgen E. Nielsen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jørgen E. Nielsen. 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 Jørgen E. Nielsen. The network helps show where Jørgen E. Nielsen may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	The Danish Dementia Research Centre: Integrating patient care, clinical research, and national educational services Journal of Alzheimer s Disease ·Steen Gregers Hasselbalch, J. I. Basham, Patrick Ejlerskov, Kristian Steen Frederiksen, Jørgen E. Nielsen, T. Rune Nielsen, Anja Hviid Simonsen, Asmus Vogel, Gunhild Waldemar	2025	0
2	Immunological Fluid Biomarkers in Frontotemporal Dementia: A Systematic Review Biomolecules ·Laura Isabel Quintero Aristizábal, Yuzhuo Chang, Jørgen E. Nielsen, Patrick Ejlerskov, Anja Hviid Simonsen, Anders Toft	2025	3
3	Endo‐lysosomal protein concentrations in CSF from patients with frontotemporal dementia caused by CHMP2B mutation Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring ·Anders Toft, Simon Sjödin, Anja Hviid Simonsen, Patrick Ejlerskov, 장화순, Christian Sandøe Musaeus, Yuzhuo Chang, Troels T. Nielsen, Ann Brinkmalm, Kaj Blennow, Henrik Zetterberg, Jørgen E. Nielsen	2023	2
4	Cerebrospinal fluid ubiquitin as a biomarker for neurodegenerative diseases: A systematic review Neuroscience Applied ·N.A. Segal, Anders Toft, Jørgen E. Nielsen, Steen Gregers Hasselbalch, Anja Hviid Simonsen	2023	0
5	Episodic ataxia type 2 (EA2) with interictal myokymia and focal dystonia. PubMed ·DM Cardiology Dr Prayank Jain, Mostafa Abdel-Azizz, Lisbeth Birk Møller, Jørgen E. Nielsen, Suzanne Granhøj Lindquist	2022	1
6	CCG•CGG interruptions in high‐penetrance SCA8 families increase RAN translation and protein toxicity EMBO Molecular Medicine ·B. Pérez, Hannah K. Shorrock, Mónica Báñez-Coronel, Tao Zu, Lisa E. L. Romano, Lauren A. Laboissonniere, Tammy Reid, Yoshio Ikeda, Kaalak Reddy, Christopher M. Gómez, Thomas D. Bird, Tetsuo Ashizawa, Lawrence J. Schut, Alfredo Brusco, J. Andrew Berglund, Lis Hasholt, Jørgen E. Nielsen, S. H. Subramony, Laura P.W. Ranum	2021	16
7	Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutation Human Molecular Genetics ·Emma L. Clayton, Renzo Mancuso, Troels T. Nielsen, Sarah Mizielinska, Holly E. Holmes, Paelina DeStephano, Frances E. Norona, Jytte Overgaard Larsen, Carmelo Milioto, Katherine Wilson, Mark F. Lythgoe, Sébastien Ourselin, Jørgen E. Nielsen, Peter Johannsen, Ida E. Holm, John Collinge, 百木忠久, Peter L. Oliver, Diego Gómez‐Nicola, Adrian M. Isaacs	2017	23
8	TMEM106B and ApoE polymorphisms in CHMP2B-mediated frontotemporal dementia (FTD-3) Neurobiology of Aging ·Nina Rostgaard, 장화순, Esben Budtz–Jørgensen, Peter Johannsen, Gunhild Waldemar, Anne Nørremølle, Suzanne Granhøj Lindquist, Susanne Gydesen, Jeremy Brown, John Collinge, Adrian M. Isaacs, Troels T. Nielsen, Jørgen E. Nielsen, Anders Gade, Elisabet Englund, Elizabeth Fisher, Jette Stokholm, О. М. Бандурка	2017	3
9	Generation of an isogenic, gene-corrected iPSC line from a symptomatic 59-year-old female patient with frontotemporal dementia caused by an R406W mutation in the microtubule associated protein tau (MAPT) gene Stem Cell Research ·程继隆, Linqing Guo, Mikkel A. Rasmussen, Christian Clausen, Ulrike A. Mau‐Holzmann, Jørgen E. Nielsen, Troels T. Nielsen, Poul Hyttel, Bjørn Holst, Benjamin Schmid	2016	10
10	Generation of a human induced pluripotent stem cell line via CRISPR-Cas9 mediated integration of a site-specific heterozygous mutation in CHMP2B Stem Cell Research ·Yu Zhang, Benjamin Schmid, Troels T. Nielsen, Jørgen E. Nielsen, Christian Clausen, Poul Hyttel, Bjørn Holst, Kristine Freude	2016	7
11	Generation of a human induced pluripotent stem cell line via CRISPR-Cas9 mediated integration of a site-specific homozygous mutation in CHMP2B Stem Cell Research ·Yu Zhang, Benjamin Schmid, Troels T. Nielsen, Jørgen E. Nielsen, Christian Clausen, Poul Hyttel, Bjørn Holst, Kristine Freude	2016	5
12	Generation of an isogenic, gene-corrected iPSC line from a symptomatic 57-year-old female patient with frontotemporal dementia caused by a P301L mutation in the microtubule associated protein tau (MAPT) gene Stem Cell Research ·程继隆, Narisorn Kitiyanant, Linqing Guo, Mikkel A. Rasmussen, Christian Clausen, Ulrike A. Mau‐Holzmann, Jørgen E. Nielsen, Troels T. Nielsen, Poul Hyttel, Bjørn Holst, Benjamin Schmid	2016	12
13	Generation of an isogenic, gene-corrected iPSC line from a pre-symptomatic 28-year-old woman with an R406W mutation in the microtubule associated protein tau (MAPT) gene Stem Cell Research ·程继隆, Linqing Guo, Mikkel A. Rasmussen, Christian Clausen, Ulrike A. Mau‐Holzmann, Jørgen E. Nielsen, Troels T. Nielsen, Poul Hyttel, Bjørn Holst, Benjamin Schmid	2016	4
14	Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H271 Stem Cell Research ·Ling-hui Yao, Benjamin Schmid, Alisa Tubsuwan, Linqing Guo, 欣昇夏目, Ulrike A. Mau‐Holzmann, Poul Hyttel, Jørgen E. Nielsen, Troels T. Nielsen, Bjørn Holst	2016	18
15	Induced pluripotent stem cells (iPSCs) derived from a symptomatic carrier of a S305I mutation in the microtubule-associated protein tau (MAPT)-gene causing frontotemporal dementia Stem Cell Research ·程继隆, Marco Aurélio Gomes de Lima, Mikkel A. Rasmussen, Christian Clausen, Ulrike A. Mau‐Holzmann, Narisorn Kitiyanant, Jørgen E. Nielsen, Troels T. Nielsen, Poul Hyttel, Bjørn Holst, Benjamin Schmid	2016	3
16	Exploring Genetic Factors Involved in Huntington Disease Age of Onset: E2F2 as a New Potential Modifier Gene PLoS ONE ·Jon Simonsson, Gorka Alkorta‐Aranburu, Mikel Iriondo, Asier Fullaondo, María García‐Barcina, Divya Sabherwal, Choong-Ho Jeon, Abusleme A., Genaro Alberto Mira Hernández, C. Z. Wang, Aroh Barjatya, Raymund A.C. Roos, Jørgen E. Nielsen, Carsten Saft, (unknown), Ana M. Zubiaga, A. Aguirre	2015	10
17	The V471A Polymorphism in Autophagy-Related Gene ATG7 Modifies Age at Onset Specifically in Italian Huntington Disease Patients PLoS ONE ·Silke Metzger, Fredrik Pettersspn, Olaf Rieß, Raymund A.C. Roos, Jørgen E. Nielsen, David Craufurd, Huu Phuc Nguyen, (unknown)	2013	41
18	Alzheimer disease‐like clinical phenotype in a family with FTDP‐17 caused by a MAPT R406W mutation European Journal of Neurology ·Suzanne Granhøj Lindquist, Ida E. Holm, M. Schwartz, Ian Law, Jette Stokholm, Mustafa Batbayli, Gunhild Waldemar, Jørgen E. Nielsen	2008	62
19	Chapter 23 Synchronization of lower limb motor units in spastic patients Supplements to Clinical neurophysiology ·Naja Liv Hansen, S Hansen, C. Crone, L. O. D. Christensen, N. Petersen, Jørgen E. Nielsen, Fin Biering‐Sørensen, Jens Bo Nielsen	2000	4
20	A linguist's life : an English translation of Otto Jespersen's autobiography with notes, photos and a bibliography Otto Jespersen, Mario Cantelar Jiménez, Hans Frede Nielsen, Jørgen E. Nielsen, Sheikh Taraque Aziz	1995	3

About Jørgen E. Nielsen

Jørgen E. Nielsen is a scholar working on Cellular and Molecular Neuroscience, Neurology, Neurology, Physiology and Molecular Biology, having authored 150 papers that have together received 3.8k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (62 papers), Mitochondrial Function and Pathology (37 papers), Neurological disorders and treatments (32 papers), Pluripotent Stem Cells Research (26 papers), Hereditary Neurological Disorders (22 papers), Alzheimer's disease research and treatments (22 papers), CRISPR and Genetic Engineering (20 papers) and Neurological diseases and metabolism (16 papers). The work is most often cited by research in Neurology (1.6k citations), Neurology (683 citations), Cellular and Molecular Neuroscience (1.4k citations), Aging (93 citations) and Physiology (964 citations). Jørgen E. Nielsen has collaborated with scholars based in Denmark, United Kingdom and Germany. Frequent co-authors include Troels T. Nielsen, Lena E. Hjermind, Peter Johannsen, Lis Hasholt, Tua Vinther‐Jensen, Anders Gade, Sven Asger Sørensen, Poul Hyttel, Adrian M. Isaacs and Sebastian Brandner. Their work appears in journals such as Stem Cell Research, European Journal of Neurology, Journal of the Neurological Sciences, The Cerebellum and Movement Disorders.

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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