Patrick Weydt

9.2k citations

90 papers · 3.6k indexed · h-index 34

Impact in

Neurology top 0.5%
- Amyotrophic Lateral Sclerosis Research
- Parkinson's Disease Mechanisms and Treatments
Genetics top 1%
- Neurogenetic and Muscular Disorders Research

Papers in ⓘ

Neurology 48
- Amyotrophic Lateral Sclerosis Research 40
- Parkinson's Disease Mechanisms and Treatments 20
Cellular and Molecular Neuroscience 37
- Genetic Neurodegenerative Diseases 26
- Neuroscience and Neuropharmacology Research 6

Co-authors: Thomas Möller (9 shared papers)Michel Kliot (5 shared papers)Soyon Hong (4 shared papers)Albert C. Ludolph (21 shared papers)Anke Witting (12 shared papers)G. Bernhard Landwehrmeyer (10 shared papers)Selma M. Soyal (4 shared papers)Wolfgang Patsch (5 shared papers)
Journals: Neuroreport (5 papers)Journal of Neurology Neurosurgery & Psychiatry (5 papers)PLoS ONE (4 papers)Human Molecular Genetics (3 papers)Nature (3 papers)
Partner nations: Germany United States France

In The Last Decade

Patrick Weydt

86 papers receiving 3.5k citations

Peers

Countries citing papers authored by Patrick Weydt

Since Specialization

Citations

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

Fields of papers citing papers by Patrick Weydt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 90 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1α in Huntington's disease neurodegeneration Cell Metabolism ·Patrick Weydt, Victor V. Pineda, Anne E Torrence, Randell T. Libby, Terrence F. Satterfield, Eduardo R. Lazarowski, Merle L. Gilbert, Gregory J. Morton, Theodor K. Bammler, Andrew D. Strand, Libin Cui, Richard P. Beyer, Courtney N. Easley, Annette C. Smith, Dimitri Krainc, Serge Luquet, Ian R. Sweet, Michael W. Schwartz, Albert R. La Spada	2006	464
2	Assessing disease onset and progression in the SOD1 mouse model of ALS Neuroreport ·Patrick Weydt, Soyon Hong, Michel Kliot, Thomas Möller	2003	186
3	A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort BMC Neurology ·(unknown), Patrick Weydt, Selma M. Soyal, G. Bernhard Landwehrmeyer, Wolfgang Patsch	2014	171
4	Neurofilament levels as biomarkers in asymptomatic and symptomatic familial amyotrophic lateral sclerosis Annals of Neurology ·Patrick Weydt, Patrick Oeckl, André Huss, Kathrin Müller, Alexander E. Volk, Jens Kühle, Antje Knehr, Peter M. Andersen, Johannes Prudlo, Petra Steinacker, Jochen H. Weishaupt, Albert C. Ludolph, Markus Otto	2015	167
5	Increased cytotoxic potential of microglia from ALS‐transgenic mice Glia ·Patrick Weydt, Eric Yuen, Bruce R. Ransom, Thomas Möller	2004	120
6	Hypothalamic atrophy is related to body mass index and age at onset in amyotrophic lateral sclerosis Journal of Neurology Neurosurgery & Psychiatry ·Martin Gorges, Pauline Vercruysse, Hans‐Peter Müller, Hans‐Jürgen Huppertz, Angela Rosenbohm, Gabriele Nagel, Patrick Weydt, Åsa Petersén, Albert C. Ludolph, Jan Kassubek, Luc Dupuis	2017	117
7	Mutual exacerbation of peroxisome proliferator‐activated receptor γ coactivator 1α deregulation and α‐synuclein oligomerization Annals of Neurology ·Judith Eschbach, Björn von Einem, Kathrin Müller, Hanna Bayer, Annika Scheffold, Brad E. Morrison, K. Lenhard Rudolph, Dietmar Rudolf Thal, Anke Witting, Patrick Weydt, Markus Otto, Michael Fauler, Birgit Liss, Pamela J. McLean, Albert R. La Spada, Albert C. Ludolph, Jochen H. Weishaupt, Karin M. Danzer	2014	106
8	The gene coding for PGC-1α modifies age at onset in Huntington's Disease Molecular Neurodegeneration ·Patrick Weydt, Selma M. Soyal, Cinzia Gellera, Stefano DiDonato, Claus Weidinger, Hannes Oberkofler, G. Bernhard Landwehrmeyer, Wolfgang Patsch	2009	106
9	Assessing disease onset and progression in the SOD1 mouse model of ALS Neuroreport ·Patrick Weydt, Soyon Hong, Michel Kliot, Thomas Möller	2003	106
10	Endocannabinoids accumulate in spinal cord of SOD1^G93A transgenic mice Journal of Neurochemistry ·Anke Witting, Patrick Weydt, Soyon Hong, Michel Kliot, Thomas Möller, Nephi Stella	2004	94
11	Novel Blood-Based Biomarkers of Cognition, Stress, and Physical or Cognitive Training in Older Adults at Risk of Dementia: Preliminary Evidence for a Role of BDNF, Irisin, and the Kynurenine Pathway Journal of Alzheimer s Disease ·Olivia C. Küster, Daria Laptinskaya, Patrick Fissler, Cathrin Schnack, Martina Zügel, Verena Nold, Franka Thurm, Sina Pleiner, Alexander Karabatsiakis, Björn von Einem, Patrick Weydt, André Liesener, Andreas Borta, Alexander Wöll, Bastian Hengerer, Iris‐Tatjana Kolassa, Christine A. F. Von Arnim	2017	90
12	Cannabinol delays symptom onset in SOD1 (G93A) transgenic mice without affecting survival Amyotrophic Lateral Sclerosis ·Patrick Weydt, Soyon Hong, Anke Witting, Thomas Möller, Nephi Stella, Michel Kliot	2005	79
13	Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers Brain ·Axel Freischmidt, Kathrin Müller, Lisa Zondler, Patrick Weydt, Alexander E. Volk, Anže Božič, Michael Walter, Michael Bonin, Benjamin Mayer, Christine A. F. Von Arnim, Markus Otto, Christoph Dieterich, Karlheinz Holzmann, Peter M. Andersen, Albert C. Ludolph, Karin M. Danzer, Jochen H. Weishaupt	2014	79
14	A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset† Human Molecular Genetics ·Selma M. Soyal, Thomas K. Felder, Simon Auer, Penelope Hahne, Hannes Oberkofler, Anke Witting, Markus Paulmichl, G. Bernhard Landwehrmeyer, Patrick Weydt, Wolfgang Patsch, (unknown)	2012	76
15	Proteomics in cerebrospinal fluid and spinal cord suggests UCHL1, MAP2 and GPNMB as biomarkers and underpins importance of transcriptional pathways in amyotrophic lateral sclerosis Acta Neuropathologica ·Patrick Oeckl, Patrick Weydt, Dietmar Rudolf Thal, Jochen H. Weishaupt, Albert C. Ludolph, Markus Otto	2019	74
16	Survey of cannabis use in patients with amyotrophic lateral sclerosis American Journal of Hospice and Palliative Medicine® ·Dagmar Amtmann, Patrick Weydt, Kurt Johnson, Mark P. Jensen, Gregory T. Carter	2004	73
17	Neuroinflammation in the pathogenesis of amyotrophic lateral sclerosis Neuroreport ·Patrick Weydt, Thomas Mo ̈ller	2005	70
18	PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis Human Molecular Genetics ·J. W. Eschbach, Birgit Schwalenstöcker, Selma M. Soyal, H Bayer, D. Wiesner, Chizuru Akimoto, Anna Christine Nilsson, A. Birve, Thomas Meyer, Luc Dupuis, Karin M. Danzer, P. M. Andersen, Anke Witting, Albert C. Ludolph, Wolfgang Patsch, Patrick Weydt	2013	69
19	Serum microRNAs in sporadic amyotrophic lateral sclerosis Neurobiology of Aging ·Axel Freischmidt, Kathrin Müller, Lisa Zondler, Patrick Weydt, Benjamin Mayer, Christine A. F. Von Arnim, Annemarie Hübers, Johannes Dorst, Markus Otto, Karlheinz Holzmann, Albert C. Ludolph, Karin M. Danzer, Jochen H. Weishaupt	2015	65
20	The Role of PGC-1α in the Pathogenesis of Neurodegenerative Disorders Current Drug Targets ·Krisztina Ròna-Vörös, Patrick Weydt	2010	61

About Patrick Weydt

Patrick Weydt is a scholar working on Neurology, Cellular and Molecular Neuroscience, Molecular Biology, Genetics and Physiology, having authored 90 papers that have together received 3.6k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (40 papers), Genetic Neurodegenerative Diseases (26 papers), Neurogenetic and Muscular Disorders Research (26 papers), Parkinson's Disease Mechanisms and Treatments (20 papers), Mitochondrial Function and Pathology (19 papers), Cannabis and Cannabinoid Research (8 papers), Adipose Tissue and Metabolism (8 papers) and Neuroscience and Neuropharmacology Research (6 papers). The work is most often cited by research in Neurology (1.7k citations), Genetics (798 citations), Cellular and Molecular Neuroscience (1.2k citations), Neurology (408 citations) and Biological Psychiatry (73 citations). Patrick Weydt has collaborated with scholars based in Germany, United States and France. Frequent co-authors include Thomas Möller, Michel Kliot, Soyon Hong, Albert C. Ludolph, Anke Witting, G. Bernhard Landwehrmeyer, Selma M. Soyal, Wolfgang Patsch, Gregory T. Carter and Jochen H. Weishaupt. Their work appears in journals such as Neuroreport, Journal of Neurology Neurosurgery & Psychiatry, PLoS ONE, Human Molecular Genetics and Nature.

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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