heiBIB: Weishaupt, Jochen H.

Weishaupt, Jochen H. Prof. Dr. med.Universität HeidelbergHeidelberg

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Publications in heiBIB

Barthel, Paula Charlotte: Beyond Huntington’s disease - late-onset chorea caused by a homozygous variant in ERCC4 / Paula C. Barthel, Bertrand Popa, Anne Ebert, Sherif A. Mohamed, Jochen Weishaupt, Julian Conrad, 2025. - 7 S. : Illustrationen
In: The cerebellum, ISSN 1473-4230. 24(2025), Artikel-ID 5, Seite 1-7
DOI: 10.1007/s12311-024-01755-1
Meyer, Thomas: SOD1 gene screening in ALS : frequency of mutations, patients’ attitudes to genetic information and transition to tofersen treatment in a multi-center program / Thomas Meyer, Peggy Schumann, Torsten Grehl, Ute Weyen, Susanne Petri, Annekathrin Rödiger, Robert S… , 2025. - 10 S.
In: Amyotrophic lateral sclerosis & frontotemporal degeneration, ISSN 2167-9223. 26(2025), 1/2, Seite 162-171
DOI: 10.1080/21678421.2024.2401131
Koch, Jan Christoph: Safety, tolerability, and efficacy of fasudil in amyotrophic lateral sclerosis (ROCK-ALS) : a phase 2, randomised, double-blind, placebo-controlled trial / Jan C. Koch, Andreas Leha, Helen Bidner, Isabell Cordts, Johannes Dorst, René Günther, Daniel Zeller… , November 2024. - 14 S. : Illustrationen
In: The lancet, ISSN 1474-4465. 23(2024), 11, Seite 1133-1146
DOI: 10.1016/S1474-4422(24)00373-9
Dash, Banaja Priyadarshini: Upregulated miR-10b-5p as a potential miRNA signature in amyotrophic lateral sclerosis patients / Banaja P. Dash, Axel Freischmidt, Anika M. Helferich, Albert C. Ludolph, Peter M. Andersen, Jochen H… , 07 November 2024. - 12 S. : Illustrationen
In: Frontiers in cellular neuroscience, ISSN 1662-5102. 18(2024), Seite 1-12
DOI: 10.3389/fncel.2024.1457704
Wiesenfarth, Maximilian: Effects of tofersen treatment in patients with <i>SOD1</i>-ALS in a “real-world” setting - a 12-month multicenter cohort study from the German early access program / Maximilian Wiesenfarth, Johannes Dorst, David Brenner, Zeynep Elmas, Özlem Parlak, Zeljko Uzelac, Ka… , March 2024. - 12 S.
In: EClinicalMedicine, ISSN 2589-5370. 69(2024), Artikel-ID 102495, Seite 1-12
DOI: 10.1016/j.eclinm.2024.102495
Brenner, David: A TBK1 variant causes autophagolysosomal and motoneuron pathology without neuroinflammation in mice / David Brenner, Kirsten Sieverding, Jahnavi Srinidhi, Susanne Zellner, Christopher Secker, Rüstem Yil… , March 22 2024. - 20 S. : Illustrationen
In: Journal of experimental medicine, ISSN 1540-9538. 221(2024), 5, Artikel-ID e20221190, Seite 1-20
DOI: 10.1084/jem.20221190
Wischnewski, Sven: Cell type mapping of inflammatory muscle diseases highlights selective myofiber vulnerability in inclusion body myositis / Sven Wischnewski, Thomas Thäwel, Chiseko Ikenaga, Anna Kocharyan, Celia Lerma-Martin, Amel Zulji, Ha… , July 2024. - 27 S. : Illustrationen
In: Nature aging, ISSN 2662-8465. 4(2024), 7 vom: Juli, Seite 969-983
DOI: 10.1038/s43587-024-00645-9
Meyer, Thomas: Clinical and patient-reported outcomes and neurofilament response during tofersen treatment in SOD1-related ALS : a multicenter observational study over 18 months / Thomas Meyer MD, Peggy Schumann MSc, Patrick Weydt MD, Susanne Petri MD, Jochen H. Weishaupt MD, Ute… , September 2024. - 13 S.
In: Muscle & nerve, ISSN 1097-4598. 70(2024), 3 vom: Sept., Seite 333-345
DOI: 10.1002/mus.28182
Meyer, Thomas: Serum neurofilament light chain in distinct phenotypes of amyotrophic lateral sclerosis : a longitudinal, multicenter study / Thomas Meyer, Marie Dreger, Torsten Grehl, Ute Weyen, Dagmar Kettemann, Patrick Weydt, René Günther,… , September 2024. - 13 S.
In: European journal of neurology, ISSN 1468-1331. 31(2024), 9, Artikel-ID e16379, Seite 1-13
DOI: 10.1111/ene.16379
Dash, Banaja Priyadarshini: An integrative miRNA-mRNA expression analysis identifies miRNA signatures associated with SOD1 and TARDBP patient-derived motor neurons / Banaja P Dash, Axel Freischmidt, Jochen H Weishaupt, Andreas Hermann, 1 August 2024. - 15 S. : Illustrationen, Diagramme
In: Human molecular genetics, ISSN 1460-2083. 33(2024), 15, Seite 1300-1314
DOI: 10.1093/hmg/ddae072
Schuster, Joachim: In-depth analysis of data from the RAS-ALS study reveals new insights in rasagiline treatment for amyotrophic lateral sclerosis / Joachim Schuster, Jens Dreyhaupt, Karla Mönkemöller, Luc Dupuis, Stéphane Dieterlé, Jochen H. Weisha… , April 2024. - 11 S. : Diagramme
In: European journal of neurology, ISSN 1468-1331. 31(2024), 4 vom: Apr., Artikel-ID e16204, Seite 1-11
DOI: 10.1111/ene.16204
Megat, Salim: Author correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes / Salim Megat, Natalia Mora, Jason Sanogo, Olga Roman, Alberto Catanese, Najwa Ouali Alami, Axel Freis… , 04 December 2023. - 3 S. : Diagramme
In: Nature Communications, ISSN 2041-1723. 14(2023), 1, Artikel-ID 8026, Seite 1-3
DOI: 10.1038/s41467-023-43710-4
Yılmaz, Rüstem: Frequency of C9orf72 and SOD1 mutations in 302 sporadic ALS patients from three German ALS centers / Rüstem Yilmaz, Torsten Grehl, Lukas Eckrich, Ines Marschalkowski, Kanchi Weishaupt, Ivan Valkadinov,… , 17 Jan 2023. - 6 S. : Illustrationen
In: Amyotrophic lateral sclerosis & frontotemporal degeneration, ISSN 2167-9223. 24(2023), 5/6, Seite 414-419
DOI: 10.1080/21678421.2023.2165946
Hebestreit, Sophie: PSEN1/SLC20A2 double mutation causes early-onset Alzheimer’s disease and primary familial brain calcification co-morbidity / Sophie Hebestreit, Janine Schwahn, Vesile Sandikci, Mate E. Maros, Ivan Valkadinov, Rüstem Yilmaz, L… , July 2023. - 5 S. : Illustrationen
In: Neurogenetics, ISSN 1364-6753. 24(2023), 3, Seite 209-213
DOI: 10.1007/s10048-023-00723-x
Kühlwein, Julia K.: ALS is imprinted in the chromatin accessibility of blood cells / Julia K. Kühlwein, Wolfgang P. Ruf, Katharina Kandler, Simon Witzel, Christina Lang, Medhanie A. Mul… , 24 April 2023. - 18 S. : Illustrationen
In: Cellular and molecular life sciences, ISSN 1420-9071. 80(2023), 5, Artikel-ID 131, Seite 1-18
DOI: 10.1007/s00018-023-04769-w
Meyer, Thomas: Neurofilament light-chain response during therapy with antisense oligonucleotide tofersen in SOD1-related ALS : treatment experience in clinical practice: clinical research short report / Thomas Meyer, Peggy Schumann, Patrick Weydt, Susanne Petri, Yasemin Koc, Susanne Spittel, Sarah Bern… , June 2023. - 7 S. : Illustrationen
In: Muscle & nerve, ISSN 1097-4598. 67(2023), 6 vom: Juni, Seite 515-521
DOI: 10.1002/mus.27818
Brockmann, Sarah J.: Mitochondrial genome study in blood of maternally inherited ALS cases / Sarah J. Brockmann, Eva Buck, Tiziana Casoli, João L. Meirelles, Wolfgang P. Ruf, Paolo Fabbietti, K… , 28 July 2023. - 13 S. : Illustrationen
In: Human genomics, ISSN 1479-7364. 17(2023), 1, Seite 1-13
DOI: 10.1186/s40246-023-00516-1
Megat, Salim: Author correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes / Salim Megat, Natalia Mora, Jason Sanogo, Olga Roman, Alberto Catanese, Najwa Ouali Alami, Axel Freis… , 04 December 2023. - 3 S. : Illustrationen
In: Nature Communications, ISSN 2041-1723. 14(2023), Artikel-ID 8026, Seite 1-3
DOI: 10.1038/s41467-023-43710-4
Dorst, Johannes: Metabolic alterations precede neurofilament changes in presymptomatic ALS gene carriers / Johannes Dorst, Patrick Weydt, David Brenner, Simon Witzel, Katharina Kandler, André Huss, Christine… , April 2023. - 10 S. : Illustrationen
In: EBioMedicine, ISSN 2352-3964. 90(2023) vom: Apr., Seite 1-10
DOI: 10.1016/j.ebiom.2023.104521
Ramachandran, Swetha: Low T-cell reactivity to TDP-43 peptides in ALS / Swetha Ramachandran, Veselin Grozdanov, Bianca Leins, Katharina Kandler, Simon Witzel, Medhanie Mula… , 21 July 2023. - 10 S. : Illustrationen
In: Frontiers in immunology, ISSN 1664-3224. 14(2023), Artikel-ID 1193507, Seite 1-10
DOI: 10.3389/fimmu.2023.1193507
Megat, Salim: Integrative genetic analysis illuminates ALS heritability and identifies risk genes / Salim Megat, Natalia Mora, Jason Sanogo, Olga Roman, Alberto Catanese, Najwa Ouali Alami, Axel Freis… , 2023. - 18 S. : Illustrationen
In: Nature Communications, ISSN 2041-1723. 14(2023), Artikel-ID 342, Seite 1-18
DOI: 10.1038/s41467-022-35724-1
Rosenbohm, Angela: Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with and Repeat Expansions : An 18-Year Study / Angela Rosenbohm, Hendrik Pott, Mirja Thomsen, Haloom Rafehi, Sabine Kaya, Silke Szymczak, Alexander… , December 2022. - 13 S.
In: Movement disorders, ISSN 1531-8257. 37(2022), 12 vom: Dez., Seite 2427-2439
DOI: 10.1002/mds.29221
Van Rheenen, Wouter: Author correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology : amendments / Wouter van Rheenen, Rick A.A. van der Spek, Mark K. Bakker, Joke J.F.A. van Vugt, Paul J. Hop, Ramon… , 31 January 2022. - 1 S.
In: Nature genetics, ISSN 1546-1718. 54(2022), 3, Seite 361-361
DOI: 10.1038/s41588-022-01020-3
McNeill, Alisdair: Predictive genetic testing for motor neuron disease: time for a guideline? : comment / Alisdair McNeill, Maria-del-Mar Amador, Hilary Bekker, Angus Clarke, Ashley Crook, Cathy Cummings, A… , 5 April 2022. - 2 S.
In: European journal of human genetics, ISSN 1476-5438. 30(2022), 6, Seite 635-636
DOI: 10.1038/s41431-022-01093-y
Schrader, Tina A.: PEX11β and FIS1 cooperate in peroxisome division independently of mitochondrial fission factor / Tina A. Schrader, Ruth E. Carmichael, Markus Islinger, Joseph L. Costello, Christian Hacker, Nina A.… , 08 July 2022. - 13 S.
In: Journal of cell science, ISSN 1477-9137. 135(2022), 13, Artikel-ID jcs259924, Seite 1-13
DOI: 10.1242/jcs.259924
Ruf, Wolfgang: Methylome analysis of ALS patients and presymptomatic mutation carriers in blood cells / Wolfgang P. Ruf, Eilis Hannon, Axel Freischmidt, Veselin Grozdanov, David Brenner, Kathrin Müller, A… , August 2022. - 9 S.
In: Neurobiology of aging, ISSN 1558-1497. 116(2022) vom: Aug., Seite 16-24
DOI: 10.1016/j.neurobiolaging.2022.04.003
Pant, Devesh C.: ALS-linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain-of-function / Devesh C Pant, Janani Parameswaran, Lu Rao, Isabel Loss, Ganesh Chilukuri, Rosanna Parlato, Liang Sh… , 23 June 2022. - 18 S. : Illustrationen
In: EMBO reports, ISSN 1469-3178. 23(2022), 8 vom: Aug., Artikel-ID e54234, Seite 1-18
DOI: 10.15252/embr.202154234
Van Schoor, Evelien: Increased pyroptosis activation in white matter microglia is associated with neuronal loss in ALS motor cortex / Evelien Van Schoor, Simona Ospitalieri, Sebastiaan Moonen, Sandra O. Tomé, Alicja Ronisz, Orkun Ok, … , 22 July 2022. - 19 S.
In: Acta neuropathologica, ISSN 1432-0533. 144(2022), 3, Seite 393-411
DOI: 10.1007/s00401-022-02466-9
Streit, Lisa: Stress induced TDP-43 mobility loss independent of stress granules / Lisa Streit, Timo Kuhn, Thomas Vomhof, Verena Bopp, Albert C. Ludolph, Jochen H. Weishaupt, J. Chris… , 19 September 2022. - 18 S. : Illustrationen
In: Nature Communications, ISSN 2041-1723. 13(2022), Artikel-ID 5480, Seite 1-18
DOI: 10.1038/s41467-022-32939-0
Opie-Martin, Sarah: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration / Sarah Opie-Martin, Alfredo Iacoangeli, Simon D. Topp, Olubunmi Abel, Keith Mayl, Puja R. Mehta, Alek… , 12 November 2022. - 9 S.
In: Nature Communications, ISSN 2041-1723. 13(2022), Artikel-ID 6901, Seite 1-9
DOI: 10.1038/s41467-022-34620-y
Siebert, Alexander: ALS-linked loss of Cyclin-F function affects HSP90 / Alexander Siebert, Vanessa Gattringer, Jochen H. Weishaupt, Christian Behrends, 16 September, 2022. - 17 S.
In: Life science alliance, ISSN 2575-1077. 5(2022), 12, Seite 1-17
DOI: 10.26508/lsa.202101359
Brenner, David: FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees / David Brenner, Kathrin Müller, Serena Lattante, Rüstem Yilmaz, Antje Knehr, Axel Freischmidt, Albert… , 2022. - 7 S.
In: Neurogenetics, ISSN 1364-6753. 23(2022), Seite 59-65
DOI: 10.1007/s10048-021-00671-4
Brenner, David: Genetik / David Brenner und Jochen H. Weishaupt, 2022. - 9 S.
In: Amyotrophe Lateralsklerose und andere Motoneuronerkrankungen. (2022), Seite 15-23
Yılmaz, Rüstem: Quadruple genetic variants in a sporadic ALS patient / Rüstem Yilmaz, Kanchi Weishaupt, Ivan Valkadinov, Antje Knehr, David Brenner, Jochen H. Weishaupt, 2022. - 4 S.
In: Molecular genetics & genomic medicine, ISSN 2324-9269. 10(2022), 7, Artikel-ID 1953, Seite 1-4
DOI: 10.1002/mgg3.1953
Osmanovic, Alma: Heterozygous DHTKD1 variants in two European cohorts of amyotrophic lateral sclerosis patients / Alma Osmanovic, Isabel Gogol, Helge Martens, Maylin Widjaja, Kathrin Müller, Olivia Schreiber-Katz, … , 2022. - 15 S.
In: Genes, ISSN 2073-4425. 13(2022), 1, Artikel-ID 84, Seite 1-15
DOI: 10.3390/genes13010084
Dash, Banaja Priyadarshini: Downstream effects of mutations in SOD1 and TARDBP converge on ene expression impairment in patient-derived motor neurons / Banaja P. Dash, Axel Freischmidt, Jochen H. Weishaupt, Andreas Hermann, 25 August 2022. - 20 S.
In: International journal of molecular sciences, ISSN 1422-0067. 23(2022), 17 vom: Aug., Artikel-ID 9652, Seite 1-20
DOI: 10.3390/ijms23179652
Buck, Eva: Increased NF-L levels in the TDP-43G298S ALS mouse model resemble NF-L levels in ALS patients / Eva Buck, Patrick Oeckl, Veselin Grozdanov, Verena Bopp, Julia K. Kühlwein, Wolfgang P. Ruf, Diana W… , 2022. - 4 S. : Illustrationen, Diagramme
In: Acta neuropathologica, ISSN 1432-0533. 144(2022), 1, Seite 161-164
DOI: 10.1007/s00401-022-02436-1
Strohm, Laura: Multi-omics profiling identifies a deregulated FUS-MAP1B axis in ALS/FTD-associated UBQLN2 mutants / Laura Strohm, Zehan Hu, Yongwon Suk, Alina Rühmkorf, Erin Sternburg, Vanessa Gattringer, Henrick Rie… , 1 July 2022. - 21 S.
In: Life science alliance, ISSN 2575-1077. 5(2022), 11, Artikel-ID e202101327, Seite 1-21
DOI: 10.26508/lsa.202101327
Steinacker, Petra: Chitotriosidase as biomarker for early stage amyotrophic lateral sclerosis : a multicenter study / Petra Steinacker, Emily Feneberg, Steffen Halbgebauer, Simon Witzel, Federico Verde, Patrick Oeckl, … , 2021. - 11 S.
In: Amyotrophic lateral sclerosis & frontotemporal degeneration, ISSN 2167-9223. 22(2021), 3/4, Seite 276-286
DOI: 10.1080/21678421.2020.1861023
Halbgebauer, Steffen: Comparison of CSF and serum neurofilament light and heavy chain as differential diagnostic biomarkers for ALS / Steffen Halbgebauer, Petra Steinacker, Federico Verde, Jochen Weishaupt, Patrick Oeckl, Christine vo… , 2021. - 7 S.
In: Journal of neurology, neurosurgery, and psychiatry, ISSN 1468-330X. 93(2021), 1, Seite 68-74
DOI: 10.1136/jnnp-2021-327129
Van Rheenen, Wouter: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology, 06 December 2021. - 13 S.
In: Nature genetics, ISSN 1546-1718. 53(2021), 12, Seite 1636-1648
DOI: 10.1038/s41588-021-00973-1
Ruf, Wolfgang: Protein binding partners of dysregulated miRNAs in Parkinson’s disease derum / Wolfgang P. Ruf, Axel Freischmidt, Veselin Grozdanov, Valerie Roth, Sarah J. Brockmann, Brit Mollenh… , 2 April 2021. - 13 S.
In: Cells, ISSN 2073-4409. 10(2021), 4, Artikel-ID 791, Seite 1-13
DOI: 10.3390/cells10040791
Freischmidt, Axel: A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis / Axel Freischmidt, Anand Goswami, Katharina Limm, Vitaly L. Zimyanin, Maria Demestre, Hannes Glaß, Ka… , 19 April 2021. - 16 S.
In: Brain, ISSN 1460-2156. 144(2021), 4, Seite 1214-1229
DOI: 10.1093/brain/awab018
Halbgebauer, Steffen: Beta-synuclein in cerebrospinal fluid as an early diagnostic marker of Alzheimer’s disease / Steffen Halbgebauer, Patrick Oeckl, Petra Steinacker, Deniz Yilmazer-Hanke, Sarah Anderl-Straub, Chr… , 2021. - 8 S.
In: Journal of neurology, neurosurgery, and psychiatry, ISSN 1468-330X. 92(2021), 4, Seite 349-356
DOI: 10.1136/jnnp-2020-324306
Kröger, Clara: Haploinsufficiency of TANK-binding kinase 1 prepones age-associated neuroinflammatory changes without causing motor neuron degeneration in aged mice / Clara Bruno, Kirsten Sieverding, Axel Freischmidt, Takashi Satoh, Paul Walther, B. Mayer, Albert C. … , August 21, 2020. - 13 S.
In: Brain communications, ISSN 2632-1297. 2(2020), 2, Artikel-ID fcaa133, Seite 1-13
DOI: 10.1093/braincomms/fcaa133
Dedeene, Lieselot: Dipeptide repeat protein and TDP-43 pathology along the hypothalamic-pituitary axis in C9orf72 and non-C9orf72 ALS and FTLD-TDP cases / Lieselot Dedeene, Evelien Van Schoor, Simona Ospitalieri, Alicja Ronisz, Jochen H. Weishaupt, Markus… , 30 August 2020. - 5 S.
In: Acta neuropathologica, ISSN 1432-0533. 140(2020), 5, Seite 777-781
DOI: 10.1007/s00401-020-02216-9
Oeckl, Patrick: Targeted mass spectrometry suggests beta-synuclein as synaptic blood marker in Alzheimer’s disease / Patrick Oeckl, Steffen Halbgebauer, Sarah Anderl-Straub, Christine A. F. von Arnim, Janine Diehl-Sch… , February 26, 2020. - 9 S.
In: Journal of proteome research, ISSN 1535-3907. 19(2020), 3, Seite 1310-1318
DOI: 10.1021/acs.jproteome.9b00824
Joilin, Greig: Identification of a potential non-coding RNA biomarker signature for amyotrophic lateral sclerosis / Greig Joilin, Elizabeth Gray, Alexander G. Thompson, Yoana Bobeva, Kevin Talbot, Jochen Weishaupt, A… , June 17, 2020. - 14 S.
In: Brain communications, ISSN 2632-1297. 2(2020), 1, Artikel-ID fcaa053, Seite 1-14
DOI: 10.1093/braincomms/fcaa053
Yılmaz, Rüstem: SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden / Rüstem Yilmaz, Kathrin Müller, David Brenner, Alexander E. Volk, Guntram Borck, Andreas Hermann, Tho… , 2020. - 7 S.
In: Neurobiology of aging, ISSN 1558-1497. 87(2020), Seite 139.e9-139.e15
DOI: 10.1016/j.neurobiolaging.2019.10.018
Müller, Hans-Peter: In vivo histopathological staging in C9orf72-associated ALS : A tract of interest DTI study / Hans-Peter Müller, Kelly Del Tredici, Dorothée Lulé, Kathrin Müller, Jochen H. Weishaupt, Albert C. … , 26 May 2020. - 6 S.
In: NeuroImage: Clinical, ISSN 2213-1582. 27(2020), Artikel-ID 102298, Seite 1-6
DOI: 10.1016/j.nicl.2020.102298
Schijven, Dick: Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy / Dick Schijven, Remi Stevelink, Mark McCormack, Wouter van Rheenen, Jurjen J. Luykx, Bobby P.C. Koele… , 18 April 2020. - 5 S.
In: Neurobiology of aging, ISSN 1558-1497. 92(2020) vom: Aug., Seite 153.e1-153.e5
DOI: 10.1016/j.neurobiolaging.2020.04.011
Barschke, Peggy: Different CSF protein profiles in amyotrophic lateral sclerosis and frontotemporal dementia with C9orf72 hexanucleotide repeat expansion / Peggy Barschke, Patrick Oeckl, Petra Steinacker, MHD Rami Al Shweiki, Jochen H Weishaupt, G Bernhard… , 4 March 2020. - 9 S.
In: Journal of neurology, neurosurgery, and psychiatry, ISSN 1468-330X. 91(2020), 5, Seite 503-511
DOI: 10.1136/jnnp-2019-322476
Oeckl, Patrick: Proteomics in cerebrospinal fluid and spinal cord suggests UCHL1, MAP2 and GPNMB as biomarkers and underpins importance of transcriptional pathways in amyotrophic lateral sclerosis / Patrick Oeckl, Patrick Weydt, Dietmar R. Thal, Jochen H. Weishaupt, Albert C. Ludolph, Markus Otto, 2020. - 16 S.
In: Acta neuropathologica, ISSN 1432-0533. 139(2020), 1, Seite 119-134
DOI: 10.1007/s00401-019-02093-x
Ludolph, Albert C.: Effect of high-caloric nutrition on survival in amyotrophic lateral sclerosis / Albert C. Ludolph, MD, Johannes Dorst, MD, Jens Dreyhaupt, PhD, Jochen H. Weishaupt, MD, Jan Kassube… , February 2020. - 11 S.
In: Annals of neurology, ISSN 1531-8249. 87(2020), 2 vom: Feb., Seite 206-216
DOI: 10.1002/ana.25661
Lulé, Dorothée: Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers : a developmental disorder / Dorothée E Lulé, Hans-Peter Müller, Julia Finsel, Patrick Weydt, Antje Knehr, Ivar Winroth, Peter An… , 27 August 2020. - 6 S.
In: Journal of neurology, neurosurgery, and psychiatry, ISSN 1468-330X. 91(2020), 11, Seite 1195-1200
DOI: 10.1136/jnnp-2020-323671
Sieverding, Kirsten: Hemizygous deletion of Tbk1 worsens neuromuscular junction pathology in TDP-43G298S transgenic mice / Kirsten Sieverding, Johannes Ulmer, Clara Bruno, Takashi Satoh, William Tsao, Axel Freischmidt, Shiz… , 2021. - 14 S.
In: Experimental neurology, ISSN 1090-2430. 335(2021), Artikel-ID 113496, Seite 1-14
DOI: 10.1016/j.expneurol.2020.113496
Freischmidt, Axel: Commentary: Effects of ALS-associated TANK binding kinase 1 mutations on protein-protein interactions and kinase activity / Axel Freischmidt, David Brenner, Albert C. Ludolph, Peter M. Andersen and Jochen H. Weishaupt, 11 September 2020. - 2 S.
In: Frontiers in neuroscience, ISSN 1662-453X. 14(2020), Artikel-ID 551006, Seite 1-2
DOI: 10.3389/fnins.2020.551006
Ouali Alami, Najwa: Multiplexed chemogenetics in astrocytes and motoneurons restore blood-spinal cord barrier in ALS / Najwa Ouali Alami, Linyun Tang, Diana Wiesner, Barbara Commisso, David Bayer, Jochen Weishaupt, Luc … , 8 September 2020. - 28 S.
In: Life science alliance, ISSN 2575-1077. 3(2020), 11, Artikel-ID 01900571, Seite 1-28
DOI: 10.26508/lsa.201900571
Michel, Detlef: Rapid, convenient and efficient kit-independent detection of SARS-CoV-2 RNA : short communication / Detlef Michel, Karin M. Danzer, Rüdiger Groß, Carina Conzelmann, Janis A. Müller, Axel Freischmidt, … , 3 September 2020. - 4 S.
In: Journal of virological methods, ISSN 1879-0984. 286(2020), Artikel-ID 113965, Seite 1-4
DOI: 10.1016/j.jviromet.2020.113965
Brenner, David: Gene specific therapies : the next therapeutic milestone in neurology / David Brenner, Albert C. Ludolph and Jochen H. Weishaupt, 2020 Sept. 8. - 13 S.
In: Neurological research and practice, ISSN 2524-3489. 2(2020), Artikel-ID 25, Seite 1-13
DOI: 10.1186/s42466-020-00075-z
Senderek, Jan: The genetic landscape of axonal neuropathies in the middle-aged and elderly : focus on MME / Jan Senderek, MD, Petra Lassuthova, PhD, Dagmara Kabzińska, PhD, Lisa Abreu, MPH, Jonathan Baets, MD… , November 3, 2020. - 17 S.
In: Neurology, ISSN 1526-632X. 95(2020,24), Seite e3163-e3179, 17 Seiten
DOI: 10.1212/WNL.0000000000011132
Bendotti, Caterina: Focus on the heterogeneity of amyotrophic lateral sclerosis / Caterina Bendotti, Valentina Bonetto, Elisabetta Pupillo, Giancarlo Logroscino, Ammar Al-Chalabi, Ch… , 25 Jun 2020. - 11 S.
In: Amyotrophic lateral sclerosis & frontotemporal degeneration, ISSN 2167-9223. 21(2020), 7/8, Seite 485-495
DOI: 10.1080/21678421.2020.1779298
Dorst, Johannes: Effect of high-caloric nutrition on serum neurofilament light chain levels in amyotrophic lateral sclerosis / Johannes Dorst, Joachim Schuster, Jens Dreyhaupt, Simon Witzel, Jochen H. Weishaupt, Jan Kassubek, U… , 2020 Aug 11. - 3 S.
In: Journal of neurology, neurosurgery, and psychiatry, ISSN 1468-330X. 91(2020), 9, Seite 1007-1009
DOI: 10.1136/jnnp-2020-323372
Tazelaar, Gijs H. P.: Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort / Gijs H. P. Tazelaar, Annelot M. Dekker, Joke J. F. A. van Vugt, Rick A. van der Spek, Henk-Jan Weste… , 2019. - 7 S.
In: Neurobiology of aging, ISSN 1558-1497. 74(2019) vom: Feb., Seite 234.e9-234.e15
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Lingor, Paul: ROCK-ALS: protocol for a randomized, placebo-controlled, double-blind phase IIa trial of safety, tolerability and efficacy of the Rho kinase (ROCK) inhibitor fasudil in amyotrophic lateral sclerosis / Paul Lingor, Markus Weber, William Camu, Tim Friede, Reinhard Hilgers, Andreas Leha, Christoph Neuwi… , 27 March 2019. - 11 S.
In: Frontiers in neurology, ISSN 1664-2295. 10(2019), Artikel-ID 293, Seite 1-11
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Lulé, Dorothée: Story of the ALS-FTD continuum retold : rather two distinct entities / Dorothée E Lulé, Helena EA Aho-Özhan, Cynthia Vázquez, Ulrike Weiland, Jochen H Weishaupt, Markus Ot… , 2019. - 4 S.
In: Journal of neurology, neurosurgery, and psychiatry, ISSN 1468-330X. 90(2019), 5, Seite 586-589
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Müller, Hans-Peter: Longitudinal diffusion tensor magnetic resonance imaging analysis at the cohort level reveals disturbed cortical and callosal microstructure with spared corticospinal tract in the TDP-43G298S ALS mouse model / Hans-Peter Müller, David Brenner, Francesco Roselli, Diana Wiesner, Alireza Abaei, Martin Gorges, Ka… , 30 August 2019. - 13 S.
In: Translational neurodegeneration, ISSN 2047-9158. 8(2019), Artikel-ID 27, Seite 1-13
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Kiechle, Martin: In vivo protein complementation demonstrates presynaptic α-synuclein oligomerization and age-dependent accumulation of 8-16-mer oligomer species / authors: Martin Kiechle, Bjoern von Einem, Lennart Höfs, Patrizia Voehringer, Veselin Grozdanov, Dan… , 26 November 2019. - 13 S.
In: Cell reports, ISSN 2211-1247. 29(2019), 9, Seite 2862-2874.e9
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Dekker, Annelot M.: Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis / Annelot M. Dekker, Frank P. Diekstra, Sara L. Pulit, Gijs H. P. Tazelaar, Rick A. van der Spek, Wout… , 11 April 2019. - 8 S.
In: Scientific reports, ISSN 2045-2322. 9(2019), Artikel-ID 5931, Seite 1-8
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Forouhideh, Yalda: A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification : letter to the editor / Yalda Forouhideh, Kathrin Müller, Wolfgang Ruf, Muhannad Assi, Tuncay Şeker, Ceren Tunca, Antje Kneh… , 12 January 2019. - 1 S.
In: Brain, ISSN 1460-2156. 142(2019), 2, Seite e4
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Naumann, Marcel: Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis / Marcel Naumann, Kevin Peikert, Rene Günther, Anneke J. van der Kooi, Eleonora Aronica, Annemarie Hüb… , 2019 Nov 4. - 11 S.
In: Annals of Clinical and Translational Neurology, ISSN 2328-9503. 6(2019), 12, Seite 2384-2394
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Brenner, David: Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations : letter to the editor / David Brenner, Angela Rosenbohm, Rüstem Yilmaz, Kathrin Müller, Torsten Grehl, Susanne Petri, Thomas… , 15 October 2019. - 1 S.
In: Brain, ISSN 1460-2156. 142(2019), 12 vom: Dez., Seite e67
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Rué, Laura: Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis / Laura Rué, Patrick Oeckl, Mieke Timmers, Annette Lenaerts, Jasmijn van der Vos, Silke Smolders, Lind… , 12 July 2019. - 15 S.
In: Acta Neuropathologica Communications, ISSN 2051-5960. 7(2019), Artikel-ID 114, Seite 1-15
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Daria, Tselmen: Genotypes of amyotrophic lateral sclerosis in Mongolia / Tselmen Daria, Kathrin Müller, Gansuvd Oidovdorj, Khandsuren Baatar, Punsaldulam Boldbaatar, Jambal … , 2019. - 3 S.
In: Journal of neurology, neurosurgery, and psychiatry, ISSN 1468-330X. 90(2019), 11 vom: Nov., Seite 1300-1302
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Brenner, David: Heterozygous Tbk1 loss has opposing effects in early and late stages of ALS in mice / David Brenner, Kirsten Sieverding, Clara Bruno, Patrick Lüningschrör, Eva Buck, Simon Mungwa, Lena F… , January 11, 2019. - 12 S.
In: Journal of experimental medicine, ISSN 1540-9538. 216(2019), 2, Seite 267-278
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Verde, Federico: Neurofilament light chain in serum for the diagnosis of amyotrophic lateral sclerosis / Federico Verde, Petra Steinacker, Jochen H Weishaupt, Jan Kassubek, Patrick Oeckl, Steffen Halbgebau… , 2019. - 8 S.
In: Journal of neurology, neurosurgery, and psychiatry, ISSN 1468-330X. 90(2019), 2, Seite 157-164
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Catanese, Alberto: Retinoic acid worsens ATG10-dependent autophagy impairment in TBK1-mutant hiPSC-derived motoneurons through SQSTM1/p62 accumulation / Alberto Catanese, Florian Olde Heuvel, Medhanie Mulaw, Maria Demestre, Julia Higelin, Gotthold Barbi… , 02 Apr 2019. - 19 S.
In: Autophagy, ISSN 1554-8635. 15(2019), 10, Seite 1719-1737
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Grozdanov, Veselin D.: Increased immune activation by pathologic α-synuclein in Parkinson's Disease / Veselin Grozdanov, PhD, Luc Bousset, PhD, Meike Hoffmeister, PhD, Corinna Bliederhaeuser, PhD, Chris… , 25 July 2019. - 14 S.
In: Annals of neurology, ISSN 1531-8249. 86(2019), 4 vom: Okt., Seite 593-606
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Brenner, David: Update on amyotrophic lateral sclerosis genetics / David Brenner, Jochen H. Weishaupt, October 2019. - 5 S.
In: Current opinion in neurology, ISSN 1473-6551. 32(2019), 5, Seite 735-739
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Dorst, Johannes: Prognostic factors in ALS : a comparison between Germany and China / Johannes Dorst, Lu Chen, Angela Rosenbohm, Jens Dreyhaupt, Annemarie Hübers, Joachim Schuster, Joche… , 2019. - 10 S. : Diagramme
In: Journal of neurology, ISSN 1432-1459. 266(2019), Seite 1516-1525
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Weishaupt, Jochen H.: Amyotrophe Lateralsklerose : neue Erkenntnisse und Therapieansätze / Jochen H. Weishaupt, Johannes Dorst, Albert C. Ludolph, 31. Oktober 2018. - 4 S.
In: Klinikarzt, ISSN 1439-3859. 47(2018), 10, Seite 468-471
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Müller, Kathrin: Comprehensive analysis of the mutation spectrum in 301 German ALS families / Kathrin Müller, David Brenner, Patrick Weydt, Thomas Meyer, Torsten Grehl, Susanne Petri, Julian Gro… , 12 April 2018. - 11 S.
In: Journal of neurology, neurosurgery, and psychiatry, ISSN 1468-330X. 89(2018), 8, Seite 817-827
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Rosenbohm, Angela: The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy / Angela Rosenbohm, Susanne Hirsch, Alexander E. Volk, Torsten Grehl, Julian Grosskreutz, Frank Hanisc… , 20 February 2018. - 11 S. : Illustrationen, Diagramme
In: Journal of neurology, ISSN 1432-1459. 265(2018), 5, Seite 1026-1036
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Helferich, Anika Marie: Dysregulation of a novel miR-1825/TBCB/TUBA4A pathway in sporadic and familial ALS / Anika M. Helferich, Sarah J. Brockmann, Jörg Reinders, Dhruva Deshpande, Karlheinz Holzmann, David B… , 20 July 2018. - 19 S.
In: Cellular and molecular life sciences, ISSN 1420-9071. 75(2018), 23, Seite 4301-4319
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Verde, Federico: Chromogranin A levels in the cerebrospinal fluid of patients with amyotrophic lateral sclerosis / Federico Verde, Petra Steinacker, Patrick Oeckl, Jochen H. Weishaupt, Angela Rosenbohm, Vincenzo Sil… , 27 February 2018. - 2 S.
In: Neurobiology of aging, ISSN 1558-1497. 67(2018), Seite 21-22
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Brockmann, Sarah J.: CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency / Sarah J. Brockmann, Axel Freischmidt, Patrick Oeckl, Kathrin Müller, Srinivas K. Ponna, Anika M. Hel… , 05 January 2018. - 10 S.
In: Human molecular genetics, ISSN 1460-2083. 27(2018), 4 vom: Feb., Seite 706-715
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Lulé, Dorothée: Cognitive phenotypes of sequential staging in amyotrophic lateral sclerosis / Dorothée Lulé, Sarah Böhm, Hans-Peter Müller, Helena Aho-Özhan, Jürgen Keller, Martin Gorges, Markus… , 31 January 2018. - 9 S.
In: Cortex, ISSN 1973-8102. 101(2018), Seite 163-171
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Volk, Alexander E.: Current knowledge and recent insights into the genetic basis of amyotrophic lateral sclerosis / Alexander E. Volk, Jochen H. Weishaupt, Peter M. Andersen, Albert C. Ludolph, Christian Kubisch, 2018 Jul 13. - 7 S.
In: Medizinische Genetik, ISSN 1863-5490. 30(2018), 2, Seite 252-258
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Brenner, David: The fecal microbiome of ALS patients / David Brenner, Andreas Hiergeist, Carolin Adis, Benjamin Mayer, André Gessner, Albert C. Ludolph, Jo… , 2018. - 6 S.
In: Neurobiology of aging, ISSN 1558-1497. 61(2018), Seite 132-137
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Naumann, Marcel: Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation / Marcel Naumann, Arun Pal, Anand Goswami, Xenia Lojewski, Julia Japtok, Anne Vehlow, Maximilian Naujo… , 23 January 2018. - 17 S.
In: Nature Communications, ISSN 2041-1723. 9(2018), Artikel-ID 335, Seite 1-17
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Brenner, David: Hot-spot KIF5A mutations cause familial ALS / David Brenner, Rüstem Yilmaz, Kathrin Müller, Torsten Grehl, Susanne Petri, Thomas Meyer, Julian Gro… , 12 January 2018. - 10 S.
In: Brain, ISSN 1460-2156. 141(2018), 3 vom: März, Seite 688-697
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Nicolas, Aude: Genome-wide analyses identify KIF5A as a novel ALS gene / authors: Aude Nicolas, Kevin P. Kenna, Alan E. Renton, Nicola Ticozzi, Faraz Faghri, Ruth Chia, Jani… , 21 March 2018. - 22 S.
In: Neuron, ISSN 1097-4199. 97(2018), 6, Seite 1268-1283.e6
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Ludolph, Albert C.: Safety and efficacy of rasagiline as an add-on therapy to riluzole in patients with amyotrophic lateral sclerosis : a randomised, double-blind, parallel-group, placebo-controlled, phase 2 trial / Albert C. Ludolph, Joachim Schuster, Johannes Dorst, Luc Dupuis, Jens Dreyhaupt, Jochen H. Weishaupt… , 2018. - 8 S.
In: The lancet, ISSN 1474-4465. 17(2018), 8, Seite 681-688
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Endo, Satoshi: Instability of C154Y variant of aldo-keto reductase 1C3 / Satoshi Endo, Sayaka Takada, Ryo P. Honda, Kathrin Müller, Jochen H. Weishaupt, Peter M. Andersen, A… , 1 Ocotober 2017. - 9 S.
In: Chemico-biological interactions, ISSN 1872-7786. 276(2017), Seite 194-202
DOI: 10.1016/j.cbi.2016.12.018
Zondler, Lisa: Impaired activation of ALS monocytes by exosomes / Lisa Zondler, Marisa S Feiler, Axel Freischmidt, Wolfgang P Ruf, Albert C Ludolph, Karin M Danzer an… , 2017. - 8 S.
In: Immunology & cell biology, ISSN 1440-1711. 95(2017), 2, Seite 207-214
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McLaughlin, Russell L.: Genetic correlation between amyotrophic lateral sclerosis and schizophrenia / Russell L. McLaughlin, Dick Schijven, Wouter van Rheenen, Kristel R. van Eijk, Margaret O’Brien, Pro… , 21 March 2017. - 12 S.
In: Nature Communications, ISSN 2041-1723. 8(2017), Artikel-ID 14774, Seite 1-12
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Freischmidt, Axel: Association of mutations in TBK1 with sporadic and familial amyotrophic lateral sclerosis and frontotemporal dementia / Axel Freischmidt, PhD, Kathrin Müller, PhD, Albert C. Ludolph, MD, Jochen H. Weishaupt, MD, Peter M.… , January 2017. - 4 S.
In: JAMA neurology, ISSN 2168-6157. 74(2017), 1 vom: Jan., Seite 110-113
DOI: 10.1001/jamaneurol.2016.3712
Khalaji, Samira: Age increases monocyte adhesion on collagen / Samira Khalaji, Lisa Zondler, Fenneke KleinJan, Ulla Nolte, Medhanie A. Mulaw, Karin M. Danzer, Joch… , 17 May 2017. - 8 S.
In: Scientific reports, ISSN 2045-2322. 7(2017), Artikel-ID 46532, Seite 1-8
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Zondler, Lisa: Proteasome impairment by α-synuclein / Lisa Zondler, Marcus Kostka, Patrick Garidel, Udo Heinzelmann, Bastian Hengerer, Benjamin Mayer, Joc… , September 25, 2017. - 14 S.
In: PLOS ONE, ISSN 1932-6203. 12(2017), 9, Artikel-ID e0184040, Seite 1-14
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Wais, Verena: The concept and diagnostic criteria of primary lateral sclerosis / Verena Wais, Angela Rosenbohm, Susanne Petri, Katja Kollewe, Andreas Hermann, Alexander Storch, Fran… , September 2017. - 8 S.
In: Acta neurologica Scandinavica, ISSN 1600-0404. 136(2017), 3, Seite 204-211
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Weydt, Patrick: Neurofilament levels as biomarkers in asymptomatic and symptomatic familial amyotrophic lateral sclerosis / Patrick Weydt, MD, Patrick Oeckl, PhD, André Huss, MSc, Kathrin Müller, PhD, Alexander E. Volk, MD, … , 2016. - 7 S. : Diagramme
In: Annals of neurology, ISSN 0364-5134. 79(2016), 1, Seite 152-158
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Helferich, Anika Marie: Commentary: Alpha-synuclein interacts with SOD1 and promotes its oligomerization / Anika M. Helferich, Pamela J. McLean, Jochen H. Weishaupt, and Karin M. Danzer, 2016 Nov 14. - 3 S.
In: Journal of neurology & neuromedicine. 1(2016), 7, Seite 28-30
Bliederhäuser, Corinna: LRRK2 contributes to monocyte dysregulation in Parkinson’s disease : letter to the editor / Corinna Bliederhaeuser, Lisa Zondler, Veselin Grozdanov, Wolfgang P. Ruf, David Brenner, Heather L. … , 24 November 2016. - 5 S.
In: Acta Neuropathologica Communications, ISSN 2051-5960. 4(2016), Artikel-ID 123, Seite 1-5
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Brenner, David: NEK1 mutations in familial amyotrophic lateral sclerosis : letter to the editor / David Brenner, Kathrin Müller, Thomas Wieland, Patrick Weydt, Sarah Böhm, Dorothée Lulé, Annemarie H… , 05 March 2016. - 4 S.
In: Brain, ISSN 1460-2156. 139(2016), 5 vom: Mai, Artikel-ID e28, Seite 1-4
DOI: 10.1093/brain/aww033
Weishaupt, Jochen H.: Common molecular pathways in amyotrophic lateral sclerosis and frontotemporal dementia : review / Jochen H. Weishaupt, Tony Hyman, Ivan Dikic, 4 August 2016. - 15 S.
In: Trends in molecular medicine, ISSN 1471-499X. 22(2016), 9, Seite 769-783
DOI: 10.1016/j.molmed.2016.07.005
Auer-Grumbach, Michaela: Rare variants in MME, encoding metalloprotease neprilysin, are linked to late-onset autosomal-dominant axonal polyneuropathies / Michaela Auer-Grumbach, Stefan Toegel, Maria Schabhüttl, Daniela Weinmann, Catharina Chiari, David L… , 1 September 2016. - 17 S.
In: The American journal of human genetics, ISSN 1537-6605. 99(2016), 3 vom: Sept., Seite 607-623
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Kenna, Kevin P.: NEK1 variants confer susceptibility to amyotrophic lateral sclerosis / Kevin P Kenna, Perry TC van Doormaal, Annelot M Dekker, Nicola Ticozzi, Brendan J Kenna, Frank P Die… , 25 July 2016. - 6 S.
In: Nature genetics, ISSN 1546-1718. 48(2016), 9 vom: Sept., Seite 1037-1042
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Van Rheenen, Wouter: Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis / Wouter van Rheenen, Marcella Rietschel, Marcus M Nöthen, Jochen H Weishaupt [und 175 weitere], 25 July 2016. - 8 S.
In: Nature genetics, ISSN 1546-1718. 48(2016), 9, Seite 1043-1048
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Kunadt, Marcel: Extracellular vesicle sorting of α-Synuclein is regulated by sumoylation / Marcel Kunadt, Katrin Eckermann, Anne Stuendl, Jing Gong, Belisa Russo, Katrin Strauss, Surya Rai, S… , 17 March 2015. - 19 S.
In: Acta neuropathologica, ISSN 1432-0533. 129(2015), 5, Seite 695-713
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Freischmidt, Axel: Serum microRNAs in sporadic amyotrophic lateral sclerosis / Axel Freischmidt, Kathrin Müller, Lisa Zondler, Patrick Weydt, Benjamin Mayer, Christine A. F. von A… , 9 June 2015. - 6 S.
In: Neurobiology of aging, ISSN 1558-1497. 36(2015), 9 vom: Sept., Seite 2660.e15-2660.e20
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Helferich, Anika Marie: α-synuclein interacts with SOD1 and promotes its oligomerization / Anika M. Helferich, Wolfgang P. Ruf, Veselin Grozdanov, Axel Freischmidt, Marisa S. Feiler, Lisa Zon… , 08 December 2015. - 16 S.
In: Molecular neurodegeneration, ISSN 1750-1326. 10(2015), Artikel-ID 66, Seite 1-16
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Feiler, Marisa S.: TDP-43 is intercellularly transmitted across axon terminals / Marisa S. Feiler, Benjamin Strobel, Axel Freischmidt, Anika M. Helferich, Julia Kappel, Bryson M. Br… , November 23, 2015. - 15 S.
In: The journal of cell biology, ISSN 1540-8140. 211(2015), 4, Seite 897-911
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Freischmidt, Axel: Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia / Axel Freischmidt, Thomas Wieland, Benjamin Richter, Wolfgang Ruf, Veronique Schaeffer, Kathrin Mülle… , 24 March 2015. - 6 S.
In: Nature neuroscience, ISSN 1546-1726. 18(2015), 5 vom: Mai, Seite 631-636
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Rizik, Naji: FXN GAA repeat expansions in amyotrophic lateral sclerosis / Naji Rizik, Axel Freischmidt, Albert C. Ludolph, Jochen H. Weishaupt, 27 January 2014. - 4 S.
In: Journal of clinical neuroscience, ISSN 1532-2653. 21(2014), 8, Seite 1319-1322
DOI: 10.1016/j.jocn.2013.10.029
Hübers, Annemarie: Amyotrophe Lateralsklerose : Diagnostik und Therapieoptionen / Annemarie Hübers, Jochen H. Weishaupt und Albert C. Ludolph, Ulm, 2014. - 9 S.
In: Medizinische Monatsschrift für Pharmazeuten. 37(2014), 10, Seite 356-364
Hübers, Annemarie: Polymerase chain reaction and Southern blot-based analysis of the C9orf72 hexanucleotide repeat in different motor neuron diseases / Annemarie Hübers, Nicolai Marroquin, Birgit Schmoll, Stefan Vielhaber, Marlies Just, Benjamin Mayer,… , 2014. - 6 S.
In: Neurobiology of aging, ISSN 1558-1497. Bd. 35.2014, 5, S. 1214.e1-1214.e6
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Krumova, Petranka: Sumoylation in neurodegenerative diseases / Petranka Krumova, Jochen H. Weishaupt, 2013. - 16 S.
In: Cellular and molecular life sciences, ISSN 1420-9071. 70(2013), 12, Seite 2123-2138
DOI: 10.1007/s00018-012-1158-3
Wagner, Jens: Anle138b : a novel oligomer modulator for disease-modifying therapy of neurodegenerative diseases such as prion and Parkinson’s disease / Jens Wagner, Sergey Ryazanov, Andrei Leonov, Johannes Levin, Song Shi, Felix Schmidt, Catharina Prix… , 19 April 2013. - 19 S.
In: Acta neuropathologica, ISSN 1432-0533. 125(2013), 6, Seite 795-813
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Ludolph, Albert C.: Amyotrophic lateral sclerosis / Albert C. Ludolph, Johannes Brettschneider, and Jochen H. Weishaupt, 2012. - 6 S.
In: Current opinion in neurology, ISSN 1473-6551. 25(2012), 5 vom: Okt., Seite 530-535
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Krumova, Petranka: Sumoylation fights “aggregopathies” / Petranka Krumova and Jochen H. Weishaupt, 15 Feb 2012. - 2 S.
In: Cell cycle, ISSN 1551-4005. 11(2012), 4, Seite 641-642
DOI: 10.4161/cc.11.4.19356
Krumova, Petranka: Sumoylation inhibits α-synuclein aggregation and toxicity / Petranka Krumova, Erik Meulmeester, Manuel Garrido, Marilyn Tirard, He-Hsuan Hsiao, Guillaume Bossis… , July 11, 2011. - 12 S.
In: The journal of cell biology, ISSN 1540-8140. 194(2011), 1, Seite 49-60
DOI: 10.1083/jcb.201010117
Weishaupt, Jochen H.: Zyklin-abhängige Kinase 5 und mitochondriale Zelltrodkaskaden bei neurodegenerativen Erkrankungen / Jochen Hans Weishaupt, 2007. - 82 Bl.
Weishaupt, Jochen H.: Untersuchung der neuronalen Glutamatrezeptorexpression im Rattenhirn während der physiologischen Entwicklung und nach Sauerstoff-Glukose- Deprivation / vorgelegt von Jochen Hans Weishaupt, 1999 [ersch.] 2000. - 117 Bl. : graph. Darst.

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