Conrad C. Weihl

8.1k total citations
100 papers, 4.0k citations indexed

About

Conrad C. Weihl is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Epidemiology. According to data from OpenAlex, Conrad C. Weihl has authored 100 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 31 papers in Cellular and Molecular Neuroscience and 26 papers in Epidemiology. Recurrent topics in Conrad C. Weihl's work include Muscle Physiology and Disorders (35 papers), Genetic Neurodegenerative Diseases (26 papers) and Endoplasmic Reticulum Stress and Disease (16 papers). Conrad C. Weihl is often cited by papers focused on Muscle Physiology and Disorders (35 papers), Genetic Neurodegenerative Diseases (26 papers) and Endoplasmic Reticulum Stress and Disease (16 papers). Conrad C. Weihl collaborates with scholars based in United States, United Kingdom and Germany. Conrad C. Weihl's co-authors include Alan Pestronk, Hemmo Meyer, Jeong-Sun Ju, Phyllis I. Hanson, Virginia Kimonis, Robert H. Baloh, Sara Miller, Glenn Lopate, Peyker Temız and Sara K. Pittman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Conrad C. Weihl

94 papers receiving 3.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Conrad C. Weihl United States 36 2.4k 1.1k 1.0k 1.0k 736 100 4.0k
Ingo Kurth Germany 31 1.6k 0.7× 838 0.7× 221 0.2× 790 0.8× 730 1.0× 110 3.5k
Steven L. Carroll United States 35 1.4k 0.6× 319 0.3× 960 0.9× 342 0.3× 1.2k 1.7× 105 3.8k
Yoko Aoki Japan 36 2.9k 1.2× 562 0.5× 546 0.5× 214 0.2× 253 0.3× 170 4.8k
Heidi Scrable United States 31 2.3k 1.0× 297 0.3× 318 0.3× 607 0.6× 290 0.4× 51 4.6k
Eiichi Tani Japan 31 1.4k 0.6× 604 0.5× 898 0.9× 232 0.2× 498 0.7× 123 3.2k
Cornelius F. Boerkoel United States 34 2.4k 1.0× 325 0.3× 292 0.3× 181 0.2× 899 1.2× 129 4.2k
John F. Staropoli United States 18 975 0.4× 498 0.4× 569 0.5× 260 0.3× 266 0.4× 29 2.0k
Angela Pyle United Kingdom 36 2.6k 1.1× 241 0.2× 470 0.5× 199 0.2× 699 0.9× 90 3.4k
Joel S. Pachter United States 39 1.5k 0.6× 640 0.6× 243 0.2× 161 0.2× 394 0.5× 76 3.7k
Pasquale A. Cancilla United States 32 1.3k 0.5× 303 0.3× 519 0.5× 357 0.3× 518 0.7× 102 3.5k

Countries citing papers authored by Conrad C. Weihl

Since Specialization
Citations

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

Fields of papers citing papers by Conrad C. Weihl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Conrad C. Weihl. 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 Conrad C. Weihl. The network helps show where Conrad C. Weihl may publish in the future.

Co-authorship network of co-authors of Conrad C. Weihl

This figure shows the co-authorship network connecting the top 25 collaborators of Conrad C. Weihl. A scholar is included among the top collaborators of Conrad C. Weihl based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Conrad C. Weihl. Conrad C. Weihl is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Weller, Shaun G., et al.. (2025). An ethanol-induced loss of the lipid droplet–associated segregase VCP/p97 leads to hepatic steatosis. The Journal of Cell Biology. 224(8).
2.
Inoue, Michio & Conrad C. Weihl. (2025). Myofibrillar myopathy: towards a mechanism-based definition as a Z-disk-opathy. Current Opinion in Neurology. 38(5). 513–523.
3.
Inoue, Michio, Divya Jayaraman, Rocío Bengoechea, et al.. (2024). Genotype‒phenotype correlation in recessive DNAJB4 myopathy. Acta Neuropathologica Communications. 12(1). 171–171. 4 indexed citations
4.
Robinson, Sarah, Andrew R. Findlay, Jil Daw, et al.. (2024). Elevated VCP ATPase Activity Correlates With Disease Onset in Multisystem Proteinopathy-1. Neurology Genetics. 10(5). e200191–e200191.
5.
Lynch, Eileen M., Sara K. Pittman, Jil Daw, et al.. (2024). Seeding-competent TDP-43 persists in human patient and mouse muscle. Science Translational Medicine. 16(775). eadp5730–eadp5730. 6 indexed citations
6.
Alfano, Lindsay N., Jordi Díaz‐Manera, Linda Lowes, et al.. (2024). Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD study. BMC Neurology. 24(1). 96–96.
7.
Paulo, João A., Jiang Zhu, Christoph S. Clemen, et al.. (2023). The p97-UBXD8 complex regulates ER-Mitochondria contact sites by altering membrane lipid saturation and composition. Nature Communications. 14(1). 638–638. 28 indexed citations
8.
Li, Chun, et al.. (2023). O07 RAN translation of expanded CGG repeat in LRP12 may contribute to oculopharyngodistal myopathy. Neuromuscular Disorders. 33. S129–S129. 2 indexed citations
9.
Findlay, Andrew R., May M. Paing, Jil Daw, et al.. (2023). DNAJB6 isoform specific knockdown: Therapeutic potential for limb girdle muscular dystrophy D1. Molecular Therapy — Nucleic Acids. 32. 937–948. 4 indexed citations
10.
Pfeffer, Gerald, et al.. (2022). Multisystem Proteinopathy Due to VCP Mutations: A Review of Clinical Heterogeneity and Genetic Diagnosis. Genes. 13(6). 963–963. 28 indexed citations
11.
Dowling, James J., Conrad C. Weihl, & Melissa J. Spencer. (2021). Molecular and cellular basis of genetically inherited skeletal muscle disorders. Nature Reviews Molecular Cell Biology. 22(11). 713–732. 67 indexed citations
12.
Palmio, Johanna, Per Harald Jonson, Michio Inoue, et al.. (2019). Mutations in the J domain of DNAJB6 cause dominant distal myopathy. Neuromuscular Disorders. 30(1). 38–46. 22 indexed citations
13.
Pajusalu, Sander, Nicole J. Lake, Geyu Zhou, et al.. (2019). Estimating prevalence for limb-girdle muscular dystrophy based on public sequencing databases. Genetics in Medicine. 21(11). 2512–2520. 57 indexed citations
14.
Cabrera‐Serrano, Macarena, Reimar Junckerstorff, Alan Pestronk, et al.. (2017). Cystinosis distal myopathy, novel clinical, pathological and genetic features. Neuromuscular Disorders. 27(9). 873–878. 7 indexed citations
15.
Evangelista, Teresinha, Conrad C. Weihl, Virginia Kimonis, et al.. (2016). 215th ENMC International Workshop VCP-related multi-system proteinopathy (IBMPFD) 13–15 November 2015, Heemskerk, The Netherlands. Neuromuscular Disorders. 26(8). 535–547. 29 indexed citations
16.
Jerath, Nivedita U., Steven A. Moore, Michael E. Shy, et al.. (2015). Rare Manifestation of a c.290 C>T, p.Gly97GluVCPMutation. SHILAP Revista de lepidopterología. 2015. 1–5. 16 indexed citations
17.
Bengoechea, Rocío, Shaughn Bell, Jieya Shao, et al.. (2013). Prion-like nuclear aggregation of TDP-43 during heat shock is regulated by HSP40/70 chaperones. Human Molecular Genetics. 23(1). 157–170. 98 indexed citations
18.
Fuentealba, Rodrigo A., Jayne Marasa, Marc I. Diamond, David Piwnica‐Worms, & Conrad C. Weihl. (2011). An aggregation sensing reporter identifies leflunomide and teriflunomide as polyglutamine aggregate inhibitors. Human Molecular Genetics. 21(3). 664–680. 26 indexed citations
19.
Temız, Peyker, Conrad C. Weihl, & Alan Pestronk. (2008). Inflammatory myopathies with mitochondrial pathology and protein aggregates. Journal of the Neurological Sciences. 278(1-2). 25–29. 77 indexed citations
20.
Weihl, Conrad C., et al.. (2000). Adenoviral Gene Transfer of Nitric Oxide Synthase Increases Cerebral Blood Flow in Rats. Neurosurgery. 47(5). 1206–1215. 21 indexed citations

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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