Daniel Darvish

2.0k citations
16 papers · 1.3k indexed · 1 hit paper · h-index 10

Daniel Darvish

16 papers receiving 1.3k citations

Hit Papers

Inclusion body myopathy associated with Paget disease of ...1.0k20042026201120182505007501000

Peers

Daniel Darvish
Comparison fields: 5 of 67
  • Neurology 524
  • Neurology 182
  • Cell Biology 299
  • Genetics 188
  • Physiology 304
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Angèle Nalbandian United States
Noemí de Luna Spain
Sarju Mehta United Kingdom
Helen Griffin United Kingdom
Josep Gámez Spain
Ruud A. Wolterman Netherlands
Ji-Ung Jung United States
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Serena Ghezzi Italy
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Citations per field
00.5×2.9×
Angèle Nalbandian · 1×
Citations per year

Countries citing papers authored by Daniel Darvish

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Darvish

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

16 of 16 papers shown
#Work
1 20137
2 201313
3 201225
4 201113
5 201127
6 201018
7 20092
8 20083
9 200810
10 2007144
11 20067
12 20061
13 20056
14
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing proteinbreakdown →
20041019
15 200219
16 200211

About Daniel Darvish

Daniel Darvish is a scholar working on Nephrology, Genetics, Gastroenterology, Epidemiology and Molecular Biology, having authored 16 papers that have together received 1.3k indexed citations. Recurring topics across this work include Inflammatory Myopathies and Dermatomyositis (11 papers), Muscle Physiology and Disorders (5 papers), Protein Kinase Regulation and GTPase Signaling (3 papers), Chronic Lymphocytic Leukemia Research (3 papers), Glycosylation and Glycoproteins Research (2 papers), Celiac Disease Research and Management (2 papers), Cardiomyopathy and Myosin Studies (2 papers) and Renal Diseases and Glomerulopathies (2 papers). The work is most often cited by research in Neurology (524 citations), Neurology (182 citations), Cell Biology (299 citations), Genetics (188 citations) and Physiology (304 citations). Daniel Darvish has collaborated with scholars based in United States, Canada and Italy. Frequent co-authors include Margaret J. Kovach, Michael P. Whyte, Sarju Mehta, Giles D. Watts, Alan Pestronk, Virginia Kimonis, Steven Mumm, Patricia M. Zerfas, Carla Ciccone and Irini Manoli. Their work appears in journals such as Molecular Genetics and Metabolism, Molecular Therapy, Nature Genetics, American Journal Of Pathology and Journal of Clinical Investigation.

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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