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Eugen Widmeier

Affiliation : Boston Children's Hospital

1Publications (affiliation in the United States)
50Total publications
2352Citations
23h-index

Research profile

Eugen Widmeier has 1 indexed publication (2017). Their work appears in “Nature Genetics”. Their most cited article, “Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly” (2017), has been cited 220 times. Their work is co-authored with at least 12 researchers, including institutions in South Korea, Singapore, Iran.

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Research areas

Renal Diseases and Glomerulopathies
Renal and related cancers
Genomics and Rare Diseases
COVID-19 Clinical Research Studies
Mechanical Circulatory Support Devices

Publications (1)

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
2017 · Nature Genetics · cited 220 times

Collaborations

Partner institutions : Harvard University · Baylor College of Medicine · Yale University · Massachusetts Institute of Technology · Massachusetts General Hospital

Co-authors’ countries : South Korea · Singapore · Iran

Co-authors

Bibliographic data from OpenAlex (open database).