Julia Hoefele

4.6k citations
65 papers · 1.5k · h-index 18

Impact in

  • Nephrology top 2%
    • Renal Diseases and Glomerulopathies
  • Genetics top 2%
    • Genetic and Kidney Cyst Diseases
    • Genetic Syndromes and Imprinting

Papers in

    • Renal and related cancers 30
    • Genetic and Kidney Cyst Diseases 17
    • Genomics and Rare Diseases 8
    • Coagulation, Bradykinin, Polyphosphates, and Angioedema 6
    • Genetic Syndromes and Imprinting 5

Julia Hoefele

58 papers receiving 1.5k citations

Peers

Julia Hoefele
Comparison fields: 5 of 73
  • Nephrology 347
  • Genetics 975
  • Immunology and Allergy 153
  • Molecular Biology 1.1k
  • Pediatrics, Perinatology and Child Health 290
Replace Géraldine Mollet with:
Géraldine Mollet France
Anita Leys Belgium
Christelle Arrondel France
Alberto Turco Italy
Albert D. Kim United States
Ryuji Fukuzawa Japan
Natalya Kaverina United States
Colin G. Miles United Kingdom
Bernward Hinkes Germany
Chiara Bacchelli United Kingdom
Julia Hoefele relative to Géraldine Mollet France Géraldine Mollet's profile →
Citations per field
00.5×3.3×
Géraldine Mollet · 1×
Citations per year

Countries citing papers authored by Julia Hoefele

Since Specialization
Citations

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

Fields of papers citing papers by Julia Hoefele

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 65 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2003244
2 2011161
3 2002153
4 2007105
5 201885
6 201585
7 201183
8 201165
9 200546
10 200239
11 201633
12 202030
13 201028
14 201327
15 202220
16 201118
17 202017
18 201317
19 201517
20 200415

About Julia Hoefele

Julia Hoefele is a scholar working on Molecular Biology, Genetics, Nephrology, Immunology and Allergy and Pediatrics, Perinatology and Child Health, having authored 65 papers that have together received 1.5k indexed citations. Recurring topics across this work include Renal and related cancers (30 papers), Renal Diseases and Glomerulopathies (20 papers), Genetic and Kidney Cyst Diseases (17 papers), Cell Adhesion Molecules Research (12 papers), Genomics and Rare Diseases (8 papers), Pediatric Urology and Nephrology Studies (7 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (6 papers) and Genetic Syndromes and Imprinting (5 papers). The work is most often cited by research in Nephrology (347 citations), Genetics (975 citations), Immunology and Allergy (153 citations), Molecular Biology (1.1k citations) and Pediatrics, Perinatology and Child Health (290 citations). Julia Hoefele has collaborated with scholars based in Germany, United States and France. Frequent co-authors include Edgar A. Otto, Friedhelm Hildebrandt, Matthias T. F. Wolf, Ralf Sudbrak, Corinne Antignac, Lutz T. Weber, Hanns‐Georg Klein, Carsten Bergmann, Richard Reinhardt and Heymut Omran. Their work appears in journals such as Pediatric Nephrology, Gene, Nephrology Dialysis Transplantation, European Journal of Human Genetics and Frontiers in Pediatrics.

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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