Bernward Hinkes

3.4k total citations
16 papers, 1.4k citations indexed

About

Bernward Hinkes is a scholar working on Molecular Biology, Nephrology and Genetics. According to data from OpenAlex, Bernward Hinkes has authored 16 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Nephrology and 4 papers in Genetics. Recurrent topics in Bernward Hinkes's work include Renal Diseases and Glomerulopathies (9 papers), Renal and related cancers (7 papers) and Renal cell carcinoma treatment (3 papers). Bernward Hinkes is often cited by papers focused on Renal Diseases and Glomerulopathies (9 papers), Renal and related cancers (7 papers) and Renal cell carcinoma treatment (3 papers). Bernward Hinkes collaborates with scholars based in Germany, United States and Türkiye. Bernward Hinkes's co-authors include Christopher N. Vlangos, Friedhelm Hildebrandt, Fatih Özaltın, Rasheed Gbadegesin, Bettina E. Mucha, K Hasselbacher, Jinhong Liu, Saskia F. Heeringa, Martin Zenker and Friedhelm Hildebrandt and has published in prestigious journals such as PLoS ONE, PEDIATRICS and Kidney International.

In The Last Decade

Bernward Hinkes

16 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bernward Hinkes Germany 15 871 736 434 282 144 16 1.4k
Laura Massella Italy 17 1.3k 1.5× 560 0.8× 397 0.9× 366 1.3× 65 0.5× 42 1.8k
Bettina E. Mucha United States 14 1.0k 1.2× 665 0.9× 225 0.5× 256 0.9× 179 1.2× 18 1.3k
Ulla Lenkkeri Finland 9 2.4k 2.7× 1.5k 2.0× 227 0.5× 417 1.5× 266 1.8× 9 2.8k
Stephen Tonna Australia 13 603 0.7× 609 0.8× 156 0.4× 94 0.3× 95 0.7× 18 1.3k
Svjetlana Lovric Germany 13 387 0.4× 297 0.4× 118 0.3× 117 0.4× 82 0.6× 26 734
Mary Donnelly United Kingdom 10 709 0.8× 414 0.6× 123 0.3× 156 0.6× 67 0.5× 10 1.2k
Géraldine Mollet France 15 367 0.4× 538 0.7× 82 0.2× 124 0.4× 54 0.4× 24 1.0k
Julia Hoefele Germany 18 347 0.4× 1.1k 1.5× 87 0.2× 200 0.7× 46 0.3× 65 1.5k
Vincent Morinière France 14 497 0.6× 806 1.1× 97 0.2× 138 0.5× 47 0.3× 27 1.3k
Paul Newey United Kingdom 18 460 0.5× 335 0.5× 70 0.2× 50 0.2× 43 0.3× 39 1.8k

Countries citing papers authored by Bernward Hinkes

Since Specialization
Citations

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

Fields of papers citing papers by Bernward Hinkes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernward Hinkes

This figure shows the co-authorship network connecting the top 25 collaborators of Bernward Hinkes. A scholar is included among the top collaborators of Bernward Hinkes 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 Bernward Hinkes. Bernward Hinkes is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Prokosch, Hans‐Ulrich, Bernward Hinkes, Antje Neubert, et al.. (2019). User-Centered Development of an Online Platform for Drug Dosing Recommendations in Pediatrics. Applied Clinical Informatics. 10(4). 570–579. 11 indexed citations
2.
Hinkes, Bernward, Karl F. Hilgers, Hanno J. Bolz, et al.. (2012). A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathy. BMC Nephrology. 13(1). 27–27. 29 indexed citations
3.
Hoff, Katja von, Bernward Hinkes, André O. von Bueren, et al.. (2011). Frequency, Risk‐Factors and Survival of Children With Atypical Teratoid Rhabdoid Tumors (AT/RT) of the CNS Diagnosed between 1988 and 2004, and Registered to the German HIT Database. Pediatric Blood & Cancer. 57(6). 978–985. 95 indexed citations
4.
Heeringa, Saskia F., Clemens Möller, Jianyang Du, et al.. (2009). A Novel TRPC6 Mutation That Causes Childhood FSGS. PLoS ONE. 4(11). e7771–e7771. 125 indexed citations
5.
Hoff, Katja von, Bernward Hinkes, Nicolas U. Gerber, et al.. (2009). Long-term outcome and clinical prognostic factors in children with medulloblastoma treated in the prospective randomised multicentre trial HIT‘91. European Journal of Cancer. 45(7). 1209–1217. 134 indexed citations
6.
Chernin, Gil, Saskia F. Heeringa, Rasheed Gbadegesin, et al.. (2008). Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome. Pediatric Nephrology. 23(9). 1455–1460. 36 indexed citations
7.
Hinkes, Bernward, Christopher N. Vlangos, Saskia F. Heeringa, et al.. (2008). Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome. Journal of the American Society of Nephrology. 19(2). 365–371. 84 indexed citations
8.
Heeringa, Saskia F., Christopher N. Vlangos, Gil Chernin, et al.. (2008). Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome. Nephrology Dialysis Transplantation. 23(11). 3527–3533. 56 indexed citations
9.
10.
Gbadegesin, Rasheed, Bernward Hinkes, Christopher N. Vlangos, et al.. (2007). Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome. Pediatric Nephrology. 22(4). 509–513. 33 indexed citations
11.
Gbadegesin, Rasheed, Bernward Hinkes, Bethan E. Hoskins, et al.. (2007). Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS). Nephrology Dialysis Transplantation. 23(4). 1291–1297. 99 indexed citations
12.
Kneitz, Susanne, Camelia‐Maria Monoranu, Stefan Rutkowski, et al.. (2007). Ependymoma gene expression profiles associated with histological subtype, proliferation, and patient survival. Acta Neuropathologica. 113(3). 325–337. 79 indexed citations
13.
Hinkes, Bernward, Bettina E. Mucha, Christopher N. Vlangos, et al.. (2007). Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (NPHS1, NPHS2, WT1, and LAMB2). PEDIATRICS. 119(4). e907–e919. 276 indexed citations
14.
Mucha, Bettina E., Fatih Özaltın, Bernward Hinkes, et al.. (2006). Mutations in the Wilms' Tumor 1 Gene Cause Isolated Steroid Resistant Nephrotic Syndrome and Occur in Exons 8 and 9. Pediatric Research. 59(2). 325–331. 88 indexed citations
15.
Hasselbacher, K, Roger C. Wiggins, Verena Matejas, et al.. (2006). Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders. Kidney International. 70(6). 1008–1012. 136 indexed citations
16.
Hinkes, Bernward, Katja von Hoff, Frank Deinlein, et al.. (2006). Childhood pineoblastoma: experiences from the prospective multicenter trials HIT-SKK87, HIT-SKK92 and HIT91. Journal of Neuro-Oncology. 81(2). 217–223. 33 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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