Florian Erger

907 total citations
24 papers, 230 citations indexed

About

Florian Erger is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Florian Erger has authored 24 papers receiving a total of 230 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Genetics and 4 papers in Nephrology. Recurrent topics in Florian Erger's work include Renal and related cancers (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic and Kidney Cyst Diseases (4 papers). Florian Erger is often cited by papers focused on Renal and related cancers (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic and Kidney Cyst Diseases (4 papers). Florian Erger collaborates with scholars based in Germany, United States and United Kingdom. Florian Erger's co-authors include Bodo B. Beck, Sander F. Garrelfs, Jaap W. Groothoff, Thomas J. Neuhaus, Graham Lipkin, Hessel Peters‐Sengers, Brigitte Adams, Pierre Cochat, Sally‐Anne Hulton and U. Gembruch and has published in prestigious journals such as Kidney International, Hypertension and Nephrology Dialysis Transplantation.

In The Last Decade

Florian Erger

21 papers receiving 218 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Florian Erger Germany	7	139	81	81	56	44	24	230
LeeLee Chu Canada	8	281 2.0×	70 0.9×	77 1.0×	34 0.6×	70 1.6×	10	341
Patrick R. van den Berg Netherlands	8	240 1.7×	62 0.8×	54 0.7×	34 0.6×	20 0.5×	8	303
Karen Ouyang United States	7	113 0.8×	35 0.4×	143 1.8×	36 0.6×	16 0.4×	17	244
Philip L. Beales United Kingdom	7	102 0.7×	48 0.6×	152 1.9×	18 0.3×	32 0.7×	8	263
Harini Ramalingam United States	8	223 1.6×	34 0.4×	114 1.4×	29 0.5×	19 0.4×	9	279
Marijn F. Stokman Netherlands	10	271 1.9×	15 0.2×	222 2.7×	37 0.7×	57 1.3×	15	360
Xingbo Cheng China	7	167 1.2×	19 0.2×	148 1.8×	9 0.2×	58 1.3×	21	295
Lihua Dong China	5	218 1.6×	49 0.6×	49 0.6×	12 0.2×	12 0.3×	9	311
Jeannine Basta United States	8	247 1.8×	53 0.7×	43 0.5×	8 0.1×	21 0.5×	10	303
Adam C. Gunning United Kingdom	7	179 1.3×	14 0.2×	151 1.9×	27 0.5×	11 0.3×	12	291

Countries citing papers authored by Florian Erger

Since Specialization

Citations

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

Fields of papers citing papers by Florian Erger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florian Erger

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

All Works

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20 of 20 papers shown

Aryal, Rajindra P., Cristina Bucci, Jamie Heimburg‐Molinaro, et al.. (2025). C1GALT1C1 ‐Associated Mosaic Disorder of Glycosylation in a Female. Journal of Inherited Metabolic Disease. 48(2). e70006–e70006.

Habbig, Sandra, Hanna Dêbiec, Dirk L. Stippel, et al.. (2025). Anti-nephrin antibodies guide living donor kidney transplantation in a pediatric patient with primary focal segmental glomerular sclerosis. Kidney International. 108(2). 321–327.

Kaufeld, Jessica, Lucas Kühne, Ulf Schönermarck, et al.. (2024). Features of Postpartum Hemorrhage-Associated Thrombotic Microangiopathy and Role of Short-Term Complement Inhibition. Kidney International Reports. 9(4). 919–928. 2 indexed citations

Erger, Florian, et al.. (2024). Biallelic Variants in LRRC45 Impair Ciliogenesis and Cause a Severe Neurological Disorder. Clinical Genetics. 107(3). 311–322.

Aryal, Rajindra P., Maxence Noël, Junwei Zeng, et al.. (2024). Cosmc regulates O-glycan extension in murine hepatocytes. Glycobiology. 34(10). 2 indexed citations

Arjune, Sita, Ron T. Gansevoort, Stephan J. L. Bakker, et al.. (2023). Copeptin in autosomal dominant polycystic kidney disease: real-world experiences from a large prospective cohort study. Clinical Kidney Journal. 16(11). 2194–2204. 6 indexed citations

Tschernoster, Nikolai, Florian Erger, Patrick R. Walsh, et al.. (2022). Unraveling Structural Rearrangements of the CFH Gene Cluster in Atypical Hemolytic Uremic Syndrome Patients Using Molecular Combing and Long-Fragment Targeted Sequencing. Journal of Molecular Diagnostics. 24(6). 619–631. 5 indexed citations

Wenzel, Andrea, Florian Erger, Julika Borde, et al.. (2022). A Low-Cost Sequencing Platform for Rapid Genotyping in ADPKD and its Impact on Clinical Care. Kidney International Reports. 8(3). 455–466. 2 indexed citations

Erger, Florian & Bodo B. Beck. (2021). A new era of treatment for primary hyperoxaluria type 1. Nature Reviews Nephrology. 17(9). 573–574. 6 indexed citations

10.

Fabretti, Francesca, Nikolai Tschernoster, Florian Erger, et al.. (2021). Expanding the Spectrum of FAT1 Nephropathies by Novel Mutations That Affect Hippo Signaling. Kidney International Reports. 6(5). 1368–1378. 10 indexed citations

11.

Netzer, Christian, et al.. (2021). Carrier testing for autosomal recessive disorders: a look at current practice in Germany. Medizinische Genetik. 33(1). 13–19. 2 indexed citations

12.

Elgizouli, Magdeldin, Jasmin Beygo, Florian Erger, et al.. (2020). The adult phenotype of Schaaf-Yang syndrome. Orphanet Journal of Rare Diseases. 15(1). 294–294. 19 indexed citations

13.

Taylan, Christina, Andrea Wenzel, Florian Erger, et al.. (2020). Case Report: Exome Sequencing Reveals LRBA Deficiency in a Patient With End-Stage Renal Disease. Frontiers in Pediatrics. 8. 42–42. 1 indexed citations

14.

Erger, Florian, Sandra Habbig, Michael S. Wiesener, et al.. (2020). cfNOMe — A single assay for comprehensive epigenetic analyses of cell-free DNA. Genome Medicine. 12(1). 54–54. 40 indexed citations

15.

Sikora, Przemysław, Marcin Zaniew, Ryszard Grenda, et al.. (2020). Still diagnosed too late and under-recognized? A first comprehensive report on primary hyperoxaluria from Poland. Polskie Archiwum Medycyny Wewnętrznej. 130(12). 1053–1063. 6 indexed citations

16.

Erger, Florian, Christine Skerka, Andrea Wenzel, et al.. (2020). Long-term data on two sisters with C3GN due to an identical, homozygous CFH mutation and autoantibodies. Clinical Nephrology. 94(4). 197–206. 1 indexed citations

17.

Erger, Florian, Christian P. Schaaf, & Christian Netzer. (2019). Which genes to assess in the NGS diagnostics of intellectual disability? The case for a consensus database-driven and expert-curated approach. Molecular and Cellular Probes. 45. 84–88. 2 indexed citations

18.

Garrelfs, Sander F., Gill Rumsby, Hessel Peters‐Sengers, et al.. (2019). Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up. Kidney International. 96(6). 1389–1399. 68 indexed citations

19.

Erger, Florian, et al.. (2018). Uniparental isodisomy as a cause of recessive Mendelian disease: a diagnostic pitfall with a quick and easy solution in medium/large NGS analyses. European Journal of Human Genetics. 26(9). 1392–1395. 9 indexed citations

20.

Erger, Florian, Nadina Ortiz Brüchle, U. Gembruch, & Klaus Zerres. (2017). Prenatal ultrasound, genotype, and outcome in a large cohort of prenatally affected patients with autosomal-recessive polycystic kidney disease and other hereditary cystic kidney diseases. Archives of Gynecology and Obstetrics. 295(4). 897–906. 18 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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