Bettina E. Mucha

2.6k total citations
18 papers, 1.3k citations indexed

About

Bettina E. Mucha is a scholar working on Molecular Biology, Nephrology and Genetics. According to data from OpenAlex, Bettina E. Mucha has authored 18 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Nephrology and 8 papers in Genetics. Recurrent topics in Bettina E. Mucha's work include Renal Diseases and Glomerulopathies (8 papers), Renal and related cancers (7 papers) and Renal cell carcinoma treatment (3 papers). Bettina E. Mucha is often cited by papers focused on Renal Diseases and Glomerulopathies (8 papers), Renal and related cancers (7 papers) and Renal cell carcinoma treatment (3 papers). Bettina E. Mucha collaborates with scholars based in United States, Germany and Canada. Bettina E. Mucha's co-authors include Friedhelm Hildebrandt, Fatih Özaltın, Bernward Hinkes, K Hasselbacher, Arno Fuchshuber, Rasheed Gbadegesin, Jinhong Liu, Christopher N. Vlangos, Michael Schultheiß and Rainer Ruf and has published in prestigious journals such as PEDIATRICS, Kidney International and Journal of the American Society of Nephrology.

In The Last Decade

Bettina E. Mucha

18 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bettina E. Mucha United States 14 1.0k 665 256 225 216 18 1.3k
Bernward Hinkes Germany 15 871 0.9× 736 1.1× 282 1.1× 434 1.9× 140 0.6× 16 1.4k
Ernie Esquivel United States 11 465 0.5× 672 1.0× 241 0.9× 93 0.4× 604 2.8× 16 1.1k
Svjetlana Lovric Germany 13 387 0.4× 297 0.4× 117 0.5× 118 0.5× 97 0.4× 26 734
Vincent Morinière France 14 497 0.5× 806 1.2× 138 0.5× 97 0.4× 452 2.1× 27 1.3k
Agnieszka Bierżyńska United Kingdom 12 456 0.4× 304 0.5× 111 0.4× 99 0.4× 94 0.4× 20 627
Chang Ying Xing China 4 733 0.7× 453 0.7× 83 0.3× 71 0.3× 191 0.9× 5 987
Jean‐Bernard Palcoux France 8 246 0.2× 168 0.3× 89 0.3× 76 0.3× 83 0.4× 12 585
Shogo Minamikawa Japan 15 159 0.2× 401 0.6× 43 0.2× 48 0.2× 177 0.8× 46 708
Britta George Germany 11 408 0.4× 277 0.4× 41 0.2× 30 0.1× 148 0.7× 20 603
Tomohiro Udagawa Japan 9 184 0.2× 198 0.3× 84 0.3× 66 0.3× 62 0.3× 25 516

Countries citing papers authored by Bettina E. Mucha

Since Specialization
Citations

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

Fields of papers citing papers by Bettina E. Mucha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bettina E. Mucha. 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 Bettina E. Mucha. The network helps show where Bettina E. Mucha may publish in the future.

Co-authorship network of co-authors of Bettina E. Mucha

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

All Works

18 of 18 papers shown
1.
Morgan, Angela, et al.. (2020). Self-limited focal epilepsy and childhood apraxia of speech with WAC pathogenic variants. European Journal of Paediatric Neurology. 30. 25–28. 8 indexed citations
2.
3.
Mucha, Bettina E., Raoul C. M. Hennekam, Sanjay M. Sisodiya, & Philippe M. Campeau. (2015). TBC1D24-Related Disorders. 10 indexed citations
4.
Capo‐Chichi, José‐Mario, Joseph Tcherkezian, Fadi F. Hamdan, et al.. (2013). Disruption of TBC1D7, a subunit of the TSC1-TSC2 protein complex, in intellectual disability and megalencephaly. Journal of Medical Genetics. 50(11). 740–744. 36 indexed citations
5.
Mucha, Bettina E., et al.. (2010). A case report of a patient with Pfeiffer syndrome, an FGRF 2 mutation (Trp290Cys) and unique ocular anterior segment findings. Ophthalmic Genetics. 31(4). 193–195. 10 indexed citations
6.
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
7.
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
8.
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
9.
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
10.
Wolf, Matthias T. F., Bettina E. Mucha, Hans Christian Hennies, et al.. (2006). Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharing. Human Genetics. 119(6). 649–658. 16 indexed citations
11.
Benz, Kerstin, Christian Plank, Kerstin Amann, et al.. (2006). Hypergonadotropic hypogonadism and renal failure due to WT1 mutation. Nephrology Dialysis Transplantation. 21(6). 1716–1718. 4 indexed citations
12.
He, Ning, Alireza Zahirieh, Brian Lee, et al.. (2006). Recessive NPHS2 (Podocin) Mutations Are Rare in Adult-Onset Idiopathic Focal Segmental Glomerulosclerosis. Clinical Journal of the American Society of Nephrology. 2(1). 31–37. 44 indexed citations
13.
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
14.
Ruf, Rainer, Anne Lichtenberger, Stephanie M. Karle, et al.. (2004). Patients with Mutations in NPHS2 (Podocin) Do Not Respond to Standard Steroid Treatment of Nephrotic Syndrome. Journal of the American Society of Nephrology. 15(3). 722–732. 282 indexed citations
15.
Ruf, Rainer, Michael Schultheiß, Anne Lichtenberger, et al.. (2004). Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome. Kidney International. 66(2). 564–570. 89 indexed citations
16.
Schultheiß, Michael, Rainer Ruf, Bettina E. Mucha, et al.. (2004). No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations. Pediatric Nephrology. 19(12). 1340–1348. 39 indexed citations
17.
Wolf, Matthias T. F., Bettina E. Mucha, Massimo Attanasio, et al.. (2003). Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains. Kidney International. 64(5). 1580–1587. 69 indexed citations
18.
Fuchshuber, Arno, Bettina E. Mucha, E. R. Baumgartner, Martin Vollmer, & Friedhelm Hildebrandt. (2000). mut0 methylmalonic acidemia: Eleven novel mutations of the methylmalonyl CoA mutase including a deletion-insertion mutation. Human Mutation. 16(2). 179–179. 29 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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