Birgit Budde

2.2k total citations
21 papers, 743 citations indexed

About

Birgit Budde is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Birgit Budde has authored 21 papers receiving a total of 743 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Cell Biology. Recurrent topics in Birgit Budde's work include Connective tissue disorders research (4 papers), Retinal Development and Disorders (4 papers) and Cellular transport and secretion (3 papers). Birgit Budde is often cited by papers focused on Connective tissue disorders research (4 papers), Retinal Development and Disorders (4 papers) and Cellular transport and secretion (3 papers). Birgit Budde collaborates with scholars based in Germany, Belgium and Switzerland. Birgit Budde's co-authors include Peter Nürnberg, Uwe Kornak, Anna Rajab, Stefan Mundlos, Janine Altmüller, Wolfgang Berger, Dirk J. Lefeber, Aikaterini Dimopoulou, Zsolt Urbán and Wim Annaert and has published in prestigious journals such as Nature Genetics, PLoS ONE and Annals of Neurology.

In The Last Decade

Birgit Budde

20 papers receiving 738 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Birgit Budde Germany 14 544 175 139 108 105 21 743
Christelle Etard Germany 15 756 1.4× 238 1.4× 156 1.1× 73 0.7× 157 1.5× 21 909
Odile Bronchain France 15 621 1.1× 159 0.9× 125 0.9× 75 0.7× 68 0.6× 28 778
Bruce Micales United States 12 817 1.5× 165 0.9× 77 0.6× 60 0.6× 91 0.9× 14 951
Wendy M. Aartsen Netherlands 13 574 1.1× 100 0.6× 153 1.1× 167 1.5× 95 0.9× 16 815
Ann E. Davidson United States 15 842 1.5× 335 1.9× 334 2.4× 93 0.9× 96 0.9× 24 1.0k
P. Daubas France 9 689 1.3× 120 0.7× 103 0.7× 92 0.9× 118 1.1× 18 873
Petra Jakobs United States 20 1.2k 2.2× 252 1.4× 163 1.2× 83 0.8× 458 4.4× 33 1.6k
Tatsuaki Kurosaki United States 13 1.1k 2.0× 211 1.2× 62 0.4× 92 0.9× 68 0.6× 24 1.3k
Zhaoxia Sun United States 10 1.0k 1.9× 251 1.4× 396 2.8× 49 0.5× 66 0.6× 16 1.3k
Mingyan Fang China 17 615 1.1× 282 1.6× 139 1.0× 177 1.6× 38 0.4× 49 1.2k

Countries citing papers authored by Birgit Budde

Since Specialization
Citations

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

Fields of papers citing papers by Birgit Budde

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Birgit Budde

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

All Works

20 of 20 papers shown
1.
Alidousty, Christina, A Becker, Elke Binot, et al.. (2023). Frequency and functional characterization of fusion genes in squamous cell carcinoma of the lung. Gene. 895. 148018–148018. 1 indexed citations
2.
Budde, Birgit, Muhammad Tariq, Zafar Ali, et al.. (2021). A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family. Genes. 12(10). 1494–1494. 4 indexed citations
3.
Budde, Birgit, Janine Altmüller, Susanne Motameny, et al.. (2020). Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss. Clinical Genetics. 98(1). 32–42. 24 indexed citations
4.
Budde, Birgit, Nataliya Di Donato, Hanno J. Bolz, et al.. (2019). First confirmatory study on PTPRQ as an autosomal dominant non-syndromic hearing loss gene. Journal of Translational Medicine. 17(1). 351–351. 12 indexed citations
5.
Gerth‐Kahlert, Christina, Marc Töteberg‐Harms, Amit K. Tiwari, et al.. (2018). Absence of Goniodysgenesis in Patients with Chromosome 13Q Microdeletion-Related Microcoria. Ophthalmology Glaucoma. 1(2). 145–147. 4 indexed citations
6.
Khan, Arif O., Birgit Budde, Peter Nürnberg, et al.. (2017). Genome‐wide linkage and sequence analysis challenge CCDC66 as a human retinal dystrophy candidate gene and support a distinct NMNAT1‐related fundus phenotype. Clinical Genetics. 93(1). 149–154. 13 indexed citations
7.
Stumpf, Maria, Ilyas Ahmad, Sarah Fischer, et al.. (2016). CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly. Molecular Genetics and Genomics. 292(2). 365–383. 18 indexed citations
8.
Budde, Birgit, Shuji Mizumoto, Christian Becker, et al.. (2015). Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3. Human Genetics. 134(7). 691–704. 25 indexed citations
9.
Désir, Julie, Naseebullah Kakar, Thomas D. Mueller, et al.. (2015). A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasia. Orphanet Journal of Rare Diseases. 10(1). 84–84. 16 indexed citations
10.
Altmüller, Janine, Birgit Budde, & Peter Nürnberg. (2013). Enrichment of target sequences for next-generation sequencing applications in research and diagnostics. Biological Chemistry. 395(2). 231–237. 32 indexed citations
11.
Knoblauch, Hans, Christian Geier, Stephanie Adams, et al.. (2009). Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation. Annals of Neurology. 67(1). 136–140. 43 indexed citations
12.
Kornak, Uwe, Hans Christian Hennies, Johannes Egerer, et al.. (2009). Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a novel RAB-6 interacting golgin. Bone. 44. S232–S232. 1 indexed citations
13.
Puk, Oliver, Claudia Dalke, Dian Soewarto, et al.. (2008). Mutation in a Novel Connexin-like Gene ( Gjf1 ) in the Mouse Affects Early Lens Development and Causes a Variable Small-Eye Phenotype. Investigative Ophthalmology & Visual Science. 49(4). 1525–1525. 23 indexed citations
14.
Kornak, Uwe, Ellen Reynders, Aikaterini Dimopoulou, et al.. (2008). Mutations in the a2-subunit of the v-type H+-ATPase impair Golgi function and cause a novel congenital disorder of glycosylation with cutix laxa. Medizinische Genetik. 20(1).
15.
Leroy, Bart P., Birgit Budde, Mariana Wittmer, et al.. (2008). A common NYX mutation in Flemish patients with X linked CSNB. British Journal of Ophthalmology. 93(5). 692–696. 17 indexed citations
16.
Rajab, Anna, Uwe Kornak, Birgit Budde, et al.. (2008). Geroderma osteodysplasticum hereditaria and wrinkly skin syndrome in 22 patients from Oman. American Journal of Medical Genetics Part A. 146A(8). 965–976. 26 indexed citations
17.
Kornak, Uwe, Ellen Reynders, Aikaterini Dimopoulou, et al.. (2007). Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2. Nature Genetics. 40(1). 32–34. 259 indexed citations
18.
Budde, Birgit, Priska Binner, Stephan Waldmüller, et al.. (2007). Noncompaction of the Ventricular Myocardium Is Associated with a De Novo Mutation in the β-Myosin Heavy Chain Gene. PLoS ONE. 2(12). e1362–e1362. 98 indexed citations
19.
Streichert, Thomas, Birgit Budde, Peter Nürnberg, et al.. (2006). Genes from Chagas Susceptibility Loci That Are Differentially Expressed in T. cruzi-Resistant Mice Are Candidates Accounting for Impaired Immunity. PLoS ONE. 1(1). e57–e57. 9 indexed citations
20.
Budde, Birgit, Silke Feil, Sergej Skosyrski, et al.. (2006). Structural and Functional Abnormalities of Retinal Ribbon Synapses due toCacna2d4Mutation. Investigative Ophthalmology & Visual Science. 47(8). 3523–3523. 103 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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