Karin Buiting

10.8k total citations
121 papers, 6.6k citations indexed

About

Karin Buiting is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Karin Buiting has authored 121 papers receiving a total of 6.6k indexed citations (citations by other indexed papers that have themselves been cited), including 114 papers in Genetics, 100 papers in Molecular Biology and 61 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Karin Buiting's work include Genetic Syndromes and Imprinting (111 papers), Epigenetics and DNA Methylation (86 papers) and Prenatal Screening and Diagnostics (61 papers). Karin Buiting is often cited by papers focused on Genetic Syndromes and Imprinting (111 papers), Epigenetics and DNA Methylation (86 papers) and Prenatal Screening and Diagnostics (61 papers). Karin Buiting collaborates with scholars based in Germany, United States and United Kingdom. Karin Buiting's co-authors include Bernhard Horsthemke, Bärbel Dittrich, Stephanie Groß, Christina Lich, Robert D. Nicholls, Charles A. Williams, Shinji Saitoh, Gabriele Gillessen‐Kaesbach, Michael Zeschnigk and Camilynn I. Brannan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Blood.

In The Last Decade

Karin Buiting

121 papers receiving 6.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karin Buiting Germany 43 5.3k 5.0k 2.6k 325 264 121 6.6k
Jill A. Rosenfeld United States 42 3.6k 0.7× 2.9k 0.6× 1.3k 0.5× 265 0.8× 111 0.4× 174 5.9k
Ian A. Glass United States 36 2.1k 0.4× 2.9k 0.6× 1.1k 0.4× 185 0.6× 110 0.4× 122 4.4k
Sau Wai Cheung United States 47 5.6k 1.1× 3.8k 0.8× 2.2k 0.9× 510 1.6× 211 0.8× 181 7.9k
Lisenka E.L.M. Vissers Netherlands 39 5.1k 1.0× 3.6k 0.7× 943 0.4× 586 1.8× 323 1.2× 98 7.7k
Trilochan Sahoo United States 36 2.8k 0.5× 1.9k 0.4× 1.1k 0.4× 241 0.7× 76 0.3× 67 4.1k
Bert B.A. de Vries Netherlands 39 5.1k 1.0× 3.6k 0.7× 785 0.3× 340 1.0× 225 0.9× 114 7.4k
C.V. Beechey United Kingdom 30 2.6k 0.5× 2.7k 0.5× 1.0k 0.4× 283 0.9× 53 0.2× 90 3.6k
Helger G. Yntema Netherlands 35 2.6k 0.5× 2.7k 0.5× 357 0.1× 346 1.1× 295 1.1× 100 4.9k
Karen Brøndum‐Nielsen Denmark 34 2.0k 0.4× 2.3k 0.5× 485 0.2× 137 0.4× 146 0.6× 137 4.1k
Hilde Van Esch Belgium 40 3.5k 0.7× 3.5k 0.7× 629 0.2× 250 0.8× 91 0.3× 148 5.6k

Countries citing papers authored by Karin Buiting

Since Specialization
Citations

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

Fields of papers citing papers by Karin Buiting

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karin Buiting

This figure shows the co-authorship network connecting the top 25 collaborators of Karin Buiting. A scholar is included among the top collaborators of Karin Buiting 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 Karin Buiting. Karin Buiting 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.
Beygo, Jasmin, et al.. (2021). Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature. Molecular Genetics & Genomic Medicine. 9(10). e1796–e1796. 3 indexed citations
2.
3.
Beygo, Jasmin, Benjamin Kamien, Jill Clayton‐Smith, et al.. (2017). Atypical Angelman syndrome due to a mosaic imprinting defect: Case reports and review of the literature. American Journal of Medical Genetics Part A. 173(3). 753–757. 18 indexed citations
4.
Buiting, Karin, Charles A. Williams, & Bernhard Horsthemke. (2016). Angelman syndrome — insights into a rare neurogenetic disorder. Nature Reviews Neurology. 12(10). 584–593. 242 indexed citations
5.
Mackay, Deborah, Thomas Eggermann, Karin Buiting, et al.. (2015). Multilocus methylation defects in imprinting disorders. BioMolecular Concepts. 6(1). 47–57. 28 indexed citations
6.
Czeschik, Johanna Christina, Peter Bauer, Karin Buiting, et al.. (2013). X-linked intellectual disability type Nascimento is a clinically distinct, probably underdiagnosed entity. Orphanet Journal of Rare Diseases. 8(1). 146–146. 17 indexed citations
7.
Horsthemke, Bernhard & Karin Buiting. (2008). Chapter 8 Genomic Imprinting and Imprinting Defects in Humans. Advances in genetics. 225–246. 49 indexed citations
8.
9.
Horsthemke, Bernhard & Karin Buiting. (2006). Imprinting defects on human chromosome 15. Cytogenetic and Genome Research. 113(1-4). 292–299. 94 indexed citations
10.
Raca, Gordana, Karin Buiting, & Soma Das. (2004). Deletion Analysis of the Imprinting Center Region in Patients with Angelman Syndrome and Prader-Willi Syndrome by Real-Time Quantitative PCR. Genetic Testing. 8(4). 387–394. 9 indexed citations
11.
Runte, Maren, Raymonda Varon, Denise Horn, Bernhard Horsthemke, & Karin Buiting. (2004). Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader?Willi syndrome. Human Genetics. 116(3). 228–230. 78 indexed citations
12.
Buiting, Karin, Stephanie Groß, Christina Lich, et al.. (2003). Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect. The American Journal of Human Genetics. 72(3). 571–577. 208 indexed citations
13.
Lerer, Israela, et al.. (2001). The 28-kb Deletion Spanning D15S63 Is a Polymorphic Variant in the Ashkenazi Jewish Population. The American Journal of Human Genetics. 68(1). 261–263. 4 indexed citations
14.
Buiting, Karin, et al.. (2000). De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch. Nature Genetics. 25(1). 74–78. 125 indexed citations
15.
Buiting, Karin, Bärbel Dittrich, Bernd Dworniczak, et al.. (1999). A 28-kb Deletion Spanning D15S63 (PW71) in Five Families: A Rare Neutral Variant?. The American Journal of Human Genetics. 65(6). 1588–1594. 7 indexed citations
16.
Gault, Judith, Misi Robinson, Ralph Berger, et al.. (1998). Genomic Organization and Partial Duplication of the Human α7 Neuronal Nicotinic Acetylcholine Receptor Gene (CHRNA7). Genomics. 52(2). 173–185. 207 indexed citations
17.
Conroy, Jeffrey M., Theresa A. Grebe, Karen D. Tsuchiya, et al.. (1997). Balanced Translocation 46, XY, t(2;15)(q37.2;q11.2) Associated with Atypical Prader-Willi Syndrome. The American Journal of Human Genetics. 61(2). 388–394. 43 indexed citations
18.
Buiting, Karin, et al.. (1996). A pseudogene for the human ribosomal protein L5 (RPL5P1) maps within an intron of the SNRPN transcription unit on human chromosome 15. Cytogenetic and Genome Research. 75(4). 224–226. 17 indexed citations
19.
Dittrich, Bärbel, Stephanie Groß, Karin Buiting, & Bernhard Horsthemke. (1993). An Ncil RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11 – 13. Human Molecular Genetics. 2(9). 1509–1509. 4 indexed citations
20.
Knoblauch, Hans, et al.. (1992). Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13. Human Genetics. 90(3). 313–5. 171 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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