Sabine M. Klauck

17.3k total citations
36 papers, 1.8k citations indexed

About

Sabine M. Klauck is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Sabine M. Klauck has authored 36 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 22 papers in Cognitive Neuroscience and 15 papers in Molecular Biology. Recurrent topics in Sabine M. Klauck's work include Genetics and Neurodevelopmental Disorders (22 papers), Autism Spectrum Disorder Research (22 papers) and Genomic variations and chromosomal abnormalities (9 papers). Sabine M. Klauck is often cited by papers focused on Genetics and Neurodevelopmental Disorders (22 papers), Autism Spectrum Disorder Research (22 papers) and Genomic variations and chromosomal abnormalities (9 papers). Sabine M. Klauck collaborates with scholars based in Germany, United Kingdom and United States. Sabine M. Klauck's co-authors include Annemarie Poustka, Kim S. Beyer, Eftichia Duketis, Fritz Poustka, Christine M. Freitag, Regina Waltes, Anthony P. Monaco, Anthony Bailey, Wouter Staal and Gabriele Schmötzer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Sabine M. Klauck

36 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sabine M. Klauck Germany 22 996 849 746 302 173 36 1.8k
Patrice L. Whitehead United States 21 842 0.8× 722 0.9× 798 1.1× 281 0.9× 180 1.0× 41 1.8k
Guiqing Cai United States 22 747 0.8× 504 0.6× 717 1.0× 214 0.7× 221 1.3× 37 1.9k
Philip J. Ebert United States 22 634 0.6× 571 0.7× 1.1k 1.5× 454 1.5× 131 0.8× 36 2.3k
Yuji Kajiwara United States 22 747 0.8× 636 0.7× 997 1.3× 367 1.2× 93 0.5× 46 2.2k
Pamela Sklar United States 8 1.3k 1.3× 587 0.7× 735 1.0× 223 0.7× 199 1.2× 8 1.9k
Jonathan Picker United States 24 1.3k 1.3× 670 0.8× 1.0k 1.3× 223 0.7× 145 0.8× 47 2.1k
Amanda Mitchell United States 23 591 0.6× 341 0.4× 1.3k 1.8× 248 0.8× 128 0.7× 59 2.3k
Lorenzo Sinibaldi Italy 20 509 0.5× 414 0.5× 447 0.6× 284 0.9× 290 1.7× 46 1.5k
B. A. Oostra Netherlands 35 2.1k 2.1× 999 1.2× 1.9k 2.5× 422 1.4× 204 1.2× 72 3.7k
Jennifer Reichert United States 15 1.5k 1.5× 1.6k 1.8× 869 1.2× 190 0.6× 256 1.5× 17 2.3k

Countries citing papers authored by Sabine M. Klauck

Since Specialization
Citations

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

Fields of papers citing papers by Sabine M. Klauck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sabine M. Klauck. 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 Sabine M. Klauck. The network helps show where Sabine M. Klauck may publish in the future.

Co-authorship network of co-authors of Sabine M. Klauck

This figure shows the co-authorship network connecting the top 25 collaborators of Sabine M. Klauck. A scholar is included among the top collaborators of Sabine M. Klauck 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 Sabine M. Klauck. Sabine M. Klauck 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.
2.
Waltes, Regina, Sabine M. Klauck, Eftichia Duketis, et al.. (2020). Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder. Translational Psychiatry. 10(1). 215–215. 12 indexed citations
3.
Waltes, Regina, Eftichia Duketis, Michael Knapp, et al.. (2014). Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders. Human Genetics. 133(6). 781–792. 51 indexed citations
4.
Chiocchetti, Andreas G., Marnie Kopp, Regina Waltes, et al.. (2014). Variants of the CNTNAP2 5′ promoter as risk factors for autism spectrum disorders: a genetic and functional approach. Molecular Psychiatry. 20(7). 839–849. 37 indexed citations
5.
Chiocchetti, Andreas G. & Sabine M. Klauck. (2011). Genetische Analysen zur Identifizierung molekularer Mechanismen bei Autismus-Spektrum-Störungen. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie. 39(2). 101–111. 1 indexed citations
6.
Holt, Richard, Gabrielle Barnby, Elena Maestrini, et al.. (2010). Linkage and candidate gene studies of autism spectrum disorders in European populations. European Journal of Human Genetics. 18(9). 1013–1019. 64 indexed citations
7.
Felder, Bärbel, Bernhard Radlwimmer, Axel Benner, et al.. (2009). FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome. American Journal of Medical Genetics Part A. 149A(5). 952–959. 30 indexed citations
8.
Freitag, Christine M., Wouter Staal, Sabine M. Klauck, Eftichia Duketis, & Regina Waltes. (2009). Genetics of autistic disorders: review and clinical implications. European Child & Adolescent Psychiatry. 19(3). 169–178. 140 indexed citations
9.
Klauck, Sabine M., Bärbel Felder, Anja Kolb‐Kokocinski, et al.. (2006). Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism. Molecular Psychiatry. 11(12). 1073–1084. 78 indexed citations
10.
Michaelovsky, Elena, Amos Frisch, Dan J. Stein, et al.. (2005). Haplotype analysis of the COMT‐ARVCF gene region in Israeli anorexia nervosa family trios. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 139B(1). 45–50. 18 indexed citations
11.
Beyer, Kim S., Francesca Blasi, Elena Bacchelli, et al.. (2002). Mutation analysis of the coding sequence of the MECP2 gene in infantile autism. Human Genetics. 111(4-5). 305–309. 67 indexed citations
12.
Klauck, Sabine M., Susan Lindsay, Kim S. Beyer, et al.. (2002). A Mutation Hot Spot for Nonspecific X-Linked Mental Retardation in the MECP2 Gene Causes the PPM-X Syndrome. The American Journal of Human Genetics. 70(4). 1034–1037. 102 indexed citations
13.
Beyer, Kim S., Sabine M. Klauck, Axel Benner, Fritz Poustka, & Annemarie Poustka. (2001). Association studies of the HOPA dodecamer duplication variant in different subtypes of autism. American Journal of Medical Genetics. 114(1). 110–115. 16 indexed citations
14.
Hallmayer, Joachim, Laura J. Bierut, T.J. Crow, et al.. (1999). Chromosomes 1, 2, and 7 workshop. American Journal of Medical Genetics. 88(3). 219–223. 10 indexed citations
15.
Paterson, Andrew D., Lynn E. DeLisi, Stephen V. Faraone, et al.. (1999). Sixth World Congress of Psychiatric Genetics X chromosome workshop. American Journal of Medical Genetics. 88(3). 279–286. 22 indexed citations
16.
Klauck, Sabine M., Ewald Münstermann, D. Rühl, et al.. (1997). Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients. Human Genetics. 100(2). 224–229. 36 indexed citations
17.
Klauck, Sabine M., et al.. (1997). A Gene in Human Chromosome Band Xq28 (GABRE) Defines a Putative New Subunit Class of the GABAANeurotransmitter Receptor. Genomics. 45(1). 1–10. 53 indexed citations
18.
Heiss, Nina S., Gernot Glöeckner, Dietmar Bächner, et al.. (1997). Genomic Structure of a Novel LIM Domain Gene (ZNF185) in Xq28 and Comparisons with the Orthologous Murine Transcript. Genomics. 43(3). 329–338. 27 indexed citations
19.
Kioschis, Petra, Ute C. Rogner, Sabine M. Klauck, et al.. (1996). A 900-kb Cosmid Contig and 10 New Transcripts within the Candidate Region for Myotubular Myopathy (MTM1). Genomics. 33(3). 365–373. 22 indexed citations
20.
Klauck, Sabine M., Jeanne B. Lawrence, John A. McNeil, et al.. (1994). Cytogenetic and fluorescence in situ hybridization studies on sporadic and hereditary tumors associated with von Hippel-Lindau syndrome (VHL). Cancer Genetics and Cytogenetics. 77(1). 1–13. 13 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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