Doris Wöhrle

783 total citations
8 papers, 619 citations indexed

About

Doris Wöhrle is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Doris Wöhrle has authored 8 papers receiving a total of 619 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Cognitive Neuroscience. Recurrent topics in Doris Wöhrle's work include Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Doris Wöhrle is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Doris Wöhrle collaborates with scholars based in Germany, Netherlands and Poland. Doris Wöhrle's co-authors include Peter Steinbach, Walther Vogel, H. Hameister, Antonella Manca, W. Vogel, K. Schiebel, Gudrun Rappold, Birgit Weiß, Walter Just and Gotthold Barbi and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Doris Wöhrle

8 papers receiving 606 citations

Peers

Countries citing papers authored by Doris Wöhrle

Since Specialization

Citations

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

Fields of papers citing papers by Doris Wöhrle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Doris Wöhrle

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

All Works

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8 of 8 papers shown

#	Work	Indexed citations
1	Does proximal myotonic myopathy show anticipation? 2008 ·Human Mutation ·Bernd Kruse, Doris Wöhrle, Peter Steinbach, Andreas Gal	5
2	Demethylation, Reactivation, and Destabilization of Human Fragile X Full-Mutation Alleles in Mouse Embryocarcinoma Cells 2001 ·The American Journal of Human Genetics ·Doris Wöhrle, (unknown), H. Hameister, W. Vogel, Peter Steinbach	110
3	Mitotic behavior of expanded CGG repeats studied on cultured cells: Further evidence for methylation‐mediated triplet repeat stability in fragile X syndrome 1999 ·American Journal of Medical Genetics ·Dieter Gläser, Doris Wöhrle, (unknown), Walther Vogel, Peter Steinbach, (unknown)	2
4	Characterization of FMR1 Promoter Elements by In Vivo-Footprinting Analysis 1997 ·The American Journal of Human Genetics ·Sabine Schwemmle, Esther de Graaff, Heidrun L. Deissler, Dieter Gläser, Doris Wöhrle, Ingo Kennerknecht, Walter Just, Ben A. Oostra, Walter Dörfler, (unknown), Peter Steinbach	48
5	A human pseudoautosomal gene, ADP/ATP translocase, escapes X–inactivation whereas a homologue on Xq is subject to X–inactivation 1993 ·Nature Genetics ·K. Schiebel, Birgit Weiß, Doris Wöhrle, Gudrun Rappold	68
6	Enhanced expression of the murine FMR1 gene during germ cell proliferation suggests a special function in both the male and the female gonad 1993 ·Human Molecular Genetics ·D. Bächner, Antonella Manca, (unknown), Doris Wöhrle, Walter Just, (unknown), H. Hameister, (unknown)	93
7	Mitotic stability of fragile X mutations in differentiated cells indicates early post–conceptional trinucleotide repeat expansion 1993 ·Nature Genetics ·Doris Wöhrle, (unknown), Walther Vogel, Peter Steinbach	153
8	A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome. 1992 ·PubMed ·Doris Wöhrle, Dieter Kotzot, Mark C. Hirst, Antonella Manca, Bernhard Korn, A. Schmidt, Gotthold Barbi, H. Rott, Annemarie Poustka, Kay E. Davies	140

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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