Sabine Purmann

504 total citations
9 papers, 314 citations indexed

About

Sabine Purmann is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Sabine Purmann has authored 9 papers receiving a total of 314 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Sabine Purmann's work include Genetics and Neurodevelopmental Disorders (3 papers), Autism Spectrum Disorder Research (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Sabine Purmann is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Autism Spectrum Disorder Research (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Sabine Purmann collaborates with scholars based in Germany, United States and Italy. Sabine Purmann's co-authors include E. Schwinger, Volker Arolt, Bertram Müller‐Myhsok, Rebekka Lencer, Achim Nolte, Manfred Schürmann, Deniz Kanber, Gabriele Gillessen‐Kaesbach, Karin Buiting and Bernhard Horsthemke and has published in prestigious journals such as Movement Disorders, Human Mutation and European Journal of Human Genetics.

In The Last Decade

Sabine Purmann

9 papers receiving 303 citations

Peers

Sabine Purmann

GENET

MB

PMH

CN

CMN

David H. Kavanagh United Kingdom

Dmitriy Niyazov United States

H. Gurling United Kingdom

M. Plante Canada

Boro Ilievski North Macedonia

M. Rietschel Germany

Outi M. Palo Finland

Miguel Angel Pujana Spain

Stephanie Newton United States

David H. Kavanagh United Kingdom

Sabine Purmann

179 ×1.0

GENET

205 ×1.6

MB

26 ×0.3

PMH

78 ×1.3

CN

61 ×1.2

CMN

Citations per year, relative to Sabine Purmann Sabine Purmann (= 1×) peers David H. Kavanagh

Countries citing papers authored by Sabine Purmann

Since Specialization

Citations

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

Fields of papers citing papers by Sabine Purmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabine Purmann

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

All Works

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9 of 9 papers shown

1.

Beygo, Jasmin, Gabriele Gillessen‐Kaesbach, Beate Albrecht, et al.. (2017). New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome. European Journal of Human Genetics. 25(8). 935–945. 31 indexed citations

2.

Buiting, Karin, Deniz Kanber, José I. Martı́n-Subero, et al.. (2008). Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprintedDLK1/GTL2gene cluster. Human Mutation. 29(9). 1141–1146. 57 indexed citations

3.

Zühlke, Christine, Elizabeth Roeder, Sabine Purmann, et al.. (2007). Homozygous myotonic dystrophy: Clinical findings in two patients and review of the literature. American Journal of Medical Genetics Part A. 143A(17). 2058–2061. 4 indexed citations

4.

Hedrich, Katja, Peter P. Pramstaller, Anja Hiller, et al.. (2005). Premutations in the FMR1 gene as a modifying factor in Parkin‐associated Parkinson's disease?. Movement Disorders. 20(8). 1060–1062. 23 indexed citations

5.

Zühlke, Christine, et al.. (1999). Linkage Disequilibrium and Haplotype Analysis in German Friedreich Ataxia Families. Human Heredity. 49(2). 90–96. 5 indexed citations

6.

Meißner, Bettina, Sabine Purmann, Martin Schürmann, et al.. (1999). hSKCa3. Psychiatric Genetics. 9(2). 91–96. 12 indexed citations

7.

Arolt, Volker, Rebekka Lencer, Sabine Purmann, et al.. (1999). Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia. American Journal of Medical Genetics. 88(6). 603–606. 3 indexed citations

8.

Arolt, Volker, et al.. (1999). Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia. American Journal of Medical Genetics. 88(6). 603–606. 36 indexed citations

9.

Arolt, Volker, Rebekka Lencer, Achim Nolte, et al.. (1996). Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease. American Journal of Medical Genetics. 67(6). 564–579. 143 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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