Bettina Lipkowitz

1.8k total citations
6 papers, 383 citations indexed

About

Bettina Lipkowitz is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Bettina Lipkowitz has authored 6 papers receiving a total of 383 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Clinical Biochemistry. Recurrent topics in Bettina Lipkowitz's work include RNA modifications and cancer (2 papers), Genetic Syndromes and Imprinting (2 papers) and RNA Research and Splicing (2 papers). Bettina Lipkowitz is often cited by papers focused on RNA modifications and cancer (2 papers), Genetic Syndromes and Imprinting (2 papers) and RNA Research and Splicing (2 papers). Bettina Lipkowitz collaborates with scholars based in Germany, United States and Iran. Bettina Lipkowitz's co-authors include Hans‐Hilger Ropers, Christine Steinhoff, Ulrike A. Nuber, Ralph Schulz, Ulf Gurok, Constance Scharff, Adrian Bird, Jacky Guy, Tim Roloff and Megan C. Holmes and has published in prestigious journals such as Journal of Neuroscience, Human Molecular Genetics and PLoS Genetics.

In The Last Decade

Bettina Lipkowitz

6 papers receiving 380 citations

Peers

Bettina Lipkowitz

MB

GENET

CN

DN

CMN

Ilaria Chiaradia United Kingdom

Liron Abuhatzira United States

Amy B. Wilfert United States

Ábel Vértesy Austria

Sui Yu China

Laëtitia Lambert France

Caroline Nava France

Victoria Harrison United Kingdom

Shino Shimada Japan

Ilaria Chiaradia United Kingdom

Bettina Lipkowitz

245 ×0.8

MB

68 ×0.4

GENET

60 ×1.0

CN

57 ×1.4

DN

79 ×2.0

CMN

Citations per year, relative to Bettina Lipkowitz Bettina Lipkowitz (= 1×) peers Ilaria Chiaradia

Countries citing papers authored by Bettina Lipkowitz

Since Specialization

Citations

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

Fields of papers citing papers by Bettina Lipkowitz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bettina Lipkowitz

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

All Works

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6 of 6 papers shown

1.

Lipkowitz, Bettina, et al.. (2019). Two isoforms of the RAC-specific guanine nucleotide exchange factor TIAM2 act oppositely on transmission ratio distortion by the mouse t-haplotype. PLoS Genetics. 15(2). e1007964–e1007964. 19 indexed citations

2.

Musante, Luciana, Kimia Kahrizi, Masoud Garshasbi, et al.. (2017). Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability. Human Mutation. 38(6). 621–636. 47 indexed citations

3.

Stehr, Henning, Masoud Garshasbi, Hao Hu, et al.. (2013). A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family. American Journal of Medical Genetics Part A. 161(8). 1915–1922. 17 indexed citations

4.

Nuber, Ulrike A., Skirmantas Kriaučionis, Tim Roloff, et al.. (2005). Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome. Human Molecular Genetics. 14(15). 2247–2256. 150 indexed citations

5.

Gurok, Ulf, Christine Steinhoff, Bettina Lipkowitz, et al.. (2004). Gene Expression Changes in the Course of Neural Progenitor Cell Differentiation. Journal of Neuroscience. 24(26). 5982–6002. 97 indexed citations

6.

Singh, Umashankar, Teruhiko Wakayama, Jun Ohgane, et al.. (2004). Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutation. Developmental Dynamics. 230(1). 149–164. 53 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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