Gertrud Eckstein

3.8k total citations · 1 hit paper
24 papers, 1.6k citations indexed

About

Gertrud Eckstein is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Gertrud Eckstein has authored 24 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Cell Biology. Recurrent topics in Gertrud Eckstein's work include Genetic Associations and Epidemiology (5 papers), Genomics and Rare Diseases (3 papers) and Skin and Cellular Biology Research (3 papers). Gertrud Eckstein is often cited by papers focused on Genetic Associations and Epidemiology (5 papers), Genomics and Rare Diseases (3 papers) and Skin and Cellular Biology Research (3 papers). Gertrud Eckstein collaborates with scholars based in Germany, Austria and Israel. Gertrud Eckstein's co-authors include Tim M. Strom, Bettina Lorenz‐Depiereux, Tobias Freilinger, Michael Pusch, Jürgen Herzog, Arn M. J. M. van den Maagdenberg, Saskia Biskup, Michel D. Ferrari, Elena Babini and Martin Dichgans and has published in prestigious journals such as The Lancet, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Gertrud Eckstein

24 papers receiving 1.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

2005 614 citations Martin Dichgans, Tobias Freilinger et al. The Lancet profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gertrud Eckstein Germany	15	556	543	432	229	223	24	1.6k
Francesco Nicita Italy	23	288 0.5×	412 0.8×	343 0.8×	99 0.4×	8 0.0×	94	1.3k
Isabel Alonso Portugal	24	197 0.4×	889 1.6×	218 0.5×	61 0.3×	25 0.1×	76	1.6k
Ella Zeldich United States	19	93 0.2×	438 0.8×	447 1.0×	126 0.6×	485 2.2×	35	1.4k
Scott C. Supowit United States	28	182 0.3×	639 1.2×	183 0.4×	126 0.6×	12 0.1×	52	1.7k
Angela J. Villar United States	13	108 0.2×	738 1.4×	736 1.7×	21 0.1×	47 0.2×	21	1.9k
Jungho Cha South Korea	23	134 0.2×	346 0.6×	59 0.1×	27 0.1×	43 0.2×	57	1.2k
Kenneth Silver Canada	18	311 0.6×	326 0.6×	108 0.3×	76 0.3×	8 0.0×	32	1.0k
Gabriel Rusanescu United States	12	55 0.1×	454 0.8×	74 0.2×	46 0.2×	73 0.3×	14	1.1k
Francesca Moro Italy	25	212 0.4×	700 1.3×	469 1.1×	281 1.2×	8 0.0×	50	1.7k
Jon Andresen United States	14	34 0.1×	331 0.6×	79 0.2×	70 0.3×	139 0.6×	23	919

Countries citing papers authored by Gertrud Eckstein

Since Specialization

Citations

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

Fields of papers citing papers by Gertrud Eckstein

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gertrud Eckstein

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

All Works

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20 of 20 papers shown

Rost, Nicolas, Gertrud Eckstein, Susann Sauer, et al.. (2024). Huntingtin CAG repeat size variations below the Huntington’s disease threshold: associations with depression, anxiety and basal ganglia structure. European Journal of Human Genetics. 33(5). 624–632. 1 indexed citations

Almeida, Gustavo P. de, Peter Lichtner, Gertrud Eckstein, et al.. (2022). Human skin-resident host T cells can persist long term after allogeneic stem cell transplantation and maintain recirculation potential. Science Immunology. 7(67). eabe2634–eabe2634. 31 indexed citations

Brunet, Theresa, Riccardo Berutti, Veronika Dill, et al.. (2022). Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. Human Molecular Genetics. 31(14). 2386–2395. 4 indexed citations

Vural, Seçil, Martina Baumgartner, Peter Lichtner, et al.. (2021). Investigation of gamma secretase gene complex mutations in German population with Hidradenitis suppurativa designate a complex polygenic heritage. Journal of the European Academy of Dermatology and Venereology. 35(6). 1386–1392. 12 indexed citations

Nath, Neetika, Lars Kaderali, Karin Klingel, et al.. (2020). Stimulation of soluble guanylyl cyclase (sGC) by riociguat attenuates heart failure and pathological cardiac remodelling. British Journal of Pharmacology. 179(11). 2430–2442. 26 indexed citations

Krenn, Martin, Ivan Milenković, Gertrud Eckstein, et al.. (2019). Adult-onset variant ataxia-telangiectasia diagnosed by exome and cDNA sequencing. Neurology Genetics. 5(4). e346–e346. 3 indexed citations

Wagner, Matias, Riccardo Berutti, Bettina Lorenz‐Depiereux, et al.. (2019). Mitochondrial DNA mutation analysis from exome sequencing—A more holistic approach in diagnostics of suspected mitochondrial disease. Journal of Inherited Metabolic Disease. 42(5). 909–917. 45 indexed citations

Umair, Muhammad, Gertrud Eckstein, Günther Rudolph, et al.. (2017). Homozygous XYLT2 variants as a cause of spondyloocular syndrome. Clinical Genetics. 93(4). 913–918. 24 indexed citations

Giehl, Kathrin, Thomas Herzinger, Hans Wolff, et al.. (2015). Eight Novel Mutations Confirm the Role of AAGAB in Punctate Palmoplantar Keratoderma Type 1 (Buschke-Fischer-Brauer) and Show Broad Phenotypic Variability. Acta Dermato Venereologica. 96(4). 468–472. 13 indexed citations

10.

Hadchouel, Alice, Thomas Wieland, Matthias Griese, et al.. (2015). Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island. The American Journal of Human Genetics. 96(5). 826–831. 76 indexed citations

11.

Smida, Jan, et al.. (2015). Genomic Heterogeneity of Osteosarcoma - Shift from Single Candidates to Functional Modules. PLoS ONE. 10(4). e0123082–e0123082. 27 indexed citations

12.

Mehta, Divya, Katharina Heim, Christian Herder, et al.. (2012). Impact of common regulatory single-nucleotide variants on gene expression profiles in whole blood. European Journal of Human Genetics. 21(1). 48–54. 25 indexed citations

13.

Giehl, Kathrin, Gertrud Eckstein, Sandra M. Pasternack, et al.. (2012). Nonsense Mutations in AAGAB Cause Punctate Palmoplantar Keratoderma Type Buschke-Fischer-Brauer. The American Journal of Human Genetics. 91(4). 754–759. 41 indexed citations

14.

Giehl, Kathrin, Michael A. Rogers, Antonellá Tosti, et al.. (2008). Pili annulati: refinement of the locus on chromosome 12q24.33 to a 2·9-Mb interval and candidate gene analysis. British Journal of Dermatology. 160(3). 527–533. 6 indexed citations

15.

Lorenz‐Depiereux, Bettina, Anna Benet‐Pagès, Gertrud Eckstein, et al.. (2006). Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3. The American Journal of Human Genetics. 78(2). 193–201. 252 indexed citations

16.

Dichgans, Martin, Tobias Freilinger, Gertrud Eckstein, et al.. (2005). Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. The Lancet. 366(9483). 371–377. 614 indexed citations breakdown →

17.

Giehl, Kathrin, Gertrud Eckstein, Anna Benet‐Pagès, et al.. (2004). A Gene Locus Responsible for the Familial Hair Shaft Abnormality Pili Annulati Maps to Chromosome 12q24.32–24.33. Journal of Investigative Dermatology. 123(6). 1073–1077. 10 indexed citations

18.

Schwab, Sibylle G., Joachim Hallmayer, Margot Albus, et al.. (2000). A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6. Molecular Psychiatry. 5(6). 638–649. 131 indexed citations

19.

Nürnberger, John I., Tatiana Foroud, Gertrud Eckstein, et al.. (1999). Chromosome 6 workshop report. American Journal of Medical Genetics. 88(3). 233–238. 32 indexed citations

20.

Schwab, Sibylle G., Gertrud Eckstein, Joachim Hallmayer, et al.. (1997). Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis. Molecular Psychiatry. 2(2). 156–160. 119 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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