Isolde Schreyer

687 total citations
10 papers, 87 citations indexed

About

Isolde Schreyer is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, Isolde Schreyer has authored 10 papers receiving a total of 87 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Plant Science and 4 papers in Molecular Biology. Recurrent topics in Isolde Schreyer's work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (5 papers) and Genomics and Chromatin Dynamics (3 papers). Isolde Schreyer is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (5 papers) and Genomics and Chromatin Dynamics (3 papers). Isolde Schreyer collaborates with scholars based in Germany, Australia and Czechia. Isolde Schreyer's co-authors include Thomas Liehr, S. St‐Pierre, Omri Bar, Kay Wilhelm, Angela Nietzel, Anita Heller, Wolfgang Fiedler, Volkmar Beensen, Anja Weise and Uwe Claussen and has published in prestigious journals such as Journal of Histochemistry & Cytochemistry, Clinical Genetics and Prenatal Diagnosis.

In The Last Decade

Isolde Schreyer

10 papers receiving 85 citations

Peers

Isolde Schreyer

GENET

PPCH

MB

PS

AI

Simon Zwolinski United Kingdom

Françoise Baverel France

Florence Démurger France

A.L. Mosca France

Catherine L. Mercer United Kingdom

Valerie Banks United States

Aldo Bonfante Italy

Elyse Mitchell United States

Emily Aston United States

Vickie Zurcher United States

Simon Zwolinski United Kingdom

Isolde Schreyer

70 ×1.0

GENET

12 ×0.4

PPCH

27 ×0.9

MB

14 ×0.5

PS

0 ×0.0

AI

Citations per year, relative to Isolde Schreyer Isolde Schreyer (= 1×) peers Simon Zwolinski

Countries citing papers authored by Isolde Schreyer

Since Specialization

Citations

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

Fields of papers citing papers by Isolde Schreyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isolde Schreyer

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

All Works

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10 of 10 papers shown

1.

Lengyel, Anna, et al.. (2022). Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes. Molecular Cytogenetics. 15(1). 19–19. 2 indexed citations

2.

Schreyer, Isolde, et al.. (2020). STX1B-related epilepsy in a 24-month-old female infant. Epilepsy & Behavior Reports. 15. 100391–100391. 1 indexed citations

3.

Liehr, Thomas, Isolde Schreyer, Alma Kuechler, et al.. (2018). Parental origin of deletions and duplications – about the necessity to check for cryptic inversions. Molecular Cytogenetics. 11(1). 20–20. 9 indexed citations

4.

Louis, Annie, et al.. (2017). X-autosome and X-Y translocations in female carriers: X-chromosome inactivation easily detectable by 5-ethynyl-2-deoxyuridine (EdU). Balkan Journal of Medical Genetics. 20(1). 87–90. 3 indexed citations

5.

Liehr, Thomas, et al.. (2017). Next generation phenotyping in Emanuel and Pallister‐Killian syndrome using computer‐aided facial dysmorphology analysis of 2D photos. Clinical Genetics. 93(2). 378–381. 35 indexed citations

6.

Tönnies, Holger, Ewa Bocian, Alma Kuechler, et al.. (2007). New Immortalized Cell Lines of Patients With Small Supernumerary Marker Chromosome. Journal of Histochemistry & Cytochemistry. 55(6). 651–660. 11 indexed citations

7.

Schreyer, Isolde, Volkmar Beensen, Karl‐Heinz Eichhorn, et al.. (2005). Dup(13)(q14.2-q14.3): Yet Another New Differential Diagnostic Aspect for Short Stature–like Phenotype. Journal of Histochemistry & Cytochemistry. 53(3). 365–366. 1 indexed citations

8.

Starke, Heike, Isolde Schreyer, Wolfgang Fiedler, et al.. (1999). Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8. Prenatal Diagnosis. 19(12). 1169–1174. 2 indexed citations

9.

Starke, Heike, Isolde Schreyer, Wolfgang Fiedler, et al.. (1999). Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8. Prenatal Diagnosis. 19(12). 1169–1174. 17 indexed citations

10.

Caspi, E, Isolde Schreyer, Peter Schreyer, Z. Weinraub, & I Tamir. (1975). Amniotic fluid volume, total phospholipids concentratio, and L/S ratio in term pregnancies.. PubMed. 46(5). 584–7. 6 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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