Caroline Scholz

440 total citations
8 papers, 127 citations indexed

About

Caroline Scholz is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Caroline Scholz has authored 8 papers receiving a total of 127 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Clinical Biochemistry. Recurrent topics in Caroline Scholz's work include Genomic variations and chromosomal abnormalities (4 papers), Genetic Syndromes and Imprinting (2 papers) and BRCA gene mutations in cancer (2 papers). Caroline Scholz is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genetic Syndromes and Imprinting (2 papers) and BRCA gene mutations in cancer (2 papers). Caroline Scholz collaborates with scholars based in Germany, Switzerland and Austria. Caroline Scholz's co-authors include Doris Steinemann, Brigitte Schlegelberger, Bernd Auber, Stephanie Schubert, Thomas Illig, Gunnar Schmidt, Vicente A. Yépez, Norbert Lorenz, Colin Davenport and Mirjana Gušić and has published in prestigious journals such as The American Journal of Human Genetics, International Journal of Cancer and Breast Cancer Research and Treatment.

In The Last Decade

Caroline Scholz

8 papers receiving 124 citations

Peers

Caroline Scholz

MB

GENET

ONCOL

CR

CB

Haley Streff United States

Monika Weisz Hubshman Israel

Jennifer L. Kemppainen United States

Joseph Porrmann Germany

William L. Macken United Kingdom

Theresa Brunet Germany

Mary Koziura United States

Rocío Rius Australia

Yael Wilnai United States

G. C. Chan United Kingdom

Haley Streff United States

Caroline Scholz

100 ×1.2

MB

93 ×1.5

GENET

16 ×1.1

ONCOL

23 ×1.5

CR

10 ×0.7

CB

Citations per year, relative to Caroline Scholz Caroline Scholz (= 1×) peers Haley Streff

Countries citing papers authored by Caroline Scholz

Since Specialization

Citations

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

Fields of papers citing papers by Caroline Scholz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Scholz

This figure shows the co-authorship network connecting the top 25 collaborators of Caroline Scholz. A scholar is included among the top collaborators of Caroline Scholz 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 Caroline Scholz. Caroline Scholz 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

1.

Gušić, Mirjana, Gudrun Schottmann, René G. Feichtinger, et al.. (2019). Bi-Allelic UQCRFS1 Variants Are Associated with Mitochondrial Complex III Deficiency, Cardiomyopathy, and Alopecia Totalis. The American Journal of Human Genetics. 106(1). 102–111. 31 indexed citations

2.

Wappenschmidt, Barbara, Brigitte Pabst, Saki Chan, et al.. (2018). A tandem duplication of BRCA1 exons 1–19 through DHX8 exon 2 in four families with hereditary breast and ovarian cancer syndrome. Breast Cancer Research and Treatment. 172(3). 561–569. 11 indexed citations

3.

Ripperger, Tim, Susanne Morlot, Thomas Illig, et al.. (2018). 12q14 microdeletion syndrome: A family with short stature and Silver-Russell syndrome (SRS)-like phenotype and review of the literature. European Journal of Medical Genetics. 61(8). 421–427. 7 indexed citations

4.

Schubert, Stephanie, Bernd Auber, Gunnar Schmidt, et al.. (2018). The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants. International Journal of Cancer. 144(11). 2683–2694. 41 indexed citations

5.

Scholz, Caroline, Doris Steinemann, Mandy Roy, et al.. (2016). NCAM2 deletion in a boy with macrocephaly and autism: Cause, association or predisposition?. European Journal of Medical Genetics. 59(10). 493–498. 13 indexed citations

6.

Schubert, Stephanie, Cordula Haas, Christine Bärtsch, et al.. (2014). Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland. Molecular and Cellular Probes. 29(1). 31–34. 5 indexed citations

7.

Classen, Carl Friedrich, Vera Riehmer, Christina Landwehr, et al.. (2013). Dissecting the genotype in syndromic intellectual disability using whole exome sequencing in addition to genome-wide copy number analysis. Human Genetics. 132(7). 825–841. 18 indexed citations

8.

Horst, J., Caroline Scholz, & Bernd Dworniczak. (1989). Phenylketonuria identification of a new frequent mutation in the phenylalanine hydroxylase gene. 195. 1 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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