Dorothea Wand

1.2k total citations
9 papers, 78 citations indexed

About

Dorothea Wand is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Dorothea Wand has authored 9 papers receiving a total of 78 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Immunology. Recurrent topics in Dorothea Wand's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), RNA regulation and disease (3 papers) and Chromosomal and Genetic Variations (2 papers). Dorothea Wand is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), RNA regulation and disease (3 papers) and Chromosomal and Genetic Variations (2 papers). Dorothea Wand collaborates with scholars based in Germany, Switzerland and United States. Dorothea Wand's co-authors include Stephanie Spranger, Krystyńa Chrzańowska, Ursula G. Froster, Julie McGaughran, Wiktor Borozdin, Jürgen Kohlhase, Elke Botzenhart, Michael J. Bamshad, Johannes R. Lemke and Albert Schinzel and has published in prestigious journals such as SHILAP Revista de lepidopterología, Muscle & Nerve and Human Mutation.

In The Last Decade

Dorothea Wand

8 papers receiving 73 citations

Peers

Dorothea Wand

MB

EPIDE

GENET

CB

SURGE

Rudel A. Saunders United States

Stasa Stankovic United Kingdom

Gillian L. Dalgliesh United Kingdom

C. Scott Gallagher United States

Karthick Natarajan Germany

Charles M. Krafchak United States

Breana Cham Singapore

Hanwei Jiang China

Michelle Steinraths Canada

Maëlle Givelet France

Rudel A. Saunders United States

Dorothea Wand

74 ×1.3

MB

18 ×0.9

EPIDE

44 ×2.6

GENET

7 ×0.4

CB

12 ×1.2

SURGE

Citations per year, relative to Dorothea Wand Dorothea Wand (= 1×) peers Rudel A. Saunders

Countries citing papers authored by Dorothea Wand

Since Specialization

Citations

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

Fields of papers citing papers by Dorothea Wand

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dorothea Wand

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

Saleh, Christian, et al.. (2020). Fragile-X-Associated Tremor/Ataxia Syndrome or Alcohol-Induced Cerebellar Degeneration? A Case Report. SHILAP Revista de lepidopterología. 12(3). 466–471. 1 indexed citations

2.

Egger, Stefan, et al.. (2020). Fehlerhafte Geschlechtsbestimmung aufgrund partieller Deletion des Y-Chromosoms. Rechtsmedizin. 30(2). 94–100. 1 indexed citations

3.

Weigel, Johannes, et al.. (2013). Low-level hyperinsulinism with hypoglycemic spells in an infant with mosaic Turner syndrome and mild Kabuki-like phenotype: a case report and review of the literature. Journal of Pediatric Endocrinology and Metabolism. 27(1-2). 165–70. 5 indexed citations

4.

Ezgü, Fatih Süheyl, Pavel Krejčı́, J. M. Graham, et al.. (2013). Phenotype–genotype correlations in patients with Marinesco–Sjögren syndrome. Clinical Genetics. 86(1). 74–84. 17 indexed citations

5.

Kornhuber, Malte, Christian Kunze, Dorothea Wand, et al.. (2011). SOX10 mutation with peripheral amyelination and developmental disturbance of axons. Muscle & Nerve. 45(2). 284–290. 8 indexed citations

6.

Wand, Dorothea, Eva Klopocki, Raoul Heller, et al.. (2011). Combined partial trisomy 11q and partial monosomy 10p in a 19‐year‐old female patient: Phenotypic and genotypic findings. American Journal of Medical Genetics Part A. 155(12). 3075–3081. 2 indexed citations

7.

Rüssel, Jörn, et al.. (2009). The 9p24.3 Breakpoint of a Constitutional t(6;9)(p12;p24) in a Patient with Chronic Lymphocytic Leukemia Maps Close to the Putative Promoter Region of the <i>DMRT2 </i>Gene. Cytogenetic and Genome Research. 125(2). 81–86. 1 indexed citations

8.

Borozdin, Wiktor, Michael J. Bamshad, Elke Botzenhart, et al.. (2006). Expanding the spectrum ofTBX5 mutations in Holt-Oram syndrome: detection of two intragenic deletions by quantitative real time PCR, and report of eight novel point mutations. Human Mutation. 27(9). 975–976. 33 indexed citations

9.

Katulski, Krzysztof, S. Bornstein, Maciej Figiel, et al.. (1998). Typical hormonal profiles are accompanied by increased immunoreactivity of theca folliculi steroid 17α-hydroxylase P450 in polycystic ovary syndrome. Journal of Endocrinological Investigation. 21(5). 304–309. 10 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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