Detlef Trost

604 total citations
20 papers, 346 citations indexed

About

Detlef Trost is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Detlef Trost has authored 20 papers receiving a total of 346 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Detlef Trost's work include Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (4 papers) and Acute Myeloid Leukemia Research (3 papers). Detlef Trost is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (4 papers) and Acute Myeloid Leukemia Research (3 papers). Detlef Trost collaborates with scholars based in France, Germany and Canada. Detlef Trost's co-authors include Brigitte Royer‐Pokora, Barbara Hildebrandt, Franz Theuring, Frauke Leenders, Hans‐Dieter Royer, Ellen Fietze, Stephan Bergmann, Manfred Dietel, Karsten Jürchott and Ralf C. Bargou and has published in prestigious journals such as Cancer Research, International Journal of Cancer and Human Mutation.

In The Last Decade

Detlef Trost

18 papers receiving 341 citations

Peers

Detlef Trost

GENET

ONCOL

PPCH

Ephrem Chin United States

Josef Davidsson Sweden

Lisa M Niswander United States

Bela Patel United States

Marco Garieri Switzerland

Lori Jukofsky United States

Chantal Farra Lebanon

Ji Yoo Kim Japan

Ebtesam Abdalla Egypt

Jürgen Groet United Kingdom

Ephrem Chin United States

Detlef Trost

256 ×1.1

155 ×1.3

GENET

25 ×0.5

ONCOL

26 ×0.5

PPCH

55 ×1.4

Citations per year, relative to Detlef Trost Detlef Trost (= 1×) peers Ephrem Chin

Countries citing papers authored by Detlef Trost

Since Specialization

Citations

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

Fields of papers citing papers by Detlef Trost

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Detlef Trost

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

Trost, Detlef, et al.. (2024). Gnathodiaphyseal dysplasia: Diagnostic clues from two fetal cases and literature review. Prenatal Diagnosis. 44(9). 1098–1104. 2 indexed citations

Benazra, Marion, Pascale Kleinfinger, Mylène Valduga, et al.. (2024). Optical genome mapping identifies a homozygous deletion in the non-coding region of the SCN9A gene in individuals from the same family with congenital insensitivity to pain. Frontiers in Genetics. 15. 1375770–1375770.

Rigonnot, Luc, et al.. (2024). The First Fetal Case of Shwachman-Diamond Syndrome Mimicking Vascular Growth Restriction. Pediatric and Developmental Pathology. 27(6). 603–607. 1 indexed citations

Volk, Valery, Bernd Auber, Detlef Trost, et al.. (2023). Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families. Acta Neuropathologica Communications. 11(1). 184–184. 2 indexed citations

Chevarin, Martin, Antonio Vitobello, Cyril Fournier, et al.. (2022). A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort. European Journal of Human Genetics. 31(7). 761–768. 6 indexed citations

Kleinfinger, Pascale, Armelle Luscan, Detlef Trost, et al.. (2022). Case Report: How whole-genome sequencing-based cell-free DNA prenatal testing can help identify a marker mhromosome. Frontiers in Genetics. 13. 926290–926290.

Kleinfinger, Pascale, Armelle Luscan, Stéphane Serero, et al.. (2022). Noninvasive Prenatal Screening for Trisomy 21 in Patients with a Vanishing Twin. Genes. 13(11). 2027–2027. 5 indexed citations

Feger, Claire, Vincent Laugel, Denys Chaigne, et al.. (2021). Pathogenic variants in KCNQ2 cause intellectual deficiency without epilepsy: Broadening the phenotypic spectrum of a potassium channelopathy. American Journal of Medical Genetics Part A. 185(6). 1803–1815. 12 indexed citations

Ebstein, Frédéric, Geoffroy Delplancq, Stéphane Auvin, et al.. (2020). Report of the first patient with a homozygous OTUD7A variant responsible for epileptic encephalopathy and related proteasome dysfunction. Clinical Genetics. 97(4). 567–575. 18 indexed citations

10.

Kleinfinger, Pascale, Armelle Luscan, Detlef Trost, et al.. (2020). Strategy for Use of Genome-Wide Non-Invasive Prenatal Testing for Rare Autosomal Aneuploidies and Unbalanced Structural Chromosomal Anomalies. Journal of Clinical Medicine. 9(8). 2466–2466. 18 indexed citations

11.

Bris, Céline, Vincent Procaccio, Patrizia Amati‐Bonneau, et al.. (2019). Deciphering exome sequencing data: Bringing mitochondrial DNA variants to light. Human Mutation. 40(12). 2430–2443. 7 indexed citations

12.

Plaisancié, Julie, Pascale Kleinfinger, Claude Cancès, et al.. (2014). Constitutional chromoanasynthesis: description of a rare chromosomal event in a patient. European Journal of Medical Genetics. 57(10). 567–570. 28 indexed citations

13.

Hoischen, Alexander, Christina Landwehr, Xiaoqi Ding, et al.. (2009). Array-CGH in unclear syndromic nephropathies identifies a microdeletion in Xq22.3-q23. Pediatric Nephrology. 24(9). 1673–1681. 8 indexed citations

14.

Trost, Detlef, Rolf Fimmers, Jörg Felsberg, et al.. (2007). Identification of genomic aberrations associated with shorter overall survival in patients with oligodendroglial tumors. International Journal of Cancer. 120(11). 2368–2376. 31 indexed citations

15.

Trost, Detlef, et al.. (2006). Molecular cytogenetic profiling of complex karyotypes in primary myelodysplastic syndromes and acute myeloid leukemia. Cancer Genetics and Cytogenetics. 165(1). 51–63. 18 indexed citations

16.

Prott, Eva‐Christina, Detlef Trost, Alexander Hoischen, et al.. (2006). Towards mapping phenotypical traits in 18p− syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation. European Journal of Human Genetics. 15(1). 35–44. 37 indexed citations

17.

Royer‐Pokora, Brigitte, et al.. (2006). Delineation by molecular cytogenetics of 5q deletion breakpoints in myelodyplastic syndromes and acute myeloid leukemia. Cancer Genetics and Cytogenetics. 167(1). 66–69. 6 indexed citations

18.

Bergmann, Stephan, Brigitte Royer‐Pokora, Ellen Fietze, et al.. (2005). YB-1 Provokes Breast Cancer through the Induction of Chromosomal Instability That Emerges from Mitotic Failure and Centrosome Amplification. Cancer Research. 65(10). 4078–4087. 120 indexed citations

19.

Schwanitz, Gesa, et al.. (2004). New trends in chromosomal investigation in children with cardiovascular malformations. Cardiology in the Young. 14(6). 622–629. 13 indexed citations

20.

Trost, Detlef, et al.. (2003). Hidden chromosomal aberrations are rare in primary myelodysplastic syndromes with evolution to acute myeloid leukaemia and normal cytogenetics. Leukemia Research. 28(2). 171–177. 14 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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