André E. Minoche

4.8k total citations · 3 hit papers
34 papers, 2.2k citations indexed

About

André E. Minoche is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, André E. Minoche has authored 34 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 14 papers in Plant Science and 11 papers in Genetics. Recurrent topics in André E. Minoche's work include Chromosomal and Genetic Variations (11 papers), Genomics and Phylogenetic Studies (8 papers) and Genomics and Rare Diseases (6 papers). André E. Minoche is often cited by papers focused on Chromosomal and Genetic Variations (11 papers), Genomics and Phylogenetic Studies (8 papers) and Genomics and Rare Diseases (6 papers). André E. Minoche collaborates with scholars based in Australia, Germany and Spain. André E. Minoche's co-authors include Heinz Himmelbauer, Juliane C. Dohm, Bernd Weißhaar, Daniela Holtgräwe, Thomas Rosleff Sörensen, Falk Zakrzewski, Mark J. Cowley, Thomas Kraft, Marcel E. Dinger and Alexander Goesmann and has published in prestigious journals such as Nature, Nature Medicine and Journal of the American College of Cardiology.

In The Last Decade

André E. Minoche

34 papers receiving 2.1k 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.

The genome of the recently domesticated crop plant sugar beet (Beta vulgaris)

2013 478 citations Juliane C. Dohm, André E. Minoche et al. profile →
Evaluation of genomic high-throughput sequencing data generated on Illumina HiSeq and Genome Analyzer systems

2011 448 citations André E. Minoche, Juliane C. Dohm et al. Genome biology profile →
Identification of a mutation in the extracellular domain of the Epidermal Growth Factor Receptor conferring cetuximab resistance in colorectal cancer

2012 367 citations André E. Minoche, Heinz Himmelbauer et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
André E. Minoche Australia	22	1.1k	742	416	319	244	34	2.2k
Bo Ding China	30	1.7k 1.5×	1.3k 1.8×	402 1.0×	231 0.7×	324 1.3×	117	3.5k
Jie Xu United States	27	1.4k 1.2×	462 0.6×	554 1.3×	209 0.7×	161 0.7×	117	2.6k
Chew Yee Ngan United States	28	1.9k 1.7×	599 0.8×	211 0.5×	634 2.0×	497 2.0×	47	2.9k
Jun Zhu China	21	783 0.7×	274 0.4×	460 1.1×	192 0.6×	340 1.4×	183	1.9k
Yi Pan China	28	1.4k 1.2×	282 0.4×	310 0.7×	171 0.5×	398 1.6×	76	2.5k
Eleanor Howe United States	7	1.4k 1.2×	558 0.8×	180 0.4×	166 0.5×	306 1.3×	9	2.4k
Rolf H. A. M. Vossen Netherlands	23	1.4k 1.3×	289 0.4×	497 1.2×	83 0.3×	278 1.1×	50	2.2k
Jaime A. Castro-Mondragón France	14	2.6k 2.3×	528 0.7×	470 1.1×	193 0.6×	581 2.4×	20	3.5k
Gabriel Mazzucchelli Belgium	29	1.2k 1.1×	269 0.4×	280 0.7×	197 0.6×	398 1.6×	97	2.7k

Countries citing papers authored by André E. Minoche

Since Specialization

Citations

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

Fields of papers citing papers by André E. Minoche

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by André E. Minoche. 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 André E. Minoche. The network helps show where André E. Minoche may publish in the future.

Co-authorship network of co-authors of André E. Minoche

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Torpy, James, Geoffrey McCowage, Sarah E. Woodfield, et al.. (2023). Quantitative ctDNA Detection in Hepatoblastoma: Implications for Precision Medicine. Cancers. 16(1). 12–12. 2 indexed citations

Davis, Ryan L., Kishore R. Kumar, Clare Puttick, et al.. (2022). Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis. Neurology. 99(7). e730–e742. 32 indexed citations

Nash, Benjamin M., Alan Ma, Gladys Ho, et al.. (2022). Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies. International Journal of Molecular Sciences. 23(7). 3905–3905. 7 indexed citations

Deng, Niantao, André E. Minoche, Kate Harvey, et al.. (2022). Deep whole genome sequencing identifies recurrent genomic alterations in commonly used breast cancer cell lines and patient-derived xenograft models. Breast Cancer Research. 24(1). 63–63. 7 indexed citations

Mallawaarachchi, Amali, Ben Lundie, Yvonne Hort, et al.. (2021). Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing. European Journal of Human Genetics. 29(5). 760–770. 30 indexed citations

Minoche, André E., Ben Lundie, Greg B. Peters, et al.. (2021). ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data. Genome Medicine. 13(1). 32–32. 38 indexed citations

Lehner, Reinhard, et al.. (2021). Assembly and characterization of the genome of chard (Beta vulgaris ssp. vulgaris var. cicla). Journal of Biotechnology. 333. 67–76. 12 indexed citations

Riley, Lisa G., Mark J. Cowley, Velimir Gayevskiy, et al.. (2020). The diagnostic utility of genome sequencing in a pediatric cohort with suspected mitochondrial disease. Genetics in Medicine. 22(7). 1254–1261. 45 indexed citations

Kim, Aryun, Kishore R. Kumar, Ryan L. Davis, et al.. (2019). Increased Diagnostic Yield of Spastic Paraplegia with or Without Cerebellar Ataxia Through Whole-Genome Sequencing. The Cerebellum. 18(4). 781–790. 27 indexed citations

10.

Bagnall, Richard D., Jodie Ingles, Marcel E. Dinger, et al.. (2018). Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy. Journal of the American College of Cardiology. 72(4). 419–429. 112 indexed citations

11.

Weißhaar, Bernd, Heinz Himmelbauer, Thomas Schmidt, et al.. (2016). Sugar Beet BeetMap-3, and Steps to Improve the Genome Assembly and Genome Sequence Annotation (W875). PUB – Publications at Bielefeld University (Bielefeld University). 1 indexed citations

12.

Mallawaarachchi, Amali, Yvonne Hort, Mark J. Cowley, et al.. (2016). Whole-genome sequencing overcomes pseudogene homology to diagnose autosomal dominant polycystic kidney disease. European Journal of Human Genetics. 24(11). 1584–1590. 58 indexed citations

13.

Kumar, Kishore R., Gautam Wali, Mahesh Kamate, et al.. (2016). Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing. Neurogenetics. 17(4). 265–270. 22 indexed citations

14.

Minoche, André E., Juliane C. Dohm, Jessica Schneider, et al.. (2015). Exploiting single-molecule transcript sequencing for eukaryotic gene prediction. Genome biology. 16(1). 184–184. 112 indexed citations

15.

Pin, Pierre A., Thomas Kraft, Juliane C. Dohm, et al.. (2014). Differential Expression Patterns of Non-Symbiotic Hemoglobins in Sugar Beet (Beta vulgaris ssp. vulgaris). Plant and Cell Physiology. 55(4). 834–844. 19 indexed citations

16.

Schmidt, Martin, André E. Minoche, Juliane C. Dohm, et al.. (2014). Cytosine Methylation of an Ancient Satellite Family in the Wild Beet <b><i>Beta procumbens</i></b>. Cytogenetic and Genome Research. 143(1-3). 157–167. 8 indexed citations

17.

Heitkam, Tony, Daniela Holtgräwe, Bernd Weißhaar, et al.. (2012). Evolutionary reshuffling in the Errantivirus lineage Elbe within the Beta vulgaris genome. The Plant Journal. 72(4). 636–651. 21 indexed citations

18.

Herrmann, Frank, Mireia Garriga-Canut, James Cotterell, et al.. (2011). p53 Gene Repair with Zinc Finger Nucleases Optimised by Yeast 1-Hybrid and Validated by Solexa Sequencing. PLoS ONE. 6(6). e20913–e20913. 31 indexed citations

19.

Minoche, André E., Juliane C. Dohm, & Heinz Himmelbauer. (2011). Evaluation of genomic high-throughput sequencing data generated on Illumina HiSeq and Genome Analyzer systems. Genome biology. 12(11). R112–R112. 448 indexed citations breakdown →

20.

Zakrzewski, Falk, Bernd Weißhaar, Jörg Fuchs, et al.. (2011). Epigenetic profiling of heterochromatic satellite DNA. Chromosoma. 120(4). 409–422. 25 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.

Explore authors with similar magnitude of impact