Artur Darmanian

1.1k total citations
15 papers, 539 citations indexed

About

Artur Darmanian is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Artur Darmanian has authored 15 papers receiving a total of 539 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Artur Darmanian's work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic Syndromes and Imprinting (4 papers). Artur Darmanian is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic Syndromes and Imprinting (4 papers). Artur Darmanian collaborates with scholars based in Australia, Germany and France. Artur Darmanian's co-authors include Richard Kefford, Helen Rizos, Graham J. Mann, Elizabeth A. Holland, Josep Malvehy, Célia Bádenas, Susana Puig, Montserrat Milà, Art Daniel and Felicity Collins and has published in prestigious journals such as Journal of Biological Chemistry, Cancer Research and Oncogene.

In The Last Decade

Artur Darmanian

15 papers receiving 493 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Artur Darmanian Australia	11	315	231	195	87	86	15	539
Robert Stobezki United States	6	303 1.0×	173 0.7×	145 0.7×	96 1.1×	79 0.9×	9	746
Muhammad B. Ekram United States	10	354 1.1×	98 0.4×	219 1.1×	69 0.8×	83 1.0×	15	484
Nora Shannon United Kingdom	6	368 1.2×	123 0.5×	206 1.1×	100 1.1×	62 0.7×	11	551
Sou‐De Cheng Taiwan	11	320 1.0×	133 0.6×	164 0.8×	47 0.5×	69 0.8×	16	494
Betty K. Martin United States	13	661 2.1×	145 0.6×	245 1.3×	231 2.7×	26 0.3×	17	799
E Emison United States	3	400 1.3×	104 0.5×	172 0.9×	76 0.9×	20 0.2×	5	681
Dirk Reutzel Germany	5	256 0.8×	57 0.2×	113 0.6×	70 0.8×	63 0.7×	5	339
Mohsen Ahmadian United States	6	503 1.6×	196 0.8×	261 1.3×	153 1.8×	11 0.1×	7	697
Lakshmi Rambhatla United States	8	572 1.8×	62 0.3×	151 0.8×	39 0.4×	56 0.7×	9	704

Countries citing papers authored by Artur Darmanian

Since Specialization

Citations

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

Fields of papers citing papers by Artur Darmanian

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Artur Darmanian

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

All Works

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15 of 15 papers shown

Wright, Dale, Artur Darmanian, Luke St Heaps, et al.. (2023). Saliva DNA: An alternative biospecimen for single nucleotide polymorphism chromosomal microarray analysis in autism. American Journal of Medical Genetics Part A. 191(12). 2913–2920. 1 indexed citations

Bennetts, Bruce, Artur Darmanian, Luke Jones, et al.. (2023). SNP chromosome microarray genotyping for detection of uniparental disomy in the clinical diagnostic laboratory. Pathology. 55(6). 818–826. 1 indexed citations

McCowage, Geoffrey, et al.. (2021). Neuroblastoma Molecular Risk-Stratification of DNA Copy Number and ALK Genotyping via Cell-Free Circulating Tumor DNA Profiling. Cancers. 13(13). 3365–3365. 10 indexed citations

Wright, Dale, et al.. (2016). Validation of a Chromosomal Microarray for Prenatal Diagnosis Using a Prospective Cohort of Pregnancies with Increased Risk for Chromosome Abnormalities. Genetic Testing and Molecular Biomarkers. 20(12). 791–798. 2 indexed citations

Ellaway, Carolyn, Gladys Ho, Elisa Bettella, et al.. (2012). 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. European Journal of Human Genetics. 21(5). 522–527. 44 indexed citations

White, Rose, Gladys Ho, Ingrid E. Scheffer, et al.. (2010). Cyclin-Dependent Kinase-Like 5 (CDKL5) Mutation Screening in Rett Syndrome and Related Disorders. Twin Research and Human Genetics. 13(2). 168–178. 27 indexed citations

Daniel, Art, et al.. (2007). An innocuous duplication of 11.2 Mb at 13q21 is gene poor: Sub‐bands of gene paucity and pervasive CNV characterize the chromosome anomalies. American Journal of Medical Genetics Part A. 143A(20). 2452–2459. 10 indexed citations

Algar, Elizabeth M., Luke St Heaps, Artur Darmanian, et al.. (2007). Paternally Inherited Submicroscopic Duplication at 11p15.5 Implicates Insulin-like Growth Factor II in Overgrowth and Wilms' Tumorigenesis. Cancer Research. 67(5). 2360–2365. 34 indexed citations

Daniel, Art, Zhanhe Wu, Artur Darmanian, et al.. (2004). Issues arising from the prenatal diagnosis of some rare trisomy mosaics—the importance of cryptic fetal mosaicism. Prenatal Diagnosis. 24(7). 524–536. 38 indexed citations

10.

Daniel, Art, et al.. (2003). Three different origins for apparent triploid/diploid mosaics. Prenatal Diagnosis. 23(7). 529–534. 32 indexed citations

11.

Daniel, Art, Elizabeth Baker, Nicole Chia, et al.. (2002). Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: A cause of minute terminal chromosomal imbalances. American Journal of Medical Genetics Part A. 117A(1). 57–64. 17 indexed citations

12.

Rizos, Helen, Susana Puig, Célia Bádenas, et al.. (2001). A melanoma-associated germline mutation in exon 1β inactivates p14ARF. Oncogene. 20(39). 5543–5547. 125 indexed citations

13.

Rizos, Helen, Artur Darmanian, Elizabeth A. Holland, Graham J. Mann, & Richard Kefford. (2001). Mutations in the INK4a/ARF Melanoma Susceptibility Locus Functionally Impair p14ARF. Journal of Biological Chemistry. 276(44). 41424–41434. 90 indexed citations

14.

Rizos, Helen, Artur Darmanian, Graham J. Mann, & Richard Kefford. (2000). Two arginine rich domains in the p14ARF tumour suppressor mediate nucleolar localization. Oncogene. 19(26). 2978–2985. 82 indexed citations

15.

Rizos, Helen, Artur Darmanian, James O. Indsto, et al.. (1999). Multiple abnormalities of the p16INK4a-pRb regulatory pathway in cultured melanoma cells. Melanoma Research. 9(1). 10–20. 26 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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