Art Daniel

3.1k total citations
56 papers, 1.9k citations indexed

About

Art Daniel is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Art Daniel has authored 56 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Genetics, 24 papers in Pediatrics, Perinatology and Child Health and 22 papers in Molecular Biology. Recurrent topics in Art Daniel's work include Genomic variations and chromosomal abnormalities (29 papers), Prenatal Screening and Diagnostics (23 papers) and Chromosomal and Genetic Variations (17 papers). Art Daniel is often cited by papers focused on Genomic variations and chromosomal abnormalities (29 papers), Prenatal Screening and Diagnostics (23 papers) and Chromosomal and Genetic Variations (17 papers). Art Daniel collaborates with scholars based in Australia, United States and Singapore. Art Daniel's co-authors include Gillian Turner, John M. Opitz, Michael Frost, Ross Brookwell, Ernest B. Hook, P.R.L.C. Lam-Po-Tang, Paul Malafiej, Mark Selikowitz, James F. Reynolds and Zhanhe Wu and has published in prestigious journals such as Nature, New England Journal of Medicine and The Journal of Pediatrics.

In The Last Decade

Art Daniel

56 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Art Daniel Australia 26 1.5k 705 617 457 195 56 1.9k
Johannes Nielsen Denmark 21 1.5k 1.0× 773 1.1× 678 1.1× 476 1.0× 98 0.5× 66 2.1k
Dorothy Pettay United States 18 1.1k 0.8× 723 1.0× 767 1.2× 390 0.9× 143 0.7× 26 1.7k
P.A. Jacobs United Kingdom 19 1.1k 0.7× 723 1.0× 336 0.5× 360 0.8× 148 0.8× 28 1.8k
A Kleczkowska Belgium 22 1.1k 0.8× 490 0.7× 439 0.7× 346 0.8× 122 0.6× 80 1.3k
Franz Binkert Switzerland 24 1.3k 0.9× 585 0.8× 932 1.5× 403 0.9× 46 0.2× 50 1.7k
R H Lindenbaum United Kingdom 20 960 0.7× 715 1.0× 529 0.9× 192 0.4× 157 0.8× 39 1.7k
J.J.M. Engelen Netherlands 23 1.1k 0.8× 680 1.0× 464 0.8× 402 0.9× 111 0.6× 92 1.7k
M Prieur France 26 1.5k 1.0× 1.4k 2.0× 449 0.7× 445 1.0× 184 0.9× 75 2.6k
Joëlle Boué France 16 991 0.7× 667 0.9× 664 1.1× 122 0.3× 388 2.0× 36 1.9k
Mark W. Steele United States 24 846 0.6× 498 0.7× 323 0.5× 229 0.5× 131 0.7× 66 1.2k

Countries citing papers authored by Art Daniel

Since Specialization
Citations

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

Fields of papers citing papers by Art Daniel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Art Daniel

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

All Works

20 of 20 papers shown
1.
2.
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
3.
Perry, Jo K., Sara Nouri, Art Daniel, et al.. (2005). Molecular distinction between true centric fission and pericentric duplication-fission. Human Genetics. 116(4). 300–310. 7 indexed citations
4.
Mahjoubi, Frouzandeh, Greg B. Peters, Paul Malafiej, et al.. (2005). An analphoid marker chromosome inv dup(15)(q26.1qter), detected during prenatal diagnosis and characterized via chromosome microdissection. Cytogenetic and Genome Research. 109(4). 485–490. 14 indexed citations
5.
6.
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
7.
Daniel, Art, Neil Athayde, Robert Ogle, et al.. (2003). Prospective ranking of the sonographic markers for aneuploidy: Data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound. Australian and New Zealand Journal of Obstetrics and Gynaecology. 43(1). 16–26. 30 indexed citations
8.
Daniel, Art & Paul Malafiej. (2003). A Series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15. American Journal of Medical Genetics Part A. 117A(3). 212–222. 44 indexed citations
9.
Daniel, Art, et al.. (2003). Three different origins for apparent triploid/diploid mosaics. Prenatal Diagnosis. 23(7). 529–534. 32 indexed citations
10.
Li, Shulan, Paul Malafiej, Brynn Levy, et al.. (2002). Chromosome 13q neocentromeres: Molecular cytogenetic characterization of three additional cases and clinical spectrum. American Journal of Medical Genetics. 110(3). 258–267. 23 indexed citations
11.
12.
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
13.
Daniel, Art, Zhanhe Wu, Bruce Bennetts, et al.. (2001). Karyotype, phenotype and parental origin in 19 cases of triploidy. Prenatal Diagnosis. 21(12). 1034–1048. 56 indexed citations
14.
Daniel, Art, et al.. (1994). Identification of marker chromosomes in thirteen patients using FISH probing. American Journal of Medical Genetics. 53(1). 8–18. 41 indexed citations
15.
Daniel, Art, et al.. (1989). Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: Data from United States and Canadian laboratories. American Journal of Medical Genetics. 33(1). 14–53. 161 indexed citations
16.
Purrello, Michele, Becky Alhadeff, K.E. Buckton, et al.. (1987). Comparison of cytologic and genetic distances between long arm subtelomeric markers of human autosome 14 suggests uneven distribution of crossing-over. Cytogenetic and Genome Research. 44(1). 32–40. 21 indexed citations
17.
Opitz, John M., Joan Fitzgerald, James F. Reynolds, et al.. (1987). The montana fetal genetic pathology program and a review of prenatal death in humans. American Journal of Medical Genetics. 28(S3). 93–112. 10 indexed citations
18.
Reynolds, James F., Art Daniel, Joan Fitzgerald, & John M. Opitz. (1987). Atypical phenotype associated with deletion (15) (pter → q11::q13 → qter). American Journal of Medical Genetics. 28(1). 55–58. 9 indexed citations
19.
Opitz, John M., et al.. (1984). Discovery of a connective tissue dysplasia in the Martin‐Bell syndrome. American Journal of Medical Genetics. 17(1). 101–109. 40 indexed citations
20.
Daniel, Art & P.R.L.C. Lam-Po-Tang. (1976). Structure and inheritance of some heterozygous Robertsonian translocation in man.. Journal of Medical Genetics. 13(5). 381–388. 45 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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