Art Daniel

3.1k citations

56 papers · 1.9k indexed · h-index 26

Impact in

Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics

Papers in ⓘ

Genetics 45
- Genomic variations and chromosomal abnormalities 29
- Genetic Syndromes and Imprinting 10
- Genetics and Neurodevelopmental Disorders 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
Pediatrics, Perinatology and Child Health 24
- Prenatal Screening and Diagnostics 23

Co-authors: Gillian Turner (6 shared papers)John M. Opitz (10 shared papers)Michael Frost (1 shared paper)Ross Brookwell (5 shared papers)Ernest B. Hook (1 shared paper)P.R.L.C. Lam-Po-Tang (5 shared papers)Paul Malafiej (8 shared papers)Mark Selikowitz (2 shared papers)
Journals: Prenatal Diagnosis (7 papers)Human Genetics (6 papers)Journal of Medical Genetics (5 papers)Cytogenetic and Genome Research (3 papers)Pathology (2 papers)
Partner nations: Australia United States Iran

In The Last Decade

Art Daniel

56 papers receiving 1.6k citations

Peers

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-authors

The 25 scholars most cited alongside Art Daniel, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Art Daniel Line = papers co-authored together Art Daniel links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 56 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	X-linked mental retardation, macro-orchidism, and the Xq27 fragile site The Journal of Pediatrics ·Gillian Turner, Art Daniel, Michael Frost	1980	206
2	Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: Data from United States and Canadian laboratories American Journal of Medical Genetics ·Art Daniel, Ernest B. Hook, Gary Wulf	1989	161
3	Heterozygous Expression of X-Linked Mental Retardation and X-Chromosome Marker Fra(X)(Q27) New England Journal of Medicine ·Gillian Turner, Ross Brookwell, Art Daniel, Mark Selikowitz, Michael Zilibowitz	1980	149
4	Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister‐Killian syndrome): Report of 11 cases American Journal of Medical Genetics ·James F. Reynolds, Art Daniel, Thaddeus E. Kelly, Susanne M. Gollin, Mark J. Stephan, John C. Carey, William N. Adkins, Mary Jane Webb, F Char, Jorge F. Jimenez, John M. Opitz, Giovanni Neri	1987	107
5	The diagnosis and frequency of X‐linked conditions in a cohort of moderately retarded males with affected brothers American Journal of Medical Genetics ·Jane Fishburn, Gillian Turner, Art Daniel, Ross Brookwell, John M. Opitz	1983	90
6	Structural differences in reciprocal translocations Human Genetics ·Art Daniel	1979	72
7	Karyotype, phenotype and parental origin in 19 cases of triploidy Prenatal Diagnosis ·Art Daniel, Zhanhe Wu, Bruce Bennetts, Howard R. Slater, R A Osborn, Julianne Jackson, Vladimir Pupko, John W. Nelson, Geoff Watson, Claire Cooke‐Yarborough, Christine Loo	2001	56
8	Structure and inheritance of some heterozygous Robertsonian translocation in man. Journal of Medical Genetics ·Art Daniel, P.R.L.C. Lam-Po-Tang	1976	45
9	The fragile X(q27) form of X‐linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes American Journal of Medical Genetics ·Ross Brookwell, Art Daniel, Gillian Turner, Jane Fishburn, John M. Opitz	1982	45
10	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 ·Art Daniel, Paul Malafiej	2003	44
11	Single Cd band in dicentric translocations with one suppressed centromere Human Genetics ·Art Daniel	1979	43
12	Identification of marker chromosomes in thirteen patients using FISH probing American Journal of Medical Genetics ·Art Daniel, Paul Malafiej, Kerrie Preece, Nicole Chia, John W. Nelson, M.F. Smith	1994	41
13	Structural differences in pericentric inversions. Application to a model of risk of recombinants Human Genetics ·Art Daniel	1981	41
14	Discovery of a connective tissue dysplasia in the Martin‐Bell syndrome American Journal of Medical Genetics ·John M. Opitz, Joan M. Westphal, Art Daniel, John M. Optiz	1984	40
15	Issues arising from the prenatal diagnosis of some rare trisomy mosaics—the importance of cryptic fetal mosaicism Prenatal Diagnosis ·Art Daniel, Zhanhe Wu, Artur Darmanian, Paul Malafiej, Varsha Tembe, Greg B. Peters, Craig H. Kennedy, Lesley C. Adès	2004	38
16	Constitutive fragile sites 1p31, 3p14, 6q26, and 16q23 and their use as controls for false‐negative results with the fragile(X) American Journal of Medical Genetics ·Art Daniel, Linda Ekblom, S M Phillips, John M. Opitz	1984	34
17	Mechanism for the Chromosome Banding Phenomenon Nature ·Art Daniel, P.R.L.C. Lam-Po-Tang	1973	34
18	Three different origins for apparent triploid/diploid mosaics Prenatal Diagnosis ·Art Daniel, Zhanhe Wu, Artur Darmanian, Felicity Collins, Julianne Jackson	2003	32
19	Theoretical bases for karyotype evolution. II. The fusion burst in man and mouse. The Japanese Journal of Genetics ·Hirotami T. Imai, Naoyuki Takahata, Takeo Maruyama, Art Daniel, Takeo Honda, Yoichi Matsuda, Kazuo Moriwaki	1988	32
20	Prenatal diagnosis in 3,000 women for chromosome, X‐linked, and metabolic disorders American Journal of Medical Genetics ·Art Daniel, Lesley Stewart, Toni Saville, Ross Brookwell, Helen Paull, Stuart Purvis‐Smith, P.R.L.C. Lam-Po-Tang, Patricia A. Jacobs, Lillian Y. F. Hsu	1982	32

About Art Daniel

Art Daniel is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Surgery, having authored 56 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (29 papers), Prenatal Screening and Diagnostics (23 papers), Chromosomal and Genetic Variations (17 papers), Genetic Syndromes and Imprinting (10 papers), Genomics and Chromatin Dynamics (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Folate and B Vitamins Research (4 papers). The work is most often cited by research in Genetics (1.5k citations), Pediatrics, Perinatology and Child Health (617 citations), Developmental Biology (27 citations), Plant Science (457 citations) and Molecular Biology (705 citations). Art Daniel has collaborated with scholars based in Australia, United States and Iran. Frequent 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. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Journal of Medical Genetics, Cytogenetic and Genome Research and Pathology.

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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