J.J.A. Holden

1.2k total citations
21 papers, 631 citations indexed

About

J.J.A. Holden is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, J.J.A. Holden has authored 21 papers receiving a total of 631 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Plant Science. Recurrent topics in J.J.A. Holden's work include Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). J.J.A. Holden is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). J.J.A. Holden collaborates with scholars based in Canada, United States and United Kingdom. J.J.A. Holden's co-authors include Elizabeth Kay‐Raining Bird, Bradley N. White, Fabìo Macciardi, Dennis R. Grayson, Huiping Zhang, Emanuela Mundo, Nancy E. Simpson, M. E. Suzanne Lewis, Evica Rajcan‐Separovic and Ying Qiao and has published in prestigious journals such as Nucleic Acids Research, JNCI Journal of the National Cancer Institute and Molecular Psychiatry.

In The Last Decade

J.J.A. Holden

20 papers receiving 599 citations

Peers

J.J.A. Holden

GENET

DEP

Nuala Sykes United Kingdom

Karola Rehnström Finland

Elizabeth Dykens United States

A. Gulhan Ercan‐Sencicek United States

Kristin Herman United States

Kristen M. West United States

S. L. Donnelly United States

Alexis Rea United States

Karen Chorney United States

Christopher J. Smith United States

Nuala Sykes United Kingdom

J.J.A. Holden

366 ×1.3

GENET

265 ×1.1

257 ×1.2

129 ×1.4

DEP

26 ×0.4

Citations per year, relative to J.J.A. Holden J.J.A. Holden (= 1×) peers Nuala Sykes

Countries citing papers authored by J.J.A. Holden

Since Specialization

Citations

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

Fields of papers citing papers by J.J.A. Holden

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.J.A. Holden. 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 J.J.A. Holden. The network helps show where J.J.A. Holden may publish in the future.

Co-authorship network of co-authors of J.J.A. Holden

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

Harvard, Chansonette, Eloi Mercier, Rita Colnaghi, et al.. (2011). Understanding the impact of 1q21.1 copy number variant. Orphanet Journal of Rare Diseases. 6(1). 54–54. 43 indexed citations

Bird, Elizabeth Kay‐Raining, et al.. (2011). Survey of bilingualism in autism spectrum disorders. International Journal of Language & Communication Disorders. 47(1). 52–64. 113 indexed citations

Qiao, Ying, Chansonette Harvard, Christine Tyson, et al.. (2010). Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics. Human Genetics. 128(2). 179–194. 19 indexed citations

Qiao, Ying, Chansonette Harvard, Mark Hildebrand, et al.. (2009). Phenomic determinants of genomic variation in autism spectrum disorders. Journal of Medical Genetics. 46(10). 680–688. 31 indexed citations

Qiao, Ying, Chansonette Harvard, Chris Fawcett, et al.. (2008). Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disability. Cytogenetic and Genome Research. 123(1-4). 79–87. 1 indexed citations

Qiao, Ying, Xudong Liu, Chansonette Harvard, et al.. (2007). Large-scale copy number variants (CNVs): Distribution in normal subjects and FISH/real-time qPCR analysis. BMC Genomics. 8(1). 167–167. 18 indexed citations

D’Amelio, Marcello, Irene Ricci, Roberto Sacco, et al.. (2005). Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions. Molecular Psychiatry. 10(11). 1006–1016. 94 indexed citations

Zhang, Huiping, et al.. (2002). Reelin gene alleles and susceptibility to autism spectrum disorders. Molecular Psychiatry. 7(9). 1012–1017. 122 indexed citations

Holden, J.J.A., Melissa Walker, Maryse Chalifoux, & Bradley N. White. (1996). Trinucleotide repeats at the FRAXF locus: Frequency and distribution in the general population. American Journal of Medical Genetics. 64(2). 424–427. 4 indexed citations

10.

Hough, Christine, Bradley N. White, & J.J.A. Holden. (1995). Characterization of a lymphoblastoid line deleted for lambda immunoglobulin genes. Immunogenetics. 41(6). 359–365.

11.

Skare, James, Bai‐Lin Wu, Venkat Pulijaal, et al.. (1993). Characterization of Three Overlapping Deletions Causing X-Linked Lymphoproliferative Disease. Genomics. 16(1). 254–255. 20 indexed citations

12.

Mulligan, Lois M., Raman Sood, Alessandra M.V. Duncan, et al.. (1989). Isolation and mapping of a polymorphic DNA sequence, DXS312, to Xq27–Xq28. Nucleic Acids Research. 17(11). 4421–4421. 3 indexed citations

13.

Hough, Margaret R., Bradley N. White, & J.J.A. Holden. (1988). Tumorigenicity of ten karyotypically distinct cell types present in the human melanoma cell line MeWo-A. Cancer Genetics and Cytogenetics. 32(1). 117–128. 2 indexed citations

14.

Goodfellow, Paul J., Alessandra M.V. Duncan, Lindsay A. Farrer, et al.. (1987). Localization and linkage of three polymorphic DNA sequences on human chromosome 20. Cytogenetic and Genome Research. 44(2-3). 112–117. 18 indexed citations

15.

Holden, J.J.A., Margaret R. Hough, Dorothy L. Reimer, & Bradley N. White. (1987). Evidence for unequal crossing-over as the mechanism for amplification of some homogeneously staining regions. Cancer Genetics and Cytogenetics. 29(1). 139–149. 10 indexed citations

16.

Riddell, D. Christie, J. B. Beckett, Arthur K. Chan, et al.. (1986). Regional localization of 18 human X-linked DNA sequences. Cytogenetic and Genome Research. 42(3). 123–128. 26 indexed citations

17.

Beckett, J. B., J.J.A. Holden, Nancy E. Simpson, Bradley N. White, & Patrick MacLeod. (1986). Localization of X-Linked Dominant Charcot-Marie-Tooth Disease (CMT 2) to Xq13. Journal of Neurogenetics. 3(4). 225–231. 40 indexed citations

18.

Goodfellow, Paul J., Bradley N. White, J.J.A. Holden, et al.. (1985). Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.. PubMed. 37(5). 890–7. 16 indexed citations

19.

Haliotis, Tina, J. A. Werkmeister, J. R. Matthews, et al.. (1984). Enhanced natural killer sensitivity with concomitant clonal selection for cells bearing homogeneously staining regions in the human melanoma cell line MeWo upon induction of differentiation with theophylline.. PubMed. 72(5). 991–8. 5 indexed citations

20.

Grigliatti, T A, Bradley N. White, G. M. Tener, et al.. (1974). Studies on the Transfer RNA Genes of Drosophila. Cold Spring Harbor Symposia on Quantitative Biology. 38(0). 461–474. 32 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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