Arabella Smith

2.8k total citations
119 papers, 1.8k citations indexed

About

Arabella Smith is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Arabella Smith has authored 119 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Genetics, 50 papers in Pediatrics, Perinatology and Child Health and 41 papers in Molecular Biology. Recurrent topics in Arabella Smith's work include Genomic variations and chromosomal abnormalities (44 papers), Genetic Syndromes and Imprinting (40 papers) and Prenatal Screening and Diagnostics (37 papers). Arabella Smith is often cited by papers focused on Genomic variations and chromosomal abnormalities (44 papers), Genetic Syndromes and Imprinting (40 papers) and Prenatal Screening and Diagnostics (37 papers). Arabella Smith collaborates with scholars based in Australia, United States and Germany. Arabella Smith's co-authors include Ronald J. Trent, Lisa Robson, Stewart Einfeld, Bruce J. Tonge, Ian S. Fraser, Trevor Woodage, Peter J. Russell, Joanne Dixon, Rodney P. Shearman and D. A. Brown and has published in prestigious journals such as New England Journal of Medicine, The Journal of Pediatrics and Fertility and Sterility.

In The Last Decade

Arabella Smith

119 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arabella Smith Australia 22 1.2k 605 591 182 132 119 1.8k
G. Shashidhar Pai United States 25 981 0.9× 796 1.3× 450 0.8× 232 1.3× 78 0.6× 55 1.9k
J P Fryns Belgium 25 1.2k 1.1× 1.1k 1.8× 430 0.7× 304 1.7× 130 1.0× 90 2.2k
Laird G. Jackson United States 30 866 0.8× 1.6k 2.6× 1.0k 1.8× 326 1.8× 163 1.2× 71 3.0k
Y. Gillerot Belgium 22 616 0.5× 740 1.2× 426 0.7× 334 1.8× 112 0.8× 74 1.8k
K Méhes Hungary 17 717 0.6× 828 1.4× 408 0.7× 152 0.8× 70 0.5× 105 1.7k
R H Lindenbaum United Kingdom 20 960 0.8× 715 1.2× 529 0.9× 253 1.4× 48 0.4× 39 1.7k
J. O. Van Hemel Netherlands 21 809 0.7× 457 0.8× 356 0.6× 109 0.6× 107 0.8× 38 1.1k
Udo Trautmann Germany 23 1.1k 0.9× 930 1.5× 328 0.6× 132 0.7× 80 0.6× 65 1.7k
Peter Miny Germany 21 629 0.5× 437 0.7× 844 1.4× 203 1.1× 80 0.6× 88 1.5k
Gordana Raca United States 18 1.1k 0.9× 586 1.0× 490 0.8× 94 0.5× 133 1.0× 62 1.7k

Countries citing papers authored by Arabella Smith

Since Specialization
Citations

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

Fields of papers citing papers by Arabella Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arabella Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Arabella Smith. A scholar is included among the top collaborators of Arabella Smith 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 Arabella Smith. Arabella Smith 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.
Alexander, Stephen I., Neil Smith, Min Hu, et al.. (2008). Chimerism and Tolerance in a Recipient of a Deceased-Donor Liver Transplant. New England Journal of Medicine. 358(4). 369–374. 110 indexed citations
2.
Kandasamy, Jothy, Arabella Smith, Sara Dı́az, Barbara Rose, & Christopher J. O’Brien. (2007). Heterogeneity of PLAG1 gene rearrangements in pleomorphic adenoma. Cancer Genetics and Cytogenetics. 177(1). 1–5. 19 indexed citations
3.
Sharma, Praveen, et al.. (2003). Hypodiploidy of 37 chromosomes in an adult patient with acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 145(2). 176–178. 3 indexed citations
4.
Smith, Arabella, Lisa Robson, Luke St Heaps, et al.. (2001). Routine fluorescence in situ hybridization with the MLL probe does not reliably detect two separate signals on one chromosome 11 in patients with trisomy 11. Cancer Genetics and Cytogenetics. 129(2). 173–176. 1 indexed citations
5.
Sharma, Praveen, et al.. (2001). Complex variant t(4;11) characterized by fluorescence in situ hybridization in infant acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 127(2). 177–180. 4 indexed citations
6.
Smith, Arabella, et al.. (1999). Frequency of Trisomy 15 and Loss of the Y Chromosome in Adult Leukemia. Cancer Genetics and Cytogenetics. 114(2). 108–111. 14 indexed citations
7.
Smith, Arabella, Lisa Robson, & Bettina M. Buchholz. (1998). Normal growth in Angelman syndrome due to paternal UPD. Clinical Genetics. 53(3). 223–225. 15 indexed citations
8.
Beange, Helen, et al.. (1997). Manifestations in institutionalised adults with Angelman syndrome due to deletion. American Journal of Medical Genetics. 70(4). 415–420. 32 indexed citations
9.
Smith, Arabella. (1997). FISH and the paediatrician. Journal of Paediatrics and Child Health. 33(5). 365–368. 2 indexed citations
10.
Smith, Arabella. (1996). Why is There No Diploid Overdose Effect in Prader-Willi Syndrome Due to Uniparental Disomy?. Acta geneticae medicae et gemellologiae twin research. 45(1-2). 179–189. 3 indexed citations
11.
Coyle, Luke, et al.. (1995). Evaluation of interphase fluorescence in situ hybridization on direct hematological bone marrow smears. Pathology. 27(1). 86–90. 4 indexed citations
12.
Robson, Lisa, et al.. (1994). Novel karyotype in the Ullrich‐Turner syndrome—45,X/46,X,r(X)/46,X,dic(X)—investigated with fluorescence in situ hybridization. American Journal of Medical Genetics. 50(3). 251–254. 5 indexed citations
13.
Woodage, Trevor, Robert W. Lindeman, Zemin Deng, et al.. (1994). Physical Mapping Studies at D15S10: Implications for Candidate Gene Identification in the Angelman Syndrome/Prader-Willi Syndrome Chromosome Region of 15q11-q13. Genomics. 19(1). 170–172. 8 indexed citations
14.
Smith, Arabella, Lisa Robson, Marie T. Mulcahy, et al.. (1993). Fluorescence in‐situ hybridisation and molecular studies used in the characterisation of a Robertsonian translocation (13q15q) in Prader‐Willi syndrome. Clinical Genetics. 43(1). 5–8. 21 indexed citations
15.
Smith, Arabella & Roy G. Beran. (1992). Chromosome fragility in the Lennox‐Gastaut epilepsy syndrome. Journal of Intellectual Disability Research. 36(5). 435–441. 1 indexed citations
16.
Bablok, L, et al.. (1990). Male infertility and its treatment: A review of over 4700 patients treated for male related infertility. International Urology and Nephrology. 22(2). 161–165. 1 indexed citations
17.
Smith, Arabella, et al.. (1990). Data on Families of Chromosome Translocation Carriers Ascertained Because of Habitual Spontaneous Abortion. Australian and New Zealand Journal of Obstetrics and Gynaecology. 30(1). 57–62. 10 indexed citations
18.
Wilcken, Bridget, Arabella Smith, & D. A. Brown. (1980). Urine screening for aminoacidopathies: Is it beneficial?. The Journal of Pediatrics. 97(3). 492–497. 43 indexed citations
19.
Smith, Arabella, et al.. (1979). An abnormal dicentric X chromosome in a patient with short stature and gonadal dysgenesis.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 22(3). 143–7. 8 indexed citations
20.
Smith, Arabella, et al.. (1979). Three Siblings with Premature Gonadal Failure. Fertility and Sterility. 32(5). 528–530. 23 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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