Lisa Robson

705 total citations
29 papers, 396 citations indexed

About

Lisa Robson is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lisa Robson has authored 29 papers receiving a total of 396 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 12 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lisa Robson's work include Genomic variations and chromosomal abnormalities (14 papers), Genetic Syndromes and Imprinting (13 papers) and Prenatal Screening and Diagnostics (7 papers). Lisa Robson is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Genetic Syndromes and Imprinting (13 papers) and Prenatal Screening and Diagnostics (7 papers). Lisa Robson collaborates with scholars based in Australia, Germany and United States. Lisa Robson's co-authors include Arabella Smith, Anne‐Marie Selzler, Erica Lenton, Roger Goldstein, Dina Brooks, A. Jauch, Tina Buchholz, Zemin Deng, Trevor Woodage and Ronald J. Trent and has published in prestigious journals such as Archives of Disease in Childhood, Journal of Medical Genetics and Patient Education and Counseling.

In The Last Decade

Lisa Robson

29 papers receiving 389 citations

Peers

Lisa Robson
P Beauvais France
Lucila Sandoval Mexico
Shivani Nazareth United States
Paulie Papavassiliou United States
Joseph M. Majure United States
Qutub H. Qazi United States
Julián Llera Argentina
Katelijne Bouman Netherlands
H. Sardemann Denmark
K Matsumiya Japan
P Beauvais France
Lisa Robson
Citations per year, relative to Lisa Robson Lisa Robson (= 1×) peers P Beauvais

Countries citing papers authored by Lisa Robson

Since Specialization
Citations

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

Fields of papers citing papers by Lisa Robson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lisa Robson

This figure shows the co-authorship network connecting the top 25 collaborators of Lisa Robson. A scholar is included among the top collaborators of Lisa Robson 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 Lisa Robson. Lisa Robson 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.
Selzler, Anne‐Marie, et al.. (2019). Self-efficacy and health-related quality of life in chronic obstructive pulmonary disease: A meta-analysis. Patient Education and Counseling. 103(4). 682–692. 64 indexed citations
2.
Cheallaigh, Clíona Ní, Aisling O’Leary, Eamon Keenan, et al.. (2017). Telementoring with project ECHO: a pilot study in Europe. BMJ Innovations. 3(3). 144–151. 35 indexed citations
3.
4.
Smith, Arabella, Luke St Heaps, & Lisa Robson. (2002). Apparently unrelated cytogenetic abnormalities among 462 probands referred for the detection of del(22q) by FISH. American Journal of Medical Genetics. 113(4). 346–350. 6 indexed citations
5.
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
6.
Robson, Lisa, et al.. (2000). 17p− Syndrome Arising from a Novel Dicentric Translocation in a Patient with Acute Myeloid Leukemia. Cancer Genetics and Cytogenetics. 118(2). 159–162. 9 indexed citations
7.
Smith, Arabella, Anna Jauch, Luke St Heaps, Lisa Robson, & Brian P. Kearney. (2000). Unbalanced translocation t(15;22) in ‘severe’ Prader–Willi syndrome. Annales de Génétique. 43(3-4). 125–130. 10 indexed citations
8.
Robinson, Lisa, et al.. (2000). A Novel Dicentric Deleted Chromosome 21 Arising from Tandem Translocation. Cancer Genetics and Cytogenetics. 121(2). 208–211. 3 indexed citations
9.
Smith, Arabella, et al.. (1999). Syndromal obesity due to paternal duplication 6(q24.3-q27). American Journal of Medical Genetics. 84(2). 125–131. 12 indexed citations
10.
Sharma, Praveen, et al.. (1999). Novel Chromosome 16 Abnormality—der(16)del(16)(q13)t(16;21)(p11.2;q22)—Associated with Acute Myeloid Leukemia. Cancer Genetics and Cytogenetics. 113(1). 25–28. 6 indexed citations
11.
Mowat, David, et al.. (1999). Duplication within chromosome 5q characterized by fluorescence in situ hybridization. American Journal of Medical Genetics. 83(5). 361–364. 7 indexed citations
12.
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
13.
Flaherty, L, et al.. (1998). A case of monosomy 21 found to be an unbalanced de novo t(5p;21q) by fluorescence in situ hybridization. Journal of Intellectual Disability Research. 42(3). 254–258. 4 indexed citations
14.
Buchholz, Tina, et al.. (1998). Evaluation of methylation analysis for diagnostic testing in 258 referrals suspected of Prader-Willi or Angelman syndromes. Human Genetics. 103(5). 535–539. 11 indexed citations
15.
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
16.
Dean, John, et al.. (1997). Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child.. Journal of Medical Genetics. 34(3). 246–249. 13 indexed citations
17.
Ogle, Robert, et al.. (1996). The Wolf-Hirschhorn syndrome in adulthood: Evaluation of a 24-year-old man with a rec(4) chromosome. American Journal of Medical Genetics. 65(2). 124–127. 12 indexed citations
18.
19.
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
20.
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

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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