Gordon Lowther

980 total citations
12 papers, 191 citations indexed

About

Gordon Lowther is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Gordon Lowther has authored 12 papers receiving a total of 191 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 2 papers in Molecular Biology. Recurrent topics in Gordon Lowther's work include Prenatal Screening and Diagnostics (5 papers), Genetic Syndromes and Imprinting (2 papers) and Acute Myeloid Leukemia Research (2 papers). Gordon Lowther is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genetic Syndromes and Imprinting (2 papers) and Acute Myeloid Leukemia Research (2 papers). Gordon Lowther collaborates with scholars based in United Kingdom, Germany and India. Gordon Lowther's co-authors include Jane Wolstenholme, E. J. Maher, Claudia Scholl, Peter Lichter, Jill M. Brown, Hartmut Döhner, Lap Chee Tsui, Janet Stewart, Antonio Cuneo and Stephen W. Scherer and has published in prestigious journals such as Blood, American Journal of Obstetrics and Gynecology and International Journal of Cancer.

In The Last Decade

Gordon Lowther

12 papers receiving 183 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gordon Lowther United Kingdom 6 69 68 60 41 30 12 191
Siân Morgan United Kingdom 8 82 1.2× 107 1.6× 117 1.9× 39 1.0× 57 1.9× 16 304
Sugandhi A. Tharapel United States 10 142 2.1× 83 1.2× 215 3.6× 13 0.3× 19 0.6× 19 337
Elisabet Lloveras Spain 8 132 1.9× 58 0.9× 153 2.5× 29 0.7× 22 0.7× 20 250
Anders Lundmark Sweden 7 67 1.0× 235 3.5× 53 0.9× 63 1.5× 27 0.9× 15 320
J A Castillejo Spain 6 27 0.4× 103 1.5× 14 0.2× 108 2.6× 12 0.4× 7 209
Elena Campos‐Sánchez Spain 8 15 0.2× 82 1.2× 21 0.3× 18 0.4× 32 1.1× 10 155
Yvonne Lisa Behrens Germany 8 21 0.3× 62 0.9× 29 0.5× 78 1.9× 17 0.6× 21 210
Petra Bilinski United States 5 32 0.5× 174 2.6× 112 1.9× 7 0.2× 64 2.1× 7 356
Blanche P. Alter United States 6 13 0.2× 215 3.2× 67 1.1× 67 1.6× 67 2.2× 9 295
Charnise Goodings United States 8 18 0.3× 94 1.4× 18 0.3× 49 1.2× 64 2.1× 11 188

Countries citing papers authored by Gordon Lowther

Since Specialization
Citations

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

Fields of papers citing papers by Gordon Lowther

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gordon Lowther

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

All Works

12 of 12 papers shown
1.
Dündar, Munis, et al.. (2001). A case of ambiguous genitalia presenting with a 45,X/46,Xr(Y)(p11.2;q11.23)/47,X,idic(Y)(p11.2),idic(Y)(p11.2) karyotype. Annales de Génétique. 44(1). 5–8. 6 indexed citations
2.
Carothers, A D, E. Boyd, Gordon Lowther, et al.. (1999). Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings. Genetic Epidemiology. 16(2). 179–190. 25 indexed citations
4.
Döhner, Konstanze, Jill M. Brown, Janet Stewart, et al.. (1998). Molecular Cytogenetic Characterization of a Critical Region in Bands 7q35-q36 Commonly Deleted in Malignant Myeloid Disorders. Blood. 92(11). 4031–4035. 68 indexed citations
5.
Döhner, Konstanze, Jill M. Brown, Janet Stewart, et al.. (1998). Molecular Cytogenetic Characterization of a Critical Region in Bands 7q35-q36 Commonly Deleted in Malignant Myeloid Disorders. Blood. 92(11). 4031–4035. 2 indexed citations
6.
Lowther, Gordon & Martin Whittle. (1997). Prenatal diagnosis in the United Kingdom--an overview.. PubMed. 5 Suppl 1. 84–9. 2 indexed citations
7.
Lowther, Gordon & Martin Whittle. (1997). Prenatal Diagnosis in the United Kingdom - An Overview. European Journal of Human Genetics. 5(Suppl. 1). 84–89. 4 indexed citations
8.
Lowther, Gordon, et al.. (1996). Long-term culture of primary breast cancer in defined medium. Breast Cancer Research and Treatment. 39(3). 247–259. 29 indexed citations
9.
Cameron, Alan D., Karl W. Murphy, M. B. McNay, et al.. (1994). Midtrimester chorionic villus sampling: An alternative approach?. American Journal of Obstetrics and Gynecology. 171(4). 1035–1037. 4 indexed citations
10.
Cameron, Alexander D., et al.. (1990). Second-trimester placental biopsy for rapid fetal karyotyping. American Journal of Obstetrics and Gynecology. 163(3). 931–934. 3 indexed citations
11.
Pratt, Norman, et al.. (1984). Non‐random chromosome changes in a herpes‐virus‐transformed syrian hamster cell line and its metastatic derivatives. International Journal of Cancer. 34(6). 849–853. 7 indexed citations
12.
Gray, Richard, Gordon Lowther, J M Littlewood, B. Middleton, & Malcolm J. Bennett. (1984). A case of 2-methylacetoacetyl CoA thiolase deficiency with coincidental chromosome abnormalities.. Journal of Medical Genetics. 21(5). 397–397. 2 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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