Lorraine Gaunt

3.2k total citations
16 papers, 368 citations indexed

About

Lorraine Gaunt is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lorraine Gaunt has authored 16 papers receiving a total of 368 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lorraine Gaunt's work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Genomics and Rare Diseases (3 papers). Lorraine Gaunt is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Genomics and Rare Diseases (3 papers). Lorraine Gaunt collaborates with scholars based in United Kingdom and United States. Lorraine Gaunt's co-authors include Dian Donnai, Anne Slavotinek, Jill Clayton‐Smith, Helen Kingston, Hazel Tinegate, Marjorie Rosenberg, William Fergusson, Samantha J.L. Knight, Jonathan Flint and R. H. A. Campbell and has published in prestigious journals such as Human Molecular Genetics, British Journal of Haematology and Developmental Medicine & Child Neurology.

In The Last Decade

Lorraine Gaunt

16 papers receiving 342 citations

Peers

Lorraine Gaunt

GENET

PPCH

NEURO

Patrick L. Wilmot United States

Jack H. Jung Canada

Helle Lybæk Norway

Nicole Maas Belgium

Britt-Marie Anderlid Sweden

Carrie Hanscom United States

Erica H. Gerkes Netherlands

T. Lukusa Belgium

Kelly E. Jackson United States

Angelika Köhler Germany

Patrick L. Wilmot United States

Lorraine Gaunt

148 ×0.6

GENET

95 ×0.7

49 ×0.5

PPCH

29 ×0.6

19 ×0.5

NEURO

Citations per year, relative to Lorraine Gaunt Lorraine Gaunt (= 1×) peers Patrick L. Wilmot

Countries citing papers authored by Lorraine Gaunt

Since Specialization

Citations

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

Fields of papers citing papers by Lorraine Gaunt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lorraine Gaunt

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

All Works

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16 of 16 papers shown

Banka, Siddharth, et al.. (2011). A novel 800 kb microduplication of chromosome 16q22.1 resulting in learning disability and epilepsy may explain phenotypic variability in a family with 15q13 microdeletion. American Journal of Medical Genetics Part A. 155(6). 1453–1457. 3 indexed citations

Whibley, Annabel, Jill Urquhart, Lionel Willatt, et al.. (2010). Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements. European Journal of Human Genetics. 18(10). 1095–1099. 35 indexed citations

Kingston, Helen, et al.. (2009). Haploinsufficiency of the nerve growth factor beta gene in a 1p13 deleted female child with an insensitivity to pain. Developmental Medicine & Child Neurology. 51(10). 833–837. 5 indexed citations

Clayton‐Smith, Jill, et al.. (2008). Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case report. Journal of Medical Case Reports. 2(1). 355–355. 6 indexed citations

Newman, William G., Sara Hamilton, J G Ayres, et al.. (2007). Array comparative genomic hybridization for diagnosis of developmental delay – an exploratory cost‐consequences analysis. Clinical Genetics. 71(3). 254–259. 21 indexed citations

Slavotinek, Anne, et al.. (2003). Two unique patients with trisomy 18 mosaicism and molecular marker studies. American Journal of Medical Genetics Part A. 117A(3). 282–288. 6 indexed citations

Stewart, Helen, et al.. (2001). De novo deletion of chromosome 18q in a baby with Harlequin ichthyosis. American Journal of Medical Genetics. 102(4). 342–345. 5 indexed citations

Slavotinek, Anne, Marjorie Rosenberg, Samantha J.L. Knight, et al.. (1999). Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres. Journal of Medical Genetics. 36(5). 405–411. 107 indexed citations

Slavotinek, Anne, Lorraine Gaunt, & Dian Donnai. (1997). Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.. Journal of Medical Genetics. 34(10). 819–826. 73 indexed citations

10.

Robinson, Jacqueline A., Helen Stewart, Lynette Moore, & Lorraine Gaunt. (1997). A case of mosaic trisomy 2 diagnosed at amniocentesis in an abnormal fetus and confirmed in multiple fetal tissues. Clinical Genetics. 51(6). 417–420. 14 indexed citations

11.

Ramsden, Simon, et al.. (1996). A Case of Angelman Syndrome Arising as a Result of a De Novo Robertsonian Translocation. Acta geneticae medicae et gemellologiae twin research. 45(1-2). 255–261. 9 indexed citations

12.

McGaughran, Julie, Lorraine Gaunt, J. F. Doré, et al.. (1996). Rubinstein-Taybi syndrome with deletions of FISH probe RT1 at 16p13.3: two UK patients.. Journal of Medical Genetics. 33(1). 82–83. 12 indexed citations

13.

Greenwood, A. D., J. Lowe, & Lorraine Gaunt. (1995). Renal carcinoma in a chimpanzee (Pan troglodytes). Veterinary Record. 137(15). 380–381. 8 indexed citations

14.

Watson, Carolyn J., Lorraine Gaunt, D. Gareth Evans, et al.. (1993). A disease-associated germline deletion maps the type 2 neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukaemia inhibitory factor locus. Human Molecular Genetics. 2(6). 701–704. 35 indexed citations

15.

Tinegate, Hazel, Lorraine Gaunt, & Peter J. Hamilton. (1983). The 5q – syndrome: an underdiagnosed form of macrocytic anaemia. British Journal of Haematology. 54(1). 103–110. 11 indexed citations

16.

Tinegate, Hazel, et al.. (1983). The 5q – syndrome: an underdiagnosed form of macrocytic anaemia. British Journal of Haematology. 54(1). 103–110. 18 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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