Rodger Palmer

1.5k total citations
20 papers, 915 citations indexed

About

Rodger Palmer is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Rodger Palmer has authored 20 papers receiving a total of 915 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 10 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Rodger Palmer's work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (3 papers) and Genetic Syndromes and Imprinting (3 papers). Rodger Palmer is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (3 papers) and Genetic Syndromes and Imprinting (3 papers). Rodger Palmer collaborates with scholars based in United Kingdom, Australia and United States. Rodger Palmer's co-authors include Deborah Morrogh, Robin Lovell‐Badge, Juan Pedro Martı́nez-Barberá, Gudrun E. Moore, Maria Cundall, Eugene Healy, Veronica A. Kinsler, Anna Thomas, Sam Loughlin and Jane Chalker and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics and Journal of Investigative Dermatology.

In The Last Decade

Rodger Palmer

20 papers receiving 887 citations

Peers

Rodger Palmer
Louise C. Wilson United Kingdom
Yves Sznajer Belgium
Christian Netzer Germany
J.H.A.M. Tuerlings Netherlands
Ann Haskins Olney United States
Isabella Torrente Italy
Boris Keren France
Annalisa Vetro Italy
Greg B. Peters Australia
Meena Balasubramanian United Kingdom
Louise C. Wilson United Kingdom
Rodger Palmer
Citations per year, relative to Rodger Palmer Rodger Palmer (= 1×) peers Louise C. Wilson

Countries citing papers authored by Rodger Palmer

Since Specialization
Citations

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

Fields of papers citing papers by Rodger Palmer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rodger Palmer

This figure shows the co-authorship network connecting the top 25 collaborators of Rodger Palmer. A scholar is included among the top collaborators of Rodger Palmer 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 Rodger Palmer. Rodger Palmer 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.
Trump, Natalie, Amy McTague, Helen Brittain, et al.. (2016). Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. Journal of Medical Genetics. 53(5). 310–317. 147 indexed citations
2.
Kinsler, Veronica A., Anna Thomas, Miho Ishida, et al.. (2013). Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS. Journal of Investigative Dermatology. 133(9). 2229–2236. 196 indexed citations
3.
Sousa, Sérgio B., Margarida Venâncio, Estelle Chanudet, et al.. (2013). Intellectual disability, unusual facial morphology and hand anomalies in sibs. American Journal of Medical Genetics Part A. 161(10). 2401–2406. 2 indexed citations
4.
Palmer, Rodger, et al.. (2012). The idic(15) syndrome: Expanding the phenotype. American Journal of Medical Genetics Part A. 158A(6). 1505–1508. 3 indexed citations
5.
Palmer, Rodger, Jonathan J. Waters, Nicholas Lench, et al.. (2012). Array comparative genomic hybridization: Results from an adult population with drug-resistant epilepsy and co-morbidities. European Journal of Medical Genetics. 55(5). 342–348. 24 indexed citations
6.
Kenny, Janna, Melissa Lees, Susan Drury, et al.. (2011). Sotos syndrome, infantile hypercalcemia, and nephrocalcinosis: a contiguous gene syndrome. Pediatric Nephrology. 26(8). 1331–1334. 24 indexed citations
7.
Alatzoglou, Kyriaki S., Christopher T. Cowell, Rodger Palmer, et al.. (2011). Increased Transactivation Associated with SOX3 Polyalanine Tract Deletion in a Patient with Hypopituitarism. Molecular Endocrinology. 25(3). 546–546. 3 indexed citations
8.
Alatzoglou, Kyriaki S., Daniel Kelberman, Christopher T. Cowell, et al.. (2011). Increased Transactivation Associated withSOX3 Polyalanine Tract Deletion in a Patient with Hypopituitarism. The Journal of Clinical Endocrinology & Metabolism. 96(4). E685–E690. 34 indexed citations
9.
Baple, Emma L., Rodger Palmer, & Raoul C. M. Hennekam. (2010). A Microdeletion at 12q24.31 Can Mimic Beckwith-Wiedemann Syndrome Neonatally. Molecular Syndromology. 1(1). 42–45. 16 indexed citations
10.
Palmer, Rodger, et al.. (2010). Evaluation of the efficacy of constitutional array‐based comparative genomic hybridization in the diagnosis of aneuploidy using genomic and amplified DNA. Journal of obstetrics and gynaecology research. 36(1). 19–26. 2 indexed citations
11.
12.
Kelberman, Daniel, Sandra C. de Castro, Shuwen Huang, et al.. (2008). SOX2 Plays a Critical Role in the Pituitary, Forebrain, and Eye during Human Embryonic Development. The Journal of Clinical Endocrinology & Metabolism. 93(5). 1865–1873. 115 indexed citations
13.
Woods‐Townsend, Kathryn, Maria Cundall, James Turton, et al.. (2005). Over- and Underdosage of SOX3 Is Associated with Infundibular Hypoplasia and Hypopituitarism. The American Journal of Human Genetics. 76(5). 833–849. 190 indexed citations
14.
Prescott, Katrina, Kathryn Woodfine, Maurice Super, et al.. (2004). A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome. Human Genetics. 116(1-2). 83–90. 22 indexed citations
15.
Woodward, Karen, Maria Cundall, Rodger Palmer, et al.. (2002). Complex chromosomal rearrangement and associated counseling issues in a family with Pelizaeus‐Merzbacher disease. American Journal of Medical Genetics Part A. 118A(1). 15–24. 12 indexed citations
16.
Martinez, Anna E., M. Malone, Peter H. Hoeger, Rodger Palmer, & John Harper. (2000). Lipoatrophic panniculitis and chromosome 10 abnormality. British Journal of Dermatology. 142(5). 1034–1039. 10 indexed citations
17.
Woodward, Karen, Rodger Palmer, Kathleen Rao, & Sue Malcolm. (1999). Prenatal diagnosis by FISH in a family with Pelizaeus–Merzbacher disease caused by duplication of the PLP gene. Prenatal Diagnosis. 19(3). 266–268. 14 indexed citations
18.
Witt, David R., Catherine Schaefer, Seunghwan Wi, et al.. (1996). Cystic fibrosis heterozygote screening in 5,161 pregnant women.. PubMed. 58(4). 823–35. 65 indexed citations
19.
Richter, M., et al.. (1991). Panniculitis: a report of four cases and literature review.. Archives of Disease in Childhood. 66(9). 1057–1060. 9 indexed citations
20.
Moore, Gudrun E., Philip Hedge, S.H. Rider, et al.. (1989). Multiple tandem 18-kb sequences clustered in the region of the acute promyelocytic leukemia breakpoint on chromosome 17. Genomics. 4(2). 152–161. 6 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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