Deborah Morrogh

2.3k total citations
13 papers, 542 citations indexed

About

Deborah Morrogh is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Deborah Morrogh has authored 13 papers receiving a total of 542 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in Deborah Morrogh's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Deborah Morrogh is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Deborah Morrogh collaborates with scholars based in United Kingdom, Netherlands and Germany. Deborah Morrogh's co-authors include Rodger Palmer, Richard H. Scott, Jane A. Hurst, Eugene Healy, Veronica A. Kinsler, Anna Thomas, Sam Loughlin, Jane Chalker, Neil Bulstrode and Miho Ishida and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Journal of Investigative Dermatology.

In The Last Decade

Deborah Morrogh

12 papers receiving 535 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Deborah Morrogh United Kingdom 9 299 247 129 83 78 13 542
Davor Lessel Germany 17 181 0.6× 523 2.1× 86 0.7× 72 0.9× 13 0.2× 44 733
James Colley United Kingdom 8 383 1.3× 241 1.0× 79 0.6× 21 0.3× 49 0.6× 13 539
Meena Balasubramanian United Kingdom 18 555 1.9× 310 1.3× 64 0.5× 63 0.8× 12 0.2× 74 802
Eveliina Jakkula Finland 10 283 0.9× 230 0.9× 32 0.2× 43 0.5× 19 0.2× 20 610
Chantal Missirian France 16 418 1.4× 404 1.6× 35 0.3× 41 0.5× 17 0.2× 39 720
Katherine Holman Australia 15 522 1.7× 529 2.1× 53 0.4× 41 0.5× 25 0.3× 31 911
Kit San Yeung Hong Kong 13 245 0.8× 252 1.0× 32 0.2× 25 0.3× 18 0.2× 29 529
Fortunato Lonardo Italy 16 350 1.2× 258 1.0× 110 0.9× 25 0.3× 12 0.2× 52 645
Jessica Gosio Canada 4 74 0.2× 232 0.9× 167 1.3× 58 0.7× 11 0.1× 5 473
Ayse Bilge Ozel United States 14 131 0.4× 245 1.0× 60 0.5× 58 0.7× 11 0.1× 26 635

Countries citing papers authored by Deborah Morrogh

Since Specialization
Citations

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

Fields of papers citing papers by Deborah Morrogh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deborah Morrogh

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

All Works

13 of 13 papers shown
1.
Demetriou, Charalambos, Miho Ishida, Emma Peskett, et al.. (2019). Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family. Journal of Dental Research. 98(6). 659–665. 5 indexed citations
2.
Giardino, Giuliana, Nesrine Radwan, Patra Koletsi, et al.. (2019). Clinical and immunological features in a cohort of patients with partial DiGeorge syndrome followed at a single center. Blood. 133(24). 2586–2596. 49 indexed citations
3.
Stabej, Polona Le Quesne, Chela James, Louise Ocaka, et al.. (2017). An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypes. Orphanet Journal of Rare Diseases. 12(1). 24–24. 14 indexed citations
4.
Coppola, Antonietta, Deborah Morrogh, Simona Balestrini, et al.. (2017). Ring Chromosome 17 Not Involving the Miller-Dieker Region: A Case with Drug-Resistant Epilepsy. Molecular Syndromology. 9(1). 38–44. 4 indexed citations
5.
6.
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
7.
Morrogh, Deborah, Nancy L. Kuntz, C. Halbert, et al.. (2014). The instability of the BTB-KELCH protein Gigaxonin causes Giant Axonal Neuropathy and constitutes a new penetrant and specific diagnostic test. Acta Neuropathologica Communications. 2(1). 47–47. 22 indexed citations
8.
Klaassens, Merel, Deborah Morrogh, Elisabeth Rosser, et al.. (2014). Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature. European Journal of Human Genetics. 23(5). 610–615. 48 indexed citations
9.
Morrogh, Deborah, et al.. (2014). Microarray Technology for the Diagnosis of Fetal Chromosomal Aberrations: Which Platform Should We Use?. Journal of Clinical Medicine. 3(2). 663–678. 13 indexed citations
10.
Czeschik, Johanna Christina, Peter Bauer, Karin Buiting, et al.. (2013). X-linked intellectual disability type Nascimento is a clinically distinct, probably underdiagnosed entity. Orphanet Journal of Rare Diseases. 8(1). 146–146. 17 indexed citations
11.
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
12.
Morrogh, Deborah, et al.. (2013). What is array CGH?. Archives of Disease in Childhood Education & Practice. 98(4). 134–135. 3 indexed citations
13.
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

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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