Diane Allingham‐Hawkins

1.5k total citations
21 papers, 607 citations indexed

About

Diane Allingham‐Hawkins is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Diane Allingham‐Hawkins has authored 21 papers receiving a total of 607 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Molecular Biology and 5 papers in Cognitive Neuroscience. Recurrent topics in Diane Allingham‐Hawkins's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Autism Spectrum Disorder Research (5 papers). Diane Allingham‐Hawkins is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Autism Spectrum Disorder Research (5 papers). Diane Allingham‐Hawkins collaborates with scholars based in Canada, United States and Portugal. Diane Allingham‐Hawkins's co-authors include Cheryl R. Greenberg, Elizabeth Spriggs, Brian J. Schmidt, Peter N. Ray, Paul E. Goss, Nancy Hamel, Corinne Serruya, Lisa Di Prospero, John Blondal and Martin Klein and has published in prestigious journals such as Neurology, JNCI Journal of the National Cancer Institute and Genetics in Medicine.

In The Last Decade

Diane Allingham‐Hawkins

21 papers receiving 596 citations

Peers

Diane Allingham‐Hawkins
Huw Dorkins United Kingdom
Soo‐Mi Park United Kingdom
Shehla Mohammed United Kingdom
Ruth Shomrat Israel
Gayle Patel United States
Avni Santani United States
Rocío Acuña‐Hidalgo United States
Julien Thévenon France
Michèle Mathieu France
Renske Olmer Netherlands
Huw Dorkins United Kingdom
Diane Allingham‐Hawkins
Citations per year, relative to Diane Allingham‐Hawkins Diane Allingham‐Hawkins (= 1×) peers Huw Dorkins

Countries citing papers authored by Diane Allingham‐Hawkins

Since Specialization
Citations

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

Fields of papers citing papers by Diane Allingham‐Hawkins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Diane Allingham‐Hawkins. 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 Diane Allingham‐Hawkins. The network helps show where Diane Allingham‐Hawkins may publish in the future.

Co-authorship network of co-authors of Diane Allingham‐Hawkins

This figure shows the co-authorship network connecting the top 25 collaborators of Diane Allingham‐Hawkins. A scholar is included among the top collaborators of Diane Allingham‐Hawkins 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 Diane Allingham‐Hawkins. Diane Allingham‐Hawkins 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.
Boyd, Brenna, He Fang, Diane Allingham‐Hawkins, et al.. (2024). Chromosomal translocation resolves a diagnostic odyssey for familial Ruvalcaba syndrome. American Journal of Medical Genetics Part A. 197(1). e63847–e63847. 2 indexed citations
2.
Suleiman, Jehan, Diane Allingham‐Hawkins, Mais Hashem, et al.. (2017). WDR45B‐related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: A consistent neurodevelopmental syndrome. Clinical Genetics. 93(2). 360–364. 30 indexed citations
3.
4.
Malhotra, Alka, Susan Levine, & Diane Allingham‐Hawkins. (2014). Whole exome sequencing for cancer – is there evidence of clinical utility?. 115–115. 3 indexed citations
5.
Allingham‐Hawkins, Diane, David Chitayat, Vincenzo Cirigliano, et al.. (2011). Prospective validation of quantitative fluorescent polymerase chain reaction for rapid detection of common aneuploidies. Genetics in Medicine. 13(2). 140–147. 14 indexed citations
6.
Allingham‐Hawkins, Diane, et al.. (2010). KIF6 p.Trp719Arg Testing to Assess Risk of Coronary Artery Disease and/or Statin Response. PLoS Currents. 2. RRN1191–RRN1191. 3 indexed citations
7.
Allingham‐Hawkins, Diane, et al.. (2010). ERCC1 Expression Analysis to Guide Therapy in Non-Small Cell Lung Cancer. PLoS Currents. 2. RRN1202–RRN1202. 18 indexed citations
8.
Allingham‐Hawkins, Diane, et al.. (2010). DecisionDx-GBM Gene Expression Assay for Prognostic Testing in Glioblastoma Multiform. PLoS Currents. 2. RRN1186–RRN1186. 6 indexed citations
9.
Lea, Andrew P., et al.. (2010). BRAF p.Val600Glu (V600E) Testing for Assessment of Treatment Options in Metastatic Colorectal Cancer. PLoS Currents. 2. RRN1187–RRN1187. 12 indexed citations
10.
Allingham‐Hawkins, Diane, et al.. (2009). Canadian College of Medical Geneticists Canadian Association of Genetic Counsellors Joint Statement on the Process of Informed Consent for Genetic Research. 2 indexed citations
11.
Allingham‐Hawkins, Diane, et al.. (2007). Vanishing Endometrial Carcinoma. International Journal of Gynecological Pathology. 26(3). 271–277. 6 indexed citations
12.
13.
Warner, Elizabeth, William D. Foulkes, Pamela J. Goodwin, et al.. (1999). Prevalence and Penetrance of BRCA1 and BRCA2 Gene Mutations in Unselected Ashkenazi Jewish Women With Breast Cancer. JNCI Journal of the National Cancer Institute. 91(14). 1241–1247. 306 indexed citations
14.
Holden, Jeanette J. A., Maire E. Percy, Diane Allingham‐Hawkins, et al.. (1999). Eighth International Workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997. American Journal of Medical Genetics. 83(4). 221–236. 3 indexed citations
15.
Allingham‐Hawkins, Diane, et al.. (1998). Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometry. American Journal of Medical Genetics. 75(2). 171–175. 6 indexed citations
16.
Allingham‐Hawkins, Diane, Charlotte A. Brown, Riyana Babul, et al.. (1996). Tissue-specific methylation differences and cognitive function in fragile X premutation females. American Journal of Medical Genetics. 64(2). 329–333. 27 indexed citations
17.
Allingham‐Hawkins, Diane, Charlotte A. Brown, Riyana Babul, et al.. (1996). Tissue‐specific methylation differences and cognitive function in fragile X premutation females. American Journal of Medical Genetics. 64(2). 329–333. 1 indexed citations
18.
Allingham‐Hawkins, Diane & Darrell J. Tomkins. (1995). Heterogeneity in Roberts syndrome. American Journal of Medical Genetics. 55(2). 188–194. 11 indexed citations
19.
Allingham‐Hawkins, Diane & Peter N. Ray. (1995). FRAXE expansion is not a common etiological factor among developmentally delayed males.. PubMed. 57(1). 72–6. 25 indexed citations
20.
Allingham‐Hawkins, Diane & Darrell J. Tomkins. (1991). Somatic cell hybridization of roberts syndrome and normal lymphoblasts resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypes. Somatic Cell and Molecular Genetics. 17(5). 455–462. 5 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Huw Dorkins Breakdown of academic impact, for papers by Soo‐Mi Park Breakdown of academic impact, for papers by Shehla Mohammed Breakdown of academic impact, for papers by Ruth Shomrat Breakdown of academic impact, for papers by Gayle Patel Breakdown of academic impact, for papers by Avni Santani Breakdown of academic impact, for papers by Rocío Acuña‐Hidalgo Breakdown of academic impact, for papers by Julien Thévenon Breakdown of academic impact, for papers by Michèle Mathieu Breakdown of academic impact, for papers by Renske Olmer
Rankless by CCL
2026