Ann Dalton

2.2k total citations
24 papers, 1.1k citations indexed

About

Ann Dalton is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Ann Dalton has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 10 papers in Molecular Biology and 6 papers in Rheumatology. Recurrent topics in Ann Dalton's work include Connective tissue disorders research (7 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Bone and Dental Protein Studies (3 papers). Ann Dalton is often cited by papers focused on Connective tissue disorders research (7 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Bone and Dental Protein Studies (3 papers). Ann Dalton collaborates with scholars based in United Kingdom, United States and Sweden. Ann Dalton's co-authors include Janice Nunn, Kim Cornish, Cary S. Kogan, Jeremy Turk, Göran Annerén, Robert P. McMahon, Edwin M. Horwitz, Uwe Ewald, Olle Ringdén and Eva Åström and has published in prestigious journals such as Blood, Journal of Hepatology and The American Journal of Gastroenterology.

In The Last Decade

Ann Dalton

24 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ann Dalton United Kingdom 16 580 334 302 242 152 24 1.1k
Helen Kingston United Kingdom 24 645 1.1× 839 2.5× 186 0.6× 202 0.8× 122 0.8× 63 1.9k
Elizabeth K. Schorry United States 27 471 0.8× 516 1.5× 170 0.6× 379 1.6× 323 2.1× 67 2.3k
Desirée du Sart Australia 26 617 1.1× 888 2.7× 394 1.3× 73 0.3× 168 1.1× 39 2.0k
Christine Verellen‐Dumoulin Belgium 21 818 1.4× 750 2.2× 174 0.6× 112 0.5× 148 1.0× 38 1.8k
A. Moseley United States 5 890 1.5× 834 2.5× 94 0.3× 91 0.4× 133 0.9× 10 1.6k
Luitgard M. Neumann Germany 20 1.0k 1.8× 708 2.1× 110 0.4× 97 0.4× 207 1.4× 46 1.7k
Kathleen A. Leppig United States 23 681 1.2× 662 2.0× 124 0.4× 95 0.4× 134 0.9× 57 2.0k
Phillip J. Dexheimer United States 19 326 0.6× 664 2.0× 80 0.3× 214 0.9× 483 3.2× 36 1.5k
Conny M.A. van Ravenswaaij Netherlands 11 676 1.2× 628 1.9× 709 2.3× 106 0.4× 379 2.5× 13 1.5k
Emilio Donti Italy 21 404 0.7× 836 2.5× 267 0.9× 145 0.6× 63 0.4× 96 1.6k

Countries citing papers authored by Ann Dalton

Since Specialization
Citations

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

Fields of papers citing papers by Ann Dalton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ann Dalton

This figure shows the co-authorship network connecting the top 25 collaborators of Ann Dalton. A scholar is included among the top collaborators of Ann Dalton 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 Ann Dalton. Ann Dalton 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.
Hassan, Lamiece, et al.. (2020). A deliberative study of public attitudes towards sharing genomic data within NHS genomic medicine services in England. Public Understanding of Science. 29(7). 702–717. 25 indexed citations
2.
Sollars, Elizabeth, C. J. Bartlett, Antonio Milano, et al.. (2019). Next Generation Sequencing in Newborn Screening in the United Kingdom National Health Service. International Journal of Neonatal Screening. 5(4). 40–40. 29 indexed citations
3.
Pollitt, Rebecca C., Vrinda Saraff, Ann Dalton, et al.. (2016). Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations. American Journal of Medical Genetics Part A. 170(12). 3150–3156. 27 indexed citations
4.
Cournane, Seán, Ann Dalton, Declan Byrne, et al.. (2015). Social deprivation, population dependency ratio and an extended hospital episode — Insights from acute medicine. European Journal of Internal Medicine. 26(9). 714–719. 10 indexed citations
5.
Simms, Roslyn, et al.. (2014). Genetic Testing in the Assessment of Living Related Kidney Donors at Risk of Autosomal Dominant Polycystic Kidney Disease. Transplantation. 99(5). 1023–1029. 16 indexed citations
6.
Balasubramanian, Meena, Bart Wagner, Luíz César Peres, et al.. (2014). Ultrastructural and histological findings on examination of skin in osteogenesis imperfecta. Clinical Dysmorphology. 24(2). 45–54. 11 indexed citations
7.
Balasubramanian, Meena, Michael Parker, Ann Dalton, et al.. (2013). Genotype–phenotype study in type V osteogenesis imperfecta. Clinical Dysmorphology. 22(3). 93–101. 32 indexed citations
8.
Kirk, Richard, et al.. (2012). Mutational analysis of the GYS2 gene in patients diagnosed with ketotic hypoglycaemia. Journal of Pediatric Endocrinology and Metabolism. 25(9-10). 963–7. 9 indexed citations
9.
Parker, Michael, Julia Rankin, Louise C. Wilson, et al.. (2011). Type 1 collagenopathy presenting with a Russell–Silver phenotype. American Journal of Medical Genetics Part A. 155(6). 1414–1418. 6 indexed citations
10.
Hewamadduma, Channa, Christopher McDermott, Janine Kirby, et al.. (2008). New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP). Neurogenetics. 10(2). 105–110. 35 indexed citations
11.
Olpin, S. E., et al.. (2007). Failure to repair the c.338C>T mutation in carnitine palmitoyl transferase 2 deficient skin fibroblasts using chimeraplasty. Molecular Genetics and Metabolism. 93(3). 347–349. 1 indexed citations
12.
Cornish, Kim, Lexin Li, Cary S. Kogan, et al.. (2007). Age-dependent cognitive changes in carriers of the fragile X syndrome. Cortex. 44(6). 628–636. 100 indexed citations
13.
Beauchamp, Nicholas, Ann Dalton, Uma Ramaswami, et al.. (2007). Glycogen storage disease type IX: High variability in clinical phenotype. Molecular Genetics and Metabolism. 92(1-2). 88–99. 90 indexed citations
14.
Pollitt, Rebecca C., et al.. (2006). Mutation analysis ofCOL1A1andCOL1A2in patients diagnosed with osteogenesis imperfecta type I-IV. Human Mutation. 27(7). 716–716. 77 indexed citations
15.
Gleeson, Dermot, et al.. (2006). HFE Genotypes in Decompensated Alcoholic Liver Disease: Phenotypic Expression and Comparison with Heavy Drinking and with Normal Controls. The American Journal of Gastroenterology. 101(2). 304–310. 25 indexed citations
16.
Blanc, Katarina Le, Cecilia Götherström, Olle Ringdén, et al.. (2005). Fetal Mesenchymal Stem-Cell Engraftment in Bone after In Utero Transplantation in a Patient with Severe Osteogenesis Imperfecta. Transplantation. 79(11). 1607–1614. 333 indexed citations
17.
Blanc, Katarina Le, Cecilia Götherström, Olle Ringdén, et al.. (2004). Mesenchymal Stem Cell Engraftment in Bone Following In Utero Transplantation in a Patient with Severe Osteogenesis Imperfecta.. Blood. 104(11). 505–505. 2 indexed citations
18.
Cornish, Kim, et al.. (2004). The emerging fragile X premutation phenotype: Evidence from the domain of social cognition. Brain and Cognition. 57(1). 53–60. 117 indexed citations
19.
Bonham, James R., Melanie Downing, & Ann Dalton. (2003). Screening for cystic fibrosis: the practice and the debate. European Journal of Pediatrics. 162(0). S42–S45. 11 indexed citations
20.
Yassaee, Vahid Reza, Sirous Zeinali, Iraj Harirchi, et al.. (2002). Novel mutations in the BRCA1 and BRCA2genes in Iranian women with early-onset breast cancer. Breast Cancer Research. 4(4). R6–R6. 41 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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