Daniel F. Wallace

3.3k total citations
88 papers, 2.2k citations indexed

About

Daniel F. Wallace is a scholar working on Hematology, Genetics and Nutrition and Dietetics. According to data from OpenAlex, Daniel F. Wallace has authored 88 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Hematology, 50 papers in Genetics and 36 papers in Nutrition and Dietetics. Recurrent topics in Daniel F. Wallace's work include Iron Metabolism and Disorders (60 papers), Hemoglobinopathies and Related Disorders (50 papers) and Trace Elements in Health (36 papers). Daniel F. Wallace is often cited by papers focused on Iron Metabolism and Disorders (60 papers), Hemoglobinopathies and Related Disorders (50 papers) and Trace Elements in Health (36 papers). Daniel F. Wallace collaborates with scholars based in Australia, United States and United Kingdom. Daniel F. Wallace's co-authors include V. Nathan Subramaniam, Gautam Rishi, Lesa Summerville, Cameron J. McDonald, James Dooley, Gregory J. Anderson, Lawrie W. Powell, Jeannette L. Dixon, David M. Frazer and Jonathan M. Harris and has published in prestigious journals such as Blood, Gastroenterology and PLoS ONE.

In The Last Decade

Daniel F. Wallace

81 papers receiving 2.2k citations

Peers

Daniel F. Wallace
Comparison fields: 5 of 126
  • Hematology 1.6k
  • Genetics 1.3k
  • Nutrition and Dietetics 1.2k
  • Molecular Biology 249
  • Rheumatology 143
Replace Saira Ahmed with:
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Juan Xiao China
Yuanyuan Shen China
Takashi Maki United States
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Martin Böttcher Germany
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Saira Ahmed United States View profile →
Citations per field, relative to Daniel F. Wallace
Daniel F. Wallace · 1×
Citations per year, relative to Daniel F. Wallace
Daniel F. Wallace · 1×

Countries citing papers authored by Daniel F. Wallace

Since Specialization
Citations

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

Fields of papers citing papers by Daniel F. Wallace

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel F. Wallace. 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 Daniel F. Wallace. The network helps show where Daniel F. Wallace may publish in the future.

Co-authorship network of co-authors of Daniel F. Wallace

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel F. Wallace. A scholar is included among the top collaborators of Daniel F. Wallace 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 Daniel F. Wallace. Daniel F. Wallace 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
# Work Indexed citations
1 0
2 0
3 10
4 46
5 9
6
The regulation of iron absorption and homeostasis
173
7
Endofin, a novel BMP-SMAD regulator of the iron-regulatory hormone, hepcidin
1
8
Analysis of IL-22 contribution to hepcidin induction and hypoferremia during the response to LPS in vivo
6
9 54
10
New genetic complexity underlying atypical iron disorders
2
11 35
12
Temporal and tissue-specific analysis of iron loading in mouse models of hereditary haemochromatosis
2
13
The Efficacy and Safety of Abatacept in SLE: Results of a 12-month Exploratory Study
15
14 124
15 22
16
Inactivation of the murine Transferrin Receptor 2 gene using the cre recombinase: loxP system
3
17 2
18 71
19
A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote
2
20
A simple genetic test identifies 90% of UK patients with haemochromatosis
6

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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