Alice Bailey

503 total citations
10 papers, 163 citations indexed

About

Alice Bailey is a scholar working on Molecular Biology, Epidemiology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Alice Bailey has authored 10 papers receiving a total of 163 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Epidemiology and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Alice Bailey's work include Congenital heart defects research (8 papers), Congenital Heart Disease Studies (7 papers) and Coronary Artery Anomalies (5 papers). Alice Bailey is often cited by papers focused on Congenital heart defects research (8 papers), Congenital Heart Disease Studies (7 papers) and Coronary Artery Anomalies (5 papers). Alice Bailey collaborates with scholars based in United States, Canada and Belgium. Alice Bailey's co-authors include Donna M. McDonald‐McGinn, Elaine H. Zackai, Beverly S. Emanuel, Kathleen E. Sullivan, Loydie A. Jerome‐Majewska, T. Blaine Crowley, Daniel E. McGinn, Somayyeh Fahiminiya, Elisabeth E. Mlynarski and David R. Lynch and has published in prestigious journals such as Scientific Reports, Journal of Allergy and Clinical Immunology and Journal of Medical Genetics.

In The Last Decade

Alice Bailey

10 papers receiving 163 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alice Bailey United States 6 115 74 49 35 18 10 163
Gabriela Ferraz Leal Brazil 10 144 1.3× 148 2.0× 38 0.8× 38 1.1× 19 1.1× 17 238
Κρινιώ Γιαννίκου Greece 10 207 1.8× 111 1.5× 27 0.6× 24 0.7× 18 1.0× 16 275
Haruka Hamanoue Japan 10 118 1.0× 84 1.1× 32 0.7× 21 0.6× 12 0.7× 23 220
Yiping Shen China 9 144 1.3× 151 2.0× 23 0.5× 21 0.6× 8 0.4× 12 275
Thomas Smol France 10 129 1.1× 70 0.9× 18 0.4× 10 0.3× 13 0.7× 34 224
Tracy Dudding‐Byth Australia 10 147 1.3× 146 2.0× 22 0.4× 15 0.4× 17 0.9× 18 272
Malin Kvarnung Sweden 7 119 1.0× 90 1.2× 62 1.3× 7 0.2× 13 0.7× 16 233
Brian Gibbs United States 5 123 1.1× 98 1.3× 25 0.5× 20 0.6× 25 1.4× 8 254
Volkan Okur United States 9 117 1.0× 112 1.5× 19 0.4× 9 0.3× 16 0.9× 15 205
Mahmoud Taleb Al‐Ali United Arab Emirates 10 174 1.5× 150 2.0× 17 0.3× 15 0.4× 12 0.7× 34 312

Countries citing papers authored by Alice Bailey

Since Specialization
Citations

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

Fields of papers citing papers by Alice Bailey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alice Bailey

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

All Works

10 of 10 papers shown
1.
Campbell, Ian M., T. Blaine Crowley, Chintan Jobaliya, et al.. (2022). Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression. Clinical Genetics. 103(1). 109–113. 4 indexed citations
2.
Crowley, T. Blaine, Ian M. Campbell, Emily J. Liebling, et al.. (2021). Distinct immune trajectories in patients with chromosome 22q11.2 deletion syndrome and immune-mediated diseases. Journal of Allergy and Clinical Immunology. 149(1). 445–450. 16 indexed citations
3.
Patel, Shrey, Sharon Edman, Daniel E. McGinn, et al.. (2021). Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome Without Intracardiac Anomalies. Pediatric Cardiology. 42(7). 1594–1600. 5 indexed citations
4.
Patel, Shrey, Donna M. McDonald‐McGinn, T. Blaine Crowley, et al.. (2021). Changes In Aortic Root Size Over Time In Patients with 22Q11.2 Deletion Syndrome. 378–379. 1 indexed citations
5.
Elden, Lisa M., T. Blaine Crowley, Daniel E. McGinn, et al.. (2020). Magnetic resonance angiography (MRA) in preoperative planning for patients with 22q11.2 deletion syndrome undergoing craniofacial and otorhinolaryngologic procedures. International Journal of Pediatric Otorhinolaryngology. 138. 110236–110236. 5 indexed citations
6.
Pastor, Steven, Oanh Tran, Eleanor Young, et al.. (2020). Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR). Scientific Reports. 10(1). 12235–12235. 18 indexed citations
7.
Edman, Sharon, Alice Bailey, Daniel E. McGinn, et al.. (2020). Cardiac evaluation of patients with 22q11.2 duplication syndrome. American Journal of Medical Genetics Part A. 185(3). 753–758. 8 indexed citations
8.
Crowley, T. Blaine, Sean Gallagher, Alice Bailey, et al.. (2020). Increased T‐cell counts in patients with 22q11.2 deletion syndrome who have anxiety. American Journal of Medical Genetics Part A. 182(7). 1815–1818. 3 indexed citations
9.
Wenger, Tara, Charlly Kao, Donna M. McDonald‐McGinn, et al.. (2016). The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder. Scientific Reports. 6(1). 19372–19372. 24 indexed citations
10.
McDonald‐McGinn, Donna M., Somayyeh Fahiminiya, Timothée Revil, et al.. (2012). Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS. Journal of Medical Genetics. 50(2). 80–90. 79 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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