Geraldine Malone

1.6k citations
14 papers · 1.3k · 1 hit paper · h-index 9

Impact in

    • Cystic Fibrosis Research Advances
    • Neonatal Respiratory Health Research
    • Tracheal and airway disorders
  • Surgery top 5%
    • Pancreatitis Pathology and Treatment
    • Gastrointestinal disorders and treatments
    • Pediatric Hepatobiliary Diseases and Treatments

Papers in

    • Cystic Fibrosis Research Advances 11
    • Neonatal Respiratory Health Research 5
    • Tracheal and airway disorders 3
    • Congenital Ear and Nasal Anomalies 2
    • Genomics and Rare Diseases 1

Geraldine Malone

14 papers receiving 1.3k citations

Geraldine Malone's Hit Papers

Mutations of the Cystic Fibrosis Gene in Patients with Chronic Pancreatitis 1998 · 795 citations
7950+9+18Years since publication250500750

Peers

Geraldine Malone
Comparison fields: 5 of 77
  • Pulmonary and Respiratory Medicine 594
  • Surgery 566
  • Oncology 277
  • Genetics 89
  • Genetics 152
Replace Weiliang Xie with:
Weiliang Xie United States
Masahiro Hata Japan
Soula Danopoulos United States
Dieter Broering Saudi Arabia
Jocelyn Celestin United States
Duncan S. Russell United States
Ulrich Wulbrand Germany
Katsunori Kawano Japan
Alecia‐Jane Twigger Australia
Mark A. Ranalli United States
Geraldine Malone relative to Weiliang Xie United States Weiliang Xie's profile →
Citations per field
00.5×2×4×6×7.5×
Weiliang Xie · 1×
Citations per year

Countries citing papers authored by Geraldine Malone

Since Specialization
Citations

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

Fields of papers citing papers by Geraldine Malone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 23 scholars most cited alongside Geraldine Malone, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Geraldine Malone Line = papers co-authored together Geraldine Malone links everyone, so they are left out of the graph.

All Works

14 of 14 papers shown
#Work
1
Mutations of the Cystic Fibrosis Gene in Patients with Chronic Pancreatitis
Hit paper breakdown →
1998795
2
Development, multiplexing, and application of ARMS tests for common mutations in the CFTR gene.
1992218
3 2000121
4 199476
5 199532
6 201831
7 199819
8 199418
9
The mutation status of PAX3 and p53 genes in medulloblastoma.
199812
10 19976
11 19944
12 20084
13 20033
14 19981

About Geraldine Malone

Geraldine Malone is a scholar working on Pulmonary and Respiratory Medicine, Genetics, Cancer Research, Pathology and Forensic Medicine and Genetics, having authored 14 papers that have together received 1.3k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (11 papers), Neonatal Respiratory Health Research (5 papers), Tracheal and airway disorders (3 papers), Congenital Ear and Nasal Anomalies (2 papers), Cancer Genomics and Diagnostics (1 paper), Genomics and Rare Diseases (1 paper), Molecular Biology Techniques and Applications (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Pulmonary and Respiratory Medicine (594 citations), Surgery (566 citations), Oncology (277 citations), Genetics (89 citations) and Genetics (152 citations). Geraldine Malone has collaborated with scholars based in United Kingdom, Belgium and Hungary. Frequent co-authors include Martin J Schwarz, Maurice Super, John E. Painter, Joan M. Braganza, M Super, Stephen F. Little, A. Haworth, Gordana Dermody, Víctor Faùndes and William Newman. Their work appears in journals such as Human Mutation, Human Genetics, European Journal of Pediatrics, International Journal of Oncology and New England Journal of Medicine.

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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