M McClure

1.2k citations
7 papers · 167 · h-index 6

Impact in

    • Congenital Ear and Nasal Anomalies
    • Cancer-related Molecular Pathways
    • Pancreatic and Hepatic Oncology Research

Papers in

    • Cystic Fibrosis Research Advances 4
    • Tracheal and airway disorders 2
    • Neonatal Respiratory Health Research 1
    • Congenital Ear and Nasal Anomalies 2
    • Genomics and Rare Diseases 1

M McClure

7 papers receiving 160 citations

Peers

M McClure
Comparison fields: 5 of 43
  • Genetics 26
  • Oncology 58
  • Pulmonary and Respiratory Medicine 56
  • Cancer Research 25
  • Genetics 29
Replace Meira Shaham with:
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Slim Mzoughi Singapore
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Citations per field
00.5×2.5×
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Citations per year

Countries citing papers authored by M McClure

Since Specialization
Citations

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

Fields of papers citing papers by M McClure

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside M McClure, 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 M McClure Line = papers co-authored together M McClure links everyone, so they are left out of the graph.

All Works

7 of 7 papers shown
#Work
1
MTS-1 (CDKN2) tumor suppressor gene deletions are a frequent event in esophagus squamous cancer and pancreatic adenocarcinoma cell lines.
199563
2 199232
3 199424
4
Mutation analysis of the cystic fibrosis transmembrane regulator gene in Native American populations of the southwest.
199216
5 198914
6 198713
7
Utility of internal markers to improve the accuracy of cystic fibrosis genotype analysis.
19925

About M McClure

M McClure is a scholar working on Pulmonary and Respiratory Medicine, Genetics, Oncology, Molecular Biology and Pathology and Forensic Medicine, having authored 7 papers that have together received 167 indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (4 papers), Tracheal and airway disorders (2 papers), Congenital Ear and Nasal Anomalies (2 papers), HER2/EGFR in Cancer Research (1 paper), DNA and Nucleic Acid Chemistry (1 paper), Cancer Genomics and Diagnostics (1 paper), Genomics and Rare Diseases (1 paper) and Neonatal Respiratory Health Research (1 paper). The work is most often cited by research in Genetics (26 citations), Oncology (58 citations), Pulmonary and Respiratory Medicine (56 citations), Cancer Research (25 citations) and Genetics (29 citations). M McClure has collaborated with scholars based in United States, Italy and Spain. Frequent co-authors include Qingyun Liu, Frank K. Fujimura, Hideo NAKAGAWA, Yu-Xin Yan, Anil K. Rustgi, Jason D. Weber, Cindy L. Vnencak‐Jones, Salmo Raskin, John A. Phillips and Winifred W. Doane. Their work appears in journals such as Genome Research, Human Genetics, Genetics, BMJ and PubMed.

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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