Mark A. McElwain

424 citations
7 papers · 294 · h-index 5

Impact in

  • Genetics top 10%
    • Genetic Syndromes and Imprinting
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases

Papers in

    • Advanced biosensing and bioanalysis techniques 1
    • Genomics and Phylogenetic Studies 1
    • Wnt/β-catenin signaling in development and cancer 1
    • Fibroblast Growth Factor Research 1
    • Genomic variations and chromosomal abnormalities 3
    • Genetics and Neurodevelopmental Disorders 1

Mark A. McElwain

6 papers receiving 290 citations

Peers

Mark A. McElwain
Comparison fields: 5 of 44
  • Genetics 191
  • Aging 6
  • Structural Biology 4
  • Molecular Biology 180
  • Pediatrics, Perinatology and Child Health 49
Replace Stephen C. Collins with:
Stephen C. Collins United States
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Fabiola Ceroni United Kingdom
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Babett Heye Germany
Satoshi Miyashita Japan
Yeon‐Joo Kang United States
Imen Chakchouk United States
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Mark A. McElwain relative to Stephen C. Collins United States Stephen C. Collins's profile →
Citations per field
00.5×3.6×
Stephen C. Collins · 1×
Citations per year

Countries citing papers authored by Mark A. McElwain

Since Specialization
Citations

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

Fields of papers citing papers by Mark A. McElwain

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark A. McElwain. 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 Mark A. McElwain. The network helps show where Mark A. McElwain may publish in the future.

Co-authors

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

All Works

7 of 7 papers shown
#Work
1 2013210
2 201537
3 200423
4 201119
5 20174
6 20221
7 20230

About Mark A. McElwain

Mark A. McElwain is a scholar working on Molecular Biology, Genetics, Cancer Research, Pediatrics, Perinatology and Child Health and Hematology, having authored 7 papers that have together received 294 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Cancer Genomics and Diagnostics (2 papers), Advanced biosensing and bioanalysis techniques (1 paper), Genomics and Phylogenetic Studies (1 paper), Wnt/β-catenin signaling in development and cancer (1 paper), Fibroblast Growth Factor Research (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Acute Myeloid Leukemia Research (1 paper). The work is most often cited by research in Genetics (191 citations), Aging (6 citations), Structural Biology (4 citations), Molecular Biology (180 citations) and Pediatrics, Perinatology and Child Health (49 citations). Mark A. McElwain has collaborated with scholars based in United States and China. Frequent co-authors include Radoje Drmanac, Brock A. Peters, Arthur L. Beaudet, Lorraine Potocki, Yaping Yang, C. Thomas Caskey, Karen W. Gripp, Christian P. Schaaf, Fan Xia and Manuel L. Gonzalez‐Garay. Their work appears in journals such as Molecular Biology of the Cell, Genome Research, Nature Genetics, PLoS ONE and Blood.

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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