Danny E. Miller

8.4k citations
95 papers · 4.2k · 3 hit papers · h-index 26

Impact in

  • Genetics top 2%
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genomics and Phylogenetic Studies
    • CRISPR and Genetic Engineering
    • Genomics and Chromatin Dynamics
    • RNA modifications and cancer
    • RNA and protein synthesis mechanisms

Papers in

    • Genomics and Rare Diseases 23
    • Genomic variations and chromosomal abnormalities 11
    • Genomics and Phylogenetic Studies 12
    • DNA Repair Mechanisms 11
    • CRISPR and Genetic Engineering 11
    • Mitochondrial Function and Pathology 5

Danny E. Miller

91 papers receiving 4.1k citations

Danny E. Miller's Hit Papers

A complete reference genome improves analysis of human genetic variation 2022 · 227 citations
2270+1+3Years since publication50010001.5k

Peers

Danny E. Miller
Comparison fields: 5 of 153
  • Genetics 1.5k
  • Molecular Biology 2.3k
  • Aging 45
  • Plant Science 954
  • Cancer Research 301
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Danny E. Miller relative to Matthew D. Rasmussen United States Matthew D. Rasmussen's profile →
Citations per field
00.5×2×4×6.1×
Matthew D. Rasmussen · 1×
Citations per year

Countries citing papers authored by Danny E. Miller

Since Specialization
Citations

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

Fields of papers citing papers by Danny E. Miller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Danny E. Miller. 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 Danny E. Miller. The network helps show where Danny E. Miller may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 95 papers — load more, or switch the sort, to bring in the rest.

#Work
1
The complete sequence of a human genome
Hit paper breakdown →
20221737
2
Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
Hit paper breakdown →
2021401
3
A complete reference genome improves analysis of human genetic variation
Hit paper breakdown →
2022227
4 2021137
5 2022123
6 2021112
7 201897
8 201892
9 202372
10 202166
11 201865
12 201664
13 201860
14 202356
15 201245
16 201444
17 202043
18 201541
19 201538
20 201933

About Danny E. Miller

Danny E. Miller is a scholar working on Genetics, Molecular Biology, Plant Science, Clinical Biochemistry and Cancer Research, having authored 95 papers that have together received 4.2k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (23 papers), Chromosomal and Genetic Variations (23 papers), Genomics and Phylogenetic Studies (12 papers), Genomic variations and chromosomal abnormalities (11 papers), DNA Repair Mechanisms (11 papers), CRISPR and Genetic Engineering (11 papers), Mitochondrial Function and Pathology (5 papers) and Microtubule and mitosis dynamics (5 papers). The work is most often cited by research in Genetics (1.5k citations), Molecular Biology (2.3k citations), Aging (45 citations), Plant Science (954 citations) and Cancer Research (301 citations). Danny E. Miller has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include R. Scott Hawley, Fuki Marie Hisama, Jennifer R. Malinowski, Timothy W. Yu, Monica R. McClain, Laurie Demmer, Hutton M. Kearney, Kandamurugu Manickam, Sawona Biswas and Lauren J. Massingham. Their work appears in journals such as Genetics, G3 Genes Genomes Genetics, The American Journal of Human Genetics, Proceedings of the National Academy of Sciences and Nature Communications.

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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