Danny E. Miller

7.7k total citations · 1 hit paper
61 papers, 1.3k citations indexed

About

Danny E. Miller is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Danny E. Miller has authored 61 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 22 papers in Genetics and 21 papers in Plant Science. Recurrent topics in Danny E. Miller's work include Chromosomal and Genetic Variations (20 papers), Genomics and Rare Diseases (13 papers) and CRISPR and Genetic Engineering (12 papers). Danny E. Miller is often cited by papers focused on Chromosomal and Genetic Variations (20 papers), Genomics and Rare Diseases (13 papers) and CRISPR and Genetic Engineering (12 papers). Danny E. Miller collaborates with scholars based in United States, Japan and France. Danny E. Miller's co-authors include R. Scott Hawley, Fuki M. Hisama, Timothy W. Yu, Lauren Massingham, Sawona Biswas, Kandamurugu Manickam, Laurie Demmer, Jennifer Malinowski, Hutton M. Kearney and Monica R. McClain and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Danny E. Miller

59 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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)

2021 288 citations Kandamurugu Manickam, Monica R. McClain et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Danny E. Miller United States	20	799	615	403	102	85	61	1.3k
Keith A. Maggert United States	17	1.6k 2.1×	426 0.7×	511 1.3×	118 1.2×	98 1.2×	28	2.0k
Györgyi Csankovszki United States	20	2.0k 2.5×	731 1.2×	339 0.8×	80 0.8×	101 1.2×	38	2.2k
Lawrence Hon United States	11	931 1.2×	493 0.8×	150 0.4×	84 0.8×	30 0.4×	17	1.6k
Kazuhiro R. Nitta Japan	13	2.8k 3.4×	504 0.8×	302 0.7×	76 0.7×	65 0.8×	30	3.1k
Paul J. Hurd United Kingdom	15	1.5k 1.9×	558 0.9×	131 0.3×	21 0.2×	129 1.5×	25	1.9k
Tuncay Baubec Switzerland	21	2.1k 2.6×	411 0.7×	707 1.8×	51 0.5×	90 1.1×	36	2.6k
Robert Johnsen Canada	19	1.2k 1.5×	854 1.4×	120 0.3×	208 2.0×	81 1.0×	38	2.1k
Matthew D. Schultz United States	11	1.6k 2.0×	568 0.9×	1.1k 2.8×	28 0.3×	70 0.8×	11	2.4k
Qian Bian China	17	1.4k 1.7×	257 0.4×	329 0.8×	119 1.2×	31 0.4×	44	1.6k
Shaying Zhao United States	23	1.0k 1.3×	550 0.9×	729 1.8×	34 0.3×	34 0.4×	33	1.6k

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-authorship network of co-authors of Danny E. Miller

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

All Works

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20 of 20 papers shown

Reyes, Monica, Barbara Gales, Agnès Linglart, et al.. (2025). Bidirectional disruption of GNAS transcripts causes broad methylation defects in pseudohypoparathyroidism type 1B. Proceedings of the National Academy of Sciences. 122(16). e2423271122–e2423271122. 2 indexed citations

Thomas, Ria, Emily Miyoshi, Hasan O. Akman, et al.. (2025). Splice-modulating antisense oligonucleotides targeting a pathogenic intronic variant in adult polyglucosan body disease correct mis-splicing and restore enzyme activity in patient cells. Nucleic Acids Research. 53(13).

Beck, Anita E., et al.. (2025). Concordance of Whole-Genome Long-Read Sequencing with Standard Clinical Testing for Prader-Willi and Angelman Syndromes. Journal of Molecular Diagnostics. 27(3). 166–176. 1 indexed citations

Hawley, R. Scott, Andrew J. Price, Hua Li, et al.. (2025). Patterns of crossover distribution in Drosophila mauritiana necessitate a re-thinking of the centromere effect on crossing over. Genetics. 230(1). 3 indexed citations

Wilderman, Andrea, Machteld Baetens, Ellen Roets, et al.. (2024). A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development. Nature Communications. 15(1). 3 indexed citations

Sala‐Torra, Olga, Lan Beppu, Danny E. Miller, et al.. (2024). Expanding the Role of SH2B3: T Cell Large Granular Lymphocytosis (LGL) and Common Variable Immune Deficiency in the Setting of Biallelic SH2B3 Mutations. Blood. 144(Supplement 1). 3919–3919. 1 indexed citations

Mallory, Benjamin J., Tara Wenger, Irene J. Chang, et al.. (2024). 3-hour genome sequencing and targeted analysis to rapidly assess genetic risk. SHILAP Revista de lepidopterología. 2. 101833–101833. 7 indexed citations

Mastrorosa, Francesco, Danny E. Miller, & Evan E. Eichler. (2023). Applications of long-read sequencing to Mendelian genetics. Genome Medicine. 15(1). 42–42. 50 indexed citations

Li, Haosheng, et al.. (2023). Heterozygous inversion breakpoints suppress meiotic crossovers by altering recombination repair outcomes. PLoS Genetics. 19(4). e1010702–e1010702. 9 indexed citations

10.

Pappas, John, et al.. (2023). CLN2 disease resulting from a novel homozygous deep intronic splice variant in TPP1 discovered using long-read sequencing. Molecular Genetics and Metabolism. 140(4). 107713–107713.

11.

Patel, Nisha, John M. Graham, Michael J. Bamshad, et al.. (2021). Further delineation of van den Ende‐Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome. American Journal of Medical Genetics Part A. 185(7). 2136–2149. 3 indexed citations

12.

Miller, Danny E.. (2021). The diagnostic odyssey: our family’s story. The American Journal of Human Genetics. 108(2). 217–218. 8 indexed citations

13.

Manickam, Kandamurugu, Monica R. McClain, Laurie Demmer, et al.. (2021). 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). Genetics in Medicine. 23(11). 2029–2037. 288 indexed citations breakdown →

14.

Miller, Danny E., Patrick Hanna, Monica Reyes, et al.. (2020). Targeted Long-Read Sequencing Identifies a Retrotransposon Insertion as a Cause of Altered GNAS Exon A/B Methylation in a Family With Autosomal Dominant Pseudohypoparathyroidism Type 1b (PHP1B). Journal of Bone and Mineral Research. 37(9). 1711–1719. 19 indexed citations

15.

Hatkevich, Talia, et al.. (2020). A pathway for error-free non-homologous end joining of resected meiotic double-strand breaks. Nucleic Acids Research. 49(2). 879–890. 12 indexed citations

16.

Miller, Danny E.. (2019). Synaptonemal Complex-Deficient Drosophila melanogaster Females Exhibit Rare DSB Repair Events, Recurrent Copy-Number Variation, and an Increased Rate of de Novo Transposable Element Movement. G3 Genes Genomes Genetics. 10(2). 525–537. 4 indexed citations

17.

Solares, Edwin, Mahul Chakraborty, Danny E. Miller, et al.. (2018). Rapid Low-Cost Assembly of the Drosophila melanogaster Reference Genome Using Low-Coverage, Long-Read Sequencing. G3 Genes Genomes Genetics. 8(10). 3143–3154. 64 indexed citations

18.

Miller, Danny E., Cynthia Staber, Julia Zeitlinger, & R. Scott Hawley. (2018). Highly Contiguous Genome Assemblies of 15 Drosophila Species Generated Using Nanopore Sequencing. G3 Genes Genomes Genetics. 8(10). 3131–3141. 94 indexed citations

19.

Miller, Danny E., et al.. (2018). Origin, Composition, and Structure of the Supernumerary B Chromosome of Drosophila melanogaster. Genetics. 210(4). 1197–1212. 21 indexed citations

20.

Chen, Xiangyu, Rima Sandhu, Beth Rockmill, et al.. (2015). Phosphorylation of the Synaptonemal Complex Protein Zip1 Regulates the Crossover/Noncrossover Decision during Yeast Meiosis. PLoS Biology. 13(12). e1002329–e1002329. 39 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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