Miyono Hendrix

636 total citations
14 papers, 499 citations indexed

About

Miyono Hendrix is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Miyono Hendrix has authored 14 papers receiving a total of 499 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Surgery. Recurrent topics in Miyono Hendrix's work include Cystic Fibrosis Research Advances (4 papers), Genomics and Rare Diseases (3 papers) and Diabetes and associated disorders (3 papers). Miyono Hendrix is often cited by papers focused on Cystic Fibrosis Research Advances (4 papers), Genomics and Rare Diseases (3 papers) and Diabetes and associated disorders (3 papers). Miyono Hendrix collaborates with scholars based in United States. Miyono Hendrix's co-authors include Sue Jinks-Robertson, Abhijit Datta, Marc Lipsitch, Suzanne K. Cordovado, Gray F. Crouse, Ainsley Nicholson, Marie C. Earley, Philip M. Farrell, Mei Baker and Laura Hancock and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Diabetes.

In The Last Decade

Miyono Hendrix

14 papers receiving 496 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Miyono Hendrix United States	10	300	118	95	81	66	14	499
Olga Nikolayeva Switzerland	4	273 0.9×	55 0.5×	55 0.6×	50 0.6×	24 0.4×	4	430
Abigail L. Savage United Kingdom	13	370 1.2×	109 0.9×	32 0.3×	93 1.1×	14 0.2×	20	531
Elena Alexandrova Italy	17	455 1.5×	114 1.0×	28 0.3×	134 1.7×	49 0.7×	47	669
Michael Wagner United States	9	269 0.9×	133 1.1×	27 0.3×	73 0.9×	25 0.4×	11	465
C Piussan France	9	371 1.2×	122 1.0×	31 0.3×	39 0.5×	20 0.3×	34	563
W.M. Henry United States	10	203 0.7×	94 0.8×	43 0.5×	22 0.3×	13 0.2×	24	444
T C Rodman United States	13	240 0.8×	100 0.8×	34 0.4×	41 0.5×	27 0.4×	16	508
Ján Radvánszky Slovakia	13	266 0.9×	202 1.7×	38 0.4×	32 0.4×	28 0.4×	33	547
Takashi Shimada Japan	13	392 1.3×	140 1.2×	28 0.3×	70 0.9×	9 0.1×	21	567
Joseph R. Dobosy United States	9	479 1.6×	98 0.8×	9 0.1×	124 1.5×	53 0.8×	9	629

Countries citing papers authored by Miyono Hendrix

Since Specialization

Citations

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

Fields of papers citing papers by Miyono Hendrix

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miyono Hendrix

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

All Works

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14 of 14 papers shown

Hendrix, Miyono, Carla Cuthbert, & Suzanne K. Cordovado. (2020). Assessing the Performance of Dried-Blood-Spot DNA Extraction Methods in Next Generation Sequencing. International Journal of Neonatal Screening. 6(2). 36–36. 9 indexed citations

Hendrix, Miyono, Stephanie L. Foster, & Suzanne K. Cordovado. (2016). Newborn Screening Quality Assurance Program for CFTR Mutation Detection and Gene Sequencing to Identify Cystic Fibrosis. SHILAP Revista de lepidopterología. 4. 4078078295–4078078295. 9 indexed citations

Baker, Mei, et al.. (2015). Improving newborn screening for cystic fibrosis using next-generation sequencing technology: a technical feasibility study. Genetics in Medicine. 18(3). 231–238. 73 indexed citations

Cordovado, Suzanne K., Miyono Hendrix, Christopher N. Greene, et al.. (2011). CFTR mutation analysis and haplotype associations in CF patients. Molecular Genetics and Metabolism. 105(2). 249–254. 30 indexed citations

Hagopian, William, Jin‐Xiong She, Beena Akolkar, et al.. (2010). Proficiency Testing of Human Leukocyte Antigen-DR and Human Leukocyte Antigen-DQ Genetic Risk Assessment for Type 1 Diabetes Using Dried Blood Spots. Journal of Diabetes Science and Technology. 4(4). 929–941. 7 indexed citations

Cordovado, Suzanne K., Marie C. Earley, Miyono Hendrix, et al.. (2009). Assessment of DNA contamination from dried blood spots and determination of DNA yield and function using archival newborn dried blood spots. Clinica Chimica Acta. 402(1-2). 107–113. 11 indexed citations

Cordovado, Suzanne K., Laura Hancock, Miyono Hendrix, Christopher N. Greene, & Patricia W. Mueller. (2009). Novel human leukocyte antigen class I and class II alleles identified by sequence-based typing in the Genetics of Kidneys in Diabetes (GoKinD) study population. Human Immunology. 70(9). 747–749. 1 indexed citations

Cordovado, Suzanne K., Yuan Zhao, James H. Warram, et al.. (2007). Nephropathy in Type 1 Diabetes Is Diminished in Carriers of HLA-DRB1*04. Diabetes. 57(2). 518–522. 18 indexed citations

Cordovado, Suzanne K., et al.. (2005). High‐resolution genotyping of HLA‐DQA1 in the GoKinD study and identification of novel alleles HLA‐DQA1*040102, HLA‐DQA1*0402 and HLA‐DQA1*0404. Tissue Antigens. 65(5). 448–458. 16 indexed citations

10.

Hancock, Laura, et al.. (2005). Identification of Two Novel DQA1 Alleles, DQA1*0107 and DQA1*0602, by Sequence-Based Typing in the GoKinD Population. Human Immunology. 66(12). 1248–1253. 7 indexed citations

11.

Cordovado, Suzanne K., et al.. (2003). High-resolution genotyping of HLA-DQA1 EXON 1, 2 and 3 and the identification of two novel alleles DQA1∗0402 and DQA1∗040102. Human Immunology. 64(10). S120–S120. 1 indexed citations

12.

Nicholson, Ainsley, Miyono Hendrix, Sue Jinks-Robertson, & Gray F. Crouse. (2000). Regulation of Mitotic Homeologous Recombination in Yeast: Functions of Mismatch Repair and Nucleotide Excision Repair Genes. Genetics. 154(1). 133–146. 95 indexed citations

13.

Datta, Abhijit, Miyono Hendrix, Marc Lipsitch, & Sue Jinks-Robertson. (1997). Dual roles for DNA sequence identity and the mismatch repair system in the regulation of mitotic crossing-over in yeast. Proceedings of the National Academy of Sciences. 94(18). 9757–9762. 192 indexed citations

14.

Smith, Wayne C., Robert M. Greenberg, Bruce G. Calman, et al.. (1995). Isolation and Expression of an Arrestin cDNA from the Horseshoe Crab Lateral Eye. Journal of Neurochemistry. 64(1). 1–13. 30 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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