Alison Millson

446 total citations
17 papers, 339 citations indexed

About

Alison Millson is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Alison Millson has authored 17 papers receiving a total of 339 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Pulmonary and Respiratory Medicine and 4 papers in Genetics. Recurrent topics in Alison Millson's work include Genomics and Rare Diseases (3 papers), Molecular Biology Techniques and Applications (3 papers) and Tracheal and airway disorders (3 papers). Alison Millson is often cited by papers focused on Genomics and Rare Diseases (3 papers), Molecular Biology Techniques and Applications (3 papers) and Tracheal and airway disorders (3 papers). Alison Millson collaborates with scholars based in United States, Canada and Germany. Alison Millson's co-authors include Elaine Lyon, Carl T. Wittwer, Mohamed Jama, Mary C. Lowery, Rachel Woods, Geneviève Pont-Kingdon, Christine E. Miller, Russell L. Maiese, Glenn H. Segal and Tae Sook Hwang and has published in prestigious journals such as Clinical Chemistry, Human Pathology and American Journal of Clinical Pathology.

In The Last Decade

Alison Millson

17 papers receiving 331 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alison Millson United States 12 155 68 64 60 58 17 339
Pavlína Plevová Czechia 11 150 1.0× 26 0.4× 114 1.8× 114 1.9× 60 1.0× 34 398
Alfons Meindl Germany 11 332 2.1× 65 1.0× 102 1.6× 21 0.3× 121 2.1× 14 490
Wendy J. Ingram Australia 7 267 1.7× 61 0.9× 62 1.0× 23 0.4× 44 0.8× 10 346
Peiwen Kuo United States 8 179 1.2× 19 0.3× 99 1.5× 34 0.6× 27 0.5× 16 370
Xiujing Gu United States 5 84 0.5× 19 0.3× 71 1.1× 54 0.9× 48 0.8× 6 413
Cláudia C. Faria Portugal 13 206 1.3× 175 2.6× 60 0.9× 40 0.7× 41 0.7× 42 429
Julia D. Mellentin United States 7 349 2.3× 67 1.0× 68 1.1× 13 0.2× 65 1.1× 7 578
Hsiang‐Chih Lu United States 8 142 0.9× 73 1.1× 60 0.9× 22 0.4× 15 0.3× 23 290
Shen-Long Howng Taiwan 11 143 0.9× 26 0.4× 27 0.4× 20 0.3× 24 0.4× 13 341
Tamar Eigler United States 11 260 1.7× 73 1.1× 67 1.0× 37 0.6× 41 0.7× 12 541

Countries citing papers authored by Alison Millson

Since Specialization
Citations

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

Fields of papers citing papers by Alison Millson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alison Millson

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

All Works

17 of 17 papers shown
1.
LaGrave, Danielle, et al.. (2016). Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder. European Journal of Medical Genetics. 59(9). 470–473. 19 indexed citations
2.
Millson, Alison, Tracey Lewis, Tina Pesaran, et al.. (2015). Processed Pseudogene Confounding Deletion/Duplication Assays for SMAD4. Journal of Molecular Diagnostics. 17(5). 576–582. 14 indexed citations
3.
Jama, Mohamed, Alison Millson, Christine E. Miller, & Elaine Lyon. (2013). Triplet Repeat Primed PCR Simplifies Testing for Huntington Disease. Journal of Molecular Diagnostics. 15(2). 255–262. 37 indexed citations
4.
Melis, Roberta, Tracy R. Lewis, Alison Millson, et al.. (2012). Copy Number Variation and Incomplete Linkage Disequilibrium Interfere with the HCP5 Genotyping Assay for Abacavir Hypersensitivity. Genetic Testing and Molecular Biomarkers. 16(9). 1111–1114. 13 indexed citations
5.
Anderson, Sharon, Bo Li, James H. Millonig, et al.. (2012). Medium chain acyl‐CoA dehydrogenase deficiency detected among Hispanics by New Jersey newborn screening. American Journal of Medical Genetics Part A. 158A(9). 2100–2105. 5 indexed citations
6.
Millson, Alison, Danielle LaGrave, Mary Willis, et al.. (2011). Chromosomal loss of 3q26.3‐3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability. American Journal of Medical Genetics Part A. 158A(1). 159–165. 20 indexed citations
7.
McDonald, Jamie, Kristy Damjanovich, Alison Millson, et al.. (2010). Molecular diagnosis in hereditary hemorrhagic telangiectasia: findings in a series tested simultaneously by sequencing and deletion/duplication analysis. Clinical Genetics. 79(4). 335–344. 47 indexed citations
8.
Pont-Kingdon, Geneviève, Rebecca L. Margraf, Kelli Sumner, et al.. (2008). Design and Application of Noncontinuously Binding Probes Used for Haplotyping and Genotyping. Clinical Chemistry. 54(6). 990–999. 6 indexed citations
9.
10.
Pont-Kingdon, Geneviève, Mohamed Jama, Christine Miller, Alison Millson, & Elaine Lyon. (2004). Long-Range (17.7 kb) Allele-Specific Polymerase Chain Reaction Method for Direct Haplotyping of R117H and IVS-8 Mutations of the Cystic Fibrosis Transmembrane Regulator Gene. Journal of Molecular Diagnostics. 6(3). 264–270. 15 indexed citations
11.
12.
Millson, Alison, Arminda Suli, L Hartung, et al.. (2003). Comparison of Two Quantitative Polymerase Chain Reaction Methods for Detecting HER2/neu Amplification. Journal of Molecular Diagnostics. 5(3). 184–190. 37 indexed citations
13.
Lyon, Elaine, Alison Millson, Mary C. Lowery, Rachel Woods, & Carl T. Wittwer. (2001). Quantification of HER2/neu Gene Amplification by Competitive PCR Using Fluorescent Melting Curve Analysis. Clinical Chemistry. 47(5). 844–851. 45 indexed citations
14.
Meadows, Cindy, et al.. (2000). Simultaneous Detection of C282Y and H63D Hemochromatosis Mutations by Dual-color Probes. Molecular Diagnosis. 5(2). 107–116. 14 indexed citations
15.
Millson, Alison, et al.. (2000). Comparison of Automated Short Tandem Repeat and Manual Variable Number of Tandem Repeat Analysis of Chimerism in Bone Marrow Transplant Patients. Diagnostic Molecular Pathology. 9(2). 91–97. 4 indexed citations
16.
Hussey, Charles E., Elaine Lyon, Alison Millson, et al.. (1999). A Rapid Practical RT-PCR-Based Approach for the Detection of the PML/RARalpha Fusion Transcript in Acute Promyelocytic Leukemia. American Journal of Clinical Pathology. 112(2). 256–262. 5 indexed citations
17.

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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