Melinda Procter

734 total citations · 1 hit paper
19 papers, 500 citations indexed

About

Melinda Procter is a scholar working on Molecular Biology, Organic Chemistry and Cell Biology. According to data from OpenAlex, Melinda Procter has authored 19 papers receiving a total of 500 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Organic Chemistry and 4 papers in Cell Biology. Recurrent topics in Melinda Procter's work include Protease and Inhibitor Mechanisms (4 papers), Click Chemistry and Applications (3 papers) and Biotin and Related Studies (3 papers). Melinda Procter is often cited by papers focused on Protease and Inhibitor Mechanisms (4 papers), Click Chemistry and Applications (3 papers) and Biotin and Related Studies (3 papers). Melinda Procter collaborates with scholars based in United States, Switzerland and Israel. Melinda Procter's co-authors include Rong Mao, Nicola Longo, Bryan L. Krock, Michael Bandell, Viktor Lukacs, Ardem Patapoutian, Ronald W. Day, Helen J. Kim, Pinar Bayrak‐Toydemir and David A. Stevenson and has published in prestigious journals such as Nature Communications, CHEST Journal and Clinical Chemistry.

In The Last Decade

Melinda Procter

19 papers receiving 491 citations

Hit Papers

Impaired PIEZO1 function in patients with a novel autosom... 2015 2026 2018 2022 2015 50 100 150 200

Peers

Melinda Procter
Victor Babich United States
Esti Liani Israel
Taotao Lao United States
Melinda Procter
Citations per year, relative to Melinda Procter Melinda Procter (= 1×) peers Anthony O. Fedele

Countries citing papers authored by Melinda Procter

Since Specialization
Citations

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

Fields of papers citing papers by Melinda Procter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Melinda Procter

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

All Works

19 of 19 papers shown
1.
Mao, Rong, et al.. (2022). Atypical presentation of Angelman syndrome with intact expressive language due to low‐level mosaicism. Molecular Genetics & Genomic Medicine. 10(10). e2018–e2018. 2 indexed citations
2.
Ballhausen, Diana, Barry Wolf, Melinda Procter, et al.. (2020). Severe Distal Motor Involvement in a Non-compliant Adult With Biotinidase Deficiency: The Necessity of Life-Long Biotin Therapy. Frontiers in Neurology. 11. 516799–516799. 3 indexed citations
3.
Ardon, Orly, Melinda Procter, Rong Mao, et al.. (2016). Creatine transporter deficiency: Novel mutations and functional studies. Molecular Genetics and Metabolism Reports. 8. 20–23. 15 indexed citations
4.
Procter, Melinda, Barry Wolf, & Rong Mao. (2016). Forty-eight novel mutations causing biotinidase deficiency. Molecular Genetics and Metabolism. 117(3). 369–372. 18 indexed citations
5.
Lukacs, Viktor, Jayanti Mathur, Rong Mao, et al.. (2015). Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia. Nature Communications. 6(1). 8329–8329. 216 indexed citations breakdown →
6.
Sumner, Kelli, Jeffrey Swensen, Melinda Procter, et al.. (2014). Noncontinuously Binding Loop-Out Primers for Avoiding Problematic DNA Sequences in PCR and Sanger Sequencing. Journal of Molecular Diagnostics. 16(5). 477–480. 3 indexed citations
7.
Ardon, Orly, et al.. (2014). Sequencing analysis of insulin receptor defects and detection of two novel mutations in INSR gene. Molecular Genetics and Metabolism Reports. 1. 71–84. 52 indexed citations
8.
Procter, Melinda, et al.. (2014). Challenging Identification of a Novel PiISF and the Rare PiMmaltonZ α1-Antitrypsin Deficiency Variants in Two Patients. American Journal of Clinical Pathology. 141(5). 742–746. 6 indexed citations
9.
Procter, Melinda, Barry Wolf, David K. Crockett, & Rong Mao. (2013). The Biotinidase Gene Variants Registry: A Paradigm Public Database. G3 Genes Genomes Genetics. 3(4). 727–731. 26 indexed citations
10.
Greene, Dina N., Melinda Procter, Patti Krautscheid, et al.. (2012). α1-Antitrypsin Deficiency in Fraternal Twins Born With Familial Spontaneous Pneumothorax. CHEST Journal. 141(1). 239–241. 6 indexed citations
11.
Pham, Hoai D., et al.. (2012). A Patient with Prolonged Paralysis. Clinical Chemistry. 58(3). 496–500. 3 indexed citations
12.
Wooderchak‐Donahue, Whitney, Cecily P. Vaughn, Lan‐Szu Chou, et al.. (2011). Verification of Multiplex Ligation-Dependent Probe Amplification Probes in the Absence of Positive Samples. Genetic Testing and Molecular Biomarkers. 15(11). 793–799. 1 indexed citations
13.
Greene, Dina N., Melinda Procter, David G. Grenache, et al.. (2011). Misclassification of an apparent alpha 1-antitrypsin “Z” deficiency variant by melting analysis. Clinica Chimica Acta. 412(15-16). 1454–1456. 5 indexed citations
14.
Procter, Melinda, et al.. (2011). Concordance of Butyrylcholinesterase Phenotype With Genotype. American Journal of Clinical Pathology. 135(2). 271–276. 14 indexed citations
15.
Curry, Cynthia J., Rong Mao, Emily Aston, et al.. (2008). Homozygous deletions of a copy number change detected by array CGH: A new cause for mental retardation?. American Journal of Medical Genetics Part A. 146A(15). 1903–1910. 10 indexed citations
16.
Bornhorst, Joshua A., et al.. (2007). Genotypes and serum concentrations of human alpha-1-antitrypsin “P” protein variants in a clinical population. Journal of Clinical Pathology. 60(10). 1124–1128. 19 indexed citations
17.
Bornhorst, Joshua A., Melinda Procter, Cindy Meadows, Edward R. Ashwood, & Rong Mao. (2007). Evaluation of an Integrative Diagnostic Algorithm for the Identification of People at Risk for α1-Antitrypsin Deficiency. American Journal of Clinical Pathology. 128(3). 482–490. 20 indexed citations
18.
Procter, Melinda, Lan‐Szu Chou, Wei Tang, Mohamed Jama, & Rong Mao. (2006). Molecular Diagnosis of Prader–Willi and Angelman Syndromes by Methylation-Specific Melting Analysis and Methylation-Specific Multiplex Ligation-Dependent Probe Amplification. Clinical Chemistry. 52(7). 1276–1283. 67 indexed citations
19.
Langer, Janine, et al.. (2004). Evaluation of the ELVIS plate method for the detection and typing of herpes simplex virus in clinical specimens. Diagnostic Microbiology and Infectious Disease. 49(3). 173–177. 14 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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