Joanne Mackey

1.7k total citations
16 papers, 781 citations indexed

About

Joanne Mackey is a scholar working on Physiology, Rheumatology and Epidemiology. According to data from OpenAlex, Joanne Mackey has authored 16 papers receiving a total of 781 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Physiology, 9 papers in Rheumatology and 4 papers in Epidemiology. Recurrent topics in Joanne Mackey's work include Lysosomal Storage Disorders Research (11 papers), Glycogen Storage Diseases and Myoclonus (7 papers) and Child Nutrition and Feeding Issues (3 papers). Joanne Mackey is often cited by papers focused on Lysosomal Storage Disorders Research (11 papers), Glycogen Storage Diseases and Myoclonus (7 papers) and Child Nutrition and Feeding Issues (3 papers). Joanne Mackey collaborates with scholars based in United States and Taiwan. Joanne Mackey's co-authors include Priya S. Kishnani, Joel Charrow, Laura E. Case, Suhrad G. Banugaria, Jennifer A. Sullivan, Russell E. Ware, John A. Phillips, Alison McVie‐Wylie, Wendy E. Smith and Joseph M. Majure and has published in prestigious journals such as Journal of Pediatric Surgery, Genetics in Medicine and American Journal of Medical Genetics.

In The Last Decade

Joanne Mackey

16 papers receiving 752 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joanne Mackey United States 12 580 439 186 152 133 16 781
Ed Wraith United Kingdom 11 718 1.2× 203 0.5× 242 1.3× 110 0.7× 149 1.1× 24 910
J E Wraith United Kingdom 11 571 1.0× 192 0.4× 233 1.3× 80 0.5× 92 0.7× 12 740
Shu-Chuan Chiang Taiwan 10 426 0.7× 197 0.4× 179 1.0× 135 0.9× 208 1.6× 20 721
F. A. Beemer Netherlands 12 293 0.5× 248 0.6× 101 0.5× 92 0.6× 232 1.7× 21 714
Zoheb B. Kazi United States 13 426 0.7× 245 0.6× 102 0.5× 121 0.8× 87 0.7× 23 548
Karen Tylee United Kingdom 16 580 1.0× 158 0.4× 259 1.4× 104 0.7× 104 0.8× 45 704
Alexander Broomfield United Kingdom 14 358 0.6× 137 0.3× 124 0.7× 81 0.5× 205 1.5× 54 613
Mislen Bauer United States 10 269 0.5× 208 0.5× 107 0.6× 75 0.5× 143 1.1× 19 561
Norberto Guelbert Argentina 16 514 0.9× 232 0.5× 216 1.2× 68 0.4× 148 1.1× 39 651
Rick Martin United States 8 989 1.7× 376 0.9× 517 2.8× 165 1.1× 118 0.9× 12 1.1k

Countries citing papers authored by Joanne Mackey

Since Specialization
Citations

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

Fields of papers citing papers by Joanne Mackey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joanne Mackey

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

All Works

16 of 16 papers shown
1.
Bali, Deeksha, Jennifer Goldstein, Suhrad G. Banugaria, et al.. (2012). Predicting cross‐reactive immunological material (CRIM) status in Pompe disease using GAA mutations: Lessons learned from 10 years of clinical laboratory testing experience. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 160C(1). 40–49. 97 indexed citations
2.
Banugaria, Suhrad G., Trusha Patel, Joanne Mackey, et al.. (2012). Persistence of high sustained antibodies to enzyme replacement therapy despite extensive immunomodulatory therapy in an infant with Pompe disease: Need for agents to target antibody-secreting plasma cells. Molecular Genetics and Metabolism. 105(4). 677–680. 55 indexed citations
3.
Bali, Deeksha, Jennifer Goldstein, Suhrad G. Banugaria, et al.. (2012). Predicting Cross Reactive Immunological Material (CRIM) Status in Pompe Disease Using GAA Mutations: Lessons Learned from 10 Years of Clinical Laboratory Testing Experience. Molecular Genetics and Metabolism. 105(2). S20–S20. 11 indexed citations
4.
El‐Gharbawy, Areeg, et al.. (2011). An individually, modified approach to desensitize infants and young children with Pompe disease, and significant reactions to alglucosidase alfa infusions. Molecular Genetics and Metabolism. 104(1-2). 118–122. 26 indexed citations
5.
Prater, Sean N., Suhrad G. Banugaria, Joanne Mackey, et al.. (2011). The clinical phenotype of Long-term infantile Pompe disease survivors. Molecular Genetics and Metabolism. 102(2). S36–S37. 1 indexed citations
6.
Case, Laura E., Dwight D. Koeberl, Sarah P. Young, et al.. (2008). Improvement with ongoing Enzyme Replacement Therapy in advanced late-onset Pompe disease: A case study. Molecular Genetics and Metabolism. 95(4). 233–235. 26 indexed citations
7.
Case, Laura E., Donald P. Frush, Stephanie DeArmey, et al.. (2007). Fractures in children with Pompe disease: a potentiallong-term complication. Pediatric Radiology. 37(5). 437–445. 24 indexed citations
8.
Ross, Allison Kinder, Jennifer S. Li, Stephanie DeArmey, et al.. (2007). Cardiac arrhythmias following anesthesia induction in infantile‐onset Pompe disease: a case series. Pediatric Anesthesia. 17(8). 738–748. 36 indexed citations
9.
Hanna, R M, Marie McDonald, Jennifer A. Sullivan, et al.. (2004). Diagnostic and treatment challenges of neuronopathic Gaucher disease: Two caseswith an intermediate phenotype. Journal of Inherited Metabolic Disease. 27(5). 687–690. 1 indexed citations
10.
Speer, Marcy C., Kristi D. Viles, Evadnie Rampersaud, et al.. (2002). T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families. American Journal of Medical Genetics. 110(3). 215–218. 15 indexed citations
11.
Worley, Gordon, John S. Wiener, Timothy M. George, et al.. (2001). Acute abdominal symptoms and signs in children and young adults with spina bifida: Ten years' experience. Journal of Pediatric Surgery. 36(9). 1381–1386. 9 indexed citations
12.
Amalfitano, Andrea, A. Resai Bengur, Richard P. Morse, et al.. (2001). Recombinant human acid α-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial. Genetics in Medicine. 3(2). 132–138. 293 indexed citations
13.
Mackey, Joanne, et al.. (2001). Frequency of Celiac Disease in Individuals with Down Syndrome in the United States. Clinical Pediatrics. 40(5). 249–252. 36 indexed citations
14.
Amalfitano, Andrea, A. Resai Bengur, Richard P. Morse, et al.. (2001). Recombinant human acid ??-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial. Genetics in Medicine. 3(2). 132–138. 73 indexed citations
15.
Nye, Jeffrey S., et al.. (1999). Possible interaction of genotypes at cystathionine β‐synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. Clinical Genetics. 56(2). 142–144. 36 indexed citations
16.

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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