Joanne Mackey

1.7k citations

16 papers · 781 indexed · h-index 12

Impact in

Rheumatology top 2%
- Glycogen Storage Diseases and Myoclonus
- Folate and B Vitamins Research
Physiology top 5%
- Lysosomal Storage Disorders Research

Papers in ⓘ

Physiology 11
- Lysosomal Storage Disorders Research 11
Rheumatology 9
- Glycogen Storage Diseases and Myoclonus 7
- Folate and B Vitamins Research 2

Co-authors: Priya S. Kishnani (12 shared papers)Laura E. Case (5 shared papers)Joel Charrow (3 shared papers)Suhrad G. Banugaria (4 shared papers)Jennifer A. Sullivan (3 shared papers)Alison McVie‐Wylie (2 shared papers)Richard P. Morse (2 shared papers)Joseph M. Majure (2 shared papers)
Journals: Molecular Genetics and Metabolism (5 papers)Genetics in Medicine (2 papers)Neurogenetics (1 paper)American Journal of Medical Genetics Part C Seminars in Medical Genetics (1 paper)Journal of Inherited Metabolic Disease (1 paper)
Partner nations: United States Taiwan

In The Last Decade

Joanne Mackey

16 papers receiving 752 citations

Peers

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-authors

The 25 scholars most cited alongside Joanne Mackey, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Joanne Mackey Line = papers co-authored together Joanne Mackey links everyone, so they are left out of the graph.

All Works

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16 of 16 papers shown

#	Work
1	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 ·Andrea Amalfitano, A. Resai Bengur, Richard P. Morse, Joseph M. Majure, Laura E. Case, Deborah L. Veerling, Joanne Mackey, Priya S. Kishnani, Wendy E. Smith, Alison McVie‐Wylie, Jennifer A. Sullivan, George Hoganson, John A. Phillips, G. Bradley Schaefer, Joel Charrow, Russell E. Ware, Edward H. Bossen, Yuan-Tsong Chen	2001	293
2	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 ·Deeksha Bali, Jennifer Goldstein, Suhrad G. Banugaria, Jian Dai, Joanne Mackey, Catherine Rehder, Priya S. Kishnani	2012	97
3	Recombinant human acid ??-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial Genetics in Medicine ·Andrea Amalfitano, A. Resai Bengur, Richard P. Morse, Joseph M. Majure, Laura E. Case, Deborah L. Veerling, Joanne Mackey, Priya S. Kishnani, Wendy E. Smith, Alison McVie‐Wylie, Jennifer A. Sullivan, George Hoganson, John A. Phillips, G. Bradley Schaefer, Joel Charrow, Russell E. Ware, Edward H. Bossen, Yuan‐Tsong Chen	2001	73
4	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 ·Suhrad G. Banugaria, Trusha Patel, Joanne Mackey, S DAS, Andrea Amalfitano, Amy S. Rosenberg, Joel Charrow, Yuqi Chen, Priya S. Kishnani	2012	55
5	The thermolabile variant of methylenetetrahydrofolate reductase (MTHFR) is not a major risk factor for neural tube defect in American Caucasians Neurogenetics ·Marcy C. Speer, Gordon Worley, Joanne Mackey, E. Melvin, W. Jerry Oakes, T George	1997	42
6	Cardiac arrhythmias following anesthesia induction in infantile‐onset Pompe disease: a case series Pediatric Anesthesia ·LUKE Y.‐J. WANG, Allison Kinder Ross, Jennifer S. Li, Stephanie DeArmey, Joanne Mackey, MaryAlice Worden, Deyanira Corzo, Claire Morgan, Priya S. Kishnani	2007	36
7	Possible interaction of genotypes at cystathionine β‐synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects Clinical Genetics ·MC Speer, Jeffrey S. Nye, David G. McLone, Gordon Worley, E. Melvin, K. Viles, Amy Franklin, Courtney Drake, Joanne Mackey, TM George, (unknown)	1999	36
8	Frequency of Celiac Disease in Individuals with Down Syndrome in the United States Clinical Pediatrics ·Joanne Mackey, William R. Treem, Gordon Worley, Anne Boney, Patricia Hart, Priya S. Kishnani	2001	36
9	An individually, modified approach to desensitize infants and young children with Pompe disease, and significant reactions to alglucosidase alfa infusions Molecular Genetics and Metabolism ·Areeg El‐Gharbawy, Joanne Mackey, Stephanie DeArmey, Greg Westby, Sherry G. Grinnell, Peggy Malovrh, Robert L. Conway, Priya S. Kishnani	2011	26
10	Improvement with ongoing Enzyme Replacement Therapy in advanced late-onset Pompe disease: A case study Molecular Genetics and Metabolism ·Laura E. Case, Dwight D. Koeberl, Sarah P. Young, Deeksha Bali, Stephanie DeArmey, Joanne Mackey, Priya S. Kishnani	2008	26
11	Fractures in children with Pompe disease: a potentiallong-term complication Pediatric Radiology ·Laura E. Case, Rabi Hanna, Donald P. Frush, Vidya Krishnamurthy, Stephanie DeArmey, Joanne Mackey, Anne Boney, Claire Morgan, Deyanira Corzo, Susan Bouchard, Thomas J. Weber, Yuan-Tsong Chen, Priya S. Kishnani	2007	24
12	T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families American Journal of Medical Genetics ·Marcy C. Speer, Elizabeth C. Melvin, Kristi D. Viles, KIM A. BAUER, Evadnie Rampersaud, Courtney Drake, Timothy M. George, David S. Enterline, Joanne Mackey, Gordon Worley, John R. Gilbert, Jeffrey S. Nye, (unknown)	2002	15
13	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 ·Deeksha Bali, Jennifer Goldstein, Suhrad G. Banugaria, Jian Dai, Joanne Mackey, Catherine Rehder, Priya S. Kishnani	2012	11
14	Acute abdominal symptoms and signs in children and young adults with spina bifida: Ten years' experience Journal of Pediatric Surgery ·Gordon Worley, John S. Wiener, Timothy M. George, Herbert E. Fuchs, Joanne Mackey, Robert D. Fitch, Keith T. Oldham	2001	9
15	Diagnostic and treatment challenges of neuronopathic Gaucher disease: Two caseswith an intermediate phenotype Journal of Inherited Metabolic Disease ·R M Hanna, Marie McDonald, Jennifer A. Sullivan, Joanne Mackey, Venkat Krishnamurthy, Priya S. Kishnani	2004	1
16	The clinical phenotype of Long-term infantile Pompe disease survivors Molecular Genetics and Metabolism ·Sean N. Prater, Suhrad G. Banugaria, Joanne Mackey, Michelle Canfield, Laura E. Case, Stephanie DeArmey, Priya S. Kishnani	2011	1

About Joanne Mackey

Joanne Mackey is a scholar working on Physiology, Rheumatology, Epidemiology, Surgery and Psychiatry and Mental health, having authored 16 papers that have together received 781 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (11 papers), Glycogen Storage Diseases and Myoclonus (7 papers), Child Nutrition and Feeding Issues (3 papers), Trypanosoma species research and implications (3 papers), Congenital Anomalies and Fetal Surgery (2 papers), Spinal Dysraphism and Malformations (2 papers), Folate and B Vitamins Research (2 papers) and Neurological diseases and metabolism (1 paper). The work is most often cited by research in Rheumatology (439 citations), Physiology (580 citations), Clinical Biochemistry (56 citations), Physiology (32 citations) and Psychiatry and Mental health (91 citations). Joanne Mackey has collaborated with scholars based in United States and Taiwan. Frequent co-authors include Priya S. Kishnani, Laura E. Case, Joel Charrow, Suhrad G. Banugaria, Jennifer A. Sullivan, Alison McVie‐Wylie, Richard P. Morse, Joseph M. Majure, A. Resai Bengur and Andrea Amalfitano. Their work appears in journals such as Molecular Genetics and Metabolism, Genetics in Medicine, Neurogenetics, American Journal of Medical Genetics Part C Seminars in Medical Genetics and Journal of Inherited Metabolic Disease.

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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