May Christine V. Malicdan

8.7k total citations
126 papers, 2.6k citations indexed

About

May Christine V. Malicdan is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, May Christine V. Malicdan has authored 126 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 35 papers in Epidemiology and 28 papers in Genetics. Recurrent topics in May Christine V. Malicdan's work include Inflammatory Myopathies and Dermatomyositis (27 papers), Muscle Physiology and Disorders (19 papers) and Cardiomyopathy and Myosin Studies (11 papers). May Christine V. Malicdan is often cited by papers focused on Inflammatory Myopathies and Dermatomyositis (27 papers), Muscle Physiology and Disorders (19 papers) and Cardiomyopathy and Myosin Studies (11 papers). May Christine V. Malicdan collaborates with scholars based in United States, Japan and Israel. May Christine V. Malicdan's co-authors include Ichizo Nishino, S. Noguchi, William A. Gahl, Ikuya Nonaka, Marjan Huizing, Yukiko Hayashi, Nuria Carrillo, Thierry Vilboux, David R. Adams and Ikuya Nonaka and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

May Christine V. Malicdan

117 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
May Christine V. Malicdan United States	29	1.5k	744	544	460	309	126	2.6k
Takayuki Morisaki Japan	34	2.1k 1.5×	399 0.5×	747 1.4×	223 0.5×	645 2.1×	154	3.7k
Stefania Petrini Italy	34	2.2k 1.5×	314 0.4×	364 0.7×	352 0.8×	312 1.0×	127	3.7k
Thomas P. Zwaka United States	24	3.3k 2.2×	746 1.0×	502 0.9×	242 0.5×	477 1.5×	47	4.9k
Philippe M. Campeau Canada	33	1.8k 1.3×	327 0.4×	1.0k 1.9×	298 0.6×	92 0.3×	123	3.3k
Reimar Abraham Italy	10	2.1k 1.4×	219 0.3×	281 0.5×	409 0.9×	199 0.6×	16	3.0k
Maria Alice Donati Italy	31	2.5k 1.7×	344 0.5×	334 0.6×	573 1.2×	371 1.2×	136	3.9k
Matthias Mueller Germany	22	1.1k 0.8×	694 0.9×	156 0.3×	176 0.4×	320 1.0×	41	2.4k
Conrad C. Weihl United States	36	2.4k 1.6×	1.0k 1.4×	205 0.4×	1.1k 2.5×	245 0.8×	100	4.0k
Robin L. Erickson United States	14	1.7k 1.2×	434 0.6×	317 0.6×	156 0.3×	127 0.4×	29	2.6k

Countries citing papers authored by May Christine V. Malicdan

Since Specialization

Citations

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

Fields of papers citing papers by May Christine V. Malicdan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by May Christine V. Malicdan. 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 May Christine V. Malicdan. The network helps show where May Christine V. Malicdan may publish in the future.

Co-authorship network of co-authors of May Christine V. Malicdan

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

All Works

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20 of 20 papers shown

Fu, Jiayu, Barbara N. Pusey, Ellen F. Macnamara, et al.. (2025). RNA sequencing driven diagnosis expands the phenotypic spectrum of NBAS deficiency. Molecular Genetics and Metabolism. 145(1). 109105–109105.

Maynard, Dawn, Bernadette R. Gochuico, Christopher K. E. Bleck, et al.. (2024). Insights into the renal pathophysiology in Hermansky‐Pudlak syndrome‐1 from urinary extracellular vesicle proteomics and a new mouse model. FEBS Letters. 599(7). 1055–1074.

Sharma, Prashant, Thomas C. Markello, Dorothy K. Grange, et al.. (2024). Biallelic germline DDX41 variants in a patient with bone dysplasia, ichthyosis, and dysmorphic features. Human Genetics. 143(12). 1445–1457.

Morimoto, Marie, Elena‐Raluca Nicoli, Joseph C. Roney, et al.. (2023). Spectrum of LYST mutations in Chediak-Higashi syndrome: a report of novel variants and a comprehensive review of the literature. Journal of Medical Genetics. 61(3). 212–223. 8 indexed citations

Pace, Raffaella De, Javier Manzella‐Lapeira, Antony Cougnoux, et al.. (2023). LYST deficiency impairs autophagic lysosome reformation in neurons and alters lysosome number and size. Cellular and Molecular Life Sciences. 80(2). 53–53. 10 indexed citations

Montaño, Carolina, Shira G. Ziegler, Manfred Boehm, et al.. (2022). Diagnosis and discovery: Insights from the NIH Undiagnosed Diseases Program. Journal of Inherited Metabolic Disease. 45(5). 907–918. 4 indexed citations

Sharma, Prashant, Elena‐Raluca Nicoli, Marie Morimoto, et al.. (2019). Chediak-Higashi syndrome: A review of the past, present, and future. Drug Discovery Today Disease Models. 31. 31–36. 25 indexed citations

Sharma, Prashant, Yan Lu, Thomas C. Markello, et al.. (2019). Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype. PLoS Genetics. 15(5). e1008143–e1008143. 18 indexed citations

Park, Joshua K., Nathan J. Coffey, William A. Gahl, et al.. (2019). Bleomycin Induces Drug Efflux in Lungs. A Pitfall for Pharmacological Studies of Pulmonary Fibrosis. American Journal of Respiratory Cell and Molecular Biology. 62(2). 178–190. 17 indexed citations

10.

Power, Bradley, Carlos R. Ferreira, Dong Chen, et al.. (2019). Hermansky-Pudlak syndrome and oculocutaneous albinism in Chinese children with pigmentation defects and easy bruising. Orphanet Journal of Rare Diseases. 14(1). 52–52. 11 indexed citations

11.

Leoyklang, Petcharat, S. Noguchi, William A. Gahl, et al.. (2018). Quantification of lectin fluorescence in GNE myopathy muscle biopsies. Muscle & Nerve. 58(2). 286–292. 12 indexed citations

12.

Brooks, Brian P., Wadih M. Zein, A. Thompson, et al.. (2018). Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single Center. Ophthalmology. 125(12). 1937–1952. 41 indexed citations

13.

Davids, Mariska, Megan Kane, Lynne A. Wolfe, et al.. (2018). Glycomics in rare diseases: from diagnosis tomechanism. Translational research. 206. 5–17. 5 indexed citations

14.

Behnam, Babak, Mariska Davids, Prashant Sharma, et al.. (2018). Novel mutations in CLN6 cause late-infantile neuronal ceroid lipofuscinosis without visual impairment in two unrelated patients. Molecular Genetics and Metabolism. 126(2). 188–195. 7 indexed citations

15.

Zhang, Yihan, Haigen Huang, Gexin Zhao, et al.. (2017). ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13. PLoS Genetics. 13(2). e1006481–e1006481. 45 indexed citations

16.

Li, Chong, Jennifer M. Brazill, Yi Zhu, et al.. (2017). Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome. Nature Communications. 8(1). 1257–1257. 65 indexed citations

17.

Stephen, Joshi, Angela Gruber, Carla Ciccone, et al.. (2017). Identification of an Alu element‐mediated deletion in the promoter region of GNE in siblings with GNE myopathy. Molecular Genetics & Genomic Medicine. 5(4). 410–417. 14 indexed citations

18.

Huizing, Marjan, May Christine V. Malicdan, Thierry Vilboux, et al.. (2015). Genetic Analysis Reveals that GNE Myopathy is an Underdiagnosed Neuromuscular Disorder (P2.044). Neurology. 84(14_supplement). 1 indexed citations

19.

Malicdan, May Christine V. & Ichizo Nishino. (2014). Central Core Disease. 4 indexed citations

20.

Malicdan, May Christine V., S. Noguchi, Yukiko Hayashi, & Ichizo Nishino. (2008). Muscle weakness correlates with muscle atrophy and precedes the development of inclusion body or rimmed vacuoles in the mouse model of DMRV/hIBM. Physiological Genomics. 35(1). 106–115. 28 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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