P. Morehart

860 total citations
15 papers, 155 citations indexed

About

P. Morehart is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, P. Morehart has authored 15 papers receiving a total of 155 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Physiology and 2 papers in Genetics. Recurrent topics in P. Morehart's work include Muscle Physiology and Disorders (7 papers), Mitochondrial Function and Pathology (3 papers) and Metabolism and Genetic Disorders (2 papers). P. Morehart is often cited by papers focused on Muscle Physiology and Disorders (7 papers), Mitochondrial Function and Pathology (3 papers) and Metabolism and Genetic Disorders (2 papers). P. Morehart collaborates with scholars based in United States, United Kingdom and Netherlands. P. Morehart's co-authors include Brenda Wong, Kevin E. Bove, Mathula Thangarajh, Robert C. Griggs, Jos G.M. Hendriksen, Michael McDermott, William B. Martens, Lili Miles, Robert D. Steiner and Erin O’Rourke and has published in prestigious journals such as Neurology, American Journal of Neuroradiology and Human Pathology.

In The Last Decade

P. Morehart

15 papers receiving 149 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
P. Morehart United States	7	102	42	18	17	17	15	155
Silvia Rota United Kingdom	11	44 0.4×	63 1.5×	21 1.2×	17 1.0×	10 0.6×	28	242
Daniel Flicker United States	5	128 1.3×	37 0.9×	16 0.9×	20 1.2×	19 1.1×	6	211
Miriam Stampfer Germany	8	51 0.5×	133 3.2×	22 1.2×	18 1.1×	10 0.6×	8	226
Julia Gräf Germany	10	51 0.5×	43 1.0×	6 0.3×	36 2.1×	7 0.4×	20	330
Katarzyna Iwanicka‐Pronicka Poland	8	113 1.1×	25 0.6×	17 0.9×	7 0.4×	48 2.8×	27	185
Cheuk Wing Fung China	9	67 0.7×	23 0.5×	7 0.4×	8 0.5×	29 1.7×	18	177
Anderson Rodrigues Brandão de Paiva Brazil	6	108 1.1×	49 1.2×	11 0.6×	11 0.6×	12 0.7×	24	243
H. Ouhabi Morocco	7	172 1.7×	22 0.5×	10 0.6×	5 0.3×	15 0.9×	21	287
Hélio Pedro United States	8	72 0.7×	50 1.2×	7 0.4×	13 0.8×	7 0.4×	14	183
Verayuth Praphanphoj Thailand	12	181 1.8×	16 0.4×	32 1.8×	4 0.2×	21 1.2×	20	328

Countries citing papers authored by P. Morehart

Since Specialization

Citations

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

Fields of papers citing papers by P. Morehart

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. Morehart

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

All Works

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15 of 15 papers shown

Wong, Kingsley, Summer B. Cook, P. Morehart, et al.. (2023). P221 A five-year review of newborn screening for spinal muscular atrophy in the state of Utah: lessons learned. Neuromuscular Disorders. 33. S90–S90. 1 indexed citations

Swank, Jacqueline M., et al.. (2020). Color‐Conscious Multicultural Mindfulness Training in the Counseling Field. Journal of Counseling & Development. 98(2). 147–158. 12 indexed citations

Thangarajh, Mathula, Jos G.M. Hendriksen, Michael McDermott, et al.. (2019). Relationships between DMD mutations and neurodevelopment in dystrophinopathy. Neurology. 93(17). e1597–e1604. 40 indexed citations

Wong, Brenda, Boryana Stamova, P. Morehart, et al.. (2015). microRNA and mRNA expression networks in Duchenne muscular dystrophy. Neuromuscular Disorders. 25. S253–S254. 1 indexed citations

Rutter, Meilan M., James J. Collins, Hemant Sawnani, et al.. (2013). P.11.10 Height predictions using ulna length are inaccurate in glucocorticoid-treated boys with Duchenne Muscular Dystrophy (DMD). Neuromuscular Disorders. 23(9-10). 801–801. 1 indexed citations

Wong, Brenda, Lauren E. Miller, Paul S. Horn, et al.. (2013). P.11.6 Functional motor changes in Duchenne Muscular Dystrophy (DMD) patients on long term daily glucocorticoid (GC) treatment. Neuromuscular Disorders. 23(9-10). 800–800. 1 indexed citations

Rutter, Meilan M., James J. Collins, Philippe Backeljauw, et al.. (2013). P.11.15 Recombinant human insulin-like growth factor-I (IGF-I) therapy in Duchenne Muscular Dystrophy (DMD): A 6-month prospective randomized controlled trial. Neuromuscular Disorders. 23(9-10). 803–803. 2 indexed citations

Wong, Brenda, et al.. (2011). P1.2 Phenotypic profile of dystrophinopathy patients with deletion of exons 3–7 of the dystrophin gene. Neuromuscular Disorders. 21(9-10). 642–642. 2 indexed citations

Guglieri, Michela, Barbara E. Herr, Elaine McColl, et al.. (2010). P3.52 FOR-DMD: double-blind randomized trial to optimize steroid regime in Duchenne Muscular Dystrophy (DMD). Neuromuscular Disorders. 20(9-10). 657–657. 1 indexed citations

10.

Collins, James J., Kevin E. Bove, David Dimmock, et al.. (2009). Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutations. Neuromuscular Disorders. 19(11). 784–787. 12 indexed citations

11.

Dinopoulos, Argirios, J. R. Gorospe, John C. Egelhoff, et al.. (2007). Discrepancy between neuroimaging findings and clinical phenotype in Alexander disease.. American Journal of Neuroradiology. 27(10). 2088–92. 13 indexed citations

12.

Wong, Brenda, et al.. (2006). G.P.10 02 Bone health in Duchenne muscular dystrophy. Neuromuscular Disorders. 16(9-10). 718–718. 1 indexed citations

13.

Miles, Lili, Michael V. Miles, Peter Tang, et al.. (2005). Muscle Coenzyme Q: A Potential Test for Mitochondrial Activity and Redox Status. Pediatric Neurology. 32(5). 318–324. 20 indexed citations

14.

Miles, Lili, et al.. (2005). Investigation of children for mitochondriopathy confirms need for strict patient selection, improved morphological criteria, and better laboratory methods. Human Pathology. 37(2). 173–184. 14 indexed citations

15.

Bennett, Robin L., P. Morehart, Erin O’Rourke, et al.. (2002). Fabry Disease in Genetic Counseling Practice: Recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling. 11(2). 121–146. 34 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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