Ann Martin - Concepedia

Author

Ann Martin

Also Known As

A. Martin, A.S. Martin, ANN MARTIN, Adrian Ramos Martín, Ann Martin, Ann S Martin, Ann S. Martin, Karin K. Lucas, Martin, Ann

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Parent Project Muscular Dystrophy RTI International RAND Corporation Indiana University – Purdue University Indianapolis University of Calgary

About

Ann Martin is an author at Parent Project Muscular Dystrophy specializing in medicine, rehabilitation, and physical therapy.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	974
2	Health Sciences	3	3	129
3	Engineering	1	1	717
4	Public Health	1	1	81
5	Applied Physiology	1	1	13

Ann Martin

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations Catherine L. Bladen, David Salgado, Soledad Monges, Human Mutation Dmd MutationsTrial PlanningEngineeringMendelian DisorderGenetic Disorder	2015	717
Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database Zaïda Koeks, Catherine L. Bladen, David Salgado, Journal of Neuromuscular Diseases	2017	171
Practical Considerations in Using Online Modified-Delphi Approaches to Engage Patients and Other Stakeholders in Clinical Practice Guideline Development Dmitry Khodyakov, Sean Grant, Brian Denger, Patient	2019	106
The TREAT-NMD Duchenne Muscular Dystrophy Registries: Conception, Design, and Utilization by Industry and Academia Catherine L. Bladen, Karen Rafferty, Volker Straub, Human Mutation Rare DiseasesDmd RegistriesDuchenne Muscular DystrophyPrecision MedicineClinical Trials	2013	103
<i>DMD</i> genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtype Richard T. Wang, Florian Barthélémy, Ann Martin, Human Mutation GeneticsGenetic EpidemiologyMolecular BiologyDisease Gene IdentificationDefined Mutation Subtype	2018	81
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats Paweł Stankiewicz, Shashikant Kulkarni, Avinash V. Dharmadhikari, Human Mutation	2011	60
Variability and trends in corticosteroid use by male United States participants with Duchenne muscular dystrophy in the Duchenne Registry Leslie Cowen, Maria Mancini, Ann Martin, BMC Neurology	2019	50
Patient and caregiver perspectives on guideline adherence: the case of endocrine and bone health recommendations for Duchenne muscular dystrophy Brian Denger, Kathi Kinnett, Ann Martin, Orphanet Journal of Rare Diseases	2019	45
Using an Online, Modified Delphi Approach to Engage Patients and Caregivers in Determining the Patient-Centeredness of Duchenne Muscular Dystrophy Care Considerations Dmitry Khodyakov, Sean Grant, Brian Denger, Medical Decision Making	2019	40
DuchenneConnect Registry Report Vanessa Maia Rangel, Ann Martin, Holly L. Peay PLoS Currents Duchenne/becker Muscular DystrophyClinical DataTranslational BioinformaticsPrecision MedicineConformance Testing	2012	33

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