Jamie L. Fraser - Concepedia

Author

Jamie L. Fraser

Children's National ORCID

Also Known As

J. Lee Fraser, Jamie L. Fraser, Jamie Fraser, Jamie L Fraser, Jamie L. Fraser, Josue Flores Daboub, Stephanie Gogarten

Publications

2.7K

Citations

H-Index

Concepts

All Affiliations

Children's National National Human Genome Research Institute University of California, San Francisco Harvard University National Institutes of Health

About

Jamie L. Fraser is an author at Children's National specializing in medicine, neurology, and health sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	1.5K
2	Health Sciences	3	3	458
3	Engineering	1	1	617
4	Public Health	1	1	28
5	Biomedical Engineering	1	1	617

Jamie L. Fraser

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
Transplantation of hypoxia-preconditioned mesenchymal stem cells improves infarcted heart function via enhanced survival of implanted cells and angiogenesis Xinyang Hu, Shan Ping Yu, Jamie L. Fraser, Journal of Thoracic and Cardiovascular Surgery Tissue EngineeringRegenerative MedicineInfarcted Heart FunctionTransplantationEngineering	2008	617
Transplantation of hypoxia preconditioned bone marrow mesenchymal stem cells enhances angiogenesis and neurogenesis after cerebral ischemia in rats Ling Wei, Jamie L. Fraser, Zhongyang Lu, Neurobiology of Disease Regenerative MedicineCerebral IschemiaDevelopmental BiologyMedicineAdult Stem Cell	2012	360
Clinical delineation and natural history of the <i>PIK3CA</i>‐related overgrowth spectrum Kim M. Keppler‐Noreuil, Julie C. Sapp, Marjorie J. Lindhurst, American Journal of Medical Genetics Part A	2014	301
Transplantation of Embryonic Stem Cells Improves Nerve Repair and Functional Recovery After Severe Sciatic Nerve Axotomy in Rats Lin Cui, Jun Jiang, Ling Wei, Stem Cells	2008	156
Diagnosis and management of osteoporosis. Stuart H. Ralston, Jamie L. Fraser PubMed Bone DiseaseSpinal FractureBone HealthOsteoarthritisFragility Fractures	2015	116
De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism María J. Guillen Sacoto, Iva A. Tchasovnikarova, Erin Torti, The American Journal of Human Genetics Neurodevelopmental DisordersAtpase ModuleDevelopmental AnomalyDevelopmental BiologyGenetic Disorder	2020	107
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, Nature	2024	93
Revised consensus statement on the preventive and symptomatic care of patients with leukodystrophies Laura Adang, Omar Sherbini, Laura J. Ball, Molecular Genetics and Metabolism MedicineRheumatologySymptomatic CareConsensus Statement	2017	71
The role of VEGF/VEGFR2 signaling in peripheral stimulation-induced cerebral neurovascular regeneration after ischemic stroke in mice Wenlei Li, Jamie L. Fraser, Shan Ping Yu, Experimental Brain Research Cerebral Vascular RegulationNeuroregenerationIschemic StrokeMedicineVascular Endothelial Growth Factor	2011	54
De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy Chiara Klöckner, Heinrich Sticht, Pia Zacher, Genetics in Medicine Epileptic EncephalopathyDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2020	46

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