Amanda L. Bergner - Concepedia

Author

Amanda L. Bergner

Johns Hopkins University ORCID

Also Known As

A. Bergner, A. L. Bergner, Amanda Bergner, Amanda L Bergner, Amanda L. Bergner, Catherine Cassiman

Publications

2.5K

Citations

H-Index

Concepts

All Affiliations

Johns Hopkins University Massachusetts General Hospital Johns Hopkins Medicine University of Alabama at Birmingham Columbia University

About

Amanda L. Bergner is an author at Johns Hopkins University specializing in medicine, neurology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	556
2	Engineering	1	1	14
3	Health Sciences	1	1	14
4	Public Health	1	1	38
5	Social Sciences	1	1	20

Amanda L. Bergner

Publications

Citations

H-Index

Page 1

	Year	Citations
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation Eric Legius, Ludwine Messiaen, P. Wolkenstein, Genetics in Medicine	2021	687
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas Arkadiusz Piotrowski, Jing Xie, Ying F Liu, Nature Genetics Developmental AnomalyRare DiseasesSomatic VariantMendelian DisorderGenetic Disorder	2013	315
Efficacy and Biomarker Study of Bevacizumab for Hearing Loss Resulting From Neurofibromatosis Type 2–Associated Vestibular Schwannomas Jaishri O. Blakeley, Xiaobu Ye, Dan G. Duda, Journal of Clinical Oncology	2016	128
Increased risk of breast cancer in women with NF1 Sara Aileen Madanikia, Amanda L. Bergner, Xiaobu Ye, American Journal of Medical Genetics Part A	2012	120
Current whole-body MRI applications in the neurofibromatoses Shivani Ahlawat, Laura M. Fayad, Muhammad Shayan Khan, Neurology	2016	85
Spectrum and Prevalence of Vasculopathy in Pediatric Neurofibromatosis Type 1 Bonnie Kaas, Thierry A.G.M. Huisman, Aylin Tekes, Journal of Child Neurology Neuro-oncologyPediatric Brain TumorsVasculitisOphthalmologyNeurological Disorder	2012	76
2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling Debra Lochner Doyle, Rawan I. Awwad, Jehannine Austin, Journal of Genetic Counseling	2016	72
Mutation analysis of <i>B3GALTL</i> in Peters Plus syndrome Linda M. Reis, Rebecca C. Tyler, Omar Abdul‐Rahman, American Journal of Medical Genetics Part A	2008	60
Patient-reported outcomes of pain and physical functioning in neurofibromatosis clinical trials Pamela L. Wolters, Staci Martin, Vanessa L. Merker, Neurology	2016	45
Introduction of sapropterin dihydrochloride as standard of care in patients with phenylketonuria Hilary J. Vernon, Celide Koerner, Maria R. Johnson, Molecular Genetics and Metabolism Sapropterin DihydrochlorideUrologyMedicineRenal PathologyChronic Kidney Disease	2010	42

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