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A. Bergner · SciRah

Researcher profile · Semantic Scholar

A. Bergner

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A. Bergner — researcher profile on SciRah

h-index: 18
Works: 40
Citations: 1,281

Most-cited papers

Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas
A. Piotrowski, Jing Xie, Y. Liu, A. Poplawski +24 more
2013Nature Genetics273 citations Open access
Semantic Scholar
Genetic testing for the epilepsies: A systematic review
B. Sheidley, Jennifer R. Malinowski, A. Bergner, Louise Bier +5 more
2021Epilepsia157 citations
Semantic Scholar
Increased Risk of Breast Cancer in Women with NF1
Sara Madanikia, A. Bergner, Xiao-Bu Ye, Jaishri O. Blakeley
2012American Journal of Medical Genetics. Part A128 citations Open access
Semantic Scholar
Efficacy and Biomarker Study of Bevacizumab for Hearing Loss Resulting From Neurofibromatosis Type 2-Associated Vestibular Schwannomas.
J. Blakeley, Xiao-Bu Ye, Du-Da G. Dan, C. Halpin +12 more
2016Journal of Clinical Oncology116 citations Open access
Semantic Scholar
Spectrum and prevalence of vasculopathy in pediatric neurofibromatosis type 1
B. Kaas, T. Huisman, A. Tekes, A. Bergner +2 more
2012Journal of Child Neurology71 citations Open access
Semantic Scholar
Mutation Analysis of B3GALTL in Peters Plus Syndrome
Linda M. Reis, Rebecca C. Tyler, O. Abdul-Rahman, Pamela Trapane +8 more
2008American Journal of Medical Genetics. Part A70 citations Open access
Semantic Scholar
2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling
D. Doyle, Rawan I. Awwad, J. Austin, Bonnie J. Baty +16 more
2016Journal of Genetic Counseling59 citations Open access
Semantic Scholar
Introduction of sapropterin dihydrochloride as standard of care in patients with phenylketonuria
Hilary J. Vernon, Celide Koerner, M. Johnson, A. Bergner +1 more
2010Molecular Genetics and Metabolism44 citations Open access
Semantic Scholar
Informed Consent for Exome Sequencing Research in Families with Genetic Disease: The Emerging Issue of Incidental Findings
A. Bergner, Juli M. Bollinger, K. Raraigh, C. Tichnell +4 more
2014American Journal of Medical Genetics. Part A39 citations Open access
Semantic Scholar
Choices for return of primary and secondary genomic research results of 790 members of families with Mendelian disease
Katie Fiallos, C. Applegate, D. Mathews, Juli M. Bollinger +2 more
2017European Journal of Human Genetics35 citations Open access
Semantic Scholar
Patient-reported outcomes of pain and physical functioning in neurofibromatosis clinical trials
P. Wolters, Staci Martin, V. Merker, James Tonsgard +10 more
2016Neurology34 citations Open access
Semantic Scholar
Clinical response to bevacizumab in schwannomatosis
J. Blakeley, K. Schreck, D. Evans, B. Korf +4 more
2014Neurology32 citations Open access
Semantic Scholar
Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results
C. Berrios, C. James, K. Raraigh, Juli M. Bollinger +4 more
2017Journal of Genetic Counseling28 citations Open access
Semantic Scholar
Genetic Counseling for Neurofibromatosis 1, Neurofibromatosis 2, and Schwannomatosis—Practice Resource of the National Society of Genetic Counselors
Heather B. Radtke, A. Bergner, Allison L. Goetsch, Caroline McGowan +2 more
2020Journal of Genetic Counseling23 citations Open access
Semantic Scholar
Health-related Quality of Life of Individuals With Neurofibromatosis Type 2: Results From the NF2 Natural History Study
V. Merker, A. Bergner, Ana-Maria Vranceanu, A. Muzikansky +2 more
2016Otology and Neurotology22 citations Open access
Semantic Scholar
Improvement in patient-reported hearing after treatment with bevacizumab in people with Neurofibromatosis Type 2
Victoria Huang, A. Bergner, C. Halpin, V. Merker +4 more
2018Otology and Neurotology19 citations Open access
Semantic Scholar
Clinical utility of exome sequencing in a pediatric epilepsy cohort
Jordana L Graifman, N. Lippa, Maureen S. Mulhern, A. Bergner +1 more
2023Epilepsia18 citations Open access
Semantic Scholar
Dystrophic Spinal Deformities in a Neurofibromatosis Type 1 Murine Model
Steven D. Rhodes, Wei Zhang, Da-Long Yang, Hao Yang +9 more
2015PLoS ONE18 citations Open access
Semantic Scholar
Metanephric Stromal Tumor Arising in a Patient With Neurofibromatosis Type 1 Syndrome
O. McDonald, Ron Rodriguez, A. Bergner, P. Argani
2011International Journal of Surgical Pathology16 citations
Semantic Scholar
The Dynamics of a Genetic Counseling Peer Supervision Group
K. Lewis, L. Erby, A. Bergner, E. K. Reed +3 more
2017Journal of Genetic Counseling15 citations Open access
Semantic Scholar
Creation of an international registry to support discovery in schwannomatosis
K. Ostrow, A. Bergner, J. Blakeley, David Evans +16 more
2017American Journal of Medical Genetics. Part A14 citations Open access
Semantic Scholar
A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination
Melanie F. Myers, A. Bergner, Laura Conway, D. Duquette +4 more
2021Journal of Genetic Counseling11 citations Open access
Semantic Scholar
Intracranial Hemorrhage as the Initial Manifestation of a Congenital Disorder of Glycosylation
R. Cohn, E. Eklund, A. Bergner, J. Casella +9 more
2006Pediatrics11 citations
Semantic Scholar
Incidental parenchymal magnetic resonance imaging findings in the brains of patients with neurofibromatosis type 2
Wendy S. Vargas, L. Heier, F. Rodriguez, A. Bergner +1 more
2014NeuroImage: Clinical9 citations Open access
Semantic Scholar
The utility of limited Spanish proficiency in interpreted genetic counseling sessions
Rebecca M. Waggoner, Nina Harkavy, L. Way, Michelle E. Florido +2 more
2023Journal of Genetic Counseling6 citations
Semantic Scholar
Knowledge and Beliefs about Epilepsy Genetics among Hispanic and Non-Hispanic Patients
Shannon Trujillo, John B. Wetmore, Itzel A. Camarillo, S. Misiewicz +9 more
2023Epilepsia5 citations Open access
Semantic Scholar
The evolution of genetic counseling graduate education in New York City during the COVID‐19 pandemic: In the eye of the storm
A. Bergner, Lindsey Alico Ecker, M. Ernst, Monika Zak Goelz +3 more
2021Journal of Genetic Counseling5 citations Open access
Semantic Scholar
NEURO/MEDICAL ONCOLOGY
P. Ambady, M. Holdhoff, C. Ferrigno, S. Grossman +496 more
20134 citations Open access
Semantic Scholar
Updated diagnostic criteria and nomenclature for Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation consensus recommendation
Scott R. Plotkin, L. Messiaen, Eric Legius, Patrice Pancza +84 more
1 citations
Semantic Scholar
Erratum: Efficacy and Biomarker Study of Bevacizumab for Hearing Loss Resulting From Neurofibromatosis Type 2-Associated Vestibular Schwannomas.
Jaishri O. Blakeley, Xiao-Bu Ye, Du-Da G. Dan, Chris Halpin +12 more
2026Journal of Clinical Oncology0 citations
Semantic Scholar
P395: Assessing the collaborative relationships among diverse stakeholders working to expand access to genetic services in Puerto Rico
Oksana Kutsa, Alissa Terry, J. Bodurtha, M. Caggana +7 more
2023Genetics in Medicine Open0 citations Open access
Semantic Scholar
EPID-16. HEREDITARY BRAIN TUMORS ARE MORE COMMON THAN YOU THINK: GERMLINE MUTATIONS IN BENIGN AND MALIGNANT PRIMARY BRAIN TUMORS
M. Jackson, H. LaDuca, A. Bergner
20170 citations Open access
Semantic Scholar
MNGO-13. GERMLINE MUTATIONS IN INDIVIDUALS WITH MENINGIOMA AND BREAST CANCER
M. Jackson, A. Bergner
20160 citations
Semantic Scholar
Improving the molecular diagnosis and treatment of epilepsy with complex genetic testing.
A. Elliott, A. Bergner
2016MLO: medical laboratory observer0 citations
Semantic Scholar
Bevacizumab Impact on Hearing Loss Due to Neurofibromatosis Type 2 Associated Vestibular Schwannomas and Associated Biomarkers (S34.004)
J. Blakeley, X. Ye, G. Duda, C. Halpin +11 more
2016Neurology0 citations
Semantic Scholar
Overview of Neurocutaneous Syndromes
A. Bergner
20150 citations
Semantic Scholar
Frequency of Gastrointestinal Problems in Neurofibromatosis Type 1: The Johns Hopkins Experience (P07.105)
D. Wolf, A. Bergner, C. Obeng, J. Blakeley
20120 citations
Semantic Scholar
Central Nervous System Vascular Complications in Children and Adults with Neurofibromatosis Type 1 (P06.014)
A. Bergner, B. Kaas, Aaron B. Chance, L. Jordan +1 more
20120 citations
Semantic Scholar
The Schwannomatosis International Database
A. Belzberg, A. Bergner, J. Blakeley
20100 citations
Semantic Scholar
905 patients with chronic sinus pain/pressure and upper respiratory symptoms: A retrospective clinical, laboratory and CT analysis
A. Bergner, R. Bergner, M. Roznowski, M. Abrahamowicz +1 more
20020 citations Open access
Semantic Scholar

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