Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Amanda L. Bergner"'
Autor:
Jordana L. Graifman, Natalie C. Lippa, Maureen S. Mulhern, Amanda L. Bergner, Tristan T. Sands
Publikováno v:
Epilepsia. 64:986-997
Autor:
Rebecca M. Waggoner, Nina Harkavy, Lorraine Way, Michelle E. Florido, Adriana Sánchez, Amanda L. Bergner
Publikováno v:
Journal of Genetic Counseling.
Autor:
Beth R. Sheidley, Jennifer Malinowski, Amanda L. Bergner, Louise Bier, David S. Gloss, Weiyi Mu, Maureen M. Mulhern, Emily J. Partack, Annapurna Poduri
Publikováno v:
Epilepsia. 63:375-387
Numerous genetic testing options for individuals with epilepsy have emerged over the past decade without clear guidelines regarding optimal testing strategies. We performed a systematic evidence review (SER) and conducted meta-analyses of the diagnos
Autor:
Monika Zak Goelz, Lindsey Alico Ecker, Michelle E. Ernst, Kristina Habermann, Randi E. Zinberg, Amanda L. Bergner, Lisa Karger
Publikováno v:
Journal of Genetic Counseling
The COVID‐19 pandemic has ravaged the globe in the past year, demanding shifts in all aspects of life including health profession education. The New York City area was the first major United States epicenter and is home to four genetic counseling g
Autor:
Ashley Cannon, Heather B. Radtke, Allison L. Goetsch, Caroline McGowan, Amanda L. Bergner, Karin Panzer
Publikováno v:
Journal of Genetic Counseling. 29:692-714
The goal of this practice resource is to provide genetic counselors and other healthcare professionals with a resource to reference when providing genetic counseling services to individuals and families undergoing evaluation for neurofibromatosis (NF
Autor:
Beverly M. Yashar, Andrea L. Durst, Melanie F. Myers, Amanda L. Bergner, Debra Duquette, Xue Zhang, MaryAnn Campion, Laura Conway
Publikováno v:
Journal of genetic counselingREFERENCES. 31(2)
Graduation from a genetic counseling graduate program accredited by the Accreditation Council of Genetic Counseling and certification obtained by passing the American Board of Genetic Counseling (ABGC) certification examination are increasingly requi
Autor:
Matthias A. Karajannis, A Taylor, Diana Baralle, Rosalie E. Ferner, A Gomes, Dave Viskochil, J Toelen, Rianne Oostenbrink, Christopher L. Moertel, Laura Papi, Conxi Lázaro, H Wu, Michael D. Wilson, Shay Ben-Shachar, Pierre Wolkenstein, Sirkku Peltonen, Plotkin, P Joly, Dominique C. Pichard, Michael Fisher, Steinke-Lange, T Frébourg, P Ciavarelli, H Hanson, Mia MacCollin, I Blanco, D Bessis, Meena Upadhyaya, C Cassiman, Dusica Babovic-Vuksanovic, Riccardi, Juha Peltonen, James H. Tonsgard, B Poppe, Katharina Wimmer, M Larralde, P Pancza, A Heiberg, Bruce R. Korf, Mautner, D. G. R. Evans, Robert Listernick, Tena Rosser, S Barbarot, Eva Trevisson, D Stevenson, M Anten, Eduard Serra, Miriam J. Smith, Christopher J Hammond, Susan M Huson, Yemima Berman, Marco Giovannini, C Mallucci, Anat Stemmer-Rachamimov, G Tadini, Robert A. Avery, N Rezende, Nicole J. Ullrich, CO Hanemann, SM Stivaros, Hildegard Kehrer-Sawatzki, A Parry, D Kroshinsky, Maurizio Clementi, JT Jordan, A Varan, Joanne Ngeow, A Mueller, G Zadeh, Michel Kalamarides, D Halliday, M Link, Elizabeth K. Schorry, Roger J. Packer, Vanessa L. Merker, David H. Gutmann, Arthur S. Aylsworth, Karin Soares Gonçalves Cunha, V-F Mautner, Amanda L. Bergner, David A. Stevenson, Eric Legius, L Le, M Ruggieri, Fred G. Barker, Ludwine Messiaen, Jan M. Friedman, J. Blakeley, Kaleb Yohay, Katherine A. Rauen, LO Rodrigues
Publikováno v:
Genetics in Medicine
Genetics in Medicine, 23(8), 1506-1513. Lippincott Williams & Wilkins
Genetics in Medicine, 23(8), 1506-1513. Lippincott Williams & Wilkins
PURPOSE: By incorporating major developments in genetics, ophthalmology, dermatology, and neuroimaging, to revise the diagnostic criteria for neurofibromatosis type 1 (NF1) and to establish diagnostic criteria for Legius syndrome (LGSS). METHODS: We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45cd2826f627d5badf189e97ab322203
https://orca.cardiff.ac.uk/id/eprint/143733/1/s41436-021-01170-5.pdf
https://orca.cardiff.ac.uk/id/eprint/143733/1/s41436-021-01170-5.pdf
Autor:
Steven D Rhodes, Wei Zhang, Dalong Yang, Hao Yang, Shi Chen, Xiaohua Wu, Xiaohong Li, Xianlin Yang, Khalid S Mohammad, Theresa A Guise, Amanda L Bergner, David A Stevenson, Feng-Chun Yang
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0119093 (2015)
Despite the high prevalence and significant morbidity of spinal anomalies in neurofibromatosis type 1 (NF1), the pathogenesis of these defects remains largely unknown. Here, we present two murine models: Nf1flox/-;PeriCre and Nf1flox/-;Col.2.3Cre mic
Externí odkaz:
https://doaj.org/article/8e12ddc01307458b87ade751dd2b6f67
Publikováno v:
Journal of genetic counselingREFERENCES. 29(2)
Through self-reflection, self-education, and with a learning mindset each of us has embarked on a personal path to understand the impact of racism in our personal and professional lives. This personal work is ongoing, though it was through our indivi
Autor:
Juli Bollinger, Crystal Tichnell, Cynthia A. James, Carolyn D. Applegate, Karen S. Raraigh, Amanda L. Bergner, Brittney Murray, Courtney Berrios
Publikováno v:
J Genet Couns
Genetic counselors working in a clinical setting may find themselves recruiting, enrolling, and returning results for genomic research, and existing clinical relationships with study participants may impact these research interactions. We present a q