Search Results - Peter D. Galer
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1
Enriching representation learning using 53 million patient notes through human phenotype ontology embedding by Maryam Daniali, Peter D. Galer, David Lewis‐Smith, Shridhar Parthasarathy, Edward Kim, Dario D. Salvucci, Jeffrey M. Miller, Scott Haag, Ingo Helbig
Published 2023Artigo -
2
Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders by Katherine Crawford, Julie Xian, Katherine L. Helbig, Peter D. Galer, Shridhar Parthasarathy, David Lewis‐Smith, Michael C. Kaufman, Eryn Fitch, Shiva Ganesan, Margaret O’Brien, Veronica Codoni, Colin A. Ellis, Laura Conway, Deanne Taylor, Roland Krause, Ingo Helbig
Published 2021Artigo -
3
Analyzing 2,589 child neurology telehealth encounters necessitated by the COVID-19 pandemic by Salvatore C. Rametta, Sara Fridinger, Alexander K. Gonzalez, Julie Xian, Peter D. Galer, Michael C. Kaufman, Marisa S. Prelack, Uzma Sharif, Mark P. Fitzgerald, Susan E. Melamed, Marissa P. Malcolm, Sudha Kilaru Kessler, Donna J. Stephenson, Brenda Banwell, Nicholas S. Abend, Ingo Helbig
Published 2020Artigo -
4
Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneurons by Chad R. Camp, Anna Vlachos, Chiara Klöckner, Ilona Krey, Tue G. Banke, Nima Shariatzadeh, Sarah M. Ruggiero, Peter D. Galer, Kristen Park, Adam Caccavano, Sarah Kimmel, Xiaoqing Yuan, Hongjie Yuan, Ingo Helbig, Tim A. Benke, Johannes R. Lemke, Kenneth A. Pelkey, Chris J. McBain, Stephen F. Traynelis
Published 2023Artigo -
5
Extracting seizure frequency from epilepsy clinic notes: a machine reading approach to natural language processing by Kevin Xie, Ryan S. Gallagher, Erin C. Conrad, Chadric O Garrick, Steven N. Baldassano, John M. Bernabei, Peter D. Galer, Nina J Ghosn, Adam Greenblatt, Tara Jennings, Alana Kornspun, Catherine V. Kulick‐Soper, Jal M Panchal, Akash R. Pattnaik, Brittany H. Scheid, Danmeng Wei, Micah Weitzman, Ramya Muthukrishnan, Joongwon Kim, Brian Litt, Colin A. Ellis, Dan Roth
Published 2022Artigo -
6
The Human Phenotype Ontology in 2021 by Sebastian Köhler, Michael Gargano, Nicolas Matentzoglu, Leigh Carmody, David Lewis‐Smith, Nicole Vasilevsky, Daniel Daniš, Ganna Balagura, Gareth Baynam, Amy Brower, Tiffany J Callahan, Christopher G. Chute, Johanna L Est, Peter D. Galer, Shiva Ganesan, Matthias Griese, Matthias Haimel, Júlia Pázmándi, Marc Hanauer, Nomi L. Harris, M. J. Hartnett, Maximilian Hastreiter, Fabian Hauck, Yongqun He, Tim Jeske, Hugh Kearney, Gerhard Kindle, Christoph Klein, Katrin Knoflach, Roland Krause, David Lagorce, Julie A. McMurry, Jillian A. Miller, Monica Muñoz‐Torres, Rebecca L. Peters, Christina Rapp, Ana Rath, Shahmir A Rind, Avi Z. Rosenberg, Michael M. Segal, Markus G. Seidel, Damian Smedley, Tomer Talmy, Yarlalu Thomas, Samuel Agyei Wiafe, Julie Xian, Zafer Yüksel, Ingo Helbig, Chris Mungall, Melissa Haendel, Peter N. Robinson
Published 2020Artigo -
7
Assessing the landscape of <i>STXBP1</i>-related disorders in 534 individuals by Julie Xian, Shridhar Parthasarathy, Sarah M. Ruggiero, Ganna Balagura, Eryn Fitch, Katherine L. Helbig, Jing Gan, Shiva Ganesan, Michael C. Kaufman, Colin A. Ellis, David Lewis‐Smith, Peter D. Galer, Kristin Cunningham, Margaret O’Brien, Mahgenn Cosico, Kate Baker, Alejandra Darling, Fernanda Veiga de Góes, Christelle Moufawad El Achkar, Jan H Doering, Francesca Furia, Ángeles García‐Cazorla, Elena Gardella, Lisa Geertjens, Courtney Klein, Anna Kolesnik, Hanna C. A. Lammertse, Jeehun Lee, Alexandra T. Mackie, Mala Misra‐Isrie, Heather E. Olson, Emma Sexton, Beth Rosen Sheidley, Lacey Smith, Luiza Sotero, Hannah Stamberger, Steffen Syrbe, Kim Marie Thalwitzer, Annemiek van Berkel, Mieke M. van Haelst, Christopher J. Yuskaitis, Sarah Weckhuysen, Benjamin L. Prosser, Charlene Son Rigby, Scott Demarest, Samuel R. Pierce, Yuehua Zhang, Rikke S. Møller, Hilgo Bruining, Annapurna Poduri, Federico Zara, Matthijs Verhage, Pasquale Striano, Ingo Helbig
Published 2021Artigo -
8
A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy by Ingo Helbig, Tania López-Hernández, Oded Shor, Peter D. Galer, Shiva Ganesan, Manuela Pendziwiat, Annika Rademacher, Colin A. Ellis, Nadja Hümpfer, Niklas Schwarz, Simone Seiffert, Joseph Peeden, Joseph Shen, Katalin Štěrbová, Trine Bjørg Hammer, Rikke S. Møller, Deepali N. Shinde, Sha Tang, Lacey Smith, Annapurna Poduri, Roland Krause, Felix Benninger, Katherine L. Helbig, Volker Haucke, Yvonne G. Weber, Rudi Balling, Nina Barišić, Stéphanie Baulac, Hande Çağlayan, Dana Craiu, Peter De Jonghe, Christel Depienne, Renzo Guerrini, Helle Hjalgrim, Dorota Hoffman‐Zacharska, Johanna Jähn, Karl Martin Klein, Bobby P.C. Koeleman, Vladimı́r Komárek, Eric LeGuern, Anna‐Elina Lehesjoki, Johannes R. Lemke, Holger Lerche, Tarja Linnankivi, Carla Marini, Patrick May, Hiltrud Muhle, Deb K. Pal, Aarno Palotie, Felix Rosenow, Susanne Schubert‐Bast, Kaja Kristine Selmer, José M. Serratosa, Sanjay M. Sisodiya, Ulrich Stephani, Pasquale Striano, Arvid Suls, Tiina Talvik, Sarah von Spiczak, Sarah Weckhuysen, Federico Zara, Paul Avillach, Anna Bartels, Sawona Biswas, Florence T. Bourgeois, Batsal Devkota, Tracy A. Glauser, Barbara Hallinan, Allison P. Heath, Joel N. Hirschhorn, Judson Kilbourn, Sek Won Kong, Ian D. Krantz, In‐Hee Lee, Kenneth D. Mandl, Eric D. Marsh, Kristen L. Sund, Deanne Taylor, Peter S. White
Published 2019Artigo
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