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Andrew C. Edmondson

pennsylvania medicine

29H-index
110Paper Count
6.5KCitation Count
Published Papers 51
Publication Date
Disease-specific growth charts capture characteristic growth patterns in children with PMM2 – CDG
err2026-04-20
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errKyriakie Sarafoglou; Christina Lam; Andrew C. Edmondson; Andrea Miller; Rodrigo T. Starosta; Aziza Zeighami; Seishu Horikoshi; Hayden Vreugdenhil; Fernando Scaglia; Tamas Kozicz; Queenie K.G. Tan; Bradley S. Miller; Iván Martínez-Duncker; Gerard T. Berry; Peter McWilliams; Eva Morava; Yaw Addo
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Targeted long-read RNA sequencing for rare disease diagnosis and variant interpretation
err2026-04-15
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errRobert Wang; Feng Wang; Nicole DeBruyne; Xinjun Ji; Nicole M. Engelhardt; Joseph Jee-Hwan Park; Amber Notaro; Samantha Gaerlan; Ryan Park; Matthew J. Schultz; Sheila Clever; Elizabeth M. McCormick; Kelsey Keith; Bobby G. Ng; Kathryn E. Kadash-Edmondson; Hudson H. Freeze; Christina T. Lam; Eva Morava; Ingo Helbig; Marni J. Falk; Rebecca D. Ganetzky; Andrew C. Edmondson; Lan Lin; Yi Xing
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Expanded Clinical Spectrum of Autosomal-Dominant STT3A-CDG
err2026-03-12
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errHamdan Al-Shahrani; Evelin Szabó; Caroline Staccone; Georgia MacDonald; Yutaka Furuta; Daniel Schecter; Andrew C. Edmondson; Anne McRae; Josh Baker; Rory J. Tinker
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L-fucose supplementation in a patient with global hypofucosylation and a mono-allelic variant in SLC35C1: Clinical improvement and assessment of biomarkers
err2026-01-01
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PREAI
errStarosta, Rodrigo T.; He, Miao; Gracie, Sara; Kierstein, Janell; Thiel, Christian; Himmelreich, Nastassja; Liu, Yupeng; Zhang, Wenyue; Edmondson, Andrew C.; Meeks, Naomi; Larson, Austin; Van Hove, Johan L. K.; Kochhar, Aaina
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Expanding the phenotype of CARS1 variants to include congenital hyperinsulinism
err2025-10-21
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errSanders, Victoria R.; Edmondson, Andrew C.; Yan, Albert C.; De Leon, Diva D.
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Incidence and prevalence of phosphomannomutase 2-congenital disorder of glycosylation: Past, present, and future
err2025-07-13
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errAndrew C. Edmondson; Tomáš Honzík; Christina Lam; Katrin Õunap; Peter McWilliams; Eva Morava
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Map of the neuronal O-glycoproteome reveals driver functions in the regulated secretory pathway
err2025-07-01
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errThomas D. Madsen; Asli B. Topaktas; Leo A. Dworkin; John Hintze; Lasse H. Hansen; Mahnaz Nikpour; Jarkko J. Lackman; Christoffer K. Goth; Göran Larson; Emily J. Shiplett; Andrew C. Edmondson; Zhaolan Zhou; Rebecca L. Miller; Hiren J. Joshi; Sergey Y. Vakhrushev; Katrine T. Schjoldager
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Goal attainment in PMM2-CDG: A new approach measuring meaningful clinical outcomes
err2025-05-01
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PREAI
errVerberkmoes, Sanne; Mazza, Gina L.; Edmondson, Andrew C.; Scaglia, Fernando; Horikoshi, Seishu; Kuschel, Bryce; Janssen, Mirian C. H.; Mousa, Jehan; Larson, Austin; Shah, Rameen; Mcdonald, Georgia; Sarafoglou, Kyriaki; Berry, Gerard; Kozicz, Tamas; Lam, Christina; Morava, Eva
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Causes of mortality in the congenital disorders of glycosylation
err2025-03-01
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PREAI
errAlharbi, Hana; Horikoshi, Seishu; Jenkins, Sabrina Malone; Scaglia, Fernando; Lam, Christina; Morava, Eva; Larson, Austin; Edmondson, Andrew C.
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Mapping the diagnostic odyssey of congenital disorders of glycosylation (CDG): insights from the community
err2024-11-01
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errGranjo, Pedro; Pascoal, Carlota; Gallego, Diana; Francisco, Rita; Jaeken, Jaak; Moors, Tristen; Edmondson, Andrew C.; Kantautas, Kristin A.; Serrano, Mercedes; Videira, Paula A.; dos Reis Ferreira, Vanessa
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Genotype/Phenotype Relationship: Lessons From 137 Patients With PMM2-CDG
err2024-10-03
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errPajusalu, Sander; Vals, Mari-Anne; Serrano, Mercedes; Witters, Peter; Cechova, Anna; Honzik, Tomas; Edmondson, Andrew C.; Ficicioglu, Can; Barone, Rita; De Lonlay, Pascale; Berat, Claire-Marine; Vuillaumier-Barrot, Sandrine; Lam, Christina; Patterson, Marc C.; Janssen, Mirian C. H.; Martins, Esmeralda; Quelhas, Dulce; Sykut-Cegielska, Jolanta; Mousa, Jehan; Urreizti, Roser; Mcwilliams, Peter; Vernhes, Frederique; Plotkin, Horacio; Morava, Eva; Ounap, Katrin
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Coagulation abnormalities and vascular complications are common in PGM1-CDG
err2024-08-01
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errRadenkovic, Silvia; Bleukx, Sofie; Engelhardt, Nicole; Eklund, Erik; Mercimek-Andrews, Saadet; Edmondson, Andrew C.; Morava, Eva
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Frontiers in congenital disorders of glycosylation consortium, a cross-sectional study report at year 5 of 280 individuals in the natural history cohort
err2024-08-01
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PREAI
errLam, Christina; Scaglia, Fernando; Berry, Gerard T.; Larson, Austin; Sarafoglou, Kyriakie; Andersson, Hans C.; Sklirou, Evgenia; Tan, Queenie K. G.; Starosta, Rodrigo T.; Sadek, Mustafa; Wolfe, Lynne; Horikoshi, Seishu; Ali, May; Barone, Rita; Campbell, Teresa; Chang, Irene J.; Coles, Kiaira; Cook, Edward; Eklund, Erik A.; Engelhardt, Nicole M.; Freeman, Mary; Friedman, Jennifer; Fu, Debbie Y. T.; Botzo, Grace; Rawls, Brandy; Hernandez, Christien; Johnsen, Christin; Keller, Kierstin; Kramer, Sara; Kuschel, Bryce; Leshinski, Angela; Martinez-Duncker, Ivan; Mazza, Gina L.; Mercimek-Andrews, Saadet; Miller, Bradley S.; Muthusamy, Karthik; Neira, Juanita; Patterson, Marc C.; Pogorelc, Natalie; Powers, Lex N.; Ramey, Elizabeth; Reinhart, Michaela; Squire, Audrey; Af, Jenny Thies; Vockley, Jerry; Vreugdenhil, Hayden; Witters, Peter; Youbi, Mehdi; Zeighami, Aziza; Zemet, Roni; Edmondson, Andrew C.; Morava, Eva
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ALG13-Congenital Disorder of Glycosylation (ALG13-CDG): Updated clinical and molecular review and clinical management guidelines
err2024-06-01
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PREAI
errShah, Rameen; Eklund, Erik A.; Radenkovic, Silvia; Sadek, Mustafa; Shammas, Ibrahim; Verberkmoes, Sanne; Ng, Bobby G.; Freeze, Hudson H.; Edmondson, Andrew C.; He, Miao; Kozicz, Tamas; Altassan, Ruqaiah; Morava, Eva
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A complement C4-derived glycopeptide is a biomarker for PMM2-CDG
err2024-04-08
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errGarapati, Kishore; Budhraja, Rohit; Saraswat, Mayank; Kim, Jinyong; Joshi, Neha; Sachdeva, Gunveen S.; Jain, Anu; Ligezka, Anna N.; Radenkovic, Silvia; Ramarajan, Madan Gopal; Udainiya, Savita; Raymond, Kimiyo; He, Miao; Lam, Christina; Larson, Austin; Edmondson, Andrew C.; Sarafoglou, Kyriakie; Larson, Nicholas B.; Freeze, Hudson H.; Schultz, Matthew J.; Kozicz, Tamas; Morava, Eva; Pandey, Akhilesh
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The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders
errBRAIN
IF11.7
err2024-03-08
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errSidpra, Jai; Sudhakar, Sniya; Biswas, Asthik; Massey, Flavia; Turchetti, Valentina; Lau, Tracy; Cook, Edward; Alvi, Javeria Raza; Elbendary, Hasnaa M.; Jewell, Jerry L.; Riva, Antonella; Orsini, Alessandro; Vignoli, Aglaia; Federico, Zara; Rosenblum, Jessica; Schoonjans, An-Sofie; de Wachter, Matthias; Alvarez, Ignacio Delgado; Felipe-Rucian, Ana; Haridy, Nourelhoda A.; Haider, Shahzad; Zaman, Mashaya; Banu, Selina; Anwaar, Najwa; Rahman, Fatima; Maqbool, Shazia; Yadav, Rashmi; Salpietro, Vincenzo; Maroofian, Reza; Patel, Rajan; Radhakrishnan, Rupa; Prabhu, Sanjay P.; Lichtenbelt, Klaske; Stewart, Helen; Murakami, Yoshiko; Lobel, Ulrike; D'Arco, Felice; Wakeling, Emma; Jones, Wendy; Hay, Eleanor; Bhate, Sanjay; Jacques, Thomas S.; Mirsky, David M.; Whitehead, Matthew T.; Zaki, Maha S.; Sultan, Tipu; Striano, Pasquale; Jansen, Anna C.; Lequin, Maarten; de Vries, Linda S.; Severino, Mariasavina; Edmondson, Andrew C.; Menzies, Lara; Campeau, Philippe M.; Houlden, Henry; McTague, Amy; Efthymiou, Stephanie; Mankad, Kshitij
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Combined PMM2-CDG and hereditary fructose intolerance in a patient with mild clinical presentation
err2023-11-01
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errHong, Xinying; Edmondson, Andrew C.; Strong, Alanna; Pomerantz, Daniel; Michl, Emma; Berry, Gerard; He, Miao
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