Andrew C. Edmondson

6.5k citations

46 papers · 939 indexed · h-index 17

Molecular Biology
Genetics top 10%
Surgery
Endocrinology, Diabetes and Metabolism top 10%
Cardiology and Cardiovascular Medicine top 10%

Co-authors: Daniel J. Rader Brent L. Nielsen Jennifer M. Kalish Sekar Kathiresan Mingyao Li Fayaz R. Khazi Éva Morava Can Fıçıcıoğlu
Topics: Glycosylation and Glycoproteins Research (16 papers)Genomics and Rare Diseases (10 papers)Metabolism and Genetic Disorders (7 papers)
Cited by: Endocrinology, Diabetes and Metabolism Clinical Biochemistry Genetics
Journals: Journal of Biological Chemistry Journal of Clinical InvestigationSHILAP Revista de lepidopterología
Partner nations: United States Hungary Saudi Arabia

In The Last Decade

Andrew C. Edmondson

41 papers receiving 933 citations

Peers

Countries citing papers authored by Andrew C. Edmondson

Since Specialization

Citations

This map shows the geographic impact of Andrew C. Edmondson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Andrew C. Edmondson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew C. Edmondson more than expected).

Fields of papers citing papers by Andrew C. Edmondson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew C. Edmondson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Andrew C. Edmondson. The network helps show where Andrew C. Edmondson may publish in the future.

Co-authorship network of co-authors of Andrew C. Edmondson

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew C. Edmondson. A scholar is included among the top collaborators of Andrew C. Edmondson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Andrew C. Edmondson. Andrew C. Edmondson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Biochemical testing for congenital disorders of glycosylation: A technical standard of the American College of Medical Genetics and Genomics (ACMG) 2025 ·Genetics in Medicine ·Patricia Hall,Christina Lam,Lynne A. Wolfe,Andrew C. Edmondson	1
2	Incidence and prevalence of phosphomannomutase 2-congenital disorder of glycosylation: Past, present, and future 2025 ·Molecular Genetics and Metabolism ·Andrew C. Edmondson,Tomáš Honzík,Christina Lam,Katrin Õunap,(unknown),Éva Morava	0
3	Cardiomyopathy, an uncommon phenotype of congenital disorders of glycosylation: Recommendations for baseline screening and follow-up evaluation 2024 ·Molecular Genetics and Metabolism ·Roni Zemet,(unknown),Andrew C. Edmondson,(unknown),(unknown),(unknown),Justin H. Berger,Kyriakie Sarafoglou,Austin Larson,Christina Lam,Éva Morava,Fernando Scaglia	4
4	Coagulation abnormalities and vascular complications are common in PGM1-CDG 2024 ·Molecular Genetics and Metabolism ·Silvia Radenkovic,(unknown),(unknown),Erik A. Eklund,Saadet Mercimek‐Andrews,Andrew C. Edmondson,Éva Morava	2
5	Combined PMM2-CDG and hereditary fructose intolerance in a patient with mild clinical presentation 2023 ·Molecular Genetics and Metabolism ·Xinying Hong,Andrew C. Edmondson,Alanna Strong,(unknown),(unknown),Gerard T. Berry,(unknown)	1
6	Thymine Hyperexcretion in a Patient with Abnormal Newborn Screen for Glutaric Aciduria Type I 2023 ·Clinical Chemistry ·Parith Wongkittichote,Andrew C. Edmondson,Xinying Hong	0
7	Coagulation abnormalities in a prospective cohort of 50 patients with PMM2-congenital disorder of glycosylation 2023 ·Molecular Genetics and Metabolism ·(unknown),Anna N. Ligezka,(unknown),Gina L. Mazza,Graeme Preston,(unknown),Wirginia Krzyściak,Christina Lam,Andrew C. Edmondson,Christin Johnsen,Tamás Kozicz,Éva Morava	8
8	Interplay of Impaired Cellular Bioenergetics and Autophagy in PMM2-CDG 2023 ·Genes ·Anna N. Ligezka,(unknown),(unknown),Fabienne C. Fiesel,Graeme Preston,Andrew C. Edmondson,Wasantha Ranatunga,Johan L.K. Van Hove,Jens O. Watzlawik,Wolfdieter Springer,Akhilesh Pandey,Éva Morava,Tamás Kozicz	11
9	Should patients with Phosphomannomutase 2-CDG (PMM2-CDG) be screened for adrenal insufficiency? 2021 ·Molecular Genetics and Metabolism ·Anna Čechová,Tomáš Honzík,Andrew C. Edmondson,Can Fıçıcıoğlu,Mercedes Serrano,Rita Barone,Pascale de Lonlay,Manuel Schiff,Peter Witters,Christina Lam,Marc C. Patterson,Mirian C. H. Janssen,(unknown),Dulce Quelhas,Jolanta Sykut‐Cegielska,Horacio Plotkin,Éva Morava,Kyriakie Sarafoglou	6
10	Expanding the phenotype, genotype and biochemical knowledge of ALG3‐CDG 2021 ·Journal of Inherited Metabolic Disease ·(unknown),Bobby G. Ng,(unknown),Jennifer Friedman,Enikö K. Pivnick,Amal Alhashem,Eissa Faqeih,Pengfei Liu,(unknown),(unknown),(unknown),(unknown),Jill A. Rosenfeld,Michael J. Bamshad,Deborah A. Nickerson,Kimiyo Raymond,Hudson H. Freeze,(unknown),Andrew C. Edmondson,Christina Lam	9
11	Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDG 2020 ·Genetics in Medicine ·Peter Witters,(unknown),Rita Barone,Katrin Õunap,Ramona Salvarinova,Sabine Grønborg,George Hoganson,Fernando Scaglia,Andrea M. Lewis,Mari Mori,Jolanta Sykut‐Cegielska,Andrew C. Edmondson,Miao He,Éva Morava	56
12	X-linked cellular mosaicism underlies age-dependent occurrence of seizure-like events in mouse models of CDKL5 deficiency disorder 2020 ·Neurobiology of Disease ·(unknown),Yue Cui,Andrew C. Edmondson,Sheng Tang,(unknown),(unknown),Eric D. Marsh,Douglas A. Coulter,Zhaolan Zhou	27
13	Gain‐of‐function mutations in SMAD4 cause a distinctive repertoire of cardiovascular phenotypes in patients with Myhre syndrome 2016 ·American Journal of Medical Genetics Part A ·Angela E. Lin,Caroline Michot,Valérie Cormier‐Daire,Thomas J. L’Ecuyer,G. Paul Matherne,Peter J. Barnes,Jennifer B. Humberson,Andrew C. Edmondson,Elaine H. Zackai,Matthew J. O’Connor,Julie Kaplan,Makram R. Ebeid,Joel B. Krier,Elizabeth L. Krieg,Brian Ghoshhajra,Mark E. Lindsay	45
14	ECHS1 Deficiency as a Cause of Severe Neonatal Lactic Acidosis 2016 ·JIMD Reports ·Rebecca Ganetzky,(unknown),Rebecca C. Ahrens‐Nicklas,Andrew C. Edmondson,Matthew A. Deardorff,Michael J. Bennett,Can Fıçıcıoğlu	27
15	Fetal akinesia deformation sequence due to a congenital disorder of glycosylation 2015 ·American Journal of Medical Genetics Part A ·Rebecca Ganetzky,Kosuke Izumi,Andrew C. Edmondson,Colleen Muraresku,Elaine H. Zackai,Matthew A. Deardorff,Jaya Ganesh	11
16	Pathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation 2011 ·SHILAP Revista de lepidopterología ·Kai Wang,Andrew C. Edmondson,Mingyao Li,Fan Gao,Atif Qasim,Joseph M. Devaney,Mary Susan Burnett,Dawn Waterworth,Vincent Mooser,Struan F.A. Grant,Stephen E. Epstein,Muredach P. Reilly,Håkon Håkonarson,Daniel J. Rader	9
17	A Gaussian copula approach for the analysis of secondary phenotypes in case-control genetic association studies 2011 ·Biostatistics ·Jing He,Hui Li,Andrew C. Edmondson,Daniel J. Rader,Mingyang Li	44
18	The T111I variant in the endothelial lipase gene and risk of coronary heart disease in three independent populations 2009 ·European Heart Journal ·Majken K. Jensen,E. B. Rimm,Kenneth J. Mukamal,Andrew C. Edmondson,Dan Rader,Ulla Vogel,Anne Tjønneland,T. I. A. Sørensen,Erik Berg Schmidt,Kim Overvad	34
19	Characterization of a mitochondrially targeted single-stranded DNA-binding protein in Arabidopsis thaliana 2005 ·Molecular Genetics and Genomics ·Andrew C. Edmondson,(unknown),Luis Álvarez,(unknown),(unknown),David A. McClellan,Anthony Maxwell,Brent L. Nielsen	39
20	An Arabidopsis homologue of bacterial RecA that complements an E. coli recA deletion is targeted to plant mitochondria 2003 ·Molecular Genetics and Genomics ·Fayaz R. Khazi,Andrew C. Edmondson,Brent L. Nielsen	42

About Andrew C. Edmondson

Andrew C. Edmondson is a scholar working on Clinical Biochemistry, Genetics and Molecular Biology, having authored 46 papers that have together received 939 indexed citations. Recurring topics across this work include Glycosylation and Glycoproteins Research (16 papers), Genomics and Rare Diseases (10 papers) and Metabolism and Genetic Disorders (7 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (184 citations), Clinical Biochemistry (72 citations) and Genetics (283 citations). Andrew C. Edmondson has collaborated with scholars based in United States, Hungary and Saudi Arabia. Frequent co-authors include Daniel J. Rader, Brent L. Nielsen, Jennifer M. Kalish, Sekar Kathiresan, Mingyao Li, Fayaz R. Khazi, Éva Morava, Can Fıçıcıoğlu, Megan L. Wolfe and Jing He. Their work appears in journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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