Sarah P. Young

5.4k total citations
105 papers, 3.8k citations indexed

About

Sarah P. Young is a scholar working on Physiology, Rheumatology and Molecular Biology. According to data from OpenAlex, Sarah P. Young has authored 105 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Physiology, 40 papers in Rheumatology and 34 papers in Molecular Biology. Recurrent topics in Sarah P. Young's work include Lysosomal Storage Disorders Research (57 papers), Glycogen Storage Diseases and Myoclonus (38 papers) and Metabolism and Genetic Disorders (22 papers). Sarah P. Young is often cited by papers focused on Lysosomal Storage Disorders Research (57 papers), Glycogen Storage Diseases and Myoclonus (38 papers) and Metabolism and Genetic Disorders (22 papers). Sarah P. Young collaborates with scholars based in United States, Canada and Singapore. Sarah P. Young's co-authors include David S. Millington, Priya S. Kishnani, Haoyue Zhang, Dwight D. Koeberl, Deeksha Bali, Baodong Sun, Andrew Bird, Yan An, Beth L. Roman and Christiane Auray‐Blais and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Development.

In The Last Decade

Sarah P. Young

101 papers receiving 3.7k citations

Peers

Countries citing papers authored by Sarah P. Young

Since Specialization

Citations

This map shows the geographic impact of Sarah P. Young'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 Sarah P. Young with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah P. Young more than expected).

Fields of papers citing papers by Sarah P. Young

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah P. Young. 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 Sarah P. Young. The network helps show where Sarah P. Young may publish in the future.

Co-authorship network of co-authors of Sarah P. Young

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah P. Young. A scholar is included among the top collaborators of Sarah P. Young 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 Sarah P. Young. Sarah P. Young 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	Lessons from late-onset Pompe disease identified by Newborn screening: A systematic review 2026 ·Molecular Genetics and Metabolism ·(unknown), (unknown), (unknown), Laura E. Case, (unknown), Sarah P. Young, (unknown)	0
2	Persistent elevations of alkaline phosphatase as an early indicator of GM1 gangliosidosis 2025 ·Molecular Genetics and Metabolism Reports ·(unknown), Monika Williams, (unknown), Rui Wei, Sarah P. Young, Areeg El‐Gharbawy, Ashlee R. Stiles	1
3	Infantile-onset Pompe disease entering adulthood: Insights from 2 decades of enzyme replacement therapy experience 2025 ·Genetics in Medicine ·(unknown), Daniel Kenney‐Jung, Grace A. Stafford, Michael D. Malinzak, Gail A. Spiridigliozzi, (unknown), (unknown), P. Brian Smith, Laura E. Case, Sarah P. Young, Harrison N. Jones, Priya S. Kishnani	1
4	Sex differences in mitochondrial free-carnitine levels in subjects at-risk and with Alzheimer’s disease in two independent study cohorts 2025 ·Molecular Psychiatry ·Benedetta Bigio, Ricardo A. S. Lima‐Filho, (unknown), Felipe Kenji Sudo, Cláudia Drummond, (unknown), Bart Vanderborght, James Beasley, Sarah P. Young, (unknown), Drew R. Jones, David L. Sultzer, Sérgio T. Ferreira, Paulo Mattos, Elizabeth Head, Fernanda Tovar‐Moll, Fernanda G. De Felice, Mychael V. Lourenco, Carla Nasca	2
5	The attenuated hepatic clearance of propionate increases cardiac oxidative stress in propionic acidemia 2024 ·Basic Research in Cardiology ·(unknown), (unknown), (unknown), (unknown), Eva Richard, Lourdes R. Desviat, Sarah P. Young, Dwight D. Koeberl, Takhar Kasumov, Xiaoxin Chen, Guofang Zhang	3
6	Intra-Articular AAV9 α-l-Iduronidase Gene Replacement in the Canine Model of Mucopolysaccharidosis Type I 2023 ·PubMed ·Raymond Wang, Shih‐hsin Kan, Haoyue Zhang, Jodi D. Smith, (unknown), Elizabeth Snella, Jackie K. Jens, Sarah P. Young, Patricia Dickson, N. Matthew Ellinwood	0
7	Intrauterine enzyme replacement therapies for lysosomal storage disorders: Current developments and promising future prospects 2023 ·Prenatal Diagnosis ·(unknown), (unknown), Billie R. Lianoglou, (unknown), (unknown), (unknown), Sarah P. Young, Deeksha Bali, (unknown), Pranesh Chakraborty, Priya S. Kishnani, Paul Harmatz, Jennifer L. Cohen, Tippi C. MacKenzie	12
8	Multidimensional predictors of antidepressant responses: Integrating mitochondrial, genetic, metabolic and environmental factors with clinical outcomes 2021 ·Neurobiology of Stress ·Carla Nasca, (unknown), Paolo De Angelis, Kathleen Watson, Jue Lin, James Beasley, Sarah P. Young, (unknown), (unknown), Benedetta Bigio, Bruce S. McEwen, Natalie Rasgon	11
9	Higher dosing of alglucosidase alfa improves outcomes in children with Pompe disease: a clinical study and review of the literature 2020 ·Genetics in Medicine ·(unknown), Laura E. Case, (unknown), Stephanie DeArmey, Harrison N. Jones, (unknown), Kanecia O. Zimmerman, Mai K. ElMallah, Sarah P. Young, Priya S. Kishnani	40
10	Diurnal variability of glucose tetrasaccharide (Glc₄) excretion in patients with glycogen storage disease type III 2020 ·JIMD Reports ·Sarah P. Young, (unknown), (unknown), (unknown), (unknown), Stephanie Austin, Priya S. Kishnani	9
11	Comparison of dermatan sulfate and heparan sulfate concentrations in serum, cerebrospinal fluid and urine in patients with mucopolysaccharidosis type I receiving intravenous and intrathecal enzyme replacement therapy 2020 ·Clinica Chimica Acta ·Haoyue Zhang, Patricia Dickson, Ashlee R. Stiles, Agnes H. Chen, Steven Q. Le, (unknown), James Beasley, David S. Millington, Sarah P. Young	6
12	Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia 2014 ·Human Molecular Genetics ·Sander M. Houten, Simone Denis, Heleen te Brinke, Aldo Jongejan, Antoine H. C. van Kampen, Eddie Bradley, Frank Baas, Raoul C. M. Hennekam, David S. Millington, Sarah P. Young, Dianne M. Frazier, Müge Güçsavaş‐Çalıkoğlu, Ronald J. A. Wanders	54
13	BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia 2013 ·The American Journal of Human Genetics ·Whitney Wooderchak‐Donahue, Jamie McDonald, Brendan O’Fallon, Paul D. Upton, Wei Li, Beth L. Roman, Sarah P. Young, (unknown), (unknown), Carmen Langa, Nicholas W. Morrell, Luisa M. Botella, Carmelo Bernabéu, David A. Stevenson, James Runo, Pınar Bayrak‐Toydemir	226
14	Atypical immunologic response in a patient with CRIM-negative Pompe disease 2011 ·Molecular Genetics and Metabolism ·Mary‐Alice Abbott, Sean N. Prater, Suhrad G. Banugaria, Susan Richards, Sarah P. Young, Amy S. Rosenberg, Priya S. Kishnani	24
15	Follow-up of a child with pyruvate dehydrogenase deficiency on a less restrictive ketogenic diet 2010 ·Molecular Genetics and Metabolism ·Areeg El‐Gharbawy, Anne Boney, Sarah P. Young, Priya S. Kishnani	16
16	Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarker 2009 ·Genetics in Medicine ·Sarah P. Young, Haoyue Zhang, Deyanira Corzo, Beth L. Thurberg, Deeksha Bali, Priya S. Kishnani, David S. Millington	72
17	Impaired clearance of accumulated lysosomal glycogen in advanced Pompe disease despite high‐level vector‐mediated transgene expression 2009 ·The Journal of Gene Medicine ·Baodong Sun, Haoyue Zhang, Andrew Bird, Songtao Li, Sarah P. Young, Dwight D. Koeberl	20
18	Correction of Multiple Striated Muscles in Murine Pompe Disease Through Adeno-associated Virus–mediated Gene Therapy 2008 ·Molecular Therapy ·Baodong Sun, Sarah P. Young, Ping Li, Chunhui Di, T. T. Brown, (unknown), Songtao Li, Andrew Bird, Zhen Yan, Richard L. Auten, Stephen D. Hauschka, Dwight D. Koeberl	60
19	Efficacy of an Adeno-associated Virus 8-Pseudotyped Vector in Glycogen Storage Disease Type II 2004 ·Molecular Therapy ·Baodong Sun, Haoyue Zhang, Luis M. Franco, Sarah P. Young, Ayn Schneider, Andrew Bird, Andrea Amalfitano, Y.-T. Chen, Dwight D. Koeberl	112
20	Liquid Chromatographic Assay for a Glucose Tetrasaccharide, a Putative Biomarker for the Diagnosis of Pompe Disease 2000 ·Analytical Biochemistry ·Yan An, Sarah P. Young, (unknown), Johan L.K. Van Hove, Yuan‐Tsong Chen, David S. Millington	51

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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