Sarah P. Young

5.4k citations

105 papers · 3.8k indexed · h-index 35

Physiology top 0.5%
- Lysosomal Storage Disorders Research 57
- Diet and metabolism studies 7
Rheumatology top 0.5%
- Glycogen Storage Diseases and Myoclonus 38
Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders 22
Genetics top 2%
Physiology top 2%
- Lysosomal Storage Disorders Research 57
- Diet and metabolism studies 7
Organic Chemistry
- Carbohydrate Chemistry and Synthesis 20
Molecular Biology
- Biochemical and Molecular Research 12
- Mitochondrial Function and Pathology 10
Epidemiology
- Trypanosoma species research and implications 9

Co-authors: David S. Millington Priya S. Kishnani Haoyue Zhang Dwight D. Koeberl Deeksha Bali Baodong Sun Andrew Bird Yan An
Cited by: Physiology Rheumatology Clinical Biochemistry
Journals: Proceedings of the National Academy of Sciences (1 paper)SHILAP Revista de lepidopterología (1 paper)Development (2 papers)
Partner nations: United States Canada Singapore

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

The 25 scholars most cited alongside Sarah P. Young, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sarah P. Young Line = papers co-authored together Sarah P. Young links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Lessons from late-onset Pompe disease identified by Newborn screening: A systematic review Molecular Genetics and Metabolism ·Myriam Boueri,Jessica Doxey,Tracy Boggs,Laura E. Case,Erica Nading,Sarah P. Young,Priya S. Kishnani	2026	0
2	Persistent elevations of alkaline phosphatase as an early indicator of GM1 gangliosidosis Molecular Genetics and Metabolism Reports ·Iskren Menkovic,Monika Williams,Neelam Makhijani,Rui Wei,Sarah P. Young,Areeg El‐Gharbawy,Ashlee R. Stiles	2025	1
3	Infantile-onset Pompe disease entering adulthood: Insights from 2 decades of enzyme replacement therapy experience Genetics in Medicine ·Neha Regmi,Daniel Kenney‐Jung,Grace A. Stafford,Michael D. Malinzak,Gail A. Spiridigliozzi,Tracy Boggs,Rebecca L. Koch,P. Brian Smith,Laura E. Case,Sarah P. Young,Harrison N. Jones,Priya S. Kishnani	2025	1
4	Sex differences in mitochondrial free-carnitine levels in subjects at-risk and with Alzheimer’s disease in two independent study cohorts Molecular Psychiatry ·Benedetta Bigio,Ricardo A. S. Lima‐Filho,Olivia Barnhill,Felipe Kenji Sudo,Cláudia Drummond,Naima Assunção,Bart Vanderborght,James Beasley,Sarah P. Young,Aryeh Korman,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	2025	2
5	The attenuated hepatic clearance of propionate increases cardiac oxidative stress in propionic acidemia Basic Research in Cardiology ·You Wang,Suhong Zhu,Wentao He,Hannah Marchuk,Eva Richard,Lourdes R. Desviat,Sarah P. Young,Dwight D. Koeberl,Takhar Kasumov,Xiaoxin Chen,Guofang Zhang	2024	3
6	Intra-Articular AAV9 α-l-Iduronidase Gene Replacement in the Canine Model of Mucopolysaccharidosis Type I PubMed ·Raymond Wang,Shih‐hsin Kan,Haoyue Zhang,Jodi D. Smith,Afshin Aminian,Elizabeth Snella,Jackie K. Jens,Sarah P. Young,Patricia Dickson,N. Matthew Ellinwood	2023	0
7	Intrauterine enzyme replacement therapies for lysosomal storage disorders: Current developments and promising future prospects Prenatal Diagnosis ·Akos Herzeg,Beltran Borges,Billie R. Lianoglou,Juan Gonzalez‐Velez,Emma Canepa,Dane Munar,Sarah P. Young,Deeksha Bali,Michel H. Gelb,Pranesh Chakraborty,Priya S. Kishnani,Paul Harmatz,Jennifer L. Cohen,Tippi C. MacKenzie	2023	12
8	Multidimensional predictors of antidepressant responses: Integrating mitochondrial, genetic, metabolic and environmental factors with clinical outcomes Neurobiology of Stress ·Carla Nasca,Olivia Barnhill,Paolo De Angelis,Kathleen Watson,Jue Lin,James Beasley,Sarah P. Young,Alison Myoraku,Josh Dobbin,Benedetta Bigio,Bruce S. McEwen,Natalie Rasgon	2021	11
9	Higher dosing of alglucosidase alfa improves outcomes in children with Pompe disease: a clinical study and review of the literature Genetics in Medicine ·Aleena Khan,Laura E. Case,Mrudu Herbert,Stephanie DeArmey,Harrison N. Jones,Kelly D. Crisp,Kanecia O. Zimmerman,Mai K. ElMallah,Sarah P. Young,Priya S. Kishnani	2020	40
10	Diurnal variability of glucose tetrasaccharide (Glc₄) excretion in patients with glycogen storage disease type III JIMD Reports ·Sarah P. Young,Aleena Khan,Ela Stefanescu,Andrea M. Seifts,Ghada Hijazi,Stephanie Austin,Priya S. Kishnani	2020	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 Clinica Chimica Acta ·Haoyue Zhang,Patricia Dickson,Ashlee R. Stiles,Agnes H. Chen,Steven Q. Le,Patricia McCaw,James Beasley,David S. Millington,Sarah P. Young	2020	6
12	Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia 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	2014	54
13	BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia 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,Parker Plant,Gyula T. Fülöp,Carmen Langa,Nicholas W. Morrell,Luisa M. Botella,Carmelo Bernabéu,David A. Stevenson,James Runo,Pınar Bayrak‐Toydemir	2013	226
14	Atypical immunologic response in a patient with CRIM-negative Pompe disease Molecular Genetics and Metabolism ·Mary‐Alice Abbott,Sean N. Prater,Suhrad G. Banugaria,Susan Richards,Sarah P. Young,Amy S. Rosenberg,Priya S. Kishnani	2011	24
15	Follow-up of a child with pyruvate dehydrogenase deficiency on a less restrictive ketogenic diet Molecular Genetics and Metabolism ·Areeg El‐Gharbawy,Anne Boney,Sarah P. Young,Priya S. Kishnani	2010	16
16	Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarker Genetics in Medicine ·Sarah P. Young,Haoyue Zhang,Deyanira Corzo,Beth L. Thurberg,Deeksha Bali,Priya S. Kishnani,David S. Millington	2009	72
17	Impaired clearance of accumulated lysosomal glycogen in advanced Pompe disease despite high‐level vector‐mediated transgene expression The Journal of Gene Medicine ·Baodong Sun,Haoyue Zhang,Andrew Bird,Songtao Li,Sarah P. Young,Dwight D. Koeberl	2009	20
18	Correction of Multiple Striated Muscles in Murine Pompe Disease Through Adeno-associated Virus–mediated Gene Therapy Molecular Therapy ·Baodong Sun,Sarah P. Young,Ping Li,Chunhui Di,T. T. Brown,Maja Z. Salva,Songtao Li,Andrew Bird,Zhen Yan,Richard L. Auten,Stephen D. Hauschka,Dwight D. Koeberl	2008	60
19	Efficacy of an Adeno-associated Virus 8-Pseudotyped Vector in Glycogen Storage Disease Type II Molecular Therapy ·Baodong Sun,Haoyue Zhang,Luis M. Franco,Sarah P. Young,Ayn Schneider,Andrew Bird,Andrea Amalfitano,Y.-T. Chen,Dwight D. Koeberl	2004	112
20	Liquid Chromatographic Assay for a Glucose Tetrasaccharide, a Putative Biomarker for the Diagnosis of Pompe Disease Analytical Biochemistry ·Yan An,Sarah P. Young,Stephen L. Hillman,Johan L.K. Van Hove,Yuan‐Tsong Chen,David S. Millington	2000	51

About Sarah P. Young

Sarah P. Young is a scholar working on Clinical Biochemistry, Rheumatology and Physiology, having authored 105 papers that have together received 3.8k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (57 papers), Glycogen Storage Diseases and Myoclonus (38 papers), Metabolism and Genetic Disorders (22 papers), Carbohydrate Chemistry and Synthesis (20 papers), Biochemical and Molecular Research (12 papers), Mitochondrial Function and Pathology (10 papers), Trypanosoma species research and implications (9 papers) and Diet and metabolism studies (7 papers). The work is most often cited by research in Physiology (2.1k citations), Rheumatology (1.1k citations) and Clinical Biochemistry (388 citations). Sarah P. Young has collaborated with scholars based in United States, Canada and Singapore. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Development.

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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