Deborah Marsden

3.1k citations

65 papers · 1.8k indexed · h-index 24

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Physiology top 5%
- Diet and metabolism studies
- Lysosomal Storage Disorders Research

Papers in

Clinical Biochemistry 40
- Metabolism and Genetic Disorders 40
Physiology 27
- Lysosomal Storage Disorders Research 17
- Diet and metabolism studies 10

Co-authors: Harvey L. Levy Cecilia Larson Arnold W. Strauss Vivian E. Shih George F. Grady Roger B. Eaton Thomas H. Zytkovicz Anne Marie Comeau
Journals: Molecular Genetics and Metabolism (17 papers)Journal of Inherited Metabolic Disease (9 papers)Genetics in Medicine (5 papers)Clinical Chemistry (3 papers)The Journal of Pediatrics (2 papers)
Partner nations: United States Netherlands United Kingdom

In The Last Decade

Deborah Marsden

61 papers receiving 1.7k citations

Peers

Countries citing papers authored by Deborah Marsden

Since Specialization

Citations

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

Fields of papers citing papers by Deborah Marsden

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah Marsden. 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 Deborah Marsden. The network helps show where Deborah Marsden may publish in the future.

Co-authors

The 25 scholars most cited alongside Deborah Marsden, 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 Deborah Marsden Line = papers co-authored together Deborah Marsden links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Mucopolysaccharidosis type VII (Sly syndrome) - What do we know? Molecular Genetics and Metabolism ·Christina Grant, العيهار أ. محمد, Deborah Marsden, Fatih Süheyl Ezgü	2024	1
2	Growth patterns in patients with mucopolysaccharidosis VII Molecular Genetics and Metabolism Reports ·Adriana M. Montaño, Agnieszka Różdżyńska‐Świątkowska, Agnieszka Jurecka, Shengzhi Zhang, Lin Zhang, Deborah Marsden, Raymond Wang, Paul Harmatz	2023	1
3	Long-term efficacy and safety of vestronidase alfa enzyme replacement therapy in pediatric subjects < 5 years with mucopolysaccharidosis VII Molecular Genetics and Metabolism ·Heather Lau, David Viskochil, Pranoot Tanpaiboon, Mitsugu Kuboki, Esmeralda Martins, Julie Taylor, A.H. Jaytissa, Lin Zhang, Agnieszka Jurecka, Deborah Marsden	2022	4
4	Impact of newborn screening on the reported incidence and clinical outcomes associated with medium- and long-chain fatty acid oxidation disorders Genetics in Medicine ·Deborah Marsden, Camille L. Bedrosian, Jerry Vockley	2021	45
5	3D printed customised external cranial plate in a patient with syndrome of trephined: ‘a case report’ SHILAP Revista de lepidopterología ·Harry Mee, Sarah L. Greasley, M.Kubendran, Christopher P. Harkin, Tuan Ruzuaini Tuan Lah, Deborah Marsden, Rachael Andrews, Ayumi Oka, B. Khanpour, Fahim Anwar, 김상윤, Carlos M. Scuderi, Joachim Dorschel, Adel Helmy	2021	7
6	The long-term safety and efficacy of vestronidase alfa, rhGUS enzyme replacement therapy, in subjects with mucopolysaccharidosis VII Molecular Genetics and Metabolism ·Raymond Wang, José Francisco da Silva Franco, العيهار أ. محمد, Esmeralda Martins, V. Reid Sutton, Chester B. Whitley, Lin Zhang, George O Obel, Deborah Marsden, Agnieszka Jurecka, Paul Harmatz	2020	25
7	Regulatory strategies for rare diseases under current global regulatory statutes: a discussion with stakeholders Orphanet Journal of Rare Diseases ·Andrew E. Mulberg, Christina Bucci‐Rechtweg, Joseph Giuliano, David Jacoby, Franklin K. Johnson, Qing Liu, Deborah Marsden, Wang Kai, Robert M. Nelson, Nita Patel, Klaus Romero, Vikram Sinha, Sheela Sitaraman, G. P. Evseeva, Fajar Pramudyastuty	2019	37
8	UX007 for the treatment of long chain-fatty acid oxidation disorders: Safety and efficacy in children and adults following 24 weeks of treatment Molecular Genetics and Metabolism ·Jerry Vockley, Barbara K. Burton, Gerard T. Berry, Nicola Longo, John G. Phillips, Amarilis Sanchez‐Valle, Pranoot Tanpaiboon, Stephanie Grünewald, Elaine Murphy, Reed Humphrey, J. Mayhew, A. Bowden, AGNES G. McCLURE, C.X. Diniz, Deborah Marsden, Emil Kakkis	2017	58
9	Clinical, Biochemical, and Molecular Features in 37 Saudi Patients with Very Long Chain Acyl CoA Dehydrogenase Deficiency JIMD Reports ·武夫岡田, Marwan Nashabat, Majid Alfadhel, Ali Alasmari, Fuad Al Mutairi, Abdulrahman Alswaid, Eissa Faqeih, Melanie Tait, Susanne Stronski, Xingru Sun, Deborah Marsden, Wafaa Eyaid	2017	16
10	Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disorders Molecular Genetics and Metabolism ·Jerry Vockley, Joel Charrow, Abhishek Divekar, 品种管理处, George A. Díaz, Elizabeth McCracken, Robert L. Conway, Gregory M. Enns, Joanne P. Starr, Xiaowei Song, José E. Abdenur, Joan Sánchez-de-Toledo, Deborah Marsden	2016	67
11	Recurrent unexplained hyperammonemia in an adolescent with arginase deficiency Clinical Biochemistry ·Yan Zhang, Yuval E. Landau, David T. Miller, Deborah Marsden, Gerard T. Berry, Mark D. Kellogg	2012	9
12	Newborn Screening Critical Reviews in Clinical Laboratory Sciences ·Inderneel Sahai, Deborah Marsden	2009	35
13	M.P.5.08 Physician reported outcomes of enzyme replacement therapy in older, severely affected patients with Pompe disease Neuromuscular Disorders ·Ans van der Ploeg, Deborah Marsden	2007	1
14	Development of a newborn screening follow-up algorithm for the diagnosis of isobutyryl-CoA dehydrogenase deficiency Genetics in Medicine ·Devin Oglesbee, Miao He, Sabrinath Prasad, Jerry Vockley, Ayesha Ahmad, Brad Angle, Barbara K. Burton, Joel Charrow, Regina Ensenauer, Can Fıçıcıoğlu, Laura Davis Keppen, Deborah Marsden, Silvia Tortorelli, Si Houn Hahn, Dietrich Matern	2007	33
15	Effect of Expanded Newborn Screening for Biochemical Genetic Disorders on Child Outcomes and Parental Stress Obstetrical & Gynecological Survey ·Susan E. Waisbren, К А Сухов, Л.В. Затонская, Mary G. Ampola, Thomas Brewster, Laurie Demmer, Roger B. Eaton, Robert M. Greenstein, Mark Korson, Cecilia Larson, Deborah Marsden, Michael E. Msall, Edwin W. Naylor, Siegfried M. Pueschel, Margretta R. Seashore, Vivian E. Shih, Harvey L. Levy	2004	10
16	Expanded Newborn Screening Pediatric Annals ·Medgyesi Ga, Deborah Marsden	2003	28
17	Arginase deficiency with lethal neonatal expression: Evidence for the glutamine hypothesis of cerebral edema The Journal of Pediatrics ·Jonathan Picker, Ana Cristina Puga, Harvey L. Levy, Deborah Marsden, Vivian E. Shih, Umberto DeGirolami, Keith L. Ligon, Stephen D. Cederbaum, Rita M. Kern, Gerald F. Cox	2003	37
18	Multicolour karyotyping The Lancet ·Charles Lee, Michael F. Murray, Patricia M. Miron, Deborah Marsden, Mira Irons, Louise Wilkins‐Haug, Cynthia C. Morton	2001	6
19	Spectrum of expression of MCAD and SCAD detected by newborn screening Journal of Inherited Metabolic Disease ·Deborah Marsden	2000	4
20	Histopathological Findings in a male with Late-Onset Ornithine Transcarbamylase Deficiency Pediatric Pathology ·Mridula V. G., Deborah Marsden, William L. Nyhan, Robert Newbury, Henry F. Krous, Mendel Tuchman	1994	17

About Deborah Marsden

Deborah Marsden is a scholar working on Clinical Biochemistry, Physiology, Pediatrics, Perinatology and Child Health, Rheumatology and Nephrology, having authored 65 papers that have together received 1.8k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (40 papers), Lysosomal Storage Disorders Research (17 papers), Mitochondrial Function and Pathology (15 papers), Neonatal Health and Biochemistry (12 papers), Diet and metabolism studies (10 papers), Glycogen Storage Diseases and Myoclonus (8 papers), Alcoholism and Thiamine Deficiency (5 papers) and Trypanosoma species research and implications (5 papers). The work is most often cited by research in Clinical Biochemistry (1.2k citations), Physiology (532 citations), Pediatrics, Perinatology and Child Health (391 citations), Rheumatology (283 citations) and Biochemistry (101 citations). Deborah Marsden has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include Harvey L. Levy, Cecilia Larson, Arnold W. Strauss, Vivian E. Shih, George F. Grady, Roger B. Eaton, Thomas H. Zytkovicz, Anne Marie Comeau, Jerry Vockley and Donna M. Johnson. Their work appears in journals such as Molecular Genetics and Metabolism, Journal of Inherited Metabolic Disease, Genetics in Medicine, Clinical Chemistry and The Journal of Pediatrics.

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