Marc C. Patterson

13.8k citations

172 papers · 6.5k indexed · h-index 46

Impact in

Physiology top 0.5%
- Lysosomal Storage Disorders Research
- Calcium signaling and nucleotide metabolism
Psychiatry and Mental health top 1%
- Child Nutrition and Feeding Issues

Papers in

Clinical Biochemistry 19
- Metabolism and Genetic Disorders 19
Physiology 70
- Lysosomal Storage Disorders Research 63

Co-authors: Marie T. Vanier Mark Walterfang Darleen Vecchio Larry A. Abel Hudson H. Freeze J. E. Wraith Frits A. Wijburg Helena Prady
Journals: Molecular Genetics and Metabolism (16 papers)Neurology (13 papers)Journal of Child Neurology (12 papers)Orphanet Journal of Rare Diseases (11 papers)Pediatric Neurology (6 papers)
Partner nations: United States United Kingdom Switzerland

In The Last Decade

Marc C. Patterson

169 papers receiving 6.4k citations

Peers

Countries citing papers authored by Marc C. Patterson

Since Specialization

Citations

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

Fields of papers citing papers by Marc C. Patterson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marc C. Patterson. 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 Marc C. Patterson. The network helps show where Marc C. Patterson may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Disease-Modifying, Neuroprotective Effect of N-Acetyl- l -Leucine in Adult and Pediatric Patients With Niemann-Pick Disease Type C Neurology ·Marc C. Patterson, Uma Ramaswami, Aimée Donald, Stefan Devoldere, Matthias Gautschi, Paul Gissen, Andreas Hahn, Simon Jones, R. Kay, Theo Harpel, Julien H. Park, 강세은, Mark Walterfang, Yuan Xiaoixa, Marianne Rohrbach, Κyriakos Martakis, Tatiana Brémovà-Ertl	2025	0
2	Progressive encephalopathy after routine 4‐month immunizations in a patient with NAXD genetic variant American Journal of Medical Genetics Part A ·de Baillou H, Ethan M. Grund, 清子松田, Marc C. Patterson, D. Corydon Hammond, Nessa Aghazadeh, Monika Binkowska-Bury	2024	1
3	A natural history study of pediatric patients with early onset of GM1 gangliosidosis, GM2 gangliosidoses, or gaucher disease type 2 (RETRIEVE) Orphanet Journal of Rare Diseases ·Bénédicte Héron, Spyros Batzios, Eugen Mengel, Tadesse Yayeh, Marc C. Patterson, Matthias Gautschi, Peter Cornelisse, Kyung Ae Yang, Barbara Schwierin, Marianne Rohrbach	2024	1
4	N-acetyl-L-leucine for Niemann-Pick type C: a multinational double-blind randomized placebo-controlled crossover study Trials ·幹逸箸方, Tatiana Brémovà-Ertl, к.м. Саникидзе, Nain Deo Novebra Simanjuntak, William Evans, Carter T. Fields, (unknown), R. Kay, M. Bessiar, Κyriakos Martakis, Marc C. Patterson, Frances M. Platt, Michael Factor, Michael Strupp	2023	13
5	Impacts and Burden of Niemann pick Type-C: a patient and caregiver perspective Orphanet Journal of Rare Diseases ·Eugen Mengel, Marc C. Patterson, Baishu Zheng, Carranza Camus, Christine í Dali, Tara Symonds, Dede Nizar Nirmawan, Kenji KOSEKI, А.П. Кутейникова, Babith	2021	6
6	Long‐term survival outcomes of patients with Niemann‐Pick disease type C receiving miglustat treatment: A large retrospective observational study Journal of Inherited Metabolic Disease ·Marc C. Patterson, William S. Garver, Idaho Soil, Jackie Imrie, Helena Jahnová, F. John Meaney, Yann Nadjar, Marie T. Vanier, Ana Maria Nascimento Damiani, Olivier Morand, D Rosenberg, Barbara Schwierin, Bénédicte Héron	2020	42
7	Secondary Narcolepsy in Children Journal of Child Neurology ·Xenia Rodríguez Obando, Jennifer Pitts, Marc C. Patterson, Robin M. Lloyd, Gesina F. Keating, Suresh Kotagal	2020	10
8	Developments in evidence creation for treatments of inborn errors of metabolism Journal of Inherited Metabolic Disease ·Sylvia Stöckler‐Ipsiroglu, Beth K. Potter, Nataliya Yuskiv, Kylie Tingley, Marc C. Patterson, Clara D.M. van Karnebeek	2020	14
9	Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood‐onset beta‐mannosidosis Molecular Genetics & Genomic Medicine ·Troy C. Lund, Weston P. Miller, Julie B. Eisengart, Wang Shuang-Yi, Laura Pollard, Deborah L. Renaud, David A. Wenger, Marc C. Patterson, Paul J. Orchard	2019	5
10	Recommendations for patient screening in ultra-rare inherited metabolic diseases: what have we learned from Niemann-Pick disease type C? Orphanet Journal of Rare Diseases ·A L Guyatt, Peter Bauer, 哲諏訪, Thomas Klopstock, Yann Nadjar, Marc C. Patterson, Matthis Synofzik, Christian J. Hendriksz	2019	11
11	Jeavons Syndrome: Clinical Features and Response to Treatment Pediatric Neurology ·Kelsey M. Smith, Verónica Almanza, Elaine Wirrell, Katherine Nickels, Eric T. Payne, Jeffrey W. Britton, Cheolsu Shin, Gregory D. Cascino, Marc C. Patterson, Lily C. Wong‐Kisiel	2018	35
12	Oculomotor and Vestibular Findings in Gaucher Disease Type 3 and Their Correlation with Neurological Findings Frontiers in Neurology ·Tatiana Brémovà-Ertl, Raphael Schiffmann, Marc C. Patterson, Nadia Belmatoug, Thierry Billette de Villemeur, Stanislavs Bardins, Claudia Frenzel, Vĕra Malinová, Magnus Persson, Vera Fatinato, Eugen Mengel, Jörg Reinke, Ralf Strobl, Michael Strupp	2018	14
13	Stable or improved neurological manifestations during miglustat therapy in patients from the international disease registry for Niemann-Pick disease type C: an observational cohort study Orphanet Journal of Rare Diseases ·(unknown), Marc C. Patterson, Eugen Mengel, Marie T. Vanier, Barbara Schwierin, Audrey Muller, Peter Cornelisse, Mercè Pineda	2015	69
14	The Niemann-Pick Disease Type C Suspicion Index: Development of a New Tool to Aid Diagnosis Christian J. Hendriksz, Mercédes Pineda, Michael Fahey, Mark Walterfang, Miriam Stampfer, Heiko Runz, Marc C. Patterson, Juan V. Torres, Stefan Kolb	2015	12
15	Disease and patient characteristics in NP-C patients: findings from an international disease registry Orphanet Journal of Rare Diseases ·Marc C. Patterson, Eugen Mengel, Frits A. Wijburg, Audrey Muller, Barbara Schwierin, Steve Luecking, Marie T. Vanier, Mercè Pineda	2013	145
16	Inborn Errors of Metabolism for Child Neurology Residents Seminars in Pediatric Neurology ·Marc C. Patterson	2011	0
17	Longitudinal investigation of the antinociceptive potency of oxycodone and morphine in the zucker rat Clinical Pharmacology & Therapeutics ·T. Wang, Н. Э. Шепель, Marc C. Patterson, Maree T. Smith	2004	1
18	Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene Journal of the Neurological Sciences ·Michelangelo Mancuso, Massimiliano Filosto, J. Clarke Stevens, Marc C. Patterson, Sara Shanske, Sindu Krishna, Salvatore DiMauro	2003	33
19	Functional significance of PMM2 mutations in mildly affected patients with congenital disorders of glycosylation Ia Genetics in Medicine ·Vibeke Westphal, A.R. Burns, Marc C. Patterson, Anne Tournay, Andrea Blumenthal, Eileen P. Treacy, Hudson H. Freeze	2001	47
20	AN INTRACRANIAL ARTERIOVENOUS MALFORMATION AND PALATAL MYOCLONUS RELATED TO PSEUDOXANTHOMA ELASTICUM Australian and New Zealand Journal of Medicine ·J. B. Chalk, Marc C. Patterson, Michael P. Pender	1989	8

About Marc C. Patterson

Marc C. Patterson is a scholar working on Clinical Biochemistry, Physiology, Psychiatry and Mental health, Rheumatology and Physiology, having authored 172 papers that have together received 6.5k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (63 papers), Metabolism and Genetic Disorders (19 papers), Carbohydrate Chemistry and Synthesis (18 papers), Child Nutrition and Feeding Issues (16 papers), Glycosylation and Glycoproteins Research (15 papers), Family and Disability Support Research (13 papers), Autoimmune and Inflammatory Disorders Research (12 papers) and Mitochondrial Function and Pathology (11 papers). The work is most often cited by research in Physiology (3.4k citations), Physiology (463 citations), Psychiatry and Mental health (882 citations), Clinical Biochemistry (387 citations) and Hematology (611 citations). Marc C. Patterson has collaborated with scholars based in United States, United Kingdom and Switzerland. Frequent co-authors include Marie T. Vanier, Mark Walterfang, Darleen Vecchio, Larry A. Abel, Hudson H. Freeze, J. E. Wraith, Frits A. Wijburg, Helena Prady, Bobby G. Ng and Erik A. Eklund. Their work appears in journals such as Molecular Genetics and Metabolism, Neurology, Journal of Child Neurology, Orphanet Journal of Rare Diseases and Pediatric Neurology.

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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