Marshall Summar

9.3k total citations
148 papers, 5.2k citations indexed

About

Marshall Summar is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Marshall Summar has authored 148 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Clinical Biochemistry, 47 papers in Molecular Biology and 35 papers in Physiology. Recurrent topics in Marshall Summar's work include Metabolism and Genetic Disorders (58 papers), Nitric Oxide and Endothelin Effects (14 papers) and Diet and metabolism studies (14 papers). Marshall Summar is often cited by papers focused on Metabolism and Genetic Disorders (58 papers), Nitric Oxide and Endothelin Effects (14 papers) and Diet and metabolism studies (14 papers). Marshall Summar collaborates with scholars based in United States, United Kingdom and Germany. Marshall Summar's co-authors include Mendel Tuchman, Andrea Gropman, Brendan Lee, Brian W. Christman, Nicholas Ah Mew, James V. Leonard, John A. Phillips, Kimberly A. Chapman, Frances Barr and Judy L. Aschner and has published in prestigious journals such as New England Journal of Medicine, The Journal of Immunology and PLoS ONE.

In The Last Decade

Marshall Summar

146 papers receiving 5.1k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Marshall Summar 2.0k 1.7k 978 835 713 148 5.2k
Wolfgang Sperl 2.3k 1.1× 4.1k 2.4× 892 0.9× 415 0.5× 415 0.6× 204 6.2k
H. Wächter 1.0k 0.5× 1.8k 1.0× 1.5k 1.5× 241 0.3× 436 0.6× 170 7.5k
Pascal Reynier 1.5k 0.8× 6.3k 3.6× 1.2k 1.3× 993 1.2× 191 0.3× 301 10.5k
Andreas Schulze 2.0k 1.0× 2.2k 1.3× 712 0.7× 656 0.8× 329 0.5× 139 5.5k
D. Rating 1.4k 0.7× 1.7k 1.0× 598 0.6× 1.9k 2.3× 271 0.4× 140 5.3k
Daniel E. Hale 2.6k 1.3× 2.7k 1.6× 901 0.9× 785 0.9× 247 0.3× 144 5.1k
Mitchell L. Halperin 812 0.4× 2.5k 1.4× 1.5k 1.5× 358 0.4× 341 0.5× 247 5.9k
Charles A. Stanley 3.3k 1.6× 5.0k 2.9× 1.7k 1.8× 1.2k 1.5× 823 1.2× 249 13.7k
P. Kay Lund 768 0.4× 1.7k 1.0× 1.0k 1.1× 205 0.2× 448 0.6× 59 4.5k
Frits A. Wijburg 2.9k 1.4× 4.1k 2.3× 6.1k 6.2× 1.1k 1.3× 504 0.7× 282 11.5k

Countries citing papers authored by Marshall Summar

Since Specialization
Citations

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

Fields of papers citing papers by Marshall Summar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marshall Summar

This figure shows the co-authorship network connecting the top 25 collaborators of Marshall Summar. A scholar is included among the top collaborators of Marshall Summar 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 Marshall Summar. Marshall Summar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Shur, Natasha, et al.. (2023). The past, present, and future of child growth monitoring: A review and primer for clinical genetics. American Journal of Medical Genetics Part A. 191(4). 948–961. 4 indexed citations
2.
Majumdar, Suvankar, James M. Chamberlain, Robert Sheppard Nickel, et al.. (2023). Design of an adaptive randomized clinical trial of intravenous citrulline for sickle cell pain crisis in the emergency department. Contemporary Clinical Trials Communications. 32. 101077–101077. 1 indexed citations
3.
Adachi, Takeya, Ayman W. El‐Hattab, Ritu Jain, et al.. (2023). Enhancing Equitable Access to Rare Disease Diagnosis and Treatment around the World: A Review of Evidence, Policies, and Challenges. International Journal of Environmental Research and Public Health. 20(6). 4732–4732. 71 indexed citations
4.
Regier, Debra S., Jennifer Weaver, Mark L. Batshaw, et al.. (2021). The Rare Disease Research Scholars Program: A training curriculum for clinical researchers with mixed methods evaluation study. PubMed. 6(1-2). 1–11. 1 indexed citations
5.
Porras, Antonio R., Kenneth N. Rosenbaum, Carlos Tor-Díez, Marshall Summar, & Marius George Linguraru. (2021). Development and evaluation of a machine learning-based point-of-care screening tool for genetic syndromes in children: a multinational retrospective study. The Lancet Digital Health. 3(10). e635–e643. 42 indexed citations
6.
Shur, Natasha, et al.. (2020). Rapid deployment of a telemedicine care model for genetics and metabolism during COVID‐19. American Journal of Medical Genetics Part A. 185(1). 68–72. 32 indexed citations
7.
Molema, Femke, Florian Gleich, Peter Burgard, et al.. (2019). Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea‐cycle disorders: On the basis of information from a European multicenter registry. Journal of Inherited Metabolic Disease. 42(6). 1162–1175. 26 indexed citations
8.
Summar, Marshall & Nicholas Ah Mew. (2018). Inborn Errors of Metabolism with Hyperammonemia. Pediatric Clinics of North America. 65(2). 231–246. 58 indexed citations
9.
Kirmse, Brian, Tzy‐Jyun Yao, Sean Hofherr, et al.. (2015). Acylcarnitine Profiles in HIV-Exposed, Uninfected Neonates in the United States. AIDS Research and Human Retroviruses. 32(4). 339–348. 13 indexed citations
10.
Fike, Candice D., Anna Dikalova, Mark R. Kaplowitz, et al.. (2014). Rescue Treatment with L-Citrulline Inhibits Hypoxia-Induced Pulmonary Hypertension in Newborn Pigs. American Journal of Respiratory Cell and Molecular Biology. 53(2). 255–264. 52 indexed citations
11.
Zhao, Qian, Kazunori Okada, Kenneth N. Rosenbaum, et al.. (2014). Digital facial dysmorphology for genetic screening: Hierarchical constrained local model using ICA. Medical Image Analysis. 18(5). 699–710. 52 indexed citations
12.
Fike, Candice D., Marta Sidoryk‐Wȩgrzynowicz, Michael Aschner, et al.. (2012). Prolonged hypoxia augments l-citrulline transport by System A in the newborn piglet pulmonary circulation. Cardiovascular Research. 95(3). 375–384. 14 indexed citations
13.
Chapman, Kimberly A. & Marshall Summar. (2011). Propionic acidemia consensus conference summary. Molecular Genetics and Metabolism. 105(1). 3–4. 10 indexed citations
14.
Gamble, Karen L., Alison A. Motsinger‐Reif, Akiko Hida, et al.. (2011). Shift Work in Nurses: Contribution of Phenotypes and Genotypes to Adaptation. PLoS ONE. 6(4). e18395–e18395. 132 indexed citations
15.
Falik‐Zaccai, Tzipora C., et al.. (2008). Population screening in a Druze community: the challenge and the reward. Genetics in Medicine. 10(12). 903–909. 31 indexed citations
16.
Mortlock, Douglas P., et al.. (2007). Assessing the Functional Characteristics of Synonymous and Nonsynonymous Mutation Candidates by Use of Large DNA Constructs. The American Journal of Human Genetics. 80(4). 740–750. 7 indexed citations
17.
Caldovic, Ljubica, Hiroki Morizono, Giselle Y. López, et al.. (2005). Late onset N-acetylglutamate synthase deficiency caused by hypomorphic alleles. Human Mutation. 25(3). 293–298. 34 indexed citations
18.
Hulgan, Todd, David W. Haas, Jonathan L. Haines, et al.. (2005). Mitochondrial haplogroups and peripheral neuropathy during antiretroviral therapy: an adult AIDS clinical trials group study. AIDS. 19(13). 1341–1349. 113 indexed citations
19.
Coleman, Rosalind, et al.. (1997). Cerebral defects and nephrogenic diabetes insipidus with the ARC syndrome: additional findings or a new syndrome (ARCC-NDI)?. PubMed. 72(3). 335–8. 29 indexed citations
20.
Jurado, L.A. Pérez, John A. Phillips, Marshall Summar, et al.. (1994). Genetic Mapping of the Human Growth Hormone-Releasing Factor Gene (GHRF) Using Two Intragenic Polymorphisms Detected by PCR Amplification. Genomics. 20(1). 132–134. 4 indexed citations

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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