Darius J. Adams

2.8k total citations
17 papers, 464 citations indexed

About

Darius J. Adams is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Darius J. Adams has authored 17 papers receiving a total of 464 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 6 papers in Physiology. Recurrent topics in Darius J. Adams's work include Metabolism and Genetic Disorders (8 papers), Mitochondrial Function and Pathology (7 papers) and Neurological diseases and metabolism (3 papers). Darius J. Adams is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Mitochondrial Function and Pathology (7 papers) and Neurological diseases and metabolism (3 papers). Darius J. Adams collaborates with scholars based in United States, France and Austria. Darius J. Adams's co-authors include David A. Clark, Richard W. Erbe, Joan E. Pellegrino, Carlos A. Saavedra‐Matiz, Michele Caggana, David Kronn, Melissa Wasserstein, Brett H. Graham, Joyce A. Kobori and Joseph Shen and has published in prestigious journals such as Hepatology, Neurology and The Journal of Pediatrics.

In The Last Decade

Darius J. Adams

16 papers receiving 451 citations

Peers

Darius J. Adams
Elena Martín‐Hernández Spain
Annette S. Feigenbaum Canada
Patrik Feyh Germany
Andrew A.M. Morris United Kingdom
Anke Schumann Germany
L. Kierat Switzerland
Yutaka Hase Japan
M.T. García‐Silva Spain
Magalie Barth France
A. E. M. Stroomer Netherlands
Elena Martín‐Hernández Spain
Darius J. Adams
Citations per year, relative to Darius J. Adams Darius J. Adams (= 1×) peers Elena Martín‐Hernández

Countries citing papers authored by Darius J. Adams

Since Specialization
Citations

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

Fields of papers citing papers by Darius J. Adams

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Darius J. Adams. 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 Darius J. Adams. The network helps show where Darius J. Adams may publish in the future.

Co-authorship network of co-authors of Darius J. Adams

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

All Works

17 of 17 papers shown
1.
Schmidt, Sarah, Hélio Pedro, Reena Jethva, et al.. (2025). Newborn Screening for Gaucher Disease: The New Jersey Experience. International Journal of Neonatal Screening. 11(2). 34–34.
2.
Adams, Darius J., et al.. (2023). Moya moya vasculopathy and MECP2 duplication syndrome. Child s Nervous System. 40(3). 809–812. 1 indexed citations
3.
Adams, Darius J., Hans C. Andersson, Kristin Lindstrom, et al.. (2021). Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics. Molecular Genetics and Metabolism Reports. 28. 100790–100790. 14 indexed citations
4.
Atwal, Paldeep S., et al.. (2020). The infantile neuroaxonal dystrophy rating scale (INAD-RS). Orphanet Journal of Rare Diseases. 15(1). 195–195. 8 indexed citations
5.
Adams, Darius J., et al.. (2020). Natural history of the oldest known females with mucopolysaccharidosis type IVA (Morquio A syndrome). American Journal of Medical Genetics Part A. 182(6). 1491–1495. 4 indexed citations
6.
Adams, Darius J., Mark Midei, Jahannaz Dastgir, et al.. (2020). Treatment of infantile neuroaxonal dystrophy with RT001: A di‐deuterated ethyl ester of linoleic acid: Report of two cases. JIMD Reports. 54(1). 54–60. 20 indexed citations
7.
Muntau, Ania C., Darius J. Adams, Amaya Bélanger-Quintana, et al.. (2019). International best practice for the evaluation of responsiveness to sapropterin dihydrochloride in patients with phenylketonuria. Molecular Genetics and Metabolism. 127(1). 1–11. 43 indexed citations
8.
9.
Vogel, Beth, Darius J. Adams, Kristin D׳Aco, et al.. (2015). Newborn screening for X-linked adrenoleukodystrophy in New York State: Diagnostic protocol, surveillance protocol and treatment guidelines. Molecular Genetics and Metabolism. 114(4). 599–603. 84 indexed citations
10.
Adams, Darius J. & David A. Clark. (2015). Common Genetic and Epigenetic Syndromes. Pediatric Clinics of North America. 62(2). 411–426. 15 indexed citations
11.
12.
Burton, Barbara K., et al.. (2010). Tetrahydrobiopterin Therapy for Phenylketonuria in Infants and Young Children. The Journal of Pediatrics. 158(3). 410–415. 23 indexed citations
13.
El‐Hattab, Ayman W., Fangyuan Li, Joseph Shen, et al.. (2010). Maternal systemic primary carnitine deficiency uncovered by newborn screening: Clinical, biochemical, and molecular aspects. Genetics in Medicine. 12(1). 19–24. 81 indexed citations
14.
Arnold, Georgianne L., Carlos A. Saavedra‐Matiz, Patricia Galvin‐Parton, et al.. (2009). Lack of genotype–phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State. Molecular Genetics and Metabolism. 99(3). 263–268. 48 indexed citations
15.
Wong, Lee-Jun, Nicola Brunetti‐Pierri, Qing Zhang, et al.. (2007). Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy. Hepatology. 46(4). 1218–1227. 94 indexed citations
16.
Rios, Angel, SUSAN A. FURDON, Darius J. Adams, & David A. Clark. (2004). RECOGNIZING THE CLINICAL FEATURES OF TRISOMY 13 SYNDROME. Advances in Neonatal Care. 4(6). 332–343. 16 indexed citations
17.
Afonina, Irina, Stephen Sanders, Igor V. Kutyavin, et al.. (2002). Single nucleotide polymorphism detection with MGB Eclipse (TM) assays. Digital Academic REpository of VU University Amsterdam (Vrije Universiteit Amsterdam). 25(3). 268–275. 3 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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