Marvin R. Natowicz

9.7k total citations
111 papers, 4.2k citations indexed

About

Marvin R. Natowicz is a scholar working on Physiology, Molecular Biology and Genetics. According to data from OpenAlex, Marvin R. Natowicz has authored 111 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Physiology, 42 papers in Molecular Biology and 27 papers in Genetics. Recurrent topics in Marvin R. Natowicz's work include Lysosomal Storage Disorders Research (37 papers), Carbohydrate Chemistry and Synthesis (17 papers) and Metabolism and Genetic Disorders (13 papers). Marvin R. Natowicz is often cited by papers focused on Lysosomal Storage Disorders Research (37 papers), Carbohydrate Chemistry and Synthesis (17 papers) and Metabolism and Genetic Disorders (13 papers). Marvin R. Natowicz collaborates with scholars based in United States, Canada and United Kingdom. Marvin R. Natowicz's co-authors include Joseph S. Alper, Jacques Baenziger, Paul R. Billings, E M Prence, Barbara L. Triggs‐Raine, Melvin A. Kohn, Jon Beckwith, Margaret de Cuevas, William S. Sly and Richard I. Kelley and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Marvin R. Natowicz

109 papers receiving 4.0k citations

Peers

Marvin R. Natowicz

GENET

PHYSI

Michael M. Kaback United States

Gail E. Herman United States

Robert D. Steiner United States

Marc C. Patterson United States

Elsa Shapiro United States

Flemming Skovby Denmark

Yin‐Hsiu Chien Taiwan

Gerald L. Feldman United States

John J. Mitchell United States

Graham Jamieson United States

Michael M. Kaback United States

Marvin R. Natowicz

1.5k ×0.8

1.6k ×1.4

GENET

1.1k ×1.1

PHYSI

302 ×0.6

346 ×0.7

Citations per year, relative to Marvin R. Natowicz Marvin R. Natowicz (= 1×) peers Michael M. Kaback

Countries citing papers authored by Marvin R. Natowicz

Since Specialization

Citations

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

Fields of papers citing papers by Marvin R. Natowicz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marvin R. Natowicz. 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 Marvin R. Natowicz. The network helps show where Marvin R. Natowicz may publish in the future.

Co-authorship network of co-authors of Marvin R. Natowicz

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

All Works

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20 of 20 papers shown

Palomaki, Glenn E., Philip Wyatt, Ross Rowsey, et al.. (2024). Numbers of prenatal cell‐free DNA screens performed: Results of a 2022 CAP exercise. Prenatal Diagnosis. 44(8). 946–952. 1 indexed citations

Smith, Alan M., Elizabeth L.R. Donley, Denise M. Ney, et al.. (2023). Metabolomic biomarkers in autism: identification of complex dysregulations of cellular bioenergetics. Frontiers in Psychiatry. 14. 1249578–1249578. 10 indexed citations

Smith, Alan M., Marvin R. Natowicz, Daniel Braas, et al.. (2020). A Metabolomics Approach to Screening for Autism Risk in the Children's Autism Metabolome Project. Autism Research. 13(8). 1270–1285. 41 indexed citations

Abraham, Joseph R., John Barnard, Heng Wang, et al.. (2019). Proteomic investigations of human HERC2 mutants: Insights into the pathobiology of a neurodevelopmental disorder. Biochemical and Biophysical Research Communications. 512(2). 421–427. 11 indexed citations

Natowicz, Marvin R., et al.. (2018). The accuracy of computer‐based diagnostic tools for the identification of concurrent genetic disorders. American Journal of Medical Genetics Part A. 176(12). 2704–2709. 6 indexed citations

Kellaris, Georgios, Shahid Mahmood Baig, I-Chun Tsai, et al.. (2018). A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative features. Human Genomics. 12(1). 11–11. 41 indexed citations

Seabra, Catarina M., Serkan Erdin, Ashok Ragavendran, et al.. (2017). A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings. American Journal of Medical Genetics Part A. 173(9). 2478–2484. 5 indexed citations

Natowicz, Marvin R., et al.. (2017). Proteomic explorations of autism spectrum disorder. Autism Research. 10(9). 1460–1469. 12 indexed citations

Natowicz, Marvin R., et al.. (2009). On treatability: considerations of treatment in the context of newborn screening.. PubMed. 19(1). 187–97. 2 indexed citations

10.

Johnson, Samantha, Nancy Kass, & Marvin R. Natowicz. (2005). Disclosure of Personal Medical Information: Differences among Parents and Affected Adults for Genetic and Nongenetic Conditions. Genetic Testing. 9(3). 269–280. 12 indexed citations

11.

Natowicz, Marvin R., et al.. (2004). Heterozygosity for Tay-Sachs and Sandhoff Diseases in Non-Jewish Americans with Ancestry from Ireland, Great Britain, or Italy. Genetic Testing. 8(2). 174–180. 10 indexed citations

12.

Natowicz, Marvin R., et al.. (2003). Rapid Prenatal Testing for Human β-Glucuronidase Deficiency (MPS VII). Genetic Testing. 7(3). 241–243. 6 indexed citations

13.

Natowicz, Marvin R. & Elaine Hiller. (2002). Addressing Consumer Grievances in Medicine: Policies and Practices of Newborn Screening Programs in the United States. Genetic Testing. 6(1). 31–38. 3 indexed citations

14.

Natowicz, Marvin R., James Evans, Richard I. Kelley, et al.. (1996). Urinary bile acids and peroxisomal bifunctional enzyme deficiency. American Journal of Medical Genetics. 63(2). 356–362. 5 indexed citations

15.

Natowicz, Marvin R. & Yu Wang. (1996). Human serum hyaluronidase: Characterization of a clinical assay. Clinica Chimica Acta. 245(1). 1–6. 25 indexed citations

16.

Street, Jackie, James Evans, & Marvin R. Natowicz. (1996). Glucuronic Acid-conjugated Dihydroxy Fatty Acids in the Urine of Patients with Generalized Peroxisomal Disorders. Journal of Biological Chemistry. 271(7). 3507–3516. 24 indexed citations

17.

Palomaki, Glenn E., Josephine Williams, James E. Haddow, & Marvin R. Natowicz. (1995). Tay‐sachs disease in persons of French‐Canadian heritage in northern New England. American Journal of Medical Genetics. 56(4). 409–412. 8 indexed citations

18.

Natowicz, Marvin R., et al.. (1994). Abnormal bile acids in the Smith‐Lemli‐Opitz syndrome. American Journal of Medical Genetics. 50(4). 364–367. 52 indexed citations

19.

Akerman, Beverly R., Julian Zielenski, Barbara L. Triggs‐Raine, et al.. (1992). A mutation common in non-jewish Tay-Sachs disease: Frequency and RNA studies. Human Mutation. 1(4). 303–309. 34 indexed citations

20.

Natowicz, Marvin R., et al.. (1991). Marked variation in blood beta-hexosaminidase in Gaucher disease. Clinica Chimica Acta. 203(1). 17–22. 10 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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