Edwin W. Naylor

3.8k total citations
66 papers, 2.8k citations indexed

About

Edwin W. Naylor is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Edwin W. Naylor has authored 66 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Clinical Biochemistry, 33 papers in Molecular Biology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Edwin W. Naylor's work include Metabolism and Genetic Disorders (41 papers), Neonatal Health and Biochemistry (14 papers) and Mitochondrial Function and Pathology (11 papers). Edwin W. Naylor is often cited by papers focused on Metabolism and Genetic Disorders (41 papers), Neonatal Health and Biochemistry (14 papers) and Mitochondrial Function and Pathology (11 papers). Edwin W. Naylor collaborates with scholars based in United States, Spain and Canada. Edwin W. Naylor's co-authors include Donald H. Chace, Johan L.K. Van Hove, Emanuel Lebenthal, Steven L Hillman, James C. DiPerna, L F Hofman, Robert Guthrie, Brenda Mitchell, Steven F. Dobrowolski and David N. Finegold and has published in prestigious journals such as Journal of Biological Chemistry, PEDIATRICS and Analytical Biochemistry.

In The Last Decade

Edwin W. Naylor

66 papers receiving 2.7k citations

Peers

Countries citing papers authored by Edwin W. Naylor

Since Specialization

Citations

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

Fields of papers citing papers by Edwin W. Naylor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edwin W. Naylor. 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 Edwin W. Naylor. The network helps show where Edwin W. Naylor may publish in the future.

Co-authorship network of co-authors of Edwin W. Naylor

This figure shows the co-authorship network connecting the top 25 collaborators of Edwin W. Naylor. A scholar is included among the top collaborators of Edwin W. Naylor 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 Edwin W. Naylor. Edwin W. Naylor 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

#	Work	Indexed citations
1	Molecular analysis using targeted next generation DNA sequencing and clinical spectrum of Mexican patients with isovaleric acidemia 2019 ·Clinica Chimica Acta ·Isabel Ibarra‐González, Cynthia Fernández‐Lainez, (unknown), (unknown), (unknown), Tanya Sokolsky, Viren Amin, (unknown), Marcela Vela‐Amieva, Edwin W. Naylor, (unknown)	10
2	Development of DNA Confirmatory and High-Risk Diagnostic Testing for Newborns Using Targeted Next-Generation DNA Sequencing 2014 ·Genetics in Medicine ·Arindam Bhattacharjee, Tanya Sokolsky, Stacia K. Wyman, Martin G. Reese, Erik G. Puffenberger, Kevin A. Strauss, (unknown), Richard B. Parad, Edwin W. Naylor	52
3	Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening 2010 ·Molecular Genetics and Metabolism ·(unknown), David N. Finegold, Edwin W. Naylor, Inderneel Sahai, Susan E. Waisbren, Harvey L. Levy	44
4	Mutations in the phenylalanine hydroxylase gene identified in 95 patients with phenylketonuria using novel systems of mutation scanning and specific genotyping based upon thermal melt profiles 2007 ·Molecular Genetics and Metabolism ·Steven F. Dobrowolski, (unknown), (unknown), (unknown), (unknown), Edwin W. Naylor, Richard Koch, Harvey L. Levy	37
5	Alternative DNA-based newborn screening for glucose-6-phosphate dehydrogenase deficiency 2005 ·Molecular Genetics and Metabolism ·Zhili Lin, (unknown), (unknown), Edwin W. Naylor	37
6	Effect of Expanded Newborn Screening for Biochemical Genetic Disorders on Child Outcomes and Parental Stress 2004 ·Obstetrical & Gynecological Survey ·Susan E. Waisbren, (unknown), (unknown), 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	10
7	The use of filter paper-dried blood spots for thyroid-antibody screening in adults 2004 ·Journal of Laboratory and Clinical Medicine ·L F Hofman, Thomas P. Foley, (unknown), Edwin W. Naylor	18
8	Real time PCR assays to detect common mutations in the biotinidase gene and application of mutational analysis to newborn screening for biotinidase deficiency 2003 ·Molecular Genetics and Metabolism ·Steven F. Dobrowolski, (unknown), Richard Banas, Edwin W. Naylor	19
9	Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutations Identified by MS/MS-Based Prospective Screening of Newborns Differ from Those Observed in Patients with Clinical Symptoms: Identification and Characterization of a New, Prevalent Mutation That Results in Mild MCAD Deficiency* 2001 ·The American Journal of Human Genetics ·Brage Storstein Andresen, (unknown), Linda P. O’Reilly, Joseph Muenzer, Shawn E. McCandless, Dianne M. Frazier, Szabolcs Udvari, Peter Bross, Inga Knudsen, (unknown), Donald H. Chace, Paul C. Engel, Edwin W. Naylor, Niels Gregersen	180
10	Immunoreactive trypsinogen levels in pediatric patients with intestinal failure awaiting intestinal transplantation 1999 ·Clinical Transplantation ·Giuseppe M. Rovera, Lúther Sigurðsson, Jorge Reyes, (unknown), Edwin W. Naylor, Samuel A. Kocoshis	2
11	Direct analysis of filter paper blood specimens for identification of Smith-Lemli-Opitz syndrome using time-of-flight secondary ion mass spectrometry 1997 ·American Journal of Medical Genetics ·Paul Zimmerman, David M. Hercules, Edwin W. Naylor	28
12	Deletion of the ferrochelatase gene in a patient with protoporphyria 1994 ·Human Molecular Genetics ·Scott T. Magness, Antonio Tugores, (unknown), Caryn Wagner-McPherson, Glen A. Evans, Edwin W. Naylor, David A. Brenner	25
13	Combined transient and peripheral defects in tetrahydrobiopterin synthesis 1991 ·The Journal of Pediatrics ·Judith Allanson, Roderick R. McInnes, (unknown), Theodore J. Tarby, Edwin W. Naylor, (unknown)	4
14	False positive alanine tolerance test results in heterozygote detection of urea cycle disorders 1989 ·The Journal of Pediatrics ·Mark L. Batshaw, Edwin W. Naylor, George Thomas	7
15	Repetitive recycling of guanosine triphosphate cyclohydrolase I for synthesis of dihydroneopterin triphosphate 1989 ·Analytical Biochemistry ·Juan Ferré, Edwin W. Naylor, K. Bruce Jacobson	4
16	Sepiapterin reductase in cultured human cells 1987 ·Biochemical and Biophysical Research Communications ·Juan Ferré, Edwin W. Naylor	8
17	Biopterin Synthesis Defects: Problems in Diagnosis 1984 ·PEDIATRICS ·George Hoganson, Stanley Berlow, Seymour Kaufman, Sheldon Milstien, (unknown), Reuben Matalon, Edwin W. Naylor, William E. Seifert	17
18	A simple screening test for reduced glutathione in filter paper spots of blood 1981 ·The Journal of Pediatrics ·Michael D. Garrick, (unknown), (unknown), Edwin W. Naylor, Robert Guthrie	2
19	Urine screening for metabolic disease in newborn infants 1980 ·The Journal of Pediatrics ·(unknown), Edwin W. Naylor, Robert Guthrie	8
20	Measurement of urinary pyrimidine bases and nucleosides by high-performance liquid chromatography 1979 ·Journal of Chromatography B Biomedical Sciences and Applications ·(unknown), Howard Tieckelmann, Edwin W. Naylor, Robert Guthrie	24

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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