Stephen D. Cederbaum

2.2k citations

39 papers · 1.6k indexed · h-index 21

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Biochemistry top 1%
- Amino Acid Enzymes and Metabolism

Papers in

Clinical Biochemistry 32
- Metabolism and Genetic Disorders 32
Biochemistry 14
- Amino Acid Enzymes and Metabolism 10
- Biochemical Acid Research Studies 5

Co-authors: Rita M. Kern John P. Blass Wayne W. Grody Wendy J. Brown P Chapoy Joseph G. Vockley C. Angelini Austin L. Shug
Journals: Molecular Genetics and Metabolism (8 papers)The Journal of Pediatrics (5 papers)Journal of Inherited Metabolic Disease (3 papers)Biochemical Genetics (3 papers)Pediatric Research (3 papers)
Partner nations: United States Australia Germany

In The Last Decade

Stephen D. Cederbaum

38 papers receiving 1.5k citations

Peers

Countries citing papers authored by Stephen D. Cederbaum

Since Specialization

Citations

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

Fields of papers citing papers by Stephen D. Cederbaum

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen D. Cederbaum. 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 Stephen D. Cederbaum. The network helps show where Stephen D. Cederbaum may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Taste-masked formulation of sodium phenylbutyrate (ACER-001) for the treatment of urea cycle disorders Molecular Genetics and Metabolism ·Stephen D. Cederbaum, Robert J. Edwards, 弘晃高梨, T. Beringer, Robert D. Steiner	2023	1
2	Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California Molecular Genetics and Metabolism ·Natalie M. Gallant, سمیه رسولی ابراهیمی فرد, Yael Wilnai, Harri Veivo, Fred Lorey, Lisa Feuchtbaum, Hao Tang, Felismina Saraiva Soares, Gregory M. Enns, Seymour Packman, Henry J. Lin, William R. Wilcox, Stephen D. Cederbaum, José E. Abdenur	2017	20
3	Analysis of cases of 3-methylcrotonyl CoA carboxylase deficiency (3-MCCD) in the California newborn screening program reported in the state database Molecular Genetics and Metabolism ·Kumud Patel, Bianca Thaís Silva do Nascimento, Stephen D. Cederbaum, Julie Neidich, Natalie M. Gallant, Fred Lorey, Lisa Feuchtbaum, Derek A. Wong	2013	18
4	Combined Hurler and Sanfilippo syndrome in a sibling pair Molecular Genetics and Metabolism ·Angela Sun, John J. Hopwood, Jerry N. Thompson, Stephen D. Cederbaum	2011	2
5	Cross-sectional multicenter study of patients with urea cycle disorders in the United States Molecular Genetics and Metabolism ·Mendel Tuchman, Brendan Lee, Uta Lichter‐Konecki, Marshall Summar, Marc Yudkoff, Stephen D. Cederbaum, Douglas S. Kerr, George A. Díaz, Du Shuangquan, Hye Seung Lee, Robert McCarter, Jeffrey P. Krischer, Mark L. Batshaw	2008	144
6	Clinical and Functional Characterization of a Human ORNT1 Mutation (T32R) in the Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) Syndrome Pediatric Research ·Manuel Graña, Rebecca Mardach, Betzabe Mogollon Portilla, Eduardo Ruiz‐Pesini, Olga Derbeneva, Lindfors Lg, Frank Zaldivar, Haruo Koizumi, Stephen D. Cederbaum	2006	20
7	Arginase deficiency with lethal neonatal expression: Evidence for the glutamine hypothesis of cerebral edema The Journal of Pediatrics ·Jonathan Picker, Ana Cristina Puga, Harvey L. Levy, Deborah Marsden, Vivian E. Shih, Umberto DeGirolami, Keith L. Ligon, Stephen D. Cederbaum, Rita M. Kern, Gerald F. Cox	2003	37
8	Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency Molecular Genetics and Metabolism ·Stephen D. Cederbaum, Samantha Koo-McCoy, Ingrid Tein, Betty Y.L. Hsu, Arupa Ganguly, Éric Vilain, Katrina M. Dipple, Ljerka Cvitanović-Šojat, Charles A. Stanley	2002	52
9	Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans Molecular Genetics and Metabolism ·Nguyễn Văn Tiến, Brage Storstein Andresen, Thomas J. Corydon, Sandro Ghisla, Yoldine Talina Jean Noel, Al‐Walid Mohsen, Stephen D. Cederbaum, Diane S. Roe, Charles R. Roe, Nicholas Lench, Jerry Vockley	2002	51
10	Laboratory evaluation of urea cycle disorders The Journal of Pediatrics ·Robert D. Steiner, Stephen D. Cederbaum	2001	39
11	Psychosocial issues and coping strategies in families affected by urea cycle disorders The Journal of Pediatrics ·Julie A. Cederbaum, Cynthia LeMons, Ala’ Sh Almehsen, Mary Ahrens, G Bodländer, Stephen D. Cederbaum	2001	32
12	Isolated Isobutyryl-CoA Dehydrogenase Deficiency: An Unrecognized Defect in Human Valine Metabolism Molecular Genetics and Metabolism ·Charles R. Roe, Stephen D. Cederbaum, Diane S. Roe, Rebecca Mardach, Alvaro Galindo, Lawrence Sweetman	1998	59
13	Cloning and Characterization of the Human Type II Arginase Gene Genomics ·Joseph G. Vockley, Christopher P. Jenkinson, Amor Tbib, Rita M. Kern, Wayne W. Grody, Stephen D. Cederbaum	1996	167
14	Deletion in Blood Mitochondrial DNA in Kearns-Sayre Syndrome Pediatric Research ·Nathan Fischel‐Ghodsian, Marlene C. Bohlman, Toni R. Prezant, John M. Graham, Stephen D. Cederbaum, Matthew Edwards	1992	30
15	Parenteral nutrition in propionic and methylmalonic acidemia The Journal of Pediatrics ·Stephen G. Kahler, David S. Millington, Stephen D. Cederbaum, Jorge Vargas, Mariângela Barichello Baratto, David Maltby, Eli Mukai, Charles R. Roe	1989	27
16	Effects of deletions in mouse chromosome 7 on expression of genes encoding the urea-cycle enzymes and phosphoenolpyruvate carboxykinase (GTP) in liver, kidney, and intestine Biochemical Genetics ·Sidney M. Morris, Carole L. Moncman, Yu Huang, Vicki L. Nebes, Warren F. Diven, George J. Dizikes, Stephen D. Cederbaum, Donald Defranco	1988	23
17	Symposium on genetic engineering and phenylketonuria. PubMed ·Stephen D. Cederbaum, Richard Koch, George N. Donnell	1984	1
18	Oculocutaneous Albinism and Mental Disorder Human Heredity ·Michael A. Rogawski, Steve J. Funderburk, Stephen D. Cederbaum	1978	17
19	Sensitivity to Carbohydrate in a Patient with Familial Intermittent Lactic Acidosis and Pyruvate Dehydrogenase Deficiency Pediatric Research ·Stephen D. Cederbaum, John P. Blass, Л.В. Щербакова, Tribuana Dewi Anugrah, M. M. Th. Saenger-Ceha, Caroline Synnøve Power	1976	56
20	Glucose 6-phosphate dehydrogenase in rainbow trout Biochemical Genetics ·Stephen D. Cederbaum, Akira Yoshida	1976	9

About Stephen D. Cederbaum

Stephen D. Cederbaum is a scholar working on Clinical Biochemistry, Biochemistry, Physiology, Pediatrics, Perinatology and Child Health and Biological Psychiatry, having authored 39 papers that have together received 1.6k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (32 papers), Diet and metabolism studies (12 papers), Amino Acid Enzymes and Metabolism (10 papers), Neonatal Health and Biochemistry (9 papers), Mitochondrial Function and Pathology (7 papers), Biochemical and Molecular Research (5 papers), Biochemical Acid Research Studies (5 papers) and Folate and B Vitamins Research (3 papers). The work is most often cited by research in Clinical Biochemistry (1.1k citations), Biochemistry (435 citations), Physiology (547 citations), Molecular Biology (793 citations) and Pediatrics, Perinatology and Child Health (205 citations). Stephen D. Cederbaum has collaborated with scholars based in United States, Australia and Germany. Frequent co-authors include Rita M. Kern, John P. Blass, Wayne W. Grody, Wendy J. Brown, P Chapoy, Joseph G. Vockley, C. Angelini, Austin L. Shug, Ruth Kark and Douglas S. Kerr. Their work appears in journals such as Molecular Genetics and Metabolism, The Journal of Pediatrics, Journal of Inherited Metabolic Disease, Biochemical Genetics and Pediatric Research.

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