Arnold W. Strauss

13.4k citations

220 papers · 10.5k indexed · h-index 58

Impact in

Clinical Biochemistry top 0.02%
- Metabolism and Genetic Disorders
Molecular Biology top 0.5%
- Mitochondrial Function and Pathology
- Peroxisome Proliferator-Activated Receptors

Papers in

Clinical Biochemistry 95
- Metabolism and Genetic Disorders 95
Molecular Biology 143
- Mitochondrial Function and Pathology 55
- Peroxisome Proliferator-Activated Receptors 31
- Biochemical and Molecular Research 25

Co-authors: Jeffrey I. Gordon Harold F. Sims Daniel P. Kelly Piero Rinaldo Zaza Khuchua Michael J. Bennett David Alpers Jamal A. Ibdah
Journals: Journal of Biological Chemistry (40 papers)Proceedings of the National Academy of Sciences (14 papers)The Journal of Pediatrics (13 papers)Journal of Inherited Metabolic Disease (11 papers)Pediatric Research (10 papers)
Partner nations: United States Germany Netherlands

In The Last Decade

Arnold W. Strauss

218 papers receiving 10.1k citations

Peers

Countries citing papers authored by Arnold W. Strauss

Since Specialization

Citations

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

Fields of papers citing papers by Arnold W. Strauss

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	The PPAR pan-agonist bezafibrate ameliorates cardiomyopathy in a mouse model of Barth syndrome Orphanet Journal of Rare Diseases ·Yan Huang, Corey Powers, Victoria Moore, Caitlin Schafer, Mindong Ren, Colin K. L. Phoon, Jeanne James, Alexander V. Glukhov, Sabzali Javadov, Frédéric M. Vaz, John L. Jefferies, Arnold W. Strauss, Zaza Khuchua	2017	42
2	Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein Muscle & Nerve ·Ute Spiekerkoetter, Michael J. Bennett, Bruria Ben‐Zeev, Arnold W. Strauss, Ingrid Tein	2003	48
3	Inborn Errors of Mitochondrial Fatty Acid Oxidation Critical Reviews in Clinical Laboratory Sciences ·Malcolm J. Bennett, Piero Rinaldo, Arnold W. Strauss	2000	87
4	Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications Seminars in Perinatology ·Arnold W. Strauss, Malcolm J. Bennett, Piero Rinaldo, Harold F. Sims, Laurie K. O'Brien, Yiwen Zhao, Beverly Gibson, Jamal A. Ibdah	1999	60
5	Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: Identification of a novel mutation The Journal of Pediatrics ·Sihoun Hahn, Eunha Lee, Jo Won Jung, Chang-Ho Hong, Hye‐Ran Yoon, Piero Rinaldo, Harold F. Sims, Beverly Gibson, Arnold W. Strauss	1999	4
6	The Molecular Basis of Congenital Cardiac Disease Seminars in Thoracic and Cardiovascular Surgery Pediatric Cardiac Surgery Annual ·Arnold W. Strauss	1998	7
7	Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlation. Journal of Clinical Investigation ·Jamal A. Ibdah, Ingrid Tein, Carlo Dionisi‐Vici, Malcolm J. Bennett, Lodewijk IJlst, B Gibson, Ronald J. A. Wanders, Arnold W. Strauss	1998	57
8	Characterization of Human and Pig Kidney Long‐Chain‐Acyl‐CoA Dehydrogenases and their Role in β‐Oxidation European Journal of Biochemistry ·Michael Eder, Franz Kräutle, Dong Yü, Petra Vock, Volker Kieweg, Jung‐Ja P. Kim, Arnold W. Strauss, Sandro Ghisla	1997	15
9	Deletion Within Chromosome 22 is Common in Patients With Absent Pulmonary Valve Syndrome The American Journal of Cardiology ·Mark C. Johnson, Arnold W. Strauss, S. Bruce Dowton, Thomas L. Spray, Charles B. Huddleston, Mary K. Wood, Rachel Slaugh, Michael S. Watson	1995	51
10	Anomalous origin of the right pulmonary artery from the aorta and CATCH 22 syndrome The Annals of Thoracic Surgery ·Mark C. Johnson, Michael S. Watson, Arnold W. Strauss, Thomas L. Spray	1995	16
11	Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency. Journal of Clinical Investigation ·J C Brackett, Harold F. Sims, Piero Rinaldo, Scott Shapiro, C K Powell, Malcolm J. Bennett, Arnold W. Strauss	1995	84
12	Inherited Cardiomyopathies New England Journal of Medicine ·Franklin H. Epstein, Daniel P. Kelly, Arnold W. Strauss	1994	213
13	A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death. Journal of Clinical Investigation ·J C Brackett, Harold F. Sims, Robert D. Steiner, M Nunge, E M Zimmerman, B deMartinville, Piero Rinaldo, Rachel Slaugh, Arnold W. Strauss	1994	36
14	Expression and Characterization of Human Mutant (Glutamic Acid304) Medium-Chain Acyl-Coenzyme A Dehydrogenase in Mammalian Cells Pediatric Research ·Alison Whelan, Arnold W. Strauss, Daniel E Male, Nancy J. Mendelsohn, Daniel P. Kelly	1993	7
15	Complete repair of total anomalous pulmonary venous connection in infancy Journal of Thoracic and Cardiovascular Surgery ·Bradley D. Raisher, James W. Grant, Thomas Martin, Arnold W. Strauss, Thomas L. Spray	1992	32
16	Expression of a Nagao-type, phosphatidylinositol-glycan anchored alkaline phosphatase in human choriocarcinomas. PubMed ·Mark E. Lowe, Arnold W. Strauss	1990	12
17	Cleavage of the PO glycoprotein of the rat peripheral nerve myelin: Tentative identification of cleavage site and evidence for the precursor-product relationship Neurochemical Research ·Harish C. Agrawal, Daya Agrawal, Arnold W. Strauss	1990	16
18	Characterization of MB creatine kinase isoform conversion in vitro and in vivo in dogs. Journal of Clinical Investigation ·Joseph J. Billadello, Héctor L. Fontanet, Arnold W. Strauss, Dana R. Abendschein	1989	19
19	Isolation and sequencing of a complementary deoxyribonucleic acid clone encoding human placental 173-estradiol dehydrogenase: Identification of the putative cofactor binding site American Journal of Obstetrics and Gynecology ·Michael J. Gast, Harold F. Sims, Gary L. Murdock, Peter M. Gast, Arnold W. Strauss	1989	40
20	Idiopathic paroxysmal ventricular tachycardia in infants and children The Journal of Pediatrics ·Antonio Hernandez, Arnold W. Strauss, Robert E. Kleiger, David Goldring	1975	29

About Arnold W. Strauss

Arnold W. Strauss is a scholar working on Clinical Biochemistry, Molecular Biology, Cell Biology, Cardiology and Cardiovascular Medicine and Biochemistry, having authored 220 papers that have together received 10.5k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (95 papers), Mitochondrial Function and Pathology (55 papers), Peroxisome Proliferator-Activated Receptors (31 papers), Biochemical and Molecular Research (25 papers), Diet and metabolism studies (18 papers), Muscle metabolism and nutrition (16 papers), Congenital Heart Disease Studies (15 papers) and Cardiomyopathy and Myosin Studies (13 papers). The work is most often cited by research in Clinical Biochemistry (3.4k citations), Molecular Biology (6.4k citations), Biochemistry (511 citations), Cardiology and Cardiovascular Medicine (1.5k citations) and Physiology (1.6k citations). Arnold W. Strauss has collaborated with scholars based in United States, Germany and Netherlands. Frequent co-authors include Jeffrey I. Gordon, Harold F. Sims, Daniel P. Kelly, Piero Rinaldo, Zaza Khuchua, Michael J. Bennett, David Alpers, Jamal A. Ibdah, Malcolm J. Bennett and R. Mark Payne. Their work appears in journals such as Journal of Biological Chemistry, Proceedings of the National Academy of Sciences, The Journal of Pediatrics, Journal of Inherited Metabolic Disease and Pediatric Research.

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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