Peter Bross

9.1k citations

150 papers · 6.4k indexed · h-index 46

Impact in

Clinical Biochemistry top 0.05%
- Metabolism and Genetic Disorders
Aging top 2%

Papers in ⓘ

Clinical Biochemistry 62
- Metabolism and Genetic Disorders 62
Aging 6

Co-authors: Niels Gregersen (67 shared papers)Brage Storstein Andresen (42 shared papers)Thomas J. Corydon (32 shared papers)Lars Bolund (37 shared papers)Rikke Katrine Jentoft Olsen (13 shared papers)Jane Christensen (10 shared papers)Johan Palmfeldt (27 shared papers)Jakob Hansen (17 shared papers)
Journals: Journal of Biological Chemistry (8 papers)Journal of Inherited Metabolic Disease (8 papers)Human Mutation (7 papers)The American Journal of Human Genetics (6 papers)Molecular Genetics and Metabolism (5 papers)
Partner nations: Denmark United States Germany

In The Last Decade

Peter Bross

148 papers receiving 6.3k citations

Peers

Countries citing papers authored by Peter Bross

Since Specialization

Citations

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

Fields of papers citing papers by Peter Bross

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter Bross. 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 Peter Bross. The network helps show where Peter Bross may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 150 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	α-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy Journal of Clinical Investigation ·Jens Mogensen, Ib Christian Klausen, Anders Kirstein Pedersen, Henrik Egeblad, Peter Bross, Torben A. Kruse, Niels Gregersen, Peter S. Hansen, Ulrik Baandrup, Anders D. Børglum	1999	284
2	Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60 The American Journal of Human Genetics ·Jens Jacob Hansen, Alexandra Dürr, Isabelle Cournu‐Rebeix, Costa Georgopoulos, Debbie Ang, Marit N. Nielsen, Claire‐Sophie Davoine, Alexis Brice, Bertrand Fontaine, Niels Gregersen, Peter Bross	2002	266
3	Protein Misfolding and Human Disease Annual Review of Genomics and Human Genetics ·Niels Gregersen, Peter Bross, Søren Vang, Jane Christensen	2006	234
4	Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency The American Journal of Human Genetics ·Brage Storstein Andresen, S. E. Olpin, Ben J. H. M. Poorthuis, H.R. Scholte, Christine Vianey‐Saban, Ronald Wanders, Lodewijk IJlst, Andrew A.M. Morris, Morteza Pourfarzam, K. Bartlett, E. R. Baumgartner, Johannis B.C. deKlerk, Lisbeth Dahl Schroeder, Thomas J. Corydon, Hans Lund, Vibeke Winter, Peter Bross, Lars Bolund, Niels Gregersen	1999	233
5	Protein misfolding and degradation in genetic diseases Human Mutation ·Peter Bross, Thomas J. Corydon, Brage Storstein Andresen, Malene M. J�rgensen, Lars Bolund, Niels Gregersen	1999	189
6	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* The American Journal of Human Genetics ·Brage Storstein Andresen, Steve F. Dobrowolski, Linda P. O’Reilly, Joseph Muenzer, Shawn E. McCandless, Dianne M. Frazier, Szabolcs Udvari, Peter Bross, Inga Knudsen, Rick Banas, Donald H. Chace, Paul C. Engel, Edwin W. Naylor, Niels Gregersen	2001	180
7	Clear relationship betweenETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency Human Mutation ·Rikke Katrine Jentoft Olsen, Brage Storstein Andresen, Ernst Christensen, Peter Bross, Flemming Skovby, Niels Gregersen	2003	174
8	Mitochondrial Hsp60 Chaperonopathy Causes an Autosomal-Recessive Neurodegenerative Disorder Linked to Brain Hypomyelination and Leukodystrophy The American Journal of Human Genetics ·Daniella Magen, Costa Georgopoulos, Peter Bross, Debbie Ang, Yardena Segev, Dorit Goldsher, Alexandra Nemirovski, Eli Shahar, Sarit Ravid, Anthony Luder, Bayan Heno, Ruth Gershoni‐Baruch, Karl Skorecki, Hanna Mandel	2008	159
9	Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship Human Mutation ·Niels Gregersen, Brage Storstein Andresen, Morten J. Corydon, Thomas J. Corydon, Rikke Katrine Jentoft Olsen, Lars Bolund, Peter Bross	2001	148
10	Protein Misfolding and Cellular Stress: An Overview Methods in molecular biology ·Niels Gregersen, Peter Bross	2010	119
11	Riboflavin Deficiency—Implications for General Human Health and Inborn Errors of Metabolism International Journal of Molecular Sciences ·Signe Mosegaard, Graziana Dipace, Peter Bross, Jasper Carlsen, Niels Gregersen, Rikke Katrine Jentoft Olsen	2020	117
12	Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter Human Genetics ·Jens Hansen, Peter Bross, Majken Westergaard, Marit Nielsen, Hans Eiberg, Anders D. Børglum, Jens Mogensen, Karsten Kristiansen, Lars Bolund, Niels Gregersen	2003	109
13	Mitochondrial fatty acid oxidation defects—remaining challenges Journal of Inherited Metabolic Disease ·Niels Gregersen, Brage Storstein Andresen, Christina B. Pedersen, Rikke Katrine Jentoft Olsen, Thomas J. Corydon, Peter Bross	2008	106
14	The Molecular Basis of Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Compound Heterozygous Patients: Is There Correlation between Genotype and Phenotype? Human Molecular Genetics ·Brage Storstein Andresen, Peter Bross, Szabolcs Udvari, J M Kirk, Glenda Gray, Stanislav Kmoch, N. Chamoles, Inga Knudsen, Vibeke Winter, Bridget Wilcken, Ichiro Yokota, K Hart, Seymour Packman, J P Harpey, Jean Marie Saudubray, Daniel E. Hale, Lars Bolund, Steen Kølvraa, Niels Gregersen	1997	105
15	Dissection of functional domains in phage fd adsorption protein Journal of Molecular Biology ·Irina Stengele, Peter Bross, Xaver Garces, Jeanette Giray, Ihab Rasched	1990	103
16	Influence of Lewis α1-3/4-L-Fucosyltransferase (FUT3) Gene Mutations on Enzyme Activity, Erythrocyte Phenotyping, and Circulating Tumor Marker Sialyl-Lewis a Levels Journal of Biological Chemistry ·Torben F. Ørntoft, Else Marie Vestergaard, Eric H. Holmes, Jørn Sinkbæk Jakobsen, Niels Grunnet, Mette Tapdrup Mortensen, Philip H. Johnson, Peter Bross, Niels Gregersen, Karna Skorstengaard, Uffe Birk Jensen, Lars Bolund, Hans Wolf	1996	102
17	Protein Misfolding and Disease Humana Press eBooks ·Peter Bross, Niels Gregersen	2003	101
18	Leptin regulation of Hsp60 impacts hypothalamic insulin signaling Journal of Clinical Investigation ·André Kleinridders, Hans P.M.M. Lauritzen, Siegfried Ussar, Jane Christensen, Marcelo A. Mori, Peter Bross, C. Ronald Kahn	2013	99
19	Ethylmalonic Aciduria Is Associated with an Amino Acid Variant of Short Chain Acyl-Coenzyme A Dehydrogenase Pediatric Research ·Morten J. Corydon, N. Gregersen, W. Lehnert, Antònia Ribes, Piero Rinaldo, Stanislav Kmoch, E. Christensen, Thomas J. Kristensen, Brage Storstein Andresen, Peter Bross, Vibeke Winter, G Martı́nez, Søren Neve, Thomas G. Jensen, Lars Bolund, Steen Kølvraa	1996	82
20	Effects of Two Mutations Detected in Medium Chain Acyl-CoA Dehydrogenase (MCAD)-deficient Patients on Folding, Oligomer Assembly, and Stability of MCAD Enzyme Journal of Biological Chemistry ·Peter Bross, Charlotte Jespersen, Thomas G. Jensen, Brage Storstein Andresen, Morten Juhl Kristensen, Vibeke Winter, Andreas Nandy, Franz Kräutle, Sandro Ghisla, Lars Bolund, Jung‐Ja P. Kim, Niels Gregersen	1995	75

About Peter Bross

Peter Bross is a scholar working on Clinical Biochemistry, Aging, Molecular Biology, Cell Biology and Biochemistry, having authored 150 papers that have together received 6.4k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (62 papers), Mitochondrial Function and Pathology (44 papers), Heat shock proteins research (34 papers), Biochemical and Molecular Research (33 papers), Endoplasmic Reticulum Stress and Disease (21 papers), Peroxisome Proliferator-Activated Receptors (16 papers), Metabolomics and Mass Spectrometry Studies (10 papers) and Enzyme Structure and Function (10 papers). The work is most often cited by research in Clinical Biochemistry (2.3k citations), Aging (141 citations), Molecular Biology (4.7k citations), Cell Biology (855 citations) and Biochemistry (262 citations). Peter Bross has collaborated with scholars based in Denmark, United States and Germany. Frequent co-authors include Niels Gregersen, Brage Storstein Andresen, Thomas J. Corydon, Lars Bolund, Rikke Katrine Jentoft Olsen, Jane Christensen, Johan Palmfeldt, Jakob Hansen, Søren Vang and Vibeke Winter. Their work appears in journals such as Journal of Biological Chemistry, Journal of Inherited Metabolic Disease, Human Mutation, The American Journal of Human Genetics and Molecular Genetics and Metabolism.

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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