John J. Mitchell

7.4k citations

134 papers · 4.2k · 1 hit paper · h-index 34

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Physiology top 2%
- Lysosomal Storage Disorders Research
- Diet and metabolism studies

Papers in

Physiology 36
- Lysosomal Storage Disorders Research 27
Molecular Biology 31
- Mitochondrial Function and Pathology 6

Co-authors: Janet Woodcock‐Mitchell (22 shared papers)Robert B. Low (15 shared papers)Charles R. Scriver (2 shared papers)Yannis Trakadis (5 shared papers)Xiao‐Jian Sun (2 shared papers)Kevin O. Leslie (7 shared papers)Barbara K. Burton (17 shared papers)Nancy Braverman (2 shared papers)
Journals: Molecular Genetics and Metabolism (21 papers)American Journal of Respiratory Cell and Molecular Biology (6 papers)Journal of Inherited Metabolic Disease (4 papers)Genetics in Medicine (3 papers)Orphanet Journal of Rare Diseases (3 papers)
Partner nations: United States Canada United Kingdom

In The Last Decade

John J. Mitchell

130 papers receiving 4.1k citations

John J. Mitchell's Hit Papers

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Phenylalanine hydroxylase deficiency: diagnosis and management guideline 2014 · 478 citations

Peers

Countries citing papers authored by John J. Mitchell

Since Specialization

Citations

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

Fields of papers citing papers by John J. Mitchell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John J. Mitchell. 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 John J. Mitchell. The network helps show where John J. Mitchell may publish in the future.

Co-authors

The 25 scholars most cited alongside John J. Mitchell, 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 John J. Mitchell Line = papers co-authored together John J. Mitchell 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 134 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Phenylalanine hydroxylase deficiency: diagnosis and management guideline Genetics in Medicine ·Jerry Vockley, Hans C. Andersson, Kevin M. Antshel, Nancy Braverman, Barbara K. Burton, Dianne M. Frazier, John J. Mitchell, Wendy E. Smith, Barry H. Thompson, Susan A. Berry Hit paper breakdown →	2014	478
2	Phenylalanine hydroxylase deficiency Genetics in Medicine ·John J. Mitchell, Yannis Trakadis, Charles R. Scriver	2011	374
3	Insulin-induced insulin receptor substrate-1 degradation is mediated by the proteasome degradation pathway. Diabetes ·Xiao‐Jian Sun, Jonathan Goldberg, Li‐Ya Qiao, John J. Mitchell	1999	191
4	Molecular Mechanism of Insulin-Induced Degradation of Insulin Receptor Substrate 1 Molecular and Cellular Biology ·Rachel Zhande, John J. Mitchell, Jiong Wu, Xiao‐Jian Sun	2002	175
5	α-Smooth muscle actin is transiently expressed in embryonic rat cardiac and skeletal muscles Differentiation ·Janet Woodcock‐Mitchell, John J. Mitchell, Robert B. Low, M Kieny, Philippe Sengel, Laura Rubbia, Omar Skalli, Brian R. Jackson, Giulio Gabbiani	1988	172
6	Twenty-year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia disease carriers in high schools. PubMed ·John J. Mitchell, A Capua, C Clow, C. R. Scriver	1996	122
7	The Morquio A Clinical Assessment Program: Baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects Molecular Genetics and Metabolism ·Paul Harmatz, Eugen Mengel, Roberto Giugliani, Vassili Valayannopoulos, Shuan-Pei Lin, Rossella Parini, Nathalie Guffon, Barbara K. Burton, Christian J. Hendriksz, John J. Mitchell, Ana María Martins, Simon Jones, Norberto Guelbert, Ashok Vellodi, Carla E. M. Hollak, Peter Slasor, Celeste Decker	2013	113
8	Identification of PEX7 as the Second Gene Involved in Refsum Disease The American Journal of Human Genetics ·Daan M. van den Brink, Pedro Brites, Janet Haasjes, Anthony S. Wierzbicki, John J. Mitchell, Michelle Lambert-Hamill, Jacqueline de Belleroche, Gerbert A. Jansen, Hans R. Waterham, Jennifer Wanders	2003	112
9	Smooth Muscle Cell Markers in Developing Rat Lung American Journal of Respiratory Cell and Molecular Biology ·John J. Mitchell, Susan E. Reynolds, Kevin O. Leslie, Robert B. Low, Janet Woodcock‐Mitchell	1990	94
10	Alpha-smooth muscle actin in parenchymal cells of bleomycin-injured rat lung. PubMed ·John J. Mitchell, Janet Woodcock‐Mitchell, Susan Reynolds, R Low, K Leslie, K B Adler, Giulio Gabbiani, Omar Skalli	1989	91
11	TNF-α and insulin, alone and synergistically, induce plasminogen activator inhibitor-1 expression in adipocytes American Journal of Physiology-Cell Physiology ·Tomohiro Sakamoto, Janet Woodcock‐Mitchell, Kousuke Marutsuka, John J. Mitchell, Burton E. Sobel, Satoshi Fujii	1999	87
12	Contractile Cells in Normal and Fibrotic Lung Humana Press eBooks ·Kenneth B. Adler, Robert B. Low, Kevin O. Leslie, John J. Mitchell, John N. Evans	1990	87
13	Neonatal diabetes, with hypoplastic pancreas, intestinal atresia and gall bladder hypoplasia: search for the aetiology of a new autosomal recessive syndrome Diabetologia ·John J. Mitchell, Zubin Punthakee, Bernard Lo, C. Bernard, Karen Chong, Catherine E. Newman, Lola Cartier, Valérie Désilets, E. Cutz, Inger Lise Skog Hansen, P Riley, Constantin Polychronakos	2004	82
14	Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B Human Mutation ·Gladys Ho, Atsushi Yonezawa, Satohiro Masuda, Ken‐ichi Inui, Keow Giak Sim, Kevin Carpenter, Rikke Katrine Jentoft Olsen, John J. Mitchell, William J. Rhead, Gregory B. Peters, John Christodoulou	2010	79
15	Alpha smooth muscle actin expression in developing and adult human lung Differentiation ·Kevin O. Leslie, John J. Mitchell, Janet Woodcock‐Mitchell, Robert B. Low	1990	78
16	Induction of Plasminogen Activator Inhibitor Type 1 and Type 1 Collagen Expression in Rat Cardiac Microvascular Endothelial Cells by Interleukin-1 and Its Dependence on Oxygen-Centered Free Radicals Circulation ·Hitoshi Okada, Janet Woodcock‐Mitchell, John J. Mitchell, Tomohiro Sakamoto, Kousuke Marutsuka, Burton E. Sobel, Satoshi Fujii	1998	74
17	Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation Sequencing Journal of Molecular Diagnostics ·Lan Qin, Jing Wang, Tian Xia, Hui Yu, Cavatina K. Truong, John J. Mitchell, Klaas J. Wierenga, William J. Craigen, Victor Wei Zhang, Lee‐Jun C. Wong	2016	67
18	UPLC-MS/MS detection of disaccharides derived from glycosaminoglycans as biomarkers of mucopolysaccharidoses Analytica Chimica Acta ·Christiane Auray‐Blais, Paméla Lavoie, Shunji Tomatsu, Vassili Valayannopoulos, John J. Mitchell, Julian Raiman, Maxime Beaudoin, Bruno Maranda, Joe T.R. Clarke	2016	54
19	Cyclic Mechanical Deformation Stimulates Human Lung Fibroblast Proliferation and Autocrine Growth Factor Activity American Journal of Respiratory Cell and Molecular Biology ·Jill E. Bishop, John J. Mitchell, P. Marlene Absher, Linda Baldor, Henry Geller, Janet Woodcock‐Mitchell, Michael J. Hamblin, Pamela Vacek, Robert B. Low	1993	53
20	What young people think and do when the option for cystic fibrosis carrier testing is available. Journal of Medical Genetics ·John J. Mitchell, C. R. Scriver, C Clow, Feige Kaplan	1993	52

About John J. Mitchell

John J. Mitchell is a scholar working on Physiology, Molecular Biology, Rheumatology, Genetics and Epidemiology, having authored 134 papers that have together received 4.2k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (27 papers), Glycogen Storage Diseases and Myoclonus (15 papers), Metabolism and Genetic Disorders (12 papers), Trypanosoma species research and implications (9 papers), Mitochondrial Function and Pathology (6 papers), Skin and Cellular Biology Research (6 papers), Folate and B Vitamins Research (5 papers) and Genomics and Rare Diseases (5 papers). The work is most often cited by research in Clinical Biochemistry (1.0k citations), Physiology (993 citations), Rheumatology (441 citations), Molecular Biology (1.5k citations) and Pulmonary and Respiratory Medicine (601 citations). John J. Mitchell has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Janet Woodcock‐Mitchell, Robert B. Low, Charles R. Scriver, Yannis Trakadis, Xiao‐Jian Sun, Kevin O. Leslie, Barbara K. Burton, Nancy Braverman, Jerry Vockley and Barry H. Thompson. Their work appears in journals such as Molecular Genetics and Metabolism, American Journal of Respiratory Cell and Molecular Biology, Journal of Inherited Metabolic Disease, Genetics in Medicine and Orphanet Journal of Rare Diseases.

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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