Clayton, Peter T.

Mutations in the gene encoding peroxisomal α-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy

Ferdinandusse, S., Denis, S., Clayton, P. T., Graham, A., Rees, J. E., Allen, J. T., McLean, B. N., Brown, A. Y., Vreken, P., Waterham, H. R., et al. (2000) · Nature Genetics

Hereditary Neurological DisordersMetabolism and Genetic Disorders

Cited by 262

Host-microbe co-metabolism dictates cancer drug efficacy in C. elegans

Scott, T. A., Quintaneiro, L. M., Norvaisas, P., Lui, P. P., Wilson, M. P., Leung, K.-Y., Herrera-Dominguez, L., Sudiwala, S., Pessia, A., Clayton, P. T., et al. (2017) · Cell

Gut microbiota and healthPharmacogenetics and Drug Metabolism

Cited by 254

Hereditary Tyrosinemia Type I: A New Clinical Classification With Difference in Prognosis on Dietary Treatment

Van Spronsen, F. J., Thomasse, Y., Smit, P. G. A., Leonard, J. V., Clayton, P. T., Fidler, V., Berger, R., & Heymans, H. S. A. (1994) · Hepatology

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 193

Peroxisomal d -hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

van Grunsven, E. G., van Berkel, E., Ijlst, L., Vreken, P., de Klerk, J. B. C., Adamski, J., Lemonde, H., Clayton, P. T., Cuebas, D. A., & Wanders, R. J. A. (1998) · Proceedings of the National Academy of Sciences

Metabolism and Genetic DisordersNeurological diseases and metabolism

Cited by 152

Mutations in SRD5B1 ( AKR1D1 ), the gene encoding Δ 4 -3-oxosteroid 5β-reductase, in hepatitis and liver failure in infancy

Lemonde, H. A., Custard, E. J., Bouquet, J., Duran, M., Overmars, H., Scambler, P. J., & Clayton, P. T. (2003) · Gut

Pediatric Hepatobiliary Diseases and TreatmentsMetabolism and Genetic Disorders

Cited by 125

Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene

Ebberink, M. S., Csanyi, B., Chong, W. K., Denis, S., Sharp, P., Mooijer, P. A. W., Dekker, C. J. M., Spooner, C., Ngu, L. H., De Sousa, C., et al. (2010) · Journal of Medical Genetics

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 94

Human Δ4-3-oxosteroid 5β-reductase (AKR1D1) deficiency and steroid metabolism

Palermo, M., Marazzi, M. G., Hughes, B. A., Stewart, P. M., Clayton, P. T., & Shackleton, C. H. L. (2008) · Steroids

Adrenal Hormones and DisordersSteroid Chemistry and Biochemistry

Cited by 55