Watkins, Paul A.

Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening

Bezman, L., Moser, A. B., Raymond, G. V., Rinaldo, P., Watkins, P. A., Smith, K. D., Kass, N. E., & Moser, H. W. (2001) · Annals of Neurology

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 324

A mouse model for X-linked adrenoleukodystrophy

Lu, J.-F., Lawler, A. M., Watkins, P. A., Powers, J. M., Moser, A. B., Moser, H. W., & Smith, K. D. (1997) · Proceedings of the National Academy of Sciences

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 293

Gene redundancy and pharmacological gene therapy: Implications for X-linked adrenoleukodystrophy

Kemp, S., Wei, H.-M., Lu, J.-F., Braiterman, L. T., McGuinness, M. C., Moser, A. B., Watkins, P. A., & Smith, K. D. (1998) · Nature Medicine

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 249

Insulin Control of Glucose Metabolism in Man

Insel, P. A., Liljenquist, J. E., Tobin, J. D., Sherwin, R. S., Watkins, P., Andres, R., & Berman, M. (1975) · Journal of Clinical Investigation

Pancreatic function and diabetesDiabetes Management and Research

Cited by 244

X-linked adrenoleukodystrophy: Genes, mutations, and phenotypes

Smith, K. D., Kemp, S., Braiterman, L. T., Lu, J.-F., Wei, H.-M., Geraghty, M., Stetten, G., Bergin, J. S., Pevsner, J., & Watkins, P. A. (1999) · Neurochemical Research

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 190

Loss-or gain-of-function mutations in ACOX1 cause axonal loss via different mechanisms

Chung, H.-L., Wangler, M. F., Marcogliese, P. C., Jo, J., Ravenscroft, T. A., Zuo, Z., Duraine, L., Sadeghzadeh, S., Li-Kroeger, D., Schmidt, R. E., et al. (2020) · Neuron

Hereditary Neurological DisordersMetabolism and Genetic Disorders

Cited by 154

Role of ALDP (ABCD1) and Mitochondria in X-Linked Adrenoleukodystrophy

McGuinness, M. C., Lu, J.-F., Zhang, H.-P., Dong, G.-X., Heinzer, A. K., Watkins, P. A., Powers, J., & Smith, K. D. (2003) · Molecular and Cellular Biology

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 147

Biochemical abnormalities in rhizomelic chondrodysplasia punctata

Hoefler, G., Hoefler, S., Watkins, P. A., Chen, W. W., Moser, A., Baldwin, V., McGillivary, B., Charrow, J., Friedman, J. M., Rutledge, L., et al. (1988) · The Journal of Pediatrics

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 133

PXA1, a possible Saccharomyces cerevisiae ortholog of the human adrenoleukodystrophy gene.

Shani, N., Watkins, P. A., & Valle, D. (1995) · Proceedings of the National Academy of Sciences

Metabolism and Genetic DisordersLipid metabolism and biosynthesis

Cited by 129

Mutational analysis of patients with X-linked adrenoleukodystrophy

Kok, F., Neumann, S., Sarde, C.-O., Zheng, S., Wu, K.-H., Wei, H.-M., Bergin, J., Watkins, P. A., Gould, S., Sack, G., et al. (1995) · Human Mutation

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 103

Peroxisomal fatty acid β-oxidation in HepG2 cells

Watkins, P. A., Ferrell, E. V., Pedersen, J. I., & Hoefler, G. (1991) · Archives of Biochemistry and Biophysics

Metabolism and Genetic DisordersLipid metabolism and biosynthesis

Cited by 86

Contiguous deletion of the X‐linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders

Corzo, D., Gibson, W., Johnson, K., Mitchell, G., LePage, G., Cox, G. F., Casey, R., Zeiss, C., Tyson, H., Cutting, G. R., et al. (2002) · The American Journal of Human Genetics

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 85

Bromocriptine Administration Reduces Hyperphagia and Adiposity and Differentially Affects Dopamine D2 Receptor and Transporter Binding in Leptin-Receptor-Deficient Zucker Rats and Rats with Diet-Induced Obesity

Davis, L. M., Michaelides, M., Cheskin, L. J., Moran, T. H., Aja, S., Watkins, P. A., Pei, Z., Contoreggi, C., McCullough, K., Hope, B., et al. (2009) · Neuroendocrinology

Regulation of Appetite and ObesityNeurotransmitter Receptor Influence on Behavior

Cited by 82

The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder

Hiebler, S., Masuda, T., Hacia, J. G., Moser, A. B., Faust, P. L., Liu, A., Chowdhury, N., Huang, N., Lauer, A., Bennett, J., et al. (2014) · Molecular Genetics and Metabolism

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 60

X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism

Wang, Y., Busin, R., Reeves, C., Bezman, L., Raymond, G., Toomer, C. J., Watkins, P. A., Snowden, A., Moser, A., Naidu, S., et al. (2011) · Molecular Genetics and Metabolism

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 58

Cerebral X‐linked adrenoleukodystrophy in a girl with Xq27‐Ter deletion

Hershkovitz, E., Narkis, G., Shorer, Z., Moser, A. B., Watkins, P. A., Moser, H. W., & Manor, E. (2002) · Annals of Neurology

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 30

Adrenoleukodystrophy: biochemical procedures in diagnosis, prevention and treatment

Watkins, P. A., Naidu, S., & Moser, H. W. (1987) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersGenetic and rare skin diseases.

Cited by 20

Expression of ALDP Is Altered in X‐linked Adrenoleukodystrophy

WATKINS, P. A., GOULD, S. J., SMITH, M. A., BRAITERMAN, L. T., WEI, H., KOK, F., MOSER, A. B., MOSER, H. W., & SMITH, K. D. (1996) · Annals of the New York Academy of Sciences

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 1