J. Laycock

A liquid chromatographic-electrospray ionization-tandem mass spectrometric method for determination of buprenorphine, its metabolite, norbuprenorphine, and a coformulant, naloxone, that is suitable for in vivo and in vitro metabolism studies.

E. Strain, R. Foltz, M. Slawson, 2002, Analytical biochemistry.

A high-performance liquid chromatographic-atmospheric pressure chemical ionization-tandem mass spectrometric method for determination of risperidone and 9-hydroxyrisperidone in human plasma.

R. Foltz, D. Moody, Wei Huang, 2004, Journal of analytical toxicology.

Electron ionization mass spectrometric analysis of 5‐nitro octaethylprophyrin: evidence for scission of the porphyrin macrocycle

R. Ocampo, H. Callot, R. Yost, 1997 .

Determination of buprenorphine in human plasma by gas chromatography-positive ion chemical ionization mass spectrometry and liquid chromatography-tandem mass spectrometry.

D J Crouch, R L Foltz, W K Bickel, 1997, Journal of analytical toxicology.

Evidence supporting the formation of 2,3-epoxy-3-methylindoline: a reactive intermediate of the pneumotoxin 3-methylindole.

G. Yost, G. Skiles, D. L. Lanza, 1998, Chemical research in toxicology.

Quantitative Small Molecule Bioanalysis Using Chip-Based NanoESI-MS/MS

Lei Zhang, J. Laycock, K. J. Miller, 2004 .

Automating bioanalytical sample analysis through enhanced system integration.

Mark Ma, Judy Y Shih, Vimal Patel, 2013, Bioanalysis.

Thioether adducts of a new imine reactive intermediate of the pneumotoxin 3-methylindole.

K. Skordos, J. Laycock, Garold S. Yost, 1998, Chemical research in toxicology.