Sarde, Claude-Olivier
Institut de génétique et de biologie moléculaire et cellulaire
7 papers on CoChatORCID 0000-0003-3839-0668
Most cited papers
- Verified
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
Mosser, J., Douar, A.-M., Sarde, C.-O., Kioschis, P., Feil, R., Moser, H., Poustka, A.-M., Mandel, J.-L., & Aubourg, P. (1993) · Nature
Metabolism and Genetic DisordersHereditary Neurological Disorders
Cited by 1,202
- Verified
A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern.
Lombard-Platet, G., Savary, S., Sarde, C. O., Mandel, J. L., & Chimini, G. (1996) · Proceedings of the National Academy of Sciences
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 222
- Verified
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
- Verified
Genomic organization of the adrenoleukodystrophy gene
Sarde, C.-O., Mosser, J., Kioschis, P., Kretz, C., Vicaire, S., Aubourg, P., Poustka, A., & Mandel, J.-L. (1994) · Genomics
Metabolism and Genetic DisordersHereditary Neurological Disorders
Cited by 82
- Verified
Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: A possible hot spot for mutations
Kemp, S., Ligtenberg, M. J. L., Vangeel, B. M., Barth, P. G., Wolterman, R. A., Schoute, F., Sarde, C. O., Mandel, J. L., Vanoost, B. A., & Bolhuis, P. A. (1994) · Biochemical and Biophysical Research Communications
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 75
- Verified
Abnormal messenger RNA expression and a missense mutation in patients with X-linked adrenoleukodystrophy
Cartier, N., Sarde, C.-O., Douar, A.-M., Mosser, J., Mandel, J.-L., & Aubourg, P. (1993) · Human Molecular Genetics
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 55
- Verified
A new human gene (DXS1357E) with ubiquitous expression, located in Xq28 adjacent to the adrenoleukodystrophy gene
Mosser, J., Sarde, C.-O., Vicaire, S., Yates, J. R. W., & Mandel, J.-L. (1994) · Genomics
Muscle Physiology and DisordersGenetics and Neurodevelopmental Disorders
Cited by 27
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free