Get started
Author

J. F. Mattéi

Observed names: J F Mattei, J F Matteï, J F Mattéi, J. -F. Mattei, J. F. MATTEI, J. F. Mattei, J.-F. Mattei, J.-F. Mattéi, J.-Fr. Mattei, J.F Mattei, J.F. Mattei, J.F. Mattéi, J.Francois Mattei, J.‐F. Mattei, JF Mattei, JF Mattéï, Mattei Jf, Mattei, J.F., Mattéi Jf
Observed institutions: Centre National de la Recherche Scientifique, Inserm, Aix-Marseille Université, Académie Nationale de Médecine, Laboratoire de Biochimie, Centre d’Immunologie de Marseille-Luminy, Centre Hospitalier Universitaire de Saint-Étienne, Hôpital de la Timone, Centre de Génétique Médicale de Marseille, Académie des Sciences Morales et Politiques, Anthropologie Bio-Culturelle, Droit, Éthique & Santé
OpenAlex ID: A5113578550
DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome
1985 · M. G. Mattei, N. Philip, et al. · Human Genetics · 309
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.
1989 · Z Rahmani, J L Blouin, et al. · Proceedings of the National Academy of Sciences · 264
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male
1983 · G. Camerino, M. G. Mattei, et al. · Nature · 165
X-Autosome translocations: Cytogenetic characteristics and their consequences
1982 · M.G. Mattei, J.F. Mattei, et al. · Human Genetics · 155
The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice
1986 · A. Dautigny, M.-G. Mattei, et al. · Nature · 154
Constitutional chromosomal breakage
1976 · F. Giraud, S. Ayme, et al. · Human Genetics · 149
Guidelines for Human Gene Nomenclature
2008 · Jean Frézal, P.J. McAlpine, et al. · Cytogenetics and Cell Genetics · 134
Localization of the human NCAM gene to band q23 of chromosome 11: the third gene coding for a cell interaction molecule mapped to the distal portion of the long arm of chromosome 11.
1986 · C Nguyen, M G Mattei, et al. · The Journal of Cell Biology · 127
Mapping of the human retinoic acid receptor to the q21 band of chromosome 17
1988 · M. -G. Mattei, M. Petkovich, et al. · Human Genetics · 112
Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis
1984 · M. G. Mattei, N. Souiah, et al. · Human Genetics · 95
Prader-Willi syndrome and chromosome 15
1983 · J. F. Mattei, M. G. Mattei, et al. · Human Genetics · 87
Structural anomalies of the X chromosome and inactivation center
1981 · M. G. Mattei, J. F. Mattei, et al. · Human Genetics · 82
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approach
1981 · M. G. Mattei, J. F. Mattei, et al. · Human Genetics · 82
X-linked mental retardation with the fragile X. A study of 15 families
1981 · J. F. Mattei, M. G. Mattei, et al. · Human Genetics · 76
The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome
1986 · M. G. Mattei, P. M. Alliel, et al. · Human Genetics · 75
Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
1986 · I Oberlé, R Heilig, et al. · Proceedings of the National Academy of Sciences · 71
Distribution of spontaneous chromosome breaks in man
2008 · M.G. Mattei, S. Ayme, et al. · Cytogenetics and Cell Genetics · 70
Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects
1976 · S. Aym�, J. F. Mattei, et al. · Human Genetics · 68
Linkage studies of X-linked mental retardation: High frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome)
1985 · K.E. Davies, M.G. Mattei, et al. · Human Genetics · 66
Origin of the extra chromosome in trisomy 21
1979 · J. F. Mattei, M. G. Mattei, et al. · Human Genetics · 64
Atelosteogenesis
1982 · P. Maroteaux, J. Spranger, et al. · American Journal of Medical Genetics · 63
Mapping of DNA markers close to the fraglle site on the human X chromosome at Xq25–3
1987 · M. Patterson, S. Kenwrick, et al. · Nucleic Acids Research · 56
Morquio syndrome: Clinical findings in 11 patients with MPS IVA and 2 patients with MPS IVB
1981 · W. Holzgreve, H. Gröbe, et al. · Human Genetics · 55
Physicians' acceptability of termination of pregnancy after prenatal diagnosis in southern france
1989 · C. Julian, P. Huard, et al. · Prenatal Diagnosis · 48
Trisomy 21 for the region 21q223: Identification by high-resolution R-banding patterns
1981 · J. F. Mattei, M. G. Mattei, et al. · Human Genetics · 47
Works count: 248
Citation count: 4,413
H-index: 35
I10-index: 90
Year
Topic
Type