| Year |
Citation |
Score |
| 2020 |
Vaidyanathan R, Schaller F, Muscatelli F, Hammock EAD. Colocalization of Oxtr with Prader-Willi Syndrome transcripts in the trigeminal ganglion of neonatal mice. Human Molecular Genetics. PMID 32420597 DOI: 10.1093/Hmg/Ddaa094 |
0.364 |
|
| 2009 |
Zanella S, Tauber M, Muscatelli F. Breathing deficits of the Prader-Willi syndrome. Respiratory Physiology & Neurobiology. 168: 119-24. PMID 19712904 DOI: 10.1016/J.Resp.2009.03.010 |
0.353 |
|
| 2006 |
Andrieu D, Meziane H, Marly F, Angelats C, Fernandez PA, Muscatelli F. Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death. Bmc Developmental Biology. 6: 56. PMID 17116257 DOI: 10.1186/1471-213X-6-56 |
0.304 |
|
| 2005 |
Le Meur E, Watrin F, Landers M, Sturny R, Lalande M, Muscatelli F. Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region. Developmental Biology. 286: 587-600. PMID 16126194 DOI: 10.1016/J.Ydbio.2005.07.030 |
0.36 |
|
| 2004 |
Landers M, Bancescu DL, Le Meur E, Rougeulle C, Glatt-Deeley H, Brannan C, Muscatelli F, Lalande M. Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn. Nucleic Acids Research. 32: 3480-92. PMID 15226413 DOI: 10.1093/Nar/Gkh670 |
0.331 |
|
| 2001 |
Runte M, Faerber C, Lich C, Zeschnigk M, Buchholz T, Smith A, Maldergem LV, Buerger J, Muscatelli F, Gillessen-Kaesbach G, Horsthemke B, Buiting K. Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15 European Journal of Human Genetics. 9: 519-526. PMID 11464243 DOI: 10.1038/Sj.Ejhg.5200661 |
0.365 |
|
| 2000 |
Muscatelli F, Abrous DN, Massacrier A, Boccaccio I, Le Moal M, Cau P, Cremer H. Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome. Human Molecular Genetics. 9: 3101-10. PMID 11115855 DOI: 10.1093/Hmg/9.20.3101 |
0.362 |
|
| 1999 |
Boccaccio I, Glatt-Deeley H, Watrin F, Roëckel N, Lalande M, Muscatelli F. The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. Human Molecular Genetics. 8: 2497-505. PMID 10556298 DOI: 10.1093/Hmg/8.13.2497 |
0.458 |
|
| 1997 |
Jay P, Rougeulle C, Massacrier A, Moncla A, Mattei MG, Malzac P, Roëckel N, Taviaux S, Lefranc JL, Cau P, Berta P, Lalande M, Muscatelli F. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nature Genetics. 17: 357-61. PMID 9354807 DOI: 10.1038/Ng1197-357 |
0.439 |
|
| 1997 |
Watrin F, Roëckel N, Lacroix L, Mignon C, Mattei MG, Disteche C, Muscatelli F. The Mouse Necdin Gene Is Expressed from the Paternal Allele Only and Lies in the 7C Region of the Mouse Chromosome 7, a Region of Conserved Synteny to the Human Prader-Willi Syndrome Region European Journal of Human Genetics. 5: 324-332. DOI: 10.1007/Bf03405936 |
0.477 |
|
| 1995 |
Muscatelli F, Strom TM, Walker AP, Zanaria E, Récan D, Meindl A, Bardoni B, Guioli S, Zehetner G, Rabl W. Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism. Nature. 372: 672-6. PMID 7990958 DOI: 10.1038/372672A0 |
0.317 |
|
| 1995 |
Muscatelli F, Walker AP, De Plaen E, Stafford AN, Monaco AP. Isolation and characterization of a MAGE gene family in the Xp21.3 region. Proceedings of the National Academy of Sciences of the United States of America. 92: 4987-91. PMID 7761436 DOI: 10.1073/Pnas.92.11.4987 |
0.326 |
|
| 1994 |
Matfin G, Sheaves R, Muscatelli F, Walker A, Monaco A, Grant D, Nwose O, Wass JAH. Gene deletion causing adrenal hypoplasia congenita and hypogonadotrophic hypogonadism. Clinical Endocrinology. 40: 807-808. PMID 8033374 DOI: 10.1111/J.1365-2265.1994.Tb02517.X |
0.31 |
|
| 1993 |
Walker AP, Muscatelli F, Monaco AP. Isolation of the human Xp21 glycerol kinase gene by positional cloning. Human Molecular Genetics. 2: 107-14. PMID 8499898 DOI: 10.1093/Hmg/2.2.107 |
0.316 |
|
| 1993 |
Mollereau C, Muscatelli F, Mattei MG, Vassart G, Parmentier M. The high-affinity interleukin 8 receptor gene (IL8RA) maps to the 2q33-q36 region of the human genome: cloning of a pseudogene (IL8RBP) for the low-affinity receptor. Genomics. 16: 248-51. PMID 8486366 DOI: 10.1006/Geno.1993.1167 |
0.361 |
|
| 1993 |
Lefebvre S, Bureau J, Muscatelli F, Mattei M, Brahic M. A new human brain cDNA molecule: assignment to chromosome 11q21-q23.1 and description of two polymorphisms studied by the polymerase chain reaction. Human Genetics. 91: 148-150. PMID 8462974 DOI: 10.1007/Bf00222715 |
0.423 |
|
| 1993 |
Moncla A, Piras L, Arbex OF, Muscatelli F, Mattei MG, Mattei JF, Fontes M. Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndrome. Human Genetics. 90: 657-60. PMID 8444473 DOI: 10.1007/Bf00202487 |
0.622 |
|
| 1993 |
Piarroux R, Azaiez R, Lossi AM, Reynier P, Muscatelli F, Gambarelli F, Fontes M, Dumon H, Quilici M. Isolation and characterization of a repetitive DNA sequence from Leishmania infantum: development of a visceral leishmaniasis polymerase chain reaction. The American Journal of Tropical Medicine and Hygiene. 49: 364-9. PMID 8372958 DOI: 10.4269/ajtmh.1993.49.364 |
0.524 |
|
| 1993 |
Schurmans S, Muscatelli F, Miot F, Mattei MG, Vassart G, Parmentier M. The OLFR1 gene encoding the HGMP07E putative olfactory receptor maps to the 17p13-->p12 region of the human genome and reveals an MspI restriction fragment length polymorphism. Cytogenetics and Cell Genetics. 63: 200-4. PMID 8097991 DOI: 10.1159/000133534 |
0.401 |
|
| 1992 |
Muscatelli F, Verna JM, Philip N, Moncla A, Mattei MG, Mattei JF, Fontes M. Physical mapping of an Xq-proximal interstitial duplication in a male. Human Genetics. 88: 691-4. PMID 1551675 DOI: 10.1007/Bf02265299 |
0.619 |
|
| 1992 |
Muscatelli F, Monaco AP, Goodfellow PN, Hors-Cayla MC, Lehrach H, Fontes M. Isolation of new probes from Xq12-->q13: an example of the screening of reference libraries with Alu-PCR products from radiation hybrids. Cytogenetics and Cell Genetics. 61: 109-13. PMID 1395715 DOI: 10.1159/000133383 |
0.596 |
|
| 1992 |
Muscatelli F, Lena D, Mettei MG, Fontes M. A male with two contiguous inactivation centers on a single X chromosome: study of X inactivation and XIST expression Human Molecular Genetics. 1: 115-119. PMID 1301147 DOI: 10.1093/Hmg/1.2.115 |
0.599 |
|
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