Robustness and power of the unified model in the analysis of quantitative measurements.

Por Demenais, F, Lathrop, M, Lalouel, J M
Publicado em 1986

Herpes simplex virus type-2 stimulates HIV-1 replication in cervical tissues: implications for HIV-1 transmission and efficacy of anti-HIV-1 microbicides

Por Rollenhagen, C, Lathrop, M J, Macura, S L, Doncel, G F, Asin, S N
Publicado em 2014

Exclusion of linkage between the collagenase gene and generalized recessive dystrophic epidermolysis bullosa phenotype.

Por Hovnanian, A, Duquesnoy, P, Amselem, S, Blanchet-Bardon, C, Lathrop, M, Dubertret, L, Goossens, M
Publicado em 1991

Further data on linkage between cystic fibrosis and 7C22 (D7S16)

Por Farrall, M, Lathrop, M, Spence, J E, Bowcock, A, Klinger, K, Tsui, L C
Publicado em 1987

HLA heterozygosity contributes to susceptibility to rheumatoid arthritis.

Por Wordsworth, P, Pile, K D, Buckely, J D, Lanchbury, J S, Ollier, B, Lathrop, M, Bell, J I
Publicado em 1992

Class II HLA-DC beta-chain DNA restriction fragments differentiate among HLA-DR2 individuals in insulin-dependent diabetes and multiple sclerosis.

Por Cohen, D, Cohen, O, Marcadet, A, Massart, C, Lathrop, M, Deschamps, I, Hors, J, Schuller, E, Dausset, J
Publicado em 1984

Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene.

Por Hovnanian, A, Duquesnoy, P, Blanchet-Bardon, C, Knowlton, R G, Amselem, S, Lathrop, M, Dubertret, L, Uitto, J, Goossens, M
Publicado em 1992

Impaired anti-pneumococcal antibody response in patients with AIDS-related persistent generalized lymphadenopathy.

Por Ballet, J J, Sulcebe, G, Couderc, L J, Danon, F, Rabian, C, Lathrop, M, Clauvel, J P, Seligmann, M
Publicado em 1987

A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci

Por Modamio-Hoybjor, S, Moreno-Pelayo, M, Mencia, A, del Castillo, I, Chardenoux, S, Morais, D, Lathrop, M, Petit, C, Moreno, F
Publicado em 2004

Etiological heterogeneity in X-linked spastic paraplegia.

Por Keppen, L D, Leppert, M F, O'Connell, P, Nakamura, Y, Stauffer, D, Lathrop, M, Lalouel, J M, White, R
Publicado em 1987

DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23

Por Moreno-Pelayo, M, Modamio-Hoybjor, S, Mencia, A, del Castillo, I, Chardenoux, S, Fernandez-Burriel, M, Lathrop, M, Petit, C, Moreno, F
Publicado em 2003

Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred.

Por Leppert, M, Breslow, J L, Wu, L, Hasstedt, S, O'Connell, P, Lathrop, M, Williams, R R, White, R, Lalouel, J M
Publicado em 1988

A gene differentially expressed in the kidney of the spontaneously hypertensive rat cosegregates with increased blood pressure.

Por Samani, N J, Lodwick, D, Vincent, M, Dubay, C, Kaiser, M A, Kelly, M P, Lo, M, Harris, J, Sassard, J, Lathrop, M
Publicado em 1993

Deletions within COL7A1 exons distant from consensus splice sites alter splicing and produce shortened polypeptides in dominant dystrophic epidermolysis bullosa.

Por Sakuntabhai, A, Hammami-Hauasli, N, Bodemer, C, Rochat, A, Prost, C, Barrandon, Y, de Prost, Y, Lathrop, M, Wojnarowska, F, Bruckner-Tuderman, L, Hovnanian, A
Publicado em 1998

Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease

Por Pelet, A, de Pontual, L, Clement-Ziza, M, Salomon, R, Mugnier, C, Matsuda, F, Lathrop, M, Munnich, A, Feingold, J, Lyonnet, S, Abel, L, Amiel, J
Publicado em 2005

Linkage of DNA probe B79a (D7S13) to cystic fibrosis

Por Wainwright, B. J., Tsui, L.-C., Leppert, M., Buchwald, M., Estivill, X., O'Connell, P., Lathrop, M., Lalouel, J.-M., White, R., Williamson, R., Farrall, M.
Publicado em 1987

Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6.

Por Delépine, M, Pociot, F, Habita, C, Hashimoto, L, Froguel, P, Rotter, J, Cambon-Thomsen, A, Deschamps, I, Djoulah, S, Weissenbach, J, Nerup, J, Lathrop, M, Julier, C
Publicado em 1997

Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibr...

Por Hovnanian, A, Rochat, A, Bodemer, C, Petit, E, Rivers, C A, Prost, C, Fraitag, S, Christiano, A M, Uitto, J, Lathrop, M, Barrandon, Y, de Prost, Y
Publicado em 1997

Network-assisted analysis of GWAS data identifies a functionally-relevant gene module for childhood-onset asthma

Por Liu, Y., Brossard, M., Sarnowski, C., Vaysse, A., Moffatt, M., Margaritte-Jeannin, P., Llinares-López, F., Dizier, M. H., Lathrop, M., Cookson, W., Bouzigon, E., Demenais, F.
Publicado no Sci Rep (2017)

A haplotype of the human CXCR1 gene protective against rapid disease progression in HIV-1(+) patients

Por Vasilescu, A., Terashima, Y., Enomoto, M., Heath, S., Poonpiriya, V., Gatanaga, H., Do, H., Diop, G., Hirtzig, T., Auewarakul, P., Lauhakirti, D., Sura, T., Charneau, P., Marullo, S., Therwath, A., Oka, S., Kanegasaki, S., Lathrop, M., Matsushima, K., Zagury, J.-F., Matsuda, F.
Publicado em 2007