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

per Demenais, F, Lathrop, M, Lalouel, J M
Publicat 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

per Rollenhagen, C, Lathrop, M J, Macura, S L, Doncel, G F, Asin, S N
Publicat 2014

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

per Hovnanian, A, Duquesnoy, P, Amselem, S, Blanchet-Bardon, C, Lathrop, M, Dubertret, L, Goossens, M
Publicat 1991

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

per Farrall, M, Lathrop, M, Spence, J E, Bowcock, A, Klinger, K, Tsui, L C
Publicat 1987

HLA heterozygosity contributes to susceptibility to rheumatoid arthritis.

per Wordsworth, P, Pile, K D, Buckely, J D, Lanchbury, J S, Ollier, B, Lathrop, M, Bell, J I
Publicat 1992

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

per Cohen, D, Cohen, O, Marcadet, A, Massart, C, Lathrop, M, Deschamps, I, Hors, J, Schuller, E, Dausset, J
Publicat 1984

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

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

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

per Ballet, J J, Sulcebe, G, Couderc, L J, Danon, F, Rabian, C, Lathrop, M, Clauvel, J P, Seligmann, M
Publicat 1987

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

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

Etiological heterogeneity in X-linked spastic paraplegia.

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

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

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

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

per Leppert, M, Breslow, J L, Wu, L, Hasstedt, S, O'Connell, P, Lathrop, M, Williams, R R, White, R, Lalouel, J M
Publicat 1988

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

per Samani, N J, Lodwick, D, Vincent, M, Dubay, C, Kaiser, M A, Kelly, M P, Lo, M, Harris, J, Sassard, J, Lathrop, M
Publicat 1993

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

per 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
Publicat 1998

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

per 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
Publicat 2005

Linkage of DNA probe B79a (D7S13) to cystic fibrosis

per 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.
Publicat 1987

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

per 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
Publicat 1997

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

per 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
Publicat 1997

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

per 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.
Publicat a Sci Rep (2017)

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

per 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.
Publicat 2007