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

nork Demenais, F, Lathrop, M, Lalouel, J M
Argitaratua 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

nork Rollenhagen, C, Lathrop, M J, Macura, S L, Doncel, G F, Asin, S N
Argitaratua 2014

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

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

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

nork Farrall, M, Lathrop, M, Spence, J E, Bowcock, A, Klinger, K, Tsui, L C
Argitaratua 1987

HLA heterozygosity contributes to susceptibility to rheumatoid arthritis.

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

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

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

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

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

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

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

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

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

Etiological heterogeneity in X-linked spastic paraplegia.

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

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

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

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

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

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

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

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

nork 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
Argitaratua 1998

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

nork 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
Argitaratua 2005

Linkage of DNA probe B79a (D7S13) to cystic fibrosis

nork 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.
Argitaratua 1987

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

nork 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
Argitaratua 1997

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

nork 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
Argitaratua 1997

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

nork 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.
Argitaratua izan da Sci Rep (2017)

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

nork 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.
Argitaratua 2007