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

מאת Demenais, F, Lathrop, M, Lalouel, J M
יצא לאור 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

מאת Rollenhagen, C, Lathrop, M J, Macura, S L, Doncel, G F, Asin, S N
יצא לאור 2014

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

מאת Hovnanian, A, Duquesnoy, P, Amselem, S, Blanchet-Bardon, C, Lathrop, M, Dubertret, L, Goossens, M
יצא לאור 1991

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

מאת Farrall, M, Lathrop, M, Spence, J E, Bowcock, A, Klinger, K, Tsui, L C
יצא לאור 1987

HLA heterozygosity contributes to susceptibility to rheumatoid arthritis.

מאת Wordsworth, P, Pile, K D, Buckely, J D, Lanchbury, J S, Ollier, B, Lathrop, M, Bell, J I
יצא לאור 1992

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

מאת Cohen, D, Cohen, O, Marcadet, A, Massart, C, Lathrop, M, Deschamps, I, Hors, J, Schuller, E, Dausset, J
יצא לאור 1984

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

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

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

מאת Ballet, J J, Sulcebe, G, Couderc, L J, Danon, F, Rabian, C, Lathrop, M, Clauvel, J P, Seligmann, M
יצא לאור 1987

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

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

Etiological heterogeneity in X-linked spastic paraplegia.

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

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

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

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

מאת Leppert, M, Breslow, J L, Wu, L, Hasstedt, S, O'Connell, P, Lathrop, M, Williams, R R, White, R, Lalouel, J M
יצא לאור 1988

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

מאת Samani, N J, Lodwick, D, Vincent, M, Dubay, C, Kaiser, M A, Kelly, M P, Lo, M, Harris, J, Sassard, J, Lathrop, M
יצא לאור 1993

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

מאת 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
יצא לאור 1998

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

מאת 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
יצא לאור 2005

Linkage of DNA probe B79a (D7S13) to cystic fibrosis

מאת 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.
יצא לאור 1987

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

מאת 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
יצא לאור 1997

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

מאת 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
יצא לאור 1997

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

מאת 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.
הוצא לאור ב Sci Rep (2017)

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

מאת 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.
יצא לאור 2007