EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome von Delépine, Marc, Nicolino, Marc, Barrett, Timothy, Golamaully, Mahamadee, Mark Lathrop, G., Julier, Cécile

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A genome-wide search for quantitative trait loci underlying asthma von Daniels, Susan E., Bhattacharrya, Sumit, James, Alan, Leaves, Nicholas I., Young, Alan, Hill, Michael R., Faux, Jennie A., Ryan, Gerrard F., le Söuef, Peter N., Lathrop, G. Mark, Musk, A. William, Cookson, William O. C. M.

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Two stage genome–wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12 von Satsangi, Jack, Parkes, Miles, Louis, Edouard, Hashimoto, Lara, Kato, Norihiro, Welsh, Ken, Terwilliger, Joseph D., Lathrop, G. Mark, Bell, John I., Jewell, Derek P.

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Identification of a Major Susceptibility Locus on Chromosome 6p and Evidence for Further Disease Loci Revealed by a Two Stage Genome-Wide Search in Psoriasis von Trembath, Richard C., Lee Clough, R., Rosbotham, Jane L., Jones, Andrew B., Camp, Richard D. R., Frodsham, Angela, Browne, Julie, Barber, Ruth, Terwilliger, Joseph, Mark Lathrop, G., Barker, Jonathan N. W. N.

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Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease von Sakuntabhai, Anavaj, Ruiz-Perez, Victor, Carter, Simon, Jacobsen, Nick, Burge, Susan, Monk, Sarah, Smith, Melanie, Munro, Colin S., O'Donovan, Michael, Craddock, Nick, Kucherlapati, Raju, Rees, Jonathan L., Owen, Mike, Lathrop, G. Mark, Monaco, Anthony P., Strachan, Tom, Hovnanian, Alain

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Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3) von Yamagata, Kazuya, Oda, Naohisa, Kaisaki, Pamela J., Menzel, Stephan, Furuta, Hiroto, Vaxillaire, Martine, Southam, Lorraine, Cox, Roger D., Lathrop, G. Mark, Boriraj, V. Vicky, Chen, Xiangna, Cox, Nancy J., Oda, Yukie, Yano, Hideki, Le Beau, Michelle M., Yamada, Shirou, Nishigori, Hidekazu, Takeda, Jun, Fajans, Stefan S., Hattersley, Andrew T., Iwasaki, Naoko, Hansen, Torben, Pedersen, Oluf, Polonsky, Kenneth S., Turner, Robert C., Velho, Gilberto, Chèvre, Jean-Claude, Froguel, Philippe, Bell, Graeme I.

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Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16 von Szepetowski, Pierre, Rochette, Jacques, Berquin, Patrick, Piussan, Charles, Lathrop, G. Mark, Monaco, Anthony P.

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Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus von Froguel, Ph, Vaxillaire, M., Sun, F., Velho, G., Zouali, H., Butel, M. O., Lesage, S., Vionnet, N., Clément, K., Fougerousse, F., Tanizawa, Y., Weissenbach, J., Beckmann, J. S., Lathrop, G. M., Passa, Ph, Permutt, M. A., Cohen, D.

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Rat Gene Mapping Using PCR-Analyzed Microsatellites von Serikawa, T, Kuramoto, T, Hilbert, P, Mori, M, Yamada, J, Dubay, C. J, Lindpainter, K, Ganten, D, Guenet, J. L, Lathrop, G. M, Beckmann, J. S

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Genomic analysis of Th1–Th2 cytokine genes in an AIDS cohort: identification of IL4 and IL10 haplotypes associated with the disease progression von Vasilescu, A, Heath, S C, Ivanova, R, Hendel, H, Do, H, Mazoyer, A, Khadivpour, E, Goutalier, F X, Khalili, K, Rappaport, J, Lathrop, G M, Matsuda, F, Zagury, J-F

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Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats von HILBERT, P, LINDPAINTNER, K, VINCENT, M, GANTEN, D, GEORGES, M, LATHROP, G. M, BECKMANN, J. S, SERIKAWA, T, SOUBRIER, F, DUBAY, C, CARTWRIGHT, P, DE GOUYON, B, JULIER, C, TAKAHASI, S

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Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q von HASHIMOTO, L, HABITA, C, FROGUEL, P, WEISSENBACH, J, LATHROP, G. M, JULIER, C, BERESSI, J. P, DELEPINE, M, BESSE, C, CAMBON-THOMSEN, A, DESCHAMPS, I, ROTTER, J. I, DJOUIAH, S, JAMES, M. R

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Localisation of atopy and β subunit of high-affinity IgE receptor (Fc∈RI) on chromosome 11q von Sandford, A.J., Shirakawa, T., Moffat, M.F., Daniels, S.E., Faux, J.A., Young, R.P., Cookson, W.O.C.M., Ra, C., Nakamura, Y., Lathrop, G.M., Hopkin, J.M.

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Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10 von Julier, Cécile, Delépine, Marc, Keavney, Bernard, Terwilliger, Joseph, Davis, S., Weeks, Daniel E., Bui, Thuan, Jeunemaître, Xavier, Velho, Gilberto, Froguel, Philippe, Ratcliffe, Peter, Corvol, Pierre, Soubrier, Florent, Mark Lathrop, G.

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Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility von Julier, C., Hyer, R. N., Davies, J., Merlin, F., Soularue, P., Briant, L., Cathelineau, G., Deschamps, I., Rotter, J. I., Froguel, P., Boitard, C., Bell, J. I., Lathrop, G. M.

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Easy calculations of lod scores and genetic risks on small computers von LATHROP, G. M, LALOUEL, J. M

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Multilocus linkage analysis in humans: detection of linkage and estimation of recombination von LATHROP, G. M, LALOUEL, J. M, JULIER, C, OTT, J

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Strategies for Multilocus Linkage Analysis in Humans von Lathrop, G. M., Lalouel, J. M., Julier, C., Ott, J.

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Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease von Kyo, K., Muto, T., Nagawa, H., Lathrop, G. M., Nakamura, Y.

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Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14 von Melki, J., Sheth, P., Abdelhak, S., Burlet, P., Bachelot, M.F., Frézal, J., Munnich, A., Lathrop, M.G.

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