Emergence of young human genes after a burst of retroposition in primates. by Marques, A, Dupanloup, I, Vinckenbosch, N, Reymond, A, Kaessmann, H

Emergence of young human genes after a burst of retroposition in primates by Marques, A, Dupanloup, I, Vinckenbosch, N, Reymond, A, Kaessmann, H

Identification of structural variation in mouse genomes. by Keane, T, Wong, K, Adams, D, Flint, J, Reymond, A, Yalcin, B

Comparison of mouse and human genomes followed by experimental verification yields an estimated 1,019 additional genes. by Guigo, R, Dermitzakis, E, Agarwal, P, Ponting, C, Parra, G, Reymond, A, Abril, J, Keibler, E, Lyle, R, Ucla, C, Antonarakis, SE, Brent, MR

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. by Jacquemont, S, Reymond, A, Zufferey, F, Harewood, L, Walters, R, Kutalik, Z, Martinet, D, Shen, Y, Valsesia, A, Beckmann, N, Thorleifsson, G, Belfiore, M, Bouquillon, S, Campion, D, de Leeuw, N, de Vries, B, Esko, T, Fernandez, B, Fernández-Aranda, F, Fernández-Real, J, Gratacòs, M, Guilmatre, A, Hoyer, J, Jarvelin, MR, Kooy, R

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus by Jacquemont, S, Reymond, A, Zufferey, F, Harewood, L, Walters, R, Kutalik, Z, Martinet, D, Shen, Y, Valsesia, A, Beckmann, N, Thorleifsson, G, Belfiore, M, Bouquillon, S, Campion, D, de Leeuw, N, de Vries, B, Esko, T, Fernandez, B, Fernández-Aranda, F, Fernández-Real, J, Gratacòs, M, Guilmatre, A, Hoyer, J, Jarvelin, M, Frank Kooy, R

The GENCODE human gene set by Searle, S., Frankish, A., Bignell, A., Aken, B., Derrien, Thomas, Diekhans, M., Harte, R., Howald, C., Kokocinski, F., Lin, M., Tress, M., Van Baren, M., Barnes, I., Hunt, T., Carvalho-Silva, D., Davidson, C., Donaldson, S., Gilbert, J., Kay, M., Lloyd, D., Loveland, J., Mudge, J., Snow, C., Vamathevan, J., Wilming, L., Brent, M., Gerstein, Mark B., Guigo, Roderic, Kellis, Manolis, Reymond, A., Zadissa, A., Valencia, A., Harrow, J., Hubbard, T.

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Mutations in MAST1 cause mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations by Tripathy, R, Leca, I, Van Dijk, T, Weiss, J, Van Bon, B, Sergaki, M, Gstrein, T, Breuss, M, Tian, G, Bahi-Buisson, N, Paciorkowski, A, Pagnamenta, A, Wenninger-Weinzierl, A, Martinez-Reza, M, Landler, L, Lise, S, Taylor, J, Terrone, G, Vitiello, G, Del Giudice, E, Brunetti-Pierri, N, D'Amico, A, Reymond, A, Voisin, N, Bernstein, J, Farrelly, E, Kini, U, Leonard, T, Valence, S, Burglen, L, Armstrong, L, Hiatt, S, Cooper, G, Aldinger, K, Dobyns, W, Mirzaa, G, Pierson, T, Baas, F, Chelly, J, Cowan, N, Keays, D