The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes von Wilkinson, B, Grepo, N, Thompson, B L, Kim, J, Wang, K, Evgrafov, O V, Lu, W, Knowles, J A, Campbell, D B

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Genome-wide association study of recurrent early-onset major depressive disorder von Shi, J, Potash, J B, Knowles, J A, Weissman, M M, Coryell, W, Scheftner, W A, Lawson, W B, DePaulo, J R, Gejman, P V, Sanders, A R, Johnson, J K, Adams, P, Chaudhury, S, Jancic, D, Evgrafov, O, Zvinyatskovskiy, A, Ertman, N, Gladis, M, Neimanas, K, Goodell, M, Hale, N, Ney, N, Verma, R, Mirel, D, Holmans, P, Levinson, D F

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A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light Gene von Mersiyanova, Irina V., Perepelov, Alexander V., Polyakov, Alexander V., Sitnikov, Vladimir F., Dadali, Elena L., Oparin, Roman B., Petrin, Alexander N., Evgrafov, Oleg V.

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Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome von Plummer, J T, Evgrafov, O V, Bergman, M Y, Friez, M, Haiman, C A, Levitt, P, Aldinger, K A

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Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study von Voyiaziakis, E, Evgrafov, O, Li, D, Yoon, H-J, Tabares, P, Samuels, J, Wang, Y, Riddle, M A, Grados, M A, Bienvenu, O J, Shugart, Y Y, Liang, K-Y, Greenberg, B D, Rasmussen, S A, Murphy, D L, Wendland, J R, McCracken, J T, Piacentini, J, Rauch, S L, Pauls, D L, Nestadt, G, Fyer, A J, Knowles, J A

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Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E von De Jonghe, Peter, Mersivanova, Irina, Nelis, Eva, Del Favero, Jurgen, Martin, Jean-Jacques, Van Broeckhoven, Christine, Evgrafov, Oleg, Timmerman, Vincent

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A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24 von TANG, Bei-Sha, WEI LUO, DAI, He-Ping, YANG, Qi-Dong, XIA, Jia-Hui, EVGRAFOV, Oleg V, KUN XIA, XIAO, Jian-Feng, HONG JIANG, LU SHEN, TANG, Jian-Guang, ZHAO, Guo-Hua, FANG CAI, QIAN PAN

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Mutation in the connexin 50 gene (GJA8) in a Russian family with zonular pulverulent cataract von Polyakov, AV, Shagina, IA, Khlebnikova, OV, Evgrafov, OV

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Mapping, cloning and genetic characterization of the region containing the Wilson disease gene von Petrukhin, K., Fischer, S. G., Pirastu, M., Tanzi, R.E., Chernov, I., Devoto, M., Brzustowicz, L. M., Cayanis, E., Vitale, E., Russo, J. J., Matseoane, D., Boukhgalter, B., Wasco, W., Figus, A. L., Loudianos, J., Cao, A., Sternlieb, I., Evgrafov, O., Parano, E., Pavone, L., Warburton, D., Ott, J., Penchaszadeh, G. K., Scheinberg, I. H., Gilliam, T.C.

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Compound Heterozygous Deletion of the PROP-1 Gene in Children with Combined Pituitary Hormone Deficiency von Fofanova, Q, Takamura, N, Kinoshita, E, Parks, J. S, Brown, M. R, Peterkova, V. A, Evgrafov, O. V, Goncharov, N. P, Bulatov, A. A, Dedov, I. I, Yamashita, S

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The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene von Tanzi, R.E., Petrukhin, K., Chernov, I., Pellequer, J.L., Wasco, W., Ross, B., Romano, D.M., Parano, E., Pavone, L., Brzustowicz, L.M., Devoto, M., Peppercorn, J., Bush, A.I., Sternlieb, I., Pirastu, M., Gusella, J.F., Evgrafov, O., Penchaszadeh, G.K., Honig, B., Edelman, I.S., Soares, M.B., Scheinberg, I.H., Gilliam, T.C.

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P26.23: The termination of pregnancy under ultrasound control in cases of bilateral renal agenesis, multicystic dysplasia and infantile polycystic disease von Teregulova, L., Zalaletdinov, A., Golovanova, N., Evgrafov, O.

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Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis von Zerjal, T, Dashnyam, B, Pandya, A, Kayser, M, Roewer, L, Santos, F R, Schiefenhövel, W, Fretwell, N, Jobling, M A, Harihara, S, Shimizu, K, Semjidmaa, D, Sajantila, A, Salo, P, Crawford, M H, Ginter, E K, Evgrafov, O V, Tyler-Smith, C

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Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features von Kalachikov, Sergey, Evgrafov, Oleg, Ross, Barbara, Winawer, Melodie, Barker-Cummings, Christie, Boneschi, Filippo Martinelli, Choi, Chang, Morozov, Pavel, Das, Kamna, Teplitskaya, Elita, Yu, Andrew, Cayanis, Eftihia, Penchaszadeh, Graciela, Kottmann, Andreas H., Pedley, Timothy A., Hauser, W. Allen, Ottman, Ruth, Gilliam, T. Conrad

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A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21 von Ismailov, S M, Fedotov, V P, Dadali, E L, Polyakov, A V, Van Broeckhoven, C, Ivanov, V I, De Jonghe, P, Timmerman, V, Evgrafov, O V

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Screening for Mutations in the Peripheral Myelin Genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth Neuropathy Patients von Mersiyanova, I V, Ismailov, S M, Polyakov, A V, Dadali, EL, Fedotov, V P, Nelis, E, Loefgren, A, Timmerman, V, Van Broeckhoven, C, Evgrafov, O V

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Targeting β-catenin/CBP interaction in breast cancer von Ring, A., Evgrafov, O., Knwoles, J., Kahn, M.

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A Third-Pass Genome Scan in Panic Disorder: Evidence for Multiple Susceptibility Loci von Fyer, Abby J., Hamilton, Steven P., Durner, Martina, Haghighi, Fatemeh, Heiman, Gary A., Costa, Ramiro, Evgrafov, Oleg, Adams, Philip, de Leon, Ada Baisre, Taveras, Nilda, Klein, Donald F., Hodge, Susan E., Weissman, Myrna M., Knowles, James A.

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Olfactory neuroepithelium-derived neural progenitor cells as a model system for investigating the molecular mechanisms of neuropsychiatric disorders von Evgrafov, Oleg V, Wrobel, Bozena B, Kang, Xin, Simpson, George, Malaspina, Dolores, Knowles, James A

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GH-1 gene splicing mutations: molecular basis of hereditary isolated growth hormone deficiency in children von Fofanova, O V, Evgrafov, O V, Polyakov, A V, Peterkova, V A, Dedov, I I

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