Search results

• 2015

  Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD

  Yu, D., Mathews, C. A., Scharf, J. M., Neale, B. M., Davis, L. K., Gamazon, E. R., Derks, E. M., Evans, P., Edlund, C. K., Crane, J., Fagerness, J. A., Osiecki, L., Gallagher, P., Gerber, G., Haddad, S., Illmann, C., McGrath, L. M., Mayerfeld, C., Arepalli, S. & Barlassina, C. & 135 others, Barr, C. L., Bellodi, L., Benarroch, F., Berrió, G. B., Bienvenu, O. J., Black, D. W., Bloch, M. H., Brentani, H., Bruun, R. D., Budman, C. L., Camarena, B., Campbell, D. D., Cappi, C., Silgado, J. C. C., Cavallini, M. C., Chavira, D. A., Chouinard, S., Cook, E. H., Cookson, M. R., Coric, V., Cullen, B., Cusi, D., Delorme, R., Denys, D., Dion, Y., Eapen, V., Egberts, K., Falkai, P., Fernandez, T., Fournier, E., Garrido, H., Geller, D., Gilbert, D. L., Girard, S. L., Grabe, H. J., Grados, M. A., Greenberg, B. D., Gross-Tsur, V., Grünblatt, E., Hardy, J., Heiman, G. A., Hemmings, S. M. J., Herrera, L. D., Hezel, D. M., Hoekstra, P. J., Jankovic, J., Kennedy, J. L., King, R. A., Konkashbaev, A. I., Kremeyer, B., Kurlan, R., Lanzagorta, N., Leboyer, M., Leckman, J. F., Lennertz, L., Liu, C., Lochner, C., Lowe, T. L., Lupoli, S., Macciardi, F., Maier, W., Manunta, P., Marconi, M., McCracken, J. T., Mesa Restrepo, S. C., Moessner, R., Moorjani, P., Morgan, J., Muller, H., Murphy, D. L., Naarden, A. L., Nurmi, E., Ochoa, W. C., Ophoff, R. A., Pakstis, A. J., Pato, M. T., Pato, C. N., Piacentini, J., Pittenger, C., Pollak, Y., Rauch, S. L., Renner, T., Reus, V. I., Richter, M. A., Riddle, M. A., Robertson, M. M., Romero, R., Rosário, M. C., Rosenberg, D., Ruhrmann, S., Sabatti, C., Salvi, E., Sampaio, A. S., Samuels, J., Sandor, P., Service, S. K., Sheppard, B., Singer, H. S., Smit, J. H., Stein, D. J., Strengman, E., Tischfield, J. A., Turiel, M., Valencia Duarte, A. V., Vallada, H., Veenstra-VanderWeele, J., Walitza, S., Wang, Y., Weale, M., Weiss, R., Wendland, J. R., Westenberg, H. G. M., Shugart, Y. Y., Hounie, A. G., Miguel, E. C., Nicolini, H., Wagner, M., Ruiz-Linares, A., Cath, D. C., McMahon, W., Posthuma, D., Oostra, B. A., Nestadt, G., Rouleau, G. A., Purcell, S., Jenike, M. A., Heutink, P., Hanna, G. L., Conti, D. V., Arnold, P. D., Freimer, N. B., Stewart, S. E., Knowles, J. A., Cox, N. J. & Pauls, D. L., Jan 2015, In: The American Journal of Psychiatry. 172, 1, p. 82-93 12 p.

  Research output: Contribution to journal › Article › peer-review

  • Genome Wide Association Study 100%
  • Obsessive-Compulsive Disorder 100%
  • Tourette Syndrome 100%
  • Single-Nucleotide Polymorphism 50%
  • Genetic Architecture 50%
  116 Citations (Scopus)
• 2013

  Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

  Lee, S. H., Ripke, S., Neale, B. M., Faraone, S. V., Purcell, S. M., Perlis, R. H., Mowry, B. J., Thapar, A., Goddard, M. E., Witte, J. S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen, O. A., Anjorin, A., Anney, R., Anttila, V., Arking, D. E. & Asherson, P. & 31 others, Azevedo, M. H., Backlund, L., Badner, J. A., Bailey, A. J., Banaschewski, T., Barchas, J. D., Barnes, M. R., Barrett, T. B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen, S. E., Berrettini, W., Breen, G., Collier, D. A., Craig, D. W., Craig, I. W., Day, R., Farmer, A. E., Fombonne, E., Freitag, C. M., Kuntsi, J., Lewis, C. M., Lowe, J. K., McGuffin, P., Parr, J. R., Sonuga-Barke, E. J. S., Young, A. H. & Cross-Disorder Group of the Psychiatric Genomics Consortium, Sept 2013, In: Nature Genetics. 45, 9, p. 984-994 11 p., N/A.

  Research output: Contribution to journal › Article › peer-review

  • Major Depressive Disorder 100%
  • Bipolar Disorder 75%
  • Attention Deficit Hyperactivity Disorder 50%
  • Pervasive Developmental Disorder 50%
  • Genotype 25%
  1752 Citations (Scopus)

• Genome-wide association analysis identifies 13 new risk loci for schizophrenia

  Ripke, S., O'dushlaine, C., Chambert, K., Moran, J. L., K??hler, A. K., Akterin, S., Bergen, S. E., Collins, A. L., Crowley, J. J., Fromer, M., Kim, Y., Lee, S. H., Magnusson, P. K. E., Sanchez, N., Stahl, E. A., Williams, S., Wray, N. R., Xia, K., Bettella, F. & Borglum, A. D. & 15 others, Bulik-sullivan, B. K., Cormican, P., Craddock, N., De Leeuw, C., Durmishi, N., Gill, M., Lin, K., Neale, B. M., Powell, J., Riley, B. P., Walters, J. T., Multicenter Genetic Studies of Schizophrenia Consortium, Psychosis Endophenotypes International Consortium, Wellcome Trust Case Consortium 2 & Purcell, S., Oct 2013, In: Nature Genetics. 45, 10, p. 1150-1159 10 p.

  Research output: Contribution to journal › Article › peer-review

  • Single Nucleotide Polymorphism 100%
  • Genome Wide Association Study 100%
  • Candidate Gene 33%
  • Genetic Divergence 33%
  • Genomics 33%
  1206 Citations (Scopus)
• 1998

  Genetic influence on language delay in two-year-old children

  Dale, P., Simonoff, E., Bishop, D., Eley, T., Oliver, B., Price, T., Purcell, S., Stevenson, J. & Plomin, R., 1 Aug 1998, In: Nature Neuroscience. 1, 4, p. 324-328 5 p.

  Research output: Contribution to journal › Article › peer-review

  • Genetic Influence 100%
  • Individual Differences 50%
  • Brain Lesions 50%
  215 Citations (Scopus)