Items where Author is "Chen, W."

2021

McCartney, D. L. and Min, J. L. and Richmond, R. C. and Lu, A. T. and Sobczyk, M. K. and Davies, G. and Broer, L. and Guo, X. and Jeong, A. and Jung, J. and Kasela, S. and Katrinli, S. and Kuo, P. L. and Matias-Garcia, P. R. and Mishra, P. P. and Nygaard, M. and Palviainen, T. and Patki, A. and Raffield, L. M. and Ratliff, S. M. and Richardson, T. G. and Robinson, O. and Soerensen, M. and Sun, D. and Tsai, P. C. and van der Zee, M. D. and Walker, R. M. and Wang, X. and Wang, Y. and Xia, R. and Xu, Z. and Yao, J. and Zhao, W. and Correa, A. and Boerwinkle, E. and Dugue, P. A. and Durda, P. and Elliott, H. R. and Gieger, C. and Genetics of DNA Methylation Consortium, and de Geus, E. J. C. and Harris, S. E. and Hemani, G. and Imboden, M. and Kahonen, M. and Kardia, S. L. R. and Kresovich, J. K. and Li, S. and Lunetta, K. L. and Mangino, M. and Mason, D. and McIntosh, A. M. and Mengel-From, J. and Moore, A. Z. and Murabito, J. M. and Nhlbi Trans-Omics for Precision Medicine Consortium, and Ollikainen, M. and Pankow, J. S. and Pedersen, N. L. and Peters, A. and Polidoro, S. and Porteous, D. J. and Raitakari, O. and Rich, S. S. and Sandler, D. P. and Sillanpaa, E. and Smith, A. K. and Southey, M. C. and Strauch, K. and Tiwari, H. and Tanaka, T. and Tillin, T. and Uitterlinden, A. G. and Van Den Berg, D. J. and van Dongen, J. and Wilson, J. G. and Wright, J. and Yet, I. and Arnett, D. and Bandinelli, S. and Bell, J. T. and Binder, A. M. and Boomsma, D. I. and Chen, W. and Christensen, K. and Conneely, K. N. and Elliott, P. and Ferrucci, L. and Fornage, M. and Hagg, S. and Hayward, C. and Irvin, M. and Kaprio, J. and Lawlor, D. A. and Lehtimaki, T. and Lohoff, F. W. and Milani, L. and Milne, R. L. and Probst-Hensch, N. and Reiner, A. P. and Ritz, B. and Rotter, J. I. and Smith, J. A. and Taylor, J. A. and van Meurs, J. B. J. and Vineis, P. and Waldenberger, M. and Deary, I. J. and Relton, C. L. and Horvath, S. and Marioni, R. E.. (2021) Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. Genome Biol, 22. p. 194.

2008

Asherson, P. and Zhou, K. and Anney, R. J. L. and Franke, B. and Buitelaar, J. and Ebstein, R. and Gill, M. and Altink, M. and Arnold, R. and Boer, F. and Brookes, K. and Buschgens, C. and Butler, L. and Cambell, D. and Chen, W. and Christiansen, H. and Feldman, L. and Fleischman, K. and Fliers, E. and Howe-Forbes, R. and Goldfarb, A. and Heise, A. and Gabriëls, I. and Johansson, L. and Lubetzki, I. and Marco, R. and Medad, S. and Minderaa, R. and Mulas, F. and Müller, U. and Mulligan, A. and Neale, B. and Rijsdijk, F. and Rabin, K. and Rommelse, N. and Sethna, V. and Sorohan, J. and Uebel, H. and Psychogiou, L. and Weeks, A. and Barrett, R. and Xu, X. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Manor, I. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H.-C. and Taylor, E. and Thompson, M. and Faraone, S. V.. (2008) A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16. Molecular Psychiatry, 13 (5). pp. 514-521.

Christiansen, H. and Chen, W. and Oades, R. D. and Asherson, P. and Taylor, E. A. and Lasky-Su, J. and Zhou, K. and Banaschewski, T. and Buschgens, C. and Franke, B. and Gabriels, I. and Manor, I. and Marco, R. and Müller, U. C. and Mulligan, A. and Psychogiou, L. and Rommelse, N. N. J. and Uebel, H. and Buitelaar, J. and Ebstein, R. P. and Eisenberg, J. and Gill, M. and Miranda, A. and Mulas, F. and Roeyers, H. and Rothenberger, A. and Sergeant, J. A. and Sonuga-Barke, E. J. S. and Steinhausen, H.-C. and Thompson, M. and Faraone, S. V.. (2008) Co-transmission of conduct problems with attention-deficit/hyperactivity disorder : familial evidence for a distinct disorder. Journal of neural transmission, Vol. 115, No. 2. pp. 163-175.

Brookes, K. J. and Neale, B. and Xu, X. and Thapar, A. and Gill, M. and Langley, K. and Hawi, Z. and Mill, J. and Taylor, E. and Franke, B. and Chen, W. and Ebstein, R. and Buitelaar, J. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Manor, I. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H. C. and Faraone, S. V. and Asherson, P.. (2008) Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 147B (1). pp. 94-99.

Xu, X. and Duman, E. A. and Aysimi, E. and Anney, R. and Brookes, K. and Franke, B. and Zhou, K. and Buschgens, C. and Chen, W. and Christiansen, H. and Eisenberg, J. and Gabriëls, I. and Manor, I. and Marco, R. and Müller, U. C. and Mulligan, A. and Rommelse, N. and Thompson, M. and Uebel, H. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Gill, M. and Miranda, A. and Mulas, F. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Taylor, E. and Faraone, S. V. and Asherson, P.. (2008) No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 7. pp. 1306-1309.

Xu, X. and Hawi, Z. and Brookes, K. J. and Anney, R. and Bellgrove, M. and Franke, B. and Barry, E. and Chen, W. and Kuntsi, J. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Fitzgerald, M. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Faraone, S. V. and Gill, M. and Asherson, P.. (2008) Replication of a rare protective allele in the noradrenaline transporter gene and ADHD. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 8. pp. 1564-1567.

2006

Brookes, K. and Xu, X. and Chen, W. and Zhou, K. and Neale, B. and Lowe, N. and Anney, R. and Aneey, R. and Franke, B. and Gill, M. and Ebstein, R. and Buitelaar, J. and Sham, P. and Campbell, D. and Knight, J. and Andreou, P. and Altink, M. and Arnold, R. and Boer, F. and Buschgens, C. and Butler, L. and Christiansen, H. and Feldman, L. and Fleischman, K. and Fliers, E. and Howe-Forbes, R. and Goldfarb, A. and Heise, A. and Gabriëls, I. and Korn-Lubetzki, I. and Johansson, L. and Marco, R. and Medad, S. and Minderaa, R. and Mulas, F. and Müller, U. and Mulligan, A. and Rabin, K. and Rommelse, N. and Sethna, V. and Sorohan, J. and Uebel, H. and Psychogiou, L. and Weeks, A. and Barrett, R. and Craig, I. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Kuntsi, J. and Manor, I. and McGuffin, P. and Miranda, A. and Oades, R. D. and Plomin, R. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H.-C. and Taylor, E. and Thompson, M. and Faraone, S. V. and Asherson, P.. (2006) The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Molecular Psychiatry, 11 (10). pp. 934-953.