Items where Author is "Rommelse, Nanda"

2012

Williams, Nigel M. and Franke, Barbara and Mick, Eric and Anney, Richard J. L. and Freitag, Christine M. and Gill, Michael and Thapar, Anita and O'Donovan, Michael C. and Owen, Michael J. and Holmans, Peter and Kent, Lindsey and Middleton, Frank and Zhang-James, Yanli and Liu, Lu and Meyer, Jobst and Nguyen, Thuy Trang and Romanos, Jasmin and Romanos, Marcel and Seitz, Christiane and Renner, Tobias J. and Walitza, Susanne and Warnke, Andreas and Palmason, Haukur and Buitelaar, Jan and Rommelse, Nanda and Vasquez, Alejandro Arias and Hawi, Ziarih and Langley, Kate and Sergeant, Joseph and Steinhausen, Hans-Christoph and Roeyers, Herbert and Biederman, Joseph and Zaharieva, Irina and Hakonarson, Hakon and Elia, Josephine and Lionel, Anath C. and Crosbie, Jennifer and Marshall, Christian R. and Schachar, Russell and Scherer, Stephen W. and Todorov, Alexandre and Smalley, Susan L. and Loo, Sandra and Nelson, Stanley and Shtir, Corina and Asherson, Philip and Reif, Andreas and Lesch, Klaus-Peter and Faraone, Stephen V.. (2012) Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder. American journal of psychiatry, Vol. 169, H. 2. pp. 195-204.

Fliers, Ellen A. and Vasquez, Alejandro Arias and Poelmans, Geert and Rommelse, Nanda and Altink, Marieke and Buschgens, Cathelijne and Asherson, Philip and Banaschewski, Tobias and Ebstein, Richard and Gill, Michael and Miranda, Ana and Mulas, Fernando and Oades, Robert D. and Roeyers, Herbert and Rothenberger, Aribert and Sergeant, Joseph and Sonuga-Barke, Edmund and Steinhausen, Hans-Christoph and Faraone, Stephen V. and Buitelaar, Jan K. and Franke, Barbara. (2012) Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function. The world journal of biological psychiatry, Vol. 13, no. 3. pp. 211-222.

2011

Rizzi, Thais S. and Arias-Vasquez, Alejandro and Rommelse, Nanda and Kuntsi, Jonna and Anney, Richard and Asherson, Philip and Buitelaar, Jan and Banaschewski, Tobias and Ebstein, Richard and Ruano, Dina and Van der Sluis, Sophie and Markunas, Christina A. and Garrett, Melanie E. and Ashley-Koch, Allison E. and Kollins, Scott H. and Anastopoulos, Arthur D. and Hansell, Narelle K. and Wright, Margaret J. and Montgomery, Grant W. and Martin, Nicholas G. and Harris, Sarah E. and Davies, Gail and Tenesa, Albert and Porteous, David J. and Starr, John M. and Deary, Ian J. and St Pourcain, Beate and Davey Smith, George and Timpson, Nicholas J. and Evans, David M. and Gill, Michael and Miranda, Ana and Mulas, Fernando and Oades, Robert D. and Roeyers, Herbert and Rothenberger, Aribert and Sergeant, Joseph and Sonuga-Barke, Edmund and Steinhausen, Hans Christoph and Taylor, Eric and Faraone, Stephen V. and Franke, Barbara and Posthuma, Danielle. (2011) The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background : evidence from a large collaborative study totaling 4,963 subjects. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 156, H. 2. pp. 145-157.

2009

Mulligan, Aisling and Anney, Richard J. L. and O'Regan, Myra and Chen, Wai and Butler, Louise and Fitzgerald, Michael and Buitelaar, Jan and Steinhausen, Hans-Christoph and Rothenberger, Aribert and Minderaa, Ruud and Nijmeijer, Judith and Hoekstra, Pieter J. and Oades, Robert D. and Roeyers, Herbert and Buschgens, Cathelijne and Christiansen, Hanna and Franke, Barbara and Gabriels, Isabel and Hartman, Catharina and Kuntsi, Jonna and Marco, Rafaela and Meidad, Sheera and Mueller, Ueli and Psychogiou, Lamprini and Rommelse, Nanda and Thompson, Margaret and Uebel, Henrik and Banaschewski, Tobias and Ebstein, Richard and Eisenberg, Jacques and Manor, Iris and Miranda, Ana and Mulas, Fernando and Sergeant, Joseph and Sonuga-Barke, Edmund and Asherson, Phil and Faraone, Stephen V. and Gill, Michael. (2009) Autism symptoms in Attention-Deficit/Hyperactivity Disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders. Journal of autism and developmental disorders, Vol. 39, H. 2. pp. 197-209.

2008

Chen, Wai and Zhou, Kaixin and Sham, Pak and Franke, Barbara and Kuntsi, Jonna and Campbell, Desmond and Fleischman, Karin and Knight, Jo and Andreou, Penny and Arnold, Renée and Altink, Marieke and Boer, Frits and Boholst, Mary Jane and Buschgens, Cathelijne and Butler, Louise and Christiansen, Hanna and Fliers, Ellen and Howe-Forbes, Raoul and Gabriëls, Isabel and Heise, Alexander and Korn-Lubetzki, Isabelle and Marco, Rafaela and Medad, She'era and Minderaa, Ruud and Müller, Ueli C. and Mulligan, Aisling and Psychogiou, Lamprini and Rommelse, Nanda and Sethna, Vaheshta and Uebel, Henrik and McGuffin, Peter and Plomin, Robert and Banaschewski, Tobias and Buitelaar, Jan and Ebstein, Richard and Eisenberg, Jacques and Gill, Michael and Manor, Iris and Miranda, Ana and Mulas, Fernando and Oades, Robert D. and Roeyers, Herbert and Rothenberger, Aribert and Sergeant, Joseph and Sonuga-Barke, Edmund and Steinhausen, Hans-Christoph and Taylor, Eric and Thompson, Margaret and Faraone, Stephen V. and Asherson, Philip. (2008) DSM-IV combined type ADHD shows familial association with sibling trait scores : a sampling strategy for QTL linkage. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 8. pp. 1450-1460.

Sonuga-Barke, Edmund J. S. and Brookes, Keeley-Joanne and Buitelaar, Jan and Anney, Richard and Bitsakou, Paraskevi and Baeyens, Dieter and Buschgens, Cathelijne and Chen, Wai and Christiansen, Hanna and Eisenberg, Jacques and Kuntsi, Jonna and Manor, Iris and Meliá, Amanda and Mulligan, Aisling and Rommelse, Nanda and Müller, Ueli C. and Uebel, Henrik and Banaschewski, Tobias and Ebstein, Richard and Franke, Barbara and Gill, Michael and Miranda, Ana and Oades, Robert D. and Roeyers, Herbert and Rothenberger, Aribert and Sergeant, Joseph and Steinhausen, Hans Christoph and Thompson, Margaret and Taylor, Eric and Asherson, Philip and Faraone, Stephen V.. (2008) Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147, H. 3. pp. 316-319.

Zhou, Kaixin and Asherson, Philip and Sham, Pak and Franke, Barbara and Anney, Richard J. L. and Buitelaar, Jan and Ebstein, Richard and Gill, Michael and Brookes, Keeley and Buschgens, Cathelijne and Campbell, Desmond and Chen, Wai and Christiansen, Hanna and Fliers, Ellen and Gabriëls, Isabel and Johansson, Lena and Marco, Rafaela and Mulas, Fernando and Müller, Ueli and Mulligan, Aisling and Neale, Benjamin M. and Rijsdijk, Fruhling and Rommelse, Nanda and Uebel, Henrik and Psychogiou, Lamprini and Xu, Xiaohui and Banaschewski, Tobias and Sonuga-Barke, Edmund and Eisenberg, Jacques and Manor, Iris and Miranda, Ana and Oades, Robert D. and Roeyers, Herbert and Rothenberger, Aribert and Sergeant, Joseph and Steinhausen, Hans-Christoph and Taylor, Eric and Thompson, Margaret and Faraone, Stephen V.. (2008) Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings. Biological psychiatry, Vol. 64, H. 7. pp. 571-576.

Anney, Richard J. L. and Hawi, Ziarih and Sheehan, Karen and Mulligan, Aisling and Pinto, Carlos and Brookes, Keeley J. and Xu, Xiaohui and Zhou, Kaixin and Franke, Barbara and Buitelaar, Jan and Vermeulen, Sita H. and Banaschewski, Tobias and Sonuga-Barke, Edmund and Ebstein, Richard and Manor, Iris and Miranda, Ana and Mulas, Fernando and Oades, Robert D. and Roeyers, Herbert and Rommelse, Nanda and Rothenberger, Aribert and Sergeant, Joseph and Steinhausen, Hans-Christoph and Taylor, Eric and Thompson, Margaret and Asherson, Philip and Faraone, Stephen V. and Gill, Michael. (2008) Parent of origin effects in attention/deficit hyperactivity disorder (ADHD) : analysis of data from the international multicenter ADHD genetics (IMAGE) program. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 8. pp. 1495-1500.