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Johnson, K. A., Kelly, S.P., Robertson, I.H., Barry, E., Mulligan, A., Daly, M, Lambert, M., McDonnell, C., Connor, T.J., Hawi, Z., Gill, M. and Bellgrove, Mark (2008) Absence of the 7-Repeat Variant of the DRD4 VNTR Is Associated With Drifting Sustained Attention in Children With ADHD But Not in Controls. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B 6: 927-937. doi:10.1002/ajmg.b.30718 224   28 Cited 31 times in Scopus31 0
Hawi, Z., Kent, L., Hill, M., Anney, R. J. L., Brookes, K. J., Barry, E., Franke, B., Banaschewski, T., Buitelaar, J., Ebstein, R., Miranda, A., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E., Steinhausen, H. -C., Faraone, S. V., Asherson, P. and Gill, M. (2010) ADHD and DAT1: Further evidence of paternal over-transmission of risk alleles and haplotype. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 153B 1: 97-102. doi:10.1002/ajmg.b.30960 45   13 Cited 14 times in Scopus14 0
Gallagher, Louise, Bellgrove, Mark A., Hawi, Ziarih, Segurado, Ricardo and Fitzgerald, Michael (2007). ADHD, Autism spectrum disorders and Tourette’s Syndrome: Investigating the evidence for clinical and genetic overlap. In Michael Fitzgerald, Mark Bellgrove and Michael Gill (Ed.), Handbook of attention deficit hyperactivity disorder (pp. 69-89) Hoboken, NJ, United States: John Wiley. 77  
Hawi, Ziarih, Matthews, Natasha, Barry, Edwina, Kirley, Aiveen, Wagner, Joseph, Wallace, Robyn H., Heussler, Helen S., Vance, Alasdair, Gill, Michael and Bellgrove, Mark A. (2013) A high density linkage disequilibrium mapping in 14 noradrenergic genes: evidence of association between SLC6A2, ADRA1B and ADHD. Psychopharmacology, 225 4: 895-902. doi:10.1007/s00213-012-2875-x 75 1 8 Cited 10 times in Scopus10 0
Hill, Matthew James, Kenny, Elaine, Roche, Siobhan, Morris, Derek W., Corvin, Aiden, Hawi, Ziarih, Gill, Michael and Anney, Richard J. L. (2011) Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: Evidence of cis-acting variation and tissue specific regulation. Psychiatric Genetics, 21 6: 281-286. doi:10.1097/YPG.0b013e328348045b 73 2 0 Cited 0 times in Scopus0 0
Cummins, T. D. R., Jacoby, O., Hawi. Z., Nandam, L. S., Byrne, M. A. V., Kim, B.-N., Wagner, J., Chambers, C. D. and Bellgrove. M A. (2013) Alpha-2A adrenergic receptor gene variants are associated with increased intra-individual variability in response time. Molecular Psychiatry, 19 9: 1031-1036. doi:10.1038/mp.2013.140 32   0 Cited 1 times in Scopus1 1
Lowe, Naomi, Barry, Edwina, Gill, Michael and Hawi, Ziarih (2009) An overview of the pharmacogenetics and molecular genetics of ADHD. Current Pharmacogenomics and Personalized Medicine, 4 3: 231-243. doi:10.2174/157016006778195106 54   Cited 5 times in Scopus5 0
Lynch, C. A., Brazil, J., Cullen, B., Coakley, D., Gill, M., Lawlor, B. A. and Hawi, Z. (2008) Apolipoprotein E promoter polymorphisms (-491A/T and -427T/C) and Alzheimer's disease: No evidence of association in the Irish population. Irish Journal of Medical Science, 177 1: 29-33. doi:10.1007/s11845-007-0098-7 26   5 Cited 5 times in Scopus5 0
Domschke, Katharina, Sheehan, Karen, Lowe, Naomi, Kirley, Aiveen, Mullins, Celine, O'Sullivan, Roderick, Freitag, Christine, Becker, Tim, Conroy, Judith, Fitzgerald, Michael, Gill, Michael and Hawi, Ziarih (2005) Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: Preferential transmission of the MAO-A 941G allele to affected children. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 134B 1: 110-114. doi:10.1002/ajmg.b.30158 68   46 Cited 48 times in Scopus48 0
Bellgrove, M. A., Hawi, Z., Kirley, A., Fitzgerald, M., Gill, M. and Robertson, I. H. (2005) Association between dopamine transporter (DATI) genotype, left-sided inattention, and an enhanced response to methylphenidate in attention-deficit hyperactivity disorder. Neuropsychopharmacology, 30 12: 2290-2297. doi:10.1038/sj.npp.1300839 70   56 Cited 59 times in Scopus59 0
Kent, L., Green, E., Hawi, Z., Kirley, A., Dudbridge, F., Lowe, N., Raybould, R., Langley, K., Bray, N., Fitzgerald, M., Owen, M. J., O'Donovan, M. C., Gill, M., Thapar, A. and Craddock, N. (2005) Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. Molecular Psychiatry, 10 10: 939-943. doi:10.1038/sj.mp.4001696 51   74 Cited 78 times in Scopus78 0
Brookes, K. J., Hawi, Z., Kirley, A., Barry, E., Gill, M. and Kent, L. (2008) Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B 8: 1531-1535. doi:10.1002/ajmg.b.30873 44   34 Cited 35 times in Scopus35 1
Barry, Edwina, Hawi, Ziarih and Kirley, Aiveen (2007). Avenues for pharmacogenetic research in ADHD. In Michael Fitzgerald, Mark Bellgrove and Michael Gill (Ed.), (pp. 355-371) Hoboken, NJ, United States: John Wiley and Sons. 33  
Neale, Benjamin M., Medland, Sarah, Ripke, Stephan, Anney, Richard J. L., Asherson, Philip, Buitelaar, Jan, Franke, Barbara, Gill, Michael, Kent, Lindsey, Holmans, Peter, Middleton, Frank, Thapar, Anita, Lesch, Klaus-Peter, Faraone, Stephen V., Daly, Mark, Nguyen, Thuy Trang, Schafer, Helmut, Steinhausen, Hans-Christoph, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Walitza, Susanne, Freitag, Christine, Meyer, Jobst, Palmason, Haukur, Rothenberger, Aribert, Hawi, Ziarih, Sergeant, Joseph, Roeyers, Herbert, Mick, Eric and Biederman, Joseph (2010) Case-control genome-wide association study of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 49 9: 906-920. doi:10.1016/j.jaac.2010.06.007 57   57 Cited 62 times in Scopus62 0
Bellgrove, Mark A., Hawi, Ziarah, Kirley, Aiveen, Gill, Michael and Robertson, Ian H. (2005) Dissecting the attention deficit hyperactivity disorder (ADHD) phenotype: Sustained attention, response variability and spatial attentional asymmetries in relation to dopamine transporter (DAT1) genotype. Neuropsychologia, 43 13: 1847-1857. doi:10.1016/j.neuropsychologia.2005.03.011 107   106 Cited 113 times in Scopus113 0
Hawi, Ziarih, Matthews, Natasha, Wagner, Joseph, Wallace, Robyn H., Butler, Tim J., Vance, Alasdair, Kent, Lindsey, Gill, Michael and Bellgrove, Mark A. (2013) DNA variation in the SNAP25 gene confers risk to ADHD and is associated with reduced expression in prefrontal cortex. PLoS One, 8 4: e60274.1-e60274.8. doi:10.1371/journal.pone.0060274 27   2 Cited 5 times in Scopus5 1
Bellgrove, M. A., Chambers, C. D., Johnson, K. A., Daibhis, A., Daly, M., Hawi, Z., Lambert, D., Gill, M. and Robertson, I. H. (2007) Dopaminergic genotype biases spatial attention in healthy children. Molecular Psychiatry, 12 8: 786-792. doi:10.1038/sj.mp.4002022 72   32 Cited 34 times in Scopus34 0
Bellgrove, Mark A., Johnson, Katherine A., Barry, Edwina, Mulligan, Aisling, Hawi, Ziarah, Gill, Michael, Robertson, Ian and Chambers, Christopher D. (2009) Dopaminergic Haplotype as a Predictor of Spatial Inattention in Children With Attention-Deficit/Hyperactivity Disorder. Archives of General Psychiatry, 66 10: 1135-1142. doi:10.1001/archgenpsychiatry.2009.120 92   18 Cited 23 times in Scopus23 0
Cummins, T. R. D., Hawi, Z., Hocking, J., Strudwick, M., Hester, R., Garavan, H., Wagner, J., Chambers, C. D. and Bellgrove, M. A. (2012) Dopamine transporter genotype predicts behavioural and neural measures of response inhibition. Molecular Psychiatry, 17 11: 1086-1092. doi:10.1038/mp.2011.104 108   11 Cited 14 times in Scopus14 1
Bellgrove, M. A., Hawi, Z., Lowe, N., Kirley, A., Robertson, I. H. and Gill, M. (2005) DRD4 gene variants and sustained attention in attention deficit hyperactivity disorder (ADHD): Effects of associated alleles at the VNTR and-521 SNP. American Journal of Medical Genetics Part B-neuropsychiatric Genetics, 136B 1: 81-86. doi:10.1002/ajmg.b.30193 64   55 Cited 61 times in Scopus61 1
Segurado, Ricardo, Bellgrove, Mark A, Manconi, Francesca, Gill, Michael and Hawi, Ziarah (2011) Epistasis between neurochemical gene polymorphisms and risk for ADHD. European Journal of Human Genetics, 19 5: 577-582. doi:10.1038/ejhg.2010.250 44   6 Cited 5 times in Scopus5 0
Park, J,, Willmott, M., Vetuz, G., Toye, C., Kirley, A., Hawi, Z., Brookes, K. J., Gill, M, and Kent, L. (2010) Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 34 4: 697-702. doi:10.1016/j.pnpbp.2010.03.029 31   28 Cited 33 times in Scopus33 10
Braet, Wouter, Johnson, Katherine A., Tobin, Claire T., Acheson, Ruth, McDonnell, Caroline, Hawi, Ziarah, Barry, Edwina, Mulligan, Aisling, Gill, Michael, Bellgrove, Mark A., Robertson, Ian H. and Garavan, Hugh (2011) fMRI activation during response inhibition and error processing: The role of the DAT1 gene in typically developing adolescents and those diagnosed with ADHD. Neuropsychologia, 49 7: 1641-1650. doi:10.1016/j.neuropsychologia.2011.01.001 55   14 Cited 16 times in Scopus16 0
Hill, M., Anney, R. J., Gill, M. and Hawi, Z. (2010) Functional analysis of intron 8 and 3' UTR variable number of tandem repeats of SLC6A3: Differential activity of intron 8 variants. Pharmacogenomics Journal, 10 5: 442-447. doi:10.1038/tpj.2009.66 36   9 Cited 11 times in Scopus11 0
Williams, Nigel M., Franke, Barbara, Mick, Eric, Anney, Richard J. L., Freitag, Christine M., Gill, Michael, Thapar, Anita, O'Donovan, Michael C., Owen, Michael J., Holmans, Peter, Kent, Lindsey, Middleton, Frank, Zhang-James, Yanli, Liu, Lu, Meyer, Jobst, Nguyen, Thuy Trang, Romanos, Jasmin, Romanos, Marcel, Seitz, Christine, Renner, Tobias J., Walitza, Susanne, Warnke, Andreas, Palmason, Haukur, Buitelaar, Jan, Rommelse, Nanda, Vasquez, Arias, Hawi, Ziarih, Langley, Kate, Sergeant, Joseph, Steinhausen, Hans-Christoph, Roeyers, Herbert, Biederman, Joseph, Zaharieva, Irina, Hakonarson, Hakon, Elia, Josephine, Lionel, Anath C., Crosbie, Jennifer, Marshall, Christian R., Schachar, Russell, Scherer, Stephen W., Todorov, Alexandre, Smalley, Susan L., Loo, Sandra, Nelson, Stanley, Shtir, Corina, Asherson, Philip, Reif, Andreas, Lesch, Klaus-Peter and Faraone, Stephen V. (2011) Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. American Journal of Psychiatry, 169 2: 195-204. doi:10.1176/appi.ajp.2011.11060822 79   74 Cited 80 times in Scopus80 0
Alsaraj, F., O'Gorman, D., McAteer, S., McDermott, J., Hawi, Z. and Sreenan, S. (2010) Haplotype association of calpain 10 gene variants with type 2 diabetes mellitus in an Irish sample. Irish Journal of Medical Science, 179 2: 269-272. doi:10.1007/s11845-010-0462-x 26   4 Cited 5 times in Scopus5 0
Stjepanovic,D., Lorenzetti, V., Yücel, M., Hawi, Z. and Bellgrove, Mark A. (2013) Human amygdala volume is predicted by common DNA variation in the stathmin and serotonin transporter genes. Translational Psychiatry, 3 e283.1-e283.6. doi:10.1038/tp.2013.41 15   2 Cited 2 times in Scopus2 2
Bellgrove, M. A., Mattingley, J. B., Hawi, Z., Mullins, C., Kirley, A., Gill, M. and Robertson, I. H. (2006) Impaired temporal resolution of visual attention and dopamine beta hydroxylase genotype in attention-deficit/hyperactivity disorder. Biological Psychiatry, 60 10: 1039-1045. doi:10.1016/j.biopsych.2006.03.062 76   15 Cited 17 times in Scopus17 0
Stergiakouli, Evangelia, Hamshere, Marian, Holmans, Peter, Langley, Kate, Zaharieva, Irina, deCODE Genetics, Psychiatric GWAS Consortium: ADHD Subgroup, Hawi, Ziarah, Kent, Lindsey, Gill, Michael, Williams, Nigel, Owen, Michael J., O'Donovan, Michael and Thapar, Anita (2011) Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. American Journal of Psychiatry, 169 2: 1-9. doi:10.1176/appi.ajp.2011.11040551 55   49 Cited 57 times in Scopus57 7
Johnson, Katherine A., Barry, Edwina, Lambert, David, Fitzgerald, Michael, McNicholas, Fiona, Kirley, Aiveen, Gill, Michae, Bellgrove, Mark A. and Hawi, Ziarih (2013) Methylphenidate side effect profile is influenced by genetic variation in the attention-deficit/hyperactivity disorder-associated CES1 gene. Journal of Child and Adolescent Psychopharmacology, 23 10: 655-664. doi:10.1089/cap.2013.0032 5   1 Cited 1 times in Scopus1 0
Hawi, Ziarih and Lowe, Naomi (2007). Molecular genetic aspects of attention deficit hyperactivity disorder. In Michael Fitzgerald, Mark Bellgrove and Michael Gill (Ed.), Handbook of attention deficit hyperactivity disorder (pp. 129-149) Hoboken, NJ, United States: John Wiley and Sons. 28  
Cristino, A. S., Williams, S. M., Hawi, Z., An, J-Y, Bellgrove, M. A., Schwartz, C. E., Costa, L. da F. and Claudianos, C. (2014) Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system. Molecular Psychiatry, 19 3: 294-301. doi:10.1038/mp.2013.16 72   12 Cited 14 times in Scopus14 21
Sheehan, Karen, Hawi. Ziarih, Gill, Michael and Kent, Lindsey (2007) No association between TPH2 gene polymorphisms and ADHD in a UK sample. Neuroscience Letters, 412 2: 105-107. doi:10.1016/j.neulet.2006.10.043 37   14 Cited 15 times in Scopus15 0
Kim, Bung-Nyun, Kim, Jae-Won, Cummins, Tarrant D. R., Bellgrove, Mark A., Hawi, Ziarih, Hong, Soon-Beom, Yang, Young-Hui, Kim, Hyo-Jin, Shin, Min-Sup, Cho, Soo-Churl, Kim, Ji-Hoon, Son, Jung-Woo, Shin, Yun-Mi, Chung, Un-Sun and Han, Doug-Hyun (2013) Norepinephrine genes predict response time variability and methylphenidate-induced changes in neuropsychological function in attention deficit hyperactivity disorder. Journal of Clinical Psychopharmacology, 33 3: 356-362. doi:10.1097/JCP.0b013e31828f9fc3 36   4 Cited 6 times in Scopus6 2
Anney, Richard J. L., Hawi, Ziarih, Sheehan, Karen, Mulligan, Aisling, Pinto, Carlos, Brookes, Keeley J., Xu, Xiaohui, Zhou, Kaixin, Franke, Barbara, Buitelaar, Jan, Vermeulen, Sita H., Banaschewski, Tobias, Sonuga-Barke, Edmund, Ebstein, Richard, Manor, Iris, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rommelse, Nanda, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans-Christoph, Taylor, Eric, Thompson, Margaret, Asherson, Philip, 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, 147B 8: 1495-1500. doi:10.1002/ajmg.b.30659 44   15 Cited 15 times in Scopus15 0
Brookes K. J., Hawi, Z., Park, J., Scott, S., Gill, M. and Kent, L. (2010) Polymorphisms of the steroid sulfatase (STS) gene are associated with attention deficit hyperactivity disorder and influence brain tissue mRNA expression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 153B 8: 1417-1424. doi:10.1002/ajmg.b.31120 33   12 Cited 11 times in Scopus11 0
Hawi, Ziarih, Segurado, Ricardo, Conroy, Judith, Sheehan, Karen, Lowe, Naomi, Kirley, Aiveen, Shields, Denis, Fitzgerald, Michael, Gallagher, Louise and Gill, Michael (2005) Preferential Transmission of Paternal Alleles at Risk Genes in Attention-Deficit/Hyperactivity Disorder. The American Society of Human Genetics, 77 6: 958-965. doi:10.1086/498174 42   46 Cited 48 times in Scopus48 0
Yang, Mao S., Cochrane, Lynne, Conroy, Judith, Hawi, Ziarah, Fitzgerald, Michael, Gallagher, Louise and Gill, Michael (2007) Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population. Psychiatric Genetics, 17 1: 39-41. doi:10.1097/YPG.0b013e3280115428 23   6 Cited 5 times in Scopus5 0
Doyle, Christopher, Brookes, Keeley, Simpson, Keeley, Park, Joanne, Scott, Sarah, Coghill, David R., Hawi, Ziarah, Kirley, Aiveen, Gill, Michael and Kent, Lindsey (2009) Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder. Neuroscience Letters, 462 2: 179-181. doi:10.1016/j.neulet.2009.06.084 36   6 Cited 6 times in Scopus6 0
Xu, X., Hawi Z., Brookes, K. J., Anney, R., Bellgrove, M., Franke, B., Barry, E., Chen, W., Kuntsi, J., Banaschewski, T., Buitelaar, J., Ebstein, R., Fitzgerald, M., Miranda, A., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E., Steinhausen, H. C., Faraone, S. V., 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, 147B 8: 1564-1567. doi:10.1002/ajmg.b.30872 31   16 Cited 17 times in Scopus17 0
Bellgrove, Mark A, Barry, Edwina, Johnson, Katherine A., Cox, Marie, Daibhis, Aoife, Daly, Michael, Hawi, Ziarih, Lambert, David, Fitzgerald, Michael, McNicholas, Fiona, Robertson, Ian H., Gill, Michael and Kirley, Aiveen (2008) Spatial Attentional Bias as a Marker of Genetic Risk, Symptom Severity, and Stimulant Response in ADHD. Neuropsychopharmacology, 33 10: 2536-2545. doi:10.1038/sj.npp.1301637 90   20 Cited 24 times in Scopus24 0
Bellgrove, Mark A., Hawi, Ziarih, Gill, Michael and Robertson, Ian H. (2006) The cognitive genetics of attention deficit hyperactivity disorder (ADHD): Sustained attention as a candidate phenotype. Cortex, 42 6: 838-845. doi:10.1016/S0010-9452(08)70426-X 83   38 Cited 48 times in Scopus48 0
Bellgrove, M. A., Domschke, K., Hawi, Z., Kirley, A., Mullins, C., Robertson, I. H. and Gill, M. (2005) The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD. Experimental Brain Research, 163 3: 352-360. doi:10.1007/s00221-004-2180-y 91   49 Cited 55 times in Scopus55 0
Sheehan, K., Lowe, N., Kirley, A., Mullins, C., Fitzgerald, M., Gill, M. and Hawi, Z. (2005) Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD. Molecular Psychiatry, 10 10: 944-949. doi:10.1038/sj.mp.4001698 35   78 Cited 87 times in Scopus87 3