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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 222   24 Cited 29 times in Scopus29 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 42   12 Cited 13 times in Scopus13 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. 74  
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 74 1 7 Cited 9 times in Scopus9 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 72 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 31   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 51   Cited 4 times in Scopus4 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 25   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 66   45 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 68   55 Cited 58 times in Scopus58 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 50   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 42   33 Cited 34 times in Scopus34 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. 32  
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 56   50 Cited 57 times in Scopus57 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.2005.03.011 105   103 Cited 109 times in Scopus109 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 4 times in Scopus4 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 69   30 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 90   16 Cited 22 times in Scopus22 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.2011.104 107   8 Cited 13 times in Scopus13 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 61   55 Cited 60 times in Scopus60 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   5 Cited 4 times in Scopus4 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 31 times in Scopus31 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 53   13 Cited 14 times in Scopus14 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 35   7 Cited 9 times in Scopus9 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 77   67 Cited 71 times in Scopus71 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 24   4 Cited 4 times in Scopus4 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   0 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 74   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 54   42 Cited 48 times in Scopus48 8
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. 26  
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 68   9 Cited 10 times in Scopus10 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 35   13 Cited 13 times in Scopus13 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 34   3 Cited 4 times in Scopus4 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 43   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 31   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 36   46 Cited 47 times in Scopus47 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 21   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 34   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 30   16 Cited 16 times in Scopus16 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 87   18 Cited 21 times in Scopus21 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 80   38 Cited 47 times in Scopus47 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 86   49 Cited 53 times in Scopus53 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 34   77 Cited 84 times in Scopus84 3