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Research Output 1990 2019

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2019
119 Citations (Scopus)

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Demontis, D., Walters, R. K., Martin, J., Manuel, M., Als, T., Agerbo, E., Baldursson, G., Belliveau, R., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Cerrato, F., Chambert, K., Churchhouse, C., Dumont, A., Eriksson, N., Gandal, M., Goldstein, J. I., Grasby, K. L., Grove, J., Gudmundsson, O. O. & 3 others, ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium & 23andMe Research Team, Jan 2019, In : Nature Genetics. 51, 1, 16 p.

Research output: Contribution to journalArticleResearchpeer-review

Intensity Matters: High-intensity Interval Exercise Enhances Motor Cortex Plasticity More Than Moderate Exercise

Andrews, S. C., Curtin, D., Hawi, Z., Wongtrakun, J., Stout, J. C. & Coxon, J. P., 1 May 2019, (Accepted/In press) In : Cerebral Cortex. 12 p., bhz075.

Research output: Contribution to journalArticleResearchpeer-review

The application of human pluripotent stem cells to model the neuronal and glial components of neurodevelopmental disorders

Lee, K. M., Hawi, Z. H., Parkington, H. C., Parish, C. L., Kumar, P. V., Polo, J. M., Bellgrove, M. A. & Tong, J., 27 Aug 2019, (Accepted/In press) In : Molecular Psychiatry. 11 p.

Research output: Contribution to journalArticleResearchpeer-review

2018

A case-control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene

Hawi, Z., Yates, H., Pinar, A., Arnatkeviciuteb, A., Johnson, B., Tong, J., Pugsley, K., Dark, C., Pauper, M., Klein, M., Heussler, H. S., Hiscock, H., Fornito, A., Tiego, J., Finlay, A., Vance, A., Gill, M., Kent, L. & Bellgrove, M. A., 18 Dec 2018, In : Translational Psychiatry. 8, 1, 8 p., 284.

Research output: Contribution to journalArticleResearchpeer-review

Open Access
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31 Citations (Scopus)

A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder

Martin, J., Walters, R. K., Demontis, D., Mattheisen, M., Lee, S. H., Robinson, E., Brikell, I., Ghirardi, L., Larsson, H., Lichtenstein, P., Eriksson, N., 23andMe Research Team, Psychiatric Genomics Consortium: ADHD Subgroup, iPSYCH–Broad ADHD Workgroup, Werge, T., Mortensen, P. B., Pedersen, M. G., Mors, O., Nordentoft, M., Hougaard, D. M. & 8 others, Bybjerg-Grauholm, J., Wray, N. R., Franke, B., Faraone, S. V., O'Donovan, M. C., Thapar, A., Børglum, A. D. & Neale, B. M., 15 Jun 2018, In : Biological Psychiatry. 83, 12, p. 1044-1053 10 p.

Research output: Contribution to journalArticleResearchpeer-review

Open Access
File
1 Citation (Scopus)

Genome-wide association study reveals novel genetic locus associated with intra-individual variability in response time

Pinar, A., Hawi, Z., Cummins, T., Johnson, B., Pauper, M., Tong, J., Tiego, J., Finlay, A., Klein, M., Franke, B., Fornito, A. & Bellgrove, M. A., 4 Oct 2018, In : Translational Psychiatry. 8, 1, 8 p., 207.

Research output: Contribution to journalArticleResearchpeer-review

Open Access
File
2017
2 Citations (Scopus)

Allelic variation in dopamine D2 receptor gene is associated with attentional impulsiveness on the Barratt Impulsiveness Scale (BIS-11)

Taylor, J. B., Cummins, T. D. R., Fox, A. M., Johnson, B. P., Tong, J. H., Visser, T. A. W., Hawi, Z. & Bellgrove, M., 20 Jan 2017, In : World Journal of Biological Psychiatry. 19, S2, p. S75-S83 9 p.

Research output: Contribution to journalArticleResearchpeer-review

7 Citations (Scopus)

Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study

Hawi, Z., Cummins, T. DR., Tong, J., Arcos-Burgos, M., Zhao, Q., Matthews, N., Newman, D. P., Johnson, B., Vance, A., Heussler, H. S., Levy, F., Easteal, S., Wray, N., Kenny, E., Morris, D., Kent, L., Gill, M. & Bellgrove, M. A., Apr 2017, In : Molecular Psychiatry. 22, p. 580-584 5 p.

Research output: Contribution to journalArticleResearchpeer-review

2016
19 Citations (Scopus)

Psychiatric gene discoveries shape evidence on ADHD's biology

Thapar, A., Martin, J., Mick, E., Arias Vásquez, A., Langley, K., Scherer, S. W., Schachar, R., Crosbie, J., Williams, N., Franke, B., Elia, J., Glessner, J., Hakonarson, H., IMAGE 2 Consortium, Owen, M. J., Faraone, S. V., O'Donovan, M. C. & Holmans, P., 1 Sep 2016, In : Molecular Psychiatry. 21, 9, p. 1202-1207 6 p.

Research output: Contribution to journalArticleResearchpeer-review

Open Access
4 Citations (Scopus)

Separating the wheat from the chaff: systematic identification of functionally relevant noncoding variants in ADHD

Tong, JHS., Hawi, Z., Dark, C., Cummins, TDR., Johnson, BP., Newman, DP., Lau, R., Vance, A., Heussler, HS., Matthews, N., Bellgrove, M. A. & Pang, KC., 1 Nov 2016, In : Molecular Psychiatry. 21, 11, p. 1589-1598 10 p.

Research output: Contribution to journalArticleResearchpeer-review

2015
14 Citations (Scopus)

An association between a dopamine transporter gene (SLC6A3) haplotype and ADHD symptom measures in nonclinical adults

Tong, J. H. S., Cummins, T., Johnson, B. P., McKinley, L-A., Pickering, H., Fanning, P., Stefanac, N., Newman, D. P., Hawi, Z. & Bellgrove, M. A., 2015, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 168, 2, p. 89 - 96 8 p.

Research output: Contribution to journalArticleResearchpeer-review

6 Citations (Scopus)

Identification and functional characterisation of a novel dopamine beta hydroxylase gene variant associated with attention deficit hyperactivity disorder

Tong, J. H. S., McKinley, L-A., Cummins, T., Johnson, B. P., Matthews, N. L., Vance, A. L. A., Heussler, H. S., Gill, M., Kent, L. S. W., Bellgrove, M. A. & Hawi, Z., 2015, In : World Journal of Biological Psychiatry. 16, 8, p. 610 - 618 9 p.

Research output: Contribution to journalArticleResearchpeer-review

2014
12 Citations (Scopus)

Alpha-2A adrenergic receptor gene variants are associated with increased intra-individual variability in response time

Cummins, T., Jacoby, O., Hawi, Z., Nandam, L. S., Byrne, M. A. V., Kim, B-N., Wagner, J., Chambers, C. D. & Bellgrove, M. A., 2014, In : Molecular Psychiatry. 19, p. 1031 - 1036 6 p.

Research output: Contribution to journalArticleResearchpeer-review

8 Citations (Scopus)

Dopamine transporter genotype is associated with a lateralized resistance to distraction during attention selection

Newman, D. P., Cummins, T., Tong, J. H. S., Johnson, B. P., Pickering, H., Fanning, P., Wagner, J., Goodrich, J. T. T., Hawi, Z., Chambers, C. D. & Bellgrove, M. A., 2014, In : Journal of Neuroscience. 34, 47, p. 15743 - 15750 8 p.

Research output: Contribution to journalArticleResearchpeer-review

96 Citations (Scopus)

Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system

Cristino, A. S., Williams, S. M., Hawi, Z., An, J. Y., Bellgrove, M. A., Schwartz, C. E., Costa, L. D. F. C. & Claudianos, C., 2014, In : Molecular Psychiatry. 19, 3, p. 294 - 301 8 p.

Research output: Contribution to journalArticleResearchpeer-review

2013
24 Citations (Scopus)

A high density linkage disequilibrium mapping in 14 noradrenergic genes: evidence of association between SLC6A2, ADRA1B and ADHD

Hawi, Z., Matthews, N., Barry, E., Kirley, A., Wagner, J., Wallace, R., Heussler, H. S., Vance, A. L. A., Gill, M. & Bellgrove, M. A., 2013, In : Psychopharmacology. 225, 4, p. 895 - 902 8 p.

Research output: Contribution to journalArticleResearchpeer-review

30 Citations (Scopus)

DNA variation in the SNAP25 gene confers risk to ADHD and Is associated with reduced expression in prefrontal cortex

Hawi, Z., Matthews, N., Wagner, J., Wallace, R., Butler, T. J., Vance, A. L. A., Kent, L. S. W., Gill, M. & Bellgrove, M. A., 2013, In : PLoS ONE. 8, 4 (Art. No. e60274 ), p. 1 - 8 8 p.

Research output: Contribution to journalArticleResearchpeer-review

Open Access
9 Citations (Scopus)

Human amygdala volume is predicted by common DNA variation in the stathmin and serotonin transporter genes

Stjepanovic, D., Lorenzetti, V., Yucel, M., Hawi, Z. & Bellgrove, M. A., 2013, In : Translational Psychiatry. 3, 3 (Art. No.: e283), p. 1 - 7 7 p.

Research output: Contribution to journalArticleResearchpeer-review

Open Access
17 Citations (Scopus)

Methylphenidate side effect profile is influenced by genetic variation in the attention-deficit/hyperactivity disorder-associated CES1 gene

Johnson, K. A., Barry, E., Lambert, D., Fitzgerald, M. F., McNicholas, F., Kirley, A., Gill, M., Bellgrove, M. A. & Hawi, Z., 2013, In : Journal of Child and Adolescent Psychopharmacology. 23, 10, p. 655 - 664 10 p.

Research output: Contribution to journalArticleResearchpeer-review

17 Citations (Scopus)

Norepinephrine genes predict response time variability and methylphenidate-induced changes in neuropsychological function in attention deficit hyperactivity disorder

Kim, B-N., Kim, J-W., Cummins, T. D., Bellgrove, M. A., Hawi, Z., Hong, S. B., Yang, Y. H., Kim, H. J., Shin, M. S., Cho, S-C., Kim, J. H., Son, J. W., Shin, Y. M., Chung, U. S. & Han, D. H., 2013, In : Journal of Clinical Psychopharmacology. 33, 3, p. 356 - 362 7 p.

Research output: Contribution to journalArticleResearchpeer-review

2012
40 Citations (Scopus)

Dopamine transporter genotype predicts behavioural and neural measures of response inhibition

Cummins, TDR., Hawi, Z., Hocking, J., Strudwick, M., Hester, R., Garavan, H., Wagner, J., Chambers, CD. & Bellgrove, MA., Nov 2012, In : Molecular Psychiatry. 17, 11, p. 1086-1092 7 p.

Research output: Contribution to journalArticleResearchpeer-review

162 Citations (Scopus)

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3

Williams, N. M. A., Franke, B., Mick, E. O., Anney, R. J., Freitag, C. M., Gill, M., Thapar, A., O'Donovan, M. C., Owen, M. J., Holmans, P. A., Kent, L. S. W., Middleton, F. A., Zhang-James, Y., Liu, L., Meyer, J. D., Nguyen, T. T., Romanos, J., Romanos, M., Seitz, C., Renner, T. J. & 29 others, Walitza, S., Warnke, A., Palmason, H. O., Buitelaar, J. K., Rommelse, N. N. J., Vasquez, A. A., Hawi, Z., Langley, K., Sergeant, J. A., Steinhausen, H. C., Roeyers, H., Biederman, J. J., Zaharieva, I. T., Hakonarson, H., Elia, J., Lionel, A. C., Crosbie, J., Marshall, C. R., Schachar, R., Scherer, S. W., Todorov, A. A., Smalley, S. L., Loo, S., Nelson, S. F., Shtir, C., Asherson, P. J., Reif, A., Lesch, K. P. & Faraone, S. V., 2012, In : American Journal of Psychiatry. 169, 2, p. 195 - 204 10 p.

Research output: Contribution to journalArticleResearchpeer-review

129 Citations (Scopus)

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD

Stergiakouli, E., Hamshere, M. L., Holmans, P. A., Langley, K., Zaharieva, I. T., Faraone, S. V., Neale, B. M., Ripke, S., Daly, M. J., Medland, S. E., Asherson, P. J., Franke, B., Steinhausen, H. C., Lesch, K. P., Freitag, C. M., Reif, A., Renner, T. J., Nguyen, T. T., Romanos, M., Romanos, J. & 38 others, Walitza, S., Schafer, H. H., Warnke, A., Meyer, J. D., Palmason, H. O., Buitelaar, J. K., Vasquez, A. A., Rommelse, N. N. J., Anney, R. J., Sergeant, J. A., Roeyers, H., Mick, E. O., Biederman, J. J., Doyle, A. E., Smalley, S. L., Loo, S., Hakonarson, H., Elia, J., Todorov, A. A., Miranda, A. L., Mulas, F., Ebstein, R. P., Rothenberger, A., Banaschewski, T., Oades, R. D., Sonuga-Barke, E. J. S., McGough, J. J., Nisenbaum, L. K., Hawi, Z., Owen, M. J., Gill, M., Middleton, F. A., Kent, L. S. W., Williams, N. M. A., Hu, X., O'Donovan, M. C., Nelson, S. F. & Thapar, A., 2012, In : American Journal of Psychiatry. 169, 2, p. 186 - 194 9 p.

Research output: Contribution to journalArticleResearchpeer-review

2011
1 Citation (Scopus)

Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation

Hill, M. J., Kenny, E. M., Roche, S., Morris, D. W., Corvin, A., Hawi, Z., Gill, M. & Anney, R. J., 2011, In : Psychiatric Genetics. 21, 6, p. 281 - 286 6 p.

Research output: Contribution to journalArticleResearchpeer-review

8 Citations (Scopus)

Epistasis between neurochemical gene polymorphisms and risk for ADHD

Segurado, R., Bellgrove, M., Manconi, F., Gill, M. & Hawi, Z., 2011, In : European Journal of Human Genetics. 19, 5, p. 577 - 582 6 p.

Research output: Contribution to journalArticleResearchpeer-review

37 Citations (Scopus)

fMRI activation during response inhibition and error processing: the role of the DAT1 gene in typically developing adolescents and those diagnosed with ADHD

Braet, W., Johnson, K., Tobin, C., Acheson, R., McDonnell, C., Hawi, Z., Barry, E., Mulligan, A., Gill, M., Bellgrove, M., Robertson, I. & Garavan, H., 2011, In : Neuropsychologia. 49, 7, p. 1641 - 1650 10 p.

Research output: Contribution to journalArticleResearchpeer-review

2010
25 Citations (Scopus)

ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype

Hawi, Z., Kent, L. S. W., Hill, M. J., Anney, R. J., Brookes, K. J., Barry, E., Franke, B., Banaschewski, T., Buitelaar, J. K., Ebstein, R. P., Miranda, A. L., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J. A., Sonuga-Barke, E. J. S., Steinhausen, H. C., Faraone, S. V., Asherson, P. J. & Gill, M., 2010, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 153, 1, p. 97 - 102 6 p.

Research output: Contribution to journalArticleResearchpeer-review

118 Citations (Scopus)

Case-control genome-wide association study of attention-deficit/ hyperactivity disorder

Neale, B. M., Medland, S. E., Ripke, S., Anney, R. J., Asherson, P. J., Buitelaar, J. K., Franke, B., Gill, M., Kent, L. S. W., Holmans, P. A., Middleton, F. A., Thapar, A., Lesch, K. P., Faraone, S. V., Daly, M. J., Nguyen, T. T., Schafer, H. H., Steinhausen, H. C., Reif, A., Renner, T. J. & 13 others, Romanos, M., Romanos, J., Warnke, A., Walitza, S., Freitag, C. M., Meyer, J. D., Palmason, H. O., Rothenberger, A., Hawi, Z., Sergeant, J. A., Roeyers, H., Mick, E. O. & Biederman, J. J., 2010, In : Journal of the American Academy of Child and Adolescent Psychiatry. 49, 9, p. 906 - 920 15 p.

Research output: Contribution to journalArticleResearchpeer-review

58 Citations (Scopus)

Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD

Park, J., Willmott, M., Vetuz, G. L., Toye, C., Kirley, A., Hawi, Z., Brookes, K. J., Gill, M. & Kent, L. S. W., 2010, In : Progress in Neuro-Psychopharmacology and Biological Psychiatry. 34, 4, p. 697 - 702 6 p.

Research output: Contribution to journalArticleResearchpeer-review

16 Citations (Scopus)

Functional analysis of intron 8 and 3' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants

Hill, M. J., Anney, R. J., Gill, M. & Hawi, Z., 2010, In : The Pharmacogenomics Journal. 10, 5, p. 442 - 447 6 p.

Research output: Contribution to journalArticleResearchpeer-review

6 Citations (Scopus)

Haplotype association of calpain 10 gene variants with type 2 diabetes mellitus in an Irish sample

Al Saraj, F., O'Gorman, D. J., McAteer, S., McDermott, J. H., Hawi, Z. & Sreenan, S. K., 2010, In : Irish Journal of Medical Science. 179, 2, p. 269 - 272 4 p.

Research output: Contribution to journalArticleResearchpeer-review

20 Citations (Scopus)

Polymorphisms of the steroid sulfatase (STS) gene are associated with attention deficit hyperactivity disorder and influence brain tissue mRNA expression

Brookes, K. J., Hawi, Z., Park, J., Scott, S. V., Gill, M. & Kent, L. S. W., 2010, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 153, 8, p. 1417 - 1424 8 p.

Research output: Contribution to journalArticleResearchpeer-review

2009
31 Citations (Scopus)

Dopaminergic haplotype as a predictor of spatial inattention in children with attention-deficit/hyperactivity disorder

Bellgrove, M. A., Johnson, K. A., Barry, E., Mulligan, A., Hawi, Z., Gill, M., Robertson, I. H. & Chambers, C. D., 2009, In : Archives of General Psychiatry. 66, 10, p. 1135 - 1142 8 p.

Research output: Contribution to journalArticleResearchpeer-review

11 Citations (Scopus)

Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder

Doyle, C., Brookes, K. J., Simpson, J., Park, J., Scott, S. V., Coghill, D. R., Hawi, Z., Kirley, A., Gill, M. & Kent, L. S. W., 2009, In : Neuroscience Letters. 462, 2, p. 179 - 181 3 p.

Research output: Contribution to journalArticleResearchpeer-review

2008
58 Citations (Scopus)

Absence of the 7-repeat variant of the DRD4 VNTR is associated with drifting sustained attention in children with ADHD but not in controls

Johnson, K. A., Kelly, S. P., Robertson, I. H., Barry, E., Mulligan, A., Daly, M., Lambert, D. B., McDonnell, C., Connor, T. J., Hawi, Z., Gill, M. & Bellgrove, M. A., 2008, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 147, 6, p. 927 - 937 11 p.

Research output: Contribution to journalArticleResearchpeer-review

7 Citations (Scopus)

Apolipoprotein e promoter polymorphisms (-491A/T and -427T/C) and Alzheimer's disease: No evidence of association in the Irish population

Lynch, C. A., Brazil, J. K., Cullen, B., Coakley, D. P., Gill, M., Lawlor, B. A. & Hawi, Z., 2008, In : Irish Journal of Medical Science. 177, 1, p. 29 - 33 5 p.

Research output: Contribution to journalArticleResearchpeer-review

51 Citations (Scopus)

Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder

Brookes, K. J., Hawi, Z., Kirley, A., Barry, E., Gill, M. & Kent, L. S. W., 2008, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 147, 8, p. 1531 - 1535 5 p.

Research output: Contribution to journalArticleResearchpeer-review

15 Citations (Scopus)

Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth

Brookes, K. J., Neale, B. M., Xu, X., Thapar, A., Gill, M., Langley, K., Hawi, Z., Mill, J. S., Taylor, E. T., Franke, B., Chen, W., Ebstein, R. P., Buitelaar, J. K., Banaschewski, T., Sonuga-Barke, E. J. S., Eisenberg, J., Manor, I., Miranda, A. L., Oades, R. D., Roeyers, H. & 5 others, Rothenberger, A., Sergeant, J. A., Steinhausen, H. C., Faraone, S. V. & Asherson, P. J., 2008, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 147, 1, p. 94 - 99 6 p.

Research output: Contribution to journalArticleResearchpeer-review

22 Citations (Scopus)

Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): Analysis of data from the international multicenter ADHD genetics (IMAGE) program

Anney, R. J., Hawi, Z., Sheehan, K., Mulligan, A., Pinto, C. M., Brookes, K. J., Xu, X., Zhou, K., Franke, B., Buitelaar, J. K., Vermeulen, S. H. H. M., Banaschewski, T., Sonuga-Barke, E. J. S., Ebstein, R. P., Manor, I., Miranda, A. L., Mulas, F., Oades, R. D., Roeyers, H., Rommelse, N. N. J. & 8 others, Rothenberger, A., Sergeant, J. A., Steinhausen, H. C., Taylor, E. T., Thompson, M. J. J., Asherson, P. J., Faraone, S. V. & Gill, M., 2008, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 147, 8, p. 1495 - 1500 6 p.

Research output: Contribution to journalArticleResearchpeer-review

23 Citations (Scopus)

Replication of a rare protective allele in the noradrenaline transporter gene and ADHD

Xu, X., Hawi, Z., Brookes, K. J., Anney, R. J., Bellgrove, M. A., Franke, B., Barry, E., Chen, W., Kuntsi, J., Banaschewski, T., Buitelaar, J. K., Ebstein, R. P., Fitzgerald, M. F., Miranda, A. L., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J. A., Sonuga-Barke, E., Steinhausen, H. C. & 3 others, Faraone, S. V., Gill, M. & Asherson, P. J., 2008, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 147, 8, p. 1564 - 1567 4 p.

Research output: Contribution to journalArticleResearchpeer-review

28 Citations (Scopus)

Spatial attentional bias as a marker of genetic risk, symptom severity, and stimulant response in ADHD

Bellgrove, M. A., Barry, E., Johnson, K. A., Cox, M. A., Daibhis, A., Daly, M., Hawi, Z., Lambert, D. B., Fitzgerald, M. F., McNicholas, F., Robertson, I. H., Gill, M. & Kirley, A., 2008, In : Neuropsychopharmacology. 33, 10, p. 2536 - 2545 10 p.

Research output: Contribution to journalArticleResearchpeer-review

2007
44 Citations (Scopus)

Dopaminergic genotype biases spatial attention in healthy children

Bellgrove, MA., Chambers, C. D., Johnson, K. A., Daibhis, A., Daly, M., Barry, E., Hawi, Z., Lambert, D., Gill, M. & Robertson, I. H., 2007, In : Molecular Psychiatry. 12, 8, p. 786-792 7 p.

Research output: Contribution to journalArticleResearchpeer-review

17 Citations (Scopus)

No association between TPH2 gene polymorphisms and ADHD in a UK sample

Sheehan, K., Hawi, Z., Gill, M. & Kent, L., 29 Jan 2007, In : Neuroscience Letters. 412, 2, p. 105-107 3 p.

Research output: Contribution to journalArticleResearchpeer-review

5 Citations (Scopus)

Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population

Yang, M. S., Cochrane, L., Conroy, J., Hawi, Z., Fitzgerald, M. F., Gallagher, L. & Gill, M., Feb 2007, In : Psychiatric Genetics. 17, 1, p. 39-41 3 p.

Research output: Contribution to journalArticleResearchpeer-review

2006
19 Citations (Scopus)

Impaired temporal resolution of visual attention and dopamine beta hydroxylase genotype in attention-deficit/hyperactivity disorder

Bellgrove, M. A., Mattingley, J. B., Hawi, Z., Mullins, C., Kirley, A., Gill, M. & Robertson, I. H., 2006, In : Biological Psychiatry. 60, 10, p. 1039 - 1045 7 p.

Research output: Contribution to journalArticleResearchpeer-review

70 Citations (Scopus)

The Cognitive Genetics of Attention Deficit Hyperactivity Disorder (ADHD): Sustained attention as a Candidate Phenotype

Bellgrove, M. A., Hawi, Z., Gill, M. & Robertson, I. H., 2006, In : Cortex. 42, p. 838 - 845 8 p.

Research output: Contribution to journalArticleResearchpeer-review

2005
62 Citations (Scopus)

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

Domschke, K., Sheehan, K., Lowe, N., Kirley, A., Mullins, C., O'Sullivan, R., Freitag, C., Becker, T., Conroy, J., Fitzgerald, M., Gill, M. & Hawi, Z., 5 Apr 2005, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 134 B, 1, p. 110-114 5 p.

Research output: Contribution to journalArticleResearchpeer-review

75 Citations (Scopus)

Association between dopamine transporter (DAT1) genotype, left-sided inattention, and an enhanced response to methylphenidate in attention-deficit hyperactivity disorder

Bellgrove, M. A., Hawi, Z., Kirley, A., Fitzgerald, M., Gill, M. & Robertson, I. H., Dec 2005, In : Neuropsychopharmacology. 30, 12, p. 2290-2297 8 p.

Research output: Contribution to journalArticleResearchpeer-review

97 Citations (Scopus)

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

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. & Craddock, N., Oct 2005, In : Molecular Psychiatry. 10, 10, p. 939-943 5 p.

Research output: Contribution to journalArticleResearchpeer-review

149 Citations (Scopus)

Dissecting the attention deficit hyperactivity disorder (ADHD) phenotype: Sustained attention, response variability and spatial attentional asymmetries in relation to dopamine transporter (DAT1) genotype

Bellgrove, M. A., Hawi, Z., Kirley, A., Gill, M. & Robertson, I. H., 2005, In : Neuropsychologia. 43, 13, p. 1847-1857 11 p.

Research output: Contribution to journalArticleResearchpeer-review