| Year |
Citation |
Score |
| 2022 |
Trubetskoy V, Pardiñas AF, Qi T, Panagiotaropoulou G, Awasthi S, Bigdeli TB, Bryois J, Chen CY, Dennison CA, Hall LS, Lam M, Watanabe K, Frei O, Ge T, Harwood JC, ... ... Gill M, et al. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. PMID 35396580 DOI: 10.1038/s41586-022-04434-5 |
0.303 |
|
| 2021 |
Gill MJ, Andreychik MR, Getty PD. Those who ignore the past are doomed…to be heartless: Lay historicist theory is associated with humane responses to the struggles and transgressions of others. Plos One. 16: e0246882. PMID 33606759 DOI: 10.1371/journal.pone.0246882 |
0.734 |
|
| 2020 |
Holland JF, Cosgrove D, Whitton L, Harold D, Corvin A, Gill M, Mothersill DO, Morris DW, Donohoe G. Effects of complement gene-set polygenic risk score on brain volume and cortical measures in patients with psychotic disorders and healthy controls. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 32918526 DOI: 10.1002/Ajmg.B.32820 |
0.389 |
|
| 2020 |
Rokita KI, Dauvermann MR, Mothersill D, Holleran L, Holland J, Costello L, Cullen C, Kane R, McKernan D, Morris DW, Kelly J, Gill M, Corvin A, Hallahan B, McDonald C, et al. Childhood trauma, parental bonding, and social cognition in patients with schizophrenia and healthy adults. Journal of Clinical Psychology. PMID 32783219 DOI: 10.1002/Jclp.23023 |
0.305 |
|
| 2020 |
Satterstrom FK, Kosmicki JA, Wang J, Breen MS, De Rubeis S, An JY, Peng M, Collins R, Grove J, Klei L, Stevens C, Reichert J, Mulhern MS, Artomov M, Gerges S, ... ... Gill M, et al. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism. Cell. PMID 31981491 DOI: 10.1016/J.Cell.2019.12.036 |
0.344 |
|
| 2020 |
Foley C, Heron EA, Harold D, Walters J, Owen M, O'Donovan M, Sebat J, Kelleher E, Mooney C, Durand A, Pinto C, Cormican P, Morris D, Donohoe G, Gill M, et al. Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study. The British Journal of Psychiatry : the Journal of Mental Science. 1-5. PMID 31964429 DOI: 10.1192/Bjp.2019.262 |
0.384 |
|
| 2019 |
Lei D, Pinaya WHL, van Amelsvoort T, Marcelis M, Donohoe G, Mothersill DO, Corvin A, Gill M, Vieira S, Huang X, Lui S, Scarpazza C, Young J, Arango C, Bullmore E, et al. Detecting schizophrenia at the level of the individual: relative diagnostic value of whole-brain images, connectome-wide functional connectivity and graph-based metrics. Psychological Medicine. 1-10. PMID 31391132 DOI: 10.1017/S0033291719001934 |
0.32 |
|
| 2019 |
Holland JF, Cosgrove D, Whitton L, Harold D, Corvin A, Gill M, Mothershill D, Morris DW, Donohoe G. Beyond C4: Analysis Of The Complement Gene Pathway Shows Enrichment For IQ In Patients With Psychotic Disorders And Healthy Controls. Genes, Brain, and Behavior. e12602. PMID 31385409 DOI: 10.1111/Gbb.12602 |
0.38 |
|
| 2019 |
Lam M, Hill WD, Trampush JW, Yu J, Knowles E, Davies G, Stahl E, Huckins L, Liewald DC, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, DeRosse P, ... ... Gill M, et al. Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. American Journal of Human Genetics. 105: 334-350. PMID 31374203 DOI: 10.1016/J.Ajhg.2019.06.012 |
0.366 |
|
| 2019 |
Baker E, Sims R, Leonenko G, Frizzati A, Harwood JC, Grozeva D, Morgan K, Passmore P, Holmes C, Powell J, ... ... Gill M, et al. Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease. Plos One. 14: e0218111. PMID 31283791 DOI: 10.1371/Journal.Pone.0218111 |
0.338 |
|
| 2019 |
Sanfeliu A, Kaufmann WE, Gill M, Guasoni P, Tropea D. Transcriptomic Studies in Mouse Models of Rett Syndrome: A Review. Neuroscience. PMID 31229631 DOI: 10.1016/J.Neuroscience.2019.06.013 |
0.323 |
|
| 2019 |
Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Trubetskoy V, Mattheisen M, Wang Y, Coleman JRI, Gaspar HA, de Leeuw CA, Steinberg S, Pavlides JMW, Trzaskowski M, Byrne EM, ... ... Gill M, et al. Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics. PMID 31043756 DOI: 10.1038/S41588-019-0397-8 |
0.392 |
|
| 2019 |
Harold D, Connolly S, Riley BP, Kendler KS, McCarthy SE, McCombie WR, Richards A, Owen MJ, O'Donovan MC, Walters J, Donohoe G, Gill M, Corvin A, et al. Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 30801977 DOI: 10.1002/Ajmg.B.32716 |
0.375 |
|
| 2019 |
Rokita K, Dauvermann MR, Mothersill D, Holleran L, Holland J, Costello L, O’Donoghue C, Cullen C, Daly-Ryan N, McDonald C, Hallahan B, Corvin A, Gill M, Donohoe G. S4. Childhood Trauma And Social Cognition In Schizophrenia Schizophrenia Bulletin. 45. DOI: 10.1093/Schbul/Sbz020.549 |
0.311 |
|
| 2019 |
Donohoe G, Holland J, Mothersill D, Corvin A, Gill M, Cosgrove D, Morris D. Su121Genetic Variation Related To Immune Function And Schizophrenia Risk: Evidence For Effects On Cognition European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.485 |
0.322 |
|
| 2019 |
Flynn M, Whitton L, Corvin A, Gill M, Donohoe G, Morrison C, Morris D. F125A Molecular Analysis Of Sdccag8, A Schizophrenia Risk Gene That Is Required For Efficient Primary Ciliogenesis European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.205 |
0.342 |
|
| 2019 |
Riley B, Corvin A, Stefansson H, Kenny E, Morris D, Donohoe G, Waddington J, Webb B, Bacanu S, Gill M, Kendler K, Stefansson K. F122Whole Genome Sequencing Of Schizophrenia In Ireland European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.202 |
0.306 |
|
| 2019 |
Hubbard L, Rees E, Morris D, Lynham A, Legge S, Harold D, Zammit S, Corvin A, Gill M, O'Donovan M, Owen M, Donohoe G, Kirov G, Pocklington A, Walters JTR. 43Rare Copy Number Variations Are Associated With Poorer Cognition In Schizophrenia European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.050 |
0.348 |
|
| 2019 |
Hawi Z, Yates H, Kent L, Gill M, Bellgrove M. A CASE-CONTROL GENOME WIDE ASSOCIATION STUDY OF CHILDHOOD ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD) European Neuropsychopharmacology. 29: S956. DOI: 10.1016/J.Euroneuro.2017.08.311 |
0.417 |
|
| 2019 |
Donohoe G, Cosgrove D, Motherills D, Harold D, Kelly S, Holleran L, Holland J, Anney R, Richards A, Owen M, O'Donovan M, Gill M, Corvin A, Morris D. Genetic Risk Variants Interacting With MIR137: Effects On Cognition, Brain Structure And Brain Function In Patients And Healthy Participants European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.06.051 |
0.359 |
|
| 2019 |
Holland J, Cosgrove D, Harold D, Whitton L, Corvin A, Gill M, Mothershill D, Morris D, Donohoe G. O51. Beyond C4: Analysis of the Complement Gene Pathway Shows Enrichment for IQ in Patients With Schizophrenia and Healthy Controls Biological Psychiatry. 85. DOI: 10.1016/J.Biopsych.2019.03.316 |
0.325 |
|
| 2018 |
Hawi Z, Yates H, Pinar A, Arnatkeviciute A, Johnson B, Tong J, Pugsley K, Dark C, Pauper M, Klein M, Heussler HS, Hiscock H, Fornito A, Tiego J, Finlay A, ... ... Gill M, et al. A case-control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene. Translational Psychiatry. 8: 284. PMID 30563984 DOI: 10.1038/S41398-018-0329-X |
0.41 |
|
| 2018 |
Maguire Á, Hargreaves A, Gill M. Coenzyme Q10 and neuropsychiatric and neurological disorders: relevance for schizophrenia. Nutritional Neuroscience. 1-14. PMID 30537908 DOI: 10.1080/1028415X.2018.1556481 |
0.33 |
|
| 2018 |
Kooij JJS, Bijlenga D, Salerno L, Jaeschke R, Bitter I, Balázs J, Thome J, Dom G, Kasper S, Nunes Filipe C, Stes S, Mohr P, Leppämäki S, Casas Brugué M, Bobes J, ... ... Gill M, et al. Updated European Consensus Statement on diagnosis and treatment of adult ADHD. European Psychiatry : the Journal of the Association of European Psychiatrists. 56: 14-34. PMID 30453134 DOI: 10.1016/J.Eurpsy.2018.11.001 |
0.307 |
|
| 2018 |
Rees E, Carrera N, Morgan J, Hambridge K, Escott-Price V, Pocklington AJ, Richards AL, Pardiñas AF, McDonald C, Donohoe G, Morris DW, Kenny E, Kelleher E, Gill M, et al. Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis. Biological Psychiatry. PMID 30420267 DOI: 10.1016/J.Biopsych.2018.08.022 |
0.328 |
|
| 2018 |
Savage JE, Jansen PR, Stringer S, Watanabe K, Bryois J, de Leeuw CA, Nagel M, Awasthi S, Barr PB, Coleman JRI, Grasby KL, Hammerschlag AR, Kaminski JA, Karlsson R, Krapohl E, ... ... Gill M, et al. Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. Nature Genetics. PMID 29942086 DOI: 10.1038/S41588-018-0152-6 |
0.399 |
|
| 2018 |
Davies G, Lam M, Harris SE, Trampush JW, Luciano M, Hill WD, Hagenaars SP, Ritchie SJ, Marioni RE, Fawns-Ritchie C, Liewald DCM, Okely JA, Ahola-Olli AV, Barnes CLK, Bertram L, ... ... Gill M, et al. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nature Communications. 9: 2098. PMID 29844566 DOI: 10.1038/S41467-018-04362-X |
0.33 |
|
| 2018 |
Wray NR, Ripke S, Mattheisen M, Trzaskowski M, Byrne EM, Abdellaoui A, Adams MJ, Agerbo E, Air TM, Andlauer TMF, Bacanu SA, Bækvad-Hansen M, Beekman AFT, Bigdeli TB, Binder EB, ... ... Gill M, et al. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics. PMID 29700475 DOI: 10.1038/S41588-018-0090-3 |
0.341 |
|
| 2018 |
Cosgrove D, Mothersill DO, Whitton L, Harold D, Kelly S, Holleran L, Holland J, Anney R, Richards A, Mantripragada K, Owen M, O'Donovan MC, Gill M, Corvin A, et al. Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 29418072 DOI: 10.1002/Ajmg.B.32620 |
0.321 |
|
| 2018 |
Donohoe G, Holland J, Mothersill D, McCarthy-Jones S, Cosgrove D, Harold D, Richards A, Mantripragada K, Owen MJ, O'Donovan MC, Gill M, Corvin A, Morris DW. Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation. Psychological Medicine. 1-10. PMID 29310738 DOI: 10.1017/S0033291717002987 |
0.303 |
|
| 2018 |
Maguire Á, Hargreaves A, Gill M. S83. The Impact Of Coenzyme Q10 On The Cognitive Deficits And Symptoms Of Schizophrenia: Protocol And Baseline Data Of A Randomised, Placebo-Controlled Study Schizophrenia Bulletin. 44. DOI: 10.1093/Schbul/Sby018.870 |
0.342 |
|
| 2017 |
Lam M, Trampush JW, Yu J, Knowles E, Davies G, Liewald DC, Starr JM, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, DeRosse P, Lundervold AJ, Steen VM, ... ... Gill M, et al. Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. Cell Reports. 21: 2597-2613. PMID 29186694 DOI: 10.1016/J.Celrep.2017.11.028 |
0.36 |
|
| 2017 |
Kelly S, Jahanshad N, Zalesky A, Kochunov P, Agartz I, Alloza C, Andreassen OA, Arango C, Banaj N, Bouix S, Bousman CA, Brouwer RM, Bruggemann J, Bustillo J, Cahn W, ... ... Gill M, et al. Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group. Molecular Psychiatry. PMID 29038599 DOI: 10.1038/Mp.2017.170 |
0.354 |
|
| 2017 |
Blokland GAM, Del Re EC, Mesholam-Gately RI, Jovicich J, Trampush JW, Keshavan MS, DeLisi LE, Walters JTR, Turner JA, Malhotra AK, Lencz T, Shenton ME, Voineskos AN, Rujescu D, Giegling I, ... ... Gill M, et al. The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project. Schizophrenia Research. PMID 28982554 DOI: 10.1016/J.Schres.2017.09.024 |
0.364 |
|
| 2017 |
Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... ... Gill M, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916 |
0.344 |
|
| 2017 |
Cosgrove D, Mothersill O, Kendall K, Konte B, Harold D, Giegling I, Hartmann A, Richards A, Mantripragada K, Owen MJ, O'Donovan MC, Gill M, Rujescu D, Walters J, Corvin A, et al. Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 28607492 DOI: 10.1038/Npp.2017.123 |
0.405 |
|
| 2017 |
Walton E, Hibar DP, van Erp TGM, Potkin SG, Roiz-Santiañez R, Crespo-Facorro B, Suarez-Pinilla P, van Haren NEM, de Zwarte SMC, Kahn RS, Cahn W, Doan NT, Jørgensen KN, Gurholt TP, Agartz I, ... ... Gill M, et al. Prefrontal cortical thinning links to negative symptoms in schizophrenia via the ENIGMA consortium. Psychological Medicine. 1-13. PMID 28545597 DOI: 10.1017/S0033291717001283 |
0.335 |
|
| 2017 |
Walton E, Hibar DP, van Erp TG, Potkin SG, Roiz-Santiañez R, Crespo-Facorro B, Suarez-Pinilla P, Van Haren NE, de Zwarte SM, Kahn RS, Cahn W, Doan NT, Jørgensen KN, Gurholt TP, Agartz I, ... ... Gill M, et al. Positive symptoms associate with cortical thinning in the superior temporal gyrus via the ENIGMA Schizophrenia consortium. Acta Psychiatrica Scandinavica. PMID 28369804 DOI: 10.1111/Acps.12718 |
0.309 |
|
| 2017 |
Bigdeli TB, Ripke S, Peterson RE, Trzaskowski M, Bacanu SA, Abdellaoui A, Andlauer TF, Beekman AT, Berger K, Blackwood DH, Boomsma DI, Breen G, Buttenschøn HN, Byrne EM, Cichon S, ... ... Gill M, et al. Genetic effects influencing risk for major depressive disorder in China and Europe. Translational Psychiatry. 7: e1074. PMID 28350396 DOI: 10.1038/Tp.2016.292 |
0.396 |
|
| 2017 |
Cosgrove D, Harold D, Mothersill O, Anney R, Hill MJ, Bray NJ, Blokland G, Petryshen T, Richards A, Mantripragada K, Owen M, O'Donovan MC, Gill M, Corvin A, et al. MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls. Translational Psychiatry. 7: e1012. PMID 28117840 DOI: 10.1038/Tp.2016.286 |
0.366 |
|
| 2017 |
Giegling I, Hosak L, Mössner R, Serretti A, Bellivier F, Claes S, Collier DA, Corrales A, DeLisi LE, Gallo C, Gill M, Kennedy JL, Leboyer M, Maier W, Marquez M, et al. Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 1-14. PMID 28112043 DOI: 10.1080/15622975.2016.1268715 |
0.36 |
|
| 2017 |
Trampush JW, Yang ML, Yu J, Knowles E, Davies G, Liewald DC, Starr JM, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, DeRosse P, Lundervold AJ, Steen VM, ... ... Gill M, et al. GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. Molecular Psychiatry. PMID 28093568 DOI: 10.1038/Mp.2016.244 |
0.381 |
|
| 2017 |
Gill M, Corvin A, Daly M, Sullivan P, Levinson D. PGC3 AIM 6 - Large Scale Wgs of Multiply Affected Pedigrees European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.459 |
0.386 |
|
| 2017 |
Sullivan P, Levinson D, Gill M. The Science of The Psychiatric Genomics Consortium (Part 1) European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.377 |
0.333 |
|
| 2016 |
Mothersill O, Tangney N, Morris DW, McCarthy H, Frodl T, Gill M, Corvin A, Donohoe G. Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia. Schizophrenia Research. PMID 27913157 DOI: 10.1016/J.Schres.2016.11.043 |
0.325 |
|
| 2016 |
Whitton L, Cosgrove D, Clarkson C, Harold D, Kendall K, Richards A, Mantripragada K, Owen MJ, O'Donovan MC, Walters J, Hartmann A, Konte B, Rujescu D, Gill M, et al. Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 27762073 DOI: 10.1002/Ajmg.B.32503 |
0.422 |
|
| 2016 |
Fabbri C, Hosak L, Mössner R, Giegling I, Mandelli L, Bellivier F, Claes S, Collier DA, Corrales A, Delisi LE, Gallo C, Gill M, Kennedy JL, Leboyer M, Lisoway A, et al. Consensus paper of the WFSBP Task Force on Genetics: Genetics, epigenetics and gene expression markers of major depressive disorder and antidepressant response. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 1-24. PMID 27603714 DOI: 10.1080/15622975.2016.1208843 |
0.337 |
|
| 2016 |
Roessner V, Banaschewski T, Becker A, Buse J, Wanderer S, Buitelaar JK, Sergeant JA, Sonuga-Barke EJ, Gill M, Manor I, Miranda A, Mulas F, Oades RD, Roeyers H, Steinhausen HC, et al. Familiality of Co-existing ADHD and Tic Disorders: Evidence from a Large Sibling Study. Frontiers in Psychology. 7: 1060. PMID 27486412 DOI: 10.3389/Fpsyg.2016.01060 |
0.335 |
|
| 2016 |
Hawi Z, Cummins TD, Tong J, Arcos-Burgos M, Zhao Q, Matthews N, Newman DP, Johnson B, Vance A, Heussler HS, Levy F, Easteal S, Wray NR, Kenny E, Morris D, ... ... Gill M, et al. Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study. Molecular Psychiatry. PMID 27457811 DOI: 10.1038/Mp.2016.117 |
0.393 |
|
| 2016 |
Tropea D, Molinos I, Petit E, Bellini S, Nagakura I, O'Tuathaigh C, Schorova L, Mitchell KJ, Waddington J, Sur M, Gill M, Corvin AP. Disrupted in schizophrenia 1 (DISC1) L100P mutants have impaired activity-dependent plasticity in vivo and in vitro. Translational Psychiatry. 6: e712. PMID 26756905 DOI: 10.1038/Tp.2015.206 |
0.343 |
|
| 2015 |
Wetterling F, McCarthy H, Tozzi L, Skokauskas N, O'Doherty JP, Mulligan A, Meaney J, Fagan AJ, Gill M, Frodl T. Impaired reward processing in the human prefrontal cortex distinguishes between persistent and remittent attention deficit hyperactivity disorder. Human Brain Mapping. PMID 26287509 DOI: 10.1002/Hbm.22944 |
0.329 |
|
| 2015 |
Lee SH, Byrne EM, Hultman CM, Kähler A, Vinkhuyzen AA, Ripke S, Andreassen OA, Frisell T, Gusev A, Hu X, Karlsson R, Mantzioris VX, McGrath JJ, Mehta D, Stahl EA, ... ... Gill M, et al. New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology. PMID 26286434 DOI: 10.1093/Ije/Dyv136 |
0.36 |
|
| 2015 |
Tozzi L, Carballedo A, Wetterling F, McCarthy H, O'Keane V, Gill M, Morris D, Fahey C, Meaney J, Frodl T. Single-Nucleotide Polymorphism of the FKBP5 Gene and Childhood Maltreatment as Predictors of Structural Changes in Brain Areas Involved in Emotional Processing in Depression. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 26076833 DOI: 10.1038/Npp.2015.170 |
0.366 |
|
| 2015 |
Tong J, McKinley LA, Cummins TD, Johnson B, Matthews N, Vance A, Heussler H, Gill M, Kent L, Bellgrove MA, Hawi Z. Identification and functional characterisation of a novel dopamine beta hydroxylase gene variant associated with attention deficit hyperactivity disorder. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 1-9. PMID 25975715 DOI: 10.3109/15622975.2015.1036771 |
0.359 |
|
| 2015 |
Trampush JW, Lencz T, Knowles E, Davies G, Guha S, Pe'er I, Liewald DC, Starr JM, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, Mukherjee S, DeRosse P, ... ... Gill M, et al. Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 168: 363-73. PMID 25951819 DOI: 10.1002/Ajmg.B.32319 |
0.345 |
|
| 2015 |
Hung CF, Breen G, Czamara D, Corre T, Wolf C, Kloiber S, Bergmann S, Craddock N, Gill M, Holsboer F, Jones L, Jones I, Korszun A, Kutalik Z, Lucae S, et al. A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder. Bmc Medicine. 13: 86. PMID 25903154 DOI: 10.1186/S12916-015-0334-3 |
0.307 |
|
| 2015 |
Jun G, Ibrahim-Verbaas CA, Vronskaya M, Lambert JC, Chung J, Naj AC, Kunkle BW, Wang LS, Bis JC, Bellenguez C, Harold D, Lunetta KL, Destefano AL, Grenier-Boley B, Sims R, ... ... Gill M, et al. A novel Alzheimer disease locus located near the gene encoding tau protein. Molecular Psychiatry. PMID 25778476 DOI: 10.1038/Mp.2015.23 |
0.354 |
|
| 2015 |
Ferentinos P, Koukounari A, Power R, Rivera M, Uher R, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Ising M, Maier W, Mors O, et al. Familiality and SNP heritability of age at onset and episodicity in major depressive disorder. Psychological Medicine. 1-11. PMID 25698070 DOI: 10.1017/S0033291715000215 |
0.345 |
|
| 2015 |
Frodl T, Szyf M, Carballedo A, Gill M, Booij L. Integrated Functional Imaging and Genetics in Depression and Anxiety European Psychiatry. 30: 119. DOI: 10.1016/S0924-9338(15)30099-7 |
0.323 |
|
| 2014 |
Merikangas AK, Segurado R, Heron EA, Anney RJ, Paterson AD, Cook EH, Pinto D, Scherer SW, Szatmari P, Gill M, Corvin AP, Gallagher L. The phenotypic manifestations of rare genic CNVs in autism spectrum disorder. Molecular Psychiatry. PMID 25421404 DOI: 10.1038/Mp.2014.150 |
0.358 |
|
| 2014 |
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, ... ... Gill M, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 515: 209-15. PMID 25363760 DOI: 10.1038/Nature13772 |
0.305 |
|
| 2014 |
Smith TF, Anastopoulos AD, Garrett ME, Arias-Vasquez A, Franke B, Oades RD, Sonuga-Barke E, Asherson P, Gill M, Buitelaar JK, Sergeant JA, Kollins SH, Faraone SV, Ashley-Koch A. Angiogenic, neurotrophic, and inflammatory system SNPs moderate the association between birth weight and ADHD symptom severity. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 691-704. PMID 25346392 DOI: 10.1002/Ajmg.B.32275 |
0.353 |
|
| 2014 |
Rose EJ, Morris DW, Fahey C, Cannon D, McDonald C, Scanlon C, Kelly S, Gill M, Corvin A, Donohoe G. The miR-137 schizophrenia susceptibility variant rs1625579 does not predict variability in brain volume in a sample of schizophrenic patients and healthy individuals. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 467-71. PMID 25044277 DOI: 10.1002/Ajmg.B.32249 |
0.324 |
|
| 2014 |
Gill MJ, Andreychik MR. The Social Explanatory Styles Questionnaire: assessing moderators of basic social-cognitive phenomena including spontaneous trait inference, the fundamental attribution error, and moral blame. Plos One. 9: e100886. PMID 25007152 DOI: 10.1371/Journal.Pone.0100886 |
0.722 |
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| 2014 |
Merikangas AK, Segurado R, Cormican P, Heron EA, Anney RJ, Moore S, Kelleher E, Hargreaves A, Anderson-Schmidt H, Gill M, Gallagher L, Corvin A. The phenotypic manifestations of rare CNVs in schizophrenia. Schizophrenia Research. 158: 255-60. PMID 24999052 DOI: 10.1016/J.Schres.2014.06.016 |
0.406 |
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| 2014 |
Mullins N, Perroud N, Uher R, Butler AW, Cohen-Woods S, Rivera M, Malki K, Euesden J, Power RA, Tansey KE, Jones L, Jones I, Craddock N, Owen MJ, Korszun A, ... Gill M, et al. Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 428-37. PMID 24964207 DOI: 10.1002/Ajmg.B.32247 |
0.353 |
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| 2014 |
Martin J, Cooper M, Hamshere ML, Pocklington A, Scherer SW, Kent L, Gill M, Owen MJ, Williams N, O'Donovan MC, Thapar A, Holmans P. Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 761-70.e26. PMID 24954825 DOI: 10.1016/J.Jaac.2014.03.004 |
0.379 |
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| 2014 |
Escott-Price V, Bellenguez C, Wang LS, Choi SH, Harold D, Jones L, Holmans P, Gerrish A, Vedernikov A, Richards A, DeStefano AL, Lambert JC, Ibrahim-Verbaas CA, Naj AC, Sims R, ... ... Gill M, et al. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. Plos One. 9: e94661. PMID 24922517 DOI: 10.1371/Journal.Pone.0094661 |
0.336 |
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| 2014 |
Mothersill O, Morris DW, Kelly S, Rose EJ, Bokde A, Reilly R, Gill M, Corvin AP, Donohoe G. Altered medial prefrontal activity during dynamic face processing in schizophrenia spectrum patients. Schizophrenia Research. 157: 225-30. PMID 24888525 DOI: 10.1016/J.Schres.2014.05.023 |
0.308 |
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| 2014 |
Nicodemus KK, Hargreaves A, Morris D, Anney R, Gill M, Corvin A, Donohoe G. Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway. Jama Psychiatry. 71: 778-85. PMID 24828433 DOI: 10.1001/Jamapsychiatry.2014.528 |
0.397 |
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| 2014 |
Kelly S, Morris DW, Mothersill O, Rose EJ, Fahey C, O'Brien C, O'Hanlon E, Gill M, Corvin AP, Donohoe G. Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants. Neuroscience Letters. 574: 6-10. PMID 24820543 DOI: 10.1016/J.Neulet.2014.05.002 |
0.34 |
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| 2014 |
McCarthy SE, Gillis J, Kramer M, Lihm J, Yoon S, Berstein Y, Mistry M, Pavlidis P, Solomon R, Ghiban E, Antoniou E, Kelleher E, O'Brien C, Donohoe G, Gill M, et al. De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability. Molecular Psychiatry. 19: 652-8. PMID 24776741 DOI: 10.1038/Mp.2014.29 |
0.407 |
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| 2014 |
Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, ... ... Gill M, et al. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics. 94: 677-94. PMID 24768552 DOI: 10.1016/J.Ajhg.2014.03.018 |
0.363 |
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| 2014 |
Heron EA, Cormican P, Donohoe G, O'Neill FA, Kendler KS, Riley BP, Gill M, Corvin AP, Morris DW. No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset. Schizophrenia Research. 154: 79-82. PMID 24560374 DOI: 10.1016/J.Schres.2014.01.038 |
0.382 |
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| 2014 |
Morris DW, Pearson RD, Cormican P, Kenny EM, O'Dushlaine CT, Perreault LP, Giannoulatou E, Tropea D, Maher BS, Wormley B, Kelleher E, Fahey C, Molinos I, Bellini S, Pirinen M, ... ... Gill M, et al. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. Human Molecular Genetics. 23: 3316-26. PMID 24474471 DOI: 10.1093/Hmg/Ddu025 |
0.404 |
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| 2014 |
O'Donoghue T, Morris DW, Fahey C, Da Costa A, Moore S, Cummings E, Leicht G, Karch S, Hoerold D, Tropea D, Foxe JJ, Gill M, Corvin A, Donohoe G. Effects of ZNF804A on auditory P300 response in schizophrenia. Translational Psychiatry. 4: e345. PMID 24424391 DOI: 10.1038/Tp.2013.115 |
0.41 |
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| 2014 |
Fahey C, Byrne S, McLaughlin R, Kenna K, Shatunov A, Donohoe G, Gill M, Al-Chalabi A, Bradley DG, Hardiman O, Corvin AP, Morris DW. Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample. Neurobiology of Aging. 35: 1510.e1-5. PMID 24411481 DOI: 10.1016/J.Neurobiolaging.2013.12.003 |
0.375 |
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| 2014 |
Lencz T, Knowles E, Davies G, Guha S, Liewald DC, Starr JM, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, Mukherjee S, DeRosse P, Lundervold A, Steen VM, ... ... Gill M, et al. Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT). Molecular Psychiatry. 19: 168-74. PMID 24342994 DOI: 10.1038/Mp.2013.166 |
0.361 |
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| 2014 |
Rose EJ, Hargreaves A, Morris D, Fahey C, Tropea D, Cummings E, Caltagirone C, Bossù P, Chiapponi C, Piras F, Spalletta G, Gill M, Corvin A, Donohoe G. Effects of a novel schizophrenia risk variant rs7914558 at CNNM2 on brain structure and attributional style. The British Journal of Psychiatry : the Journal of Mental Science. 204: 115-21. PMID 24311551 DOI: 10.1192/Bjp.Bp.113.131359 |
0.386 |
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| 2014 |
Hargreaves A, Anney R, O'Dushlaine C, Nicodemus KK, Gill M, Corvin A, Morris D, Donohoe G. The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis. Psychological Medicine. 44: 2177-87. PMID 24284030 DOI: 10.1017/S0033291713002663 |
0.399 |
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| 2014 |
Rees E, Kirov G, Sanders A, Walters JT, Chambert KD, Shi J, Szatkiewicz J, O'Dushlaine C, Richards AL, Green EK, Jones I, Davies G, Legge SE, Moran JL, Pato C, ... ... Gill M, et al. Evidence that duplications of 22q11.2 protect against schizophrenia. Molecular Psychiatry. 19: 37-40. PMID 24217254 DOI: 10.1038/Mp.2013.156 |
0.368 |
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| 2014 |
Ferentinos P, Rivera M, Ising M, Spain SL, Cohen-Woods S, Butler AW, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Maier W, Mors O, et al. Investigating the genetic variation underlying episodicity in major depressive disorder: suggestive evidence for a bipolar contribution. Journal of Affective Disorders. 155: 81-9. PMID 24215895 DOI: 10.1016/J.Jad.2013.10.027 |
0.367 |
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| 2014 |
Rees E, Walters JT, Chambert KD, O'Dushlaine C, Szatkiewicz J, Richards AL, Georgieva L, Mahoney-Davies G, Legge SE, Moran JL, Genovese G, Levinson D, Morris DW, Cormican P, Kendler KS, ... ... Gill M, et al. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Human Molecular Genetics. 23: 1669-76. PMID 24163246 DOI: 10.1093/Hmg/Ddt540 |
0.395 |
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| 2014 |
Kenny EM, Cormican P, Furlong S, Heron E, Kenny G, Fahey C, Kelleher E, Ennis S, Tropea D, Anney R, Corvin AP, Donohoe G, Gallagher L, Gill M, Morris DW. Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders. Molecular Psychiatry. 19: 872-9. PMID 24126926 DOI: 10.1038/Mp.2013.127 |
0.386 |
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| 2014 |
Luo XJ, Li M, Huang L, Steinberg S, Mattheisen M, Liang G, Donohoe G, Shi Y, Chen C, Yue W, Alkelai A, Lerer B, Li Z, Yi Q, Rietschel M, ... ... Gill M, et al. Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene. Molecular Psychiatry. 19: 774-83. PMID 23958956 DOI: 10.1038/Mp.2013.103 |
0.403 |
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| 2014 |
Li M, Luo XJ, Rietschel M, Lewis CM, Mattheisen M, Müller-Myhsok B, Jamain S, Leboyer M, Landén M, Thompson PM, Cichon S, Nöthen MM, Schulze TG, Sullivan PF, Bergen SE, ... ... Gill M, et al. Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Molecular Psychiatry. 19: 452-61. PMID 23568192 DOI: 10.1038/Mp.2013.37 |
0.402 |
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| 2014 |
Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, Lin K, Papiol S, Huttenlocher J, Sigurdsson E, Vassos E, Giegling I, Breuer R, Fraser G, ... ... Gill M, et al. Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry. 19: 108-14. PMID 23164818 DOI: 10.1038/Mp.2012.157 |
0.422 |
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| 2014 |
Cosgrove D, Morris D, Anney R, Hargreaves A, Gill M, Corvin A, Donohoe G. Polygenic scores from the MiR137 pathway explain variability in cognitive performance in patients with schizophrenia and controls Frontiers in Neuroscience. 8. DOI: 10.3389/Conf.Fnins.2014.87.00013 |
0.348 |
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| 2014 |
Gill M, Anney R, Mulligan A. Overlap between ADHD and autism - Clinical and genetic evidence Current Psychiatry Reviews. 10: 143-155. DOI: 10.2174/1573400510666140319235755 |
0.331 |
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| 2014 |
Corvin A, Morris D, Pearson R, Cormican P, Kenny E, O'Neill F, Kendler K, Gill M, Riley B, Spencer C. 4:45 Pm Common And Rare Risk Variants Implicate Pak Signaling In The Molecular Etiology Of Schizophrenia Schizophrenia Research. 153. DOI: 10.1016/S0920-9964(14)70194-X |
0.336 |
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| 2013 |
Johnson KA, Barry E, Lambert D, Fitzgerald M, McNicholas F, Kirley A, Gill M, Bellgrove MA, Hawi Z. 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: 655-64. PMID 24350812 DOI: 10.1089/Cap.2013.0032 |
0.405 |
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| 2013 |
Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, DeStafano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thorton-Wells TA, Jones N, Smith AV, Chouraki V, ... ... Gill M, et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nature Genetics. 45: 1452-8. PMID 24162737 DOI: 10.1038/Ng.2802 |
0.327 |
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| 2013 |
Bralten J, Franke B, Waldman I, Rommelse N, Hartman C, Asherson P, Banaschewski T, Ebstein RP, Gill M, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant JA, Oosterlaan J, et al. Candidate genetic pathways for attention-deficit/hyperactivity disorder (ADHD) show association to hyperactive/impulsive symptoms in children with ADHD. Journal of the American Academy of Child and Adolescent Psychiatry. 52: 1204-1212.e1. PMID 24157394 DOI: 10.1016/J.Jaac.2013.08.020 |
0.382 |
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| 2013 |
McCarthy H, Skokauskas N, Mulligan A, Donohoe G, Mullins D, Kelly J, Johnson K, Fagan A, Gill M, Meaney J, Frodl T. Attention network hypoconnectivity with default and affective network hyperconnectivity in adults diagnosed with attention-deficit/hyperactivity disorder in childhood. Jama Psychiatry. 70: 1329-37. PMID 24132732 DOI: 10.1001/Jamapsychiatry.2013.2174 |
0.321 |
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| 2013 |
Schosser A, Butler AW, Uher R, Ng MY, Cohen-Woods S, Craddock N, Owen MJ, Korszun A, Gill M, Rice J, Hauser J, Henigsberg N, Maier W, Mors O, Placentino A, et al. Genome-wide association study of co-occurring anxiety in major depression. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 14: 611-21. PMID 24047446 DOI: 10.3109/15622975.2013.782107 |
0.335 |
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| 2013 |
Ripke S, O'Dushlaine C, Chambert K, Moran JL, Kähler AK, Akterin S, Bergen SE, Collins AL, Crowley JJ, Fromer M, Kim Y, Lee SH, Magnusson PK, Sanchez N, Stahl EA, ... ... Gill M, et al. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nature Genetics. 45: 1150-9. PMID 23974872 DOI: 10.1038/Ng.2742 |
0.424 |
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| 2013 |
Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, ... ... Gill M, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-94. PMID 23933821 DOI: 10.1038/Ng.2711 |
0.374 |
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| 2013 |
Walters JT, Rujescu D, Franke B, Giegling I, Vásquez AA, Hargreaves A, Russo G, Morris DW, Hoogman M, Da Costa A, Moskvina V, Fernández G, Gill M, Corvin A, O'Donovan MC, et al. The role of the major histocompatibility complex region in cognition and brain structure: a schizophrenia GWAS follow-up. The American Journal of Psychiatry. 170: 877-85. PMID 23903335 DOI: 10.1176/Appi.Ajp.2013.12020226 |
0.397 |
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| 2013 |
Power RA, Cohen-Woods S, Ng MY, Butler AW, Craddock N, Korszun A, Jones L, Jones I, Gill M, Rice JP, Maier W, Zobel A, Mors O, Placentino A, Rietschel M, et al. Genome-wide association analysis accounting for environmental factors through propensity-score matching: application to stressful live events in major depressive disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 521-9. PMID 23857890 DOI: 10.1002/Ajmg.B.32180 |
0.307 |
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| 2013 |
Rose EJ, Morris DW, Hargreaves A, Fahey C, Greene C, Garavan H, Gill M, Corvin A, Donohoe G. Neural effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 530-7. PMID 23839771 DOI: 10.1002/Ajmg.B.32182 |
0.387 |
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| 2013 |
Hamshere ML, Stergiakouli E, Langley K, Martin J, Holmans P, Kent L, Owen MJ, Gill M, Thapar A, O'Donovan M, Craddock N. Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia. The British Journal of Psychiatry : the Journal of Mental Science. 203: 107-11. PMID 23703318 DOI: 10.1192/Bjp.Bp.112.117432 |
0.415 |
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| 2013 |
Hawi Z, Matthews N, Wagner J, Wallace RH, Butler TJ, Vance A, Kent L, Gill M, Bellgrove MA. DNA variation in the SNAP25 gene confers risk to ADHD and is associated with reduced expression in prefrontal cortex. Plos One. 8: e60274. PMID 23593184 DOI: 10.1371/Journal.Pone.0060274 |
0.389 |
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| 2013 |
Robertson DA, Hargreaves A, Kelleher EB, Morris D, Gill M, Corvin A, Donohoe G. Social dysfunction in schizophrenia: an investigation of the GAF scale's sensitivity to deficits in social cognition. Schizophrenia Research. 146: 363-5. PMID 23422729 DOI: 10.1016/J.Schres.2013.01.016 |
0.343 |
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| 2013 |
Carballedo A, Morris D, Zill P, Fahey C, Reinhold E, Meisenzahl E, Bondy B, Gill M, Möller HJ, Frodl T. Brain-derived neurotrophic factor Val66Met polymorphism and early life adversity affect hippocampal volume. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 183-90. PMID 23341118 DOI: 10.1002/Ajmg.B.32130 |
0.34 |
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| 2013 |
Guha S, Rees E, Darvasi A, Ivanov D, Ikeda M, Bergen SE, Magnusson PK, Cormican P, Morris D, Gill M, Cichon S, Rosenfeld JA, Lee A, Gregersen PK, Kane JM, et al. Implication of a rare deletion at distal 16p11.2 in schizophrenia. Jama Psychiatry. 70: 253-60. PMID 23325106 DOI: 10.1001/2013.Jamapsychiatry.71 |
0.411 |
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| 2013 |
Donohoe G, Walters J, Hargreaves A, Rose EJ, Morris DW, Fahey C, Bellini S, Cummins E, Giegling I, Hartmann AM, Möller HJ, Muglia P, Owen MJ, Gill M, O'Donovan MC, et al. Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253. Genes, Brain, and Behavior. 12: 203-9. PMID 23320435 DOI: 10.1111/Gbb.12016 |
0.4 |
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| 2013 |
Power RA, Wingenbach T, Cohen-Woods S, Uher R, Ng MY, Butler AW, Ising M, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Maier W, et al. Estimating the heritability of reporting stressful life events captured by common genetic variants. Psychological Medicine. 43: 1965-71. PMID 23237013 DOI: 10.1017/S0033291712002589 |
0.351 |
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| 2013 |
Vorstman JA, Anney RJ, Derks EM, Gallagher L, Gill M, de Jonge MV, van Engeland H, Kahn RS, Ophoff RA. No evidence that common genetic risk variation is shared between schizophrenia and autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 55-60. PMID 23193033 DOI: 10.1002/Ajmg.B.32121 |
0.405 |
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| 2013 |
Hawi Z, Matthews N, Barry E, Kirley A, Wagner J, Wallace RH, Heussler HS, Vance A, Gill M, Bellgrove MA. A high density linkage disequilibrium mapping in 14 noradrenergic genes: evidence of association between SLC6A2, ADRA1B and ADHD. Psychopharmacology. 225: 895-902. PMID 23052569 DOI: 10.1007/S00213-012-2875-X |
0.39 |
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| 2013 |
Gill MJ, Andreychik MR, Getty PD. More than a lack of control: external explanations can evoke compassion for outgroups by increasing perceptions of suffering (independent of perceived control). Personality & Social Psychology Bulletin. 39: 73-87. PMID 23041610 DOI: 10.1177/0146167212460281 |
0.723 |
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| 2013 |
Cummings E, Donohoe G, Hargreaves A, Moore S, Fahey C, Dinan TG, McDonald C, O'Callaghan E, O'Neill FA, Waddington JL, Murphy KC, Morris DW, Gill M, Corvin A. Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137. Neuroscience Letters. 532: 33-8. PMID 22982201 DOI: 10.1016/J.Neulet.2012.08.065 |
0.381 |
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| 2013 |
Kuntsi J, Frazier-Wood AC, Banaschewski T, Gill M, Miranda A, Oades RD, Roeyers H, Rothenberger A, Steinhausen HC, van der Meere JJ, Faraone SV, Asherson P, Rijsdijk F. Genetic analysis of reaction time variability: room for improvement? Psychological Medicine. 43: 1323-33. PMID 22975296 DOI: 10.1017/S0033291712002061 |
0.341 |
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| 2013 |
Hamshere ML, Walters JT, Smith R, Richards AL, Green E, Grozeva D, Jones I, Forty L, Jones L, Gordon-Smith K, Riley B, O'Neill FA, O'Neill T, Kendler KS, Sklar P, ... ... Gill M, et al. Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. Molecular Psychiatry. 18: 708-12. PMID 22614287 DOI: 10.1038/Mp.2012.67 |
0.418 |
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| 2013 |
Mulligan A, Anney R, Butler L, O'Regan M, Richardson T, Tulewicz EM, Fitzgerald M, Gill M. Home environment: association with hyperactivity/impulsivity in children with ADHD and their non-ADHD siblings. Child: Care, Health and Development. 39: 202-12. PMID 22168816 DOI: 10.1111/J.1365-2214.2011.01345.X |
0.313 |
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| 2013 |
Rucker JJ, Breen G, Pinto D, Pedroso I, Lewis CM, Cohen-Woods S, Uher R, Schosser A, Rivera M, Aitchison KJ, Craddock N, Owen MJ, Jones L, Jones I, Korszun A, ... ... Gill M, et al. Genome-wide association analysis of copy number variation in recurrent depressive disorder. Molecular Psychiatry. 18: 183-9. PMID 22042228 DOI: 10.1038/Mp.2011.144 |
0.347 |
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| 2013 |
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, ... ... Gill M, et al. Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Nature Genetics. 45: 712-712. DOI: 10.1038/Ng0613-712A |
0.301 |
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| 2013 |
Hamshere ML, Walters JTR, Smith R, Richards AL, Green E, Grozeva D, Jones I, Forty L, Jones L, Gordon-Smith K, Riley B, O'Neill T, Kendler KS, Sklar P, Purcell S, ... ... Gill M, et al. Erratum: Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC (Molecular Psychiatry (2013) 18 (738) DOI: 10.1038/mp.2012.89) Molecular Psychiatry. 18. DOI: 10.1038/Mp.2012.89 |
0.356 |
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| 2012 |
Gill M. Developmental psychopathology: the role of structural variation in the genome. Development and Psychopathology. 24: 1319-34. PMID 23062300 DOI: 10.1017/S0954579412000739 |
0.4 |
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| 2012 |
Donohoe G, Duignan A, Hargreaves A, Morris DW, Rose E, Robertson D, Cummings E, Moore S, Gill M, Corvin A. Social cognition in bipolar disorder versus schizophrenia: comparability in mental state decoding deficits. Bipolar Disorders. 14: 743-8. PMID 23020773 DOI: 10.1111/Bdi.12011 |
0.33 |
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| 2012 |
Power RA, Keers R, Ng MY, Butler AW, Uher R, Cohen-Woods S, Ising M, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Hauser J, et al. Dissecting the genetic heterogeneity of depression through age at onset. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 859-68. PMID 22915352 DOI: 10.1002/Ajmg.B.32093 |
0.36 |
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| 2012 |
Bermingham R, Carballedo A, Lisiecka D, Fagan A, Morris D, Fahey C, Donohoe G, Meaney J, Gill M, Frodl T. Effect of genetic variant in BICC1 on functional and structural brain changes in depression. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 37: 2855-62. PMID 22910460 DOI: 10.1038/Npp.2012.158 |
0.348 |
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| 2012 |
Banaschewski T, Jennen-Steinmetz C, Brandeis D, Buitelaar JK, Kuntsi J, Poustka L, Sergeant JA, Sonuga-Barke EJ, Frazier-Wood AC, Albrecht B, Chen W, Uebel H, Schlotz W, van der Meere JJ, Gill M, et al. Neuropsychological correlates of emotional lability in children with ADHD. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 53: 1139-48. PMID 22882111 DOI: 10.1111/J.1469-7610.2012.02596.X |
0.326 |
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| 2012 |
Rose EJ, Morris DW, Fahey C, Robertson IH, Greene C, O'Doherty J, Newell FN, Garavan H, McGrath J, Bokde A, Tropea D, Gill M, Corvin AP, Donohoe G. The effect of the neurogranin schizophrenia risk variant rs12807809 on brain structure and function. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 15: 296-303. PMID 22856365 DOI: 10.1017/Thg.2012.7 |
0.379 |
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| 2012 |
Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, ... ... Gill M, et al. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics. 21: 4781-92. PMID 22843504 DOI: 10.1093/Hmg/Dds301 |
0.384 |
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| 2012 |
Sakrikar D, Mazei-Robison MS, Mergy MA, Richtand NW, Han Q, Hamilton PJ, Bowton E, Galli A, Veenstra-Vanderweele J, Gill M, Blakely RD. Attention deficit/hyperactivity disorder-derived coding variation in the dopamine transporter disrupts microdomain targeting and trafficking regulation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 5385-97. PMID 22514303 DOI: 10.1523/Jneurosci.6033-11.2012 |
0.305 |
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| 2012 |
Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM, Toro R, Appel K, Bartecek R, Bergmann Ø, Bernard M, Brown AA, Cannon DM, Chakravarty MM, Christoforou A, ... ... Gill M, et al. Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics. 44: 552-61. PMID 22504417 DOI: 10.1038/Ng.2250 |
0.36 |
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| 2012 |
Williams NM, Franke B, Mick E, Anney RJ, Freitag CM, Gill M, Thapar A, O'Donovan MC, Owen MJ, Holmans P, Kent L, Middleton F, Zhang-James Y, Liu L, Meyer J, et al. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. The American Journal of Psychiatry. 169: 195-204. PMID 22420048 DOI: 10.1176/Appi.Ajp.2011.11060822 |
0.398 |
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| 2012 |
Stergiakouli E, Hamshere M, Holmans P, Langley K, Zaharieva I, Hawi Z, Kent L, Gill M, Williams N, Owen MJ, O'Donovan M, Thapar A. Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. The American Journal of Psychiatry. 169: 186-94. PMID 22420046 DOI: 10.1176/Appi.Ajp.2011.11040551 |
0.416 |
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| 2012 |
Gilks WP, Hill M, Gill M, Donohoe G, Corvin AP, Morris DW. Functional investigation of a schizophrenia GWAS signal at the CDC42 gene. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 13: 550-4. PMID 22385474 DOI: 10.3109/15622975.2012.666359 |
0.386 |
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| 2012 |
Corvin A, Donohoe G, Hargreaves A, Gallagher L, Gill M. The cognitive genetics of neuropsychiatric disorders. Current Topics in Behavioral Neurosciences. 12: 579-613. PMID 22367920 DOI: 10.1007/7854_2011_188 |
0.365 |
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| 2012 |
Proitsi P, Lupton MK, Dudbridge F, Tsolaki M, Hamilton G, Daniilidou M, Pritchard M, Lord K, Martin BM, Johnson J, Craig D, Todd S, McGuinness B, Hollingworth P, Harold D, ... ... Gill M, et al. Alzheimer's disease and age-related macular degeneration have different genetic models for complement gene variation. Neurobiology of Aging. 33: 1843.e9-17. PMID 22300950 DOI: 10.1016/J.Neurobiolaging.2011.12.036 |
0.322 |
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| 2012 |
Rose EJ, Greene C, Kelly S, Morris DW, Robertson IH, Fahey C, Jacobson S, O'Doherty J, Newell FN, McGrath J, Bokde A, Garavan H, Frodl T, Gill M, Corvin AP, et al. The NOS1 variant rs6490121 is associated with variation in prefrontal function and grey matter density in healthy individuals. Neuroimage. 60: 614-22. PMID 22227051 DOI: 10.1016/J.Neuroimage.2011.12.054 |
0.377 |
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| 2012 |
Toplak ME, Sorge GB, Flora DB, Chen W, Banaschewski T, Buitelaar J, Ebstein R, Eisenberg J, Franke B, Gill M, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, et al. The hierarchical factor model of ADHD: invariant across age and national groupings? Journal of Child Psychology and Psychiatry, and Allied Disciplines. 53: 292-303. PMID 22084976 DOI: 10.1111/J.1469-7610.2011.02500.X |
0.302 |
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| 2012 |
Gerrish A, Russo G, Richards A, Moskvina V, Ivanov D, Harold D, Sims R, Abraham R, Hollingworth P, Chapman J, Hamshere M, Pahwa JS, Dowzell K, Williams A, Jones N, ... ... Gill M, et al. The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 28: 377-87. PMID 22027014 DOI: 10.3233/Jad-2011-110824 |
0.389 |
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| 2012 |
Hollingworth P, Sweet R, Sims R, Harold D, Russo G, Abraham R, Stretton A, Jones N, Gerrish A, Chapman J, Ivanov D, Moskvina V, Lovestone S, Priotsi P, Lupton M, ... ... Gill M, et al. Genome-wide association study of Alzheimer's disease with psychotic symptoms. Molecular Psychiatry. 17: 1316-27. PMID 22005930 DOI: 10.1016/J.Jalz.2011.05.516 |
0.32 |
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| 2012 |
Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, ... ... Gill M, et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics. 131: 565-79. PMID 21996756 DOI: 10.1007/S00439-011-1094-6 |
0.405 |
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| 2012 |
Jablensky A, Angelicheva D, Donohoe GJ, Cruickshank M, Azmanov DN, Morris DW, McRae A, Weickert CS, Carter KW, Chandler D, Alexandrov B, Usheva A, Morar B, Verbrugghe PL, Filipovska A, ... ... Gill M, et al. Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia. Molecular Psychiatry. 17: 1328-39. PMID 21968932 DOI: 10.1038/Mp.2011.129 |
0.373 |
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| 2012 |
Hargreaves A, Morris DW, Rose E, Fahey C, Moore S, Cummings E, Tropea D, Gill M, Corvin A, Donohoe G. ZNF804A and social cognition in patients with schizophrenia and healthy controls. Molecular Psychiatry. 17: 118-9. PMID 21876541 DOI: 10.1038/Mp.2011.102 |
0.328 |
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| 2012 |
Badner JA, Koller D, Foroud T, Edenberg H, Nurnberger JI, Zandi PP, Willour VL, McMahon FJ, Potash JB, Hamshere M, Grozeva D, Green E, Kirov G, Jones I, Jones L, ... ... Gill M, et al. Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. Molecular Psychiatry. 17: 818-26. PMID 21769101 DOI: 10.1038/Mp.2011.89 |
0.379 |
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| 2012 |
O'Donoghue T, Morris DW, Fahey C, Da Costa A, Foxe JJ, Hoerold D, Tropea D, Gill M, Corvin A, Donohoe G. A NOS1 variant implicated in cognitive performance influences evoked neural responses during a high density EEG study of early visual perception. Human Brain Mapping. 33: 1202-11. PMID 21520349 DOI: 10.1002/Hbm.21281 |
0.373 |
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| 2012 |
Rivera M, Cohen-Woods S, Kapur K, Breen G, Ng MY, Butler AW, Craddock N, Gill M, Korszun A, Maier W, Mors O, Owen MJ, Preisig M, Bergmann S, Tozzi F, et al. Depressive disorder moderates the effect of the FTO gene on body mass index. Molecular Psychiatry. 17: 604-11. PMID 21502950 DOI: 10.1038/Mp.2011.45 |
0.334 |
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| 2012 |
Fliers EA, Vasquez AA, Poelmans G, Rommelse N, Altink M, Buschgens C, Asherson P, Banaschewski T, Ebstein R, Gill M, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, et al. Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 13: 211-22. PMID 21473668 DOI: 10.3109/15622975.2011.560279 |
0.356 |
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| 2012 |
Proitsi P, Lupton MK, Reeves SJ, Hamilton G, Archer N, Martin BM, Iyegbe C, Hollingworth P, Lawlor B, Gill M, Brayne C, Rubinsztein DC, Owen MJ, Williams J, Lovestone S, et al. Association of serotonin and dopamine gene pathways with behavioral subphenotypes in dementia. Neurobiology of Aging. 33: 791-803. PMID 20685009 DOI: 10.1016/J.Neurobiolaging.2010.06.011 |
0.34 |
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| 2012 |
Vorstman l, Anney R, Derks E, Gallagher L, Gill M, Jonge Md, Engeland Hv, Kahn R, Ophoff R. Poster #112 NO EVIDENCE THAT COMMON GENETIC RISK VARIANTS ARE SHARED BETWEEN SCHIZOPHRENIA AND AUTISM Schizophrenia Research. 136. DOI: 10.1016/S0920-9964(12)70945-3 |
0.367 |
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| 2012 |
Hargreaves A, Morris DW, Emma R, Gill M, Corvin A, Donohoe G. Poster #116 ZNF804A AND SOCIAL COGNITION IN PATIENTS WITH SCHIZOPHRENIA AND HEALTHY PARTICIPANTS Schizophrenia Research. 136. DOI: 10.1016/S0920-9964(12)70688-6 |
0.343 |
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| 2011 |
Malhotra D, McCarthy S, Michaelson JJ, Vacic V, Burdick KE, Yoon S, Cichon S, Corvin A, Gary S, Gershon ES, Gill M, Karayiorgou M, Kelsoe JR, Krastoshevsky O, Krause V, et al. High frequencies of de novo CNVs in bipolar disorder and schizophrenia. Neuron. 72: 951-63. PMID 22196331 DOI: 10.1016/J.Neuron.2011.11.007 |
0.377 |
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| 2011 |
Rünker AE, O'Tuathaigh C, Dunleavy M, Morris DW, Little GE, Corvin AP, Gill M, Henshall DC, Waddington JL, Mitchell KJ. Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathology. Plos One. 6: e26488. PMID 22132072 DOI: 10.1371/Journal.Pone.0026488 |
0.353 |
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| 2011 |
Sims R, Dwyer S, Harold D, Gerrish A, Hollingworth P, Chapman J, Jones N, Abraham R, Ivanov D, Pahwa JS, Moskvina V, Dowzell K, Thomas C, Stretton A, Lovestone S, ... ... Gill M, et al. No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 764-71. PMID 21812096 DOI: 10.1002/Ajmg.B.31216 |
0.304 |
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| 2011 |
Schosser A, Butler AW, Ising M, Perroud N, Uher R, Ng MY, Cohen-Woods S, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Maier W, et al. Genomewide association scan of suicidal thoughts and behaviour in major depression. Plos One. 6: e20690. PMID 21750702 DOI: 10.1371/Journal.Pone.0020690 |
0.307 |
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| 2011 |
Dagdan E, Morris DW, Campbell M, Hill M, Rothermundt M, Kästner F, Hohoff C, von Eiff C, Krakowitzky P, Gill M, McKeon P, Roche S. Functional assessment of a promoter polymorphism in S100B, a putative risk variant for bipolar disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 691-9. PMID 21714070 DOI: 10.1002/Ajmg.B.31211 |
0.37 |
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| 2011 |
Hill MJ, Kenny E, Roche S, Morris DW, Corvin A, Hawi Z, Gill M, Anney RJ. Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation. Psychiatric Genetics. 21: 281-6. PMID 21642896 DOI: 10.1097/Ypg.0B013E328348045B |
0.348 |
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| 2011 |
Anney RJ, Kenny EM, O'Dushlaine C, Yaspan BL, Parkhomenka E, Buxbaum JD, Sutcliffe J, Gill M, Gallagher L, Buxbaum JD, Sutcliffe J, Gill M, Gallagher L. Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders. European Journal of Human Genetics : Ejhg. 19: 1082-9. PMID 21522181 DOI: 10.1038/Ejhg.2011.75 |
0.377 |
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| 2011 |
Sonuga-Barke EJ, Kumsta R, Schlotz W, Lasky-Su J, Marco R, Miranda A, Mulas F, Oades RD, Banaschewski T, Mueller U, Andreou P, Christiansen H, Gabriels I, Uebel H, Kuntsi J, ... ... Gill M, et al. A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings. Biological Psychiatry. 70: 230-6. PMID 21497794 DOI: 10.1016/J.Biopsych.2011.01.040 |
0.381 |
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| 2011 |
Müller UC, Asherson P, Banaschewski T, Buitelaar JK, Ebstein RP, Eisenberg J, Gill M, Manor I, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant JA, Sonuga-Barke EJ, Thompson M, et al. The impact of study design and diagnostic approach in a large multi-centre ADHD study: Part 2: Dimensional measures of psychopathology and intelligence. Bmc Psychiatry. 11: 55. PMID 21473746 DOI: 10.1186/1471-244X-11-55 |
0.334 |
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| 2011 |
Müller UC, Asherson P, Banaschewski T, Buitelaar JK, Ebstein RP, Eisenberg J, Gill M, Manor I, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant JA, Sonuga-Barke EJ, Thompson M, et al. The impact of study design and diagnostic approach in a large multi-centre ADHD study. Part 1: ADHD symptom patterns. Bmc Psychiatry. 11: 54. PMID 21473745 DOI: 10.1186/1471-244X-11-54 |
0.32 |
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| 2011 |
Hollingworth P, Harold D, Sims R, Gerrish A, Lambert JC, Carrasquillo MM, Abraham R, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Jones N, Stretton A, Thomas C, Richards A, ... ... Gill M, et al. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nature Genetics. 43: 429-35. PMID 21460840 DOI: 10.1038/Ng.803 |
0.313 |
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| 2011 |
Tansey KE, Hill MJ, Cochrane LE, Gill M, Anney RJ, Gallagher L. Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism. Molecular Autism. 2: 3. PMID 21453499 DOI: 10.1186/2040-2392-2-3 |
0.339 |
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| 2011 |
Segurado R, Bellgrove MA, Manconi F, Gill M, Hawi Z. Epistasis between neurochemical gene polymorphisms and risk for ADHD. European Journal of Human Genetics : Ejhg. 19: 577-82. PMID 21368917 DOI: 10.1038/Ejhg.2010.250 |
0.407 |
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| 2011 |
Vacic V, McCarthy S, Malhotra D, Murray F, Chou HH, Peoples A, Makarov V, Yoon S, Bhandari A, Corominas R, Iakoucheva LM, Krastoshevsky O, Krause V, Larach-Walters V, Welsh DK, ... ... Gill M, et al. Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia. Nature. 471: 499-503. PMID 21346763 DOI: 10.1038/Nature09884 |
0.374 |
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| 2011 |
Rizzi TS, Arias-Vasquez A, Rommelse N, Kuntsi J, Anney R, Asherson P, Buitelaar J, Banaschewski T, Ebstein R, Ruano D, Van der Sluis S, Markunas CA, Garrett ME, Ashley-Koch AE, Kollins SH, ... ... Gill M, et al. 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 : the Official Publication of the International Society of Psychiatric Genetics. 156: 145-57. PMID 21302343 DOI: 10.1002/Ajmg.B.31149 |
0.409 |
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| 2011 |
Heron EA, O'dushlaine C, Segurado R, Gallagher L, Gill M. Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data Biostatistics. 12: 445-461. PMID 21252078 DOI: 10.1093/Biostatistics/Kxq072 |
0.316 |
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| 2011 |
Braet W, Johnson KA, Tobin CT, Acheson R, McDonnell C, Hawi Z, Barry E, Mulligan A, Gill M, Bellgrove MA, Robertson IH, Garavan H. 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: 1641-50. PMID 21232548 DOI: 10.1016/J.Neuropsychologia.2011.01.001 |
0.344 |
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| 2011 |
Donohoe G, Walters J, Morris DW, Da Costa A, Rose E, Hargreaves A, Maher K, Hayes E, Giegling I, Hartmann AM, Möller HJ, Muglia P, Moskvina V, Owen MJ, O'Donovan MC, ... Gill M, et al. A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809. Schizophrenia Research. 125: 304-6. PMID 21112188 DOI: 10.1016/J.Schres.2010.10.019 |
0.378 |
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| 2011 |
Donohoe G, Rose E, Frodl T, Morris D, Spoletini I, Adriano F, Bernardini S, Caltagirone C, Bossù P, Gill M, Corvin AP, Spalletta G. ZNF804A risk allele is associated with relatively intact gray matter volume in patients with schizophrenia. Neuroimage. 54: 2132-7. PMID 20934520 DOI: 10.1016/J.Neuroimage.2010.09.089 |
0.363 |
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| 2011 |
Chen X, Lee G, Maher BS, Fanous AH, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan PF, Shi J, Levinson DF, Gejman PV, Sanders A, Duan J, Owen MJ, ... ... Gill M, et al. GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Molecular Psychiatry. 16: 1117-29. PMID 20838396 DOI: 10.1038/Mp.2010.96 |
0.404 |
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| 2011 |
Wood AC, Rijsdijk F, Johnson KA, Andreou P, Albrecht B, Arias-Vasquez A, Buitelaar JK, McLoughlin G, Rommelse NN, Sergeant JA, Sonuga-Barke EJ, Uebel H, van der Meere JJ, Banaschewski T, Gill M, et al. The relationship between ADHD and key cognitive phenotypes is not mediated by shared familial effects with IQ. Psychological Medicine. 41: 861-71. PMID 20522277 DOI: 10.1017/S003329171000108X |
0.348 |
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| 2011 |
Williams HJ, Norton N, Dwyer S, Moskvina V, Nikolov I, Carroll L, Georgieva L, Williams NM, Morris DW, Quinn EM, Giegling I, Ikeda M, Wood J, Lencz T, Hultman C, ... ... Gill M, et al. Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. Molecular Psychiatry. 16: 429-41. PMID 20368704 DOI: 10.1038/Mp.2010.36 |
0.429 |
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| 2011 |
O'Dushlaine C, Kenny E, Heron E, Donohoe G, Gill M, Morris D, Corvin A. Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility. Molecular Psychiatry. 16: 286-92. PMID 20157312 DOI: 10.1038/Mp.2010.7 |
0.406 |
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| 2011 |
Vacic V, McCarthy S, Malhotra D, Murray F, Chou HH, Peoples A, Makarov V, Yoon S, Bhandari A, Corominas R, Iakoucheva LM, Krastoshevsky O, Krause V, Larach-Walters V, Welsh DK, ... ... Gill M, et al. Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia (Nature (2011) 471 (499-501)) Nature. 474: 114. DOI: 10.1038/Nature10088 |
0.34 |
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| 2011 |
Donohoe G, Rose EJ, Morris D, Hargreaves A, Gill M, Corvin A. S20-02 - Follow up of schizophrenia gwas based on cognitive performance, high density eeg, and structural brain imaging European Psychiatry. 26: 2083-2083. DOI: 10.1016/S0924-9338(11)73786-5 |
0.4 |
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| 2010 |
Cochrane LE, Tansey KE, Gill M, Gallagher L, Anney RJ. Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample. Autism Research : Official Journal of the International Society For Autism Research. 3: 342-4. PMID 21182210 DOI: 10.1002/Aur.157 |
0.373 |
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| 2010 |
Kuntsi J, Wood AC, Rijsdijk F, Johnson KA, Andreou P, Albrecht B, Arias-Vasquez A, Buitelaar JK, McLoughlin G, Rommelse NN, Sergeant JA, Sonuga-Barke EJ, Uebel H, van der Meere JJ, Banaschewski T, ... Gill M, et al. Separation of cognitive impairments in attention-deficit/hyperactivity disorder into 2 familial factors. Archives of General Psychiatry. 67: 1159-67. PMID 21041617 DOI: 10.1001/Archgenpsychiatry.2010.139 |
0.333 |
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| 2010 |
Butler AW, Breen G, Tozzi F, Craddock N, Gill M, Korszun A, Maier W, Middleton LT, Mors O, Owen MJ, Perry J, Preisig M, Rice JP, Rietschel M, Jones L, et al. A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 1465-73. PMID 20886545 DOI: 10.1002/Ajmg.B.31127 |
0.327 |
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| 2010 |
Brookes KJ, Hawi Z, Park J, Scott S, Gill M, Kent L. 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 : the Official Publication of the International Society of Psychiatric Genetics. 153: 1417-24. PMID 20862695 DOI: 10.1002/Ajmg.B.31120 |
0.393 |
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| 2010 |
Neale BM, Medland S, Ripke S, Anney RJ, Asherson P, Buitelaar J, Franke B, Gill M, Kent L, Holmans P, Middleton F, Thapar A, Lesch KP, Faraone SV, Daly M, et al. Case-control genome-wide association study of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry. 49: 906-20. PMID 20732627 DOI: 10.1016/J.Jaac.2010.06.007 |
0.433 |
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| 2010 |
Neale BM, Medland SE, Ripke S, Asherson P, Franke B, Lesch KP, Faraone SV, Nguyen TT, Schäfer H, Holmans P, Daly M, Steinhausen HC, Freitag C, Reif A, Renner TJ, ... ... Gill M, et al. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry. 49: 884-97. PMID 20732625 DOI: 10.1016/J.Jaac.2010.06.008 |
0.398 |
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| 2010 |
Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, ... ... Gill M, et al. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. 19: 4072-82. PMID 20663923 DOI: 10.1093/Hmg/Ddq307 |
0.394 |
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| 2010 |
Correia CT, Coutinho AM, Sequeira AF, Sousa IG, Lourenço Venda L, Almeida JP, Abreu RL, Lobo C, Miguel TS, Conroy J, Cochrane L, Gallagher L, Gill M, Ennis S, Oliveira GG, et al. Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism. Genes, Brain, and Behavior. 9: 841-8. PMID 20662941 DOI: 10.1111/J.1601-183X.2010.00627.X |
0.339 |
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| 2010 |
Quinn EM, Hill M, Anney R, Gill M, Corvin AP, Morris DW. Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression. Bipolar Disorders. 12: 440-5. PMID 20636642 DOI: 10.1111/J.1399-5618.2010.00817.X |
0.352 |
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| 2010 |
Nijmeijer JS, Arias-Vásquez A, Rommelse NN, Altink ME, Anney RJ, Asherson P, Banaschewski T, Buschgens CJ, Fliers EA, Gill M, Minderaa RB, Poustka L, Sergeant JA, Buitelaar JK, Franke B, et al. Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach. Journal of the American Academy of Child and Adolescent Psychiatry. 49: 675-85. PMID 20610137 DOI: 10.1016/J.Jaac.2010.03.015 |
0.374 |
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| 2010 |
Walters JT, Corvin A, Owen MJ, Williams H, Dragovic M, Quinn EM, Judge R, Smith DJ, Norton N, Giegling I, Hartmann AM, Möller HJ, Muglia P, Moskvina V, Dwyer S, ... ... Gill M, et al. Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia. Archives of General Psychiatry. 67: 692-700. PMID 20603450 DOI: 10.1001/Archgenpsychiatry.2010.81 |
0.373 |
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| 2010 |
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, ... ... Gill M, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 466: 368-72. PMID 20531469 DOI: 10.1038/Nature09146 |
0.368 |
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| 2010 |
Spalletta G, Morris D, Angelucci F, Rubino I, Spoletini I, Bria P, Martinotti G, Siracusano A, Bonaviri G, Bernardini S, Caltagirone C, Bossù P, Donohoe G, Gill M, Corvin A. BDNF Val66Met polymorphism is associated with aggressive behavior in schizophrenia European Psychiatry. 25: 311-313. PMID 20430595 DOI: 10.1016/J.Eurpsy.2009.10.008 |
0.354 |
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| 2010 |
Greene CM, Robertson IH, Gill M, Bellgrove MA. Dopaminergic genotype influences spatial bias in healthy adults. Neuropsychologia. 48: 2458-64. PMID 20430042 DOI: 10.1016/J.Neuropsychologia.2010.04.019 |
0.308 |
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| 2010 |
Aebi M, Müller UC, Asherson P, Banaschewski T, Buitelaar J, Ebstein R, Eisenberg J, Gill M, Manor I, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, et al. Predictability of oppositional defiant disorder and symptom dimensions in children and adolescents with ADHD combined type. Psychological Medicine. 40: 2089-100. PMID 20380783 DOI: 10.1017/S0033291710000590 |
0.318 |
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| 2010 |
Park J, Willmott M, Vetuz G, Toye C, Kirley A, Hawi Z, Brookes KJ, Gill M, Kent L. Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 34: 697-702. PMID 20347913 DOI: 10.1016/J.Pnpbp.2010.03.029 |
0.397 |
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| 2010 |
Tansey KE, Brookes KJ, Hill MJ, Cochrane LE, Gill M, Skuse D, Correia C, Vicente A, Kent L, Gallagher L, Anney RJ. Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies. Neuroscience Letters. 474: 163-7. PMID 20303388 DOI: 10.1016/J.Neulet.2010.03.035 |
0.388 |
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| 2010 |
Sobanski E, Banaschewski T, Asherson P, Buitelaar J, Chen W, Franke B, Holtmann M, Krumm B, Sergeant J, Sonuga-Barke E, Stringaris A, Taylor E, Anney R, Ebstein RP, Gill M, et al. Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 51: 915-23. PMID 20132417 DOI: 10.1111/J.1469-7610.2010.02217.X |
0.322 |
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| 2010 |
Hill MJ, Anney RJ, Gill M, Hawi Z. Functional analysis of intron 8 and 3' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants. Pharmacogenomics Journal. 10: 442-447. PMID 20029387 DOI: 10.1038/Tpj.2009.66 |
0.352 |
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| 2010 |
Gilks WP, Allott EH, Donohoe G, Cummings E, Gill M, Corvin AP, Morris DW. Replicated genetic evidence supports a role for HOMER2 in schizophrenia. Neuroscience Letters. 468: 229-33. PMID 19914345 DOI: 10.1016/J.Neulet.2009.11.003 |
0.421 |
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| 2010 |
Gill M, Donohoe G, Corvin A. What have the genomics ever done for the psychoses Psychological Medicine. 40: 529-540. PMID 19818200 DOI: 10.1017/S0033291709991139 |
0.399 |
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| 2010 |
Donohoe G, Frodl T, Morris D, Spoletini I, Cannon DM, Cherubini A, Caltagirone C, Bossù P, McDonald C, Gill M, Corvin AP, Spalletta G. Reduced occipital and prefrontal brain volumes in dysbindin-associated schizophrenia. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 35: 368-73. PMID 19794403 DOI: 10.1038/Npp.2009.140 |
0.353 |
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| 2010 |
Carroll LS, Williams NM, Moskvina V, Russell E, Norton N, Williams HJ, Peirce T, Georgieva L, Dwyer S, Grozeva D, Greene E, Farmer A, McGuffin P, Morris DW, Corvin A, ... Gill M, et al. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha. Molecular Psychiatry. 15: 1101-11. PMID 19786960 DOI: 10.1038/Mp.2009.96 |
0.405 |
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| 2010 |
Hawi Z, Kent L, Hill M, Anney RJ, Brookes KJ, Barry E, Franke B, Banaschewski T, Buitelaar J, Ebstein R, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, ... ... Gill M, et al. ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 97-102. PMID 19388000 DOI: 10.1002/Ajmg.B.30960 |
0.358 |
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| 2009 |
Haq F, Behan C, McGlade N, Mulkerrin U, O'Callaghan E, Kinsella A, Corvin A, Donohoe G, Gill M. Factors that influence patients' attitudes to antipsychotic medication. Irish Journal of Psychological Medicine. 26: 6-11. PMID 30282274 DOI: 10.1017/S0790966700000045 |
0.311 |
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| 2009 |
McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O, Krause V, Kumar RA, Grozeva D, Malhotra D, Walsh T, ... ... Gill M, et al. Microduplications of 16p11.2 are associated with schizophrenia. Nature Genetics. 41: 1223-7. PMID 19855392 DOI: 10.1038/Ng.474 |
0.369 |
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| 2009 |
Weiss LA, Arking DE, Daly MJ, Chakravarti A, Brune CW, West K, O'Connor A, Hilton G, Tomlinson RL, West AB, Cook EH, Green T, Chang SC, Gabriel S, Gates C, ... ... Gill M, et al. A genome-wide linkage and association scan reveals novel loci for autism Nature. 461: 802-808. PMID 19812673 DOI: 10.1038/Nature08490 |
0.404 |
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| 2009 |
Bellgrove MA, Johnson KA, Barry E, Mulligan A, Hawi Z, Gill M, Robertson I, Chambers CD. Dopaminergic haplotype as a predictor of spatial inattention in children with attention-deficit/hyperactivity disorder. Archives of General Psychiatry. 66: 1135-42. PMID 19805704 DOI: 10.1001/Archgenpsychiatry.2009.120 |
0.334 |
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| 2009 |
Donohoe G, Walters J, Morris DW, Quinn EM, Judge R, Norton N, Giegling I, Hartmann AM, Möller HJ, Muglia P, Williams H, Moskvina V, Peel R, O'Donoghue T, Owen MJ, ... ... Gill M, et al. Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects. Archives of General Psychiatry. 66: 1045-54. PMID 19805695 DOI: 10.1001/Archgenpsychiatry.2009.139 |
0.395 |
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| 2009 |
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, ... ... Gill M, et al. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nature Genetics. 41: 1088-93. PMID 19734902 DOI: 10.1038/Ng.440 |
0.341 |
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| 2009 |
Andreychik MR, Gill MJ. Ingroup identity moderates the impact of social explanations on intergroup attitudes: external explanations are not inherently prosocial. Personality & Social Psychology Bulletin. 35: 1632-45. PMID 19721101 DOI: 10.1177/0146167209345285 |
0.717 |
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| 2009 |
Hamshere ML, Schulze TG, Schumacher J, Corvin A, Owen MJ, Jamra RA, Propping P, Maier W, Orozco y Diaz G, Mayoral F, Rivas F, Jones I, Jones L, Kirov G, Gill M, et al. Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31. Bipolar Disorders. 11: 610-20. PMID 19689503 DOI: 10.1111/J.1399-5618.2009.00736.X |
0.395 |
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| 2009 |
O'Dushlaine C, Kenny E, Heron EA, Segurado R, Gill M, Morris DW, Corvin A. The SNP ratio test: pathway analysis of genome-wide association datasets. Bioinformatics (Oxford, England). 25: 2762-3. PMID 19620097 DOI: 10.1093/Bioinformatics/Btp448 |
0.333 |
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| 2009 |
Doyle C, Brookes K, Simpson J, Park J, Scott S, Coghill DR, Hawi Z, Kirley A, Gill M, Kent L. Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder. Neuroscience Letters. 462: 179-81. PMID 19576958 DOI: 10.1016/J.Neulet.2009.06.084 |
0.408 |
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| 2009 |
Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Ruderfer DM, McQuillin A, Morris DW, Oĝdushlaine CT, Corvin A, Holmans PA, Oĝdonovan MC, MacGregor S, Gurling H, ... ... Gill M, et al. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder Nature. 460: 748-752. PMID 19571811 DOI: 10.1038/Nature08185 |
0.404 |
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| 2009 |
Marco R, Miranda A, Schlotz W, Melia A, Mulligan A, Müller U, Andreou P, Butler L, Christiansen H, Gabriels I, Medad S, Albrecht B, Uebel H, Asherson P, Banaschewski T, ... Gill M, et al. Delay and reward choice in ADHD: an experimental test of the role of delay aversion. Neuropsychology. 23: 367-80. PMID 19413450 DOI: 10.1037/A0014914 |
0.313 |
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| 2009 |
Correia C, Coutinho AM, Almeida J, Lontro R, Lobo C, Miguel TS, Martins M, Gallagher L, Conroy J, Gill M, Oliveira G, Vicente AM. Association of the alpha4 integrin subunit gene (ITGA4) with autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 1147-51. PMID 19259978 DOI: 10.1002/Ajmg.B.30940 |
0.397 |
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| 2009 |
Greene CM, Bellgrove MA, Gill M, Robertson IH. Noradrenergic genotype predicts lapses in sustained attention. Neuropsychologia. 47: 591-4. PMID 18973765 DOI: 10.1016/J.Neuropsychologia.2008.10.003 |
0.306 |
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| 2009 |
Conroy J, Cochrane L, Anney RJ, Sutcliffe JS, Carthy P, Dunlop A, Mullarkey M, O'hici B, Green AJ, Ennis S, Gill M, Gallagher L. Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 535-44. PMID 18846500 DOI: 10.1002/Ajmg.B.30854 |
0.376 |
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| 2009 |
O'Donovan MC, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, ... ... Gill M, et al. Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2. Molecular Psychiatry. 14: 30-6. PMID 18813210 DOI: 10.1038/Mp.2008.108 |
0.402 |
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| 2009 |
O'Gráda C, Barry S, McGlade N, Behan C, Haq F, Hayden J, O'Donoghue T, Peel R, Morris DW, O'Callaghan E, Gill M, Corvin AP, Dinan TG, Donohoe G. Does the ability to sustain attention underlie symptom severity in schizophrenia? Schizophrenia Research. 107: 319-23. PMID 18768299 DOI: 10.1016/J.Schres.2008.07.013 |
0.33 |
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| 2009 |
Mulligan A, Anney RJ, O'Regan M, Chen W, Butler L, Fitzgerald M, Buitelaar J, Steinhausen HC, Rothenberger A, Minderaa R, Nijmeijer J, Hoekstra PJ, Oades RD, Roeyers H, Buschgens C, ... ... Gill M, et al. 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. 39: 197-209. PMID 18642069 DOI: 10.1007/S10803-008-0621-3 |
0.325 |
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| 2009 |
Morgan AR, Hollingworth P, Abraham R, Lovestone S, Brayne C, Rubinsztein DC, Lynch A, Lawlor B, Gill M, O'Donovan MC, Owen MJ, Williams J. Association analysis of dynamin-binding protein (DNMBP) on chromosome 10q with late onset Alzheimer's disease in a large caucasian UK sample. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 61-4. PMID 18452187 DOI: 10.1002/Ajmg.B.30768 |
0.353 |
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| 2009 |
Proitsi P, Lupton M, Reeves S, Hamilton G, Archer N, Martin B, hollingworth P, Lawlord B, Gill M, Owen MJ, Williams J, Lovestone S, Powell J. Genes of the serotonergic and dopaminergic pathways and their interaction affect the expression of Behavioural and Psychological Symptoms in Dementia (BPSD). Nature Precedings. DOI: 10.1038/Npre.2009.3896.1 |
0.301 |
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| 2009 |
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, ... ... Gill M, et al. Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Nature Genetics. 41: 1156-1156. DOI: 10.1038/Ng1009-1156D |
0.301 |
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| 2009 |
Braet W, Johnson K, Tobin C, Acheson R, McDonnell C, Hawi Z, Barry E, Mulligan A, Gill M, Bellgrove M, Robertson I, Garavan H. Increased fMRI activation during response inhibition, and decreased activation during error processing is associated with possession of the 10-repeat allele of the DAT1 gene: a genetic imaging study investigating the role of the DAT1 gene in Attention Deficit Hyperactivity disorder Neuroimage. 47: S161. DOI: 10.1016/S1053-8119(09)71700-8 |
0.368 |
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| 2009 |
Gerrish A, Harold D, Sims R, Abraham R, Hollingworth P, Hamshere M, Lovestone S, Brayne C, Gill M, Lawlor B, Passmore P, Nothen M, Mayer W, Livingston G, Bass N, et al. P4-124: An examination of previously reported Alzheimer candidate genes within a large genome-wide association dataset Alzheimer's & Dementia. 5: P468-P468. DOI: 10.1016/J.Jalz.2009.04.792 |
0.324 |
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| 2009 |
Hollingworth P, Sims R, Abraham R, Harold D, Gerrish A, Hamshere M, Lovestone S, Brayne C, Gill M, Lawlor B, Passmore P, Nothen M, Mayer W, Livingston G, Bass N, et al. P4-121: Genome-wide association study of Alzheimer's with psychotic symptoms Alzheimer's & Dementia. 5: P467-P467. DOI: 10.1016/J.Jalz.2009.04.789 |
0.304 |
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| 2009 |
Sims R, Hollingworth P, Abraham R, Harold D, Holmans P, Lovestone S, Powell J, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Craig D, Passmore P, Nöthen M, Mayer W, et al. P4-120: Investigating psychosis candidate genes in Alzheimer's disease with psychosis using genome-wide association studies Alzheimer's & Dementia. 5: P466-P467. DOI: 10.1016/J.Jalz.2009.04.788 |
0.337 |
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| 2008 |
Altink ME, Arias-Vásquez A, Franke B, Slaats-Willemse DI, Buschgens CJ, Rommelse NN, Fliers EA, Anney R, Brookes KJ, Chen W, Gill M, Mulligan A, Sonuga-Barke E, Thompson M, Sergeant JA, et al. The dopamine receptor D4 7-repeat allele and prenatal smoking in ADHD-affected children and their unaffected siblings: no gene-environment interaction. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 49: 1053-60. PMID 19017022 DOI: 10.1111/J.1469-7610.2008.01998.X |
0.328 |
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| 2008 |
Zhou K, Dempfle A, Arcos-Burgos M, Bakker SC, Banaschewski T, Biederman J, Buitelaar J, Castellanos FX, Doyle A, Ebstein RP, Ekholm J, Forabosco P, Franke B, Freitag C, Friedel S, ... Gill M, et al. Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1392-8. PMID 18988193 DOI: 10.1002/Ajmg.B.30878 |
0.375 |
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| 2008 |
Neale BM, Lasky-Su J, Anney R, Franke B, Zhou K, Maller JB, Vasquez AA, Asherson P, Chen W, Banaschewski T, Buitelaar J, Ebstein R, Gill M, Miranda A, Oades RD, et al. Genome-wide association scan of attention deficit hyperactivity disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1337-44. PMID 18980221 DOI: 10.1002/Ajmg.B.30866 |
0.423 |
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| 2008 |
Anney RJ, Lasky-Su J, O'Dúshláine C, Kenny E, Neale BM, Mulligan A, Franke B, Zhou K, Chen W, Christiansen H, Arias-Vásquez A, Banaschewski T, Buitelaar J, Ebstein R, Miranda A, ... ... Gill M, et al. Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1369-78. PMID 18951430 DOI: 10.1002/Ajmg.B.30871 |
0.372 |
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| 2008 |
Oades RD, Lasky-Su J, Christiansen H, Faraone SV, Sonuga-Barke EJ, Banaschewski T, Chen W, Anney RJ, Buitelaar JK, Ebstein RP, Franke B, Gill M, Miranda A, Roeyers H, Rothenberger A, et al. The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysis. Behavioral and Brain Functions : Bbf. 4: 48. PMID 18937842 DOI: 10.1186/1744-9081-4-48 |
0.385 |
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| 2008 |
Brookes KJ, Hawi Z, Kirley A, Barry E, Gill M, Kent L. Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1531-5. PMID 18937300 DOI: 10.1002/Ajmg.B.30873 |
0.39 |
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| 2008 |
Xu X, Hawi Z, Brookes KJ, Anney R, Bellgrove M, Franke B, Barry E, Chen W, Kuntsi J, Banaschewski T, Buitelaar J, Ebstein R, Fitzgerald M, Miranda A, Oades RD, ... ... Gill M, et al. Replication of a rare protective allele in the noradrenaline transporter gene and ADHD. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1564-7. PMID 18937296 DOI: 10.1002/Ajmg.B.30872 |
0.393 |
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| 2008 |
Lasky-Su J, Anney RJ, Neale BM, Franke B, Zhou K, Maller JB, Vasquez AA, Chen W, Asherson P, Buitelaar J, Banaschewski T, Ebstein R, Gill M, Miranda A, Mulas F, et al. Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1355-8. PMID 18937294 DOI: 10.1002/Ajmg.B.30869 |
0.407 |
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| 2008 |
Sonuga-Barke EJS, Lasky-Su J, Neale BM, Oades R, Chen W, Franke B, Buitelaar J, Banaschewski T, Ebstein R, Gill M, Anney R, Miranda A, Mulas F, Roeyers H, Rothenberger A, et al. Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 147: 1359-1368. PMID 18846501 DOI: 10.1002/Ajmg.B.30860 |
0.393 |
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| 2008 |
Lasky-Su J, Neale BM, Franke B, Anney RJ, Zhou K, Maller JB, Vasquez AA, Chen W, Asherson P, Buitelaar J, Banaschewski T, Ebstein R, Gill M, Miranda A, Mulas F, et al. Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1345-54. PMID 18821565 DOI: 10.1002/Ajmg.B.30867 |
0.422 |
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| 2008 |
Donohoe G, Spoletini I, McGlade N, Behan C, Hayden J, O'Donoghue T, Peel R, Haq F, Walker C, O'Callaghan E, Spalletta G, Gill M, Corvin A. Are relational style and neuropsychological performance predictors of social attributions in chronic schizophrenia? Psychiatry Research. 161: 19-27. PMID 18789541 DOI: 10.1016/J.Psychres.2007.10.001 |
0.35 |
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| 2008 |
Mefford HC, Sharp AJ, Baker C, Itsara A, Jiang Z, Buysse K, Huang S, Maloney VK, Crolla JA, Baralle D, Collins A, Mercer C, Norga K, de Ravel T, Devriendt K, ... ... Gill M, et al. Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. The New England Journal of Medicine. 359: 1685-99. PMID 18784092 DOI: 10.1056/Nejmoa0805384 |
0.303 |
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| 2008 |
Ferreira MA, O'Donovan MC, Meng YA, Jones IR, Ruderfer DM, Jones L, Fan J, Kirov G, Perlis RH, Green EK, Smoller JW, Grozeva D, Stone J, Nikolov I, Chambert K, ... ... Gill M, et al. Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. Nature Genetics. 40: 1056-8. PMID 18711365 DOI: 10.1038/Ng.209 |
0.358 |
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| 2008 |
O'Donovan MC, Craddock N, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, ... ... Gill M, et al. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nature Genetics. 40: 1053-5. PMID 18677311 DOI: 10.1038/Ng.201 |
0.367 |
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| 2008 |
Brookes KJ, Xu X, Anney R, Franke B, Zhou K, Chen W, Banaschewski T, Buitelaar J, Ebstein R, Eisenberg J, Gill M, Miranda A, Oades RD, Roeyers H, Rothenberger A, et al. Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1519-23. PMID 18668530 DOI: 10.1002/Ajmg.B.30782 |
0.412 |
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| 2008 |
Stone JL, O'Donovan MC, Gurling H, Kirov GK, Blackwood DHR, Corvin A, Craddock NJ, Gill M, Hultman CM, Lichtenstein P, McQuillin A, Pato CN, Ruderfer DM, Owen MJ, St Clair D, et al. Rare chromosomal deletions and duplications increase risk of schizophrenia Nature. 455: 237-241. PMID 18668038 DOI: 10.1038/Nature07239 |
0.411 |
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| 2008 |
Anney RJ, Kenny E, O'Dushlaine CT, Lasky-Su J, Franke B, Morris DW, Neale BM, Asherson P, Faraone SV, Gill M. Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1379-86. PMID 18663727 DOI: 10.1002/Ajmg.B.30836 |
0.334 |
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| 2008 |
Zhou K, Chen W, Buitelaar J, Banaschewski T, Oades RD, Franke B, Sonuga-Barke E, Ebstein R, Eisenberg J, Gill M, Manor I, Miranda A, Mulas F, Roeyers H, Rothenberger A, et al. Genetic heterogeneity in ADHD: DAT1 gene only affects probands without CD. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1481-7. PMID 18553640 DOI: 10.1002/Ajmg.B.30644 |
0.318 |
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| 2008 |
Xu X, Duman EA, Aysimi E, Anney R, Brookes K, Franke B, Zhou K, Buschgens C, Chen W, Christiansen H, Eisenberg J, Gabriëls I, Manor I, Marco R, Müller UC, ... ... Gill M, et al. 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 : the Official Publication of the International Society of Psychiatric Genetics. 147: 1306-9. PMID 18452186 DOI: 10.1002/Ajmg.B.30737 |
0.391 |
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| 2008 |
Zhou K, Asherson P, Sham P, Franke B, Anney RJ, Buitelaar J, Ebstein R, Gill M, Brookes K, Buschgens C, Campbell D, Chen W, Christiansen H, Fliers E, Gabriëls I, et al. Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings. Biological Psychiatry. 64: 571-6. PMID 18439570 DOI: 10.1016/J.Biopsych.2008.02.024 |
0.378 |
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| 2008 |
Johnson KA, Kelly SP, Robertson IH, Barry E, Mulligan A, Daly M, Lambert D, McDonnell C, Connor TJ, Hawi Z, Gill M, Bellgrove MA. 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 : the Official Publication of the International Society of Psychiatric Genetics. 147: 927-37. PMID 18361436 DOI: 10.1002/Ajmg.B.30718 |
0.323 |
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| 2008 |
Yang MS, Morris DW, Donohoe G, Kenny E, O'Dushalaine CT, Schwaiger S, Nangle JM, Clarke S, Scully P, Quinn J, Meagher D, Baldwin P, Crumlish N, O'Callaghan E, Waddington JL, ... Gill M, et al. Chitinase-3-like 1 (CHI3L1) gene and schizophrenia: genetic association and a potential functional mechanism. Biological Psychiatry. 64: 98-103. PMID 18281018 DOI: 10.1016/J.Biopsych.2007.12.012 |
0.441 |
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| 2008 |
Christiansen H, Chen W, Oades RD, Asherson P, Taylor EA, Lasky-Su J, Zhou K, Banaschewski T, Buschgens C, Franke B, Gabriels I, Manor I, Marco R, Müller UC, Mulligan A, ... ... Gill M, et al. Co-transmission of conduct problems with attention-deficit/hyperactivity disorder: familial evidence for a distinct disorder. Journal of Neural Transmission (Vienna, Austria : 1996). 115: 163-75. PMID 18200434 DOI: 10.1007/S00702-007-0837-Y |
0.345 |
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| 2008 |
Mulligan A, Gill M, Fitzgerald M. A case of ADHD and a major Y chromosome abnormality Journal of Attention Disorders. 12: 103-105. PMID 18192621 DOI: 10.1177/1087054707311220 |
0.327 |
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| 2008 |
Chen W, Zhou K, Sham P, Franke B, Kuntsi J, Campbell D, Fleischman K, Knight J, Andreou P, Arnold R, Altink M, Boer F, Boholst MJ, Buschgens C, Butler L, ... ... Gill M, et al. 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 : the Official Publication of the International Society of Psychiatric Genetics. 147: 1450-60. PMID 18189238 DOI: 10.1002/Ajmg.B.30672 |
0.359 |
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| 2008 |
Asherson P, Zhou K, Anney RJ, Franke B, Buitelaar J, Ebstein R, Gill M, Altink M, Arnold R, Boer F, Brookes K, Buschgens C, Butler L, Cambell D, Chen W, et al. A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16. Molecular Psychiatry. 13: 514-21. PMID 18180756 DOI: 10.1038/Sj.Mp.4002140 |
0.349 |
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| 2008 |
Morgan AR, Hamilton G, Turic D, Jehu L, Harold D, Abraham R, Hollingworth P, Moskvina V, Brayne C, Rubinsztein DC, Lynch A, Lawlor B, Gill M, O'Donovan M, Powell J, et al. Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 727-31. PMID 18163421 DOI: 10.1002/Ajmg.B.30670 |
0.376 |
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| 2008 |
Anney RJ, Hawi Z, Sheehan K, Mulligan A, Pinto C, Brookes KJ, Xu X, Zhou K, Franke B, Buitelaar J, Vermeulen SH, Banaschewski T, Sonuga-Barke E, Ebstein R, Manor I, ... ... Gill M, et al. 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 : the Official Publication of the International Society of Psychiatric Genetics. 147: 1495-500. PMID 18163388 DOI: 10.1002/Ajmg.B.30659 |
0.348 |
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| 2008 |
Corvin A, Donohoe G, Nangle JM, Schwaiger S, Morris D, Gill M. A dysbindin risk haplotype associated with less severe manic-type symptoms in psychosis. Neuroscience Letters. 431: 146-9. PMID 18162312 DOI: 10.1016/J.Neulet.2007.11.031 |
0.415 |
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| 2008 |
Lynch CA, Brazil JK, Cullen B, Coakley DP, Gill M, Lawlor BA, Hawi Z. 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: 29-33. PMID 18057979 DOI: 10.1007/S11845-007-0098-7 |
0.309 |
|
| 2008 |
Bellgrove MA, Barry E, Johnson KA, Cox M, Dáibhis A, Daly M, Hawi Z, Lambert D, Fitzgerald M, McNicholas F, Robertson IH, Gill M, Kirley A. Spatial attentional bias as a marker of genetic risk, symptom severity, and stimulant response in ADHD. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 33: 2536-45. PMID 18046306 DOI: 10.1038/Sj.Npp.1301637 |
0.353 |
|
| 2008 |
Sonuga-Barke EJ, Brookes KJ, Buitelaar J, Anney R, Bitsakou P, Baeyens D, Buschgens C, Chen W, Christiansen H, Eisenberg J, Kuntsi J, Manor I, Meliá A, Mulligan A, Rommelse N, ... ... Gill M, et al. 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 : the Official Publication of the International Society of Psychiatric Genetics. 147: 316-9. PMID 18023044 DOI: 10.1002/Ajmg.B.30596 |
0.395 |
|
| 2008 |
Donohoe G, Morris DW, De Sanctis P, Magno E, Montesi JL, Garavan HP, Robertson IH, Javitt DC, Gill M, Corvin AP, Foxe JJ. Early visual processing deficits in dysbindin-associated schizophrenia. Biological Psychiatry. 63: 484-9. PMID 17945199 DOI: 10.1016/J.Biopsych.2007.07.022 |
0.39 |
|
| 2008 |
Neale BM, Sham PC, Purcell S, Banaschewski T, Buitelaar J, Franke B, Sonuga-Barke E, Ebstein R, Eisenberg J, Mulligan A, Gill M, Manor I, Miranda A, Mulas F, Oades RD, et al. Population differences in the International Multi-Centre ADHD Gene Project. Genetic Epidemiology. 32: 98-107. PMID 17868146 DOI: 10.1002/Gepi.20265 |
0.332 |
|
| 2008 |
Morris DW, Murphy K, Kenny N, Purcell SM, McGhee KA, Schwaiger S, Nangle JM, Donohoe G, Clarke S, Scully P, Quinn J, Meagher D, Baldwin P, Crumlish N, O'Callaghan E, ... ... Gill M, et al. Dysbindin (DTNBP1) and the biogenesis of lysosome-related organelles complex 1 (BLOC-1): main and epistatic gene effects are potential contributors to schizophrenia susceptibility. Biological Psychiatry. 63: 24-31. PMID 17618940 DOI: 10.1016/J.Biopsych.2006.12.025 |
0.356 |
|
| 2008 |
Brookes KJ, Neale B, Xu X, Thapar A, Gill M, Langley K, Hawi Z, Mill J, Taylor E, Franke B, Chen W, Ebstein R, Buitelaar J, Banaschewski T, Sonuga-Barke E, et al. Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 94-9. PMID 17525975 DOI: 10.1002/Ajmg.B.30562 |
0.383 |
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| 2008 |
Behan C, McGlade N, Haq F, Kinsella A, Gill M, Corvin A, O'Callaghan E. Physical health and attendance at primary care in people with schizophrenia Irish Journal of Psychological Medicine. 25: 57-60. DOI: 10.1017/S0790966700010958 |
0.31 |
|
| 2008 |
Mitchell K, Runker A, Little G, O'Tuathaigh C, Dunleavy M, Morris D, Corvin A, Gill M, Henshall D, Waddington J. Semaphorin And Plexin Genes Specify Limbic And Cortical Connectivity And Are Implicated In The Etiology Of Schizophrenia Schizophrenia Research. 102: 26-27. DOI: 10.1016/S0920-9964(08)70084-7 |
0.34 |
|
| 2008 |
Sanders J, Johnson KA, Garavan H, Gill M, Gallagher L. A review of neuropsychological and neuroimaging research in autistic spectrum disorders: Attention, inhibition and cognitive flexibility Research in Autism Spectrum Disorders. 2: 1-16. DOI: 10.1016/J.Rasd.2007.03.005 |
0.328 |
|
| 2007 |
Corvin A, Donohoe G, McGhee K, Murphy K, Kenny N, Schwaiger S, Nangle JM, Morris D, Gill M. d-Amino acid oxidase (DAO) genotype and mood symptomatology in schizophrenia Neuroscience Letters. 426: 97-100. PMID 17890006 DOI: 10.1016/J.Neulet.2007.09.002 |
0.397 |
|
| 2007 |
Sanders J, Gill M. Unravelling the genome: a review of molecular genetic research in schizophrenia. Irish Journal of Medical Science. 176: 5-9. PMID 17849516 DOI: 10.1007/S11845-007-0004-3 |
0.352 |
|
| 2007 |
Waddington JL, Corvin AP, Donohoe G, O'Tuathaigh CM, Mitchell KJ, Gill M. Functional genomics and schizophrenia: endophenotypes and mutant models. The Psychiatric Clinics of North America. 30: 365-99. PMID 17720028 DOI: 10.1016/J.Psc.2007.04.011 |
0.355 |
|
| 2007 |
Jones I, Hamshere M, Nangle JM, Bennett P, Green E, Heron J, Segurado R, Lambert D, Holmans P, Corvin A, Owen M, Jones L, Gill M, Craddock N. Bipolar affective puerperal psychosis: genome-wide significant evidence for linkage to chromosome 16. The American Journal of Psychiatry. 164: 1099-104. PMID 17606662 DOI: 10.1176/Appi.Ajp.164.7.1099 |
0.371 |
|
| 2007 |
Lasky-Su J, Banaschewski T, Buitelaar J, Franke B, Brookes K, Sonuga-Barke E, Ebstein R, Eisenberg J, Gill M, Manor I, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, et al. Partial replication of a DRD4 association in ADHD individuals using a statistically derived quantitative trait for ADHD in a family-based association test. Biological Psychiatry. 62: 985-90. PMID 17560555 DOI: 10.1016/J.Biopsych.2007.03.006 |
0.38 |
|
| 2007 |
Corvin A, McGhee KA, Murphy K, Donohoe G, Nangle JM, Schwaiger S, Kenny N, Clarke S, Meagher D, Quinn J, Scully P, Baldwin P, Browne D, Walsh C, Waddington JL, ... ... Gill M, et al. Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sample American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 144: 949-953. PMID 17492767 DOI: 10.1002/Ajmg.B.30452 |
0.406 |
|
| 2007 |
Donohoe G, Morris DW, Robertson IH, Clarke S, McGhee KA, Schwaiger S, Nangle JM, Gill M, Corvin A. Variance in facial recognition performance associated with BDNF in schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 578-9. PMID 17450558 DOI: 10.1002/Ajmg.B.30382 |
0.331 |
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| 2007 |
Johnson KA, Robertson IH, Kelly SP, Silk TJ, Barry E, Dáibhis A, Watchorn A, Keavey M, Fitzgerald M, Gallagher L, Gill M, Bellgrove MA. Dissociation in performance of children with ADHD and high-functioning autism on a task of sustained attention. Neuropsychologia. 45: 2234-45. PMID 17433378 DOI: 10.1016/J.Neuropsychologia.2007.02.019 |
0.314 |
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| 2007 |
Asherson P, Brookes K, Franke B, Chen W, Gill M, Ebstein RP, Buitelaar J, Banaschewski T, Sonuga-Barke E, Eisenberg J, Manor I, Miranda A, Oades RD, Roeyers H, Rothenberger A, et al. Confirmation that a specific haplotype of the dopamine transporter gene is associated with combined-type ADHD. The American Journal of Psychiatry. 164: 674-7. PMID 17403983 DOI: 10.1176/Appi.Ajp.164.4.674 |
0.347 |
|
| 2007 |
Morgan AR, Turic D, Jehu L, Hamilton G, Hollingworth P, Moskvina V, Jones L, Lovestone S, Brayne C, Rubinsztein DC, Lawlor B, Gill M, O'Donovan MC, Owen MJ, Williams J. Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 762-70. PMID 17373700 DOI: 10.1002/Ajmg.B.30509 |
0.355 |
|
| 2007 |
Grupe A, Abraham R, Li Y, Rowland C, Hollingworth P, Morgan A, Jehu L, Segurado R, Stone D, Schadt E, Karnoub M, Nowotny P, Tacey K, Catanese J, Sninsky J, ... ... Gill M, et al. Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants. Human Molecular Genetics. 16: 865-73. PMID 17317784 DOI: 10.1093/Hmg/Ddm031 |
0.374 |
|
| 2007 |
Yang MS, Gill M. A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 25: 69-85. PMID 17236739 DOI: 10.1016/J.Ijdevneu.2006.12.002 |
0.369 |
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| 2007 |
Thapar A, Langley K, Asherson P, Gill M. Gene-environment interplay in attention-deficit hyperactivity disorder and the importance of a developmental perspective. The British Journal of Psychiatry : the Journal of Mental Science. 190: 1-3. PMID 17197648 DOI: 10.1192/Bjp.Bp.106.027003 |
0.37 |
|
| 2007 |
Yang MS, Cochrane L, Conroy J, Hawi Z, Fitzgerald M, Gallagher L, Gill M. Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population Psychiatric Genetics. 17: 39-41. PMID 17167344 DOI: 10.1097/Ypg.0B013E3280115428 |
0.355 |
|
| 2007 |
Johnson KA, Kelly SP, Bellgrove MA, Barry E, Cox M, Gill M, Robertson IH. Response variability in attention deficit hyperactivity disorder: evidence for neuropsychological heterogeneity. Neuropsychologia. 45: 630-8. PMID 17157885 DOI: 10.1016/J.Neuropsychologia.2006.03.034 |
0.3 |
|
| 2007 |
Sheehan K, Hawi Z, Gill M, Kent L. No association between TPH2 gene polymorphisms and ADHD in a UK sample. Neuroscience Letters. 412: 105-7. PMID 17123708 DOI: 10.1016/J.Neulet.2006.10.043 |
0.37 |
|
| 2007 |
Donohoe G, Morris DW, Clarke S, McGhee KA, Schwaiger S, Nangle JM, Garavan H, Robertson IH, Gill M, Corvin A. Variance in neurocognitive performance is associated with dysbindin-1 in schizophrenia: a preliminary study. Neuropsychologia. 45: 454-8. PMID 16930638 DOI: 10.1016/J.Neuropsychologia.2006.06.016 |
0.388 |
|
| 2006 |
Bellgrove MA, Hawi Z, Gill M, Robertson IH. The cognitive genetics of attention deficit hyperactivity disorder (ADHD): sustained attention as a candidate phenotype. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 42: 838-45. PMID 17131588 DOI: 10.1016/S0010-9452(08)70426-X |
0.373 |
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| 2006 |
Donohoe G, Reilly R, Clarke S, Meredith S, Green B, Morris D, Gill M, Corvin A, Garavan H, Robertson IH. Do antisaccade deficits in schizophrenia provide evidence of a specific inhibitory function? Journal of the International Neuropsychological Society : Jins. 12: 901-6. PMID 17064452 DOI: 10.1017/S135561770606108X |
0.336 |
|
| 2006 |
Brookes K, Xu X, Chen W, Zhou K, Neale B, Lowe N, Anney R, Aneey R, Franke B, Gill M, Ebstein R, Buitelaar J, Sham P, Campbell D, Knight J, et al. 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: 934-53. PMID 16894395 DOI: 10.1038/Sj.Mp.4001869 |
0.412 |
|
| 2006 |
Bellgrove MA, Mattingley JB, Hawi Z, Mullins C, Kirley A, Gill M, Robertson IH. Impaired temporal resolution of visual attention and dopamine beta hydroxylase genotype in attention-deficit/hyperactivity disorder. Biological Psychiatry. 60: 1039-45. PMID 16876143 DOI: 10.1016/J.Biopsych.2006.03.062 |
0.332 |
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| 2006 |
Donohoe G, Clarke S, Morris D, Nangle JM, Schwaiger S, Gill M, Corvin A, Robertson IH. Are deficits in executive sub-processes simply reflecting more general cognitive decline in schizophrenia? Schizophrenia Research. 85: 168-73. PMID 16716568 DOI: 10.1016/J.Schres.2006.03.041 |
0.33 |
|
| 2006 |
Nangle JM, Clarke S, Morris DW, Schwaiger S, McGhee KA, Kenny N, Murphy K, Gill M, Corvin A, Donohoe G. Neurocognition and suicidal behaviour in an Irish population with major psychotic disorders. Schizophrenia Research. 85: 196-200. PMID 16690256 DOI: 10.1016/J.Schres.2006.03.035 |
0.352 |
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| 2006 |
Talkowski ME, Seltman H, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin AP, Deshpande SN, Egan MF, Gill M, Kendler KS, Kirov G, Heston LL, et al. Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biological Psychiatry. 60: 152-62. PMID 16631129 DOI: 10.1016/J.Biopsych.2006.02.015 |
0.411 |
|
| 2006 |
Norton N, Moskvina V, Morris DW, Bray NJ, Zammit S, Williams NM, Williams HJ, Preece AC, Dwyer S, Wilkinson JC, Spurlock G, Kirov G, Buckland P, Waddington JL, Gill M, et al. Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 96-101. PMID 16249994 DOI: 10.1002/Ajmg.B.30236 |
0.397 |
|
| 2006 |
Lowe N, Barry E, Gill M, Hawi Z. An overview of the pharmacogenetics and molecular genetics of ADHD Current Pharmacogenomics. 4: 231-243. DOI: 10.2174/157016006778195106 |
0.376 |
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| 2006 |
Segurado R, Hawi Z, Gill M. Reply to Joober and Sengupta American Journal of Human Genetics. 79: 766-768. DOI: 10.1086/507588 |
0.378 |
|
| 2006 |
Brookes K, Xu X, Chen W, Zhou K, Neale B, Lowe N, Anney R, Franke B, Gill M, Ebstein R, Buitelaar J, Sham P, Campbell D, Knight J, Andreou P, et al. Erratum: 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: 1139-1139. DOI: 10.1038/Sj.Mp.4001902 |
0.358 |
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| 2006 |
Sheehan K, Lowe N, Kirley A, Mullins C, Fitzgerald M, Gill M, Hawi Z. Erratum: Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD (Molecular Psychiatry (2005) 10 (944-949) DOI: 10.1038/sj.mp.4001698) Molecular Psychiatry. 11: 221-221. DOI: 10.1038/Sj.Mp.4001771 |
0.323 |
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| 2005 |
Hawi Z, Segurado R, Conroy J, Sheehan K, Lowe N, Kirley A, Shields D, Fitzgerald M, Gallagher L, Gill M. Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder American Journal of Human Genetics. 77: 958-965. PMID 16380908 DOI: 10.1086/498174 |
0.392 |
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| 2005 |
Segurado R, Conroy J, Meally E, Fitzgerald M, Gill M, Gallagher L. Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31 American Journal of Psychiatry. 162: 2182-2184. PMID 16263864 DOI: 10.1176/Appi.Ajp.162.11.2182 |
0.404 |
|
| 2005 |
Hamshere ML, Bennett P, Williams N, Segurado R, Cardno A, Norton N, Lambert D, Williams H, Kirov G, Corvin A, Holmans P, Jones L, Jones I, Gill M, O'Donovan MC, et al. Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13. Archives of General Psychiatry. 62: 1081-8. PMID 16203953 DOI: 10.1001/Archpsyc.62.10.1081 |
0.401 |
|
| 2005 |
McGuffin P, Knight J, Breen G, Brewster S, Boyd PR, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen MJ, Perry J, Preisig M, Reich T, et al. Whole genome linkage scan of recurrent depressive disorder from the depression network study. Human Molecular Genetics. 14: 3337-45. PMID 16203746 DOI: 10.1093/Hmg/Ddi363 |
0.333 |
|
| 2005 |
McQueen MB, Devlin B, Faraone SV, Nimgaonkar VL, Sklar P, Smoller JW, Abou Jamra R, Albus M, Bacanu SA, Baron M, Barrett TB, Berrettini W, Blacker D, Byerley W, Cichon S, ... ... Gill M, et al. Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q. American Journal of Human Genetics. 77: 582-95. PMID 16175504 DOI: 10.1086/491603 |
0.357 |
|
| 2005 |
Bellgrove MA, Hawi Z, Kirley A, Gill M, Robertson IH. 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: 1847-57. PMID 16168728 DOI: 10.1016/J.Neuropsychologia.2005.03.011 |
0.35 |
|
| 2005 |
Bellgrove MA, Hawi Z, Kirley A, Fitzgerald M, Gill M, Robertson IH. Association between dopamine transporter (DAT1) genotype, left-sided inattention, and an enhanced response to methylphenidate in attention-deficit hyperactivity disorder. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 30: 2290-7. PMID 16123773 DOI: 10.1038/Sj.Npp.1300839 |
0.344 |
|
| 2005 |
McGhee KA, Morris DW, Schwaiger S, Nangle JM, Donohoe G, Clarke S, Meagher D, Quinn J, Scully P, Waddington JL, Gill M, Corvin A. Investigation of the apolipoprotein-L (APOL) gene family and schizophrenia using a novel DNA pooling strategy for public database SNPs. Schizophrenia Research. 76: 231-8. PMID 15949655 DOI: 10.1016/J.Schres.2005.01.006 |
0.399 |
|
| 2005 |
Lambert D, Middle F, Hamshere ML, Segurado R, Raybould R, Corvin A, Green E, O'Mahony E, Nikolov I, Mulcahy T, Haque S, Bort S, Bennett P, Norton N, Owen MJ, ... ... Gill M, et al. Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22. Molecular Psychiatry. 10: 831-41. PMID 15940300 DOI: 10.1038/Sj.Mp.4001684 |
0.315 |
|
| 2005 |
Kent L, Green E, Hawi Z, Kirley A, Dudbridge F, Lowe N, Raybould R, Langley K, Bray N, Fitzgerald M, Owen MJ, O'Donovan MC, Gill M, Thapar A, Craddock N. 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: 939-43. PMID 15940292 DOI: 10.1038/Sj.Mp.4001696 |
0.373 |
|
| 2005 |
Sheehan K, Lowe N, Kirley A, Mullins C, Fitzgerald M, Gill M, Hawi Z. Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD Molecular Psychiatry. 10: 944-949. PMID 15940290 DOI: 10.1038/Sj.Mp.4001698 |
0.406 |
|
| 2005 |
Bellgrove MA, Hawi Z, Lowe N, Kirley A, Robertson IH, Gill M. 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 : the Official Publication of the International Society of Psychiatric Genetics. 136: 81-6. PMID 15909295 DOI: 10.1002/Ajmg.B.30193 |
0.395 |
|
| 2005 |
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. 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. 134: 110-114. PMID 15717295 DOI: 10.1002/Ajmg.B.30158 |
0.375 |
|
| 2005 |
Bellgrove MA, Domschke K, Hawi Z, Kirley A, Mullins C, Robertson IH, Gill M. The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD. Experimental Brain Research. 163: 352-60. PMID 15654584 DOI: 10.1007/S00221-004-2180-Y |
0.378 |
|
| 2004 |
Lowe N, Kirley A, Mullins C, Fitzgerald M, Gill M, Hawi Z. Multiple marker analysis at the promoter region of the DRD4 gene and ADHD: evidence of linkage and association with the SNP -616. American Journal of Medical Genetics. 131: 33-37. PMID 15389764 DOI: 10.1002/Ajmg.B.30071 |
0.387 |
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| 2004 |
Kirley A, Lowe N, Mullins C, McCarron M, Daly G, Waldman I, Fitzgerald M, Gill M, Hawi Z. Phenotype studies of the DRD4 gene polymorphisms in ADHD: association with oppositional defiant disorder and positive family history. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 131: 38-42. PMID 15389763 DOI: 10.1002/Ajmg.B.30072 |
0.398 |
|
| 2004 |
Williams NM, Preece A, Morris DW, Spurlock G, Bray NJ, Stephens M, Norton N, Williams H, Clement M, Dwyer S, Curran C, Wilkinson J, Moskvina V, Waddington JL, Gill M, et al. Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1). Archives of General Psychiatry. 61: 336-44. PMID 15066891 DOI: 10.1001/Archpsyc.61.4.336 |
0.355 |
|
| 2004 |
Corvin AP, Morris DW, McGhee K, Schwaiger S, Scully P, Quinn J, Meagher D, Clair DS, Waddington JL, Gill M. Confirmation and refinement of an 'at-risk' haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus. Molecular Psychiatry. 9: 208-13. PMID 14966480 DOI: 10.1038/Sj.Mp.4001412 |
0.395 |
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| 2004 |
Morris DW, Rodgers A, McGhee KA, Schwaiger S, Scully P, Quinn J, Meagher D, Waddington JL, Gill M, Corvin AP. Confirming RGS4 as a susceptibility gene for schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 125: 50-3. PMID 14755443 DOI: 10.1002/Ajmg.B.20109 |
0.387 |
|
| 2004 |
Lowe N, Kirley A, Hawi Z, Sham P, Wickham H, Kratochvil CJ, Smith SD, Lee SY, Levy F, Kent L, Middle F, Rohde LA, Roman T, Tahir E, Yazgan Y, ... ... Gill M, et al. Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes. American Journal of Human Genetics. 74: 348-56. PMID 14732906 DOI: 10.1086/381561 |
0.41 |
|
| 2004 |
Conroy J, Meally E, Kearney G, Fitzgerald M, Gill M, Gallagher L. Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population. Molecular Psychiatry. 9: 587-593. PMID 14708029 DOI: 10.1038/Sj.Mp.4001459 |
0.382 |
|
| 2004 |
Gallagher L, Hawi Z, Kearney G, Fitzgerald M, Gill M. No association between allelic variants of HOXA1/HOXB1 and autism. American Journal of Medical Genetics. 124: 64-67. PMID 14681917 DOI: 10.1002/Ajmg.B.20094 |
0.375 |
|
| 2003 |
Hawi Z, Kirley A, Lowe N, Fitzgerald M, Gill M. Recent genetic advances in ADHD and diagnostic and therapeutic prospects. Expert Review of Neurotherapeutics. 3: 453-464. PMID 19810930 DOI: 10.1586/14737175.3.4.453 |
0.359 |
|
| 2003 |
Hawi Z, Sheehan K, Lynch A, Evans I, Lowe N, Lawlor B, Gill M. Late onset Alzheimer's disease and apolipoprotein association in the Irish population: relative risk and attributable fraction. Irish Journal of Medical Science. 172: 74-76. PMID 12930057 DOI: 10.1007/Bf02915251 |
0.301 |
|
| 2003 |
Kirley A, Lowe N, Hawi Z, Mullins C, Daly G, Waldman I, McCarron M, O'Donnell D, Fitzgerald M, Gill M. Association of the 480 bp DAT1 allele with methylphenidate response in a sample of Irish children with ADHD. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 121: 50-4. PMID 12898575 DOI: 10.1002/Ajmg.B.20071 |
0.367 |
|
| 2003 |
Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. American Journal of Human Genetics. 73: 49-62. PMID 12802785 DOI: 10.1086/376547 |
0.352 |
|
| 2003 |
Gallagher L, Becker K, Kearney G, Dunlop A, Stallings R, Green A, Fitzgerald M, Gill M. Brief report: A case of autism associated with del(2)(q32.1q32.2) or (q32.2q32.3). Journal of Autism and Developmental Disorders. 33: 105-8. PMID 12708586 DOI: 10.1023/A:1022242807513 |
0.354 |
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| 2003 |
Hawi Z, Lowe N, Kirley A, Gruenhage F, Nöthen M, Greenwood T, Kelsoe J, Fitzgerald M, Gill M. Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these loci. Molecular Psychiatry. 8: 299-308. PMID 12660802 DOI: 10.1038/Sj.Mp.4001290 |
0.392 |
|
| 2003 |
Morris DW, McGhee KA, Schwaiger S, Scully P, Quinn J, Meagher D, Waddington JL, Gill M, Corvin AP. No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study. Schizophrenia Research. 60: 167-72. PMID 12591580 DOI: 10.1016/S0920-9964(02)00527-3 |
0.384 |
|
| 2002 |
Lambert D, Gill M. Evaluation of parent-of-origin effect in bipolar affective disorder relating to susceptibility loci on chromosome 18. Bipolar Disorders. 4: 31-32. PMID 12479673 DOI: 10.1034/J.1399-5618.4.S1.7.X |
0.305 |
|
| 2002 |
Kirley A, Hawi Z, Daly G, McCarron M, Mullins C, Millar N, Waldman I, Fitzgerald M, Gill M. Dopaminergic system genes in ADHD: toward a biological hypothesis. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 27: 607-19. PMID 12377397 DOI: 10.1016/S0893-133X(02)00315-9 |
0.378 |
|
| 2002 |
Brophy K, Hawi Z, Kirley A, Fitzgerald M, Gill M. Synaptosomal-associated protein 25 (SNAP-25) and attention deficit hyperactivity disorder (ADHD): Evidence of linkage and association in the Irish population Molecular Psychiatry. 7: 913-917. PMID 12232787 DOI: 10.1038/Sj.Mp.4001092 |
0.348 |
|
| 2002 |
Kent L, Doerry U, Hardy E, Parmar R, Gingell K, Hawi Z, Kirley A, Lowe N, Fitzgerald M, Gill M, Craddock N. Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): analysis and pooled analysis. Molecular Psychiatry. 7: 908-12. PMID 12232786 DOI: 10.1038/Sj.Mp.4001100 |
0.372 |
|
| 2002 |
McEvoy B, Hawi Z, Fitzgerald M, Gill M. No evidence of linkage or association between the norepinephrine transporter (NET) gene polymorphisms and ADHD in the Irish population. American Journal of Medical Genetics. 114: 665-666. PMID 12210284 DOI: 10.1002/Ajmg.10416 |
0.345 |
|
| 2002 |
Hawi Z, Dring M, Kirley A, Foley D, Kent L, Craddock N, Asherson P, Curran S, Gould A, Richards S, Lawson D, Pay H, Turic D, Langley K, Owen M, ... ... Gill M, et al. Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample. Molecular Psychiatry. 7: 718-25. PMID 12192616 DOI: 10.1038/Sj.Mp.4001048 |
0.378 |
|
| 2002 |
Abood Z, Sharkey A, Webb M, Kelly A, Gill M. Are patients with bipolar affective disorder socially disadvantaged? A comparison with a control group. Bipolar Disorders. 4: 243-248. PMID 12190713 DOI: 10.1034/J.1399-5618.2002.01184.X |
0.333 |
|
| 2002 |
Wickham H, Walsh C, Asherson P, Gill M, Owen MJ, McGuffin P, Murray R, Sham P. Familiality of clinical characteristics in schizophrenia. Journal of Psychiatric Research. 36: 325-9. PMID 12127600 DOI: 10.1016/S0022-3956(02)00008-0 |
0.349 |
|
| 2002 |
Holmes J, Payton A, Barrett J, Harrington R, McGuffin P, Owen M, Ollier W, Worthington J, Gill M, Kirley A, Hawi Z, Fitzgerald M, Asherson P, Curran S, Mill J, et al. Association of DRD4 in children with ADHD and comorbid conduct problems. American Journal of Medical Genetics. 114: 150-3. PMID 11857575 DOI: 10.1002/Ajmg.10149 |
0.343 |
|
| 2002 |
Bennett P, Segurado R, Jones I, Bort S, McCandless F, Lambert D, Heron J, Comerford C, Middle F, Corvin A, Pelios G, Kirov G, Larsen B, Mulcahy T, Williams N, ... ... Gill M, et al. The Wellcome trust UK-Irish bipolar affective disorder sibling-pair genome screen: first stage report. Molecular Psychiatry. 7: 189-200. PMID 11840312 DOI: 10.1038/Sj.Mp.4000957 |
0.34 |
|
| 2002 |
Mulligan A, Webb M, Gill M. A variant of nymphomania in association with obsessive-compulsive disorder Irish Journal of Psychological Medicine. 19: 96-98. DOI: 10.1017/S0790966700007163 |
0.308 |
|
| 2001 |
Kent L, Green E, Holmes J, Thapar A, Gill M, Hawi Z, Fitzgerald M, Asherson P, Curran S, Mills J, Payton A, Craddock N. No association between CHRNA7 microsatellite markers and attention-deficit hyperactivity disorder. American Journal of Medical Genetics. 105: 686-9. PMID 11803515 DOI: 10.1002/Ajmg.1553 |
0.361 |
|
| 2001 |
Hawi Z, Foley D, Kirley A, McCarron M, Fitzgerald M, Gill M. Dopa decarboxylase gene polymorphisms and attention deficit hyperactivity disorder (ADHD): no evidence for association in the Irish population Molecular Psychiatry. 6: 420-424. PMID 11443526 DOI: 10.1038/Sj.Mp.4000903 |
0.4 |
|
| 2001 |
Reilly JL, Murphy PT, Byrne M, Larkin C, Gill M, O'Callaghan E, Lane A. Dermatoglyphic fluctuating asymmetry and atypical handedness in schizophrenia Schizophrenia Research. 50: 159-168. PMID 11439236 DOI: 10.1016/S0920-9964(00)00044-X |
0.345 |
|
| 2001 |
Kent L, Middle F, Hawi Z, Fitzgerald M, Gill M, Feehan C, Craddock NJ. Nicotinic acetylcholine receptor α4 subunit gene polymorphism and attention deficit hyperactivity disorder Psychiatric Genetics. 11: 37-40. PMID 11409698 DOI: 10.1097/00041444-200103000-00007 |
0.325 |
|
| 2001 |
Lowe N, Hawi Z, Fitzgerald M, Gill M. No evidence of linkage or association between ADHD and DXS7 locus in Irish population. American Journal of Medical Genetics. 105: 394-395. PMID 11378856 DOI: 10.1002/Ajmg.1357 |
0.323 |
|
| 2001 |
Wickham H, Walsh C, Asherson P, Taylor C, Sigmundson T, Gill M, Owen MJ, McGuffin P, Murray R, Sham P. Familiality of symptom dimensions in schizophrenia Schizophrenia Research. 47: 223-232. PMID 11278139 DOI: 10.1016/S0920-9964(00)00098-0 |
0.351 |
|
| 2001 |
Kent L, Hardy E, Hawzi Z, Fitzgerald M, Kirley A, Gill M, Craddock NJ. A significant association of serotonin transporter polymorphism haplotypes in attention deficit hyperactivity disorder (ADHD) American Journal of Medical Genetics. 105: 574-575. DOI: 10.1002/Ajmg.1592 |
0.354 |
|
| 2000 |
Messas GP, Gentil V, Gill M, Murray R, Vallada HP. Lack of gender effect on familial schizophrenia: a Brazilian study Arquivos De Neuro-Psiquiatria. 58: 494-498. PMID 10920412 DOI: 10.1590/S0004-282X2000000300015 |
0.341 |
|
| 2000 |
Hawi Z, Millar N, Daly G, Fitzgerald M, Gill M. No association between catechol-O-methyltransferase (COMT) gene polymorphism and attention deficit hyperactivity disorder (ADHD) in an Irish sample. American Journal of Medical Genetics. 96: 282-284. PMID 10898900 DOI: 10.1002/1096-8628(20000612)96:3<282::Aid-Ajmg9>3.0.Co;2-R |
0.382 |
|
| 2000 |
Hawi Z, McCarron M, Kirley A, Daly G, Fitzgerald M, Gill M. No association of the dopamine DRD4 receptor (DRD4) gene polymorphism with attention deficit hyperactivity disorder (ADHD) in the Irish population. American Journal of Medical Genetics. 96: 268-272. PMID 10898897 DOI: 10.1002/1096-8628(20000612)96:3<268::AID-AJMG6>3.0.CO;2 |
0.37 |
|
| 1999 |
Tyrrell J, Cosgrave M, McPherson J, Hawi Z, Trulock V, Calvert J, Lawlor B, Gill M. Presenilin 1 and alpha-1-antichymotrypsin polymorphisms in Down syndrome: no effect on the presence of dementia. American Journal of Medical Genetics. 88: 616-20. PMID 10581479 DOI: 10.1002/(Sici)1096-8628(19991215)88:6<616::Aid-Ajmg8>3.0.Co;2-I |
0.312 |
|
| 1999 |
Hawi Z, Mynett-Johnson L, Murphy V, Straub RE, Kendler KS, Walsh D, McKeon P, Gill M. No evidence to support the association of the potassium channel gene hSKCa3 CAG repeat with schizophrenia or bipolar disorder in the Irish population. Molecular Psychiatry. 4: 488-91. PMID 10523823 DOI: 10.1038/Sj.Mp.4000560 |
0.419 |
|
| 1999 |
Bowen T, Kirov G, Gill M, Spurlock G, Vallada HP, Murray RM, McGuffin P, Collier DA, Owen MJ, Craddock N. Linkage studies of bipolar disorder with chromosome 18 markers American Journal of Medical Genetics - Neuropsychiatric Genetics. 88: 503-509. PMID 10490707 DOI: 10.1002/(Sici)1096-8628(19991015)88:5<503::Aid-Ajmg13>3.0.Co;2-U |
0.351 |
|
| 1999 |
Rees MI, Fenton I, Williams NM, Holmans P, Norton N, Cardno A, Asherson P, Spurlock G, Roberts E, Parfitt E, Mant R, Vallada H, Dawson E, Li MW, Collier DA, ... ... Gill M, et al. Autosome search for schizophrenia susceptibility genes in multiply affected families. Molecular Psychiatry. 4: 353-9. PMID 10483052 DOI: 10.1038/Sj.Mp.4000521 |
0.363 |
|
| 1999 |
Hawi Z, Gibson S, Straub RE, Walsh D, Kendler KS, Gill M. Schizophrenia and HLA: No association with PCR-SSOP typed classical loci in a large Irish familial sample. American Journal of Medical Genetics. 88: 422-9. PMID 10402512 DOI: 10.1002/(SICI)1096-8628(19990820)88:4<422::AID-AJMG22>3.0.CO;2-# |
0.34 |
|
| 1999 |
Gibson S, Hawi Z, Straub RE, Walsh D, Kendler KS, Gill M. HLA and schizophrenia: refutation of reported associations with A9 (A23/A24), DR4, and DQbeta1*0602. American Journal of Medical Genetics. 88: 416-21. PMID 10402511 DOI: 10.1002/(Sici)1096-8628(19990820)88:4<416::Aid-Ajmg21>3.0.Co;2-S |
0.336 |
|
| 1999 |
Daly G, Hawi Z, Fitzgerald M, Gill M. Mapping susceptibility loci in attention deficit hyperactivity disorder: preferential transmission of parental alleles at DAT1, DBH and DRD5 to affected children Molecular Psychiatry. 4: 192-196. PMID 10208453 DOI: 10.1038/Sj.Mp.4000510 |
0.333 |
|
| 1999 |
Hawi Z, Mynett-Johnson L, Gill M, Murphy V, Straubl RE, Kendler KS, Walsh D, Machen F, Connell H, McKeon P, Shields D. Pseudoautosomal gene Psychiatric Genetics. 9: 129-134. DOI: 10.1097/00041444-199909000-00003 |
0.409 |
|
| 1999 |
Nugent E, Hawi Z, Lowe N, Kirley A, Fitzgerald MF, Gill M. Attention Deficit Hyperactivity Disorder (ADHD) and 5-HT2C receptor: A slight increase in the transmission of Cys23 to ADHD cases American Journal of Medical Genetics. 105. DOI: 10.1002/Ajmg.1595/Pdf |
0.306 |
|
| 1998 |
Hawi Z, Straub RE, O'Neill A, Kendler KS, Walsh D, Gill M. No linkage or linkage disequilibrium between brain-derived neurotrophic factor (BDNF) dinucleotide repeat polymorphism and schizophrenia in Irish families. Psychiatry Research. 81: 111-6. PMID 9858028 DOI: 10.1016/S0165-1781(98)00076-6 |
0.366 |
|
| 1998 |
Vallada HP, Vasques L, Curtis D, Zatz M, Kirov G, Lauriano V, Gentil V, Murray RM, McGuffin P, Owen M, Gill M, Craddock N, Collier DA. Linkage analysis between bipolar affective disorder and markers on chromosome X. Psychiatric Genetics. 8: 183-6. PMID 9800220 DOI: 10.1097/00041444-199800830-00008 |
0.35 |
|
| 1998 |
Vallada H, Curtis D, Sham P, Kunugi H, Zhao J, Murray R, McGuffin P, Nanko S, Owen M, Gill M, Collier D, Antonarakis S, Housman D, Kazazian H, Nestadt G, et al. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12 Schizophrenia Research. 32: 115-121. PMID 9713907 DOI: 10.1016/S0920-9964(98)00048-6 |
0.414 |
|
| 1998 |
Wright P, Dawson E, Donaldson PT, Underhill JA, Sham PC, Zhao J, Gill M, Nanko S, Owen MJ, McGuffin P, Murray RM. A transmission/disequilibrium study of the DRB1*04 gene locus on chromosome 6p21.3 with schizophrenia. Schizophrenia Research. 32: 75-80. PMID 9713901 DOI: 10.1016/S0920-9964(98)00050-4 |
0.413 |
|
| 1998 |
Hawi Z, McCabe U, Straub RE, O'Neill A, Kendler KS, Walsh D, Gill M. Examination of new and reported data of the DRD3/MscI polymorphism: no support for the proposed association with schizophrenia. Molecular Psychiatry. 3: 150-5. PMID 9577839 DOI: 10.1038/Sj.Mp.4000362 |
0.408 |
|
| 1998 |
Hawi Z, Gill M. Report on the Fifth International Congress of Psychiatric Genetics Molecular Psychiatry. 3: 109-111. PMID 9577833 DOI: 10.1038/Sj.Mp.4000361 |
0.369 |
|
| 1998 |
Gill M, Richards T. Meeting the challenge of genetic advance: Requires rigorous navigation between laboratory, clinic, and society Bmj. 316: 570-570. PMID 9518896 DOI: 10.1136/Bmj.316.7131.570 |
0.341 |
|
| 1998 |
Spurlock G, Williams J, McGuffin P, Aschauer HN, Lenzinger E, Fuchs K, Sieghart WC, Meszaros K, Fathi N, Laurent C, Mallet J, Macciardi F, Pedrini S, Gill M, Hawi Z, et al. European Multicentre Association Study of Schizophrenia: a study of the DRD2 Ser311Cys and DRD3 Ser9Gly polymorphisms. American Journal of Medical Genetics. 81: 24-8. PMID 9514583 DOI: 10.1002/(Sici)1096-8628(19980207)81:1<24::Aid-Ajmg5>3.0.Co;2-N |
0.404 |
|
| 1997 |
Kunugi H, Vallada HP, Sham PC, Hoda F, Arranz MJ, Li T, Nanko S, Murray RM, McGuffin P, Owen M, Gill M, Collier DA. Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families. Psychiatric Genetics. 7: 97-101. PMID 9323320 DOI: 10.1097/00041444-199723000-00001 |
0.421 |
|
| 1997 |
Kunugi H, Vallada HP, Hoda F, Kirov G, Gill M, Aitchison KJ, Ball D, Arranz MJ, Murray RM, Collier DA. No evidence for an association of affective disorders with high- or low-activity allele of catechol-o-methyltransferase gene. Biological Psychiatry. 42: 282-5. PMID 9270905 DOI: 10.1016/S0006-3223(96)00366-6 |
0.349 |
|
| 1997 |
Hawi Z, Myakishev MV, Straub RE, O'Neill A, Kendler KS, Walsh D, Gill M. No association or linkage between the 5-HT2a/T102C polymorphism and schizophrenia in Irish families. American Journal of Medical Genetics. 74: 370-3. PMID 9259371 DOI: 10.1002/(Sici)1096-8628(19970725)74:4<370::Aid-Ajmg6>3.0.Co;2-T |
0.415 |
|
| 1997 |
Gill M, Daly G, Heron S, Hawi Z, Fitzgerald M. Confirmation Of Association Between Attention Deficit Hyperactivity Disorder And A Dopamine Transporter Polymorphism Molecular Psychiatry. 2: 311-313. PMID 9246671 DOI: 10.1038/Sj.Mp.4000290 |
0.352 |
|
| 1997 |
Ashworth A, Abusaad I, Walsh C, Nanko S, Murray RM, Asherson P, McGuffin P, Gill M, Owen MJ, Collier DA. Linkage analysis of the fragile X gene FMR-1 and schizophrenia: no evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat. Psychiatric Genetics. 6: 81-6. PMID 8840394 DOI: 10.1097/00041444-199622000-00008 |
0.374 |
|
| 1997 |
Gill M, Hawi Z, Webb M. Homozygous mutation at cytochrome P4502D6 in an individual with schizophrenia: Implications for antipsychotic drugs, side effects and compliance Irish Journal of Psychological Medicine. 14: 38-39. DOI: 10.1017/S0790966700002925 |
0.313 |
|
| 1997 |
Spurlock G, Williams J, McGuffin P, Mallet J, Nöthen M, Gill M, Aschauer H, Adlfsson R, Macciardi F, Owen MJ. Meta-analysis of association studies between schizophrenia and polymorphisms of the 5-hydroxytryptamine type 2A receptor gene Schizophrenia Research. 24: 91. DOI: 10.1016/S0920-9964(97)82247-5 |
0.352 |
|
| 1997 |
Wright P, Dawson E, Donaldson PT, Underhill JA, Sham PC, Gill M, Nanko S, Owen MJ, McGuffin P, Murray RM. Evidence from a transmission/disequilibrium study that alleles of the DRB1*04 gene on chromosome 6p21.3 may protect against schizophrenia Schizophrenia Research. 24: 51. DOI: 10.1016/S0920-9964(97)82145-7 |
0.368 |
|
| 1996 |
Gill M, Hawi Z, O'Neill FA, Walsh D, Straub RE, Kendler KS. Neurotrophin-3 gene polymorphisms and schizophrenia: no evidence for linkage or association. Psychiatric Genetics. 6: 183-6. PMID 9149322 DOI: 10.1097/00041444-199624000-00002 |
0.421 |
|
| 1996 |
Vallada H, Craddock N, Vasques L, Curtis D, Kirov G, Lauriano V, Gentil V, Passos-Bueno R, Murray RM, Zatz M, McGuffin P, Powell JF, Gill M, Owen M, Collier DA. Linkage studies in bipolar affective disorder with markers on chromosome 21. Journal of Affective Disorders. 41: 217-21. PMID 8988454 DOI: 10.1016/S0165-0327(96)00055-9 |
0.356 |
|
| 1996 |
Wildenauer DB, Schwab SG, Albus M, Hallmayer J, Lerer B, Maier W, Blackwood D, Muir W, Clair DS, Morris S, Moises HW, Yang L, Kristbjarnarson H, Helgason T, Wiese C, ... ... Gill M, et al. Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study American Journal of Medical Genetics. 67: 580-594. PMID 8950417 DOI: 10.1002/(Sici)1096-8628(19961122)67:6<580::Aid-Ajmg11>3.0.Co;2-P |
0.33 |
|
| 1996 |
Kunugi H, Curtis D, Vallada HP, Nanko S, Powell JF, Murray RM, McGuffin P, Owen MJ, Gill M, Collier DA. A linkage study of schizophrenia with DNA markers from chromosome 8p21-p22 in 25 multiplex families. Schizophrenia Research. 22: 61-8. PMID 8908691 DOI: 10.1016/0920-9964(96)00048-5 |
0.367 |
|
| 1996 |
Parfitt E, Asherson P, Roberts E, Mant R, Nanko S, Gill M, McGuffin P, Owen M. No evidence for linkage between schizophrenia and eight microsatellite markers on chromosome 19. Human Heredity. 46: 191-6. PMID 8807320 DOI: 10.1159/000154352 |
0.365 |
|
| 1996 |
Vallada H, Curtis D, Sham PC, Murray RM, McGuffin P, Nanko S, Gill M, Owen M, Collier DA. Chromosome 22 markers demonstrate transmission disequilibrium with schizophrenia. Psychiatric Genetics. 5: 127-30. PMID 8746411 DOI: 10.1097/00041444-199505030-00005 |
0.365 |
|
| 1996 |
Gill M, Vallada H, Collier D, Sham P, Holmans P, Murray R, McGuffin P, Nanko S, Owen M, Antonarakis S, Housman D, Kazazian H, Nestadt G, Pulver AE, Straub RE, et al. A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). American Journal of Medical Genetics. 67: 40-5. PMID 8678112 DOI: 10.1002/(Sici)1096-8628(19960216)67:1<40::Aid-Ajmg6>3.0.Co;2-W |
0.363 |
|
| 1996 |
Shaikh S, Collier DA, Sham PC, Ball D, Aitchison K, Vallada H, Smith I, Gill M, Kerwin RW. Allelic association between a Ser-9-Gly polymorphism in the dopamine D3 receptor gene and schizophrenia. Human Genetics. 97: 714-9. PMID 8641685 DOI: 10.1007/Bf02346178 |
0.407 |
|
| 1996 |
Williams J, Spurlock G, McGuffin P, Mallet J, Nöthen MM, Gill M, Aschauer H, Nylander PO, Macciardi F, Owen MJ. Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. European Multicentre Association Study of Schizophrenia (EMASS) Group. Lancet (London, England). 347: 1294-6. PMID 8622505 DOI: 10.1016/S0140-6736(96)90939-3 |
0.377 |
|
| 1996 |
Okoro C, Bell R, Sham P, Nanko S, Asherson P, Owen M, Gill M, McGuffin P, Murray RM, Collier D. No evidence for linkage between the X-chromosome marker DXS7 and schizophrenia. American Journal of Medical Genetics. 60: 461-4. PMID 8546163 DOI: 10.1002/Ajmg.1320600520 |
0.362 |
|
| 1996 |
Williams J, Spurlock G, McGuffin P, Mallet J, Nothen M, Gill M, Aschauer H, Nylander P-, Macciardi F, Owen MJ. Assocation between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2A receptor gene Psychiatric Genetics. 6: 145. DOI: 10.1097/00041444-199623000-00030 |
0.327 |
|
| 1996 |
Murphy KC, Gill M. Recent developments in the genetics of schizophrenia Irish Journal of Psychological Medicine. 13: 151-154. DOI: 10.1017/S0790966700004432 |
0.339 |
|
| 1996 |
Gill M, Hawi Z, Gibson S, Kendler K, Straub R, Walsh D. Testing candidate gene hypotheses in schizophrenia European Psychiatry. 11: 221s. DOI: 10.1016/0924-9338(96)88651-2 |
0.34 |
|
| 1995 |
Shaikh S, Collier DA, Sham P, Pilowsky L, Sharma T, Lin LK, Crocq MA, Gill M, Kerwin R. Analysis of clozapine response and polymorphisms of the dopamine D4 receptor gene (DRD4) in schizophrenic patients American Journal of Medical Genetics. 60: 541-545. PMID 8825892 DOI: 10.1002/Ajmg.1320600611 |
0.333 |
|
| 1995 |
Dawson E, Gill M, Curtis D, Castle D, Hunt N, Murray R, Powell J. Genetic association between alleles of pancreatic phospholipase A2 gene and bipolar affective disorder. Psychiatric Genetics. 5: 177-180. PMID 8750360 DOI: 10.1097/00041444-199524000-00005 |
0.362 |
|
| 1995 |
Lin MW, Curtis D, Williams N, Arranz M, Nanko S, Collier D, McGuffin P, Murray R, Owen M, Gill M. Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Psychiatric Genetics. 5: 117-26. PMID 8746410 DOI: 10.1097/00041444-199505030-00004 |
0.351 |
|
| 1995 |
Dawson E, Powell JF, Sham P, Shaikh S, Taylor C, Clements A, Asherson P, Sargeant M, Collier D, Nanko S, Whatley S, Murray R, McGuffin P, Owen M, Gill M. Systematic search for major genes in schizophrenia: Methodological issues and results from chromosome 12 American Journal of Medical Genetics - Neuropsychiatric Genetics. 60: 424-433. PMID 8546156 DOI: 10.1002/Ajmg.1320600513 |
0.371 |
|
| 1995 |
Arranz M, Sharma T, Sham P, Kerwin R, Nanko S, Owen M, Gill M, Collier D. Schizophrenia and the androgen receptor gene: report of a sibship showing co-segregation with Reifenstein syndrome but no evidence for linkage in 23 multiply affected families. American Journal of Medical Genetics. 60: 377-81. PMID 8546149 DOI: 10.1002/Ajmg.1320600506 |
0.361 |
|
| 1995 |
Lim LC, Nöthen MM, Körner J, Rietschel M, Castle D, Hunt N, Propping P, Murray R, Gill M. No evidence of association between dopamine D4 receptor variants and bipolar affective disorder. American Journal of Medical Genetics. 54: 259-63. PMID 7810585 DOI: 10.1002/Ajmg.1320540314 |
0.357 |
|
| 1995 |
Arranz MJ, Dawson E, Shaikh S, Sham P, Sharma T, Aitchison K, Crocq MA, Gill M, Kerwin R, Collier DA. Cytochrome P4502D6 genotype does not determine response to clozapine. British Journal of Clinical Pharmacology. 39: 417-20. PMID 7640149 DOI: 10.1111/J.1365-2125.1995.Tb04471.X |
0.312 |
|
| 1995 |
Lim LCC, Powell J, Sham P, Castle D, Hunt N, Murray R, Gill M. Evidence for a genetic association between alleles of monoamine oxidase a gene and bipolar affective disorder American Journal of Medical Genetics. 60: 325-331. PMID 7485270 DOI: 10.1002/Ajmg.1320600413 |
0.404 |
|
| 1995 |
Dawson E, Parfitt E, Roberts Q, Daniels J, Lim L, Sham P, Nöthen M, Propping P, Lanczik M, Maier W, Reuner U, Weissenbach J, Gill M, Powell J, McGuffin P, et al. Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1. American Journal of Medical Genetics. 60: 94-102. PMID 7485258 DOI: 10.1002/Ajmg.1320600203 |
0.353 |
|
| 1995 |
Vallada HP, Gill M, Sham P, Lim LC, Nanko S, Asherson P, Murray RM, McGuffin P, Owen M, Collier D. Linkage studies on chromosome 22 in familial schizophrenia. American Journal of Medical Genetics. 60: 139-46. PMID 7485248 DOI: 10.1002/Ajmg.1320600210 |
0.382 |
|
| 1994 |
Asherson P, Mant R, Taylor C, Sargeant M, Collier D, Clements A, Nanko S, Whatley S, Gill M, McGuffin P. Failure to find linkage between schizophrenia and genetic markers on chromosome 21. American Journal of Medical Genetics. 48: 161-5. PMID 8291572 DOI: 10.1002/Ajmg.1320480310 |
0.384 |
|
| 1994 |
Shaikh S, Gill M, Owen M, Asherson P, McGuffin P, Nanko S, Murray RM, Collier DA. Failure to find linkage between a functional polymorphism in the dopamine D4 receptor gene and schizophrenia. American Journal of Medical Genetics. 54: 8-11. PMID 8178839 DOI: 10.1002/Ajmg.1320540104 |
0.362 |
|
| 1994 |
Craddock N, Dawson E, Burge S, Parfitt L, Mant B, Roberts Q, Daniels J, Gill M, McGuffin P, Powell J. The gene for Darier's disease maps to chromosome 12q23-q24.1. Human Molecular Genetics. 2: 1941-3. PMID 8129825 DOI: 10.1093/Hmg/2.11.1941 |
0.332 |
|
| 1994 |
Asherson P, Walsh C, Williams J, Sargeant M, Taylor C, Clements A, Gill M, Owen M, McGuffin P. Imprinting and anticipation. Are they relevant to genetic studies of schizophrenia? The British Journal of Psychiatry : the Journal of Mental Science. 164: 619-24. PMID 7921711 DOI: 10.1192/Bjp.164.5.619 |
0.354 |
|
| 1994 |
Nanko S, Fukuda R, Hattori M, Sasaki T, Dai XY, Gill M, Kuwata S, Shibata Y, Kazamatsuri H. No evidence of linkage or allelic association of schizophrenia with DNA markers at pericentric region of chromosome 9. Biological Psychiatry. 36: 589-594. PMID 7833423 DOI: 10.1016/0006-3223(94)90069-8 |
0.392 |
|
| 1994 |
Korner J, Rietschel M, Hunt N, Castle D, Gill M, Nothen MM, Craddock NJ, Daniels J, Owen MJ, Fimmers R, Fritze J, Moller HJ, Propping P. Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German-British sample of manic depressive patients and controls. Psychiatric Genetics. 4: 167-176. PMID 7719703 DOI: 10.1097/00041444-199400430-00007 |
0.353 |
|
| 1994 |
Dawson E, Powell JF, Nothen MM, Crocq MA, Lanczik M, Korner J, Rietschel M, Van Os J, Wright P, Gill M. An association study of debrisoquine hydroxylase (CYP2D6) polymorphisms in schizophrenia Psychiatric Genetics. 4: 215-218. PMID 7712118 DOI: 10.1097/00041444-199400440-00005 |
0.362 |
|
| 1993 |
Gill M, McGuffin P, Parfitt E, Mant R, Asherson P, Collier D, Vallada H, Powell J, Shaikh S, Taylor C. A linkage study of schizophrenia with DNA markers from the long arm of chromosome 11. Psychological Medicine. 23: 27-44. PMID 8475213 DOI: 10.1016/0920-9964(92)90084-I |
0.4 |
|
| 1993 |
Zatz M, Vallada H, Melo MS, Passos-Bueno MR, Vieira AH, Vainzof M, Gill M, Gentil V. Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain? Journal of Medical Genetics. 30: 131-4. PMID 8445617 DOI: 10.1136/Jmg.30.2.131 |
0.396 |
|
| 1993 |
Wright P, Gill M, Murray RM. Schizophrenia: Genetics and the maternal immune response to viral infection American Journal of Medical Genetics. 48: 40-46. PMID 8357035 DOI: 10.1002/Ajmg.1320480110 |
0.319 |
|
| 1993 |
Nanko S, Sasaki T, Fukuda R, Hattori M, Dai XY, Kazamatsuri H, Kuwata S, Juji T, Gill M. A study of the association between schizophrenia and the dopamine D3 receptor gene. Human Genetics. 92: 336-338. PMID 8225313 DOI: 10.1007/Bf01247330 |
0.405 |
|
| 1993 |
Shaikh S, Ball D, Craddock NJ, Castle D, Hunt N, Mant R, Owen MJ, Collier D, Gill M. The dopamine D3 receptor gene: no association with bipolar affective disorder. Journal of Medical Genetics. 30: 308-309. PMID 8098068 DOI: 10.1136/Jmg.30.4.308 |
0.387 |
|
| 1993 |
Lim LC, Gurling H, Curtis D, Brynjolfsson J, Petursson H, Gill M. Linkage between tyrosine hydroxylase gene and affective disorder cannot be excluded in two of six pedigrees. American Journal of Medical Genetics. 48: 223-8. PMID 7907843 DOI: 10.1002/Ajmg.1320480410 |
0.378 |
|
| 1993 |
Collier D, Abusaad I, Ashworth A, Clements A, Gill M, Nanko S, Owen M, Walsh C. Is there a link between schizophrenia and mutations at the fragile-X gene, FMR-1? Schizophrenia Research. 9: 115-116. DOI: 10.1016/0920-9964(93)90162-C |
0.314 |
|
| 1992 |
Asherson P, Parfitt E, Sargeant M, Tidmarsh S, Buckland P, Taylor C, Clements A, Gill M, McGuffin P, Owen M. No evidence for a pseudoautosomal locus for schizophrenia. Linkage analysis of multiply affected families. The British Journal of Psychiatry : the Journal of Mental Science. 161: 63-8. PMID 1638331 DOI: 10.1192/Bjp.161.1.63 |
0.378 |
|
| 1992 |
Gill M, Castle D, Duggan C. Cosegregation of Christmas disease and major affective disorder in a pedigree. British Journal of Psychiatry. 160: 112-114. PMID 1543989 DOI: 10.1192/Bjp.160.1.112 |
0.322 |
|
| 1992 |
Owen MJ, Gill M. Looking for genes in schizophrenia. Clinical Neuropharmacology. 222A-223A. PMID 1498819 DOI: 10.1097/00002826-199201001-00116 |
0.34 |
|
| 1992 |
Owen MJ, Mant R, Parfitt E, Williams J, Asherson P, O'Mahoney G, Van Os J, Llewellyn D, Collier D, Gill M. No association between RFLPs at the porphobilinogen deaminase gene and schizophrenia. Human Genetics. 90: 131-2. PMID 1358782 DOI: 10.1007/Bf00210756 |
0.393 |
|
| 1992 |
Vallada H, Collier D, Dawson E, Owen MJ, Nanko S, Murray R, Gill M. Debrisoquine 4-hydroxylase (CYP2D) locus and possible susceptibility to schizophrenia. The Lancet. 340: 181-182. PMID 1352597 DOI: 10.1016/0140-6736(92)93266-P |
0.343 |
|
| 1992 |
Walsh C, Hicks AA, Sham P, Castle D, Hunt N, Clements A, Sander T, Murray R, Darlison MG, Gill M. GABAA receptor subunit genes as candidate genes for bipolar affective disorder—an association analysis Psychiatric Genetics. 2: 239-248. DOI: 10.1097/00041444-199210000-00002 |
0.303 |
|
| 1992 |
Collier D, Gill M, Nanko S, Owen MJ, Vallada H. Linkage analysis of schizophrenia on chromosome 22 Schizophrenia Research. 6: 89-90. DOI: 10.1016/0920-9964(92)90085-J |
0.326 |
|
| 1991 |
Gill M, Castle D, Hunt N, Clements A, Sham P, Murray RM. Tyrosine hydroxylase polymorphisms and bipolar affective disorder. Journal of Psychiatric Research. 25: 179-184. PMID 1685750 DOI: 10.1016/0022-3956(91)90022-3 |
0.374 |
|
| 1991 |
Gill M, Daggers A, Collier D, Hett G, Nanko S, Pilowski L, Taylor C, Murray R. Linkage map of schizophrenia 11q Schizophrenia Research. 4: 258. DOI: 10.1016/0920-9964(91)90110-D |
0.306 |
|
| 1989 |
Gill M, Taylor C, Murray RM. Schizophrenia Research: Attempting to integrate genetics, neurodevelopment and nosology International Review of Psychiatry. 1: 277-286. DOI: 10.3109/09540268909089421 |
0.381 |
|
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