L. Kent

发表

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

S. Baron-Cohen, S. Wheelwright, F. Dudbridge, 2009, Autism research : official journal of the International Society for Autism Research.

Methylphenidate improves response inhibition but not reflection–impulsivity in children with attention deficit hyperactivity disorder (ADHD)

Danielle C. Turner, B. Sahakian, L. Clark, 2008, Psychopharmacology.

The Effects of Methylphenidate on Decision Making in Attention-Deficit/Hyperactivity Disorder

Andrew D. Blackwell, Karen D. Ersche, Luke Clark, 2008, Biological Psychiatry.

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, American journal of human genetics.

Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes.

Jan K Buitelaar, Florence Levy, Michael Gill, 2004, American journal of human genetics.

Sex-specific serum biomarker patterns in adults with Asperger's syndrome

S Baron-Cohen, Michael D. Spain, S. Baron-Cohen, 2011, Molecular Psychiatry.

Is there a relationship between attention deficit hyperactivity disorder and bipolar disorder?

N. Craddock, L. Kent, 2003, Journal of affective disorders.

ADHD and DAT1: Further evidence of paternal over‐transmission of risk alleles and haplotype

B. Franke, M. Gill, R. Anney, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Beckwith Weidemann syndrome: A behavioral phenotype–genotype study

S. Bowdin, L. Kent, E. Maher, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT1B receptor gene in 273 nuclear families from a multi-centre sample

M. Gill, N. Craddock, M. Owen, 2001, Molecular Psychiatry.

The genetic contribution of the NO system at the glutamatergic post-synapse to schizophrenia: Further evidence and meta-analysis

C. Freitag, K. Lesch, J. Sanjuán, 2014, European Neuropsychopharmacology.

A shared polygenic contribution between childhood ADHD and adult schizophrenia

M. Gill, N. Craddock, M. Owen, 2013 .

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

M. Gill, L. Kent, Z. Hawi, 2007, Neuroscience Letters.

Investigating the Presence of the History of Medicine in North American Medical Education: Can One of the Medical Humanities Concisely Integrate with Biomedical and Clinical Content with Reference to Clinical Competencies?

Peter J. Ward, L. Kent, Peter J Ward, 2020, Medical Science Educator.

Prescribing practices of community child and adolescent psychiatrists

L. Kent, U. Doerry, 2003 .

Comorbidity of autistic spectrum disorders in children with Down syndrome.

L. Kent, M. Paul, Joanne Evans, 1999 .

Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.

Susanne Walitza, Aribert Rothenberger, Stephan Ripke, 2010, Journal of the American Academy of Child and Adolescent Psychiatry.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

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

Alicia R. Martin, N. Eriksson, N. Wray, 2017, Biological Psychiatry.

High Loading of Polygenic Risk for ADHD in Children With Comorbid Aggression

B. Franke, M. Owen, R. Anney, 2013, The American journal of psychiatry.

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Susanne Walitza, Aribert Rothenberger, Takeshi Sakurai, 2011, Nature Genetics.

A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures

J. Talcott, C. Hulme, M. Rice, 2021, medRxiv.

Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia

M. Gill, N. Craddock, M. Owen, 2013, British Journal of Psychiatry.

GLRB allelic variation associated with agoraphobic cognitions, increased startle response and fear network activation: a potential neurogenetic pathway to panic disorder

S. Cichon, L. Kiemeney, M. Nöthen, 2017, Molecular Psychiatry.

Clinical implications of psychiatric genetics in the new millennium -- nightmare or nirvana?

N. Craddock, I. Jones, L. Kent, 2001 .

Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

M. S. Artigas, B. Franke, O. Andreassen, 2021, Nature Communications.

Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants

S. Scherer, M. Gill, M. Owen, 2014, Journal of the American Academy of Child and Adolescent Psychiatry.

Polymorphisms of the Steroid Sulfatase [STS] Gene are Associated With Attention Deficit Hyperactivity Disorder and Influence Brain Tissue mRNA Expression

M. Gill, L. Kent, Z. Hawi, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Allelic variation in CRHR1 predisposes to panic disorder: evidence for biased fear processing

G. Alpers, A. Jansen, A. Hamm, 2016, Molecular Psychiatry.

Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3

Susanne Walitza, Herbert Roeyers, Peter Holmans, 2012, The American journal of psychiatry.

Comorbidity of autistic spectrum disorders in children with Down syndrome

L. Kent, M. Paul, L Kent, 1999, Developmental medicine and child neurology.

Autism in Down's Syndrome: Three Case Reports

L. Kent, Joanne Evans, D. Perry, 1998 .

Maternal and child psychological sequelae in paediatric burn injuries.

L. Kent, H. King, R. Cochrane, 2000, Burns : journal of the International Society for Burn Injuries.

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

M. Gill, T. Cummins, M. Bellgrove, 2015, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Identification and functional characterisation of a novel dopamine beta hydroxylase gene variant associated with ADHD

M. Gill, T. Cummins, A. Vance, 2015 .

DNA Variation in the SNAP25 Gene Confers Risk to ADHD and Is Associated with Reduced Expression in Prefrontal Cortex

M. Gill, M. Bellgrove, A. Vance, 2013, PloS one.

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

M. Daly, B. Franke, M. Gill, 2010, Journal of the American Academy of Child and Adolescent Psychiatry.

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

Michael Gill, M. Gill, D. Coghill, 2009, Neuroscience Letters.

Association study of a SNAP-25 microsatellite and attention deficit hyperactivity disorder.

J. Mill, P. Asherson, S. Curran, 2002, American journal of medical genetics.

Evidence to suggest biased phenotypes in children with Attention Deficit Hyperactivity Disorder from completely ascertained trios

N. Craddock, M. Owen, M. Hamshere, 2002, Molecular Psychiatry.

Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): analysis and pooled analysis

M. Gill, N. Craddock, M. Fitzgerald, 2002, Molecular Psychiatry.

Nicotinic acetylcholine receptor alpha4 subunit gene polymorphism and attention deficit hyperactivity disorder.

C Feehan, M. Gill, N. Craddock, 2001, Psychiatric genetics.

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

M. Gill, L. Kent, Z. Hawi, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits

L. Willatt, J. Yates, E. Weisblatt, 2008, Journal of Medical Genetics.

Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samples

J. Mill, E. Simonoff, P. Asherson, 2001, Molecular Psychiatry.

Attention deficit hyperactivity disorder (ADHD) and the dopamine D4 receptor gene: evidence of association but no linkage in a UK sample

J. Mill, P. Sham, P. Asherson, 2001, Molecular Psychiatry.

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

M. Gill, M. Bellgrove, A. Fornito, 2018, Translational Psychiatry.

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

Daniel P. Newman, N. Wray, M. Gill, 2017, Molecular Psychiatry.

Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD

M. Gill, M. Owen, M. O’Donovan, 2012, The American journal of psychiatry.

Allelic variation in CRHR 1 predisposes to panic disorder by biasing towards fear

G. Alpers, A. Jansen, A. Hamm, 2015 .

Variations in the human cannabinoid receptor (CNR1) gene modulate striatal responses to happy faces

E. Bullmore, S. Baron-Cohen, J. Suckling, 2006, The European journal of neuroscience.

Nicotinic acetylcholine receptor α4 subunit gene polymorphism and attention deficit hyperactivity disorder

M. Gill, N. Craddock, M. Fitzgerald, 2001 .

Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD

N. Craddock, M. Owen, A. Thapar, 2004, Molecular Psychiatry.

Recent advances in the genetics of attention deficit hyperactivity disorder

L. Kent, 2004, Current psychiatry reports.

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

M. Gill, N. Craddock, M. Owen, 2005, Molecular Psychiatry.

An investigation of mitochondrial haplogroups in autism

L. Gallagher, P. Chinnery, L. Kent, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The DRD4 receptor Exon 3 VNTR and 5′ SNP variants and mRNA expression in human post‐mortem brain tissue

L. Kent, K. Brookes, J. Simpson, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Methylphenidate improves response inhibition but not reflection – impulsivity in children with attention deficit hyperactivity disorder ( ADHD )

B. Sahakian, L. Clark, A. Blackwell, 2008 .

No association between CHRNA7 microsatellite markers and attention-deficit hyperactivity disorder.

M. Gill, N. Craddock, E. Green, 2001, American journal of medical genetics.

Testing for gene × environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior

N. Craddock, P. Holmans, F. Rice, 2008 .

Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: Genetic and molecular studies

D. Skuse, M. Gill, L. Gallagher, 2010, Neuroscience Letters.

Insights into the control of attentional set in ADHD using the attentional blink paradigm.

G. Humphreys, L. Kent, D. J. Mason, 2005, Journal of child psychology and psychiatry, and allied disciplines.

Exploring selective attention in ADHD: visual search through space and time.

G. Humphreys, L. Kent, D. J. Mason, 2003, Journal of child psychology and psychiatry, and allied disciplines.

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

M. Gill, L. Kent, Z. Hawi, 2010, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

An investigation of the neurotrophic factor genes GDNF, NGF, and NT3 in susceptibility to ADHD

F. Dudbridge, L. Kent, Zahoor Syed, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

On the role of NOS1 ex1f‐VNTR in ADHD—allelic, subgroup, and meta‐analysis

B. Franke, K. Lesch, B. Cormand, 2015, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.

Visual search, singleton capture, and the control of attentional set in ADHD

Glyn W Humphreys, G. Humphreys, L. Kent, 2004, Cognitive neuropsychology.

A systematic review and meta-analysis of robotic versus laparoscopic partial liver resection

L. Kent, S. Froghi, A. Aydın, 2017 .

Genetics of affective disorders.

N. Craddock, I. Jones, L. Kent, 2002 .

Eyelid myoclonia with absences: phenomenology in children

L. Kent, W. Whitehouse, A. Blake, 1998, Seizure.

Out-Patient Clinic Attendance Consent from Children and Young People: Ethical Aspects and Practical Considerations

L. Kent, M. Paul, D. Foreman, 2000 .