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1
المؤلفون: Michael Conlon O'Donovan, N. Craddock, Anita Thapar, Kate Langley, M. van den Bree, Frances Rice, M. J. Owen, Lindsey Kent, Peter Holmans, D. Turic
المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :49-53
مصطلحات موضوعية: Alcohol Drinking, Genotype, Birth weight, Poison control, Linkage Disequilibrium, Cellular and Molecular Neuroscience, Pregnancy, mental disorders, Injury prevention, Birth Weight, Humans, Medicine, Attention deficit hyperactivity disorder, Gene–environment interaction, Child, Genetics (clinical), business.industry, Smoking, Antisocial Personality Disorder, medicine.disease, Psychiatry and Mental health, Attention Deficit Disorder with Hyperactivity, Maternal Exposure, Conduct disorder, Sample size determination, Female, business, Clinical psychology
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2
المؤلفون: Paul Hollingworth, Nigel J. Cairns, Lynnette J. Cook, David C. Rubinsztein, Edith Terrenoire, Simon Lovestone, Carol Brayne, Amanda J. Edmondson, Luke Jehu, Pamela Moore, Catherine Foy, Nicola Archer, Lin Wang, Sarah Walter, John Powell, John H. Xuereb, Julie Williams, D. Turic, John Grimley Evans, Luk W. Ho
المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :5-8
مصطلحات موضوعية: Male, Candidate gene, Genotype, Biology, Choline O-Acetyltransferase, Cellular and Molecular Neuroscience, chemistry.chemical_compound, Gene Frequency, Gene interaction, Alzheimer Disease, Odds Ratio, Humans, Genetic Predisposition to Disease, Allele, Alleles, Genetics (clinical), Butyrylcholinesterase, Aged, Genetics, Chi-Square Distribution, Polymorphism, Genetic, Acetylcholinesterase, Choline acetyltransferase, Psychiatry and Mental health, chemistry, Case-Control Studies, Cholinergic, Female
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3
المؤلفون: Kate Langley, Michael Conlon O'Donovan, T. Peirce, D. Turic, Anita Thapar, M. J. Owen, S. Mills, M. van den Bree
المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :7-10
مصطلحات موضوعية: Male, Adolescent, Single-nucleotide polymorphism, Minisatellite Repeats, Biology, Polymorphism, Single Nucleotide, Cellular and Molecular Neuroscience, Polymorphism (computer science), mental disorders, Genotype, Humans, Allele, Child, Genetics (clinical), Dopamine transporter, Genetics, Dopamine Plasma Membrane Transport Proteins, Haplotype, Promoter, Odds ratio, Psychiatry and Mental health, Attention Deficit Disorder with Hyperactivity, Methylphenidate, biology.protein, Central Nervous System Stimulants, Female
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4
المؤلفون: Corinne Lendon, Sarah Walter, D. Turic, John Grimley Evans, Antonia L. Pritchard, Amanda J. Edmondson, Lynnette J. Cook, Pamela Moore, Nigel J. Cairns, Alison Taylor, Helen Lemmon, John H. Xuereb, Catherine Foy, Luk W. Ho, Paul Hollingworth, Julie Williams, David M. A. Mann, David C. Rubinsztein, Michael John Owen, Luke Jehu, Simon Lovestone, Nicola Archer, David St Clair, Carol Brayne, John Powell
المصدر: Neuroscience Letters. 358:142-146
مصطلحات موضوعية: Male, medicine.medical_specialty, Candidate gene, Genotype, Receptors, Nicotinic, Biology, Alzheimer Disease, Internal medicine, Confidence Intervals, Odds Ratio, medicine, Humans, Receptor, Alleles, Aged, Genetic association, Acetylcholine receptor, Chi-Square Distribution, Polymorphism, Genetic, General Neuroscience, Odds ratio, medicine.disease, Nicotinic acetylcholine receptor, Nicotinic agonist, Endocrinology, Female, Alzheimer's disease
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5
المؤلفون: D. Turic, Robert Plomin, Julie Williams, L Hill, Michael Conlon O'Donovan, M. Stephens, Michael John Owen, Darko Turic
المصدر: Molecular Psychiatry. 9:582-586
مصطلحات موضوعية: Genotype, Offspring, Intelligence, Population, Polymorphism, Single Nucleotide, Cellular and Molecular Neuroscience, Cognition, Polymorphism (computer science), Humans, Aldehyde dehydrogenase 5 family, member A1, Allele, education, Molecular Biology, Genetics, education.field_of_study, Polymorphism, Genetic, Wechsler Scales, DNA, Exons, Aldehyde Oxidoreductases, Minor allele frequency, Succinate-semialdehyde dehydrogenase, Psychiatry and Mental health, Succinate-Semialdehyde Dehydrogenase, Psychology
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6
المؤلفون: Kate Langley, Lindsey Kent, Sophie Mills, D. Turic, Nicholas John Craddock, M. Stephens, Deborah C. Lawson, Michael John Owen, C. Govan, M. van den Bree, Anita Thapar, Nigel Williams, Michael Conlon O'Donovan
المصدر: Molecular Psychiatry. 9:169-173
مصطلحات موضوعية: Male, Candidate gene, Adolescent, Genetic Linkage, Polymorphism, Single Nucleotide, Receptors, N-Methyl-D-Aspartate, Cellular and Molecular Neuroscience, Genetic linkage, Genetic variation, medicine, Humans, Attention deficit hyperactivity disorder, Child, Molecular Biology, Genetic association, Genetics, biology, Haplotype, medicine.disease, Psychiatry and Mental health, Attention Deficit Disorder with Hyperactivity, Child, Preschool, biology.protein, GRIN2A, Female, Gene polymorphism, Chromosomes, Human, Pair 16, Follow-Up Studies
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7
المؤلفون: Michael Conlon O'Donovan, Anita Thapar, D. Turic, Michael John Owen, George Kirov, Kate Langley
المصدر: American Journal of Medical Genetics. :68-72
مصطلحات موضوعية: Genetics, Candidate gene, Exon, G protein, GTP-Binding Protein alpha Subunits, mental disorders, Haplotype, Alpha (ethology), Biology, Genotyping, Gene, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b97dd73ab144926970651c24aab95858
https://doi.org/10.1002/ajmg.b.20173 -
8
المؤلفون: Peter Holmans, Joanne Norton, John Hardy, Kit Lau, Jolanda van Hengel, Gillian Hamilton, Pamela Moore, Luke Jehu, C. Lendon, Andrew Grupe, Sarah Walter, Kristina Tacey, Stuart Pickering-Brown, Takeshi Iwatsubo, Daniel Woo, Richard Killick, Meredith Womick, John Powell, Victoria L. Busby, Paul Hollingworth, Denise Harold, Danielle Compton, Petra Nowotny, Alison Goate, Lisa Doil, Barbara Janssens, David M. A. Mann, John C. Morris, Frans van Roy, Amanda J. Myers, Lesley Jones, Safa Al-Saraj, Michael John Owen, Simon Lovestone, Nicola Archer, Catherine Foy, Michael Conlon O'Donovan, Scott Smemo, Julie Williams, Steven Goossens, D. Turic
المصدر: NeuroMolecular Medicine. 5:133-146
مصطلحات موضوعية: Male, Apolipoprotein E, Beta-catenin, Genotype, Genetic Linkage, DNA Mutational Analysis, Gene Expression, Single-nucleotide polymorphism, Locus (genetics), Biology, Cell Line, Mice, Cellular and Molecular Neuroscience, Gene Frequency, Alzheimer Disease, Proto-Oncogene Proteins, Animals, Humans, SNP, Genetic Testing, Allele, Gene, Aged, Aged, 80 and over, Brain Chemistry, Genetics, Amyloid beta-Peptides, Polymorphism, Genetic, Chromosomes, Human, Pair 10, Wnt signaling pathway, Brain, Chromosome Mapping, Molecular biology, Wnt Proteins, Alternative Splicing, Cytoskeletal Proteins, Neurology, Case-Control Studies, biology.protein, Molecular Medicine, Female, alpha Catenin, Signal Transduction
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9
المؤلفون: Ian W. Craig, Lee A. Thompson, D. Turic, Robert Plomin, Peter McGuffin, Pak C. Sham, Shaun Purcell, Michael John Owen, L Hill, David Lubinski, Paul J. Fisher
المصدر: Behavior Genetics. 31:497-509
مصطلحات موضوعية: Genetics, Linkage disequilibrium, Genetic marker, False positive paradox, Genome Scan, Single-nucleotide polymorphism, Transmission disequilibrium test, Biology, Quantitative trait locus, Genotyping, Genetics (clinical), Ecology, Evolution, Behavior and Systematics
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10
المؤلفون: L Hill, David Ball, David Lubinski, Paul J. Fisher, Nigel Williams, Camilla Persson Benbow, Michael J. Chorney, Philip Asherson, Peter McGuffin, Ian W. Craig, Michael John Owen, D. Turic, Karen Chorney, Thalia C. Eley, Robert Plomin
المصدر: Scopus-Elsevier
مصطلحات موضوعية: Adolescent, Genotype, Quantitative trait locus, Biology, White People, chemistry.chemical_compound, Cognition, Gene Frequency, Gene mapping, Genetics, Humans, False Positive Reactions, Allele, Child, False Negative Reactions, Molecular Biology, Gene, Genetics (clinical), Intelligence Tests, Reproducibility of Results, Chromosome, DNA, General Medicine, Chromosome 4, Genetic Techniques, chemistry, Genetic marker, Chromosomes, Human, Pair 4, Microsatellite Repeats
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a90a0c4238c2b2ad62d3f7c8437c111e
https://doi.org/10.1093/hmg/8.5.915