نتائج البحث - "genomic disorders"

1

Depressive symptom clusters are differentially associated with atherosclerotic disease

المؤلفون: Nitin Purandare, Radboud M. Marijnissen, J. de Graaf, Suzanne Holewijn, Boudewijn A.A. Bus, Barbara Franke, M. den Heijer, R.C. Oude Voshaar, Jan K. Buitelaar

المساهمون: Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE)

المصدر: Psychological Medicine, 41, 7, pp. 1419-28
Psychological Medicine, 41, 1419-28
Psychological Medicine, 41(7), 1419-1428. Cambridge University Press

مصطلحات موضوعية: Carotid Artery Diseases, Male, 110 012 Social cognition of verbal communication, Heart disease, Perception and Actions Mental Health [DCN 1], LATE-LIFE DEPRESSION, Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], INTIMA-MEDIA THICKNESS, Coronary artery disease, Hormonal regulation Molecular epidemiology [IGMD 6], Myocardial infarction, Applied Psychology, Depression (differential diagnoses), Subclinical infection, Netherlands, Principal Component Analysis, CARDIOVASCULAR PROGNOSIS, Late life depression, Middle Aged, Psychiatry and Mental health, depression, Cardiology, cognitive-affective, CAROTID ATHEROSCLEROSIS, CORONARY-ARTERY-DISEASE, Female, Functional Neurogenomics [DCN 2], medicine.medical_specialty, Health aging / healthy living [IGMD 5], factor analysis, HEART-DISEASE, elderly, 150 000 MR Techniques in Brain Function, Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular epidemiology [NCEBP 1], Internal medicine, medicine, Humans, VASCULAR DEPRESSION, Aged, Psychiatric Status Rating Scales, Depressive Disorder, business.industry, Vascular disease, somatic-affective, MAJOR DEPRESSION, medicine.disease, CARDIAC EVENTS, Intima-media thickness, MYOCARDIAL-INFARCTION, intima-media thickness (IMT), atherosclerosis, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9db9945212085cf84ee6a056d806efcaTest
https://research.rug.nl/en/publications/36b60b0d-5e60-4570-a7bc-c72bc4382d20Test

2

Human cognitive flexibility depends on dopamine D2 receptor signaling

المؤلفون: Marieke E. van der Schaaf, Dirk E. M. Geurts, Roshan Cools, Robbert J. Verkes, Martine R. van Schouwenburg, Esther Aarts, Mieke van Holstein, Barbara Franke

المصدر: Psychopharmacology, 218, 567-78
Psychopharmacology
Psychopharmacology, 218, 3, pp. 567-78

مصطلحات موضوعية: SLC6A3, Adult, Male, Adolescent, Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], Striatum, Biology, Cognitive flexibility, Genomic disorders and inherited multi-system disorders [IGMD 3], Young Adult, DAT1, Cognition, Double-Blind Method, Dopamine, Dopamine receptor D2, Perception and Action [DCN 1], medicine, Humans, Bromocriptine, Original Investigation, Pharmacology, Dopamine Plasma Membrane Transport Proteins, Cross-Over Studies, Polymorphism, Genetic, Receptors, Dopamine D2, Set switching, Tandem Repeat Sequences, Dopamine receptor, Dopamine Agonists, Dopamine Antagonists, Female, Sulpiride, 170 000 Motivational & Cognitive Control, Functional Neurogenomics [DCN 2], Neuroscience, Signal Transduction, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb14609f645ef2a9b3416794540f40e6Test
https://doi.org/10.1007/s00213-011-2340-2Test

3

Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness

المؤلفون: Ingason, Andrés, Kirov, George, Giegling, Ina, Hansen, Thomas, Isles, Anthony R., Jakobsen, Klaus D., Kristinsson, Kari T., le Roux, Louise, Gustafsson, Omar, Craddock, Nick, Möller, Hans-Jürgen, McQuillin, Andrew, Muglia, Pierandrea, Cichon, Sven, Rietschel, Marcella, Ophoff, Roel A., Djurovic, Srdjan, Andreassen, Ole A., Pietiläinen, Olli P. H., Peltonen, Leena, Dempster, Emma, Collier, David A., St Clair, David, Rasmussen, Henrik B., Glenthøj, Birte Y., Kiemeney, Lambertus A., Franke, Barbara, Tosato, Sarah, Bonetto, Chiara, Saemundsen, Evald, Hreidarsson, Stefán J., Nöthen, Markus M., Gurling, Hugh, O'Donovan, Michael C., Owen, Michael J., Sigurdsson, Engilbert, Petursson, Hannes, Stefansson, Hreinn, Rujescu, Dan, Stefansson, Kari, Werge, Thomas, Linszen, Don

المساهمون: ANS - Amsterdam Neuroscience, Adult Psychiatry, Psychiatrie & Neuropsychologie, RS: MHeNs School for Mental Health and Neuroscience, Research Institute of Biological Psychiatry, Mental Health Center Sct. Hans, Copenhagen University Hospital, Roskilde, Denmark.

المصدر: American journal of psychiatry, 168(4), 408-417. American Psychiatric Association
ResearcherID
American Journal of Psychiatry, 168(4), 408-417. American Psychiatric Publishing, Inc.
American Journal of Psychiatry, 168, 408-17
American Journal of Psychiatry; Vol 168
American Journal of Psychiatry
American Journal of Psychiatry, 168, 4, pp. 408-17

مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Genetics and epigenetic pathways of disease [NCMLS 6], Adolescent, DNA Copy Number Variations, Genotype, Denmark, Mothers, Schizoaffective disorder, Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], Article, Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular epidemiology [NCEBP 1], Young Adult, 03 medical and health sciences, 0302 clinical medicine, Angelman syndrome, Gene duplication, medicine, Humans, Copy-number variation, Age of Onset, Child, Genetic Association Studies, Molecular epidemiology Aetiology, screening and detection [NCEBP 1], 030304 developmental biology, Psychiatry, Genetics, Chromosomes, Human, Pair 15, 0303 health sciences, Great Britain, Uniparental Disomy, medicine.disease, United Kingdom, Uniparental disomy, 3. Good health, Blotting, Southern, Psychiatry and Mental health, Psychotic Disorders, Schizophrenia, Autism, Female, Age of onset, Psychology, Functional Neurogenomics [DCN 2], Prader-Willi Syndrome, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f815f1a9a0441a65855fbd37275ec161Test
https://doi.org/10.1176/appi.ajp.2010.09111660Test

4

Sequence variants at CYP1A1–CYP1A2 and AHR associate with coffee consumption

المصدر: Human Molecular Genetics
Human Molecular Genetics, 20, 2071-7
Human Molecular Genetics, 20, 10, pp. 2071-7

مصطلحات موضوعية: Male, Genome-wide association study, Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], Coffee, chemistry.chemical_compound, 0302 clinical medicine, Association Studies Article, Promoter Regions, Genetic, Genetics (clinical), Genetics, 0303 health sciences, education.field_of_study, biology, General Medicine, Middle Aged, 3. Good health, Female, Caffeine, Functional Neurogenomics [DCN 2], Adult, Population, Drinking Behavior, Single-nucleotide polymorphism, Models, Biological, Polymorphism, Single Nucleotide, Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular epidemiology [NCEBP 1], 03 medical and health sciences, Sex Factors, Cytochrome P-450 CYP1A2, Cytochrome P-450 CYP1A1, Humans, education, Molecular Biology, Alleles, Molecular epidemiology Aetiology, screening and detection [NCEBP 1], Aged, 030304 developmental biology, Genetic association, Chromosomes, Human, Pair 15, Hormonal regulation [IGMD 6], CYP1A2, Genetic Variation, Heritability, Aryl hydrocarbon receptor, Receptors, Aryl Hydrocarbon, chemistry, biology.protein, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76c0957e178cea624a096b7abf1f49e7Test
https://doi.org/10.1093/hmg/ddr086Test

5

A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings

المساهمون: University of Zurich, Sonuga-Barke, E J S

المصدر: Sonuga-Barke, E J S, Kumsta, R, Schlotz, W, Lasky-Su, J, Marco, R, Miranda, A, Mulas, F, Oades, R D, Banaschewski, T, Mueller, U, Andreou, P, Christiansen, H, Gabriels, I, Uebel, H, Kuntsi, J, Franke, B, Buitelaar, J, Ebstein, R, Gill, M, Anney, R, Roeyers, H, Rothenberger, A, Sergeant, J, Steinhausen, H C, Asherson, P & Faraone, S V 2011, ' A Functional Variant of the Serotonin Transporter Gene (SLC6A4) Moderates Impulsive Choice in Attention-Deficit/Hyperactivity Disorder Boys and Siblings ', Biological Psychiatry, vol. 70, no. 3, pp. 230-6 . https://doi.org/10.1016/j.biopsych.2011.01.040Test
BIOLOGICAL PSYCHIATRY
Biological Psychiatry, 70, 3, pp. 230-6
Biological Psychiatry, 70, 230-6

مصطلحات موضوعية: DEFICIT HYPERACTIVITY DISORDER, Medizin, Social Sciences, impulsivity, 610 Medicine & health, CHILDREN, Single-nucleotide polymorphism, Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], attention-deficit/hyperactivity disorder, Impulsivity, COMBINED-TYPE ADHD, REACTION-TIME PERFORMANCE, Developmental psychology, Genomic disorders and inherited multi-system disorders [IGMD 3], DOPAMINE, 03 medical and health sciences, 0302 clinical medicine, Dopamine, medicine, Attention deficit hyperactivity disorder, ddc:610, Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, Allele, Biological Psychiatry, Serotonin transporter, 030304 developmental biology, Dopamine transporter, Genetics, Mental Health [NCEBP 9], 0303 health sciences, DELAY AVERSION, biology, TRYPTOPHAN DEPLETION, ASSOCIATION, 10058 Department of Child and Adolescent Psychiatry, medicine.disease, POLYMORPHISM, 5-HTTLPR (SLC6A4), 5-HTTLPR, biology.protein, CRITERION VALIDITY, medicine.symptom, DAT1 (SLC6A3), Psychology, 2803 Biological Psychiatry, Functional Neurogenomics [DCN 2], 030217 neurology & neurosurgery, medicine.drug

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54817db18a57bf5e45119337ec0a5a46Test
https://doi.org/10.1016/j.biopsych.2011.01.040Test

6

Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: a meta-analysis in four European populations

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 156, 5, pp. 600-12
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 156, 600-12

مصطلحات موضوعية: Adult, Male, 110 012 Social cognition of verbal communication, Dopamine, Population, Perception and Actions Mental Health [DCN 1], Context (language use), Minisatellite Repeats, Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], White People, 150 000 MR Techniques in Brain Function, Genomic disorders and inherited multi-system disorders [IGMD 3], Cellular and Molecular Neuroscience, Gene interaction, Risk Factors, mental disorders, medicine, Humans, Attention deficit hyperactivity disorder, Genetic Testing, education, Genetics (clinical), Psychiatric genetics, Molecular epidemiology Aetiology, screening and detection [NCEBP 1], Genetics, Dopamine Plasma Membrane Transport Proteins, education.field_of_study, Polymorphism, Genetic, business.industry, Receptors, Dopamine D4, Haplotype, Case-control study, Middle Aged, medicine.disease, Europe, Psychiatry and Mental health, Haplotypes, Attention Deficit Disorder with Hyperactivity, Case-Control Studies, Meta-analysis, Female, business, Functional Neurogenomics [DCN 2]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d962b274953fa4e99e851c28e0b166c7Test
https://doi.org/10.1002/ajmg.b.31202Test

7

Motor problems in Prader–Willi syndrome: A systematic review on body composition and neuromuscular functioning

المؤلفون: Linda Reus, Leo A. van Vlimmeren, Maria W.G. Nijhuis-van der Sanden, Machiel J. Zwarts, Barto J. Otten, Michèl A.A.P. Willemsen

المصدر: Neuroscience and Biobehavioral Reviews, 35, 3, pp. 956-69
Neuroscience and Biobehavioral Reviews, 35, 956-69

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Weakness, Movement disorders, Prader–Willi syndrome, Cognitive Neuroscience, Quality of nursing and allied health care [NCEBP 6], Neuromuscular Junction, Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], Muscle mass, Growth hormone, Body composition, Neuromuscular junction, Fat mass, Behavioral Neuroscience, Physical medicine and rehabilitation, Internal medicine, medicine, Humans, Human Movement & Fatigue [NCEBP 10], Movement Disorders, business.industry, Quality of nursing and allied health care Genomic disorders and inherited multi-system disorders [NCEBP 6], nutritional and metabolic diseases, Hypotonia, nervous system diseases, Mitochondrial medicine [IGMD 8], Neuropsychology and Physiological Psychology, medicine.anatomical_structure, Endocrinology, Systematic review, Lean body mass, medicine.symptom, business, Functional Neurogenomics [DCN 2], Prader-Willi Syndrome

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fae0a60bd232db0e025e460186cd12d9Test
https://doi.org/10.1016/j.neubiorev.2010.10.015Test

8

Nitric oxide synthase genotype modulation of impulsivity and ventral striatal activity in adult ADHD patients and healthy comparison subjects

المؤلفون: Marcel P. Zwiers, Barbara Franke, Marlies Naber, Marten Onnink, Cornelis C. Kan, Esther Aarts, Jan K. Buitelaar, Dorine Slaats-Willemse, Martine Hoogman, Roshan Cools

المصدر: American Journal of Psychiatry, 168, 1099-106
American Journal of Psychiatry, 168, 10, pp. 1099-106
American Journal of Psychiatry

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Candidate gene, Genotype, NOS1, Nitric Oxide Synthase Type I, Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], Neuropsychological Tests, Impulsivity, Brain mapping, Basal Ganglia, Genomic disorders and inherited multi-system disorders [IGMD 3], Internal medicine, Basal ganglia, mental disorders, medicine, Image Processing, Computer-Assisted, Attention deficit hyperactivity disorder, Humans, Allele, Alleles, Brain Mapping, Middle Aged, medicine.disease, Magnetic Resonance Imaging, Psychiatry and Mental health, Endocrinology, Phenotype, Attention Deficit Disorder with Hyperactivity, Tandem Repeat Sequences, Impulsive Behavior, Female, medicine.symptom, Psychology, Neuroscience, 170 000 Motivational & Cognitive Control, Functional Neurogenomics [DCN 2]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5e04279cdf5fd4863c4e48941ff01d0Test
https://hdl.handle.net/2066/96147Test

9

A review on cognitive and brain endophenotypes that may be common in autism spectrum disorder and attention-deficit/hyperactivity disorder and facilitate the search for pleiotropic genes

المؤلفون: Hilde M. Geurts, Catharina A. Hartman, Jan K. Buitelaar, Nanda Rommelse, Barbara Franke

المساهمون: Brein en Cognitie (Psychologie, FMG)

المصدر: Neuroscience and Biobehavioral Reviews, 35, 1363-96
Neuroscience and Biobehavioral Reviews, 35(6), 1363-1396. Elsevier
Neuroscience and Biobehavioral Reviews, 35, 6, pp. 1363-96

مصطلحات موضوعية: 110 012 Social cognition of verbal communication, Perception and Actions Mental Health [DCN 1], Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], Behavioral Neuroscience, Cognition, DEFICIT-HYPERACTIVITY DISORDER, Perception and Action [DCN 1], EEG, Autism spectrum disorder, Child, AND/OR PDD-NOS, CARD SORTING TEST, Brain, Genetic Pleiotropy, HIGH-FUNCTIONING AUTISM, Endophenotype, Neuropsychology and Physiological Psychology, Phenotype, VOXEL-BASED MORPHOMETRY, DTI, Psychology, RESPONSE-INHIBITION, Functional Neurogenomics [DCN 2], MRI, Endophenotypes, Cognitive Neuroscience, PERVASIVE DEVELOPMENTAL DISORDER, CORTICAL THICKNESS ANALYSIS, Mental health [NCEBP 9], behavioral disciplines and activities, Genomic disorders and inherited multi-system disorders [IGMD 3], FIGURES TASK-PERFORMANCE, Neuropsychology, mental disorders, medicine, Pervasive developmental disorder, Genetics, Attention deficit hyperactivity disorder, Humans, INFORMATION-PROCESSING SPEED, medicine.disease, Developmental disorder, High-functioning autism, Attention-deficit/hyperactivity disorder, Attention Deficit Disorder with Hyperactivity, Child Development Disorders, Pervasive, Autism, Neurocognitive, Neuroscience

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bac5d1469494203180fdb8d120781fd9Test
https://doi.org/10.1016/j.neubiorev.2011.02.015Test

10

Integrated genome-wide association study findings: identification of a neurodevelopmental network for attention deficit hyperactivity disorder

المؤلفون: Jan K. Buitelaar, David L. Pauls, Barbara Franke, Geert Poelmans

المصدر: American Journal of Psychiatry, 168, 365-77
American Journal of Psychiatry, 168, 4, pp. 365-77

مصطلحات موضوعية: Adult, Candidate gene, 110 012 Social cognition of verbal communication, DNA Copy Number Variations, Perception and Actions Mental Health [DCN 1], Single-nucleotide polymorphism, Genome-wide association study, Computational biology, Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], Polymorphism, Single Nucleotide, behavioral disciplines and activities, 150 000 MR Techniques in Brain Function, Genomic disorders and inherited multi-system disorders [IGMD 3], mental disorders, medicine, Neurites, Attention deficit hyperactivity disorder, Animals, Humans, Genetic Predisposition to Disease, Copy-number variation, Genes, Developmental, Child, Genetic association, Genetics, Brain, medicine.disease, Psychiatry and Mental health, Attention Deficit Disorder with Hyperactivity, Etiology, Identification (biology), Psychology, Functional Neurogenomics [DCN 2], Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9051e618a758061ba17bbbe8d9d5e53Test
https://doi.org/10.1176/appi.ajp.2010.10070948Test

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