نتائج البحث - "Marieke E. Altink"

المصدر: Journal of attention disorders, 18(6), 521-531. SAGE Publications Inc.
Journal of Attention Disorders, 18(6), 521-531. SAGE Publications Inc.
Thissen, A J A M, Rommelse, N N J, Altink, M E, Oosterlaan, J & Buitelaar, J 2014, ' Parent-of-Origin Effects in ADHD: Distinct Influences of Paternal and Maternal ADHD on Neuropsychological Functioning in Offspring ', Journal of Attention Disorders, vol. 18, no. 6, pp. 521-531 . https://doi.org/10.1177/1087054712443159Test

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bab00d17d4bd86558dc6e2adf950c751Test
https://research.vu.nl/en/publications/b71ea21c-0673-4880-87bd-bb6841ea5cffTest

6

Quantitative Linkage for Autism Spectrum Disorders Symptoms in Attention-Deficit/Hyperactivity Disorder

المؤلفون: Catharina A. Hartman, Alejandro Arias-Vasquez, Cathelijne J. M. Buschgens, Ellen A. Fliers, Nanda Rommelse, Marieke E. Altink, Jan K. Buitelaar, Barbara Franke, Joseph A. Sergeant, Judith S. Nijmeijer, Ruud B. Minderaa, Pieter J. Hoekstra

المساهمون: Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), Life Course Epidemiology (LCE)

المصدر: Journal of Autism and Developmental Disorders, 44(7), 1671-1680. SPRINGER/PLENUM PUBLISHERS
Journal of Autism and Developmental Disorders, 44, 1671-80
Journal of Autism and Developmental Disorders, 44, 7, pp. 1671-80

مصطلحات موضوعية: Male, Candidate gene, medicine.medical_specialty, Genetic Linkage, DEFICIT HYPERACTIVITY DISORDER, Locus (genetics), SIB PAIRS, Comorbidity, Quantitative trait locus, ASD, TWIN SAMPLE, Genetic linkage, Surveys and Questionnaires, Developmental and Educational Psychology, medicine, Genetics, GENETIC INFLUENCES, Attention deficit hyperactivity disorder, Humans, ADHD, Attention, SOCIAL-BEHAVIOR, Psychiatry, Child, Genetic association, GENERAL-POPULATION, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], WILLIAMS-BEUREN-SYNDROME, Chromosome Mapping, medicine.disease, GENOME, Autism spectrum disorder, Attention Deficit Disorder with Hyperactivity, Child Development Disorders, Pervasive, Autism, Female, Psychology, Chromosomes, Human, Pair 7, TRAITS, SCAN, Clinical psychology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6018d6e68cea5b0ae029b2acc20f9e0Test
https://doi.org/10.1007/s10803-014-2039-4Test

7

Perinatal risk factors interacting with catechol O-methyltransferase and the serotonin transporter gene predict ASD symptoms in children with ADHD

المؤلفون: Pieter J. Hoekstra, Frank C. Verhulst, Judith S. Nijmeijer, Joseph A. Sergeant, Ruud B. Minderaa, Johan Ormel, Barbara Franke, Catharina A. Hartman, Jan K. Buitelaar, Cathelijne J. M. Buschgens, Marieke E. Altink, Ellen A. Fliers, Nanda Rommelse

المصدر: Journal of Child Psychology and Psychiatry. 51:1242-1250

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::31da0d3da7ebcf9c0be9375996641cf1Test
https://doi.org/10.1111/j.1469-7610.2010.02277.xTest

8

ADHD and Poor Motor Performance From a Family Genetic Perspective

المؤلفون: Sita H. Vermeulen, Stephen V. Faraone, Fruhling Rijsdijk, Joseph Sergeant, Ellen A. Fliers, Marieke E. Altink, N.N.J. Rommelse, Cathelijne J. M. Buschgens, Barbara Franke, Jan Buitelaar

المساهمون: Clinical Neuropsychology

المصدر: Journal of the American Academy of Child and Adolescent Psychiatry, 48(1), 25-34. Elsevier Limited
Fliers, E, Vermeulen, S, Rijsdijk, F, Altink, M, Buschgens, C, Rommelse, N, Faraone, S, Sergeant, J A, Buitelaar, J & Franke, B 2009, ' ADHD and Poor Motor Performance From a Family Genetic Perspective ', Journal of the American Academy of Child and Adolescent Psychiatry, vol. 48, no. 1, pp. 25-34 . https://doi.org/10.1097/CHI.0b013e31818b1ca2Test
Journal of the American Academy of Child and Adolescent Psychiatry, 48, 25-34
Journal of the American Academy of Child and Adolescent Psychiatry, 48, 1, pp. 25-34

مصطلحات موضوعية: medicine.medical_specialty, 110 012 Social cognition of verbal communication, Genetics and epigenetic pathways of disease [NCMLS 6], Apraxias, Disease, Neurological disorder, Mental health [NCEBP 9], Severity of Illness Index, behavioral disciplines and activities, Structural equation modeling, 150 000 MR Techniques in Brain Function, Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular epidemiology [NCEBP 1], Translational research [ONCOL 3], Surveys and Questionnaires, Severity of illness, mental disorders, Developmental and Educational Psychology, medicine, Perception and Action [DCN 1], Attention deficit hyperactivity disorder, Humans, Sibling, Psychiatry, Child, Psychomotor learning, medicine.disease, Psychiatry and Mental health, El Niño, Attention Deficit Disorder with Hyperactivity, Psychomotor Disorders, Psychology, Functional Neurogenomics [DCN 2]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12c4c00f885c91bb7ea98b709a383435Test
https://hdl.handle.net/1871/17555Test

9

A review and analysis of the relationship between neuropsychological measures andDAT1in ADHD

المؤلفون: Stephen V. Faraone, Jan K. Buitelaar, Marieke E. Altink, Alejandro Arias-Vásquez, Barbara Franke, Jaap Oosterlaan, Nanda Rommelse, Joseph A. Sergeant, Ellen A. Fliers, Cathelijne J. M. Buschgens

المساهمون: Clinical Neuropsychology

المصدر: American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 1536-46
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 8, pp. 1536-46
Rommelse, N N J, Altink, M E, Vasquez, A A, Buschgens, C J M, Fliers, E, Faraone, S V, Buitelaar, J K, Sergeant, J A, Franke, B & Oosterlaan, J 2008, ' A review and analysis of the relationship between neuropsychological measures and DAT1 in ADHD ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 147B, no. 8, pp. 1536-1546 . https://doi.org/10.1002/ajmg.b.30848Test
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B(8), 1536-1546. Wiley-Liss Inc.

مصطلحات موضوعية: Male, 110 012 Social cognition of verbal communication, Genetics and epigenetic pathways of disease [NCMLS 6], Neuropsychological Tests, Neuroinformatics [DCN 3], Linkage Disequilibrium, 0302 clinical medicine, Perception and Action [DCN 1], Medicine, Young adult, Child, Prefrontal cortex, 3' Untranslated Regions, Genetics (clinical), biology, Neuropsychology, Cognition, Executive functions, Psychiatry and Mental health, Child, Preschool, Female, Functional Neurogenomics [DCN 2], Clinical psychology, Adolescent, Genotype, Polymorphism, Single Nucleotide, Mental health [NCEBP 9], White People, 150 000 MR Techniques in Brain Function, Genomic disorders and inherited multi-system disorders [IGMD 3], Young Adult, 03 medical and health sciences, Cellular and Molecular Neuroscience, SDG 3 - Good Health and Well-being, Cognitive neurosciences [UMCN 3.2], mental disorders, Humans, Sibling, Dopamine transporter, Dopamine Plasma Membrane Transport Proteins, business.industry, Siblings, Introns, 030227 psychiatry, Haplotypes, Genetic defects of metabolism [UMCN 5.1], Attention Deficit Disorder with Hyperactivity, Endophenotype, Linear Models, biology.protein, 5' Untranslated Regions, business, 030217 neurology & neurosurgery, Microsatellite Repeats

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6c078224413b63e5a6dfb700bfa46acTest
https://doi.org/10.1002/ajmg.b.30848Test

10

Support for an independent familial segregation of executive and intelligence endophenotypes in ADHD families

المؤلفون: Nanda Rommelse, Marieke E. Altink, Cathelijne J. M. Buschgens, Jaap Oosterlaan, Jan K. Buitelaar, Joseph A. Sergeant

المساهمون: Other departments, Clinical Neuropsychology

المصدر: Psychological medicine, 38(11), 1595-1606. Cambridge University Press
Psychological Medicine, 38, 1595-606
Psychological Medicine, 38(11), 1595-1606. Cambridge University Press
Rommelse, N N J, Altink, M E, Oosterlaan, J, Buschgens, C, Buitelaar, J & Sergeant, J A 2008, ' Support for an independent familial segregation of executive and intelligence endophenotypes in ADHD families ', Psychological Medicine, vol. 38, no. 11, pp. 1595-1606 . https://doi.org/10.1017/S0033291708002869Test
Psychological Medicine, 38, 11, pp. 1595-606

مصطلحات موضوعية: Male, Adolescent, Psychometrics, Intelligence, Quantitative Trait Loci, Neuroinformatics [DCN 3], Neuropsychological Tests, Verbal learning, Mental health [NCEBP 9], Developmental psychology, 03 medical and health sciences, 0302 clinical medicine, Cognitive neurosciences [UMCN 3.2], Perception and Action [DCN 1], medicine, Humans, Attention deficit hyperactivity disorder, Attention, Sibling, Child, Applied Psychology, Intelligence quotient, Working memory, Siblings, Verbal Learning, medicine.disease, Verbal reasoning, Executive functions, 030227 psychiatry, Inhibition, Psychological, Psychiatry and Mental health, Memory, Short-Term, Phenotype, Pattern Recognition, Visual, Attention Deficit Disorder with Hyperactivity, Endophenotype, Female, Cognition Disorders, Psychology, Psychomotor Performance, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bbfd3e5762376b50a6da87ea915a576Test
https://doi.org/10.1017/S0033291708002869Test

تنقيح النتائج