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1. Psychiatrische Störungen bei Kindern ausländischer Arbeitnehmer
: eine epidemiologische Untersuchung
by Poustka, Fritz
1984, ISBN 9783432938714, Volume Bd. 27., 136
Psychiatry, Transcultural | Child mental health | Children of migrant laborers
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2. Keine Lösung in Sicht: Ein Kommentar von Prof. Dr. Med. Fritz Poustka
by Poustka, Fritz
Deutsche Apotheker Zeitung, ISSN 0011-9857, 2016, Volume 156, Issue 14
Journal Article
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3. Basic approaches to genetic and molecularbiological developmental psychiatry
by Poustka, Fritz and Elliger, Tilman J
1994, Library of psychiatry., ISBN 9783861282099, 188
Child psychiatry | Developmental psychobiology
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4. Full Text A structural neural deficit in adolescents with conduct disorder and its association with lack of empathy
by Sterzer, Philipp and Stadler, Christina and Poustka, Fritz and Kleinschmidt, Andreas
NeuroImage, ISSN 1053-8119, 08/2007, Volume 37, Issue 1, pp. 335 - 342
The goal of this study was to determine whether brain regions implicated in emotion processing show structural alterations in adolescents with conduct disorder... 
Conduct disorder | Empathy | Amygdala | Aggression | Insular cortex | Voxel-based morphometry | empathy | amygdala | RECOGNITION | ANTERIOR CINGULATE | voxel-based morphometry | MECHANISMS | aggression | conduct disorder | NEUROSCIENCES | NEUROIMAGING | CHILDREN | HYPERACTIVITY DISORDER | insular cortex | DISTRESS CUES | ANTISOCIAL-BEHAVIOR | ALEXITHYMIA | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | BRAIN | FACIAL EXPRESSIONS | Aggression - physiology | Emotions - physiology | Conduct Disorder - diagnosis | Humans | Cerebral Cortex - pathology | Personality Assessment | Male | Reference Values | Attention Deficit Disorder with Hyperactivity - pathology | Statistics as Topic | Amygdala - pathology | Magnetic Resonance Imaging | Conduct Disorder - pathology | Dominance, Cerebral - physiology | Image Processing, Computer-Assisted | Social Behavior | Adolescent | Attention Deficit Disorder with Hyperactivity - diagnosis | Frontal Lobe - pathology | Attention deficit disorder | Teenagers | Anxieties | Index Medicus
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5. Full Text Autism spectrum disorders: Sex differences in autistic behaviour domains and coexisting psychopathology
by Holtmann, Martin and Bölte, Sven and Poustka, Fritz
Developmental Medicine and Child Neurology, ISSN 0012-1622, 05/2007, Volume 49, Issue 5, pp. 361 - 366
The purpose of the present study was to examine possible differences between high-functioning males and females with autism spectrum disorder (ASD) regarding... 
MALE BRAIN | INTERVIEW | LIABILITY | FEMALES | PEDIATRICS | RELIABILITY | GERMAN FORM | MALES | PERVASIVE DEVELOPMENTAL DISORDERS | CLINICAL NEUROLOGY | CHILDREN | Cognitive Processes | Child Behavior Checklist | Check Lists | Interaction | Parents | Attention | Severity (of Disability) | Interpersonal Relationship | Autism | Gender Differences | Communication Skills | Comparative Analysis | Child Behavior | Behavior Problems | Pervasive Developmental Disorders | Psychopathology | Interpersonal Competence | Symptoms (Individual Disorders) | Antisocial Behavior | Disability Evaluation | Mental Disorders - epidemiology | Comorbidity | Humans | Child, Preschool | Personality Assessment | Male | Autistic Disorder - epidemiology | Stereotyped Behavior | Adolescent | Sex Factors | Adult | Female | Autistic Disorder - diagnosis | Mental Disorders - diagnosis | Child | Interpersonal Relations | Communication | Index Medicus
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6. Gesundheitsschäden bei Kindern durch Tiefflüge und andere Umwelteinflüsse
: vegetative Reaktionen und psychische Auffälligkeiten im Entwicklungsalter
by Poustka, F and Schmeck, K and Verein für Wasser-, Boden- und Lufthygiene (Germany)
1996, Schriftenreihe der Vereins für Wasser-, Boden- und Lufthygiene, ISBN 3437251686, Volume 97., 171, [2]
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7. Full Text Functional impact of global rare copy number variation in autism spectrum disorders
by Gillberg, Christopher and Kolevzon, Alexander and Nelson, Stanley F and Sansom, Katherine and Casallo, Guillermo and Miller, Judith and Brennan, Sean and Leboyer, Marion and Bacchelli, Elena and Delorme, Richard and Fombonne, Eric and Hallmayer, Joachim and Green, Jonathan and Pickles, Andrew and Heron, Elizabeth A and Salt, Jeff and Battaglia, Agatino and Klauck, Sabine M and McDougle, Christopher J and Mahoney, William and Noor, Abdul and Cytrynbaum, Cheryl and Sato, Daisuke and Almeida, Joana and Korvatska, Olena and Dawson, Geraldine and Bierut, Laura J and Coon, Hilary and Rickaby, Jessica and Freitag, Christine M and Roeder, Kathryn and Bader, Gary D and Wijsman, Ellen M and Vincent, John B and Hakonarson, Hakon and Segurado, Ricardo and Paton, Tara and Roge, Bernadette and Ennis, Sean and Kim, Cecilia and Monaco, Anthony P and Paterson, Andrew D and Crossett, Andrew and McGrath, Jane and Carson, Andrew R and Le Couteur, Ann and Cook, Edwin H and Chung, Brian H.Y and Cuccaro, Michael L and Van Engeland, Herman and Conroy, Judith and Holt, Richard and Strawbridge, Christina and Kustanovich, Vlad and Migita, Ohsuke and Stoppioni, Vera and Igliozzi, Roberta and Poustka, Fritz and Stein, Olaf and Posey, David J and Sheffield, Val C and Duque, Frederico and Parrini, Barbara and Berney, Tom and Hus, Vanessa and Baird, Gillian and Duketis, Eftichia and Soorya, Latha and Corsello, Christina and Drmic, Irene and Sousa, Inês and Abrahams, Brett S and Thomson, Susanne and Lajonchere, Clara M and Tsiantis, John and Pinto, Dalila and Green, Andrew and Hughes, Gillian and Mantoulan, Carine and Betancur, Catalina and Volkmar, Fred and Poustka, Annemarie and Shah, Naisha and Bryson, Susan E and Munson, Jeff and Tancredi, Raffaella and Nygren, Gudrun and Wittemeyer, Kerstin and Merikangas, Alison and Oliveira, Guiomar and Farrar, Penny and Maestrini, Elena and Liu, Xiao-Qing and Gallagher, Louise and McConachie, Helen and Zurawiecki, Danielle and Schellenberg, Gerard D and Glessner, Joseph T and Lord, Catherine and Piven, Joseph and ... and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi and Göteborgs universitet and Gothenburg University and Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry and Sahlgrenska Academy
Nature, ISSN 0028-0836, 07/2010, Volume 466, Issue 7304, pp. 368 - 372
The autism spectrum disorders (ASDs) are a group of conditions characterized by impairments in reciprocal social interaction and communication, and the... 
COMPLEX | SNP GENOTYPING DATA | HIDDEN-MARKOV MODEL | MULTIDISCIPLINARY SCIENCES | LOCI | GENETIC DISORDER | MUTATIONS | LINKAGE | ASSOCIATION | ANCESTRY | REVEALS | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Signal Transduction | Child Development Disorders, Pervasive - pathology | Humans | Child Development Disorders, Pervasive - physiopathology | DNA Copy Number Variations - genetics | Case-Control Studies | Europe - ethnology | Child Development Disorders, Pervasive - genetics | Social Behavior | Child | Cell Movement | Cytoprotection | Confidence intervals | Autism | Genetics | Genes | Quality control | Reproduction | Disorders | Disabilities | Arrays | Loci | Index Medicus | Genetic Predisposition to Disease | Europe | Gene Dosage | DNA Copy Number Variations | Life Sciences | Child Development Disorders, Pervasive | Pervasive | Child Development Disorders | Ethnology | Physiopathology | Pathology | Psykiatri | Psychiatry
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8. Full Text Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
by Pinto, Dalila and Delaby, Elsa and Merico, Daniele and Barbosa, Mafalda and Merikangas, Alison and Klei, Lambertus and Thiruvahindrapuram, Bhooma and Xu, Xiao and Ziman, Robert and Wang, Zhuozhi and Vorstman, Jacob A.S and Thompson, Ann and Regan, Regina and Pilorge, Marion and Pellecchia, Giovanna and Pagnamenta, Alistair T and Oliveira, Guiomar and Oliveira, Bárbara and Marshall, Christian R and Magalhaes, Tiago R and Lowe, Jennifer K and Howe, Jennifer L and Griswold, Anthony J and Gilbert, John and Duketis, Eftichia and Dombroski, Beth A and De Jonge, Maretha V and Cuccaro, Michael and Crawford, Emily L and Correia, Catarina T and Conroy, Judith and Conceição, Inês C and Chiocchetti, Andreas G and Casey, Graham and Casey, Jillian P and Cai, Guiqing and Cabrol, Christelle and Bolshakova, Nadia and Bacchelli, Elena and Anney, Richard and Gallinger, Steven and Cotterchio, Michelle and Zwaigenbaum, Lonnie and Wittemeyer, Kerstin and Wing, Kirsty and Wallace, Simon and van Engeland, Herman and Tryfon, Ana and Thomson, Susanne and Soorya, Latha and Rogé, Bernadette and Roberts, Wendy and Poustka, Fritz and Mouga, Susana and Minshew, Nancy and McInnes, L. Alison and McGrew, Susan G and Lord, Catherine and Leboyer, Marion and Le Couteur, Ann S and Kolevzon, Alexander and Jiménez González, Patricia and Jacob, Suma and Holt, Richard and Guter, Stephen and Green, Jonathan and Green, Andrew and Gillberg, Christopher and Fernandez, Bridget A and Duque, Frederico and Delorme, Richard and Dawson, Geraldine and Chaste, Pauline and Café, Cátia and Brennan, Sean and Bourgeron, Thomas and Bolton, Patrick F and Bölte, Sven and Bernier, Raphael and Baird, Gillian and Bailey, Anthony J and Anagnostou, Evdokia and Almeida, Joana and Wijsman, Ellen M and Vieland, Veronica J and Vicente, Astrid M and Schellenberg, Gerard D and Pericak-Vance, Margaret and Paterson, Andrew D and Parr, Jeremy R and Nurnberger, John I and Monaco, Anthony P and Maestrini, Elena and Klauck, Sabine M and Hakonarson, Hakon and Haines, Jonathan L and Geschwind, Daniel H and Freitag, Christine M and Folstein, Susan E and Ennis, Sean and ... and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
The American Journal of Human Genetics, ISSN 0002-9297, 05/2014, Volume 94, Issue 5, pp. 677 - 694
Rare copy-number variation (CNV) is an important source of risk for autism spectrum disorders (ASDs). We analyzed 2,446 ASD-affected families and confirmed an... 
INTELLECTUAL DISABILITY | DUPLICATIONS | DE-NOVO MUTATIONS | PHENOTYPE ONTOLOGY | GENETICS & HEREDITY | FRAGILE-X-SYNDROME | RISK | COPY NUMBER VARIANTS | STRUCTURAL VARIATION | DELETIONS | GENOME-WIDE ASSOCIATION | Sequence Deletion | Metabolic Networks and Pathways - genetics | Multigene Family | Child Development Disorders, Pervasive - genetics | Pedigree | Humans | Female | Male | Gene Regulatory Networks | Child | DNA Copy Number Variations | Genetic research | Autism | Genetic code | Genetic aspects | Research | Genetic variation | Proteins | Chromatin | Learning disabilities | Genes | Neurological disorders | Index Medicus | Life Sciences | Genetics | Psykiatri | Psychiatry
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9. Full Text The recognition of facial affect in autistic and schizophrenic subjects and their first-degree relatives
by BÖLTE, SVEN and POUSTKA, FRITZ
Psychological Medicine, ISSN 0033-2917, 7/2003, Volume 33, Issue 5, pp. 907 - 915
Background. Autism and schizophrenia are considered to be substantially influenced by genetic factors. The endophenotype of both disorders probably also... 
WEAK CENTRAL COHERENCE | DIAGNOSTIC INTERVIEW | PSYCHIATRY | PARENTS | ASPERGER-SYNDROME | PSYCHOLOGY, CLINICAL | PERVASIVE DEVELOPMENTAL DISORDERS | PSYCHOLOGY | CHILDREN | NONPSYCHOTIC RELATIVES | COGNITIVE PHENOTYPE | DEFICITS | FACE | Autistic Disorder - genetics | Humans | Middle Aged | Parents | Facial Expression | Male | Psychometrics | Schizophrenic Psychology | Affect | Schizophrenia - genetics | Schizophrenia - diagnosis | Adolescent | Adult | Female | Autistic Disorder - diagnosis | Recognition (Psychology) | Task Performance and Analysis | Siblings | Index Medicus
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10. Full Text Sex differences in cognitive domains and their clinical correlates in higher-functioning autism spectrum disorders
by Bölte, Sven and Duketis, Eftichia and Poustka, Fritz and Holtmann, Martin
Autism, ISSN 1362-3613, 7/2011, Volume 15, Issue 4, pp. 497 - 511
Despite the skewed sex ratio, few studies have addressed possible cognitive sex differences in autism spectrum disorders (ASDs). This study compared visual... 
neuropsychology | PDD | attention | gender | savant | executive function | TEST-PERFORMANCE | BEHAVIOR | PSYCHOLOGY, DEVELOPMENTAL | ASPERGER-SYNDROME | CHILDREN | PERCEPTION | PEOPLE | CARD SORTING TEST | DEFICITS | GIRLS | Cognitive Processes | Correlation | Attention | Block Design Test | Males | Autism Diagnostic Observation Schedule | Interpersonal Relationship | Autism | Gender Differences | Interpersonal Communication | Behavior Problems | Pervasive Developmental Disorders | Cognitive Ability | Visual Perception | Females | Asperger Syndrome | Siblings | Humans | Male | Cognition | Case-Control Studies | Neuropsychological Tests | Child Development Disorders, Pervasive - psychology | Stereotyped Behavior | Adolescent | Sex Factors | Female | Psychological Tests | Child | Executive Function | Autistic spectrum disorders | Sex differences | Gender differences | Stereotypes | Visual attention | Autistic children | Sex ratio | Executive function | Cognitive ability | Stereotyped behavior | Visual perception | Index Medicus
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11. Full Text Autistic Traits and Autism Spectrum Disorders: The Clinical Validity of Two Measures Presuming a Continuum of Social Communication Skills
by Bölte, Sven and Westerwald, Eva and Holtmann, Martin and Freitag, Christine and Poustka, Fritz
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 1/2011, Volume 41, Issue 1, pp. 66 - 72
Research indicates that autism is the extreme end of a continuously distributed trait. The Social Responsiveness Scale (SRS) and the Social and Communication... 
Pediatrics | PDD | Screening | Neurosciences | Child and School Psychology | Questionnaire | Diagnostics | Psychology | Assessment | Psychometrics | Public Health/Gesundheitswesen | Screening; Questionnaire | PSYCHOLOGY, DEVELOPMENTAL | RELIABILITY | QUOTIENT | COMPETENCE | GERMAN FORM | HERITABILITY | CHILDREN | GENERAL-POPULATION | INTERVIEW | OBSERVATION-SCHEDULE ADOS | VERSION | Autism | Validity | Communication Skills | Interpersonal Communication | Pervasive Developmental Disorders | Check Lists | Communication Disorders | Screening Tests | Test Validity | Symptoms (Individual Disorders) | Reproducibility of Results | Humans | Male | Child Development Disorders, Pervasive - psychology | Social Behavior | Sensitivity and Specificity | Adolescent | Child Development Disorders, Pervasive - diagnosis | Female | ROC Curve | Surveys and Questionnaires | Child | Interpersonal Relations | Communication | Index Medicus | Original Paper
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12. Full Text Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
by Weiner, Daniel J and Wigdor, Emilie M and Ripke, Stephan and Walters, Raymond K and Kosmicki, Jack A and Grove, Jakob and Samocha, Kaitlin E and Goldstein, Jacqueline I and Okbay, Aysu and Bybjerg-Grauholm, Jonas and Werge, Thomas and Hougaard, David M and Taylor, Jacob and Skuse, David and Devlin, Bernie and Anney, Richard and Sanders, Stephan J and Bishop, Somer and Mortensen, Preben Bo and Børglum, Anders D and Smith, George Davey and Daly, Mark J and Robinson, Elise B and Bækvad-Hansen, Marie and Dumont, Ashley and Hansen, Christine and Hansen, Thomas F and Howrigan, Daniel and Mattheisen, Manuel and Moran, Jennifer and Mors, Ole and Nordentoft, Merete and Nørgaard-Pedersen, Bent and Poterba, Timothy and Poulsen, Jesper and Stevens, Christine and Anttila, Verneri and Holmans, Peter and Huang, Hailiang and Klei, Lambertus and Lee, Phil H and Medland, Sarah E and Neale, Benjamin and Weiss, Lauren A and Zwaigenbaum, Lonnie and Yu, Timothy W and Wittemeyer, Kerstin and Willsey, A Jeremy and Wijsman, Ellen M and Wassink, Thomas H and Waltes, Regina and Walsh, Christopher A and Wallace, Simon and Vorstman, Jacob A. S and Vieland, Veronica J and Vicente, Astrid M and Van Engeland, Herman and Tsang, Kathryn and Thompson, Ann P and Szatmari, Peter and Svantesson, Oscar and Steinberg, Stacy and Stefansson, Kari and Stefansson, Hreinn and State, Matthew W and Soorya, Latha and Silagadze, Teimuraz and Scherer, Stephen W and Schellenberg, Gerard D and Sandin, Sven and Saemundsen, Evald and Rouleau, Guy A and Rogé, Bernadette and Roeder, Kathryn and Roberts, Wendy and Reichert, Jennifer and Reichenberg, Abraham and Rehnström, Karola and Regan, Regina and Poustka, Fritz and Poultney, Christopher S and Piven, Joseph and Pinto, Dalila and Pericak-Vance, Margaret A and Pejovic-Milovancevic, Milica and Pedersen, Marianne G and Pedersen, Carsten B and Paterson, Andrew D and Parr, Jeremy R and Pagnamenta, Alistair T and Oliveira, Guiomar and Nurnberger, John I and Murtha, Michael T and Mouga, Susana and Morrow, Eric M and DeLuca, Daniel Moreno and Monaco, Anthony P and Minshew, Nancy and Merikangas, Alison and McMahon, William M and ... and Psychiat Genomics Consortium and iPSYCH-Broad Autism Grp and iPSYCH-Broad Autism Group and Psychiatric Genomics Consortium Autism Group and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Nature Genetics, ISSN 1061-4036, 07/2017, Volume 49, Issue 7, pp. 978 - 985
Autism spectrum disorder (ASD) risk is influenced by common polygenic and de novo variation. We aimed to clarify the influence of polygenic risk for ASD and to... 
DE-NOVO | VARIANTS | GENETIC RISK | GENETICS & HEREDITY | MUTATIONS | SIMONS SIMPLEX COLLECTION | GENOME-WIDE ASSOCIATION | INSIGHTS | Autism Spectrum Disorder - genetics | Sequence Deletion | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Risk Factors | Family Health | Genetics, Behavioral | Male | Educational Status | Intelligence - genetics | Multifactorial Inheritance | Intellectual Disability - genetics | Genetic Variation | Phenotype | Ethnic Groups - genetics | Schizophrenia - genetics | Autism Spectrum Disorder - epidemiology | Adult | Female | Child | Cohort Studies | Family | Genetic aspects | Genetic transformation | Research | Risk factors | Pervasive developmental disorders | Mental disorders | Intellectual disabilities | Disorders | Schizophrenia | Risk | Genomes | Cases (containers) | Subgroups | Educational attainment | Children & youth | Proteins | Studies | Consortia | Autism | Parents & parenting | Etiology | Population | Mutation | Children | Psychiatry | Index Medicus | Life Sciences | Neurons and Cognition | Neurologi | disease | biology | insights | variants | Genetics & Heredity | de-novo | Neurology | mutations | general-population | genetic risk | genome-wide association | loci
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