J. Hallmayer

Angeline M. Loh, R. Kaneva, S. MacGregor, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Beyond a Binary Classification of Sex: An Examination of Brain Sex Differentiation, Psychopathology, and Genotype.

Lester W. Mackey, I. Gotlib, J. Hallmayer, 2019, Journal of the American Academy of Child and Adolescent Psychiatry.

Network effects of the neuropsychiatric 15q13.3 microdeletion on the transcriptome and epigenome in human induced neurons

W. Wong, A. Urban, J. Hallmayer, 2019, bioRxiv.

Genetics of autism: characteristics of affected and unaffected children from 37 multiplex families.

H. Kraemer, L. Lotspeich, W. McMahon, 1994, American journal of medical genetics.

Failure to find cytogenetic abnormalities in autistic children whose parents grew up near plastics manufacturing sites

H. Kraemer, L. Lotspeich, J. Hallmayer, 1993, Journal of autism and developmental disorders.

Hepatitis A virus link to atopic disease

N. Risch, P. Underhill, L. Cavalli-Sforza, 2003 .

Determination of RNA content in postischemic gerbil brain byin situ hybridization

K. Hossmann, J. Hallmayer, A. Starzinski-Powitz, 1989, Metabolic Brain Disease.

Cyclical Changes of Homicide Rates

J. Hallmayer, D. Rock, D. Greenberg, 2003, Journal of interpersonal violence.

Using iPS cells to investigate cardiac phenotypes in patients with Timothy Syndrome

Jonathan A. Bernstein, Masayuki Yazawa, Brian Hsueh, 2011, Nature.

Sleep Disturbances in Individuals With Phelan‐McDermid Syndrome: Correlation With Caregivers' Sleep Quality and Daytime Functioning

J. Hallmayer, J. Bernstein, D. Bro, 2017, Sleep.

Common variants in P2RY11 are associated with narcolepsy

Christian Gieger, Poul Jennum, Thomas Meitinger, 2010, Nature Genetics.

Erratum: Common variants in P2RY11 are associated with narcolepsy

C. Gieger, N. Risch, P. Kwok, 2011, Nature Genetics.

Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8.

L. Siever, M. Daly, T. Sigmundsson, 1996, American journal of medical genetics.

A genomic screen of autism: evidence for a multilocus etiology.

Courtney A. Harper, P Nicholas, N Risch, 1999, American journal of human genetics.

Genetics of Late-Life Mental, Physical, and Cognitive Function

R. O'Hara, J. Hallmayer, Josh T Jordan, 2016 .

Angiotensin-converting enzyme activity and the ACE Alu polymorphism in autosomal dominant polycystic kidney disease.

L. Beilin, J. Hallmayer, V. Burke, 2001, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophrenia

L. Palmer, J. Badcock, A. Jablensky, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic and environmental influences on structural brain measures in twins with autism spectrum disorder

L. Lazzeroni, A. Reiss, M. Raman, 2019, Molecular Psychiatry.

Genetic and environmental influences on corticostriatal circuits in twins with autism

L. Lazzeroni, A. Reiss, M. Raman, 2020, Journal of psychiatry & neuroscience : JPN.

A proton MR spectroscopy study of the thalamus in twins with autism spectrum disorder

L. Lazzeroni, A. Reiss, M. Raman, 2018, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Protein kinase C inhibition: a target for treatment of mania.

J. Hallmayer, Mina Hah, 2008, Current psychiatry reports.

Familial Psoriasis and HLA-B: Unambiguous Support for Linkage in 97 Published Families

S. Hodge, J. Hallmayer, J. Mansbridge, 1998, Human Heredity.

Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.

H. Kraemer, L. Lotspeich, W. McMahon, 1999, American journal of medical genetics.

Brain Development in School-Age and Adolescent Girls: Effects of Turner Syndrome, Estrogen Therapy, and Genomic Imprinting

A. Reiss, J. Hallmayer, D. Hong, 2020, Biological Psychiatry.

Catatonia in a psychiatric intensive care facility: incidence and response to benzodiazepines.

J. Hallmayer, D. Schwartz, J. Lee, 2000, Annals of clinical psychiatry : official journal of the American Academy of Clinical Psychiatrists.

Genomic Imprinting Effects of the X Chromosome on Brain Morphology

A. Reiss, M. Raman, J. Hallmayer, 2013, The Journal of Neuroscience.

Catechol-O-Methyltransferase Val158Met Polymorphism Moderates Anterior Cingulate Volume in Posttraumatic Stress Disorder

S. Eliez, J. Hallmayer, D. Kaloupek, 2011, Biological Psychiatry.

Interacting and paradoxical forces in neuroscience and society

J. Illes, J. Hallmayer, Jennifer S. Singh, 2007, Nature Reviews Neuroscience.

Protein and Polyamine Metabolism in Reversible Cerebral Ischemia of Gerbils

W. Paschen, K. Hossmann, J. Hallmayer, 1991 .

Polyamine metabolism in reversible cerebral ischemia of Mongolian gerbils

W. Paschen, G. Mies, J. Hallmayer, 1988, Metabolic Brain Disease.

Low dose of barbiturates for prevention of hippocampal lesions after brief ischemic episodes

G. Mies, K. Hossmann, J. Hallmayer, 2004, Acta Neuropathologica.

Regional changes of polyamine profiles after reversible cerebral ischemia in mongolian gerbils: Effects of nimodipine and barbiturate

W. Paschen, J. Hallmayer, G. Röhn, 1988, Neurochemical Pathology.

The seasonal risk for deliberate self-harm. Determined by place of birth, but occurrence determined by place of residence.

J. Hallmayer, D. Rock, 2008, Crisis.

Association of Anxiety Symptoms in Offspring of Bipolar Parents with Serotonin Transporter-Linked Polymorphic Region (5-HTTLPR) Genotype.

K. Chang, J. Hallmayer, Eunjoo Kim, 2015, Journal of child and adolescent psychopharmacology.

Individuals with Autism Spectrum Disorders Have Equal Success Rate But Require Longer Periods of Systematic Desensitization than Control Patients to Complete Ambulatory Polysomnography.

L. Lotspeich, R. O'Hara, A. Hardan, 2016, Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.

Impact of case fatality on the seasonality of suicidal behaviour

J. Hallmayer, D. Rock, D. Greenberg, 2005, Psychiatry Research.

APOE-epsilon4 and APOE -491A polymorphisms in individuals with subjective memory loss.

R. Martins, Hans Förstl, S. Laws, 2002, Molecular psychiatry.

Lack of linkage between schizophrenia and markers at the telomeric end of the pseudoautosomal region of the sex chromosomes

W. Maier, M. Ackenheil, D. Lichtermann, 1995, Biological Psychiatry.

Erratum: Narcolepsy is strongly associated with the T-cell receptor alpha locus

C. Gieger, N. Risch, P. Kwok, 2009, Nature Genetics.

Autism and the chemical connection

H. Kraemer, L. Lotspeich, J. Hallmayer, 1994, Journal of autism and developmental disorders.

Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysis.

W. Maier, B. Lerer, D. Lichtermann, 1998, American journal of human genetics.

Narcolepsy is strongly associated with the TCR alpha locus

C. Gieger, N. Risch, P. Kwok, 2009, Nature Genetics.

A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6

M. Rietschel, P. Falkai, W. Maier, 2000, Molecular Psychiatry.

Rediscovering an old friend: a role for insulin growth factor-2 in reducing neurodegeneration, decreasing amyloid beta, and improving memory

R. O'Hara, J. Hallmayer, 2019, International Psychogeriatrics.

Perinatal factors and the development of autism: a population study.

J. Hallmayer, N. de Klerk, C. Bower, 2004, Archives of general psychiatry.

SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients

R. Dolmetsch, T. Portmann, J. Hallmayer, 2013, Nature.

Cortisol, cytokines, and hippocampal volume interactions in the elderly

H. Kraemer, F. Dhabhar, M. Weiner, 2014, Front. Aging Neurosci..

Prenatal and perinatal risk factors in a twin study of autism spectrum disorders.

C. Lajonchere, L. Lotspeich, R. O'Hara, 2013, Journal of psychiatric research.

Integrated functional genomic analyses of Klinefelter and Turner syndromes reveal global network effects of altered X chromosome dosage

W. Wong, A. Urban, A. Reiss, 2020, Proceedings of the National Academy of Sciences.

Genomic imprinting effects on cognitive and social abilities in prepubertal girls with Turner syndrome.

A. Reiss, J. Hallmayer, D. Hong, 2012, The Journal of clinical endocrinology and metabolism.

No evidence of linkage between the dopamine D2 receptor gene and schizophrenia

W. Maier, M. Ackenheil, D. Lichtermann, 1994, Psychiatry Research.

Exclusion of linkage between the serotonin2 receptor and schizophrenia in a large Swedish kindred.

K. Kidd, L. Cavalli-Sforza, J. Kennedy, 1992, Archives of general psychiatry.

Evidence against linkage of schizophrenia to chromosome 5q11-q13 markers in systematically ascertained families

W. Maier, M. Ackenheil, D. Lichtermann, 1992, Biological Psychiatry.

Chromosomes 1, 2, and 7 workshop.

J. Hallmayer, 1999, American journal of medical genetics.

Identification of Human Neuronal Protein Complexes Reveals Biochemical Activities and Convergent Mechanisms of Action in Autism Spectrum Disorders.

Zhihai Ma, A. Urban, Ke Jin, 2015, Cell systems.

Using iPS cell-derived neurons to uncover cellular phenotypes associated with Timothy Syndrome

D. Geschwind, R. Dolmetsch, T. Palmer, 2011, Nature Medicine.

On the twin risk in autism.

N. Risch, J. Hallmayer, L. Croen, 2002, American journal of human genetics.

DQB1*0602 and DQA1*0102 (DQ1) are better markers than DR2 for narcolepsy in Caucasian and black Americans.

P. Underhill, C. Guilleminault, E. Mignot, 1994, Sleep.

Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIα gene (PIP5K2A) with schizophrenia

W. Maier, P. Sklar, T. Becker, 2006, Molecular Psychiatry.

Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families.

Margot Albus, Marcella Rietschel, Michael Knapp, 2003, American journal of human genetics.

Linkage analysis of candidate regions using a composite neurocognitive phenotype correlated with schizophrenia

M. Woodbury, P. Michie, A. Jablensky, 2003, Molecular Psychiatry.

The epidemiology of the genetic liability for schizophrenia.

J. Hallmayer, Joachim Hallmayer, 2000, The Australian and New Zealand journal of psychiatry.

Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis.

M. Rietschel, W. Maier, K. Kanyas, 1998, American journal of medical genetics.

Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24

A. Hristova, L. Middleton, J. Hallmayer, 1996, Nature Genetics.

Genetic heterogeneity of polycystic kidney disease in Bulgaria

J. Hallmayer, L. Kalaydjieva, B. Dworniczak, 1994, Human Genetics.

Extensive polymorphism of a (CA)n microsatellite located in the HLA-DQA1/DQB1 class II region.

E. Mignot, J. Hallmayer, J. Kalil, 1995, Human immunology.

Association of tumor necrosis factor alpha gene -G308A polymorphism with schizophrenia

M. Rietschel, T. Schulze, W. Maier, 2003, Schizophrenia Research.

An investigation into sub‐telomeric deletions of chromosome 22 and pervasive developmental disorders

W. Hill, J. Hallmayer, B. Petterson, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Narcolepsy risk loci are enriched in immune cells and suggest autoimmune modulation of the T cell receptor repertoire

Chun Jimmie Ye, M. Rivas, M. Perola, 2018, bioRxiv.

Using iPS cells to investigate cardiac phenotypes in patients with Timothy Syndrome

R. Dolmetsch, Brian Hsueh, J. Hallmayer, 2012 .

Integration of neural and epigenetic contributions to posttraumatic stress symptoms: The role of hippocampal volume and glucocorticoid receptor gene methylation

Salil Soman, Ruth O'Hara, D. M. Lyons, 2018, PloS one.

Increased activation product of complement 4 protein in plasma of individuals with schizophrenia

C. Sabatti, A. Urban, D. Levinson, 2021, Translational Psychiatry.

Neuronal defects in a human cellular model of 22q11.2 deletion syndrome

D. Geschwind, J. Rapoport, R. Dolmetsch, 2020, Nature Medicine.

Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib–pair linkage analysis

Margot Albus, Richard P. Ebstein, Wolfgang Maier, 1995, Nature Genetics.

Genome-wide molecular effects of the neuropsychiatric 16p11 CNVs in an iPSC-to-iN neuronal model

A. Urban, Bo Zhou, Steve S. Ho, 2020, bioRxiv.

Neuronal defects in a human cellular model of 22q11.2 deletion syndrome

D. Geschwind, J. Rapoport, R. Dolmetsch, 2020, Nature medicine.

Assembly of Functional Forebrain Spheroids from Human Pluripotent Cells

H. C. Fan, L. Steinmetz, J. Huguenard, 2017 .

Twins with KBG Syndrome and Autism

L. Lotspeich, J. Hallmayer, Jennifer M. Phillips, 2009, Journal of autism and developmental disorders.

Increasing seasonality of suicide in Australia 1970–1999

J. Hallmayer, D. Rock, D. Greenberg, 2003, Psychiatry Research.

A Pilot Study of Antidepressant-Induced Mania in Pediatric Bipolar Disorder: Characteristics, Risk Factors, and the Serotonin Transporter Gene

K. Chang, J. Hallmayer, M. Howe, 2006, Biological Psychiatry.

Aging of persons with neurodevelopmental disabilities

Christina F. Chick, J. Hallmayer, L. Anker, 2020 .

Season–of–birth as a risk factor for the seasonality of suicidal behaviour

J. Hallmayer, D. Rock, D. Greenberg, 2006, European Archives of Psychiatry and Clinical Neuroscience.

Perinatal Factors and the Development of Autism

J. Hallmayer, N. Klerk, C. Bower, 2015 .

Linkage analysis between pericentrometric markers on chromosome 18 and bipolar disorder: A replication test

W. Maier, B. Bondy, M. Ackenheil, 1995, Psychiatry Research.

Trends in US Autism Research Funding

L. Lazzeroni, J. Illes, J. Hallmayer, 2009, Journal of autism and developmental disorders.

Intronic Single Nucleotide Polymorphisms of Engrailed Homeobox 2 Modulate the Disease Vulnerability of Autism in a Han Chinese Population

Pinchen Yang, J. Hallmayer, F. Lung, 2010, Neuropsychobiology.

Male-to-male transmission in extended pedigrees with multiple cases of autism.

L. Lotspeich, W. McMahon, J. Hallmayer, 1996, American journal of medical genetics.

Molecular analysis and test of linkage between the FMR-1 gene and infantile autism in multiplex families.

H. Kraemer, L. Lotspeich, W. McMahon, 1994, American journal of human genetics.

Preliminary study of anxiety symptoms, family dysfunction, and the brain-derived neurotrophic factor (BDNF) Val66Met genotype in offspring of parents with bipolar disorder.

K. Chang, Seung-Chul Hong, J. Hallmayer, 2015, Journal of psychiatric research.

Blood levels of brain derived neurotrophic factor in women with bipolar disorder and healthy control women.

H. Kenna, N. Rasgon, T. Ketter, 2014, Journal of affective disorders.

Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome

Fumiko Hoeft, Doron Gothelf, S. Antonarakis, 2007, Human brain mapping.

22q11 deletion syndrome in childhood onset schizophrenia: an update

A. Addington, J. Rapoport, N. Gogtay, 2004, Molecular Psychiatry.

Characterizing regression in Phelan McDermid Syndrome (22q13 deletion syndrome).

A. Urban, R. O'Hara, J. Hallmayer, 2017, Journal of psychiatric research.

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.

Fabian Grubert, T. Wieland, A. Urban, 2012, Human molecular genetics.

COMT genotype affects prefrontal white matter pathways in children and adolescents

Gary H. Glover, Lee M. Perry, Roland Bammer, 2010, NeuroImage.

Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy

F. Mastaglia, N. Laing, J. Hallmayer, 1999, Journal of neurology, neurosurgery, and psychiatry.

Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis

W. Maier, B. Lerer, D. Lichtermann, 1997, Molecular Psychiatry.

A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients

R. Dolmetsch, J. Rubenstein, D. Madison, 2016, eLife.

Investigation of linkage and association/linkage disequilibrium of HLA A-, DQA1-, DQB1-, and DRB1-alleles in 69 sib-pair- and 89 trio-families with schizophrenia.

M. Rietschel, W. Maier, B. Lerer, 2002, American journal of medical genetics.

Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls

Eric S. Lander, Margot Albus, Michael J. Owen, 2001, Nature Genetics.

The complex mutation pattern of a microsatellite.

L. Jin, E. Mignot, J. Hallmayer, 1997, Genome research.

Mutation rate varies among alleles at a microsatellite locus: phylogenetic evidence.

L. Jin, E. Mignot, J. Hallmayer, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Genetic and demographic predisposing factors associated with pediatric sleepwalking in the Philadelphia Neurodevelopmental Cohort

J. Hallmayer, S. Nishino, Manpreet K. Singh, 2021, Journal of the Neurological Sciences.

Serotonin transporter polymorphism, depressive symptoms, and emotional impulsivity among advanced breast cancer patients

C. Carver, J. Hallmayer, D. Spiegel, 2018, Supportive Care in Cancer.

Getting our AKT together in schizophrenia?

J. Hallmayer, Joachim Hallmayer, 2004, Nature Genetics.

HPA Axis Reactivity: A Mechanism Underlying the Associations Among 5-HTTLPR, Stress, and Depression

I. Gotlib, J. Joormann, K. Minor, 2008, Biological Psychiatry.

Effects of X Chromosome Monosomy and Genomic Imprinting on Observational Markers of Social Anxiety in Prepubertal Girls with Turner Syndrome

A. Reiss, S. Hall, J. Hallmayer, 2021, Journal of autism and developmental disorders.

Corticotropin-releasing factor 1 receptor haplotype and cognitive features of major depression

A. Schatzberg, I. Gotlib, J. Keller, 2018, Translational Psychiatry.

Apolipoprotein E promotes the binding and uptake of β-amyloid into Chinese hamster ovary cells in an isoform-specific manner

R. Martins, D. Small, J. Hallmayer, 1999, Neuroscience.

Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents trios

M. Rietschel, W. Maier, B. Lerer, 1999, Molecular Psychiatry.

Morbid Risks in Relatives of Affective, Schizoaffective, and Schizophrenic Patients — Results of a Family Study

D. Lichtermann, J. Hallmayer, J. Minges, 1990 .

A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies).

A. Pérez-Lezaun, J. Hallmayer, L. Kalaydjieva, 1999, American Journal of Human Genetics.

A linkage study of affective disorders in two Bulgarian Gypsy families: results for candidate regions on chromosomes 18 and 21.

R. Kaneva, V. Milanova, A. Jablensky, 1998, Psychiatric genetics.

Searching for susceptibility genes in schizophrenia by genetic linkage analysis.

N. Risch, W. Maier, R. Ebstein, 1996, Cold Spring Harbor symposia on quantitative biology.

Genetic and Environmental Influences on Lobar Brain Structures in Twins With Autism.

L. Lazzeroni, A. Reiss, M. Raman, 2019, Cerebral cortex.

The Epidemiology of the Genetic Liability for Schizophrenia

J. Hallmayer, 2000 .

Network Effects of the 15q13.3 Microdeletion on the Transcriptome and Epigenome in Human-Induced Neurons

W. Wong, A. Urban, R. Pattni, 2020, Biological Psychiatry.

No evidence for segregation distortion in females in a sample of 72 families with schizophrenia with potential linkage to chromosome 10p14-p11.

J. Hallmayer, D. Wildenauer, S. Schwab, 1999, American journal of medical genetics.

Austism and the X Chromosome: Multipoint sib-Pair Analysis

L. Lotspeich, W. McMahon, N. Risch, 1996 .

Potential linkage for schizophrenia on chromosome 22q12-q13: a replication study.

R. Fimmers, W. Maier, R. Ebstein, 1995, American journal of medical genetics.

Genetic identity of Marinesco–Sjögren/myoglobinuria and CCFDN syndromes

J. Hallmayer, L. Kalaydjieva, H. Lochmüller, 2002, Neurology.

Serotonin transporter polymorphism, memory and hippocampal volume in the elderly: association and interaction with cortisol

H. Kraemer, A. Schatzberg, M. Weiner, 2007, Molecular Psychiatry.

The effect of insulin and glucose on the plasma concentration of Alzheimer's amyloid precursor protein

R. Martins, K. Taddei, J. Hallmayer, 1999, Neuroscience.

The -491AA polymorphism in the APOE gene is associated with increased plasma apoE levels in Alzheimer's disease.

R. Martins, W. Brooks, S. Laws, 1999, Neuroreport.

Genome Wide Analysis of Narcolepsy in China Implicates Novel Immune Loci and Reveals Changes in Association Prior to Versus After the 2009 H1N1 Influenza Pandemic

E. Mignot, F. Han, T. Pollmächer, 2013, PLoS genetics.

Atypical antipsychotic medication in preschool children

J. Hallmayer, 2007, Current psychiatry reports.

Age at onset: important marker of genetic heterogeneity in Alzheimer's disease

R. Martins, J. Hallmayer, 2004, The Pharmacogenomics Journal.

Plasma oxytocin concentrations and OXTR polymorphisms predict social impairments in children with and without autism spectrum disorder

K. J. Parker, Antonio Y Hardan, Joseph P Garner, 2014, Proceedings of the National Academy of Sciences.

Insulin resistance and hippocampal volume in women at risk for Alzheimer's disease

A. Reiss, H. Kenna, N. Rasgon, 2011, Neurobiology of Aging.

Telomere length and cortisol reactivity in children of depressed mothers

Natalie L. Colich, O. Wolkowitz, Jue Lin, 2014, Molecular Psychiatry.

Brain health registry GenePool study: A novel approach to online genetics research

J. Yesavage, M. Weiner, R. O'Hara, 2021, Alzheimer's & dementia.

5-HTTLPR short allele, resilience, and successful aging in older adults.

C. Depp, D. Jeste, W. Thompson, 2012, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

Preparing the Next Generation of Academic Researchers During the Pandemic: Lessons from a National Mental Health Research Postdoctoral Fellowship

J. Hallmayer, N. Hantke, L. Anker, 2022, Academic Psychiatry.

ImmunoChip Study Implicates Antigen Presentation to T Cells in Narcolepsy

C. Gieger, P. Deloukas, C. Wijmenga, 2013, PLoS genetics.

Evidence that the butyryl-cholinesterase K variant can protect against late-onset Alzheimer's disease

R. Martins, D. Small, W. Brooks, 1999 .

Narcolepsy is strongly associated with the T-cell receptor alpha locus (vol 41, pg 708, 2009)

Christian Gieger, Thomas Meitinger, Emmanuel Mignot, 2014 .

COMT genotype, gender and cognition in community-dwelling, older adults

R. O'Hara, J. Hallmayer, Xiaoyan Lin, 2006, Neuroscience Letters.

Anomalous prefrontal-limbic activation and connectivity in youth at high-risk for bipolar disorder.

A. Reiss, K. Chang, A. Garrett, 2017, Journal of affective disorders.

Apolipoprotein E and obstructive sleep apnea: evaluating whether a candidate gene explains a linkage peak

S. Redline, R. Elston, E. Mignot, 2006, Genetic epidemiology.

Connectivity underlying emotion conflict regulation in older adults with 5-HTTLPR short allele: a preliminary investigation.

A. Etkin, R. O'Hara, J. Hallmayer, 2014, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

Healthy young women with serotonin transporter SS polymorphism show a pro-inflammatory bias under resting and stress conditions

Janice R. Kuo, Michael D. Edge, J. Gross, 2010, Brain, Behavior, and Immunity.

Serotonin transporter polymorphism predicts waking cortisol in young girls

I. Gotlib, J. Joormann, J. Hallmayer, 2009, Psychoneuroendocrinology.

Oxytocin receptor gene polymorphism (rs2254298) interacts with familial risk for psychopathology to predict symptoms of depression and anxiety in adolescent girls

K. J. Parker, Ian H. Gotlib, Christian E. Waugh, 2011, Psychoneuroendocrinology.

Serotonin transporter polymorphism and stress: A view across the lifespan

R. O'Hara, J. Hallmayer, R. O’Hara, 2007, Current psychiatry reports.

The seasonal relationship between assault and homicide in England and Wales.

Kevin Judd, K. Judd, J. Hallmayer, 2008, Injury.

Brief Report: Effect of Maternal Age on Severity of Autism

L. Lotspeich, J. Hallmayer, J. Grether, 2007, Journal of autism and developmental disorders.

Can autism, language and coordination disorders be differentiated based on ability profiles?

J. Piek, J. Hallmayer, M. Dyck, 2007, European Child & Adolescent Psychiatry.

The Relationship Between Symptoms and Abilities in Autism

J. Piek, J. Hallmayer, M. Dyck, 2007 .

Association of interleukin‐1 polymorphisms with Alzheimer's disease in Australia

R. Martins, W. Brooks, R. Hedley, 2002, Annals of neurology.

Circadian clock gene polymorphisms and sleep-wake disturbance in Alzheimer disease.

Philippe Robert, Art Noda, Beatriz Hernandez, 2011, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

Incidental brain MRI findings in an autism twin study

A. Hardan, J. Hallmayer, Sue C. Cleveland, 2017, Autism research : official journal of the International Society for Autism Research.

Psychiatric genetics: What to expect

J. Hallmayer, 2004, Current psychiatry reports.

Sleep-wake disorders in Alzheimer’s disease: further genetic analyses in relation to objective sleep measures

J. Yesavage, L. Williams, A. Goldstein-Piekarski, 2019, International Psychogeriatrics.

18P — A susceptibility locus for affective and schizophrenic disorder?

W. Maier, B. Lerer, M. Ackenheil, 1996 .

Atypical neuroleptic medication and psychosis in adolescence

J. Hallmayer, 2004 .

Regional profile of polyamines in reversible cerebral ischemia of Mongolian gerbils.

W. Paschen, J. Hallmayer, G. Mies, 1987, Neurochemical pathology.

Relationship between putrescine content and density of ischemic cell damage in the brain of mongolian gerbils: effect of nimodipine and barbiturate

W. Paschen, J. Hallmayer, G. Röhn, 2004, Acta Neuropathologica.

Brain-derived neurotrophic factor val66met genotype and early life stress effects upon bipolar course.

Sheri L. Johnson, T. Ketter, J. Hallmayer, 2013, Journal of psychiatric research.

Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy

Chun Jimmie Ye, M. Perola, J. Pritchard, 2023, Nature communications.

Molecular Analysis andTestofLinkage between theFMR-IGene andInfantile AutisminMultiplex Families

L. Lotspeich, W. McMahon, J. Hallmayer, 1994 .

APOE-ε4 and APOE −491A polymorphisms in individuals with subjective memory loss

R. Martins, Hans Förstl, S. Laws, 2002, Molecular Psychiatry.

Common variants in P 2 RY 11 are associated with narcolepsy

C. Gieger, N. Risch, P. Kwok, 2010 .

Association of alleles carried at TNFA -850 and BAT1-22 with Alzheimer's disease

R. Martins, W. Brooks, G. Broe, 2008, Journal of Neuroinflammation.

A potential susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia

M. Rietschel, W. Maier, K. Kanyas, 1998 .

Integrated systems analysis reveals a molecular network underlying autism spectrum disorders

Zhihai Ma, Shuchun Zhao, A. Urban, 2014 .

Association between presenilin-1 Glu318Gly mutation and familial Alzheimer's disease in the Australian population

N. Relkin, R. Martins, W. Brooks, 2002, Molecular Psychiatry.

Relationship between lipid metabolism and plasma concentration of amyloid precursor protein and apolipoprotein E

R. Martins, K. Taddei, S. Gandy, 1999 .

Genetic heritability and shared environmental factors among twin pairs with autism.

C. Lajonchere, L. Lotspeich, N. Risch, 2011, Archives of General Psychiatry.

Integrated systems analysis reveals a molecular network underlying autism spectrum disorders

Zhihai Ma, Shuchun Zhao, A. Urban, 2014, Molecular Systems Biology.

Coming of age of genetic investigations in late-life mental health.

J. Hallmayer, R. O’Hara, 2014, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

Using iPS cells to investigate cardiac phenotypes in patients with Timothy Syndrome

R. Dolmetsch, Brian Hsueh, J. Hallmayer, 2011, Nature.

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy.

Fabian Grubert, T. Wieland, A. Urban, 2012, Human molecular genetics.

Healthy young women with serotonin transporter SS polymorphism show a pro-inflammatory bias under resting and stress conditions

Janice R. Kuo, Michael D. Edge, J. Gross, 2010, Brain, Behavior, and Immunity.

Oxytocin receptor gene polymorphism (rs2254298) interacts with familial risk for psychopathology to predict symptoms of depression and anxiety in adolescent girls

K. J. Parker, Christian E. Waugh, I. Gotlib, 2011, Psychoneuroendocrinology.

Prenatal and perinatal risk factors in a twin study of autism spectrum disorders.

C. Lajonchere, L. Lotspeich, S. Ozonoff, 2014, Journal of psychiatric research.

Repetitive transcranial magnetic stimulation over temporoparietal cortices in the treatment of refractory auditory hallucinations in patients with schizophrenia

J. Hallmayer, 2005, Current psychiatry reports.

O09 - The natural history of a microsatellite located in the HLA DQ region

E. Mignot, J. Hallmayer, A. Kimura, 1996 .

Twins with KBG Syndrome and Autism

L. Lotspeich, J. Hallmayer, Jennifer M. Phillips, 2009, Journal of autism and developmental disorders.

Serotonin transporter polymorphism is associated with increased apnea–hypopnea index in older adults

R. O'Hara, J. Hallmayer, C. Schröder, 2014, International journal of geriatric psychiatry.

Genome scan for autosomal genes conferring risk to schizophrenia in a German/ Israeli sample

M. Rietschel, W. Maier, B. Lerer, 1998 .

Polyamines in cerebral ischemia.

W. Paschen, R. Schmidt-Kastner, J. Hallmayer, 1988, Neurochemical pathology.