G. Nestadt

S. E. Stewart, R. Delorme, E. Cook, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Significant linkage to compulsive hoarding on chromosome 14 in families with obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study.

V. Willour, S. Rauch, D. Murphy, 2007, The American journal of psychiatry.

Brain regions associated with olfactory dysfunction in first episode psychosis patients

Jennifer M. Coughlin, A. Faria, A. Sawa, 2022, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Criteria for Diagnosing Reversible Dementia Caused by Depression: Validation by 2-year Follow-up

P. Rabins, G. Nestadt, A. Merchant, 1984, British Journal of Psychiatry.

Genetics of OCD

G. Nestadt, M. Grados, J. Samuels, 2010 .

Lifetime and 1-month prevalence rates of intermittent explosive disorder in a community sample.

E. Coccaro, G. Nestadt, J. Samuels, 2004, The Journal of clinical psychiatry.

Incidence of obsessive-compulsive disorder in adults.

G. Nestadt, W. Eaton, O. Bienvenu, 1998, The Journal of nervous and mental disease.

The relationship between the Five-Factor Model and latent DSM-IV personality disorder dimensions

P. Costa, F. Hsu, G. Nestadt, 2008 .

Epidemiology and genetics of obsessive-compulsive disorder

G. Nestadt, J. Samuels, 1997 .

The longitudinal relationship between personality disorder dimensions and global functioning in a community-residing population

P. Costa, F. Hsu, G. Nestadt, 2004, Psychological Medicine.

Epidemiology of personality disorders

G. Nestadt, O. Bienvenu, J. Samuels, 2001, Current psychiatry reports.

Prevalence of Treated and Untreated DSM‐III Schizophrenia Results of a Two‐Stage Community Survey

M. Folstein, J. Anthony, G. Nestadt, 1985, The Journal of nervous and mental disease.

Agoraphobia in adults: Incidence and longitudinal relationship with panic

M. Stein, G. Nestadt, W. Eaton, 2006, British Journal of Psychiatry.

Gender differences in genetic linkage and association on 11p15 in obsessive–compulsive disorder families

S. Rauch, D. Murphy, B. Greenberg, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Psychiatrists' ascertained treatment needs for mental disorders in a population-based sample.

G. Nestadt, W. Eaton, O. Bienvenu, 2007, Psychiatric services.

Obsessive-compulsive symptoms in schizophrenia

G. Nestadt, J. Samuels, A. Pulver, 1993, Schizophrenia Research.

Personality disorders and traits as predictors of incident cardiovascular disease: findings from the 23-year follow-up of the Baltimore ECA study.

K. Bandeen-Roche, G. Nestadt, W. Eaton, 2010, Psychosomatics.

Interobserver Reliability of a “Standardized Psychiatric Examination” (SPE) for Case Ascertainment (DSM‐III)

M. Folstein, P. McHugh, G. Nestadt, 1988, The Journal of nervous and mental disease.

An epidemiological study of histrionic personality disorder

M. Folstein, P. McHugh, G. Nestadt, 1990, Psychological Medicine.

Personality disorder traits as predictors of subsequent first-onset panic disorder or agoraphobia.

M. Stein, G. Nestadt, W. Eaton, 2009, Comprehensive psychiatry.

Personality Disorder in Later Life: A Community Study

P. Rabins, P. McHugh, G. Nestadt, 1994, British Journal of Psychiatry.

Replication study supports evidence for linkage to 9p24 in obsessive-compulsive disorder.

V. Willour, Y. Shugart, R. Hoehn-Saric, 2004, American journal of human genetics.

A family study of obsessive compulsive disorder

R. Hoehn-Saric, G. Nestadt, O. Bienvenu, 2001 .

Self-reported executive function and hoarding in adults with obsessive-compulsive disorder.

D. Murphy, B. Greenberg, A. Fyer, 2018, Comprehensive psychiatry.

Rare plus common SERT variants in obsessive-compulsive disorder

V. Willour, D. Murphy, Y. Shugart, 2007, Molecular Psychiatry.

Cross-cultural differences in the perception and understanding of obsessive-compulsive disorder in East Asian and Western cultures

G. Nestadt, J. Samuels, L. Doerfler, 2018 .

Comprehensive family‐based association study of the glutamate transporter gene SLC1A1 in obsessive‐compulsive disorder

S. Rauch, B. Greenberg, A. Fyer, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

SEASON OF BIRTH IN OBSESSIVE‐COMPULSIVE DISORDER

G. Nestadt, T. Lan, P. Chou, 2014, Depression and anxiety.

Is obsessive–compulsive disorder an anxiety disorder, and what, if any, are spectrum conditions? A family study perspective

S. Rauch, D. Murphy, B. Greenberg, 2011, Psychological Medicine.

Evidence for potential relationship between SLC1A1 and a putative genetic linkage region on chromosome 14q to obsessive‐compulsive disorder with compulsive hoarding

S. Rauch, D. Murphy, B. Greenberg, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Familiality of Factor Analysis-Derived YBOCS Dimensions in OCD-Affected Sibling Pairs from the OCD Collaborative Genetics Study

Benjamin D. Greenberg, Ying Wang, Gregor Hasler, 2007, Biological Psychiatry.

Overview of genetics and obsessive–compulsive disorder

H. Nicolini, J. Kennedy, G. Nestadt, 2009, Psychiatry Research.

Genetic association of FKBP5 and CRHR1 with cortisol response to acute psychosocial stress in healthy adults

Pamela B. Mahon, J. Potash, P. Zandi, 2013, Psychopharmacology.

An indirect test of the new mutation hypothesis associating advanced paternal age with the etiology of schizophrenia

J. McGrath, G. Nestadt, A. Pulver, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12

R. Murray, H. Pétursson, D. Collier, 1998, Schizophrenia Research.

The serotonin transporter gene polymorphism (SLC6A4) and risk for psychiatric morbidity and comorbidity in the Baltimore ECA follow-up study.

G. Nestadt, W. Eaton, J. Samuels, 2020, Comprehensive psychiatry.

Health and mental health problems of homeless men and women in Baltimore.

R M Royall, R. Royall, G. Nestadt, 1989, JAMA.

Obsessive–compulsive disorder: subclassification based on co-morbidity

S. Rauch, D. Murphy, B. Greenberg, 2008, Psychological Medicine.

Genome-wide association study of multiplex schizophrenia pedigrees.

Jianxin Shi, Stephan Ripke, Pablo V Gejman, 2012, The American journal of psychiatry.

Meta-analysis of 32 genome-wide linkage studies of schizophrenia

E M Wijsman, G Kalsi, T Sigmundsson, 2009, Molecular Psychiatry.

Age at first birth in women is genetically associated with increased risk of schizophrenia

Hoffmann, Hartmann, Roussos, 2017, Scientific Reports.

Genetics of obsessive-compulsive disorder.

G. Nestadt, M. Grados, J. Samuels, 2010, The Psychiatric clinics of North America.

Clinical correlates of recurrent major depression in obsessive–compulsive disorder

P. Cannistraro, R. Hoehn-Saric, G. Nestadt, 2004, Depression and anxiety.

Relationship between personality disorder dimensions and verbal memory functioning in a community population

P. Costa, G. Nestadt, W. Eaton, 2012, Psychiatry Research.

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

C. Stefanis, A. Chakravarti, D. Housman, 1998, Nature Genetics.

Exclusion criteria of DSM-III. A study of co-occurrence of hierarchy-free syndromes.

L. George, G. Nestadt, C. Holzer, 1984, Archives of general psychiatry.

Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

Hunna J. Watson, Ryan L. Collins, Dan J Stein, 2019, bioRxiv.

Genome-wide association study identifies new locus associated with OCD

Dan J Stein, Ben D. Greenberg, M. S. Artigas, 2021, medRxiv.

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Wei Cheng, Jianxin Shi, Elvira Bramon, 2016, Nature Genetics.

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

R. Shprintzen, B. Morrow, M. Karayiorgou, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.

Dan J Stein, F. A. Schroeder, S. E. Stewart, 2014, Journal of the American Academy of Child and Adolescent Psychiatry.

Sex-specific involvement of the Notch–JAG pathway in social recognition

Jennifer M. Coughlin, A. Sawa, G. Nestadt, 2022, Translational Psychiatry.

Schizophrenia: a genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes.

J. Ott, D. Housman, S. Antonarakis, 1995, American journal of medical genetics.

Multicenter linkage study of schizophrenia loci on chromosome 22q

M. O’Donovan, W. Maier, J. Mallet, 2004, Molecular Psychiatry.

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Michael F. Green, Max W. Y. Lam, Catherine A. Sugar, 2022, Nature.

De Novo Variation in Bipolar Disorder

P. Zandi, M. Pirooznia, G. Nestadt, 2019, Molecular Psychiatry.

Linkage and association on 8p21.2‐p21.1 in schizophrenia

D. Avramopoulos, M. Fallin, G. Nestadt, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A polygenic resilience score moderates the genetic risk for schizophrenia

M. Pirinen, P. Donnelly, C. Spencer, 2019, Molecular Psychiatry.

No evidence for linkage between schizophrenia and markers at chromosome 15q13-14.

D. Housman, G. Nestadt, A. Pulver, 1999, American journal of medical genetics.

Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3.

D. Housman, S. Antonarakis, M. Karayiorgou, 1995, American journal of medical genetics.

Exome sequencing in obsessive–compulsive disorder reveals a burden of rare damaging coding variants

B. Greenberg, A. Fyer, Anthony W. Zoghbi, 2021, Nature Neuroscience.

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Benjamin A. Logsdon, Hae Kyung Im, Solveig K Sieberts, 2019, Nature Genetics.

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

John P. Rice, Robert M. Maier, C. Spencer, 2020, Biological Psychiatry.

Monoamine oxidase A regulates antisocial personality in whites with no history of physical abuse.

Yu-Jen Cheng, Paul Costa, Karen Bandeen-Roche, 2011, Comprehensive psychiatry.

Genome‐wide association study of schizophrenia in Ashkenazi Jews

Vladimir Vacic, Ingo Ruczinski, Mehdi Pirooznia, 2015, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia.

J. McGrath, D. Avramopoulos, M. Fallin, 2009, American journal of human genetics.

Implicates Neuregulin 3 in Schizophrenia

J. McGrath, D. Avramopoulos, M. Fallin, 2009 .

Genetic heterogeneity in schizophrenia II: conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q

J. McGrath, G. Nestadt, Y. Chiu, 2002, Molecular Psychiatry.

Multiple variants aggregate in the neuregulin signaling pathway in a subset of schizophrenia patients

P. Wong, J. McGrath, D. Avramopoulos, 2013, Translational Psychiatry.

Complement genes contribute sex-biased vulnerability in diverse illnesses

Simon C. Potter, Christopher W. Whelan, M. Pirinen, 2020, Nature.

Genome-wide Association Study of Pediatric Obsessive-Compulsive Traits: Shared Genetic Risk between Traits and Disorder

Dan J Stein, Ben D. Greenberg, R. Delorme, 2019, bioRxiv.

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

Denis C. Bauer, Annelot M. Dekker, Ashley R. Jones, 2017, Nature Communications.

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives.

D. Housman, R. Shprintzen, S. Antonarakis, 1994, The Journal of nervous and mental disease.

Follow-up of a report of a potential linkage for schizophrenia on chromosome 22q12-q13.1: Part 2.

D. Housman, S. Antonarakis, M. Karayiorgou, 1994, American journal of medical genetics.

The relationship of obsessive–compulsive disorder to possible spectrum disorders: results from a family study

R. Hoehn-Saric, G. Nestadt, O. Bienvenu, 2000, Biological Psychiatry.

The epidemiology of psychiatrist-ascertained depression and DSM-III depressive disorders Results from the Eastern Baltimore Mental Health Survey Clinical

M. Folstein, P. McHugh, C. Brown, 1992, Psychological Medicine.

Personality dimensions and criminal arrest.

P. Costa, G. Nestadt, W. Eaton, 2004, Comprehensive psychiatry.

Prevalence and correlates of personality disorders in a community sample.

P. Costa, G. Nestadt, W. Eaton, 2002, The British journal of psychiatry : the journal of mental science.

Psychiatric comorbidity in the Baltimore ECA follow-up study: the matrix approach

G. Nestadt, W. Eaton, O. Bienvenu, 2021, Social Psychiatry and Psychiatric Epidemiology.

Association between a serotonin transporter promoter polymorphism (5HTTLPR) and personality disorder traits in a community sample.

G. Nestadt, W. Eaton, O. Bienvenu, 2011, Journal of psychiatric research.

Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD

B. Greenberg, A. Fyer, J. Knowles, 2017, European Neuropsychopharmacology.

Stage II follow-up on a linkage scan for bipolar disorder in the Ashkenazim provides suggestive evidence for chromosome 12p and the GRIN2B gene

J. McGrath, D. Avramopoulos, M. Fallin, 2007, Genetics in Medicine.

Specialty knowledge and competency standards for pharmacotherapy for adult obsessive-compulsive disorder

D. Stein, K. Phillips, E. Storch, 2021, Psychiatry Research.

Genetics of perinatal obsessive–compulsive disorder

G. Nestadt, J. Samuels, L. Standeven, 2020 .

B. Greenberg, J. Knowles, Y. Shugart, 2019, Journal of child and adolescent psychopharmacology.

Genetics of obsessive-compulsive disorder

G. Nestadt, J. Samuels, B. Viswanath, 2019, Indian journal of psychiatry.

Examination of the Shared Genetic Basis of Anorexia Nervosa and Obsessive-Compulsive Disorder

G. Breen, M. Kas, J. Knowles, 2017, bioRxiv.

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

S. E. Stewart, C. Sabatti, N. Freimer, 2015, The American journal of psychiatry.

Significant linkage to compulsive hoarding on chromosome 14 in families with obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study.

V. Willour, S. Rauch, D. Murphy, 2007, The American journal of psychiatry.

Identification of Sequence Variants and Analysis of the Role of the Catechol-O-Methyl-Transferase Gene in Schizophrenia Susceptibility

D. Housman, S. Antonarakis, M. Karayiorgou, 1998, Biological Psychiatry.

Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD)

D. Murphy, B. Greenberg, A. Fyer, 2017, Front. Mol. Neurosci..

Familiality of novel factorial dimensions of schizophrenia.

J. McGrath, D. Avramopoulos, M. Fallin, 2009, Archives of general psychiatry.

No Major Schizophrenia Locus Detected on Chromosome 1q in a Large Multicenter Sample

M. Owen, M. O’Donovan, P. Holmans, 2002, Science.

No missense mutation of WKL1 in a subgroup of probands with schizophrenia

D. Stephan, G. Nestadt, J. Meyer, 2002, Molecular Psychiatry.

Screening for Psychosis in the General Population with a Self‐Report Interview

G. Nestadt, W. Eaton, J. Anthony, 1991, The Journal of nervous and mental disease.

Contributions of Olfactory and Neuropsychological Assessment to the Diagnosis of First-Episode Schizophrenia

A. Sawa, D. Schretlen, G. Nestadt, 2019, Neuropsychology.

Infection and Inflammation in Schizophrenia and Bipolar Disorder: A Genome Wide Study for Interactions with Genetic Variation

R. Yolken, I. Ruczinski, D. Avramopoulos, 2015, PloS one.

Homeobox genes in obsessive‐compulsive disorder

S. Rauch, B. Greenberg, A. Fyer, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Five latent factors underlying schizophrenia: analysis and relationship to illnesses in relatives.

J. McGrath, M. Fallin, G. Nestadt, 2004, Schizophrenia bulletin.

A multimodal study of a first episode psychosis cohort: potential markers of antipsychotic treatment resistance

Jennifer M. Coughlin, A. Faria, P. Barker, 2021, bioRxiv.

Effects of desipramine maintenance on cocaine self-administration by humans.

G D Pearlson, M W Fischman, R W Foltin, 1990, The Journal of pharmacology and experimental therapeutics.

Schizophrenia susceptibility and chromosome 6p24–22

J. Ott, D. Housman, S. Antonarakis, 1995, Nature Genetics.

Should OCD be classified as an anxiety disorder in DSM‐V?

Dan J Stein, S. Rauch, K. Phillips, 2010, Depression and anxiety.

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

R. Murray, D. Collier, M. Gill, 1996, American journal of medical genetics.

Linkage and sib-pair analysis reveal a potential schizophrenia susceptibility gene on chromosome 13q32:

A. Chakravarti, D. Housman, S. Antonarakis, 1996 .

The relationship of mental and behavioral disorders to all-cause mortality in a 27-year follow-up of 4 epidemiologic catchment area samples.

Kimberly B. Roth, A. Muñoz, R. Crum, 2013, American journal of epidemiology.

Population-based study of first onset and chronicity in major depressive disorder.

P. Zandi, G. Nestadt, W. Eaton, 2008, Archives of general psychiatry.

Normal personality traits and comorbidity among phobic, panic and major depressive disorders

P. Costa, G. Nestadt, W. Eaton, 2001, Psychiatry Research.

Comparison of the lay Diagnostic Interview Schedule and a standardized psychiatric diagnosis. Experience in eastern Baltimore.

M. Folstein, J. Anthony, G. Nestadt, 1985, Archives of general psychiatry.

Whole genome association analysis of treatment response in obsessive-compulsive disorder

D. Murphy, B. Greenberg, A. Fyer, 2015, Molecular Psychiatry.

Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus.

D. Housman, S. Antonarakis, M. Karayiorgou, 1996, Cold Spring Harbor symposia on quantitative biology.

Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21.

D. Housman, S. Antonarakis, K. Chandy, 1999, American journal of medical genetics.

An investigation of doubt in obsessive-compulsive disorder.

S. E. Stewart, D. Murphy, B. Greenberg, 2017, Comprehensive psychiatry.

Hoarding in Children and Adolescents with Obsessive-Compulsive Disorder.

S. E. Stewart, D. Murphy, B. Greenberg, 2014, Journal of obsessive-compulsive and related disorders.

Prevalence and correlates of hoarding behavior in a community-based sample.

G. Nestadt, W. Eaton, O. Bienvenu, 2008, Behaviour research and therapy.

Neuroimaging signature associated with symptom exacerbation in early-stage psychosis

Jennifer M. Coughlin, A. Faria, A. Sawa, 2021 .

Assessment of DSM-III personality structure in a general-population survey.

M. Folstein, P. McHugh, G. Nestadt, 1994, Comprehensive psychiatry.

Further development of YBOCS dimensions in the OCD Collaborative Genetics Study: Symptoms vs. categories

V. Willour, S. Rauch, D. Murphy, 2008, Psychiatry Research.

The Johns Hopkins University Collaborative Schizophrenia Study: an epidemiologic-genetic approach to test the heterogeneity hypothesis and identify schizophrenia susceptibility genes.

D. Housman, S. Antonarakis, M. Karayiorgou, 1996, Cold Spring Harbor symposia on quantitative biology.

Assessing Brain Metabolism With 7-T Proton Magnetic Resonance Spectroscopy in Patients With First-Episode Psychosis

Jennifer M. Coughlin, P. Barker, A. Sawa, 2019, JAMA psychiatry.

Association of SLC6A4 variants with obsessive-compulsive disorder in a large multi-center US family study

S. Rauch, D. Murphy, B. Greenberg, 2009, Molecular Psychiatry.

Trichotillomania comorbidity in a sample enriched for familial obsessive-compulsive disorder.

S. Rauch, B. Greenberg, J. Knowles, 2019, Comprehensive psychiatry.

Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Kristen K. Dang, D. A. Lewis, C. Spencer, 2019, Nature Genetics.

An investigation of COVID-19 related worry in a United States population sample

G. Nestadt, O. Bienvenu, J. Samuels, 2021, Journal of Psychiatric Research.

Contamination-related behaviors, obsessions, and compulsions during the COVID-19 pandemic in a United States population sample

G. Nestadt, O. Bienvenu, J. Samuels, 2021, Journal of Psychiatric Research.

Identification and Functional Studies of Regulatory Variants Responsible for the Association of NRG3 with a Delusion Phenotype in Schizophrenia

M. Taub, A. Sawa, J. McGrath, 2015, Molecular Neuropsychiatry.

Is Persistent Motor or Vocal Tic Disorder a Milder Form of Tourette Syndrome?

B. Greenberg, J. Knowles, J. McCracken, 2021, Movement disorders : official journal of the Movement Disorder Society.

The familial phenotype of obsessive-compulsive disorder in relation to tic disorders: the Hopkins OCD family study

R. Hoehn-Saric, G. Nestadt, O. Bienvenu, 2001, Biological Psychiatry.

The OCD collaborative genetics study: Methods and sample description

V. Willour, S. Rauch, B. Greenberg, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Social and Communication Difficulties and Obsessive-Compulsive Disorder

R. Landa, R. Hoehn-Saric, G. Nestadt, 2008, Psychopathology.

Complex segregation analysis provides compelling evidence for a major gene underlying obsessive-compulsive disorder and for heterogeneity by sex.

T. Beaty, Y. Shugart, R. Hoehn-Saric, 2000, American journal of human genetics.

Association of obsessive‐compulsive disorder and pathological gambling with Huntington's disease in an Italian pedigree: possible association with Huntington's disease mutation

G. Nestadt, M. Morris, R. Mennella, 1998, Acta psychiatrica Scandinavica.

Complement genes contribute sex-biased vulnerability in diverse disorders

Christopher W. Whelan, M. Pirinen, C. Spencer, 2020, Nature.

A transdiagnostic perspective of constructs underlying obsessive-compulsive and related disorders: An international Delphi consensus study

Dan J Stein, Leonardo Franklin Fontenelle, S. Rauch, 2020, The Australian and New Zealand journal of psychiatry.

DSM-III compulsive personality disorder: an epidemiological survey

M. Folstein, P. McHugh, G. Nestadt, 1991, Psychological Medicine.

DSM-III personality disorders in the community.

M. Folstein, P. McHugh, G. Nestadt, 1994, The American journal of psychiatry.

Parental bonding and hoarding in obsessive-compulsive disorder.

S. E. Stewart, D. Murphy, B. Greenberg, 2017, Comprehensive psychiatry.

The relationship between the five-factor model and latent Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition personality disorder dimensions.

Fang-Chi Hsu, William W Eaton, P. Costa, 2008, Comprehensive psychiatry.

C9orf72 hexanucleotide repeat expansions are not a common cause of obsessive-compulsive disorder

B. Traynor, G. Nestadt, B. Maher, 2017, Journal of the Neurological Sciences.

Prevalence and correlates of lifetime suicide attempt in obsessive-compulsive disorder with major depression.

S. E. Stewart, B. Greenberg, A. Fyer, 2023, Journal of psychiatric research.

Obsessive-Compulsive Disorder Issues Pertinent to Women

G. Nestadt, 2008, Women's health.

Proton magnetic resonance spectroscopy in obsessive-compulsive disorder: A pilot investigation comparing treatment responders and non-responders

Mari A. Smith, P. Barker, M. Schlund, 2007, Psychiatry Research: Neuroimaging.

Ethnicity, Education, and the Temporal Stability of Personality Traits In the East Baltimore Epidemiologic Catchment Area Study.

P. Costa, R. McCrae, A. Terracciano, 2008, Journal of research in personality.

Personality and cognitive decline in the Baltimore Epidemiologic Catchment Area follow-up study.

Jeanine M. Parisi, P. Costa, G. Nestadt, 2014, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

Eastern Baltimore Mental Health Survey Clinical Reappraisal

M. Folstein, J. Anthony, G. Nestadt, 2012 .

Sapap3 and pathological grooming in humans: Results from the OCD collaborative genetics study

V. Willour, S. Rauch, D. Murphy, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The relationship of pathologic skin picking to obsessive-compulsive disorder.

R. Hoehn-Saric, G. Nestadt, O. Bienvenu, 2001, The Journal of nervous and mental disease.

Face processing of social cognition in patients with first episode psychosis: Its deficits and association with the right subcallosal anterior cingulate cortex

Jennifer M. Coughlin, A. Faria, J. Miyata, 2021, Schizophrenia Research.

University of Groningen Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder Eating Disorders Working Group of the Psychiatric Genomics Consortium

G. Breen, M. Kas, J. Knowles, 2018 .

Latent structure of the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition personality disorder criteria.

P. Costa, F. Hsu, G. Nestadt, 2006, Comprehensive psychiatry.

General personality dimensions, impairment and treatment response in obsessive-compulsive disorder.

S. E. Stewart, D. Murphy, B. Greenberg, 2019, Personality and mental health.

Personality disorders and normal personality dimensions in obsessive-compulsive disorder

P. Costa, R. Hoehn-Saric, G. Nestadt, 2000, British Journal of Psychiatry.

ADHD and executive functioning deficits in OCD youths who hoard.

S. E. Stewart, D. Murphy, B. Greenberg, 2016, Journal of psychiatric research.

The identification of OCD-related subgroups based on comorbidity

A. Addington, R. Hoehn-Saric, G. Nestadt, 2003, Biological Psychiatry.

The relationship between obsessive–compulsive disorder and anxiety and affective disorders: results from the Johns Hopkins OCD Family Study

R. Hoehn-Saric, G. Nestadt, O. Bienvenu, 2001, Psychological Medicine.

Hoarding in obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study.

V. Willour, S. Rauch, D. Murphy, 2007, Behaviour research and therapy.

Sex-specific clinical correlates of hoarding in obsessive-compulsive disorder.

S. Rauch, D. Murphy, B. Greenberg, 2008, Behaviour research and therapy.

Dementia: case ascertainment in a community survey.

M. Folstein, J. Anthony, S. Bassett, 1991, Journal of gerontology.

Dependent personality, separation anxiety disorder and other anxiety disorders in OCD.

S. Rauch, D. Murphy, B. Greenberg, 2016, Personality and mental health.

Five-factor model personality traits as predictors of incident coronary heart disease in the community: a 10.5-year cohort study based on the Baltimore epidemiologic catchment area follow-up study.

G. Nestadt, W. Eaton, O. Bienvenu, 2014, Psychosomatics.

Hoarding in obsessive compulsive disorder: results from a case-control study.

R. Hoehn-Saric, G. Nestadt, O. Bienvenu, 2002, Behaviour research and therapy.

Longitudinal changes in brain metabolites in healthy controls and patients with first episode psychosis: a 7-Tesla MRS study

D. Geman, L. Younes, A. Sawa, 2023, Molecular Psychiatry.

Factor analysis of the Yale–Brown Obsessive Compulsive Scale in a family study of obsessive–compulsive disorder

Y. Shugart, R. Hoehn-Saric, G. Nestadt, 2007, Depression and anxiety.

Familial aggregation of panic disturbances in Parkinson's disease.

P. Rabins, L. Marsh, G. Nestadt, 2011, The Journal of neuropsychiatry and clinical neurosciences.

The General Health Questionnaire by Interview: Performance in Relation to Recent Use of Health Services

D. Ford, G. Nestadt, J. Anthony, 1989, Medical care.

Cognitive Impairment in the Non-elderly: Validation of a New Tool to Assess Intellectual Disability in Community and Clinical Populations

P. Rabins, G. Nestadt, W. Eaton, 2007 .

Peripartum complications associated with obsessive compulsive disorder exacerbation during pregnancy.

G. Nestadt, J. Samuels, C. Holingue, 2021, Journal of obsessive-compulsive and related disorders.

The association between parental bonding and obsessive compulsive disorder in offspring at high familial risk.

Y. Shugart, G. Nestadt, O. Bienvenu, 2008, Journal of affective disorders.

Influences of parenting on normal personality traits

P. Costa, G. Nestadt, W. Eaton, 2002, Psychiatry Research.

Separation anxiety disorder in OCD

S. Rauch, D. Murphy, B. Greenberg, 2011, Depression and anxiety.

Adult antisocial personality traits are associated with experiences of low parental care and maternal overprotection

P. Costa, G. Nestadt, W. Eaton, 2002, Acta psychiatrica Scandinavica.

Longitudinal changes in brain metabolites in healthy subjects and patients with first episode psychosis (FEP): a 7-Tesla MRS study

Jennifer M. Coughlin, D. Geman, L. Younes, 2020, bioRxiv.

The detection of mental disorders in the community using a 20‐item interview version of the General Health Questionnaire

G. Nestadt, J. Samuels, J. Anthony, 1994, Acta psychiatrica Scandinavica.

A family‐based association study of the glutamate transporter gene SLC1A1 in obsessive–compulsive disorder in 378 families

S. Rauch, B. Greenberg, A. Fyer, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Neuroimaging alterations and relapse in early-stage psychosis

Jennifer M. Coughlin, A. Faria, A. Sawa, 2021, bioRxiv.

Longitudinal relationships between personality disorder dimensions and depression in a community sample

G. Nestadt, W. Eaton, O. Bienvenu, 2018, Neurology, Psychiatry and Brain Research.

Concordance between personality disorder assessment methods

P. Costa, K. Bandeen-Roche, G. Nestadt, 2011, Psychological Medicine.

The stability of DSM personality disorders over twelve to eighteen years.

P. Costa, K. Bandeen-Roche, G. Nestadt, 2010, Journal of psychiatric research.

Demographic and clinical characteristics associated with treatment status in family members with obsessive‐compulsive disorder

V. Willour, S. Rauch, B. Greenberg, 2008, Depression and anxiety.

Obsessive–Compulsive Personality Disorder: A Review

E. Hollander, P. Costa, D. Shapiro, 2005 .

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Sara B. Linker, Evan Z. Macosko, Thomas G. Gilgenast, 2023, Cell genomics.

Partition Volume and Regional Binding Potentials of Serotonin Receptor and Transporter Ligands

A. Gjedde, D. Wong, P. Cumming, 2001 .

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.

John P. Rice, Simon C. Potter, Melissa J. Green, 2018, Cell.

Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.

Han Xu, Stephan Ripke, Chongzhi Zang, 2014, American journal of human genetics.

OBSESSIVE–COMPULSIVE DISORDER AND FEMALE REPRODUCTIVE CYCLE EVENTS: RESULTS FROM THE OCD AND REPRODUCTION COLLABORATIVE STUDY

D. Denys, G. Nestadt, Ying Wang, 2014, Depression and anxiety.

Biological Insights From 108 Schizophrenia-Associated Genetic Loci

C. Spencer, K. Davis, P. Visscher, 2014, Nature.

Clinical correlates and genetic linkage of social and communication difficulties in families with obsessive–compulsive disorder: Results from the OCD Collaborative Genetics Study

S. Rauch, D. Murphy, B. Greenberg, 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

OBSESSIVE–COMPULSIVE PERSONALITY DISORDER: EVIDENCE FOR TWO DIMENSIONS

S. Rauch, J. Knowles, Benjamin D. Greenberg, 2016, Depression and anxiety.

Schizophrenia genetic variants are not associated with intelligence

A F Terwisscha van Scheltinga, S C Bakker, N E M van Haren, 2013, Psychological Medicine.

A family study of obsessive-compulsive disorder.

R. Hoehn-Saric, G. Nestadt, O. Bienvenu, 1992, Archives of general psychiatry.

Utility of the Leyton Obsessional Inventory to distinguish OCD and OCPD

G. Nestadt, O. Bienvenu, M. Riddle, 2007, Depression and anxiety.

Validating a dimension of doubt in decision-making: A proposed endophenotype for obsessive-compulsive disorder

M. Shuler, V. Chib, A. Bakker, 2019, PloS one.

Association of SLC1A1 gene polymorphism with obsessive compulsive disorder in a sample from southern India.

G. Nestadt, S. Ganesh, Y. Reddy, 2020, Experimental and clinical psychopharmacology.

A screen of SLC1A1 for OCD‐related alleles

S. Rauch, D. Murphy, B. Greenberg, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

N. Wray, H. Stefánsson, D. Rujescu, 2019, Nature Genetics.

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

P. Visscher, J. Sebat, D. Malhotra, 2016, Nature Genetics.

A family‐based association study of the glutamate transporter gene SLC1A1 in obsessive–compulsive disorder in 378 families

A. Fyer, Benjamin D. Greenberg, G. Nestadt, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A family study of obsessive-compulsive disorder.

R. Hoehn-Saric, G. Nestadt, O. Bienvenu, 1992, Archives of general psychiatry.

Parental bonding and hoarding in obsessive-compulsive disorder.

S. E. Stewart, D. Murphy, B. Greenberg, 2017, Comprehensive psychiatry.

OBSESSIVE–COMPULSIVE DISORDER AND FEMALE REPRODUCTIVE CYCLE EVENTS: RESULTS FROM THE OCD AND REPRODUCTION COLLABORATIVE STUDY

D. Denys, G. Nestadt, Ying Wang, 2014, Depression and anxiety.

Obsessive-compulsive disorder: defining the phenotype.

G. Nestadt, O. Bienvenu, M. Riddle, 2002, The Journal of clinical psychiatry.

Schizophrenia genetic variants are not associated with intelligence

P. Donnelly, P. Visscher, H. Stefánsson, 2013, Psychological Medicine.

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia.

J. McGrath, D. Avramopoulos, M. Fallin, 2009, American journal of human genetics.

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts.

John P. Rice, Warren W. Kretzschmar, Robert M. Maier, 2021, Biological psychiatry.

Use of Selective Serotonin Reuptake Inhibitors and Risks of Stroke in Patients with Obsessive Compulsive Disorder: A Population-Based Study

G. Nestadt, T. Lan, Min-Wei Huang, 2016, PloS one.

Monoamine oxidase A regulates antisocial personality in whites with no history of physical abuse.

V. Willour, P. Zandi, P. Costa, 2011, Comprehensive psychiatry.

Age at first birth in women is genetically associated with increased risk of schizophrenia

Eric, H. Stefánsson, S. Steinberg, 2020 .

e-Publications@Marquette e-Publications@Marquette

Leonardo Franklin Fontenelle, D. Stein, C. Soriano-Mas, 2022 .

Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder

E. Zeggini, D. Rujescu, S. Cichon, 2020 .

Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder

Dan J Stein, S. E. Stewart, R. Delorme, 2021, Translational Psychiatry.

Genetic association of FKBP5 and CRHR1 with cortisol response to acute psychosocial stress in healthy adults

Pamela B. Mahon, J. Potash, P. Zandi, 2012, Psychopharmacology.

Clinical correlates and genetic linkage of social and communication difficulties in families with obsessive–compulsive disorder: Results from the OCD Collaborative Genetics Study

S. E. Stewart, S. Rauch, D. Murphy, 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Gender differences in genetic linkage and association on 11p15 in obsessive–compulsive disorder families

Obsessions and compulsions in the community

M. Folstein, P. McHugh, G. Nestadt, 1994, Acta psychiatrica Scandinavica.

DSM-ffl Personality Disorders in the Community

M. Folstein, P. McHugh, G. Nestadt, 1994 .

The relationship of mental and behavioral disorders to all-cause mortality in a 27-year follow-up of 4 epidemiologic catchment area samples.

A. Muñoz, R. Crum, J. Anthony, 2013, American journal of epidemiology.

Genome-wide association study identiﬁes new locus associated with OCD

Laurent F. Thomas, Jason A. Elias, Zachary F. Gerring, 2022 .

Analysis of shared heritability in common disorders of the brain

Janice M. Fullerton, Thomas W. Mühleisen, C. Sudlow, 2018, Science.

Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia