J. Roos

发表

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia

S. Levy, I. Ionita-Laza, Bin Xu, 2012, Nature Genetics.

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

Chiara Sabatti, Andrew Collins, Proton Rahman, 2006, Nature Genetics.

Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans

Gonçalo R Abecasis, Maria Karayiorgou, G. Abecasis, 2009, Proceedings of the National Academy of Sciences.

Loss of function variants contribute to schizophrenia risk and point to SETD 1 A as a candidate susceptibility gene

I. Ionita-Laza, Bin Xu, M. Karayiorgou, 2015 .

Testing the effectiveness of existing psycho-educational material (The Alliance Programme) for patients suffering from schizophrenia in the South African context.

M. Snyman, J. Roos, J. M. Pooe, 2010, African journal of psychiatry.

Loss-of-Function Variants in Schizophrenia Risk and SETD1A as a Candidate Susceptibility Gene

I. Ionita-Laza, Bin Xu, M. Karayiorgou, 2014, Neuron.

LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells

D. Geschwind, D. Rujescu, P. Muglia, 2007, Molecular Psychiatry.

Family history identifies sporadic schizoaffective disorder as a subtype for genetic studies

M. Karayiorgou, J. Roos, Nicolaas J van der Merwe, 2020, The South African journal of psychiatry : SAJP : the journal of the Society of Psychiatrists of South Africa.

Prevalence and clinical characteristics of obsessive-compulsive disorder and obsessive compulsive symptoms in Afrikaner schizophrenia and schizoaffective disorder patients.

M. Karayiorgou, J. Roos, B. Nel, 2008, African journal of psychiatry.

Multiple affected Afrikaner families in a schizophrenia genetic study : environmental risk factors in interaction with genotypes : original article

M. Karayiorgou, J. Roos, H. Pretorius, 2004 .

A comparison study of early non-psychotic deviant behavior in Afrikaner and US patients with schizophrenia or schizoaffective disorder

M. Karayiorgou, C. Sobin, J. Roos, 2003, Psychiatry Research.

Medical students on the value of role models for developing ‘soft skills’ - “That’s the way you do it”

C. Kruger, J. Roos, C. W. V. Staden, 2006 .

Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging.

E. Bertini, M. Karayiorgou, S. Lalani, 2019, American journal of human genetics.

Exome sequencing supports a de novo mutational paradigm for schizophrenia

S. Levy, Bin Xu, M. Karayiorgou, 2011, Nature Genetics.

Clinical characteristics and premorbid variables in childhood-onset schizophrenia: a descriptive study of twelve cases from a schizophrenia founder population.

J. Roos, A. Ladikos, J. L. Roos, 2009, African journal of psychiatry.

Weskoppies Hospital, founded 1892--the early years.

J. Roos, C. Plug, 1992, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Personality traits, brief recurrent depression and attempted suicide.

J. Roos, W. Bodemer, H. Pretorius, 1994, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

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

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

Strong association of de novo copy number mutations with sporadic schizophrenia

Joseph A. Gogos, Shawn Levy, Maria Karayiorgou, 2008, Nature Genetics.

Fine Mapping on Chromosome 13q32–34 and Brain Expression Analysis Implicates MYO16 in Schizophrenia

G. Abecasis, Bin Xu, M. Karayiorgou, 2014, Neuropsychopharmacology.

Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autism

Vladimir Makarov, J. Buxbaum, I. Ionita-Laza, 2013, Proceedings of the National Academy of Sciences.

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

Ellen M Wijsman, Christina Sobin, Maria Karayiorgou, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Advancing paternal age at birth is associated with poorer social functioning earlier and later in life of schizophrenia patients in a founder population

J. Roos, A. M. D. Plessis, R. Ehlers, 2016, Psychiatry Research.

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

D. Geschwind, D. Rujescu, P. Muglia, 2007, Molecular Psychiatry.

Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1.

Gonçalo R Abecasis, Maria Karayiorgou, Kimberly F Doheny, 2004, American journal of human genetics.

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

G. Abecasis, J. Rapoport, S. Heath, 2002, Proceedings of the National Academy of Sciences of the United States of America.

A Retrospective Review of 1018 Suicide Cases From the Capital City of South Africa for the Period 1997–2000

G. Saayman, J. Roos, R. Blumenthal, 2004, The American journal of forensic medicine and pathology.

Training undergraduate medical students in 'soft skills' - a qualitative research project at the University of Pretoria : guest editorial

C. Kruger, J. Roos, C. W. V. Staden, 2006 .

Psychiatric and Other Contributing Factors in Homicide-Suicide Cases, from Northern Gauteng, South Africa Over a Six-Year Period

J. Roos, J. M. Pooe, C. Kotzé, 2018 .

Nogo Receptor 1 (RTN4R) as a Candidate Gene for Schizophrenia: Analysis Using Human and Mouse Genetic Approaches

G. Abecasis, A. Woodroffe, M. Karayiorgou, 2007, PloS one.

Phenotypic characterization and genealogical tracing in an Afrikaner schizophrenia database

G. Abecasis, M. Karayiorgou, S. L. Lundy, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Extended intermarker linkage disequilibrium in the Afrikaners.

E. Wijsman, M. Karayiorgou, J. Gogos, 2002, Genome research.

Can we close the barn door before the horses get out? A case study of high genetic loading and subsequent development of psychosis.

J. Roos, A. Ladikos, M. Lombard, 2011, African journal of psychiatry.

Genetics of schizophrenia: communicating scientific findings in the clinical setting.

J. Roos, 2011, African journal of psychiatry.

The perceptions of adult psychiatric inpatients with major depressive disorder towards occupational therapy activity-based groups

J. Roos, Enos M Ramano, M. de Beer, 2021, The South African journal of psychiatry : SAJP : the journal of the Society of Psychiatrists of South Africa.

Psychoneuroimmunology: from philosophy, intuition, and folklore to a recognized science

M. Viljoen, J. Roos, W. Bodemer, 2003 .

Profile of mortality of patients admitted to Weskoppies Psychiatric Hospital in South Africa over a 5-year period (2001-2005).

P. Rheeder, J. Roos, N. Khamker, 2010, African journal of psychiatry.

Exome sequencing supports a de novo mutational paradigm for schizophrenia

S. Levy, Bin Xu, M. Karayiorgou, 2011, Nature Genetics.

Early non-psychotic deviant behaviour as an endophenotypic marker in bipolar disorder, schizo-affective disorder and schizophrenia

M. Karayiorgou, J. Roos, J. Levin, 2005 .

The neurobiological basis of fear: a concise review

M. Viljoen, J. Roos, A. Panzer, 2007 .

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

D. Geschwind, D. Rujescu, P. Muglia, 2007, Molecular Psychiatry.

Methodological limitations to a study on interpersonal therapy

C. Kruger, J. Roos, M. Bohmer, 2013 .

Assessment of the frequency of the 22q11 deletion in Afrikaner schizophrenic patients

M. Karayiorgou, J. Roos, H. Pretorius, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans

G. Abecasis, A. Woodroffe, Bin Xu, 2009, Proceedings of the National Academy of Sciences.