Overview of studies implicating common alleles, structural variants or rare variants of CNTNAP2 in psychiatric disorders.

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

Gregor, A.
Albrecht, B.
Bader, I.
Bijlsma, E.
Ekici, A.
Engels, H.
Hackmann, K.
Horn, D.
Hoyer, J.
Klapecki, J.
Kohlhase, J.
Maystadt, I.
Nagl, S.
Prott, E.
Tinschert, S.
Ullmann, R.
Wohlleber, E.
Woods, G.
Reis, A.
Rauch, A.
Zweier, C.

January 2011

BACKGROUND: Heterozygous copy-number and missense variants in CNTNAP2 and NRXN1 have repeatedly been...

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

Friedman, J. I.
Vrijenhoek, T.
Markx, S.
Janssen, I. M.
Van der Vliet, W. A.
Faas, B. H. W.
Knoers, N. V.
Cahn, W.
Kahn, R. S.
Edelmann, L.
Davis, K. L.
Silverman, J. M.
Brunner, H. G.
Van Kessel, A. Geurts
Wijmenga, C.
Ophoff, R. A.
Veltman, J. A.

March 2008

A homozygous mutation of the CNTNAP2 gene has been associated with a syndrome of focal epilepsy, men...

Recurrent CNVs disrupt three candidate genes in schizophrenia patients

Vrijenhoek, Terry
Buizer-Voskamp, Jacobine E
van der Stelt, Inge
Strengman, Eric
Genetic Risk and Outcome in Psychosis (GROUP) Consortium
Sabatti, Chiara
Geurts van Kessel, Ad
Brunner, Han G
Ophoff, Roel A
Veltman, Joris A

October 2008

Schizophrenia is a severe psychiatric disease with complex etiology, affecting approximately 1% of t...

Common SNPs in CNTNAP2 previously reported to be associated in psychiatric diseases, and their evidence for association in PGC datasets.

Claudio Toma (381011)
Kerrie D. Pierce (6157751)
Alex D. Shaw (540155)
Anna Heath (540156)
Philip B. Mitchell (423708)
Peter R. Schofield (123807)
Janice M. Fullerton (320844)

January 2019

Common SNPs in CNTNAP2 previously reported to be associated in psychiatric diseases, and their evide...

Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders

Claudio Toma (381011)
Kerrie D. Pierce (6157751)
Alex D. Shaw (540155)
Anna Heath (540156)
Philip B. Mitchell (423708)
Peter R. Schofield (123807)
Janice M. Fullerton (320844)

January 2019

The contactin-associated protein-like 2 (CNTNAP2) gene is a member of the neurexin superfamily. CNTN...

Gene-based tests for association of CNTNAP2 across seven psychiatric disorders using GWAS summary statistics of the PGC data sets.

Claudio Toma (381011)
Kerrie D. Pierce (6157751)
Alex D. Shaw (540155)
Anna Heath (540156)
Philip B. Mitchell (423708)
Peter R. Schofield (123807)
Janice M. Fullerton (320844)

January 2019

Gene-based tests for association of CNTNAP2 across seven psychiatric disorders using GWAS summary st...

Shining a light on CNTNAP2:complex functions to complex disorders

Rodenas-Cuadrado, Pedro
Ho, Joses
Vernes, Sonja C

February 2014

The genetic basis of complex neurological disorders involving language are poorly understood, partly...

Shining a light on CNTNAP2: Complex functions to complex disorders

Rodenas-Cuadrado, P.
Ho, J.
Vernes, S.

January 2014

The genetic basis of complex neurological disorders involving language are poorly understood, partly...

Overview of heterozygous CNVs spanning the CNTNAP2 gene across several diseases.

Claudio Toma (381011)
Kerrie D. Pierce (6157751)
Alex D. Shaw (540155)
Anna Heath (540156)
Philip B. Mitchell (423708)
Peter R. Schofield (123807)
Janice M. Fullerton (320844)

January 2019

Abbreviations: ID (Intellectual disability), ASD (autism spectrum disorder), SCZ (schizophrenia), BD...

Genome-wide association analyses on complex diseases: from single-nucleotide polymorphism to copy numbervariation

Wong, Hoi-man, Emily.
黃凱敏.

January 2013

Complex diseases, unlike Mendialian diseases, are often characterized by genetic heterogeneity and m...

What a psychiatrist needs to know about copy number variants

Kirov, George
Rees, Elliott
Walters, James Tynan Rhys

May 2015

Copy number variants (CNVs) are structural changes in chromosomes that result in deletions, duplicat...

Copy Number Variations and Psychiatric Disorders

Chao, Yu-Lin
Chien, Wei-Hsien
Liao, Hsiao-Mei
Fang, Jye-Siung
Chen, Chia-Hsiang

September 2009

AbstractCopy number variations (CNVs) are gains and losses of DMA segments in the human genome, and ...

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

Malhotra, Dheeraj
Sebat, Jonathan

March 2012

The genetic bases of neuropsychiatric disorders are beginning to yield to scientific inquiry. Genome...

Comprehensive survey of CNVs influencing gene expression in the human brain and its implications for pathophysiology

Mehta, D.
Iwamoto, K.
Ueda, J.
Bundo, M.
Adati, N.
Kojima, T.
Kato, T.

February 2014

Copy number variations (CNVs) contribute to neuropsychiatric diseases, which may be partly mediated ...

Recurrent CNVs disrupt three candidate genes in schizophrenia patients.

Vrijenhoek, T.
Buizer-Voskamp, J.E.
Stelt, I. van der
Strengman, E.
Sabatti, C.
Geurts van Kessel, A.H.M.
Brunner, H.G.
Ophoff, R.A.
Veltman, J.A.

January 2008

Contains fulltext : 71232.pdf (publisher's version ) (Closed access)Schizophrenia ...

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

Gregor, A.
Albrecht, B.
Bader, I.
Bijlsma, E.
Ekici, A.
Engels, H.
Hackmann, K.
Horn, D.
Hoyer, J.
Klapecki, J.
Kohlhase, J.
Maystadt, I.
Nagl, S.
Prott, E.
Tinschert, S.
Ullmann, R.
Wohlleber, E.
Woods, G.
Reis, A.
Rauch, A.
Zweier, C.

January 2011

BACKGROUND: Heterozygous copy-number and missense variants in CNTNAP2 and NRXN1 have repeatedly been...

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

Friedman, J. I.
Vrijenhoek, T.
Markx, S.
Janssen, I. M.
Van der Vliet, W. A.
Faas, B. H. W.
Knoers, N. V.
Cahn, W.
Kahn, R. S.
Edelmann, L.
Davis, K. L.
Silverman, J. M.
Brunner, H. G.
Van Kessel, A. Geurts
Wijmenga, C.
Ophoff, R. A.
Veltman, J. A.

March 2008

A homozygous mutation of the CNTNAP2 gene has been associated with a syndrome of focal epilepsy, men...

Recurrent CNVs disrupt three candidate genes in schizophrenia patients

Vrijenhoek, Terry
Buizer-Voskamp, Jacobine E
van der Stelt, Inge
Strengman, Eric
Genetic Risk and Outcome in Psychosis (GROUP) Consortium
Sabatti, Chiara
Geurts van Kessel, Ad
Brunner, Han G
Ophoff, Roel A
Veltman, Joris A

October 2008

Schizophrenia is a severe psychiatric disease with complex etiology, affecting approximately 1% of t...

Common SNPs in CNTNAP2 previously reported to be associated in psychiatric diseases, and their evidence for association in PGC datasets.

Claudio Toma (381011)
Kerrie D. Pierce (6157751)
Alex D. Shaw (540155)
Anna Heath (540156)
Philip B. Mitchell (423708)
Peter R. Schofield (123807)
Janice M. Fullerton (320844)

January 2019

Common SNPs in CNTNAP2 previously reported to be associated in psychiatric diseases, and their evide...

Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders

Claudio Toma (381011)
Kerrie D. Pierce (6157751)
Alex D. Shaw (540155)
Anna Heath (540156)
Philip B. Mitchell (423708)
Peter R. Schofield (123807)
Janice M. Fullerton (320844)

January 2019

The contactin-associated protein-like 2 (CNTNAP2) gene is a member of the neurexin superfamily. CNTN...

Gene-based tests for association of CNTNAP2 across seven psychiatric disorders using GWAS summary statistics of the PGC data sets.

Claudio Toma (381011)
Kerrie D. Pierce (6157751)
Alex D. Shaw (540155)
Anna Heath (540156)
Philip B. Mitchell (423708)
Peter R. Schofield (123807)
Janice M. Fullerton (320844)

January 2019

Gene-based tests for association of CNTNAP2 across seven psychiatric disorders using GWAS summary st...

Shining a light on CNTNAP2:complex functions to complex disorders

Rodenas-Cuadrado, Pedro
Ho, Joses
Vernes, Sonja C

February 2014

The genetic basis of complex neurological disorders involving language are poorly understood, partly...

Shining a light on CNTNAP2: Complex functions to complex disorders

Rodenas-Cuadrado, P.
Ho, J.
Vernes, S.

January 2014

The genetic basis of complex neurological disorders involving language are poorly understood, partly...

Overview of heterozygous CNVs spanning the CNTNAP2 gene across several diseases.

Claudio Toma (381011)
Kerrie D. Pierce (6157751)
Alex D. Shaw (540155)
Anna Heath (540156)
Philip B. Mitchell (423708)
Peter R. Schofield (123807)
Janice M. Fullerton (320844)

January 2019

Abbreviations: ID (Intellectual disability), ASD (autism spectrum disorder), SCZ (schizophrenia), BD...

Genome-wide association analyses on complex diseases: from single-nucleotide polymorphism to copy numbervariation

Wong, Hoi-man, Emily.
黃凱敏.

January 2013

Complex diseases, unlike Mendialian diseases, are often characterized by genetic heterogeneity and m...

What a psychiatrist needs to know about copy number variants

Kirov, George
Rees, Elliott
Walters, James Tynan Rhys

May 2015

Copy number variants (CNVs) are structural changes in chromosomes that result in deletions, duplicat...

Copy Number Variations and Psychiatric Disorders

Chao, Yu-Lin
Chien, Wei-Hsien
Liao, Hsiao-Mei
Fang, Jye-Siung
Chen, Chia-Hsiang

September 2009

AbstractCopy number variations (CNVs) are gains and losses of DMA segments in the human genome, and ...

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

Malhotra, Dheeraj
Sebat, Jonathan

March 2012

The genetic bases of neuropsychiatric disorders are beginning to yield to scientific inquiry. Genome...

Comprehensive survey of CNVs influencing gene expression in the human brain and its implications for pathophysiology

Mehta, D.
Iwamoto, K.
Ueda, J.
Bundo, M.
Adati, N.
Kojima, T.
Kato, T.

February 2014

Copy number variations (CNVs) contribute to neuropsychiatric diseases, which may be partly mediated ...

Recurrent CNVs disrupt three candidate genes in schizophrenia patients.

Vrijenhoek, T.
Buizer-Voskamp, J.E.
Stelt, I. van der
Strengman, E.
Sabatti, C.
Geurts van Kessel, A.H.M.
Brunner, H.G.
Ophoff, R.A.
Veltman, J.A.

January 2008

Contains fulltext : 71232.pdf (publisher's version ) (Closed access)Schizophrenia ...

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

Gregor, A.
Albrecht, B.
Bader, I.
Bijlsma, E.
Ekici, A.
Engels, H.
Hackmann, K.
Horn, D.
Hoyer, J.
Klapecki, J.
Kohlhase, J.
Maystadt, I.
Nagl, S.
Prott, E.
Tinschert, S.
Ullmann, R.
Wohlleber, E.
Woods, G.
Reis, A.
Rauch, A.
Zweier, C.

January 2011

BACKGROUND: Heterozygous copy-number and missense variants in CNTNAP2 and NRXN1 have repeatedly been...

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

Friedman, J. I.
Vrijenhoek, T.
Markx, S.
Janssen, I. M.
Van der Vliet, W. A.
Faas, B. H. W.
Knoers, N. V.
Cahn, W.
Kahn, R. S.
Edelmann, L.
Davis, K. L.
Silverman, J. M.
Brunner, H. G.
Van Kessel, A. Geurts
Wijmenga, C.
Ophoff, R. A.
Veltman, J. A.

March 2008

A homozygous mutation of the CNTNAP2 gene has been associated with a syndrome of focal epilepsy, men...

Recurrent CNVs disrupt three candidate genes in schizophrenia patients

Vrijenhoek, Terry
Buizer-Voskamp, Jacobine E
van der Stelt, Inge
Strengman, Eric
Genetic Risk and Outcome in Psychosis (GROUP) Consortium
Sabatti, Chiara
Geurts van Kessel, Ad
Brunner, Han G
Ophoff, Roel A
Veltman, Joris A

October 2008

Schizophrenia is a severe psychiatric disease with complex etiology, affecting approximately 1% of t...

Overview of studies implicating common alleles, structural variants or rare variants of <i>CNTNAP2</i> in psychiatric disorders.

Abstract

Extracted data

Overview of studies implicating common alleles, structural variants or rare variants of <i>CNTNAP2</i> in psychiatric disorders.

Abstract

Extracted data

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