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

A genome-wide investigation of SNPs and CNVs in schizophrenia.

NEED AC
GE D
WEALE ME
MAIA J
FENG S
HEINZEN EL
SHIANNA KV
YOON W
KASPERAVICI
TE D
M. GENNARELLI
STRITTMATTER WJ
BONVICINI C
ROSSI G
JAYATHILAKE K
COLA PA
MCEVOY JP
KEEFE RS
FISHER EM
ST JEAN PL
GIEGLING I
HARTMANN AM
MÖLLER HJ
RUPPERT A
FRASER G
CROMBIE C
MIDDLETON LT
ST CLAIR D
ROSES AD
MUGLIA P
FRANCKS C
RUJESCU D
MELTZER HY
GOLDSTEIN DB

January 2009

We report a genome-wide assessment of single nucleotide polymorphisms (SNPs) and copy number variant...

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

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

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

Vrijenhoek, Terry
Buizer-Voskamp, Jacobine E.
van der Stelt, Inge
Strengman, Eric
Sabatti, Chiara
van Kessel, Ad Geurts
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...

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...

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

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

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...

Defining the contribution of CNTNAP2 to autism susceptibility.

Srirangan Sampath
Shambu Bhat
Simone Gupta
Ashley O'Connor
Andrew B West
Dan E Arking
Aravinda Chakravarti

Multiple lines of genetic evidence suggest a role for CNTNAP2 in autism. To assess its population im...

Defining the Contribution of CNTNAP2 to Autism

Srirangan Sampath
Shambu Bhat
Simone Gupta
Andrew B. West
Dan E
Arking Aravinda Chakravarti

January 2013

Multiple lines of genetic evidence suggest a role for CNTNAP2 in autism. To assess its population im...

CNTNAP2 polymorphisms and structural brain connectivity: A diffusion-tensor imaging study

Clemm von Hohenberg, Christian
Wigand, Marlene C.
Kubicki, Marek R.
Leicht, Gregor
Giegling, Ina
Karch, Susanne
Hartmann, Annette M.
Konte, Bettina
Friedl, Marion
Ballinger, Thomas
Eckbo, Ryan
Bouix, Sylvain
Jäger, Lorenz
Shenton, Martha Elizabeth
Rujescu, Dan
Mulert, Christoph

September 2016

CNTNAP2 is a gene on chromosome 7 that has shown associations with autism andschizophrenia, and ther...

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...

Association of SNPs with CP in ICP cases (n = 434) and control (n = 1288) subjects.

Anil K. Giri (2183608)
Shallu Midha (2183606)
Priyanka Banerjee (485749)
Ankita Agrawal (2183614)
Syed Jafar Mehdi (2183618)
Rajan Dhingra (2183616)
Ismeet Kaur (2183612)
Ramesh Kumar G. (2183624)
Ritika Lakhotia (2183620)
Saurabh Ghosh (1234137)
Kshaunish Das (2183604)
Samir Mohindra (2183602)
Surinder Rana (2183626)
Deepak K. Bhasin (2183610)
Pramod K. Garg (2183622)
Dwaipayan Bharadwaj (126561)

January 2016

Association of SNPs with CP in ICP cases (n = 434) and control (n = 1288) subjects.</p

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...

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...

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

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

January 2008

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

Defining the Contribution of CNTNAP2 to Autism Susceptibility

Srirangan Sampath (473610)
Shambu Bhat (473611)
Simone Gupta (473612)
Ashley O’Connor (473613)
Andrew B. West (185211)
Dan E. Arking (143354)
Aravinda Chakravarti (77021)

October 2013

<div>Multiple lines of genetic evidence suggest a role for CNTNAP2 in autism. To assess it...

A genome-wide investigation of SNPs and CNVs in schizophrenia.

NEED AC
GE D
WEALE ME
MAIA J
FENG S
HEINZEN EL
SHIANNA KV
YOON W
KASPERAVICI
TE D
M. GENNARELLI
STRITTMATTER WJ
BONVICINI C
ROSSI G
JAYATHILAKE K
COLA PA
MCEVOY JP
KEEFE RS
FISHER EM
ST JEAN PL
GIEGLING I
HARTMANN AM
MÖLLER HJ
RUPPERT A
FRASER G
CROMBIE C
MIDDLETON LT
ST CLAIR D
ROSES AD
MUGLIA P
FRANCKS C
RUJESCU D
MELTZER HY
GOLDSTEIN DB

January 2009

We report a genome-wide assessment of single nucleotide polymorphisms (SNPs) and copy number variant...

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

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

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

Vrijenhoek, Terry
Buizer-Voskamp, Jacobine E.
van der Stelt, Inge
Strengman, Eric
Sabatti, Chiara
van Kessel, Ad Geurts
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...

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...

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

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

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...

Defining the contribution of CNTNAP2 to autism susceptibility.

Srirangan Sampath
Shambu Bhat
Simone Gupta
Ashley O'Connor
Andrew B West
Dan E Arking
Aravinda Chakravarti

Multiple lines of genetic evidence suggest a role for CNTNAP2 in autism. To assess its population im...

Defining the Contribution of CNTNAP2 to Autism

Srirangan Sampath
Shambu Bhat
Simone Gupta
Andrew B. West
Dan E
Arking Aravinda Chakravarti

January 2013

Multiple lines of genetic evidence suggest a role for CNTNAP2 in autism. To assess its population im...

CNTNAP2 polymorphisms and structural brain connectivity: A diffusion-tensor imaging study

Clemm von Hohenberg, Christian
Wigand, Marlene C.
Kubicki, Marek R.
Leicht, Gregor
Giegling, Ina
Karch, Susanne
Hartmann, Annette M.
Konte, Bettina
Friedl, Marion
Ballinger, Thomas
Eckbo, Ryan
Bouix, Sylvain
Jäger, Lorenz
Shenton, Martha Elizabeth
Rujescu, Dan
Mulert, Christoph

September 2016

CNTNAP2 is a gene on chromosome 7 that has shown associations with autism andschizophrenia, and ther...

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...

Association of SNPs with CP in ICP cases (n = 434) and control (n = 1288) subjects.

Anil K. Giri (2183608)
Shallu Midha (2183606)
Priyanka Banerjee (485749)
Ankita Agrawal (2183614)
Syed Jafar Mehdi (2183618)
Rajan Dhingra (2183616)
Ismeet Kaur (2183612)
Ramesh Kumar G. (2183624)
Ritika Lakhotia (2183620)
Saurabh Ghosh (1234137)
Kshaunish Das (2183604)
Samir Mohindra (2183602)
Surinder Rana (2183626)
Deepak K. Bhasin (2183610)
Pramod K. Garg (2183622)
Dwaipayan Bharadwaj (126561)

January 2016

Association of SNPs with CP in ICP cases (n = 434) and control (n = 1288) subjects.</p

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...

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...

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

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

January 2008

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

Defining the Contribution of CNTNAP2 to Autism Susceptibility

Srirangan Sampath (473610)
Shambu Bhat (473611)
Simone Gupta (473612)
Ashley O’Connor (473613)
Andrew B. West (185211)
Dan E. Arking (143354)
Aravinda Chakravarti (77021)

October 2013

<div>Multiple lines of genetic evidence suggest a role for CNTNAP2 in autism. To assess it...

A genome-wide investigation of SNPs and CNVs in schizophrenia.

NEED AC
GE D
WEALE ME
MAIA J
FENG S
HEINZEN EL
SHIANNA KV
YOON W
KASPERAVICI
TE D
M. GENNARELLI
STRITTMATTER WJ
BONVICINI C
ROSSI G
JAYATHILAKE K
COLA PA
MCEVOY JP
KEEFE RS
FISHER EM
ST JEAN PL
GIEGLING I
HARTMANN AM
MÖLLER HJ
RUPPERT A
FRASER G
CROMBIE C
MIDDLETON LT
ST CLAIR D
ROSES AD
MUGLIA P
FRANCKS C
RUJESCU D
MELTZER HY
GOLDSTEIN DB

January 2009

We report a genome-wide assessment of single nucleotide polymorphisms (SNPs) and copy number variant...

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

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

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

Vrijenhoek, Terry
Buizer-Voskamp, Jacobine E.
van der Stelt, Inge
Strengman, Eric
Sabatti, Chiara
van Kessel, Ad Geurts
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 <i>CNTNAP2</i> previously reported to be associated in psychiatric diseases, and their evidence for association in PGC datasets.

Abstract

Extracted data

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

Abstract

Extracted data

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