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Title: A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder

Authors:
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Publication Date:
Sponsoring Org.:
USDOE National Nuclear Security Administration (NNSA)
OSTI Identifier:
1227571
Grant/Contract Number:  
20110516ECR
Resource Type:
Published Article
Journal Name:
American Journal of Human Genetics
Additional Journal Information:
Journal Name: American Journal of Human Genetics Journal Volume: 95 Journal Issue: 6; Journal ID: ISSN 0002-9297
Publisher:
Elsevier
Country of Publication:
United States
Language:
English

Citation Formats

Duan, Jubao, Shi, Jianxin, Fiorentino, Alessia, Leites, Catherine, Chen, Xiangning, Moy, Winton, Chen, Jingchun, Alexandrov, Boian S., Usheva, Anny, He, Deli, Freda, Jessica, O’Brien, Niamh L., McQuillin, Andrew, Sanders, Alan R., Gershon, Elliot S., DeLisi, Lynn E., Bishop, Alan R., Gurling, Hugh M. D., Pato, Michele T., Levinson, Douglas F., Kendler, Kenneth S., Pato, Carlos N., Gejman, Pablo V., Gejman, Pablo V., Sanders, Alan R., Duan, Jubao, Levinson, Douglas F., Shi, Jianxin, Buccola, Nancy G., Mowry, Bryan J., Freedman, Robert, Olincy, Ann, Amin, Farooq, Black, Donald W., Silverman, Jeremy M., Byerley, William F., Svrakic, Dragan M., Cloninger, C. Robert, Pato, Michele T., Sobell, Janet L., Medeiros, Helena, Abbott, Colony, Skar, Brooke, Buckley, Peter F., Bromet, Evelyn J., Escamilla, Michael A., Fanous, Ayman H., Lehrer, Douglas S., Macciardi, Fabio, Malaspina, Dolores, McCarroll, Steve A., Marder, Stephen R., Moran, Jennifer, Morley, Christopher P., Nicolini, Humberto, Perkins, Diana O., Purcell, Shaun M., Rapaport, Mark H., Sklar, Pamela, Smoller, Jordan W., Knowles, James A., and Pato, Carlos N. A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder. United States: N. p., 2014. Web. doi:10.1016/j.ajhg.2014.11.001.
Duan, Jubao, Shi, Jianxin, Fiorentino, Alessia, Leites, Catherine, Chen, Xiangning, Moy, Winton, Chen, Jingchun, Alexandrov, Boian S., Usheva, Anny, He, Deli, Freda, Jessica, O’Brien, Niamh L., McQuillin, Andrew, Sanders, Alan R., Gershon, Elliot S., DeLisi, Lynn E., Bishop, Alan R., Gurling, Hugh M. D., Pato, Michele T., Levinson, Douglas F., Kendler, Kenneth S., Pato, Carlos N., Gejman, Pablo V., Gejman, Pablo V., Sanders, Alan R., Duan, Jubao, Levinson, Douglas F., Shi, Jianxin, Buccola, Nancy G., Mowry, Bryan J., Freedman, Robert, Olincy, Ann, Amin, Farooq, Black, Donald W., Silverman, Jeremy M., Byerley, William F., Svrakic, Dragan M., Cloninger, C. Robert, Pato, Michele T., Sobell, Janet L., Medeiros, Helena, Abbott, Colony, Skar, Brooke, Buckley, Peter F., Bromet, Evelyn J., Escamilla, Michael A., Fanous, Ayman H., Lehrer, Douglas S., Macciardi, Fabio, Malaspina, Dolores, McCarroll, Steve A., Marder, Stephen R., Moran, Jennifer, Morley, Christopher P., Nicolini, Humberto, Perkins, Diana O., Purcell, Shaun M., Rapaport, Mark H., Sklar, Pamela, Smoller, Jordan W., Knowles, James A., & Pato, Carlos N. A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder. United States. https://doi.org/10.1016/j.ajhg.2014.11.001
Duan, Jubao, Shi, Jianxin, Fiorentino, Alessia, Leites, Catherine, Chen, Xiangning, Moy, Winton, Chen, Jingchun, Alexandrov, Boian S., Usheva, Anny, He, Deli, Freda, Jessica, O’Brien, Niamh L., McQuillin, Andrew, Sanders, Alan R., Gershon, Elliot S., DeLisi, Lynn E., Bishop, Alan R., Gurling, Hugh M. D., Pato, Michele T., Levinson, Douglas F., Kendler, Kenneth S., Pato, Carlos N., Gejman, Pablo V., Gejman, Pablo V., Sanders, Alan R., Duan, Jubao, Levinson, Douglas F., Shi, Jianxin, Buccola, Nancy G., Mowry, Bryan J., Freedman, Robert, Olincy, Ann, Amin, Farooq, Black, Donald W., Silverman, Jeremy M., Byerley, William F., Svrakic, Dragan M., Cloninger, C. Robert, Pato, Michele T., Sobell, Janet L., Medeiros, Helena, Abbott, Colony, Skar, Brooke, Buckley, Peter F., Bromet, Evelyn J., Escamilla, Michael A., Fanous, Ayman H., Lehrer, Douglas S., Macciardi, Fabio, Malaspina, Dolores, McCarroll, Steve A., Marder, Stephen R., Moran, Jennifer, Morley, Christopher P., Nicolini, Humberto, Perkins, Diana O., Purcell, Shaun M., Rapaport, Mark H., Sklar, Pamela, Smoller, Jordan W., Knowles, James A., and Pato, Carlos N. Mon . "A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder". United States. https://doi.org/10.1016/j.ajhg.2014.11.001.
@article{osti_1227571,
title = {A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder},
author = {Duan, Jubao and Shi, Jianxin and Fiorentino, Alessia and Leites, Catherine and Chen, Xiangning and Moy, Winton and Chen, Jingchun and Alexandrov, Boian S. and Usheva, Anny and He, Deli and Freda, Jessica and O’Brien, Niamh L. and McQuillin, Andrew and Sanders, Alan R. and Gershon, Elliot S. and DeLisi, Lynn E. and Bishop, Alan R. and Gurling, Hugh M. D. and Pato, Michele T. and Levinson, Douglas F. and Kendler, Kenneth S. and Pato, Carlos N. and Gejman, Pablo V. and Gejman, Pablo V. and Sanders, Alan R. and Duan, Jubao and Levinson, Douglas F. and Shi, Jianxin and Buccola, Nancy G. and Mowry, Bryan J. and Freedman, Robert and Olincy, Ann and Amin, Farooq and Black, Donald W. and Silverman, Jeremy M. and Byerley, William F. and Svrakic, Dragan M. and Cloninger, C. Robert and Pato, Michele T. and Sobell, Janet L. and Medeiros, Helena and Abbott, Colony and Skar, Brooke and Buckley, Peter F. and Bromet, Evelyn J. and Escamilla, Michael A. and Fanous, Ayman H. and Lehrer, Douglas S. and Macciardi, Fabio and Malaspina, Dolores and McCarroll, Steve A. and Marder, Stephen R. and Moran, Jennifer and Morley, Christopher P. and Nicolini, Humberto and Perkins, Diana O. and Purcell, Shaun M. and Rapaport, Mark H. and Sklar, Pamela and Smoller, Jordan W. and Knowles, James A. and Pato, Carlos N.},
abstractNote = {},
doi = {10.1016/j.ajhg.2014.11.001},
journal = {American Journal of Human Genetics},
number = 6,
volume = 95,
place = {United States},
year = {Mon Dec 01 00:00:00 EST 2014},
month = {Mon Dec 01 00:00:00 EST 2014}
}

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https://doi.org/10.1016/j.ajhg.2014.11.001

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