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[{(tBu2Me)2Si}3Li4]2-: An aggregated dianion of a 1,1-dilithiosilane with a unique structural motif.

Angewandte Chemie (International ed. in English)

Bravo-Zhivotovskii D, Ruderfer I, Melamed S, Botoshansky M, Schmidt A, Apeloig Y.
PMID: 16703642
Angew Chem Int Ed Engl. 2006 Jun 19;45(25):4157-9. doi: 10.1002/anie.200600308.

No abstract available.

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Bravo-Zhivotovskii D, Ruderfer I, Melamed S, et al. [{(tBu2Me)2Si}3Li4]2-: An aggregated dianion of a 1,1-dilithiosilane with a unique structural motif. Angew Chem Int Ed Engl. 2006;45(25):4157-9doi: 10.1002/anie.200600308.
Bravo-Zhivotovskii, D., Ruderfer, I., Melamed, S., Botoshansky, M., Schmidt, A., & Apeloig, Y. (2006). [{(tBu2Me)2Si}3Li4]2-: An aggregated dianion of a 1,1-dilithiosilane with a unique structural motif. Angewandte Chemie (International ed. in English), 45(25), 4157-9. https://doi.org/10.1002/anie.200600308
Bravo-Zhivotovskii, Dmitry, et al. "[{(tBu2Me)2Si}3Li4]2-: An aggregated dianion of a 1,1-dilithiosilane with a unique structural motif." Angewandte Chemie (International ed. in English) vol. 45,25 (2006): 4157-9. doi: https://doi.org/10.1002/anie.200600308
Bravo-Zhivotovskii D, Ruderfer I, Melamed S, Botoshansky M, Schmidt A, Apeloig Y. [{(tBu2Me)2Si}3Li4]2-: An aggregated dianion of a 1,1-dilithiosilane with a unique structural motif. Angew Chem Int Ed Engl. 2006 Jun 19;45(25):4157-9. doi: 10.1002/anie.200600308. PMID: 16703642.
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Expanding cultural and ancestral representation in psychiatric genetic studies.

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology

Kang J, Ruderfer DM.
PMID: 32296136
Neuropsychopharmacology. 2020 Sep;45(10):1593-1594. doi: 10.1038/s41386-020-0676-1. Epub 2020 Apr 15.

No abstract available.

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Kang J, Ruderfer DM. Expanding cultural and ancestral representation in psychiatric genetic studies. Neuropsychopharmacology. 2020;45(10):1593-1594doi: 10.1038/s41386-020-0676-1.
Kang, J., & Ruderfer, D. M. (2020). Expanding cultural and ancestral representation in psychiatric genetic studies. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 45(10), 1593-1594. https://doi.org/10.1038/s41386-020-0676-1
Kang, Jooeun, and Ruderfer, Douglas M. "Expanding cultural and ancestral representation in psychiatric genetic studies." Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology vol. 45,10 (2020): 1593-1594. doi: https://doi.org/10.1038/s41386-020-0676-1
Kang J, Ruderfer DM. Expanding cultural and ancestral representation in psychiatric genetic studies. Neuropsychopharmacology. 2020 Sep;45(10):1593-1594. doi: 10.1038/s41386-020-0676-1. Epub 2020 Apr 15. PMID: 32296136; PMCID: PMC7609284.
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Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.

Nature genetics

Huckins LM, Dobbyn A, Ruderfer DM, Hoffman G, Wang W, Pardiñas AF, Rajagopal VM, Als TD, T Nguyen H, Girdhar K, Boocock J, Roussos P, Fromer M, Kramer R, Domenici E, Gamazon ER, Purcell S, Demontis D, Børglum AD, Walters JTR, O'Donovan MC, Sullivan P, Owen MJ, Devlin B, Sieberts SK, Cox NJ, Im HK, Sklar P, Stahl EA.
PMID: 31086353
Nat Genet. 2019 Jun;51(6):1068. doi: 10.1038/s41588-019-0435-6.

In the HTML version of the article originally published, the author group 'The Schizophrenia Working Group of the Psychiatric Genomics Consortium' was displayed incorrectly. The error has been corrected in the HTML version of the article.

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Huckins LM, Dobbyn A, Ruderfer DM, et al. Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nat Genet. 2019;51(6):1068doi: 10.1038/s41588-019-0435-6.
Huckins, L. M., Dobbyn, A., Ruderfer, D. M., Hoffman, G., Wang, W., Pardiñas, A. F., Rajagopal, V. M., Als, T. D., T Nguyen, H., Girdhar, K., Boocock, J., Roussos, P., Fromer, M., Kramer, R., Domenici, E., Gamazon, E. R., Purcell, S., Demontis, D., Børglum, A. D., Walters, J. T. R., O'Donovan, M. C., Sullivan, P., Owen, M. J., Devlin, B., Sieberts, S. K., Cox, N. J., Im, H. K., Sklar, P., & Stahl, E. A. (2019). Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature genetics, 51(6), 1068. https://doi.org/10.1038/s41588-019-0435-6
Huckins, Laura M, et al. "Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk." Nature genetics vol. 51,6 (2019): 1068. doi: https://doi.org/10.1038/s41588-019-0435-6
Huckins LM, Dobbyn A, Ruderfer DM, Hoffman G, Wang W, Pardiñas AF, Rajagopal VM, Als TD, T Nguyen H, Girdhar K, Boocock J, Roussos P, Fromer M, Kramer R, Domenici E, Gamazon ER, Purcell S, Demontis D, Børglum AD, Walters JTR, O'Donovan MC, Sullivan P, Owen MJ, Devlin B, Sieberts SK, Cox NJ, Im HK, Sklar P, Stahl EA. Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nat Genet. 2019 Jun;51(6):1068. doi: 10.1038/s41588-019-0435-6. PMID: 31086353.
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Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease.

Molecular psychiatry

Dennis J, Sealock J, Levinson RT, Farber-Eger E, Franco J, Fong S, Straub P, Hucks D, Song WL, Linton MF, Fontanillas P, Elson SL, Ruderfer D, Abdellaoui A, Sanchez-Roige S, Palmer AA, Boomsma DI, Cox NJ, Chen G, Mosley JD, Wells QS, Davis LK.
PMID: 31796895
Mol Psychiatry. 2021 Aug;26(8):4254-4264. doi: 10.1038/s41380-019-0614-y. Epub 2019 Dec 03.

Major depressive disorder (MDD) and loneliness are phenotypically and genetically correlated with coronary artery disease (CAD), but whether these associations are explained by pleiotropic genetic variants or shared comorbidities is unclear. To tease apart these scenarios, we first assessed...

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Dennis J, Sealock J, Levinson RT, et al. Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease. Mol Psychiatry. 2019;26(8):4254-4264doi: 10.1038/s41380-019-0614-y.
Dennis, J., Sealock, J., Levinson, R. T., Farber-Eger, E., Franco, J., Fong, S., Straub, P., Hucks, D., Song, W. L., Linton, M. F., Fontanillas, P., Elson, S. L., Ruderfer, D., Abdellaoui, A., Sanchez-Roige, S., Palmer, A. A., Boomsma, D. I., Cox, N. J., Chen, G., Mosley, J. D., Wells, Q. S., & Davis, L. K. (2021). Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease. Molecular psychiatry, 26(8), 4254-4264. https://doi.org/10.1038/s41380-019-0614-y
Dennis, Jessica, et al. "Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease." Molecular psychiatry vol. 26,8 (2021): 4254-4264. doi: https://doi.org/10.1038/s41380-019-0614-y
Dennis J, Sealock J, Levinson RT, Farber-Eger E, Franco J, Fong S, Straub P, Hucks D, Song WL, Linton MF, Fontanillas P, Elson SL, Ruderfer D, Abdellaoui A, Sanchez-Roige S, Palmer AA, Boomsma DI, Cox NJ, Chen G, Mosley JD, Wells QS, Davis LK. Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease. Mol Psychiatry. 2021 Aug;26(8):4254-4264. doi: 10.1038/s41380-019-0614-y. Epub 2019 Dec 03. PMID: 31796895; PMCID: PMC7266730.
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Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

Nature genetics

Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, MacCabe JH, McCarroll SA, Baune BT, Breen G, Byrne EM, Dannlowski U, Eley TC, Hayward C, Martin NG, McIntosh AM, Plomin R, Porteous DJ, Wray NR, Caballero A, Geschwind DH, Huckins LM, Ruderfer DM, Santiago E, Sklar P, Stahl EA, Won H, Agerbo E, Als TD, Andreassen OA, Bækvad-Hansen M, Mortensen PB, Pedersen CB, Børglum AD, Bybjerg-Grauholm J, Djurovic S, Durmishi N, Pedersen MG, Golimbet V, Grove J, Hougaard DM, Mattheisen M, Molden E, Mors O, Nordentoft M, Pejovic-Milovancevic M, Sigurdsson E, Silagadze T, Hansen CS, Stefansson K, Stefansson H, Steinberg S, Tosato S, Werge T, Collier DA, Rujescu D, Kirov G, Owen MJ, O'Donovan MC, Walters JTR.
PMID: 31160808
Nat Genet. 2019 Jul;51(7):1193. doi: 10.1038/s41588-019-0450-7.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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Pardiñas AF, Holmans P, Pocklington AJ, et al. Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nat Genet. 2019;51(7):1193doi: 10.1038/s41588-019-0450-7.
Pardiñas, A. F., Holmans, P., Pocklington, A. J., Escott-Price, V., Ripke, S., Carrera, N., Legge, S. E., Bishop, S., Cameron, D., Hamshere, M. L., Han, J., Hubbard, L., Lynham, A., Mantripragada, K., Rees, E., MacCabe, J. H., McCarroll, S. A., Baune, B. T., Breen, G., Byrne, E. M., Dannlowski, U., Eley, T. C., Hayward, C., Martin, N. G., McIntosh, A. M., Plomin, R., Porteous, D. J., Wray, N. R., Caballero, A., Geschwind, D. H., Huckins, L. M., Ruderfer, D. M., Santiago, E., Sklar, P., Stahl, E. A., Won, H., Agerbo, E., Als, T. D., Andreassen, O. A., Bækvad-Hansen, M., Mortensen, P. B., Pedersen, C. B., Børglum, A. D., Bybjerg-Grauholm, J., Djurovic, S., Durmishi, N., Pedersen, M. G., Golimbet, V., Grove, J., Hougaard, D. M., Mattheisen, M., Molden, E., Mors, O., Nordentoft, M., Pejovic-Milovancevic, M., Sigurdsson, E., Silagadze, T., Hansen, C. S., Stefansson, K., Stefansson, H., Steinberg, S., Tosato, S., Werge, T., Collier, D. A., Rujescu, D., Kirov, G., Owen, M. J., O'Donovan, M. C., & Walters, J. T. R. (2019). Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature genetics, 51(7), 1193. https://doi.org/10.1038/s41588-019-0450-7
Pardiñas, Antonio F, et al. "Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection." Nature genetics vol. 51,7 (2019): 1193. doi: https://doi.org/10.1038/s41588-019-0450-7
Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, MacCabe JH, McCarroll SA, Baune BT, Breen G, Byrne EM, Dannlowski U, Eley TC, Hayward C, Martin NG, McIntosh AM, Plomin R, Porteous DJ, Wray NR, Caballero A, Geschwind DH, Huckins LM, Ruderfer DM, Santiago E, Sklar P, Stahl EA, Won H, Agerbo E, Als TD, Andreassen OA, Bækvad-Hansen M, Mortensen PB, Pedersen CB, Børglum AD, Bybjerg-Grauholm J, Djurovic S, Durmishi N, Pedersen MG, Golimbet V, Grove J, Hougaard DM, Mattheisen M, Molden E, Mors O, Nordentoft M, Pejovic-Milovancevic M, Sigurdsson E, Silagadze T, Hansen CS, Stefansson K, Stefansson H, Steinberg S, Tosato S, Werge T, Collier DA, Rujescu D, Kirov G, Owen MJ, O'Donovan MC, Walters JTR. Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nat Genet. 2019 Jul;51(7):1193. doi: 10.1038/s41588-019-0450-7. PMID: 31160808.
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Learning Opportunities for Drug Repositioning via GWAS and PheWAS Findings.

AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science

Yin W, Gao C, Xu Y, Li B, Ruderfer DM, Chen Y.
PMID: 29888080
AMIA Jt Summits Transl Sci Proc. 2018 May 18;2017:237-246. eCollection 2018.

Drug repositioning for available medications can be preferred over traditional drug development, which requires substantially more effort to uncover new insights into medications and diseases. Genome-Wide Association Studies (GWAS) and Phenome-Wide Association Studies (PheWAS) are two complimentary methods for...

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Yin W, Gao C, Xu Y, et al. Learning Opportunities for Drug Repositioning via GWAS and PheWAS Findings. AMIA Jt Summits Transl Sci Proc. 2018;2017:237-246
Yin, W., Gao, C., Xu, Y., Li, B., Ruderfer, D. M., & Chen, Y. (2018). Learning Opportunities for Drug Repositioning via GWAS and PheWAS Findings. AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science, 2017237-246.
Yin, Wen, et al. "Learning Opportunities for Drug Repositioning via GWAS and PheWAS Findings." AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science vol. 2017 (2018): 237-246.
Yin W, Gao C, Xu Y, Li B, Ruderfer DM, Chen Y. Learning Opportunities for Drug Repositioning via GWAS and PheWAS Findings. AMIA Jt Summits Transl Sci Proc. 2018 May 18;2017:237-246. eCollection 2018. PMID: 29888080; PMCID: PMC5961790.
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Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors.

Biological psychiatry

Mullins N, Kang J, Campos AI, Coleman JRI, Edwards AC, Galfalvy H, Levey DF, Lori A, Shabalin A, Starnawska A, Su MH, Watson HJ, Adams M, Awasthi S, Gandal M, Hafferty JD, Hishimoto A, Kim M, Okazaki S, Otsuka I, Ripke S, Ware EB, Bergen AW, Berrettini WH, Bohus M, Brandt H, Chang X, Chen WJ, Chen HC, Crawford S, Crow S, DiBlasi E, Duriez P, Fernández-Aranda F, Fichter MM, Gallinger S, Glatt SJ, Gorwood P, Guo Y, Hakonarson H, Halmi KA, Hwu HG, Jain S, Jamain S, Jiménez-Murcia S, Johnson C, Kaplan AS, Kaye WH, Keel PK, Kennedy JL, Klump KL, Li D, Liao SC, Lieb K, Lilenfeld L, Liu CM, Magistretti PJ, Marshall CR, Mitchell JE, Monson ET, Myers RM, Pinto D, Powers A, Ramoz N, Roepke S, Rozanov V, Scherer SW, Schmahl C, Sokolowski M, Strober M, Thornton LM, Treasure J, Tsuang MT, Witt SH, Woodside DB, Yilmaz Z, Zillich L, Adolfsson R, Agartz I, Air TM, Alda M, Alfredsson L, Andreassen OA, Anjorin A, Appadurai V, Soler Artigas M, Van der Auwera S, Azevedo MH, Bass N, Bau CHD, Baune BT, Bellivier F, Berger K, Biernacka JM, Bigdeli TB, Binder EB, Boehnke M, Boks MP, Bosch R, Braff DL, Bryant R, Budde M, Byrne EM, Cahn W, Casas M, Castelao E, Cervilla JA, Chaumette B, Cichon S, Corvin A, Craddock N, Craig D, Degenhardt F, Djurovic S, Edenberg HJ, Fanous AH, Foo JC, Forstner AJ, Frye M, Fullerton JM, Gatt JM, Gejman PV, Giegling I, Grabe HJ, Green MJ, Grevet EH, Grigoroiu-Serbanescu M, Gutierrez B, Guzman-Parra J, Hamilton SP, Hamshere ML, Hartmann A, Hauser J, Heilmann-Heimbach S, Hoffmann P, Ising M, Jones I, Jones LA, Jonsson L, Kahn RS, Kelsoe JR, Kendler KS, Kloiber S, Koenen KC, Kogevinas M, Konte B, Krebs MO, Landén M, Lawrence J, Leboyer M, Lee PH, Levinson DF, Liao C, Lissowska J, Lucae S, Mayoral F, McElroy SL, McGrath P, McGuffin P, McQuillin A, Medland SE, Mehta D, Melle I, Milaneschi Y, Mitchell PB, Molina E, Morken G, Mortensen PB, Müller-Myhsok B, Nievergelt C, Nimgaonkar V, Nöthen MM, O'Donovan MC, Ophoff RA, Owen MJ, Pato C, Pato MT, Penninx BWJH, Pimm J, Pistis G, Potash JB, Power RA, Preisig M, Quested D, Ramos-Quiroga JA, Reif A, Ribasés M, Richarte V, Rietschel M, Rivera M, Roberts A, Roberts G, Rouleau GA, Rovaris DL, Rujescu D, Sánchez-Mora C, Sanders AR, Schofield PR, Schulze TG, Scott LJ, Serretti A, Shi J, Shyn SI, Sirignano L, Sklar P, Smeland OB, Smoller JW, Sonuga-Barke EJS, Spalletta G, Strauss JS, Świątkowska B, Trzaskowski M, Turecki G, Vilar-Ribó L, Vincent JB, Völzke H, Walters JTR, Shannon Weickert C, Weickert TW, Weissman MM, Williams LM, Wray NR, Zai CC, Ashley-Koch AE, Beckham JC, Hauser ER, Hauser MA, Kimbrel NA, Lindquist JH, McMahon B, Oslin DW, Qin X, Agerbo E, Børglum AD, Breen G, Erlangsen A, Esko T, Gelernter J, Hougaard DM, Kessler RC, Kranzler HR, Li QS, Martin NG, McIntosh AM, Mors O, Nordentoft M, Olsen CM, Porteous D, Ursano RJ, Wasserman D, Werge T, Whiteman DC, Bulik CM, Coon H, Demontis D, Docherty AR, Kuo PH, Lewis CM, Mann JJ, Rentería ME, Smith DJ, Stahl EA, Stein MB, Streit F, Willour V, Ruderfer DM.
PMID: 34861974
Biol Psychiatry. 2021 Sep 09; doi: 10.1016/j.biopsych.2021.05.029. Epub 2021 Sep 09.

BACKGROUND: Suicide is a leading cause of death worldwide, and nonfatal suicide attempts, which occur far more frequently, are a major source of disability and social and economic burden. Both have substantial genetic etiology, which is partially shared and...

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Mullins N, Kang J, Campos AI, et al. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biol Psychiatry. 2021;doi: 10.1016/j.biopsych.2021.05.029.
Mullins, N., Kang, J., Campos, A. I., Coleman, J. R. I., Edwards, A. C., Galfalvy, H., Levey, D. F., Lori, A., Shabalin, A., Starnawska, A., Su, M. H., Watson, H. J., Adams, M., Awasthi, S., Gandal, M., Hafferty, J. D., Hishimoto, A., Kim, M., Okazaki, S., Otsuka, I., Ripke, S., Ware, E. B., Bergen, A. W., Berrettini, W. H., Bohus, M., Brandt, H., Chang, X., Chen, W. J., Chen, H. C., Crawford, S., Crow, S., DiBlasi, E., Duriez, P., Fernández-Aranda, F., Fichter, M. M., Gallinger, S., Glatt, S. J., Gorwood, P., Guo, Y., Hakonarson, H., Halmi, K. A., Hwu, H. G., Jain, S., Jamain, S., Jiménez-Murcia, S., Johnson, C., Kaplan, A. S., Kaye, W. H., Keel, P. K., Kennedy, J. L., Klump, K. L., Li, D., Liao, S. C., Lieb, K., Lilenfeld, L., Liu, C. M., Magistretti, P. J., Marshall, C. R., Mitchell, J. E., Monson, E. T., Myers, R. M., Pinto, D., Powers, A., Ramoz, N., Roepke, S., Rozanov, V., Scherer, S. W., Schmahl, C., Sokolowski, M., Strober, M., Thornton, L. M., Treasure, J., Tsuang, M. T., Witt, S. H., Woodside, D. B., Yilmaz, Z., Zillich, L., Adolfsson, R., Agartz, I., Air, T. M., Alda, M., Alfredsson, L., Andreassen, O. A., Anjorin, A., Appadurai, V., Soler Artigas, M., Van der Auwera, S., Azevedo, M. H., Bass, N., Bau, C. H. D., Baune, B. T., Bellivier, F., Berger, K., Biernacka, J. M., Bigdeli, T. B., Binder, E. B., Boehnke, M., Boks, M. P., Bosch, R., Braff, D. L., Bryant, R., Budde, M., Byrne, E. M., Cahn, W., Casas, M., Castelao, E., Cervilla, J. A., Chaumette, B., Cichon, S., Corvin, A., Craddock, N., Craig, D., Degenhardt, F., Djurovic, S., Edenberg, H. J., Fanous, A. H., Foo, J. C., Forstner, A. J., Frye, M., Fullerton, J. M., Gatt, J. M., Gejman, P. V., Giegling, I., Grabe, H. J., Green, M. J., Grevet, E. H., Grigoroiu-Serbanescu, M., Gutierrez, B., Guzman-Parra, J., Hamilton, S. P., Hamshere, M. L., Hartmann, A., Hauser, J., Heilmann-Heimbach, S., Hoffmann, P., Ising, M., Jones, I., Jones, L. A., Jonsson, L., Kahn, R. S., Kelsoe, J. R., Kendler, K. S., Kloiber, S., Koenen, K. C., Kogevinas, M., Konte, B., Krebs, M. O., Landén, M., Lawrence, J., Leboyer, M., Lee, P. H., Levinson, D. F., Liao, C., Lissowska, J., Lucae, S., Mayoral, F., McElroy, S. L., McGrath, P., McGuffin, P., McQuillin, A., Medland, S. E., Mehta, D., Melle, I., Milaneschi, Y., Mitchell, P. B., Molina, E., Morken, G., Mortensen, P. B., Müller-Myhsok, B., Nievergelt, C., Nimgaonkar, V., Nöthen, M. M., O'Donovan, M. C., Ophoff, R. A., Owen, M. J., Pato, C., Pato, M. T., Penninx, B. W. J. H., Pimm, J., Pistis, G., Potash, J. B., Power, R. A., Preisig, M., Quested, D., Ramos-Quiroga, J. A., Reif, A., Ribasés, M., Richarte, V., Rietschel, M., Rivera, M., Roberts, A., Roberts, G., Rouleau, G. A., Rovaris, D. L., Rujescu, D., Sánchez-Mora, C., Sanders, A. R., Schofield, P. R., Schulze, T. G., Scott, L. J., Serretti, A., Shi, J., Shyn, S. I., Sirignano, L., Sklar, P., Smeland, O. B., Smoller, J. W., Sonuga-Barke, E. J. S., Spalletta, G., Strauss, J. S., Świątkowska, B., Trzaskowski, M., Turecki, G., Vilar-Ribó, L., Vincent, J. B., Völzke, H., Walters, J. T. R., Shannon Weickert, C., Weickert, T. W., Weissman, M. M., Williams, L. M., Wray, N. R., Zai, C. C., Ashley-Koch, A. E., Beckham, J. C., Hauser, E. R., Hauser, M. A., Kimbrel, N. A., Lindquist, J. H., McMahon, B., Oslin, D. W., Qin, X., Agerbo, E., Børglum, A. D., Breen, G., Erlangsen, A., Esko, T., Gelernter, J., Hougaard, D. M., Kessler, R. C., Kranzler, H. R., Li, Q. S., Martin, N. G., McIntosh, A. M., Mors, O., Nordentoft, M., Olsen, C. M., Porteous, D., Ursano, R. J., Wasserman, D., Werge, T., Whiteman, D. C., Bulik, C. M., Coon, H., Demontis, D., Docherty, A. R., Kuo, P. H., Lewis, C. M., Mann, J. J., Rentería, M. E., Smith, D. J., Stahl, E. A., Stein, M. B., Streit, F., Willour, V., & Ruderfer, D. M. (2021). Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biological psychiatry, . https://doi.org/10.1016/j.biopsych.2021.05.029
Mullins, Niamh, et al. "Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors." Biological psychiatry vol. (2021). doi: https://doi.org/10.1016/j.biopsych.2021.05.029
Mullins N, Kang J, Campos AI, Coleman JRI, Edwards AC, Galfalvy H, Levey DF, Lori A, Shabalin A, Starnawska A, Su MH, Watson HJ, Adams M, Awasthi S, Gandal M, Hafferty JD, Hishimoto A, Kim M, Okazaki S, Otsuka I, Ripke S, Ware EB, Bergen AW, Berrettini WH, Bohus M, Brandt H, Chang X, Chen WJ, Chen HC, Crawford S, Crow S, DiBlasi E, Duriez P, Fernández-Aranda F, Fichter MM, Gallinger S, Glatt SJ, Gorwood P, Guo Y, Hakonarson H, Halmi KA, Hwu HG, Jain S, Jamain S, Jiménez-Murcia S, Johnson C, Kaplan AS, Kaye WH, Keel PK, Kennedy JL, Klump KL, Li D, Liao SC, Lieb K, Lilenfeld L, Liu CM, Magistretti PJ, Marshall CR, Mitchell JE, Monson ET, Myers RM, Pinto D, Powers A, Ramoz N, Roepke S, Rozanov V, Scherer SW, Schmahl C, Sokolowski M, Strober M, Thornton LM, Treasure J, Tsuang MT, Witt SH, Woodside DB, Yilmaz Z, Zillich L, Adolfsson R, Agartz I, Air TM, Alda M, Alfredsson L, Andreassen OA, Anjorin A, Appadurai V, Soler Artigas M, Van der Auwera S, Azevedo MH, Bass N, Bau CHD, Baune BT, Bellivier F, Berger K, Biernacka JM, Bigdeli TB, Binder EB, Boehnke M, Boks MP, Bosch R, Braff DL, Bryant R, Budde M, Byrne EM, Cahn W, Casas M, Castelao E, Cervilla JA, Chaumette B, Cichon S, Corvin A, Craddock N, Craig D, Degenhardt F, Djurovic S, Edenberg HJ, Fanous AH, Foo JC, Forstner AJ, Frye M, Fullerton JM, Gatt JM, Gejman PV, Giegling I, Grabe HJ, Green MJ, Grevet EH, Grigoroiu-Serbanescu M, Gutierrez B, Guzman-Parra J, Hamilton SP, Hamshere ML, Hartmann A, Hauser J, Heilmann-Heimbach S, Hoffmann P, Ising M, Jones I, Jones LA, Jonsson L, Kahn RS, Kelsoe JR, Kendler KS, Kloiber S, Koenen KC, Kogevinas M, Konte B, Krebs MO, Landén M, Lawrence J, Leboyer M, Lee PH, Levinson DF, Liao C, Lissowska J, Lucae S, Mayoral F, McElroy SL, McGrath P, McGuffin P, McQuillin A, Medland SE, Mehta D, Melle I, Milaneschi Y, Mitchell PB, Molina E, Morken G, Mortensen PB, Müller-Myhsok B, Nievergelt C, Nimgaonkar V, Nöthen MM, O'Donovan MC, Ophoff RA, Owen MJ, Pato C, Pato MT, Penninx BWJH, Pimm J, Pistis G, Potash JB, Power RA, Preisig M, Quested D, Ramos-Quiroga JA, Reif A, Ribasés M, Richarte V, Rietschel M, Rivera M, Roberts A, Roberts G, Rouleau GA, Rovaris DL, Rujescu D, Sánchez-Mora C, Sanders AR, Schofield PR, Schulze TG, Scott LJ, Serretti A, Shi J, Shyn SI, Sirignano L, Sklar P, Smeland OB, Smoller JW, Sonuga-Barke EJS, Spalletta G, Strauss JS, Świątkowska B, Trzaskowski M, Turecki G, Vilar-Ribó L, Vincent JB, Völzke H, Walters JTR, Shannon Weickert C, Weickert TW, Weissman MM, Williams LM, Wray NR, Zai CC, Ashley-Koch AE, Beckham JC, Hauser ER, Hauser MA, Kimbrel NA, Lindquist JH, McMahon B, Oslin DW, Qin X, Agerbo E, Børglum AD, Breen G, Erlangsen A, Esko T, Gelernter J, Hougaard DM, Kessler RC, Kranzler HR, Li QS, Martin NG, McIntosh AM, Mors O, Nordentoft M, Olsen CM, Porteous D, Ursano RJ, Wasserman D, Werge T, Whiteman DC, Bulik CM, Coon H, Demontis D, Docherty AR, Kuo PH, Lewis CM, Mann JJ, Rentería ME, Smith DJ, Stahl EA, Stein MB, Streit F, Willour V, Ruderfer DM. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biol Psychiatry. 2021 Sep 09; doi: 10.1016/j.biopsych.2021.05.029. Epub 2021 Sep 09. PMID: 34861974.
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Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.

Molecular psychiatry

Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, Shen L, Thai K, Zawistowski M, Zhuang Y, Abecasis G, Akil H, Bergen S, Burmeister M, Chapman S, DelaBastide M, Juréus A, Kang HM, Kwok PY, Li JZ, Levy SE, Monson ET, Moran J, Sobell J, Watson S, Willour V, Zöllner S, Adolfsson R, Blackwood D, Boehnke M, Breen G, Corvin A, Craddock N, DiFlorio A, Hultman CM, Landen M, Lewis C, McCarroll SA, Richard McCombie W, McGuffin P, McIntosh A, McQuillin A, Morris D, Myers RM, O'Donovan M, Ophoff R, Boks M, Kahn R, Ouwehand W, Owen M, Pato C, Pato M, Posthuma D, Potash JB, Reif A, Sklar P, Smoller J, Sullivan PF, Vincent J, Walters J, Neale B, Purcell S, Risch N, Schaefer C, Stahl EA, Zandi PP, Scott LJ.
PMID: 33674754
Mol Psychiatry. 2021 Sep;26(9):5251. doi: 10.1038/s41380-021-01063-8.

No abstract available.

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Jia X, Goes FS, Locke AE, et al. Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Mol Psychiatry. 2021;26(9):5251doi: 10.1038/s41380-021-01063-8.
Jia, X., Goes, F. S., Locke, A. E., Palmer, D., Wang, W., Cohen-Woods, S., Genovese, G., Jackson, A. U., Jiang, C., Kvale, M., Mullins, N., Nguyen, H., Pirooznia, M., Rivera, M., Ruderfer, D. M., Shen, L., Thai, K., Zawistowski, M., Zhuang, Y., Abecasis, G., Akil, H., Bergen, S., Burmeister, M., Chapman, S., DelaBastide, M., Juréus, A., Kang, H. M., Kwok, P. Y., Li, J. Z., Levy, S. E., Monson, E. T., Moran, J., Sobell, J., Watson, S., Willour, V., Zöllner, S., Adolfsson, R., Blackwood, D., Boehnke, M., Breen, G., Corvin, A., Craddock, N., DiFlorio, A., Hultman, C. M., Landen, M., Lewis, C., McCarroll, S. A., Richard McCombie, W., McGuffin, P., McIntosh, A., McQuillin, A., Morris, D., Myers, R. M., O'Donovan, M., Ophoff, R., Boks, M., Kahn, R., Ouwehand, W., Owen, M., Pato, C., Pato, M., Posthuma, D., Potash, J. B., Reif, A., Sklar, P., Smoller, J., Sullivan, P. F., Vincent, J., Walters, J., Neale, B., Purcell, S., Risch, N., Schaefer, C., Stahl, E. A., Zandi, P. P., & Scott, L. J. (2021). Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular psychiatry, 26(9), 5251. https://doi.org/10.1038/s41380-021-01063-8
Jia, Xiaoming, et al. "Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder." Molecular psychiatry vol. 26,9 (2021): 5251. doi: https://doi.org/10.1038/s41380-021-01063-8
Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, Shen L, Thai K, Zawistowski M, Zhuang Y, Abecasis G, Akil H, Bergen S, Burmeister M, Chapman S, DelaBastide M, Juréus A, Kang HM, Kwok PY, Li JZ, Levy SE, Monson ET, Moran J, Sobell J, Watson S, Willour V, Zöllner S, Adolfsson R, Blackwood D, Boehnke M, Breen G, Corvin A, Craddock N, DiFlorio A, Hultman CM, Landen M, Lewis C, McCarroll SA, Richard McCombie W, McGuffin P, McIntosh A, McQuillin A, Morris D, Myers RM, O'Donovan M, Ophoff R, Boks M, Kahn R, Ouwehand W, Owen M, Pato C, Pato M, Posthuma D, Potash JB, Reif A, Sklar P, Smoller J, Sullivan PF, Vincent J, Walters J, Neale B, Purcell S, Risch N, Schaefer C, Stahl EA, Zandi PP, Scott LJ. Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Mol Psychiatry. 2021 Sep;26(9):5251. doi: 10.1038/s41380-021-01063-8. PMID: 33674754.
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Clinical Impact of Plasma Metagenomic Next-generation Sequencing in a Large Pediatric Cohort.

The Pediatric infectious disease journal

Niles DT, Revell PA, Ruderfer D, Marquez L, McNeil JC, Palazzi DL.
PMID: 34845152
Pediatr Infect Dis J. 2021 Nov 26; doi: 10.1097/INF.0000000000003395. Epub 2021 Nov 26.

BACKGROUND: Plasma metagenomic next-generation sequencing (mNGS) has the potential to detect thousands of different organisms with a single test. There are limited data on the real-world impact of mNGS and even less guidance on the types of patients and...

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Niles DT, Revell PA, Ruderfer D, et al. Clinical Impact of Plasma Metagenomic Next-generation Sequencing in a Large Pediatric Cohort. Pediatr Infect Dis J. 2021;doi: 10.1097/INF.0000000000003395.
Niles, D. T., Revell, P. A., Ruderfer, D., Marquez, L., McNeil, J. C., & Palazzi, D. L. (2021). Clinical Impact of Plasma Metagenomic Next-generation Sequencing in a Large Pediatric Cohort. The Pediatric infectious disease journal, . https://doi.org/10.1097/INF.0000000000003395
Niles, Denver T, et al. "Clinical Impact of Plasma Metagenomic Next-generation Sequencing in a Large Pediatric Cohort." The Pediatric infectious disease journal vol. (2021). doi: https://doi.org/10.1097/INF.0000000000003395
Niles DT, Revell PA, Ruderfer D, Marquez L, McNeil JC, Palazzi DL. Clinical Impact of Plasma Metagenomic Next-generation Sequencing in a Large Pediatric Cohort. Pediatr Infect Dis J. 2021 Nov 26; doi: 10.1097/INF.0000000000003395. Epub 2021 Nov 26. PMID: 34845152.
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Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.

Scientific reports

Gorski M, Most PJV, Teumer A, Chu AY, Li M, Mijatovic V, Nolte IM, Cocca M, Taliun D, Gomez F, Li Y, Tayo B, Tin A, Feitosa MF, Aspelund T, Attia J, Biffar R, Bochud M, Boerwinkle E, Borecki I, Bottinger EP, Chen MH, Chouraki V, Ciullo M, Coresh J, Cornelis MC, Curhan GC, Adamo AP, Dehghan A, Dengler L, Ding J, Eiriksdottir G, Endlich K, Enroth S, Esko T, Franco OH, Gasparini P, Gieger C, Girotto G, Gottesman O, Gudnason V, Gyllensten U, Hancock SJ, Harris TB, Helmer C, Höllerer S, Hofer E, Hofman A, Holliday EG, Homuth G, Hu FB, Huth C, Hutri-Kähönen N, Hwang SJ, Imboden M, Johansson Å, Kähönen M, König W, Kramer H, Krämer BK, Kumar A, Kutalik Z, Lambert JC, Launer LJ, Lehtimäki T, de Borst MH, Navis G, Swertz M, Liu Y, Lohman K, Loos RJF, Lu Y, Lyytikäinen LP, McEvoy MA, Meisinger C, Meitinger T, Metspalu A, Metzger M, Mihailov E, Mitchell P, Nauck M, Oldehinkel AJ, Olden M, Wjh Penninx B, Pistis G, Pramstaller PP, Probst-Hensch N, Raitakari OT, Rettig R, Ridker PM, Rivadeneira F, Robino A, Rosas SE, Ruderfer D, Ruggiero D, Saba Y, Sala C, Schmidt H, Schmidt R, Scott RJ, Sedaghat S, Smith AV, Sorice R, Stengel B, Stracke S, Strauch K, Toniolo D, Uitterlinden AG, Ulivi S, Viikari JS, Völker U, Vollenweider P, Völzke H, Vuckovic D, Waldenberger M, Wang JJ, Yang Q, Chasman DI, Tromp G, Snieder H, Heid IM, Fox CS, Köttgen A, Pattaro C, Böger CA, Fuchsberger C.
PMID: 28548086
Sci Rep. 2017 May 26;7:46835. doi: 10.1038/srep46835.

This corrects the article DOI: 10.1038/srep45040.

Cite
Gorski M, Most PJV, Teumer A, et al. Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Sci Rep. 2017;7:46835doi: 10.1038/srep46835.
Gorski, M., Most, P. J. V., Teumer, A., Chu, A. Y., Li, M., Mijatovic, V., Nolte, I. M., Cocca, M., Taliun, D., Gomez, F., Li, Y., Tayo, B., Tin, A., Feitosa, M. F., Aspelund, T., Attia, J., Biffar, R., Bochud, M., Boerwinkle, E., Borecki, I., Bottinger, E. P., Chen, M. H., Chouraki, V., Ciullo, M., Coresh, J., Cornelis, M. C., Curhan, G. C., Adamo, A. P., Dehghan, A., Dengler, L., Ding, J., Eiriksdottir, G., Endlich, K., Enroth, S., Esko, T., Franco, O. H., Gasparini, P., Gieger, C., Girotto, G., Gottesman, O., Gudnason, V., Gyllensten, U., Hancock, S. J., Harris, T. B., Helmer, C., Höllerer, S., Hofer, E., Hofman, A., Holliday, E. G., Homuth, G., Hu, F. B., Huth, C., Hutri-Kähönen, N., Hwang, S. J., Imboden, M., Johansson, �. �., Kähönen, M., König, W., Kramer, H., Krämer, B. K., Kumar, A., Kutalik, Z., Lambert, J. C., Launer, L. J., Lehtimäki, T., de Borst, M. H., Navis, G., Swertz, M., Liu, Y., Lohman, K., Loos, R. J. F., Lu, Y., Lyytikäinen, L. P., McEvoy, M. A., Meisinger, C., Meitinger, T., Metspalu, A., Metzger, M., Mihailov, E., Mitchell, P., Nauck, M., Oldehinkel, A. J., Olden, M., Wjh Penninx, B., Pistis, G., Pramstaller, P. P., Probst-Hensch, N., Raitakari, O. T., Rettig, R., Ridker, P. M., Rivadeneira, F., Robino, A., Rosas, S. E., Ruderfer, D., Ruggiero, D., Saba, Y., Sala, C., Schmidt, H., Schmidt, R., Scott, R. J., Sedaghat, S., Smith, A. V., Sorice, R., Stengel, B., Stracke, S., Strauch, K., Toniolo, D., Uitterlinden, A. G., Ulivi, S., Viikari, J. S., Völker, U., Vollenweider, P., Völzke, H., Vuckovic, D., Waldenberger, M., Wang, J. J., Yang, Q., Chasman, D. I., Tromp, G., Snieder, H., Heid, I. M., Fox, C. S., Köttgen, A., Pattaro, C., Böger, C. A., & Fuchsberger, C. (2017). Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Scientific reports, 746835. https://doi.org/10.1038/srep46835
Gorski, Mathias, et al. "Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function." Scientific reports vol. 7 (2017): 46835. doi: https://doi.org/10.1038/srep46835
Gorski M, Most PJV, Teumer A, Chu AY, Li M, Mijatovic V, Nolte IM, Cocca M, Taliun D, Gomez F, Li Y, Tayo B, Tin A, Feitosa MF, Aspelund T, Attia J, Biffar R, Bochud M, Boerwinkle E, Borecki I, Bottinger EP, Chen MH, Chouraki V, Ciullo M, Coresh J, Cornelis MC, Curhan GC, Adamo AP, Dehghan A, Dengler L, Ding J, Eiriksdottir G, Endlich K, Enroth S, Esko T, Franco OH, Gasparini P, Gieger C, Girotto G, Gottesman O, Gudnason V, Gyllensten U, Hancock SJ, Harris TB, Helmer C, Höllerer S, Hofer E, Hofman A, Holliday EG, Homuth G, Hu FB, Huth C, Hutri-Kähönen N, Hwang SJ, Imboden M, Johansson Å, Kähönen M, König W, Kramer H, Krämer BK, Kumar A, Kutalik Z, Lambert JC, Launer LJ, Lehtimäki T, de Borst MH, Navis G, Swertz M, Liu Y, Lohman K, Loos RJF, Lu Y, Lyytikäinen LP, McEvoy MA, Meisinger C, Meitinger T, Metspalu A, Metzger M, Mihailov E, Mitchell P, Nauck M, Oldehinkel AJ, Olden M, Wjh Penninx B, Pistis G, Pramstaller PP, Probst-Hensch N, Raitakari OT, Rettig R, Ridker PM, Rivadeneira F, Robino A, Rosas SE, Ruderfer D, Ruggiero D, Saba Y, Sala C, Schmidt H, Schmidt R, Scott RJ, Sedaghat S, Smith AV, Sorice R, Stengel B, Stracke S, Strauch K, Toniolo D, Uitterlinden AG, Ulivi S, Viikari JS, Völker U, Vollenweider P, Völzke H, Vuckovic D, Waldenberger M, Wang JJ, Yang Q, Chasman DI, Tromp G, Snieder H, Heid IM, Fox CS, Köttgen A, Pattaro C, Böger CA, Fuchsberger C. Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Sci Rep. 2017 May 26;7:46835. doi: 10.1038/srep46835. PMID: 28548086; PMCID: PMC5445557.
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Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity.

Archives of general psychiatry

Ernst C, Marshall CR, Shen Y, Metcalfe K, Rosenfeld J, Hodge JC, Torres A, Blumenthal I, Chiang C, Pillalamarri V, Crapper L, Diallo AB, Ruderfer D, Pereira S, Sklar P, Purcell S, Wildin RS, Spencer AC, Quade BF, Harris DJ, Lemyre E, Wu BL, Stavropoulos DJ, Geraghty MT, Shaffer LG, Morton CC, Scherer SW, Gusella JF, Talkowski ME.
PMID: 23044507
Arch Gen Psychiatry. 2012 Dec;69(12):1238-46. doi: 10.1001/archgenpsychiatry.2012.660.

CONTEXT Brain-derived neurotrophic factor (BDNF) is suspected of being a causative factor in psychiatric disorders based on case reports or studies involving large structural anomalies. OBJECTIVE To determine the involvement of BDNF in human psychopathology. DESIGN Case-control study. SETTING...

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Ernst C, Marshall CR, Shen Y, et al. Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity. Arch Gen Psychiatry. 2012;69(12):1238-46doi: 10.1001/archgenpsychiatry.2012.660.
Ernst, C., Marshall, C. R., Shen, Y., Metcalfe, K., Rosenfeld, J., Hodge, J. C., Torres, A., Blumenthal, I., Chiang, C., Pillalamarri, V., Crapper, L., Diallo, A. B., Ruderfer, D., Pereira, S., Sklar, P., Purcell, S., Wildin, R. S., Spencer, A. C., Quade, B. F., Harris, D. J., Lemyre, E., Wu, B. L., Stavropoulos, D. J., Geraghty, M. T., Shaffer, L. G., Morton, C. C., Scherer, S. W., Gusella, J. F., & Talkowski, M. E. (2012). Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity. Archives of general psychiatry, 69(12), 1238-46. https://doi.org/10.1001/archgenpsychiatry.2012.660
Ernst, Carl, et al. "Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity." Archives of general psychiatry vol. 69,12 (2012): 1238-46. doi: https://doi.org/10.1001/archgenpsychiatry.2012.660
Ernst C, Marshall CR, Shen Y, Metcalfe K, Rosenfeld J, Hodge JC, Torres A, Blumenthal I, Chiang C, Pillalamarri V, Crapper L, Diallo AB, Ruderfer D, Pereira S, Sklar P, Purcell S, Wildin RS, Spencer AC, Quade BF, Harris DJ, Lemyre E, Wu BL, Stavropoulos DJ, Geraghty MT, Shaffer LG, Morton CC, Scherer SW, Gusella JF, Talkowski ME. Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity. Arch Gen Psychiatry. 2012 Dec;69(12):1238-46. doi: 10.1001/archgenpsychiatry.2012.660. PMID: 23044507; PMCID: PMC3590016.
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Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.

Molecular psychiatry

Song J, Bergen SE, Di Florio A, Karlsson R, Charney A, Ruderfer DM, Stahl EA, Chambert KD, Moran JL, Gordon-Smith K, Forty L, Green EK, Jones I, Jones L, Scolnick EM, Sklar P, Smoller JW, Lichtenstein P, Hultman C, Craddock N, Landén M.
PMID: 28194006
Mol Psychiatry. 2017 Aug;22(8):1223. doi: 10.1038/mp.2016.246. Epub 2017 Feb 14.

This corrects the article DOI: 10.1038/mp.2015.165.

Cite
Song J, Bergen SE, Di Florio A, et al. Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder. Mol Psychiatry. 2017;22(8):1223doi: 10.1038/mp.2016.246.
Song, J., Bergen, S. E., Di Florio, A., Karlsson, R., Charney, A., Ruderfer, D. M., Stahl, E. A., Chambert, K. D., Moran, J. L., Gordon-Smith, K., Forty, L., Green, E. K., Jones, I., Jones, L., Scolnick, E. M., Sklar, P., Smoller, J. W., Lichtenstein, P., Hultman, C., Craddock, N., & Landén, M. (2017). Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder. Molecular psychiatry, 22(8), 1223. https://doi.org/10.1038/mp.2016.246
Song, J, et al. "Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder." Molecular psychiatry vol. 22,8 (2017): 1223. doi: https://doi.org/10.1038/mp.2016.246
Song J, Bergen SE, Di Florio A, Karlsson R, Charney A, Ruderfer DM, Stahl EA, Chambert KD, Moran JL, Gordon-Smith K, Forty L, Green EK, Jones I, Jones L, Scolnick EM, Sklar P, Smoller JW, Lichtenstein P, Hultman C, Craddock N, Landén M. Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder. Mol Psychiatry. 2017 Aug;22(8):1223. doi: 10.1038/mp.2016.246. Epub 2017 Feb 14. PMID: 28194006; PMCID: PMC7608474.
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