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Familial risk and heritability of intellectual disability: a population-based cohort study in Sweden.

Journal of child psychology and psychiatry, and allied disciplines

Lichtenstein P, Tideman M, Sullivan PF, Serlachius E, Larsson H, Kuja-Halkola R, Butwicka A.
PMID: 34921396
J Child Psychol Psychiatry. 2021 Dec 18; doi: 10.1111/jcpp.13560. Epub 2021 Dec 18.

BACKGROUND: Intellectual disability (ID) aggregates in families, but factors affecting individual risk and heritability estimates remain unknown.METHODS: A population-based family cohort study of 4,165,785 individuals born 1973-2013 in Sweden, including 37,787 ID individuals and their relatives. The relative risks...

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Lichtenstein P, Tideman M, Sullivan PF, et al. Familial risk and heritability of intellectual disability: a population-based cohort study in Sweden. J Child Psychol Psychiatry. 2021;doi: 10.1111/jcpp.13560.
Lichtenstein, P., Tideman, M., Sullivan, P. F., Serlachius, E., Larsson, H., Kuja-Halkola, R., & Butwicka, A. (2021). Familial risk and heritability of intellectual disability: a population-based cohort study in Sweden. Journal of child psychology and psychiatry, and allied disciplines, . https://doi.org/10.1111/jcpp.13560
Lichtenstein, Paul, et al. "Familial risk and heritability of intellectual disability: a population-based cohort study in Sweden." Journal of child psychology and psychiatry, and allied disciplines vol. (2021). doi: https://doi.org/10.1111/jcpp.13560
Lichtenstein P, Tideman M, Sullivan PF, Serlachius E, Larsson H, Kuja-Halkola R, Butwicka A. Familial risk and heritability of intellectual disability: a population-based cohort study in Sweden. J Child Psychol Psychiatry. 2021 Dec 18; doi: 10.1111/jcpp.13560. Epub 2021 Dec 18. PMID: 34921396.
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The state of the science in psychiatric genomics.

Psychological medicine

Sullivan PF, Kendler KS.
PMID: 33431078
Psychol Med. 2021 Oct;51(13):2145-2147. doi: 10.1017/S0033291720004900. Epub 2021 Jan 12.

No abstract available.

Cite
Sullivan PF, Kendler KS. The state of the science in psychiatric genomics. Psychol Med. 2021;51(13):2145-2147doi: 10.1017/S0033291720004900.
Sullivan, P. F., & Kendler, K. S. (2021). The state of the science in psychiatric genomics. Psychological medicine, 51(13), 2145-2147. https://doi.org/10.1017/S0033291720004900
Sullivan, Patrick F, and Kendler, Kenneth S. "The state of the science in psychiatric genomics." Psychological medicine vol. 51,13 (2021): 2145-2147. doi: https://doi.org/10.1017/S0033291720004900
Sullivan PF, Kendler KS. The state of the science in psychiatric genomics. Psychol Med. 2021 Oct;51(13):2145-2147. doi: 10.1017/S0033291720004900. Epub 2021 Jan 12. PMID: 33431078.
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Editorial overview: Rare CNV disorders and neuropsychiatric phenotypes: opportunities, challenges, solutions.

Current opinion in genetics & development

Mulle JG, Sullivan PF, Hjerling-Leffler J.
PMID: 34059379
Curr Opin Genet Dev. 2021 Jun;68:iii-ix. doi: 10.1016/j.gde.2021.05.002. Epub 2021 May 28.

No abstract available.

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Mulle JG, Sullivan PF, Hjerling-Leffler J. Editorial overview: Rare CNV disorders and neuropsychiatric phenotypes: opportunities, challenges, solutions. Curr Opin Genet Dev. 2021;68:iii-ixdoi: 10.1016/j.gde.2021.05.002.
Mulle, J. G., Sullivan, P. F., & Hjerling-Leffler, J. (2021). Editorial overview: Rare CNV disorders and neuropsychiatric phenotypes: opportunities, challenges, solutions. Current opinion in genetics & development, 68iii-ix. https://doi.org/10.1016/j.gde.2021.05.002
Mulle, Jennifer Gladys, et al. "Editorial overview: Rare CNV disorders and neuropsychiatric phenotypes: opportunities, challenges, solutions." Current opinion in genetics & development vol. 68 (2021): iii-ix. doi: https://doi.org/10.1016/j.gde.2021.05.002
Mulle JG, Sullivan PF, Hjerling-Leffler J. Editorial overview: Rare CNV disorders and neuropsychiatric phenotypes: opportunities, challenges, solutions. Curr Opin Genet Dev. 2021 Jun;68:iii-ix. doi: 10.1016/j.gde.2021.05.002. Epub 2021 May 28. PMID: 34059379.
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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population.

Nature neuroscience

Ganna A, Genovese G, Howrigan DP, Byrnes A, Kurki M, Zekavat SM, Whelan CW, Kals M, Nivard MG, Bloemendal A, Bloom JM, Goldstein JI, Poterba T, Seed C, Handsaker RE, Natarajan P, Mägi R, Gage D, Robinson EB, Metspalu A, Salomaa V, Suvisaari J, Purcell SM, Sklar P, Kathiresan S, Daly MJ, McCarroll SA, Sullivan PF, Palotie A, Esko T, Hultman C, Neale BM.
PMID: 27694993
Nat Neurosci. 2016 Dec;19(12):1563-1565. doi: 10.1038/nn.4404. Epub 2016 Oct 03.

Disruptive, damaging ultra-rare variants in highly constrained genes are enriched in individuals with neurodevelopmental disorders. In the general population, this class of variants was associated with a decrease in years of education (YOE). This effect was stronger among highly...

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Ganna A, Genovese G, Howrigan DP, et al. Ultra-rare disruptive and damaging mutations influence educational attainment in the general population. Nat Neurosci. 2016;19(12):1563-1565doi: 10.1038/nn.4404.
Ganna, A., Genovese, G., Howrigan, D. P., Byrnes, A., Kurki, M., Zekavat, S. M., Whelan, C. W., Kals, M., Nivard, M. G., Bloemendal, A., Bloom, J. M., Goldstein, J. I., Poterba, T., Seed, C., Handsaker, R. E., Natarajan, P., Mägi, R., Gage, D., Robinson, E. B., Metspalu, A., Salomaa, V., Suvisaari, J., Purcell, S. M., Sklar, P., Kathiresan, S., Daly, M. J., McCarroll, S. A., Sullivan, P. F., Palotie, A., Esko, T., Hultman, C., & Neale, B. M. (2016). Ultra-rare disruptive and damaging mutations influence educational attainment in the general population. Nature neuroscience, 19(12), 1563-1565. https://doi.org/10.1038/nn.4404
Ganna, Andrea, et al. "Ultra-rare disruptive and damaging mutations influence educational attainment in the general population." Nature neuroscience vol. 19,12 (2016): 1563-1565. doi: https://doi.org/10.1038/nn.4404
Ganna A, Genovese G, Howrigan DP, Byrnes A, Kurki M, Zekavat SM, Whelan CW, Kals M, Nivard MG, Bloemendal A, Bloom JM, Goldstein JI, Poterba T, Seed C, Handsaker RE, Natarajan P, Mägi R, Gage D, Robinson EB, Metspalu A, Salomaa V, Suvisaari J, Purcell SM, Sklar P, Kathiresan S, Daly MJ, McCarroll SA, Sullivan PF, Palotie A, Esko T, Hultman C, Neale BM. Ultra-rare disruptive and damaging mutations influence educational attainment in the general population. Nat Neurosci. 2016 Dec;19(12):1563-1565. doi: 10.1038/nn.4404. Epub 2016 Oct 03. PMID: 27694993; PMCID: PMC5127781.
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Don't give up on GWAS.

Molecular psychiatry

Sullivan P.
PMID: 21826059
Mol Psychiatry. 2012 Jan;17(1):2-3. doi: 10.1038/mp.2011.94. Epub 2011 Aug 09.

No abstract available.

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Sullivan P. Don't give up on GWAS. Mol Psychiatry. 2011;17(1):2-3doi: 10.1038/mp.2011.94.
Sullivan, P. (2012). Don't give up on GWAS. Molecular psychiatry, 17(1), 2-3. https://doi.org/10.1038/mp.2011.94
Sullivan, P. "Don't give up on GWAS." Molecular psychiatry vol. 17,1 (2012): 2-3. doi: https://doi.org/10.1038/mp.2011.94
Sullivan P. Don't give up on GWAS. Mol Psychiatry. 2012 Jan;17(1):2-3. doi: 10.1038/mp.2011.94. Epub 2011 Aug 09. PMID: 21826059; PMCID: PMC4187109.
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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: 33483695
Mol Psychiatry. 2021 Sep;26(9):5239-5250. doi: 10.1038/s41380-020-01006-9. Epub 2021 Jan 22.

Bipolar disorder (BD) is a serious mental illness with substantial common variant heritability. However, the role of rare coding variation in BD is not well established. We examined the protein-coding (exonic) sequences of 3,987 unrelated individuals with BD and...

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Jia X, Goes FS, Locke AE, et al. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Mol Psychiatry. 2021;26(9):5239-5250doi: 10.1038/s41380-020-01006-9.
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). Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular psychiatry, 26(9), 5239-5250. https://doi.org/10.1038/s41380-020-01006-9
Jia, Xiaoming, et al. "Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder." Molecular psychiatry vol. 26,9 (2021): 5239-5250. doi: https://doi.org/10.1038/s41380-020-01006-9
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. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Mol Psychiatry. 2021 Sep;26(9):5239-5250. doi: 10.1038/s41380-020-01006-9. Epub 2021 Jan 22. PMID: 33483695; PMCID: PMC8295400.
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Genetic association of FMRP targets with psychiatric disorders.

Molecular psychiatry

Clifton NE, Rees E, Holmans PA, Pardiñas AF, Harwood JC, Di Florio A, Kirov G, Walters JTR, O'Donovan MC, Owen MJ, Hall J, Pocklington AJ.
PMID: 33077856
Mol Psychiatry. 2021 Jul;26(7):2977-2990. doi: 10.1038/s41380-020-00912-2. Epub 2020 Oct 19.

Genes encoding the mRNA targets of fragile X mental retardation protein (FMRP) are enriched for genetic association with psychiatric disorders. However, many FMRP targets possess functions that are themselves genetically associated with psychiatric disorders, including synaptic transmission and plasticity,...

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Clifton NE, Rees E, Holmans PA, et al. Genetic association of FMRP targets with psychiatric disorders. Mol Psychiatry. 2020;26(7):2977-2990doi: 10.1038/s41380-020-00912-2.
Clifton, N. E., Rees, E., Holmans, P. A., Pardiñas, A. F., Harwood, J. C., Di Florio, A., Kirov, G., Walters, J. T. R., O'Donovan, M. C., Owen, M. J., Hall, J., & Pocklington, A. J. (2021). Genetic association of FMRP targets with psychiatric disorders. Molecular psychiatry, 26(7), 2977-2990. https://doi.org/10.1038/s41380-020-00912-2
Clifton, Nicholas E, et al. "Genetic association of FMRP targets with psychiatric disorders." Molecular psychiatry vol. 26,7 (2021): 2977-2990. doi: https://doi.org/10.1038/s41380-020-00912-2
Clifton NE, Rees E, Holmans PA, Pardiñas AF, Harwood JC, Di Florio A, Kirov G, Walters JTR, O'Donovan MC, Owen MJ, Hall J, Pocklington AJ. Genetic association of FMRP targets with psychiatric disorders. Mol Psychiatry. 2021 Jul;26(7):2977-2990. doi: 10.1038/s41380-020-00912-2. Epub 2020 Oct 19. PMID: 33077856; PMCID: PMC8505260.
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Genetic heterogeneity and subtypes of major depression.

Molecular psychiatry

Nguyen TD, Harder A, Xiong Y, Kowalec K, Hägg S, Cai N, Kuja-Halkola R, Dalman C, Sullivan PF, Lu Y.
PMID: 34997191
Mol Psychiatry. 2022 Jan 08; doi: 10.1038/s41380-021-01413-6. Epub 2022 Jan 08.

Major depression (MD) is a heterogeneous disorder; however, the extent to which genetic factors distinguish MD patient subgroups (genetic heterogeneity) remains uncertain. This study sought evidence for genetic heterogeneity in MD. Using UK Biobank cohort, the authors defined 16...

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Nguyen TD, Harder A, Xiong Y, et al. Genetic heterogeneity and subtypes of major depression. Mol Psychiatry. 2022;doi: 10.1038/s41380-021-01413-6.
Nguyen, T. D., Harder, A., Xiong, Y., Kowalec, K., Hägg, S., Cai, N., Kuja-Halkola, R., Dalman, C., Sullivan, P. F., & Lu, Y. (2022). Genetic heterogeneity and subtypes of major depression. Molecular psychiatry, . https://doi.org/10.1038/s41380-021-01413-6
Nguyen, Thuy-Dung, et al. "Genetic heterogeneity and subtypes of major depression." Molecular psychiatry vol. (2022). doi: https://doi.org/10.1038/s41380-021-01413-6
Nguyen TD, Harder A, Xiong Y, Kowalec K, Hägg S, Cai N, Kuja-Halkola R, Dalman C, Sullivan PF, Lu Y. Genetic heterogeneity and subtypes of major depression. Mol Psychiatry. 2022 Jan 08; doi: 10.1038/s41380-021-01413-6. Epub 2022 Jan 08. PMID: 34997191.
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The state of the science in psychiatric genomics.

Psychological medicine

Sullivan PF, Kendler KS.
PMID: 33431078
Psychol Med. 2021 Oct;51(13):2145-2147. doi: 10.1017/S0033291720004900. Epub 2021 Jan 12.

No abstract available.

Cite
Sullivan PF, Kendler KS. The state of the science in psychiatric genomics. Psychol Med. 2021;51(13):2145-2147doi: 10.1017/S0033291720004900.
Sullivan, P. F., & Kendler, K. S. (2021). The state of the science in psychiatric genomics. Psychological medicine, 51(13), 2145-2147. https://doi.org/10.1017/S0033291720004900
Sullivan, Patrick F, and Kendler, Kenneth S. "The state of the science in psychiatric genomics." Psychological medicine vol. 51,13 (2021): 2145-2147. doi: https://doi.org/10.1017/S0033291720004900
Sullivan PF, Kendler KS. The state of the science in psychiatric genomics. Psychol Med. 2021 Oct;51(13):2145-2147. doi: 10.1017/S0033291720004900. Epub 2021 Jan 12. PMID: 33431078.
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DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia.

eLife

Hannon E, Dempster EL, Mansell G, Burrage J, Bass N, Bohlken MM, Corvin A, Curtis CJ, Dempster D, Di Forti M, Dinan TG, Donohoe G, Gaughran F, Gill M, Gillespie A, Gunasinghe C, Hulshoff HE, Hultman CM, Johansson V, Kahn RS, Kaprio J, Kenis G, Kowalec K, MacCabe J, McDonald C, McQuillin A, Morris DW, Murphy KC, Mustard CJ, Nenadic I, O'Donovan MC, Quattrone D, Richards AL, Rutten BP, St Clair D, Therman S, Toulopoulou T, Van Os J, Waddington JL, Sullivan P, Vassos E, Breen G, Collier DA, Murray RM, Schalkwyk LS, Mill J.
PMID: 33646943
Elife. 2021 Feb 26;10. doi: 10.7554/eLife.58430.

We performed a systematic analysis of blood DNA methylation profiles from 4483 participants from seven independent cohorts identifying differentially methylated positions (DMPs) associated with psychosis, schizophrenia, and treatment-resistant schizophrenia. Psychosis cases were characterized by significant differences in measures of...

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Hannon E, Dempster EL, Mansell G, et al. DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia. Elife. 2021;10doi: 10.7554/eLife.58430.
Hannon, E., Dempster, E. L., Mansell, G., Burrage, J., Bass, N., Bohlken, M. M., Corvin, A., Curtis, C. J., Dempster, D., Di Forti, M., Dinan, T. G., Donohoe, G., Gaughran, F., Gill, M., Gillespie, A., Gunasinghe, C., Hulshoff, H. E., Hultman, C. M., Johansson, V., Kahn, R. S., Kaprio, J., Kenis, G., Kowalec, K., MacCabe, J., McDonald, C., McQuillin, A., Morris, D. W., Murphy, K. C., Mustard, C. J., Nenadic, I., O'Donovan, M. C., Quattrone, D., Richards, A. L., Rutten, B. P., St Clair, D., Therman, S., Toulopoulou, T., Van Os, J., Waddington, J. L., Sullivan, P., Vassos, E., Breen, G., Collier, D. A., Murray, R. M., Schalkwyk, L. S., & Mill, J. (2021). DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia. eLife, 10. https://doi.org/10.7554/eLife.58430
Hannon, Eilis, et al. "DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia." eLife vol. 10 (2021). doi: https://doi.org/10.7554/eLife.58430
Hannon E, Dempster EL, Mansell G, Burrage J, Bass N, Bohlken MM, Corvin A, Curtis CJ, Dempster D, Di Forti M, Dinan TG, Donohoe G, Gaughran F, Gill M, Gillespie A, Gunasinghe C, Hulshoff HE, Hultman CM, Johansson V, Kahn RS, Kaprio J, Kenis G, Kowalec K, MacCabe J, McDonald C, McQuillin A, Morris DW, Murphy KC, Mustard CJ, Nenadic I, O'Donovan MC, Quattrone D, Richards AL, Rutten BP, St Clair D, Therman S, Toulopoulou T, Van Os J, Waddington JL, Sullivan P, Vassos E, Breen G, Collier DA, Murray RM, Schalkwyk LS, Mill J. DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia. Elife. 2021 Feb 26;10. doi: 10.7554/eLife.58430. PMID: 33646943; PMCID: PMC8009672.
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