Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 14 entries
Sorted by: Best Match Show Resources per page
Multiple comparisons in studies of gene x gene and gene x environment interaction.

American journal of human genetics

Kraft P.
PMID: 14973784
Am J Hum Genet. 2004 Mar;74(3):582-4; author reply 584-5. doi: 10.1086/382051.

No abstract available.

Cite
Kraft P. Multiple comparisons in studies of gene x gene and gene x environment interaction. Am J Hum Genet. 2004;74(3):582-4; author reply 584-5doi: 10.1086/382051.
Kraft, P. (2004). Multiple comparisons in studies of gene x gene and gene x environment interaction. American journal of human genetics, 74(3), 582-4; author reply 584-5. https://doi.org/10.1086/382051
Kraft, Peter. "Multiple comparisons in studies of gene x gene and gene x environment interaction." American journal of human genetics vol. 74,3 (2004): 582-4; author reply 584-5. doi: https://doi.org/10.1086/382051
Kraft P. Multiple comparisons in studies of gene x gene and gene x environment interaction. Am J Hum Genet. 2004 Mar;74(3):582-4; author reply 584-5. doi: 10.1086/382051. PMID: 14973784; PMCID: PMC1182271.
Copy Download .nbib Format: NLM
10 Years of GWAS Discovery: Biology, Function, and Translation.

American journal of human genetics

Visscher PM, Wray NR, Zhang Q, Sklar P, McCarthy MI, Brown MA, Yang J.
PMID: 28686856
Am J Hum Genet. 2017 Jul 06;101(1):5-22. doi: 10.1016/j.ajhg.2017.06.005.

Application of the experimental design of genome-wide association studies (GWASs) is now 10 years old (young), and here we review the remarkable range of discoveries it has facilitated in population and complex-trait genetics, the biology of diseases, and translation...

Cite
Visscher PM, Wray NR, Zhang Q, et al. 10 Years of GWAS Discovery: Biology, Function, and Translation. Am J Hum Genet. 2017;101(1):5-22doi: 10.1016/j.ajhg.2017.06.005.
Visscher, P. M., Wray, N. R., Zhang, Q., Sklar, P., McCarthy, M. I., Brown, M. A., & Yang, J. (2017). 10 Years of GWAS Discovery: Biology, Function, and Translation. American journal of human genetics, 101(1), 5-22. https://doi.org/10.1016/j.ajhg.2017.06.005
Visscher, Peter M, et al. "10 Years of GWAS Discovery: Biology, Function, and Translation." American journal of human genetics vol. 101,1 (2017): 5-22. doi: https://doi.org/10.1016/j.ajhg.2017.06.005
Visscher PM, Wray NR, Zhang Q, Sklar P, McCarthy MI, Brown MA, Yang J. 10 Years of GWAS Discovery: Biology, Function, and Translation. Am J Hum Genet. 2017 Jul 06;101(1):5-22. doi: 10.1016/j.ajhg.2017.06.005. PMID: 28686856; PMCID: PMC5501872.
Copy Download .nbib Format: NLM
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium.

Behavior genetics

van den Berg SM, de Moor MH, Verweij KJ, Krueger RF, Luciano M, Arias Vasquez A, Matteson LK, Derringer J, Esko T, Amin N, Gordon SD, Hansell NK, Hart AB, Seppälä I, Huffman JE, Konte B, Lahti J, Lee M, Miller M, Nutile T, Tanaka T, Teumer A, Viktorin A, Wedenoja J, Abdellaoui A, Abecasis GR, Adkins DE, Agrawal A, Allik J, Appel K, Bigdeli TB, Busonero F, Campbell H, Costa PT, Smith GD, Davies G, de Wit H, Ding J, Engelhardt BE, Eriksson JG, Fedko IO, Ferrucci L, Franke B, Giegling I, Grucza R, Hartmann AM, Heath AC, Heinonen K, Henders AK, Homuth G, Hottenga JJ, Iacono WG, Janzing J, Jokela M, Karlsson R, Kemp JP, Kirkpatrick MG, Latvala A, Lehtimäki T, Liewald DC, Madden PA, Magri C, Magnusson PK, Marten J, Maschio A, Mbarek H, Medland SE, Mihailov E, Milaneschi Y, Montgomery GW, Nauck M, Nivard MG, Ouwens KG, Palotie A, Pettersson E, Polasek O, Qian Y, Pulkki-Råback L, Raitakari OT, Realo A, Rose RJ, Ruggiero D, Schmidt CO, Slutske WS, Sorice R, Starr JM, St Pourcain B, Sutin AR, Timpson NJ, Trochet H, Vermeulen S, Vuoksimaa E, Widen E, Wouda J, Wright MJ, Zgaga L, Porteous D, Minelli A, Palmer AA, Rujescu D, Ciullo M, Hayward C, Rudan I, Metspalu A, Kaprio J, Deary IJ, Räikkönen K, Wilson JF, Keltikangas-Järvinen L, Bierut LJ, Hettema JM, Grabe HJ, Penninx BW, van Duijn CM, Evans DM, Schlessinger D, Pedersen NL, Terracciano A, McGue M, Martin NG, Boomsma DI.
PMID: 26362575
Behav Genet. 2016 Mar;46(2):170-82. doi: 10.1007/s10519-015-9735-5. Epub 2015 Sep 11.

Extraversion is a relatively stable and heritable personality trait associated with numerous psychosocial, lifestyle and health outcomes. Despite its substantial heritability, no genetic variants have been detected in previous genome-wide association (GWA) studies, which may be due to relatively...

Cite
van den Berg SM, de Moor MH, Verweij KJ, et al. Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behav Genet. 2015;46(2):170-82doi: 10.1007/s10519-015-9735-5.
van den Berg, S. M., de Moor, M. H., Verweij, K. J., Krueger, R. F., Luciano, M., Arias Vasquez, A., Matteson, L. K., Derringer, J., Esko, T., Amin, N., Gordon, S. D., Hansell, N. K., Hart, A. B., Seppälä, I., Huffman, J. E., Konte, B., Lahti, J., Lee, M., Miller, M., Nutile, T., Tanaka, T., Teumer, A., Viktorin, A., Wedenoja, J., Abdellaoui, A., Abecasis, G. R., Adkins, D. E., Agrawal, A., Allik, J., Appel, K., Bigdeli, T. B., Busonero, F., Campbell, H., Costa, P. T., Smith, G. D., Davies, G., de Wit, H., Ding, J., Engelhardt, B. E., Eriksson, J. G., Fedko, I. O., Ferrucci, L., Franke, B., Giegling, I., Grucza, R., Hartmann, A. M., Heath, A. C., Heinonen, K., Henders, A. K., Homuth, G., Hottenga, J. J., Iacono, W. G., Janzing, J., Jokela, M., Karlsson, R., Kemp, J. P., Kirkpatrick, M. G., Latvala, A., Lehtimäki, T., Liewald, D. C., Madden, P. A., Magri, C., Magnusson, P. K., Marten, J., Maschio, A., Mbarek, H., Medland, S. E., Mihailov, E., Milaneschi, Y., Montgomery, G. W., Nauck, M., Nivard, M. G., Ouwens, K. G., Palotie, A., Pettersson, E., Polasek, O., Qian, Y., Pulkki-Råback, L., Raitakari, O. T., Realo, A., Rose, R. J., Ruggiero, D., Schmidt, C. O., Slutske, W. S., Sorice, R., Starr, J. M., St Pourcain, B., Sutin, A. R., Timpson, N. J., Trochet, H., Vermeulen, S., Vuoksimaa, E., Widen, E., Wouda, J., Wright, M. J., Zgaga, L., Porteous, D., Minelli, A., Palmer, A. A., Rujescu, D., Ciullo, M., Hayward, C., Rudan, I., Metspalu, A., Kaprio, J., Deary, I. J., Räikkönen, K., Wilson, J. F., Keltikangas-Järvinen, L., Bierut, L. J., Hettema, J. M., Grabe, H. J., Penninx, B. W., van Duijn, C. M., Evans, D. M., Schlessinger, D., Pedersen, N. L., Terracciano, A., McGue, M., Martin, N. G., & Boomsma, D. I. (2016). Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behavior genetics, 46(2), 170-82. https://doi.org/10.1007/s10519-015-9735-5
van den Berg, Stéphanie M, et al. "Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium." Behavior genetics vol. 46,2 (2016): 170-82. doi: https://doi.org/10.1007/s10519-015-9735-5
van den Berg SM, de Moor MH, Verweij KJ, Krueger RF, Luciano M, Arias Vasquez A, Matteson LK, Derringer J, Esko T, Amin N, Gordon SD, Hansell NK, Hart AB, Seppälä I, Huffman JE, Konte B, Lahti J, Lee M, Miller M, Nutile T, Tanaka T, Teumer A, Viktorin A, Wedenoja J, Abdellaoui A, Abecasis GR, Adkins DE, Agrawal A, Allik J, Appel K, Bigdeli TB, Busonero F, Campbell H, Costa PT, Smith GD, Davies G, de Wit H, Ding J, Engelhardt BE, Eriksson JG, Fedko IO, Ferrucci L, Franke B, Giegling I, Grucza R, Hartmann AM, Heath AC, Heinonen K, Henders AK, Homuth G, Hottenga JJ, Iacono WG, Janzing J, Jokela M, Karlsson R, Kemp JP, Kirkpatrick MG, Latvala A, Lehtimäki T, Liewald DC, Madden PA, Magri C, Magnusson PK, Marten J, Maschio A, Mbarek H, Medland SE, Mihailov E, Milaneschi Y, Montgomery GW, Nauck M, Nivard MG, Ouwens KG, Palotie A, Pettersson E, Polasek O, Qian Y, Pulkki-Råback L, Raitakari OT, Realo A, Rose RJ, Ruggiero D, Schmidt CO, Slutske WS, Sorice R, Starr JM, St Pourcain B, Sutin AR, Timpson NJ, Trochet H, Vermeulen S, Vuoksimaa E, Widen E, Wouda J, Wright MJ, Zgaga L, Porteous D, Minelli A, Palmer AA, Rujescu D, Ciullo M, Hayward C, Rudan I, Metspalu A, Kaprio J, Deary IJ, Räikkönen K, Wilson JF, Keltikangas-Järvinen L, Bierut LJ, Hettema JM, Grabe HJ, Penninx BW, van Duijn CM, Evans DM, Schlessinger D, Pedersen NL, Terracciano A, McGue M, Martin NG, Boomsma DI. Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behav Genet. 2016 Mar;46(2):170-82. doi: 10.1007/s10519-015-9735-5. Epub 2015 Sep 11. PMID: 26362575; PMCID: PMC4751159.
Copy Download .nbib Format: NLM
Age dependency of the polygenic risk score for colorectal cancer.

American journal of human genetics

Li S, Hopper JL.
PMID: 33667395
Am J Hum Genet. 2021 Mar 04;108(3):525-526. doi: 10.1016/j.ajhg.2021.02.002.

No abstract available.

Cite
Li S, Hopper JL. Age dependency of the polygenic risk score for colorectal cancer. Am J Hum Genet. 2021;108(3):525-526doi: 10.1016/j.ajhg.2021.02.002.
Li, S., & Hopper, J. L. (2021). Age dependency of the polygenic risk score for colorectal cancer. American journal of human genetics, 108(3), 525-526. https://doi.org/10.1016/j.ajhg.2021.02.002
Li, Shuai, and Hopper, John L. "Age dependency of the polygenic risk score for colorectal cancer." American journal of human genetics vol. 108,3 (2021): 525-526. doi: https://doi.org/10.1016/j.ajhg.2021.02.002
Li S, Hopper JL. Age dependency of the polygenic risk score for colorectal cancer. Am J Hum Genet. 2021 Mar 04;108(3):525-526. doi: 10.1016/j.ajhg.2021.02.002. PMID: 33667395; PMCID: PMC8008484.
Copy Download .nbib Format: NLM
Psychiatric Genetics Begins to Find Its Footing.

The American journal of psychiatry

Smoller JW.
PMID: 31366225
Am J Psychiatry. 2019 Aug 01;176(8):609-614. doi: 10.1176/appi.ajp.2019.19060643.

No abstract available.

Cite
Smoller JW. Psychiatric Genetics Begins to Find Its Footing. Am J Psychiatry. 2019;176(8):609-614doi: 10.1176/appi.ajp.2019.19060643.
Smoller, J. W. (2019). Psychiatric Genetics Begins to Find Its Footing. The American journal of psychiatry, 176(8), 609-614. https://doi.org/10.1176/appi.ajp.2019.19060643
Smoller, Jordan W. "Psychiatric Genetics Begins to Find Its Footing." The American journal of psychiatry vol. 176,8 (2019): 609-614. doi: https://doi.org/10.1176/appi.ajp.2019.19060643
Smoller JW. Psychiatric Genetics Begins to Find Its Footing. Am J Psychiatry. 2019 Aug 01;176(8):609-614. doi: 10.1176/appi.ajp.2019.19060643. PMID: 31366225.
Copy Download .nbib Format: NLM
The role of genetics in subjective well-being.

Nature human behaviour

Røysamb E, Nes RB.
PMID: 30932049
Nat Hum Behav. 2019 Jan;3(1):3. doi: 10.1038/s41562-018-0494-1.

No abstract available.

Cite
Røysamb E, Nes RB. The role of genetics in subjective well-being. Nat Hum Behav. 2019;3(1):3doi: 10.1038/s41562-018-0494-1.
Røysamb, E., & Nes, R. B. (2019). The role of genetics in subjective well-being. Nature human behaviour, 3(1), 3. https://doi.org/10.1038/s41562-018-0494-1
Røysamb, Espen, and Nes, Ragnhild B. "The role of genetics in subjective well-being." Nature human behaviour vol. 3,1 (2019): 3. doi: https://doi.org/10.1038/s41562-018-0494-1
Røysamb E, Nes RB. The role of genetics in subjective well-being. Nat Hum Behav. 2019 Jan;3(1):3. doi: 10.1038/s41562-018-0494-1. PMID: 30932049.
Copy Download .nbib Format: NLM
Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening.

Genetics in medicine : official journal of the American College of Medical Genetics

Lu T, Zhou S, Wu H, Forgetta V, Greenwood CMT, Richards JB.
PMID: 33110269
Genet Med. 2021 Mar;23(3):508-515. doi: 10.1038/s41436-020-01007-7. Epub 2020 Oct 28.

PURPOSE: Identifying rare genetic causes of common diseases can improve diagnostic and treatment strategies, but incurs high costs. We tested whether individuals with common disease and low polygenic risk score (PRS) for that disease generated from less expensive genome-wide...

Cite
Lu T, Zhou S, Wu H, et al. Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening. Genet Med. 2020;23(3):508-515doi: 10.1038/s41436-020-01007-7.
Lu, T., Zhou, S., Wu, H., Forgetta, V., Greenwood, C. M. T., & Richards, J. B. (2021). Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening. Genetics in medicine : official journal of the American College of Medical Genetics, 23(3), 508-515. https://doi.org/10.1038/s41436-020-01007-7
Lu, Tianyuan, et al. "Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening." Genetics in medicine : official journal of the American College of Medical Genetics vol. 23,3 (2021): 508-515. doi: https://doi.org/10.1038/s41436-020-01007-7
Lu T, Zhou S, Wu H, Forgetta V, Greenwood CMT, Richards JB. Individuals with common diseases but with a low polygenic risk score could be prioritized for rare variant screening. Genet Med. 2021 Mar;23(3):508-515. doi: 10.1038/s41436-020-01007-7. Epub 2020 Oct 28. PMID: 33110269.
Copy Download .nbib Format: NLM
Assessing the evidence for shared genetic risks across psychiatric disorders and traits.

Psychological medicine

Martin J, Taylor MJ, Lichtenstein P.
PMID: 29198204
Psychol Med. 2018 Aug;48(11):1759-1774. doi: 10.1017/S0033291717003440. Epub 2017 Dec 04.

Genetic influences play a significant role in risk for psychiatric disorders, prompting numerous endeavors to further understand their underlying genetic architecture. In this paper, we summarize and review evidence from traditional twin studies and more recent genome-wide molecular genetic...

Cite
Martin J, Taylor MJ, Lichtenstein P. Assessing the evidence for shared genetic risks across psychiatric disorders and traits. Psychol Med. 2017;48(11):1759-1774doi: 10.1017/S0033291717003440.
Martin, J., Taylor, M. J., & Lichtenstein, P. (2018). Assessing the evidence for shared genetic risks across psychiatric disorders and traits. Psychological medicine, 48(11), 1759-1774. https://doi.org/10.1017/S0033291717003440
Martin, Joanna, et al. "Assessing the evidence for shared genetic risks across psychiatric disorders and traits." Psychological medicine vol. 48,11 (2018): 1759-1774. doi: https://doi.org/10.1017/S0033291717003440
Martin J, Taylor MJ, Lichtenstein P. Assessing the evidence for shared genetic risks across psychiatric disorders and traits. Psychol Med. 2018 Aug;48(11):1759-1774. doi: 10.1017/S0033291717003440. Epub 2017 Dec 04. PMID: 29198204; PMCID: PMC6088770.
Copy Download .nbib Format: NLM
Genetic Studies of Mental Illness: Are Children Being Left Behind?.

Journal of the American Academy of Child and Adolescent Psychiatry

Posner J, Biezonski D, Pieper S, Duarte CS.
PMID: 33385509
J Am Acad Child Adolesc Psychiatry. 2021 Jun;60(6):672-674. doi: 10.1016/j.jaac.2020.12.031. Epub 2020 Dec 29.

Understanding the genetic architecture of psychiatric disorders is paramount to linking psychopathologies to their genetic underpinnings. In turn, this knowledge can inform strategies for identifying high-risk individuals, early intervention, and development of personalized treatment approaches.

Cite
Posner J, Biezonski D, Pieper S, et al. Genetic Studies of Mental Illness: Are Children Being Left Behind?. J Am Acad Child Adolesc Psychiatry. 2020;60(6):672-674doi: 10.1016/j.jaac.2020.12.031.
Posner, J., Biezonski, D., Pieper, S., & Duarte, C. S. (2021). Genetic Studies of Mental Illness: Are Children Being Left Behind?. Journal of the American Academy of Child and Adolescent Psychiatry, 60(6), 672-674. https://doi.org/10.1016/j.jaac.2020.12.031
Posner, Jonathan, et al. "Genetic Studies of Mental Illness: Are Children Being Left Behind?." Journal of the American Academy of Child and Adolescent Psychiatry vol. 60,6 (2021): 672-674. doi: https://doi.org/10.1016/j.jaac.2020.12.031
Posner J, Biezonski D, Pieper S, Duarte CS. Genetic Studies of Mental Illness: Are Children Being Left Behind?. J Am Acad Child Adolesc Psychiatry. 2021 Jun;60(6):672-674. doi: 10.1016/j.jaac.2020.12.031. Epub 2020 Dec 29. PMID: 33385509; PMCID: PMC8184577.
Copy Download .nbib Format: NLM
Polygenic risk scores, prediction of psychiatric disorders, and the health of all of us.

The lancet. Psychiatry

Parens E, Matthews L, Appelbaum PS.
PMID: 32445683
Lancet Psychiatry. 2020 Jun;7(6):481. doi: 10.1016/S2215-0366(20)30185-1. Epub 2020 May 20.

No abstract available.

Cite
Parens E, Matthews L, Appelbaum PS. Polygenic risk scores, prediction of psychiatric disorders, and the health of all of us. Lancet Psychiatry. 2020;7(6):481doi: 10.1016/S2215-0366(20)30185-1.
Parens, E., Matthews, L., & Appelbaum, P. S. (2020). Polygenic risk scores, prediction of psychiatric disorders, and the health of all of us. The lancet. Psychiatry, 7(6), 481. https://doi.org/10.1016/S2215-0366(20)30185-1
Parens, Erik, et al. "Polygenic risk scores, prediction of psychiatric disorders, and the health of all of us." The lancet. Psychiatry vol. 7,6 (2020): 481. doi: https://doi.org/10.1016/S2215-0366(20)30185-1
Parens E, Matthews L, Appelbaum PS. Polygenic risk scores, prediction of psychiatric disorders, and the health of all of us. Lancet Psychiatry. 2020 Jun;7(6):481. doi: 10.1016/S2215-0366(20)30185-1. Epub 2020 May 20. PMID: 32445683.
Copy Download .nbib Format: NLM
What genome-wide association studies reveal about the association between intelligence and physical health, illness, and mortality.

Current opinion in psychology

Deary IJ, Harris SE, Hill WD.
PMID: 30071465
Curr Opin Psychol. 2019 Jun;27:6-12. doi: 10.1016/j.copsyc.2018.07.005. Epub 2018 Jul 23.

The associations between higher intelligence test scores from early life and later good health, fewer illnesses, and longer life are recent discoveries. Researchers are mapping the extent of these associations and trying to understanding them. Part of the intelligence-health...

Cite
Deary IJ, Harris SE, Hill WD. What genome-wide association studies reveal about the association between intelligence and physical health, illness, and mortality. Curr Opin Psychol. 2018;27:6-12doi: 10.1016/j.copsyc.2018.07.005.
Deary, I. J., Harris, S. E., & Hill, W. D. (2019). What genome-wide association studies reveal about the association between intelligence and physical health, illness, and mortality. Current opinion in psychology, 276-12. https://doi.org/10.1016/j.copsyc.2018.07.005
Deary, Ian J, et al. "What genome-wide association studies reveal about the association between intelligence and physical health, illness, and mortality." Current opinion in psychology vol. 27 (2019): 6-12. doi: https://doi.org/10.1016/j.copsyc.2018.07.005
Deary IJ, Harris SE, Hill WD. What genome-wide association studies reveal about the association between intelligence and physical health, illness, and mortality. Curr Opin Psychol. 2019 Jun;27:6-12. doi: 10.1016/j.copsyc.2018.07.005. Epub 2018 Jul 23. PMID: 30071465; PMCID: PMC6624475.
Copy Download .nbib Format: NLM
Clinical use of current polygenic risk scores may exacerbate health disparities.

Nature genetics

Martin AR, Kanai M, Kamatani Y, Okada Y, Neale BM, Daly MJ.
PMID: 30926966
Nat Genet. 2019 Apr;51(4):584-591. doi: 10.1038/s41588-019-0379-x. Epub 2019 Mar 29.

Polygenic risk scores (PRS) are poised to improve biomedical outcomes via precision medicine. However, the major ethical and scientific challenge surrounding clinical implementation of PRS is that those available today are several times more accurate in individuals of European...

Cite
Martin AR, Kanai M, Kamatani Y, et al. Clinical use of current polygenic risk scores may exacerbate health disparities. Nat Genet. 2019;51(4):584-591doi: 10.1038/s41588-019-0379-x.
Martin, A. R., Kanai, M., Kamatani, Y., Okada, Y., Neale, B. M., & Daly, M. J. (2019). Clinical use of current polygenic risk scores may exacerbate health disparities. Nature genetics, 51(4), 584-591. https://doi.org/10.1038/s41588-019-0379-x
Martin, Alicia R, et al. "Clinical use of current polygenic risk scores may exacerbate health disparities." Nature genetics vol. 51,4 (2019): 584-591. doi: https://doi.org/10.1038/s41588-019-0379-x
Martin AR, Kanai M, Kamatani Y, Okada Y, Neale BM, Daly MJ. Clinical use of current polygenic risk scores may exacerbate health disparities. Nat Genet. 2019 Apr;51(4):584-591. doi: 10.1038/s41588-019-0379-x. Epub 2019 Mar 29. PMID: 30926966; PMCID: PMC6563838.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 14 entries