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Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders.

JAMA psychiatry

Calle Sánchez X, Helenius D, Bybjerg-Grauholm J, Pedersen C, Hougaard DM, Børglum AD, Nordentoft M, Mors O, Mortensen PB, Geschwind DH, Montalbano S, Raznahan A, Thompson WK, Ingason A, Werge T.
PMID: 34817560
JAMA Psychiatry. 2022 Jan 01;79(1):59-69. doi: 10.1001/jamapsychiatry.2021.3392.

IMPORTANCE: Although the association between several recurrent genomic copy number variants (CNVs) and mental disorders has been studied for more than a decade, unbiased, population-based estimates of the prevalence, disease risks and trajectories, fertility, and mortality to contrast chromosomal...

Cite
Calle Sánchez X, Helenius D, Bybjerg-Grauholm J, et al. Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders. JAMA Psychiatry. 2022;79(1):59-69doi: 10.1001/jamapsychiatry.2021.3392.
Calle Sánchez, X., Helenius, D., Bybjerg-Grauholm, J., Pedersen, C., Hougaard, D. M., Børglum, A. D., Nordentoft, M., Mors, O., Mortensen, P. B., Geschwind, D. H., Montalbano, S., Raznahan, A., Thompson, W. K., Ingason, A., & Werge, T. (2022). Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders. JAMA psychiatry, 79(1), 59-69. https://doi.org/10.1001/jamapsychiatry.2021.3392
Calle Sánchez, Xabier, et al. "Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders." JAMA psychiatry vol. 79,1 (2022): 59-69. doi: https://doi.org/10.1001/jamapsychiatry.2021.3392
Calle Sánchez X, Helenius D, Bybjerg-Grauholm J, Pedersen C, Hougaard DM, Børglum AD, Nordentoft M, Mors O, Mortensen PB, Geschwind DH, Montalbano S, Raznahan A, Thompson WK, Ingason A, Werge T. Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders. JAMA Psychiatry. 2022 Jan 01;79(1):59-69. doi: 10.1001/jamapsychiatry.2021.3392. PMID: 34817560.
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EWAS of Monozygotic Twins Implicate a Role of mTOR Pathway in Pathogenesis of Tic Spectrum Disorder.

Genes

Hildonen M, Levy AM, Hansen CS, Bybjerg-Grauholm J, Skytthe A, Debes NM, Tan Q, Tümer Z.
PMID: 34680906
Genes (Basel). 2021 Sep 26;12(10). doi: 10.3390/genes12101510.

Tic spectrum disorder (TSD) is an umbrella term which includes Gilles de la Tourette syndrome (GTS) and chronic tic disorder (CTD). They are considered highly heritable, yet the genetic components remain largely unknown. In this study we aimed to...

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Hildonen M, Levy AM, Hansen CS, et al. EWAS of Monozygotic Twins Implicate a Role of mTOR Pathway in Pathogenesis of Tic Spectrum Disorder. Genes (Basel). 2021;12(10)doi: 10.3390/genes12101510.
Hildonen, M., Levy, A. M., Hansen, C. S., Bybjerg-Grauholm, J., Skytthe, A., Debes, N. M., Tan, Q., & Tümer, Z. (2021). EWAS of Monozygotic Twins Implicate a Role of mTOR Pathway in Pathogenesis of Tic Spectrum Disorder. Genes, 12(10), . https://doi.org/10.3390/genes12101510
Hildonen, Mathis, et al. "EWAS of Monozygotic Twins Implicate a Role of mTOR Pathway in Pathogenesis of Tic Spectrum Disorder." Genes vol. 12,10 (2021). doi: https://doi.org/10.3390/genes12101510
Hildonen M, Levy AM, Hansen CS, Bybjerg-Grauholm J, Skytthe A, Debes NM, Tan Q, Tümer Z. EWAS of Monozygotic Twins Implicate a Role of mTOR Pathway in Pathogenesis of Tic Spectrum Disorder. Genes (Basel). 2021 Sep 26;12(10). doi: 10.3390/genes12101510. PMID: 34680906; PMCID: PMC8535383.
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Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder.

European journal of human genetics : EJHG

Nudel R, Benros ME, Krebs MD, Allesøe RL, Lemvigh CK, Bybjerg-Grauholm J, Børglum AD, Daly MJ, Nordentoft M, Mors O, Hougaard DM, Mortensen PB, Buil A, Werge T, Rasmussen S, Thompson WK.
PMID: 33293699
Eur J Hum Genet. 2021 Aug;29(8):1316. doi: 10.1038/s41431-020-00772-y.

No abstract available.

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Nudel R, Benros ME, Krebs MD, et al. Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder. Eur J Hum Genet. 2021;29(8):1316doi: 10.1038/s41431-020-00772-y.
Nudel, R., Benros, M. E., Krebs, M. D., Allesøe, R. L., Lemvigh, C. K., Bybjerg-Grauholm, J., Børglum, A. D., Daly, M. J., Nordentoft, M., Mors, O., Hougaard, D. M., Mortensen, P. B., Buil, A., Werge, T., Rasmussen, S., & Thompson, W. K. (2021). Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder. European journal of human genetics : EJHG, 29(8), 1316. https://doi.org/10.1038/s41431-020-00772-y
Nudel, Ron, et al. "Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder." European journal of human genetics : EJHG vol. 29,8 (2021): 1316. doi: https://doi.org/10.1038/s41431-020-00772-y
Nudel R, Benros ME, Krebs MD, Allesøe RL, Lemvigh CK, Bybjerg-Grauholm J, Børglum AD, Daly MJ, Nordentoft M, Mors O, Hougaard DM, Mortensen PB, Buil A, Werge T, Rasmussen S, Thompson WK. Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder. Eur J Hum Genet. 2021 Aug;29(8):1316. doi: 10.1038/s41431-020-00772-y. PMID: 33293699; PMCID: PMC8385069.
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Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder.

Nature communications

Demontis D, Walters RK, Rajagopal VM, Waldman ID, Grove J, Als TD, Dalsgaard S, Ribasés M, Bybjerg-Grauholm J, Bækvad-Hansen M, Werge T, Nordentoft M, Mors O, Mortensen PB, Cormand B, Hougaard DM, Neale BM, Franke B, Faraone SV, Børglum AD.
PMID: 33589642
Nat Commun. 2021 Feb 15;12(1):1166. doi: 10.1038/s41467-021-21566-w.

No abstract available.

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Demontis D, Walters RK, Rajagopal VM, et al. Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Nat Commun. 2021;12(1):1166doi: 10.1038/s41467-021-21566-w.
Demontis, D., Walters, R. K., Rajagopal, V. M., Waldman, I. D., Grove, J., Als, T. D., Dalsgaard, S., Ribasés, M., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Werge, T., Nordentoft, M., Mors, O., Mortensen, P. B., Cormand, B., Hougaard, D. M., Neale, B. M., Franke, B., Faraone, S. V., & Børglum, A. D. (2021). Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Nature communications, 12(1), 1166. https://doi.org/10.1038/s41467-021-21566-w
Demontis, Ditte, et al. "Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder." Nature communications vol. 12,1 (2021): 1166. doi: https://doi.org/10.1038/s41467-021-21566-w
Demontis D, Walters RK, Rajagopal VM, Waldman ID, Grove J, Als TD, Dalsgaard S, Ribasés M, Bybjerg-Grauholm J, Bækvad-Hansen M, Werge T, Nordentoft M, Mors O, Mortensen PB, Cormand B, Hougaard DM, Neale BM, Franke B, Faraone SV, Børglum AD. Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Nat Commun. 2021 Feb 15;12(1):1166. doi: 10.1038/s41467-021-21566-w. PMID: 33589642; PMCID: PMC7884673.
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Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders.

JAMA psychiatry

Calle Sánchez X, Helenius D, Bybjerg-Grauholm J, Pedersen C, Hougaard DM, Børglum AD, Nordentoft M, Mors O, Mortensen PB, Geschwind DH, Montalbano S, Raznahan A, Thompson WK, Ingason A, Werge T.
PMID: 34817560
JAMA Psychiatry. 2022 Jan 01;79(1):59-69. doi: 10.1001/jamapsychiatry.2021.3392.

IMPORTANCE: Although the association between several recurrent genomic copy number variants (CNVs) and mental disorders has been studied for more than a decade, unbiased, population-based estimates of the prevalence, disease risks and trajectories, fertility, and mortality to contrast chromosomal...

Cite
Calle Sánchez X, Helenius D, Bybjerg-Grauholm J, et al. Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders. JAMA Psychiatry. 2022;79(1):59-69doi: 10.1001/jamapsychiatry.2021.3392.
Calle Sánchez, X., Helenius, D., Bybjerg-Grauholm, J., Pedersen, C., Hougaard, D. M., Børglum, A. D., Nordentoft, M., Mors, O., Mortensen, P. B., Geschwind, D. H., Montalbano, S., Raznahan, A., Thompson, W. K., Ingason, A., & Werge, T. (2022). Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders. JAMA psychiatry, 79(1), 59-69. https://doi.org/10.1001/jamapsychiatry.2021.3392
Calle Sánchez, Xabier, et al. "Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders." JAMA psychiatry vol. 79,1 (2022): 59-69. doi: https://doi.org/10.1001/jamapsychiatry.2021.3392
Calle Sánchez X, Helenius D, Bybjerg-Grauholm J, Pedersen C, Hougaard DM, Børglum AD, Nordentoft M, Mors O, Mortensen PB, Geschwind DH, Montalbano S, Raznahan A, Thompson WK, Ingason A, Werge T. Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders. JAMA Psychiatry. 2022 Jan 01;79(1):59-69. doi: 10.1001/jamapsychiatry.2021.3392. PMID: 34817560.
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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.

Cite
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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Polygenic liability, stressful life events and risk for secondary-treated depression in early life: a nationwide register-based case-cohort study.

Psychological medicine

Musliner KL, Andersen KK, Agerbo E, Albiñana C, Vilhjalmsson BJ, Rajagopal VM, Bybjerg-Grauholm J, Bækved-Hansen M, Pedersen CB, Pedersen MG, Munk-Olsen T, Benros ME, Als TD, Grove J, Werge T, Børglum AD, Hougaard DM, Mors O, Nordentoft M, Mortensen PB, Suppli NP.
PMID: 33949298
Psychol Med. 2021 May 05;1-10. doi: 10.1017/S0033291721001410. Epub 2021 May 05.

BACKGROUND: In this study, we examined the relationship between polygenic liability for depression and number of stressful life events (SLEs) as risk factors for early-onset depression treated in inpatient, outpatient or emergency room settings at psychiatric hospitals in Denmark.METHODS:...

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Musliner KL, Andersen KK, Agerbo E, et al. Polygenic liability, stressful life events and risk for secondary-treated depression in early life: a nationwide register-based case-cohort study. Psychol Med. 2021;1-10doi: 10.1017/S0033291721001410.
Musliner, K. L., Andersen, K. K., Agerbo, E., Albiñana, C., Vilhjalmsson, B. J., Rajagopal, V. M., Bybjerg-Grauholm, J., Bækved-Hansen, M., Pedersen, C. B., Pedersen, M. G., Munk-Olsen, T., Benros, M. E., Als, T. D., Grove, J., Werge, T., Børglum, A. D., Hougaard, D. M., Mors, O., Nordentoft, M., Mortensen, P. B., & Suppli, N. P. (2021). Polygenic liability, stressful life events and risk for secondary-treated depression in early life: a nationwide register-based case-cohort study. Psychological medicine, 1-10. https://doi.org/10.1017/S0033291721001410
Musliner, Katherine L, et al. "Polygenic liability, stressful life events and risk for secondary-treated depression in early life: a nationwide register-based case-cohort study." Psychological medicine vol. (2021): 1-10. doi: https://doi.org/10.1017/S0033291721001410
Musliner KL, Andersen KK, Agerbo E, Albiñana C, Vilhjalmsson BJ, Rajagopal VM, Bybjerg-Grauholm J, Bækved-Hansen M, Pedersen CB, Pedersen MG, Munk-Olsen T, Benros ME, Als TD, Grove J, Werge T, Børglum AD, Hougaard DM, Mors O, Nordentoft M, Mortensen PB, Suppli NP. Polygenic liability, stressful life events and risk for secondary-treated depression in early life: a nationwide register-based case-cohort study. Psychol Med. 2021 May 05;1-10. doi: 10.1017/S0033291721001410. Epub 2021 May 05. PMID: 33949298.
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Epidemiological characterisation of the first 785 SARS-CoV-2 Omicron variant cases in Denmark, December 2021.

Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin

Espenhain L, Funk T, Overvad M, Edslev SM, Fonager J, Ingham AC, Rasmussen M, Madsen SL, Espersen CH, Sieber RN, Stegger M, Gunalan V, Wilkowski B, Larsen NB, Legarth R, Cohen AS, Nielsen F, Lam JUH, Lavik KE, Karakis M, Spiess K, Marving E, Nielsen C, Wiid Svarrer C, Bybjerg-Grauholm J, Olsen SS, Jensen A, Krause TG, Müller L.
PMID: 34915977
Euro Surveill. 2021 Dec;26(50). doi: 10.2807/1560-7917.ES.2021.26.50.2101146.

By 9 December 2021, 785 SARS-CoV-2 Omicron variant cases have been identified in Denmark. Most cases were fully (76%) or booster-vaccinated (7.1%); 34 (4.3%) had a previous SARS-CoV-2 infection. The majority of cases with available information reported symptoms (509/666;...

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Espenhain L, Funk T, Overvad M, et al. Epidemiological characterisation of the first 785 SARS-CoV-2 Omicron variant cases in Denmark, December 2021. Euro Surveill. 2021;26(50)doi: 10.2807/1560-7917.ES.2021.26.50.2101146.
Espenhain, L., Funk, T., Overvad, M., Edslev, S. M., Fonager, J., Ingham, A. C., Rasmussen, M., Madsen, S. L., Espersen, C. H., Sieber, R. N., Stegger, M., Gunalan, V., Wilkowski, B., Larsen, N. B., Legarth, R., Cohen, A. S., Nielsen, F., Lam, J. U. H., Lavik, K. E., Karakis, M., Spiess, K., Marving, E., Nielsen, C., Wiid Svarrer, C., Bybjerg-Grauholm, J., Olsen, S. S., Jensen, A., Krause, T. G., & Müller, L. (2021). Epidemiological characterisation of the first 785 SARS-CoV-2 Omicron variant cases in Denmark, December 2021. Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin, 26(50), . https://doi.org/10.2807/1560-7917.ES.2021.26.50.2101146
Espenhain, Laura, et al. "Epidemiological characterisation of the first 785 SARS-CoV-2 Omicron variant cases in Denmark, December 2021." Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin vol. 26,50 (2021). doi: https://doi.org/10.2807/1560-7917.ES.2021.26.50.2101146
Espenhain L, Funk T, Overvad M, Edslev SM, Fonager J, Ingham AC, Rasmussen M, Madsen SL, Espersen CH, Sieber RN, Stegger M, Gunalan V, Wilkowski B, Larsen NB, Legarth R, Cohen AS, Nielsen F, Lam JUH, Lavik KE, Karakis M, Spiess K, Marving E, Nielsen C, Wiid Svarrer C, Bybjerg-Grauholm J, Olsen SS, Jensen A, Krause TG, Müller L. Epidemiological characterisation of the first 785 SARS-CoV-2 Omicron variant cases in Denmark, December 2021. Euro Surveill. 2021 Dec;26(50). doi: 10.2807/1560-7917.ES.2021.26.50.2101146. PMID: 34915977.
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Development of a Multiplex Real-Time PCR Assay for the Newborn Screening of SCID, SMA, and XLA.

International journal of neonatal screening

Gutierrez-Mateo C, Timonen A, Vaahtera K, Jaakkola M, Hougaard DM, Bybjerg-Grauholm J, Baekvad-Hansen M, Adamsen D, Filippov G, Dallaire S, Goldfarb D, Schoener D, Wu R.
PMID: 33072998
Int J Neonatal Screen. 2019 Nov 02;5(4):39. doi: 10.3390/ijns5040039. eCollection 2019 Dec.

Numerous studies have shown evidence supporting the benefits of universal newborn screening for primary immunodeficiencies (PID) and for Spinal Muscular Atrophy (SMA). We have developed a four-plex, real-time PCR assay to screen for Severe Combined Immune Deficiencies (SCID), X-linked...

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Gutierrez-Mateo C, Timonen A, Vaahtera K, et al. Development of a Multiplex Real-Time PCR Assay for the Newborn Screening of SCID, SMA, and XLA. Int J Neonatal Screen. 2019;5(4):39doi: 10.3390/ijns5040039.
Gutierrez-Mateo, C., Timonen, A., Vaahtera, K., Jaakkola, M., Hougaard, D. M., Bybjerg-Grauholm, J., Baekvad-Hansen, M., Adamsen, D., Filippov, G., Dallaire, S., Goldfarb, D., Schoener, D., & Wu, R. (2019). Development of a Multiplex Real-Time PCR Assay for the Newborn Screening of SCID, SMA, and XLA. International journal of neonatal screening, 5(4), 39. https://doi.org/10.3390/ijns5040039
Gutierrez-Mateo, Cristina, et al. "Development of a Multiplex Real-Time PCR Assay for the Newborn Screening of SCID, SMA, and XLA." International journal of neonatal screening vol. 5,4 (2019): 39. doi: https://doi.org/10.3390/ijns5040039
Gutierrez-Mateo C, Timonen A, Vaahtera K, Jaakkola M, Hougaard DM, Bybjerg-Grauholm J, Baekvad-Hansen M, Adamsen D, Filippov G, Dallaire S, Goldfarb D, Schoener D, Wu R. Development of a Multiplex Real-Time PCR Assay for the Newborn Screening of SCID, SMA, and XLA. Int J Neonatal Screen. 2019 Nov 02;5(4):39. doi: 10.3390/ijns5040039. eCollection 2019 Dec. PMID: 33072998; PMCID: PMC7510252.
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Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status.

JAMA psychiatry

Agerbo E, Trabjerg BB, Børglum AD, Schork AJ, Vilhjálmsson BJ, Pedersen CB, Hakulinen C, Albiñana C, Hougaard DM, Grove J, McGrath JJ, Bybjerg-Grauholm J, Mors O, Plana-Ripoll O, Werge T, Wray NR, Mortensen PB, Musliner KL.
PMID: 33439215
JAMA Psychiatry. 2021 Apr 01;78(4):387-397. doi: 10.1001/jamapsychiatry.2020.4172.

IMPORTANCE: Combining information on polygenic risk scores (PRSs) with other known risk factors could potentially improve the identification of risk of depression in the general population. However, to our knowledge, no study has estimated the association of PRS with...

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Agerbo E, Trabjerg BB, Børglum AD, et al. Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status. JAMA Psychiatry. 2021;78(4):387-397doi: 10.1001/jamapsychiatry.2020.4172.
Agerbo, E., Trabjerg, B. B., Børglum, A. D., Schork, A. J., Vilhjálmsson, B. J., Pedersen, C. B., Hakulinen, C., Albiñana, C., Hougaard, D. M., Grove, J., McGrath, J. J., Bybjerg-Grauholm, J., Mors, O., Plana-Ripoll, O., Werge, T., Wray, N. R., Mortensen, P. B., & Musliner, K. L. (2021). Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status. JAMA psychiatry, 78(4), 387-397. https://doi.org/10.1001/jamapsychiatry.2020.4172
Agerbo, Esben, et al. "Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status." JAMA psychiatry vol. 78,4 (2021): 387-397. doi: https://doi.org/10.1001/jamapsychiatry.2020.4172
Agerbo E, Trabjerg BB, Børglum AD, Schork AJ, Vilhjálmsson BJ, Pedersen CB, Hakulinen C, Albiñana C, Hougaard DM, Grove J, McGrath JJ, Bybjerg-Grauholm J, Mors O, Plana-Ripoll O, Werge T, Wray NR, Mortensen PB, Musliner KL. Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status. JAMA Psychiatry. 2021 Apr 01;78(4):387-397. doi: 10.1001/jamapsychiatry.2020.4172. PMID: 33439215; PMCID: PMC7807393.
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Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders.

JAMA psychiatry

Calle Sánchez X, Helenius D, Bybjerg-Grauholm J, Pedersen C, Hougaard DM, Børglum AD, Nordentoft M, Mors O, Mortensen PB, Geschwind DH, Montalbano S, Raznahan A, Thompson WK, Ingason A, Werge T.
PMID: 34817560
JAMA Psychiatry. 2021 Nov 24; doi: 10.1001/jamapsychiatry.2021.3392. Epub 2021 Nov 24.

IMPORTANCE: Although the association between several recurrent genomic copy number variants (CNVs) and mental disorders has been studied for more than a decade, unbiased, population-based estimates of the prevalence, disease risks and trajectories, fertility, and mortality to contrast chromosomal...

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Calle Sánchez X, Helenius D, Bybjerg-Grauholm J, et al. Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders. JAMA Psychiatry. 2021;doi: 10.1001/jamapsychiatry.2021.3392.
Calle Sánchez, X., Helenius, D., Bybjerg-Grauholm, J., Pedersen, C., Hougaard, D. M., Børglum, A. D., Nordentoft, M., Mors, O., Mortensen, P. B., Geschwind, D. H., Montalbano, S., Raznahan, A., Thompson, W. K., Ingason, A., & Werge, T. (2021). Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders. JAMA psychiatry, . https://doi.org/10.1001/jamapsychiatry.2021.3392
Calle Sánchez, Xabier, et al. "Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders." JAMA psychiatry vol. (2021). doi: https://doi.org/10.1001/jamapsychiatry.2021.3392
Calle Sánchez X, Helenius D, Bybjerg-Grauholm J, Pedersen C, Hougaard DM, Børglum AD, Nordentoft M, Mors O, Mortensen PB, Geschwind DH, Montalbano S, Raznahan A, Thompson WK, Ingason A, Werge T. Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders. JAMA Psychiatry. 2021 Nov 24; doi: 10.1001/jamapsychiatry.2021.3392. Epub 2021 Nov 24. PMID: 34817560.
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Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status.

JAMA psychiatry

Agerbo E, Trabjerg BB, Børglum AD, Schork AJ, Vilhjálmsson BJ, Pedersen CB, Hakulinen C, Albiñana C, Hougaard DM, Grove J, McGrath JJ, Bybjerg-Grauholm J, Mors O, Plana-Ripoll O, Werge T, Wray NR, Mortensen PB, Musliner KL.
PMID: 33439215
JAMA Psychiatry. 2021 Apr 01;78(4):387-397. doi: 10.1001/jamapsychiatry.2020.4172.

IMPORTANCE: Combining information on polygenic risk scores (PRSs) with other known risk factors could potentially improve the identification of risk of depression in the general population. However, to our knowledge, no study has estimated the association of PRS with...

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Agerbo E, Trabjerg BB, Børglum AD, et al. Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status. JAMA Psychiatry. 2021;78(4):387-397doi: 10.1001/jamapsychiatry.2020.4172.
Agerbo, E., Trabjerg, B. B., Børglum, A. D., Schork, A. J., Vilhjálmsson, B. J., Pedersen, C. B., Hakulinen, C., Albiñana, C., Hougaard, D. M., Grove, J., McGrath, J. J., Bybjerg-Grauholm, J., Mors, O., Plana-Ripoll, O., Werge, T., Wray, N. R., Mortensen, P. B., & Musliner, K. L. (2021). Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status. JAMA psychiatry, 78(4), 387-397. https://doi.org/10.1001/jamapsychiatry.2020.4172
Agerbo, Esben, et al. "Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status." JAMA psychiatry vol. 78,4 (2021): 387-397. doi: https://doi.org/10.1001/jamapsychiatry.2020.4172
Agerbo E, Trabjerg BB, Børglum AD, Schork AJ, Vilhjálmsson BJ, Pedersen CB, Hakulinen C, Albiñana C, Hougaard DM, Grove J, McGrath JJ, Bybjerg-Grauholm J, Mors O, Plana-Ripoll O, Werge T, Wray NR, Mortensen PB, Musliner KL. Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status. JAMA Psychiatry. 2021 Apr 01;78(4):387-397. doi: 10.1001/jamapsychiatry.2020.4172. PMID: 33439215; PMCID: PMC7807393.
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