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Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.

Molecular psychiatry

Cleynen I, Engchuan W, Hestand MS, Heung T, Holleman AM, Johnston HR, Monfeuga T, McDonald-McGinn DM, Gur RE, Morrow BE, Swillen A, Vorstman JAS, Bearden CE, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, Warren ST, Owen MJ, Chopra P, Cutler DJ, Duncan R, Kotlar AV, Mulle JG, Voss AJ, Zwick ME, Diacou A, Golden A, Guo T, Lin JR, Wang T, Zhang Z, Zhao Y, Marshall C, Merico D, Jin A, Lilley B, Salmons HI, Tran O, Holmans P, Pardinas A, Walters JTR, Demaerel W, Boot E, Butcher NJ, Costain GA, Lowther C, Evers R, van Amelsvoort TAMJ, van Duin E, Vingerhoets C, Breckpot J, Devriendt K, Vergaelen E, Vogels A, Crowley TB, McGinn DE, Moss EM, Sharkus RJ, Unolt M, Zackai EH, Calkins ME, Gallagher RS, Gur RC, Tang SX, Fritsch R, Ornstein C, Repetto GM, Breetvelt E, Duijff SN, Fiksinski A, Moss H, Niarchou M, Murphy KC, Prasad SE, Daly EM, Gudbrandsen M, Murphy CM, Murphy DG, Buzzanca A, Fabio FD, Digilio MC, Pontillo M, Marino B, Vicari S, Coleman K, Cubells JF, Ousley OY, Carmel M, Gothelf D, Mekori-Domachevsky E, Michaelovsky E, Weinberger R, Weizman A, Kushan L, Jalbrzikowski M, Armando M, Eliez S, Sandini C, Schneider M, Béna FS, Antshel KM, Fremont W, Kates WR, Belzeaux R, Busa T, Philip N, Campbell LE, McCabe KL, Hooper SR, Schoch K, Shashi V, Simon TJ, Tassone F, Arango C, Fraguas D, García-Miñaúr S, Morey-Canyelles J, Rosell J, Suñer DH, Raventos-Simic J, Epstein MP, Williams NM, Bassett AS.
PMID: 32015465
Mol Psychiatry. 2021 Aug;26(8):4496-4510. doi: 10.1038/s41380-020-0654-3. Epub 2020 Feb 03.

Schizophrenia occurs in about one in four individuals with 22q11.2 deletion syndrome (22q11.2DS). The aim of this International Brain and Behavior 22q11.2DS Consortium (IBBC) study was to identify genetic factors that contribute to schizophrenia, in addition to the ~20-fold...

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Cleynen I, Engchuan W, Hestand MS, et al. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Mol Psychiatry. 2020;26(8):4496-4510doi: 10.1038/s41380-020-0654-3.
Cleynen, I., Engchuan, W., Hestand, M. S., Heung, T., Holleman, A. M., Johnston, H. R., Monfeuga, T., McDonald-McGinn, D. M., Gur, R. E., Morrow, B. E., Swillen, A., Vorstman, J. A. S., Bearden, C. E., Chow, E. W. C., van den Bree, M., Emanuel, B. S., Vermeesch, J. R., Warren, S. T., Owen, M. J., Chopra, P., Cutler, D. J., Duncan, R., Kotlar, A. V., Mulle, J. G., Voss, A. J., Zwick, M. E., Diacou, A., Golden, A., Guo, T., Lin, J. R., Wang, T., Zhang, Z., Zhao, Y., Marshall, C., Merico, D., Jin, A., Lilley, B., Salmons, H. I., Tran, O., Holmans, P., Pardinas, A., Walters, J. T. R., Demaerel, W., Boot, E., Butcher, N. J., Costain, G. A., Lowther, C., Evers, R., van Amelsvoort, T. A. M. J., van Duin, E., Vingerhoets, C., Breckpot, J., Devriendt, K., Vergaelen, E., Vogels, A., Crowley, T. B., McGinn, D. E., Moss, E. M., Sharkus, R. J., Unolt, M., Zackai, E. H., Calkins, M. E., Gallagher, R. S., Gur, R. C., Tang, S. X., Fritsch, R., Ornstein, C., Repetto, G. M., Breetvelt, E., Duijff, S. N., Fiksinski, A., Moss, H., Niarchou, M., Murphy, K. C., Prasad, S. E., Daly, E. M., Gudbrandsen, M., Murphy, C. M., Murphy, D. G., Buzzanca, A., Fabio, F. D., Digilio, M. C., Pontillo, M., Marino, B., Vicari, S., Coleman, K., Cubells, J. F., Ousley, O. Y., Carmel, M., Gothelf, D., Mekori-Domachevsky, E., Michaelovsky, E., Weinberger, R., Weizman, A., Kushan, L., Jalbrzikowski, M., Armando, M., Eliez, S., Sandini, C., Schneider, M., Béna, F. S., Antshel, K. M., Fremont, W., Kates, W. R., Belzeaux, R., Busa, T., Philip, N., Campbell, L. E., McCabe, K. L., Hooper, S. R., Schoch, K., Shashi, V., Simon, T. J., Tassone, F., Arango, C., Fraguas, D., García-Miñaúr, S., Morey-Canyelles, J., Rosell, J., Suñer, D. H., Raventos-Simic, J., Epstein, M. P., Williams, N. M., & Bassett, A. S. (2021). Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular psychiatry, 26(8), 4496-4510. https://doi.org/10.1038/s41380-020-0654-3
Cleynen, Isabelle, et al. "Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion." Molecular psychiatry vol. 26,8 (2021): 4496-4510. doi: https://doi.org/10.1038/s41380-020-0654-3
Cleynen I, Engchuan W, Hestand MS, Heung T, Holleman AM, Johnston HR, Monfeuga T, McDonald-McGinn DM, Gur RE, Morrow BE, Swillen A, Vorstman JAS, Bearden CE, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, Warren ST, Owen MJ, Chopra P, Cutler DJ, Duncan R, Kotlar AV, Mulle JG, Voss AJ, Zwick ME, Diacou A, Golden A, Guo T, Lin JR, Wang T, Zhang Z, Zhao Y, Marshall C, Merico D, Jin A, Lilley B, Salmons HI, Tran O, Holmans P, Pardinas A, Walters JTR, Demaerel W, Boot E, Butcher NJ, Costain GA, Lowther C, Evers R, van Amelsvoort TAMJ, van Duin E, Vingerhoets C, Breckpot J, Devriendt K, Vergaelen E, Vogels A, Crowley TB, McGinn DE, Moss EM, Sharkus RJ, Unolt M, Zackai EH, Calkins ME, Gallagher RS, Gur RC, Tang SX, Fritsch R, Ornstein C, Repetto GM, Breetvelt E, Duijff SN, Fiksinski A, Moss H, Niarchou M, Murphy KC, Prasad SE, Daly EM, Gudbrandsen M, Murphy CM, Murphy DG, Buzzanca A, Fabio FD, Digilio MC, Pontillo M, Marino B, Vicari S, Coleman K, Cubells JF, Ousley OY, Carmel M, Gothelf D, Mekori-Domachevsky E, Michaelovsky E, Weinberger R, Weizman A, Kushan L, Jalbrzikowski M, Armando M, Eliez S, Sandini C, Schneider M, Béna FS, Antshel KM, Fremont W, Kates WR, Belzeaux R, Busa T, Philip N, Campbell LE, McCabe KL, Hooper SR, Schoch K, Shashi V, Simon TJ, Tassone F, Arango C, Fraguas D, García-Miñaúr S, Morey-Canyelles J, Rosell J, Suñer DH, Raventos-Simic J, Epstein MP, Williams NM, Bassett AS. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Mol Psychiatry. 2021 Aug;26(8):4496-4510. doi: 10.1038/s41380-020-0654-3. Epub 2020 Feb 03. PMID: 32015465; PMCID: PMC7396297.
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Phylogeny of the tribe Abrotrichini (Cricetidae, Sigmodontinae): integrating morphological and molecular evidence into a new classification.

Cladistics : the international journal of the Willi Hennig Society

Teta P, Cañón C, Patterson BD, Pardiñas UFJ.
PMID: 34710969
Cladistics. 2017 Apr;33(2):153-182. doi: 10.1111/cla.12164. Epub 2016 Apr 28.

The tribe Abrotrichini (five genera and 14 living species) is a small clade within the speciose subfamily Sigmodontinae (Rodentia, Cricetidae), representing one of the extant successful radiations of mammals at southern high latitudes of the Neotropics. Its distribution is...

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Teta P, Cañón C, Patterson BD, et al. Phylogeny of the tribe Abrotrichini (Cricetidae, Sigmodontinae): integrating morphological and molecular evidence into a new classification. Cladistics. 2016;33(2):153-182doi: 10.1111/cla.12164.
Teta, P., Cañón, C., Patterson, B. D., & Pardiñas, U. F. J. (2017). Phylogeny of the tribe Abrotrichini (Cricetidae, Sigmodontinae): integrating morphological and molecular evidence into a new classification. Cladistics : the international journal of the Willi Hennig Society, 33(2), 153-182. https://doi.org/10.1111/cla.12164
Teta, Pablo, et al. "Phylogeny of the tribe Abrotrichini (Cricetidae, Sigmodontinae): integrating morphological and molecular evidence into a new classification." Cladistics : the international journal of the Willi Hennig Society vol. 33,2 (2017): 153-182. doi: https://doi.org/10.1111/cla.12164
Teta P, Cañón C, Patterson BD, Pardiñas UFJ. Phylogeny of the tribe Abrotrichini (Cricetidae, Sigmodontinae): integrating morphological and molecular evidence into a new classification. Cladistics. 2017 Apr;33(2):153-182. doi: 10.1111/cla.12164. Epub 2016 Apr 28. PMID: 34710969.
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Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study.

BJPsych open

Kendall KM, John A, Lee SC, Rees E, Pardiñas AF, Banos MDP, Owen MJ, O'Donovan MC, Kirov G, Lloyd K, Jones I, Legge SE, Walters JTR.
PMID: 33168126
BJPsych Open. 2020 Nov 10;6(6):e139. doi: 10.1192/bjo.2020.42.

BACKGROUND: Individuals with schizophrenia are at higher risk of physical illnesses, which are a major contributor to their 20-year reduced life expectancy. It is currently unknown what causes the increased risk of physical illness in schizophrenia.AIMS: To link genetic...

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Kendall KM, John A, Lee SC, et al. Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study. BJPsych Open. 2020;6(6):e139doi: 10.1192/bjo.2020.42.
Kendall, K. M., John, A., Lee, S. C., Rees, E., Pardiñas, A. F., Banos, M. D. P., Owen, M. J., O'Donovan, M. C., Kirov, G., Lloyd, K., Jones, I., Legge, S. E., & Walters, J. T. R. (2020). Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study. BJPsych open, 6(6), e139. https://doi.org/10.1192/bjo.2020.42
Kendall, Kimberley M, et al. "Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study." BJPsych open vol. 6,6 (2020): e139. doi: https://doi.org/10.1192/bjo.2020.42
Kendall KM, John A, Lee SC, Rees E, Pardiñas AF, Banos MDP, Owen MJ, O'Donovan MC, Kirov G, Lloyd K, Jones I, Legge SE, Walters JTR. Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study. BJPsych Open. 2020 Nov 10;6(6):e139. doi: 10.1192/bjo.2020.42. PMID: 33168126; PMCID: PMC7745237.
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Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants.

Nature communications

Sanders B, D'Andrea D, Collins MO, Rees E, Steward TGJ, Zhu Y, Chapman G, Legge SE, Pardiñas AF, Harwood AJ, Gray WP, O'Donovan MC, Owen MJ, Errington AC, Blake DJ, Whitcomb DJ, Pocklington AJ, Shin E.
PMID: 35031607
Nat Commun. 2022 Jan 14;13(1):27. doi: 10.1038/s41467-021-27601-0.

Coordinated programs of gene expression drive brain development. It is unclear which transcriptional programs, in which cell-types, are affected in neuropsychiatric disorders such as schizophrenia. Here we integrate human genetics with transcriptomic data from differentiation of human embryonic stem...

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Sanders B, D'Andrea D, Collins MO, et al. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nat Commun. 2022;13(1):27doi: 10.1038/s41467-021-27601-0.
Sanders, B., D'Andrea, D., Collins, M. O., Rees, E., Steward, T. G. J., Zhu, Y., Chapman, G., Legge, S. E., Pardiñas, A. F., Harwood, A. J., Gray, W. P., O'Donovan, M. C., Owen, M. J., Errington, A. C., Blake, D. J., Whitcomb, D. J., Pocklington, A. J., & Shin, E. (2022). Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nature communications, 13(1), 27. https://doi.org/10.1038/s41467-021-27601-0
Sanders, Bret, et al. "Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants." Nature communications vol. 13,1 (2022): 27. doi: https://doi.org/10.1038/s41467-021-27601-0
Sanders B, D'Andrea D, Collins MO, Rees E, Steward TGJ, Zhu Y, Chapman G, Legge SE, Pardiñas AF, Harwood AJ, Gray WP, O'Donovan MC, Owen MJ, Errington AC, Blake DJ, Whitcomb DJ, Pocklington AJ, Shin E. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nat Commun. 2022 Jan 14;13(1):27. doi: 10.1038/s41467-021-27601-0. PMID: 35031607.
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Elevated serum progesterone does not impact euploidy rates in PGT-A patients.

Journal of assisted reproduction and genetics

Pardiñas ML, Nohales M, Labarta E, De Los Santos JM, Mercader A, Remohí J, Bosch E, De Los Santos MJ.
PMID: 34008094
J Assist Reprod Genet. 2021 Jul;38(7):1819-1826. doi: 10.1007/s10815-021-02197-y. Epub 2021 May 18.

PURPOSE: Some women undergoing stimulated cycles have elevated serum progesterone (P) on the day of ovulation trigger, but its effect on embryo quality is unclear. We analyze embryo quality among patients with high and low serum P undergoing preimplantation...

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Pardiñas ML, Nohales M, Labarta E, et al. Elevated serum progesterone does not impact euploidy rates in PGT-A patients. J Assist Reprod Genet. 2021;38(7):1819-1826doi: 10.1007/s10815-021-02197-y.
Pardiñas, M. L., Nohales, M., Labarta, E., De Los Santos, J. M., Mercader, A., Remohí, J., Bosch, E., & De Los Santos, M. J. (2021). Elevated serum progesterone does not impact euploidy rates in PGT-A patients. Journal of assisted reproduction and genetics, 38(7), 1819-1826. https://doi.org/10.1007/s10815-021-02197-y
Pardiñas, Maria Luisa, et al. "Elevated serum progesterone does not impact euploidy rates in PGT-A patients." Journal of assisted reproduction and genetics vol. 38,7 (2021): 1819-1826. doi: https://doi.org/10.1007/s10815-021-02197-y
Pardiñas ML, Nohales M, Labarta E, De Los Santos JM, Mercader A, Remohí J, Bosch E, De Los Santos MJ. Elevated serum progesterone does not impact euploidy rates in PGT-A patients. J Assist Reprod Genet. 2021 Jul;38(7):1819-1826. doi: 10.1007/s10815-021-02197-y. Epub 2021 May 18. PMID: 34008094; PMCID: PMC8324650.
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Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia.

JAMA psychiatry

Legge SE, Cardno AG, Allardyce J, Dennison C, Hubbard L, Pardiñas AF, Richards A, Rees E, Di Florio A, Escott-Price V, Zammit S, Holmans P, Owen MJ, O'Donovan MC, Walters JTR.
PMID: 34347035
JAMA Psychiatry. 2021 Oct 01;78(10):1143-1151. doi: 10.1001/jamapsychiatry.2021.1961.

IMPORTANCE: Schizophrenia is a clinically heterogeneous disorder. It is currently unclear how variability in symptom dimensions and cognitive ability is associated with genetic liability for schizophrenia.OBJECTIVE: To determine whether phenotypic dimensions within schizophrenia are associated with genetic liability to...

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Legge SE, Cardno AG, Allardyce J, et al. Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia. JAMA Psychiatry. 2021;78(10):1143-1151doi: 10.1001/jamapsychiatry.2021.1961.
Legge, S. E., Cardno, A. G., Allardyce, J., Dennison, C., Hubbard, L., Pardiñas, A. F., Richards, A., Rees, E., Di Florio, A., Escott-Price, V., Zammit, S., Holmans, P., Owen, M. J., O'Donovan, M. C., & Walters, J. T. R. (2021). Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia. JAMA psychiatry, 78(10), 1143-1151. https://doi.org/10.1001/jamapsychiatry.2021.1961
Legge, Sophie E, et al. "Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia." JAMA psychiatry vol. 78,10 (2021): 1143-1151. doi: https://doi.org/10.1001/jamapsychiatry.2021.1961
Legge SE, Cardno AG, Allardyce J, Dennison C, Hubbard L, Pardiñas AF, Richards A, Rees E, Di Florio A, Escott-Price V, Zammit S, Holmans P, Owen MJ, O'Donovan MC, Walters JTR. Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia. JAMA Psychiatry. 2021 Oct 01;78(10):1143-1151. doi: 10.1001/jamapsychiatry.2021.1961. PMID: 34347035; PMCID: PMC8340009.
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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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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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Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.

Molecular psychiatry

Legge SE, Hamshere ML, Ripke S, Pardinas AF, Goldstein JI, Rees E, Richards AL, Leonenko G, Jorskog LF, Chambert KD, Collier DA, Genovese G, Giegling I, Holmans P, Jonasdottir A, Kirov G, McCarroll SA, MacCabe JH, Mantripragada K, Moran JL, Neale BM, Stefansson H, Rujescu D, Daly MJ, Sullivan PF, Owen MJ, O'Donovan MC, Walters JTR.
PMID: 27502474
Mol Psychiatry. 2017 Oct;22(10):1509. doi: 10.1038/mp.2016.137. Epub 2016 Aug 09.

This corrects the article DOI: 10.1038/mp.2016.97.

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Legge SE, Hamshere ML, Ripke S, et al. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Mol Psychiatry. 2016;22(10):1509doi: 10.1038/mp.2016.137.
Legge, S. E., Hamshere, M. L., Ripke, S., Pardinas, A. F., Goldstein, J. I., Rees, E., Richards, A. L., Leonenko, G., Jorskog, L. F., Chambert, K. D., Collier, D. A., Genovese, G., Giegling, I., Holmans, P., Jonasdottir, A., Kirov, G., McCarroll, S. A., MacCabe, J. H., Mantripragada, K., Moran, J. L., Neale, B. M., Stefansson, H., Rujescu, D., Daly, M. J., Sullivan, P. F., Owen, M. J., O'Donovan, M. C., & Walters, J. T. R. (2017). Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Molecular psychiatry, 22(10), 1509. https://doi.org/10.1038/mp.2016.137
Legge, S E, et al. "Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia." Molecular psychiatry vol. 22,10 (2017): 1509. doi: https://doi.org/10.1038/mp.2016.137
Legge SE, Hamshere ML, Ripke S, Pardinas AF, Goldstein JI, Rees E, Richards AL, Leonenko G, Jorskog LF, Chambert KD, Collier DA, Genovese G, Giegling I, Holmans P, Jonasdottir A, Kirov G, McCarroll SA, MacCabe JH, Mantripragada K, Moran JL, Neale BM, Stefansson H, Rujescu D, Daly MJ, Sullivan PF, Owen MJ, O'Donovan MC, Walters JTR. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Mol Psychiatry. 2017 Oct;22(10):1509. doi: 10.1038/mp.2016.137. Epub 2016 Aug 09. PMID: 27502474; PMCID: PMC5622123.
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Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014.

Psychiatric genetics

Aas M, Blokland GA, Chawner SJ, Choi SW, Estrada J, Forsingdal A, Friedrich M, Ganesham S, Hall L, Haslinger D, Huckins L, Loken E, Malan-Müller S, Martin J, Misiewicz Z, Pagliaroli L, Pardiñas AF, Pisanu C, Quadri G, Santoro ML, Shaw AD, Ranlund S, Song J, Tesli M, Tropeano M, van der Voet M, Wolfe K, Cormack FK, DeLisi L.
PMID: 26565519
Psychiatr Genet. 2016 Feb;26(1):1-47. doi: 10.1097/YPG.0000000000000112.

The XXII World Congress of Psychiatric Genetics, sponsored by the International Society of Psychiatric Genetics, took place in Copenhagen, Denmark, on 12-16 October 2014. A total of 883 participants gathered to discuss the latest findings in the field. The...

Cite
Aas M, Blokland GA, Chawner SJ, et al. Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014. Psychiatr Genet. 2016;26(1):1-47doi: 10.1097/YPG.0000000000000112.
Aas, M., Blokland, G. A., Chawner, S. J., Choi, S. W., Estrada, J., Forsingdal, A., Friedrich, M., Ganesham, S., Hall, L., Haslinger, D., Huckins, L., Loken, E., Malan-Müller, S., Martin, J., Misiewicz, Z., Pagliaroli, L., Pardiñas, A. F., Pisanu, C., Quadri, G., Santoro, M. L., Shaw, A. D., Ranlund, S., Song, J., Tesli, M., Tropeano, M., van der Voet, M., Wolfe, K., Cormack, F. K., & DeLisi, L. (2016). Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014. Psychiatric genetics, 26(1), 1-47. https://doi.org/10.1097/YPG.0000000000000112
Aas, Monica, et al. "Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014." Psychiatric genetics vol. 26,1 (2016): 1-47. doi: https://doi.org/10.1097/YPG.0000000000000112
Aas M, Blokland GA, Chawner SJ, Choi SW, Estrada J, Forsingdal A, Friedrich M, Ganesham S, Hall L, Haslinger D, Huckins L, Loken E, Malan-Müller S, Martin J, Misiewicz Z, Pagliaroli L, Pardiñas AF, Pisanu C, Quadri G, Santoro ML, Shaw AD, Ranlund S, Song J, Tesli M, Tropeano M, van der Voet M, Wolfe K, Cormack FK, DeLisi L. Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014. Psychiatr Genet. 2016 Feb;26(1):1-47. doi: 10.1097/YPG.0000000000000112. PMID: 26565519; PMCID: PMC6519121.
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Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM.

Psychological medicine

Pettersson E, Lichtenstein P, Larsson H, Song J, Agrawal A, Børglum AD, Bulik CM, Daly MJ, Davis LK, Demontis D, Edenberg HJ, Grove J, Gelernter J, Neale BM, Pardiñas AF, Stahl E, Walters JTR, Walters R, Sullivan PF, Posthuma D, Polderman TJC.
PMID: 30334498
Psychol Med. 2019 Jan;49(2):351. doi: 10.1017/S0033291718002945. Epub 2018 Oct 18.

No abstract available.

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Pettersson E, Lichtenstein P, Larsson H, et al. Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM. Psychol Med. 2018;49(2):351doi: 10.1017/S0033291718002945.
Pettersson, E., Lichtenstein, P., Larsson, H., Song, J., Agrawal, A., Børglum, A. D., Bulik, C. M., Daly, M. J., Davis, L. K., Demontis, D., Edenberg, H. J., Grove, J., Gelernter, J., Neale, B. M., Pardiñas, A. F., Stahl, E., Walters, J. T. R., Walters, R., Sullivan, P. F., Posthuma, D., & Polderman, T. J. C. (2019). Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM. Psychological medicine, 49(2), 351. https://doi.org/10.1017/S0033291718002945
Pettersson, E, et al. "Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM." Psychological medicine vol. 49,2 (2019): 351. doi: https://doi.org/10.1017/S0033291718002945
Pettersson E, Lichtenstein P, Larsson H, Song J, Agrawal A, Børglum AD, Bulik CM, Daly MJ, Davis LK, Demontis D, Edenberg HJ, Grove J, Gelernter J, Neale BM, Pardiñas AF, Stahl E, Walters JTR, Walters R, Sullivan PF, Posthuma D, Polderman TJC. Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM. Psychol Med. 2019 Jan;49(2):351. doi: 10.1017/S0033291718002945. Epub 2018 Oct 18. PMID: 30334498; PMCID: PMC8054319.
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Pharmacogenomics: A road ahead for precision medicine in psychiatry.

Neuron

Pardiñas AF, Owen MJ, Walters JTR.
PMID: 34619094
Neuron. 2021 Dec 15;109(24):3914-3929. doi: 10.1016/j.neuron.2021.09.011. Epub 2021 Oct 06.

Psychiatric genomics is providing insights into the nature of psychiatric conditions that in time should identify new drug targets and improve patient care. Less attention has been paid to psychiatric pharmacogenomics research, despite its potential to deliver more rapid...

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Pardiñas AF, Owen MJ, Walters JTR. Pharmacogenomics: A road ahead for precision medicine in psychiatry. Neuron. 2021;109(24):3914-3929doi: 10.1016/j.neuron.2021.09.011.
Pardiñas, A. F., Owen, M. J., & Walters, J. T. R. (2021). Pharmacogenomics: A road ahead for precision medicine in psychiatry. Neuron, 109(24), 3914-3929. https://doi.org/10.1016/j.neuron.2021.09.011
Pardiñas, Antonio F, et al. "Pharmacogenomics: A road ahead for precision medicine in psychiatry." Neuron vol. 109,24 (2021): 3914-3929. doi: https://doi.org/10.1016/j.neuron.2021.09.011
Pardiñas AF, Owen MJ, Walters JTR. Pharmacogenomics: A road ahead for precision medicine in psychiatry. Neuron. 2021 Dec 15;109(24):3914-3929. doi: 10.1016/j.neuron.2021.09.011. Epub 2021 Oct 06. PMID: 34619094.
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