نتائج البحث - "Monaco, A.P."

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33057169; info:eu-repo/semantics/altIdentifier/wos/WOS:000577244500002; info:eu-repo/semantics/altIdentifier/isbn/1359-4184; info:eu-repo/semantics; https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=60321Test; urn:isbn:1359-4184; urn:issn:1359-4184; urn:issn:1476-5578

الإتاحة: https://doi.org/10.1038/s41380-020-00898-xTest
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=60321Test

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3

دورية أكاديمية

Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

المصدر: Nature Genetics, 55, 3, pp. 520

مصطلحات موضوعية: 150 000 MR Techniques in Brain Function, Neuroinformatics

العلاقة: https://repository.ubn.ru.nl//bitstream/handle/2066/293728/293728.pdfTest; https://repository.ubn.ru.nl/handle/2066/293728Test

الإتاحة: https://doi.org/10.1038/s41588-023-01336-8Test
https://repository.ubn.ru.nl//bitstream/handle/2066/293728/293728.pdfTest
https://repository.ubn.ru.nl/handle/2066/293728Test

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4

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

المؤلفون: Price, K.M., Wigg, K.G., Eising, E., Feng, Y, Blokland, K., Wilkinson, M., Kerr, E.N., Guger, S.L., Abbondanza, F., Allegrini, A.G., Andlauer, T.F.M., Bates, T.C., Bernard, M., Bonte, M., Boomsma, D.I., Bourgeron, T., Brandeis, D., Carreiras, M., Ceroni, F., Csépe, V., Dale, P.S., DeFries, J.C., Jong, P.F. de, Démonet, J.F., Zeeuw, E.L. de, Franken, M.-C.J., Francks, C., Gerritse, M.L., Gialluisi, A., Gordon, S.D., Gruen, J.R., Hayiou-Thomas, M.E., Hernández-Cabrera, J., Hottenga, J.-J., Hulme, C., Jansen, P.R., Kere, J., Koomar, T., Landerl, K., Leonard, G.T., Liao, Z., Luciano, M., Lyytinen, H., Martin, N.G., Martinelli, A., Maurer, U., Michaelson, J.J., Mirza-Schreiber, N., Moll, K., Monaco, A.P., Morgan, A.T., Müller-Myhsok, B., Newbury, D.F., Nöthen, M.M., Olson, R.K., Paracchini, S., Paus, T., Pausova, Z., Pennell, C.E., Pennington, B.F., Plomin, R.J., Ramus, F., Reilly, S., Richer, L., Rimfeld, K., Schulte-Körne, G., Shapland, C.Y., Simpson, N.H., Smith, S.D., Snowling, M.J., St Pourcain, B., Stein, J.F., Talcott, J.B., Tiemeier, H., Tomblin, J.B., Truong, D.T., Bergen, E. van, Schroeff, M.P. van der, Donkelaar, M.M.J. van, Verhoef, E., Wang, C.A., Watkins, K.E., Whitehouse, A.J.O., Willcutt, E.G., Wright, M.J., Zhu, G., Fisher, S.E., Lovett, M.W., Strug, L.J., Barr, C.L.

المساهمون: University of St Andrews. School of Medicine, University of St Andrews. Centre for Biophotonics, University of St Andrews. Biomedical Sciences Research Complex, University of St Andrews. Institute of Behavioural and Neural Sciences, University of St Andrews. St Andrews Bioinformatics Unit, University of St Andrews. Cellular Medicine Division, STEMM - Stem Cells and Metabolism Research Program, Juha Kere / Principal Investigator, Research Programs Unit, University of Helsinki, Consortium, Quantitative Trait Working Group of the GenLang, European Commission, Otorhinolaryngology and Head and Neck Surgery, Child and Adolescent Psychiatry / Psychology, RS: FPN CN 7, Language, Biological Psychology, Amsterdam Reproduction & Development, APH - Mental Health, APH - Methodology, APH - Health Behaviors & Chronic Diseases, APH - Personalized Medicine, Complex Trait Genetics, Amsterdam Neuroscience - Complex Trait Genetics, LEARN! - Educational neuroscience, learning and development, Human genetics

المصدر: Translational Psychiatry, 12, 1-9
Translational Psychiatry, 12(1):495. Nature Publishing Group
2022, ' Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities ', Translational Psychiatry, vol. 12, 495 . https://doi.org/10.1038/s41398-022-02250-zTest
Translational Psychiatry, 12 (1)
Quantitative Trait Working Group of the GenLang Consortium 2022, ' Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities ', Translational psychiatry, vol. 12, no. 1, 495 . https://doi.org/10.1038/s41398-022-02250-zTest
Price, K M, Wigg, K G, Eising, E, Boomsma, D I, de Zeeuw, E L, Hottenga, J J, Jansen, P R, van Bergen, E, Lovett, M W, Strug, L J, Barr, C L & Quantitative Trait Working Group of the GenLang Consortium 2022, ' Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities ', Translational Psychiatry, vol. 12, 495, pp. 1-9 . https://doi.org/10.1038/s41398-022-02250-zTest
Translational Psychiatry, 12:495, 1-9. Nature Publishing Group
Translational Psychiatry
Transl. Psychiatry 12:495 (2022)
Translational Psychiatry, 12, 1, pp. 1-9
Translational psychiatry, 12(1):495

مصطلحات موضوعية: Neuroinformatics, single nucleotide, Candidate gene, Autism Spectrum Disorder, Developmental dyslexia, autism spectrum disorder, QH426 Genetics, Polymorphism, Single Nucleotide, Neuronal migration, 3124 Neurology and psychiatry, polymorphism, Dyslexia, Cellular and Molecular Neuroscience, All institutes and research themes of the Radboud University Medical Center, problem solving, SDG 3 - Good Health and Well-being, dyslexia, Humans, Kiaa0319, Family, humans, Children, QH426, Problem Solving, Biological Psychiatry, MCC, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], genome-wide association study, Dyx1c1, Plasma-membrane, 3rd-DAS, Psychiatry and Mental health, Susceptibility, RC0321, SDG 4 - Quality Education, RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry, Genome-Wide Association Study, Knockout mice

وصف الملف: application/pdf; application/application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8f62675903a80cd867fe01fb5f19891Test
https://hdl.handle.net/10023/26639Test

5

دورية أكاديمية

The DCDC2 deletion is not a risk factor for dyslexia

المؤلفون: Scerri, T.S., Macpherson, E., Martinelli, Angela, Wa, W.C., Monaco, A.P., Stein, John, Zheng, M., Ho, C. S., McBride, C., Snowling, Margaret J., Hulme, Charles, Hayiou-Thomas, Marianna E., Waye, M.M.Y., Talcott, Joel B., Paracchini, Silvia

مصطلحات موضوعية: DCDC2 protein, human, microtubule associated protein

وصف الملف: application/pdf

العلاقة: https://acuresearchbank.acu.edu.au/item/8v49v/the-dcdc2-deletion-is-not-a-risk-factor-for-dyslexiaTest; https://acuresearchbank.acu.edu.au/download/f751e3a0eeb633b775ad770a4afc0aa46c1cddda5fd45fbae1f9b00e6e0e4be6/205287/OA_Scerri_2017_The_DCDC2_deletion_is_not_a.pdfTest; https://doi.org/10.1038/tp.2017.151Test; Scerri, T.S., Macpherson, E., Martinelli, Angela, Wa, W.C., Monaco, A.P., Stein, John, Zheng, M., Ho, C. S., McBride, C., Snowling, Margaret J., Hulme, Charles, Hayiou-Thomas, Marianna E., Waye, M.M.Y., Talcott, Joel B. and Paracchini, Silvia. (2017). The DCDC2 deletion is not a risk factor for dyslexia. Translational Psychiatry. 7(7), pp. 1 - 7. https://doi.org/10.1038/tp.2017.151Test

الإتاحة: https://doi.org/10.1038/tp.2017.151Test
https://acuresearchbank.acu.edu.au/download/f751e3a0eeb633b775ad770a4afc0aa46c1cddda5fd45fbae1f9b00e6e0e4be6/205287/OA_Scerri_2017_The_DCDC2_deletion_is_not_a.pdfTest

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النص الكامل

6

دورية أكاديمية

Discovery of 42 genome-wide significant loci associated with dyslexia

المصدر: Nature Genetics, 54, 11, pp. 1621-1629

مصطلحات موضوعية: All institutes and research themes of the Radboud University Medical Center, Neuroinformatics, Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience

العلاقة: https://repository.ubn.ru.nl//bitstream/handle/2066/284950/284950.pdfTest; https://repository.ubn.ru.nl/handle/2066/284950Test; http://dx.doi.org/10.1038/s41588-022-01192-yTest

الإتاحة: https://doi.org/10.1038/s41588-022-01192-yTest
https://repository.ubn.ru.nl//bitstream/handle/2066/284950/284950.pdfTest
https://repository.ubn.ru.nl/handle/2066/284950Test

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7

دورية أكاديمية

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

المصدر: Becker , J , Czamara , D , Scerri , T S , Ramus , F , Csepe , V , Talcott , J B , Stein , J , Morris , A , Ludwig , K U , Hoffmann , P , Honbolygo , F , Toth , D , Fauchereau , F , Bogliotti , C , Iannuzzi , S , Chaix , Y , Valdois , S , Billard , C , George , F , Soares-Boucaud , I , Gerard , C L , van der Mark , S , Schulz , E , Vaessen ....

الإتاحة: https://doi.org/10.1038/ejhg.2013.199Test
https://cris.maastrichtuniversity.nl/en/publications/de830a93-60db-4b66-9fcd-2fd9d0d2953aTest

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8

دورية أكاديمية

Genome-wide screening for DNA variants associated with reading and language traits

وصف الملف: application/pdf

العلاقة: https://publications.aston.ac.uk/id/eprint/23689/1/Genome_wide_screening_for_DNA_variants_associated_with_reading_and_language_traits.pdfTest; Gialluisi, A., Newbury, D.F., Wilcutt, E.G., Olson, R.K., DeFries, J.C., Brandler, W.M., Pennington, B.F., Smith, S.D., Scerri, T.S., Simpson, N.H., SLI Consortium, Luciano, M., Evans, D.M., Bates, T.C., Stein, J.F., Talcott, J.B. , Monaco, A.P., Paracchini, S., Francks, C. and Fisher, S.E. (2014). Genome-wide screening for DNA variants associated with reading and language traits. Genes, Brain and Behavior, 13 (7), 686–701.

الإتاحة: https://publications.aston.ac.uk/id/eprint/23689Test/
https://publications.aston.ac.uk/id/eprint/23689/1/Genome_wide_screening_for_DNA_variants_associated_with_reading_and_language_traits.pdfTest

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9

دورية أكاديمية

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

المؤلفون: Hadley, D., Wu, Z.L., Kao, C., Kini, A., Mohamed-Hadley, A., Thomas, K., Vazquez, L., Qiu, H., Mentch, F., Pellegrino, R., Kim, C., Connolly, J., Glessner, J., Hakonarson, H., Pinto, D., Merikangas, A., Klei, L., Vorstman, J.A., Thompson, A., Regan, R., Pagnamenta, A.T., Oliveira, B., Magalhaes, T.R., Gilbert, J., Duketis, E., De Jonge, M.V., Cuccaro, M., Correia, C.T., Conroy, J., Conceição, I.C., Chiocchetti, A.G., Casey, J.P., Bolshakova, N., Bacchelli, E., Anney, R., Zwaigenbaum, L., Wittemeyer, K., Wallace, S., Engeland, Hv, Soorya, L., Rogé, B., Roberts, W., Poustka, F., Mouga, S., Minshew, N., McGrew, S.G., Lord, C., Leboyer, M., Le Couteur, A.S., Kolevzon, A., Jacob, S., Guter, S., Green, J., Green, A., Gillberg, C., Fernandez, B.A., Duque, F., Delorme, R., Dawson, G., Café, C., Brennan, S., Bourgeron, T., Bolton, P.F., Bölte, S., Bernier, R., Baird, G., Bailey, A.J., Anagnostou, E., Almeida, J., Wijsman, E.M., Vieland, V.J., Vicente, A.M., Schellenberg, G.D., Pericak-Vance, M., Paterson, A.D., Parr, J.R., Oliveira, G., Correia, C., Nurnberger, J.I., Monaco, A.P., Maestrini, E., Klauck, S.M., Haines, J.L., Geschwind, D.H., Freitag, C.M., Folstein, S.E., Ennis, S., Coon, H., Battaglia, A., Szatmari, P., Sutcliffe, J.S., Hallmayer, J., Gill, M., Cook, E.H., Buxbaum, J.D., Devlin, B., Gallagher, L., Betancur, C., Scherer, S.W.

مصطلحات موضوعية: Perturbações do Desenvolvimento Infantil e Saúde Mental, Autism

العلاقة: Nat Commun. 2014 Jun 13;5:4074. doi:10.1038/ncomms5074.; http://hdl.handle.net/10400.18/2440Test; ncomms5074

الإتاحة: https://doi.org/10.1038/ncomms5074Test
http://hdl.handle.net/10400.18/2440Test

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النص الكامل

10

دورية أكاديمية

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

المؤلفون: Lee, S.H., Ripke, S., Neale, B., Faraone, S.V., Purcell, S.M., Perlis, R.H., Mowry, B. J., Thapar, A., Goddard, M.E., Witte, J.S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen, O.A., Anjorin, A., Anney, R., Anttila, V., Arking, D.E., Asherson, P., Azevedo, M.H., Backlund, L., Badner, J.A., Bailey, A.J., Banaschewski, T., Barchas, J.D., Barnes, M.R., Barrett, T.B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen, S.E., Berrettini, W., Betancur, C., Bettecken, T., Biederman, J, Binder, E.B., Black, D.W., Blackwood, D.H., Bloss, C.S., Boehnke, M., Boomsma, D.I., Breen, G., Breuer, R., Bruggeman, R., Cormican, P., Buccola, N.G., Buitelaar, J.K., Bunney, W.E., Buxbaum, J.D., Byerley, W. F., Byrne, E.M., Caesar, S., Cahn, W., Cantor, R.M., Casas, M., Chakravarti, A., Chambert, K., Choudhury, K., Cichon, S., Cloninger, C. R., Collier, D.A., Cook, E.H., Coon, H., Corman, B., Corvin, A., Coryell, W.H., Craig, D.W., Craig, I.W., Crosbie, J., Cuccaro, M.L., Curtis, D., Czamara, D., Datta, S., Dawson, G., Day, R., de Geus, E.J.C., Degenhardt, F., Djurovic, S., Donohoe, G., Doyle, A.E., Duan, J., Dudbridge, F., Duketis, E., Ebstein, R.P., Edenberg, H.J., Elia, J., Ennis, S., Etain, B., Fanous, A., Farmer, A.E., Ferrier, I.N., Flickinger, M., Fombonne, E., Foroud, T., Frank, J., Franke, B., Fraser, C., Freedman, R., Freimer, N.B., Freitag, C., Friedl, M., Frisén, L., Gallagher, L., Gejman, P.V., Georgieva, L., Gershon, E.S., Geschwind, D.H., Giegling, I., Gill, M., Gordon, S.D., Gordon-Smith, K., Green, E.K., Greenwood, T.A., Grice, D.E., Gross, M., Grozeva, D., Guan, W., Gurling, H., de Haan, L., Haines, J.L., Hakonarson, H., Hallmayer, J., Hamilton, S.P., Hamshere, M.L., Hansen, T.F., Hartmann, A.M., Hautzinger, M., Heath, A.C., Henders, A.K., Herms, S., Hickie, I.B., Hipolito, M., Hoefels, S., Holmans, P.A., Holsboer, F., Hoogendijk, W.J.G., Hottenga, J.J., Hultman, C. M., Hus, V., Ingason, A., Ising, M., Jamain, S., Jones, E.G., Jones, I., Jones, L., Tzeng, J.Y., Kähler, A.K., Kahn, R.S., Kandaswamy, R., Keller, M.C., Kennedy, J.L., Kenny, E., Kent, L., Kim, Y., Kirov, G. K., Klauck, S.M., Klei, L., Knowles, J.A., Kohli, M.A., Koller, D.L., Konte, B., Korszun, A., Krabbendam, L., Krasucki, R., Kuntsi, J., Kwan, P., Landén, M., Langstrom, N., Lathrop, M., Lawrence, J., Lawson, W.B., Leboyer, M., Ledbetter, D.H., Lee, P.H., Lencz, T., Lesch, K.P., Levinson, D.F., Lewis, C.M., Li, J., Lichtenstein, P., Lieberman, J. A., Lin, D.Y., Linszen, D.H., Liu, C., Lohoff, F.W., Loo, S.K., Lord, C., Lowe, J.K., Lucae, S., MacIntyre, D.J., Madden, P.A.F., Maestrini, E., Magnusson, P.K.E., Mahon, P.B., Maier, W., Malhotra, A.K., Mane, S.M., Martin, C.L., Martin, N.G., Mattheisen, M., Matthews, K., Mattingsdal, M., McCarroll, S.A., McGhee, K.A., McGough, J.J., McGrath, P.J., McGuffin, P., McInnis, M.G., McIntosh, A., McKinney, R., McLean, A.W., McMahon, F.J., McMahon, W.M., McQuillin, A., Medeiros, H., Medland, S.E., Meier, S., Melle, I., Meng, F., Meyer, J., Middeldorp, C.M., Middleton, L., Milanova, V., Miranda, A., Monaco, A.P., Montgomery, G.W., Moran, J.L., Moreno-De Luca, D., Morken, G., Morris, D.W., Morrow, E.M., Moskvina, V., Muglia, P., Mühleisen, T.W., Muir, W.J., Müller-Myhsok, B., Murtha, M., Myers, R.M., Myin-Germeys, I., Neale, M.C., Nelson, S.F., Nievergelt, C.M., Nikolov, I., Nimgaonkar, V.L., Nolen, W.A., Nöthen, M.M., Nurnberger, J.I., Nwulia, E.A., Nyholt, DR, O'Dushlaine, C., Oades, R.D., Olincy, A., Oliveira, G., Olsen, L., Ophoff, R.A., Osby, U., Owen, M.J., Palotie, A., Parr, J.R., Paterson, A.D., Pato, C.N., Pato, M.T., Penninx, B.W.J.H., Pergadia, M.L., Pericak-Vance, M.A., Pickard, B.S., Pimm, J., Piven, J., Posthuma, D., Potash, J.B., Poustka, F., Propping, P., Puri, V., Quested, D., Quinn, E.M., Ramos-Quiroga, J.A., Rasmussen, H.B., Raychaudhuri, S., Rehnström, K., Reif, A., Ribasés, M., Rice, J.P., Rietschel, M., Roeder, K., Roeyers, H., Rossin, L., Rothenberger, A., Rouleau, G., Ruderfer, D., Rujescu, D., Sanders, A.R., Sanders, S.J., Santangelo, S., Sergeant, J.A., Schachar, R., Schalling, M., Schatzberg, A.F., Scheftner, W.A., Schellenberg, G.D., Scherer, S.W., Schork, N.J., Schulze, T.G., Schumacher, J., Schwarz, M., Scolnick, E., Scott, L.J., Shi, J., Shilling, P.D., Shyn, S.I., Silverman, J.M., Slager, S.L., Smalley, S.L., Smit, J.H., Smith, E.N., Sonuga-Barke, E.J., St Clair, D., State, M., Steffens, M, Steinhausen, H.C., Strauss, J., Strohmaier, J., Stroup, T.S., Sutcliffe, J., Szatmari, P., Szelinger, S., Thirumalai, S., Thompson, R.C., Todorov, A.A., Tozzi, F., Treutlein, J., Uhr, M., van den Oord, E.J.C.G., Grootheest, G., van Os, J., Vicente, A., Vieland, V., Vincent, J.B., Visscher, P.M., Walsh, C.A., Wassink, T.H., Watson, S.J., Weissman, M.M., Werge, T., Wienker, T.F., Wijsman, E.M., Willemsen, G., Williams, N., Willsey, A.J., Witt, S.H., Xu, W., Young, A.H., Yu, T.W., Zammit, S., Zandi, P.P., Zhang, P., Zitman, F.G., Zöllner, S., Devlin, B., Kelsoe, J., Sklar, P., Daly, M.J., O'Donovan, M.C., Craddock, N., Sullivan, P.F., Smoller, J.W., Kendler, K.S., Wray, N.R.

المصدر: Lee , S H , Ripke , S , Neale , B , Faraone , S V , Purcell , S M , Perlis , R H , Mowry , B J , Thapar , A , Goddard , M E , Witte , J S , Absher , D , Agartz , I , Akil , H , Amin , F , Andreassen , O A , Anjorin , A , Anney , R , Anttila , V , Arking , D E , Asherson , P , Azevedo , M H , Backlund , L , Badner ....

مصطلحات موضوعية: /dk/atira/pure/keywords/cohort_studies/netherlands_twin_register_ntr_, name=Netherlands Twin Register (NTR)

العلاقة: https://research.vu.nl/en/publications/8c8d48dc-ec34-412f-afa9-22425051d8c7Test

الإتاحة: https://doi.org/10.1038/ng.2711Test
https://research.vu.nl/en/publications/8c8d48dc-ec34-412f-afa9-22425051d8c7Test
https://hdl.handle.net/1871.1/8c8d48dc-ec34-412f-afa9-22425051d8c7Test

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