المؤلفون: Strange, A, Riley, BP, Spencer, CCA, Morris, DW, Pirinen, M, O'Dushlaine, CT, Su, Z, Maher, BS, Freeman, C, Cormican, P, Bellenguez, C, Kenny, EM, Band, G, Wormley, B, Donohoe, G, Dilthey, A, Moutsianas, L, Quinn, E, Edkins, S, Judge, R, Coleman, K, Hunt, S, Tropea, D, Roche, S, Cummings, L, Kelleher, E, McKeon, P, Dinan, T, McDonald, C, Murphy, KC, O'Callaghan, E, O'Neill, FA, Waddington, JL, Walsh, D, Giannoulatou, E, Langford, C, Deloukas, P, Gray, E, Dronov, S, Potter, S, Pearson, R, Vukcevic, D, Tashakkori-Ghanbaria, A, Blackwell, JM, Bramon, E, Brown, MA, Casas, JP, Duncanson, A, Jankowski, J, Markus, HS, Mathew, CG, Palmer, CNA, Plomin, R, Rautanen, A, Sawcer, SJ, Trembath, RC, Viswanathan, AC, Wood, NW, Stone, J, Scolnick, E, Purcell, S, Sklar, P, Ripke, S, Walters, J, Owen, MJ, O'Donovan, MC, Peltonen, L, McVean, G, Kendler, KS, Gill, M, Donnelly, P, Corvin, A, Conso, ISG, Consortium, SGENE, Psychiat, SWG, Consor, WTCC

مصطلحات موضوعية: Adult, Male, Genotype, Locus (genetics), Single-nucleotide polymorphism, Genome-wide association study, Human leukocyte antigen, HLA-C Antigens, Major histocompatibility complex, Polymorphism, Single Nucleotide, Article, HLA-C, Calcium Channels, T-Type, Young Adult, Risk Factors, Databases, Genetic, tourette-syndrome, SNP, Humans, genetics, Genetic Predisposition to Disease, Allele, gene, Biological Psychiatry, Aged, Genetics, cacna1i, breakpoint, Aged, 80 and over, biology, deletions, polygene score, classical hla alleles, Middle Aged, hlac, major histocompatibility complex, disruption, biology.protein, Schizophrenia, Female, immp2l, Ireland, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23e8bbf922165b49717a20a692f07464Test
https://ora.ox.ac.uk/objects/uuid:b0a3e288-eee7-4632-8d42-2baf2178e2ddTest

المؤلفون: Rees, Elliott, Kirov, George, Walters, James Tynan Rhys, Richards, Alexander, Howrigan, D., Kavanagh, D. H., Pocklington, Andrew, Fromer, M., Ruderfer, D..M., Georgieva, Lyudmila, Carrera, Noa, Gormley, P., Palta, P., Williams, H., Dwyer, S., Johnson, J. S., Roussos, P., Barker, D. D., Banks, E., Milanova, V., Rose, S .A., Chambert, K., Mahajan, M, Scolnick, E. M., Moran, J. L., Tsuang, M. T., Glatt, S. J., Chen, W. J., Hwu, H.-G., Faraone, Stephen V., Roe, Cheri A., Chandler, Sharon D., Liu, Chih-Min, Liu, Chen-Chung, Yeh, Ling-Ling, Ouyang, Wen-Chen, Chan, Hung-Yu, Chen, Chun-Ying, Neale, B. M., Palotie, A., Sklar, P., Purcell, S. M., McCarroll, S .A., Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon

المساهمون: Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders

المصدر: Translational Psychiatry
Translational psychiatry, vol 5, iss 7

مصطلحات موضوعية: Nonsynonymous substitution, Male, INTELLECTUAL DISABILITY, LOCI, Genome-wide association study, Voltage-Gated Sodium Channels, VARIANTS, Compound heterozygosity, 3124 Neurology and psychiatry, 0302 clinical medicine, Gene Frequency, 2.1 Biological and endogenous factors, Medicine, Psychology, Exome, HOMOZYGOSITY, Aetiology, Exome sequencing, Genetics, Psychiatry, RISK, 0303 health sciences, Homozygote, Serious Mental Illness, Psychiatry and Mental health, Mental Health, Public Health and Health Services, Female, Original Article, Taiwanese Trios Exome Sequencing Consortium, Life Sciences & Biomedicine, Heterozygote, Genotype, Intellectual and Developmental Disabilities (IDD), Clinical Sciences, Genes, Recessive, 03 medical and health sciences, Cellular and Molecular Neuroscience, Clinical Research, Recessive, Humans, Family, Genetic Predisposition to Disease, Allele, GENOME-WIDE ASSOCIATION, AUTISM, Allele frequency, Biological Psychiatry, 030304 developmental biology, SPECTRUM, Science & Technology, business.industry, Human Genome, Brain Disorders, Minor allele frequency, CONSANGUINITY, Genes, DE-NOVO MUTATIONS, Case-Control Studies, RC0321, Schizophrenia, business, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b192092c4e6fde38c1b01cefd08b6b6Test
https://pubmed.ncbi.nlm.nih.gov/26196440Test

المؤلفون: Aj, Schork, Wk, Thompson, Pham P, Torkamani A, Jc, Roddey, Pf, Sullivan, Jr, Kelsoe, Donovan Mc, O., Furberg H, Tobacco and Genetics Consortium, Bipolar Disorder Psychiatric Genomics Consortium, Schizophrenia Psychiatric Genomics Consortium, Nj, Schork, Oa, Andreassen, Am, Dale, Absher D, Agudo A, Almgren P, Ardissino D, Tl, Assimes, Bandinelli S, Barzan L, Bencko V, Benhamou S, Ej, Benjamin, Bernardinelli L, Bis J, Boehnke M, Boerwinkle E, Di, Boomsma, Brennan P, Canova C, Castellsagué X, Chanock S, Chasman D, Di, Conway, Dackor J, Ej, Geus, Duan J, Elosua R, Everett B, Fabianova E, Ferrucci L, Foretova L, Sp, Fortmann, Franceschini N, Frayling T, Furberg C, Pv, Gejman, Groop L, Gu F, Guralnik J, Se, Hankinson, Haritunians T, Healy C, Hofman A, Holcátová I, Dj, Hunter, Sj, Hwang, Jp, Ioannidis, Iribarren C, Au, Jackson, Janout V, Kaprio J, Kim Y, Kjaerheim K, Jw, Knowles, Kraft P, Ladenvall C, Lagiou P, Lanthrop M, Lerman C, Df, Levinson, Levy D, Md, Li, Dy, Lin, Eh, Lips, Lissowska J, Lowry R, Lucas G, Tv, Macfarlane, Maes H, Pm, Mannucci, Mates D, Mauri F, Ja, Mcgovern, Jd, Mckay, McKnight B, Melander O, Pa, Merlini, Milaneschi Y, Kl, Mohlke, Donnell Cj, O., Pare G, Bw, Penninx, Perry J, Posthuma D, Sr, Preis, Psaty B, Quertermous T, Vs, Ramachandran, Richiardi L, Ridker P, Rose J, Rudnai P, Salomaa V, Ar, Sanders, Sm, Schwartz, Shi J, Jh, Smit, Hm, Stringham, Szeszenia-Dabrowska N, Tanaka T, Taylor K, Thacker E, Thornton L, Tiemeier H, Tuomilehto J, Ag, Uitterlinden, Cm, Duijn, Jm, Vink, Vogelzangs N, Bf, Voight, Walter S, Willemsen G, Zaridze D, Znaor A, Akil H, Anjorin A, Backlund L, Ja, Badner, Jd, Barchas, Tb, Barrett, Bass N, Bauer M, Bellivier F, Se, Bergen, Berrettini W, Blackwood D, Cs, Bloss, Breen G, Breuer R, We, Bunner, Burmeister M, Byerley W, Caesar S, Chambert K, Cichon S, St Clair D, Da, Collier, Corvin A, Wh, Coryell, Craddock N, Dw, Craig, Daly M, Day R, Degenhardt F, Djurovic S, Dudbridge F, Hj, Edenberg, Elkin A, Etain B, Ae, Farmer, Ma, Ferreira, Ferrier I, Flickinger M, Foroud T, Frank J, Fraser C, Frisén L, Es, Gershon, Gill M, Gordon-Smith K, Ek, Green, Ta, Greenwood, Grozeva D, Guan W, Gurling H, Ó, Gustafsson, Ml, Hamshere, Hautzinger M, Herms S, Hipolito M, Pa, Holmans, Cm, Hultman, Jamain S, Eg, Jones, Jones I, Jones L, Kandaswamy R, Jl, Kennedy, Gk, Kirov, Dl, Koller, Kwan P, Landén M, Langstrom N, Lathrop M, Lawrence J, Wb, Lawson, Leboyer M, Ph, Lee, Li J, Lichtenstein P, Lin D, Liu C, Fw, Lohoff, Lucae S, Pb, Mahon, Maier W, Ng, Martin, Mattheisen M, Matthews K, Mattingsdal M, Ka, Mcghee, McGuffin P, Mg, Mcinnis, McIntosh A, McKinney R, Aw, Mclean, Fj, Mcmahon, McQuillin A, Meier S, Melle I, Meng F, Pb, Mitchell, Gw, Montgomery, Moran J, Morken G, Dw, Morris, Moskvina V, Muglia P, Tw, Mühleisen, Wj, Muir, Müller-Myhsok B, Rm, Myers, Cm, Nievergelt, Nikolov I, Nimgaonkar V, Mm, Nöthen, Ji, Nurnberger, Ea, Nwulia, O'Dushlaine C, Osby U, Óskarsson H, Mj, Owen, Petursson H, Bs, Pickard, Porgeirsson P, Jb, Potash, Propping P, Sm, Purcell, Quinn E, Raychaudhuri S, Rice J, Rietschel M, Ruderfer D, Schalling M, Af, Schatzberg, Wa, Scheftner, Pr, Schofield, Tg, Schulze, Schumacher J, Mm, Schwarz, Scolnick E, Lj, Scott, Pd, Shilling, Sigurdsson E, Sklar P, En, Smith, Stefansson H, Stefansson K, Steffens M, Steinberg S, Strauss J, Strohmaier J, Szelinger S, Rc, Thompson, Tozzi F, Treutlein J, Jb, Vincent, Sj, Watson, Tf, Wienker, Williamson R, Sh, Witt, Wright A, Xu W, Ah, Young, Pp, Zandi, Zhang P, Zöllner S, Agartz I, Albus M, Alexander M, Rl, Amdur, Amin F, Bitter I, Dw, Black, Ad, Børglum, Ma, Brown, Bruggeman R, Ng, Buccola, Wf, Byerley, Cahn W, Rm, Cantor, Vj, Carr, Sv, Catts, Choudhury K, Cloninger C, Cormican P, Pa, Danoy, Datta S, DeHert M, Demontis D, Dikeos D, Donnelly P, Donohoe G, Duong L, Dwyer S, Fanous A, Fink-Jensen A, Freedman R, Nb, Freimer, Friedl M, Georgieva L, Giegling I, Glenthøj B, Godard S, Golimbet V, de Haan L, Hansen M, Hansen T, Am, Hartmann, Fa, Henskens, Dm, Hougaard, Ingason A, Av, Jablensky, Kd, Jakobsen, Jay M, Eg, Jönsson, Jürgens G, Rs, Kahn, Mc, Keller, Ks, Kendler, Kenis G, Kenny E, Konnerth H, Konte B, Krabbendam L, Krasucki R, Vk, Lasseter, Laurent C, Lencz T, Lerer F, Ky, Liang, Ja, Lieberman, Dh, Linszen, Lönnqvist J, Cm, Loughland, Aw, Maclean, Bs, Maher, Ak, Malhotra, Mallet J, Malloy P, Jj, Mcgrath, McLean DE, Pt, Michie, Milanova V, Mors O, Pb, Mortensen, Bj, Mowry, Myin-Germeys I, Neale B, Da, Nertney, Nestadt G, Nielsen J, Nordentoft M, Norton N, O'Neill F, Olincy A, Olsen L, Ra, Ophoff, Tf, Ørntoft, van Os J, Pantelis C, Papadimitriou G, Cn, Pato, Mt, Pato, Peltonen L, Pickard B, Op, Pietiläinen, Pimm J, Ae, Pulver, Puri V, Digby Quested, Hb, Rasmussen, Jm, Réthelyi, Ribble R, Bp, Riley, Rossin L, Ruggeri M, Rujescu D, Schall U, Sg, Schwab, Rj, Scott, Jm, Silverman, Cc, Spencer, Strange A, Strengman E, Stroup T, Suvisaari J, Terenius L, Thirumalai S, Timm S, Toncheva D, Tosato S, Ej, Den Oord, Veldink J, Pm, Visscher, Walsh D, Ag, Wang, Werge T, Wiersma D, Db, Wildenauer, Hj, Williams, Nm, Williams, van Winkel R, Wormley B.

المساهمون: Biological Psychology, Functional Genomics, Educational Neuroscience, Neuroscience Campus Amsterdam - Brain Mechanisms in Health & Disease, LEARN! - Social cognition and learning, Biophotonics and Medical Imaging, LEARN! - Brain, learning and development, Neuroscience Campus Amsterdam - Neurobiology of Mental Health, EMGO+ - Mental Health, Neuroscience Campus Amsterdam - Brain Imaging Technology, LaserLaB - Biophotonics and Microscopy, ANS - Amsterdam Neuroscience, Adult Psychiatry, Psychiatry, Human genetics, Epidemiology and Data Science, NCA - Brain mechanisms in health and disease, NCA - Neurobiology of mental health, EMGO - Mental health, NCA - Brain imaging technology, Psychiatrie & Neuropsychologie, RS: MHeNs School for Mental Health and Neuroscience, Gibson, Greg, Germeys, Inez, van Winkel, Ruud, De Hert, Marc

المصدر: PLoS genetics, vol 9, iss 4
PLoS Genetics
Schork, AJ; Thompson, WK; Pham, P; Torkamani, A; Roddey, JC; Sullivan, PF; et al.(2013). All SNPs are not created equal: Genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. PLoS Genetics, 9(4). doi: 10.1371/journal.pgen.1003449. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/9xc7s4vrTest
Schork, A J, Thompson, W K, Pham, P, Torkamani, A, Roddey, J C, Sullivan, P F, Kelsoe, J, O'Donovan, M C, Furberg, H, Absher, D, Agudo, A, Almgren, P, Ardissino, D, Assimes, T L, Bandinelli, S, Barzan, L, Bencko, V, Benhamou, S, Benjamin, E J, Bernardinelli, L, Bis, J, Boehnke, M, Boerwinkle, E, Boomsma, D I, Brennan, P, Canova, C, Castellsagué, X, Chanock, S, Chasman, D I, Conway, D I, Dackor, J, de Geus, E J C, Duan, J, Elosua, R, Everett, B, Fabianova, E, Ferrucci, L, Foretova, L, Fortmann, S P, Franceschini, N, Frayling, T M, Furberg, C, Gejman, P V, Groop, L, Gu, F, Guralnik, J, Hankinson, S E, Haritunians, T, Healy, C, Hofman, A, Holcátová, I, Hunter, D J, Hwang, S J, Ioannidis, J P A, Iribarren, C, Jackson, A U, Janout, V, Kaprio, J, Kim, Y, Kjaerheim, K, Knowles, J W, Kraft, P, Ladenvall, C, Lagiou, P, Lanthrop, M, Lerman, C, Levinson, D F, Levy, D, Li, M D, Lin, D Y, Lips, E H, Lissowska, J, Lowry, R B, Lucas, G, Macfarlane, T V, Maes, H H M, Mannucci, P M, Mates, D, Mauri, F, McGovern, J A, McKay, J D, McKnight, B, Melander, O, Merlini, P A, Milaneschi, Y, Mohlke, K L, O'Donnell, C J, Pare, G, Penninx, B W J H, Perry, J R B, Posthuma, D, Preis, S R, Psaty, B, Quertermous, T, Ramachandran, V S, Richiardi, L, Ridker, P M, Rose, J, Rudnai, P, Salomaa, V, Sanders, A R, Schwartz, S M, Shi, J, Smit, J H, Stringham, H M, Szeszenia-Dabrowska, N, Tanaka, T, Taylor, K, Thacker, E E, Thornton, L, Tiemeier, H, Tuomilehto, J, Uitterlinden, A G, van Duijn, C M, Vink, J M, Vogelzangs, N, Voight, B F, Walter, S, Willemsen, G, Zaridze, D, Znaor, A, Akil, H, Anjorin, A, Backlund, L, Badner, J A, Barchas, J D, Barrett, T, Bass, N, Bauer, M, Bellivier, F, Bergen, S E, Berrettini, W, Blackwood, D, Bloss, C S, Breen, G, Breuer, R, Bunner, W E, Burmeister, M, Byerley, W F, Caesar, S, Chambert, K, Cichon, S, St Clair, D, Collier, D A, Corvin, A, Coryell, W H, Craddock, N, Craig, D W, Daly, M, Day, R, Degenhardt, F, Djurovic, S, Dudbridge, F, Edenberg, H J, Elkin, A, Etain, B, Farmer, A E, Ferreira, M A, Ferrier, I, Flickinger, M, Foroud, T, Frank, J, Fraser, C, Frisén, L, Gershon, E S, Gill, M, Gordon-Smith, K, Green, E K, Greenwood, T A, Grozeva, D, Guan, W, Gurling, H, Gustafsson, O, Hamshere, M L, Hautzinger, M, Herms, S, Hipolito, M, Holmans, P A, Hultman, C M, Jamain, S, Jones, E G, Jones, I, Jones, L, Kandaswamy, R, Kennedy, J L, Kirov, G K, Koller, D L, Kwan, P, Landén, M, Langstrom, N, Lathrop, M, Lawrence, J, Lawson, W B, Leboyer, M, Lee, P H, Li, J, Lichtenstein, P, Lin, D, Liu, C, Lohoff, F W, Lucae, S, Mahon, P B, Maier, W, Martin, N G, Mattheisen, M, Matthews, K, Mattingsdal, M, McGhee, K A, McGuffin, P, McInnis, M G, McIntosh, A, McKinney, R, McLean, A W, McMahon, F J, McQuillin, A, Meier, S, Melle, I, Meng, F, Mitchell, P B, Montgomery, G W, Moran, J, Morken, G, Morris, D W, Moskvina, V, Muglia, P, Mühleisen, T W, Muir, W J, Müller-Myhsok, B, Myers, R M, Nievergelt, C M, Nikolov, I, Nimgaonkar, V L, Nöthen, M M, Nurnberger, J I, Nwulia, E A, O'Dushlaine, C, Osby, U, Óskarsson, H, Owen, M J, Petursson, H, Pickard, B S, Porgeirsson, P, Potash, J B, Propping, P, Purcell, S M, Quinn, E, Raychaudhuri, S, Rice, J, Rietschel, M, Ruderfer, D, Schalling, M, Schatzberg, A F, Scheftner, W A, Schofield, P R, Schulze, T G, Schumacher, J, Schwarz, M M, Scolnick, E, Scott, L J, Shilling, P D, Sigurdsson, E, Sklar, P, Smith, E N, Stefansson, H, Stefansson, K, Steffens, M, Steinberg, S, Strauss, J, Strohmaier, J, Szelinger, S, Thompson, R C, Tozzi, F, Treutlein, J, Vincent, J B, Watson, S J, Wienker, T F, Williamson, R, Witt, S H, Wright, A, Xu, W, Young, A H, Zandi, P P, Zhang, P, Zöllner, S, Agartz, I, Albus, M, Alexander, M, Amdur, R L, Amin, F, Bitter, I, Black, D W, Børglum, A D, Brown, M A, Bruggeman, R, Buccola, N G, Cahn, W, Cantor, R M, Carr, V J, Catts, S V, Choudhury, K, Cloninger, C R, Cormican, P, Danoy, P A, Datta, S, DeHert, M, Demontis, D, Dikeos, D, Donnelly, P, Donohoe, G, Duong, L, Dwyer, S, Fanous, A, Fink-Jensen, A, Freedman, R, Freimer, N B, Friedl, M, Georgieva, L, Giegling, I, Glenthoj, B, Godard, S, Golimbet, V, de Haan, L, Hansen, M, Hansen, T, Hartmann, A M, Henskens, F A, Hougaard, D M, Ingason, A, Jablensky, A V, Jakobsen, K D, Jay, M, Jönsson, E G, Jürgens, G, Kahn, R S, Keller, M C, Kendler, K S, Kenis, G, Kenny, E, Konnerth, H, Konte, B, Krabbendam, L, Krasucki, R, Lasseter, V K, Laurent, C, Lencz, T, Lerer, F B, Liang, K Y, Lieberman, J A, Linszen, D H, Lönnqvist, J, Loughland, C M, Maclean, A W, Maher, B S, Malhotra, A K, Mallet, J, Malloy, P, McGrath, J J, McLean, D E, Michie, P T, Milanova, V, Mors, O, Mortensen, P B, Mowry, B J, Myin-Germeys, I, Neale, B, Nertney, D A, Nestadt, G, Nielsen, J, Nordentoft, M, Norton, N, O'Neill, F, Olincy, A, Olsen, L, Ophoff, R A, Orntoft, T F, van Os, J, Pantelis, C, Papadimitriou, G, Pato, C N, Peltonen, L, Pickard, B, Pietilainen, O P, Pimm, J, Pulver, A E, Puri, V, Quested, D, Rasmussen, H B, Rethelyi, J M, Ribble, R, Riley, B P, Rossin, L, Ruggeri, M, Rujescu, D, Schall, U, Schwab, S G, Scott, R J, Silverman, J M, Spencer, C C, Strange, A, Strengman, E, Stroup, T S, Suvisaari, J, Terenius, L, Thirumalai, S, Timm, S, Toncheva, D, Tosato, S, van den Oord, E J, Veldink, J, Visscher, P M, Walsh, D, Wang, A G, Werge, T, Wiersma, D, Wildenauer, D B, Williams, H J, Williams, N M, van Winkel, R, Wormley, B, Zammit, S, Schork, N J, Andreassen, O A & Dale, A M 2013, ' All SNPs are not created equal: Genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs ', PLoS Genetics, vol. 9, no. 4, e1003449, pp. e1003449 . https://doi.org/10.1371/journal.pgen.1003449Test
BASE-Bielefeld Academic Search Engine
PLoS Genetics, Vol 9, Iss 4, p e1003449 (2013)
PLoS Genetics, 9(4):e1003449. Public Library of Science
PLoS genetics, 9(4). Public Library of Science
Plos Genetics, 9(4):e1003449. Public Library of Science

مصطلحات موضوعية: False discovery rate, Netherlands Twin Register (NTR), Cancer Research, Linkage disequilibrium, Genome-wide association study, Linkage Disequilibrium, 0302 clinical medicine, 2.1 Biological and endogenous factors, Aetiology, Genetics (clinical), Genetics, 0303 health sciences, Statistics, Genomics, Single Nucleotide, Genome Scans, Tobacco and Genetics Consortium, Functional Genomics, Phenotype, complex trait, Research Article, Bipolar Disorder Psychiatric Genomics Consortium, lcsh:QH426-470, SNP, Single-nucleotide polymorphism, Computational biology, Biostatistics, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, "genome-wide association study", Genome Analysis Tools, Clinical Research, Schizophrenia Psychiatric Genomics Consortium, Genome-Wide Association Studies, Humans, Genetic Predisposition to Disease, Statistical Methods, Polymorphism, Molecular Biology, Genetic Association Studies, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Genetic association, Linkage (software), Human Genome, Computational Biology, Human Genetics, Heritability, R1, schizophrenia, lcsh:Genetics, Schizophrenia, Mathematics, 030217 neurology & neurosurgery, Genome-Wide Association Study, Developmental Biology

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الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dbecf9afc07529e710d6735ed9014c9Test
https://escholarship.org/uc/item/9xc7s4vrTest

المؤلفون: Sklar, Pamela, Ferreira, M. A. R., Craddock, N., Meng, Y., Douglas Ruderfer, Fran, J., Daly, M. J., Holmans, P., O Donovan, M., Scolnick, E. M., Corvin, A. P., Blackwood, D. H., Gurling, H. M., Purcell, S. M.

المصدر: ResearcherID

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6532957b6d11da7f5c034155875231e5Test
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000265144200306&KeyUID=WOS:000265144200306Test