Odorant-binding protein: localization to nasal glands and secretions.

由 Pevsner, J, Sklar, P B, Snyder, S H
出版 1986

Odorant-binding protein and its mRNA are localized to lateral nasal gland implying a carrier function.

由 Pevsner, J, Hwang, P M, Sklar, P B, Venable, J C, Snyder, S H
出版 1988

Population genetic study of the brain-derived neurotrophic factor (BDNF) gene

由 Petryshen, TL, Sabeti, PC, Aldinger, KA, Fry, B, Fan, JB, Schaffner, SF, Waggoner, SG, Tahl, AR, Sklar, P
出版 2009

Analysis of BENCHMRK 1 & 2 using PhenoSense® assay for darunavir (DRV/r) resistance and exploration of functional monotherapy with RAL vs DRV

由 Rockstroh, J, Eron, J, Cooper, D, Steigbigel, R, Nguyen, BY, Xu, X, Wan, H, Rodgers, A, Miller, M, Leavitt, R, Sklar, P, Teppler, H
出版 2010

Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder

由 Bergen, SE, O’Dushlaine, CT, Ripke, S, Lee, PH, Ruderfer, DM, Akterin, S, Moran, JL, Chambert, KD, Handsaker, RE, Backlund, L, Ösby, U, McCarroll, S, Landen, M, Scolnick, EM, Magnusson, PKE, Lichtenstein, P, Hultman, CM, Purcell, SM, Sklar, P, Sullivan, PF
出版 2012

A genome-wide association study of kynurenic acid in cerebrospinal fluid: implications for psychosis and cognitive impairment in bipolar disorder

由 Sellgren, CM, Kegel, ME, Bergen, SE, Ekman, CJ, Olsson, S, Larsson, M, Vawter, MP, Backlund, L, Sullivan, PF, Sklar, P, Smoller, JW, Magnusson, PKE, Hultman, CM, Walther-Jallow, L, Svensson, CI, Lichtenstein, P, Schalling, M, Engberg, G, Erhardt, S, Landén, M
發表在 Mol Psychiatry (2013)

Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci

由 Andreassen, O A, Harbo, H F, Wang, Y, Thompson, W K, Schork, A J, Mattingsdal, M, Zuber, V, Bettella, F, Ripke, S, Kelsoe, J R, Kendler, K S, O'Donovan, M C, Sklar, P, McEvoy, L K, Desikan, R S, Lie, B A, Djurovic, S, Dale, A M
發表在 Mol Psychiatry (2015)

Copy number variation in bipolar disorder

由 Green, E K, Rees, E, Walters, J T R, Smith, K-G, Forty, L, Grozeva, D, Moran, J L, Sklar, P, Ripke, S, Chambert, K D, Genovese, G, McCarroll, S A, Jones, I, Jones, L, Owen, M J, O'Donovan, M C, Craddock, N, Kirov, G
發表在 Mol Psychiatry (2016)

Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder

由 Lee, P H, Perlis, R H, Jung, J-Y, Byrne, E M, Rueckert, E, Siburian, R, Haddad, S, Mayerfeld, C E, Heath, A C, Pergadia, M L, Madden, P A F, Boomsma, D I, Penninx, B W, Sklar, P, Martin, N G, Wray, N R, Purcell, S M, Smoller, J W
出版 2012

A genome-wide association study of kynurenic acid in cerebrospinal fluid: implications for psychosis and cognitive impairment in bipolar disorder

由 Sellgren, C M, Kegel, M E, Bergen, S E, Ekman, C J, Olsson, S, Larsson, M, Vawter, M P, Backlund, L, Sullivan, P F, Sklar, P, Smoller, J W, Magnusson, P K E, Hultman, C M, Walther-Jallow, L, Svensson, C I, Lichtenstein, P, Schalling, M, Engberg, G, Erhardt, S, Landén, M
發表在 Mol Psychiatry (2016)

Erratum: Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder

由 Song, J, Bergen, S E, Di Florio, A, Karlsson, R, Charney, A, Ruderfer, D M, Stahl, E A, Chambert, K D, Moran, J L, Gordon-Smith, K, Forty, L, Green, E K, Jones, I, Jones, L, Scolnick, E M, Sklar, P, Smoller, J W, Lichtenstein, P, Hultman, C, Craddock, N, Landén, M
發表在 Mol Psychiatry (2017)

Polygenic dissection of the bipolar phenotype

由 Hamshere, M. L., O’Donovan, M. C., Jones, I. R., Jones, L., Kirov, G., Green, E. K., Moskvina, V., Grozeva, D., Bass, N., McQuillin, A., Gurling, H., St Clair, D., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Sklar, P., Purcell, S., Holmans, P. A., Owen, M. J., Craddock, N.
出版 2011

Genomewide Linkage Analysis of Bipolar Disorder by Use of a High-Density Single-Nucleotide–Polymorphism (SNP) Genotyping Assay: A Comparison with Microsatellite Marker Assays and F...

由 Middleton, F. A., Pato, M. T., Gentile, K. L., Morley, C. P., Zhao, X., Eisener, A. F., Brown, A., Petryshen, T. L., Kirby, A. N., Medeiros, H., Carvalho, C., Macedo, A., Dourado, A., Coelho, I., Valente, J., Soares, M. J., Ferreira, C. P., Lei, M., Azevedo, M. H., Kennedy, J. L., Daly, M. J., Sklar, P., Pato, C. N.
出版 2004

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

由 Kirov, G, Pocklington, A J, Holmans, P, Ivanov, D, Ikeda, M, Ruderfer, D, Moran, J, Chambert, K, Toncheva, D, Georgieva, L, Grozeva, D, Fjodorova, M, Wollerton, R, Rees, E, Nikolov, I, van de Lagemaat, L N, Bayés, À, Fernandez, E, Olason, P I, Böttcher, Y, Komiyama, N H, Collins, M O, Choudhary, J, Stefansson, K, Stefansson, H, Grant, S G N, Purcell, S, Sklar, P, O'Donovan, M C, Owen, M J
出版 2012

Whole-genome Association Study of Bipolar Disorder

由 Sklar, P, Smoller, JW, Fan, J, Ferreira, MAR, Perlis, RH, Chambert, K, Nimgaonkar, VL, McQueen, MB, Faraone, SV, Kirby, A, de Bakker, PIW, Ogdie, MN, Thase, ME, Sachs, GS, Todd-Brown, K, Gabriel, SB, Sougnez, C, Gates, C, Blumenstiel, B, Defelice, M, Ardlie, KG, Franklin, J, Muir, WJ, McGhee, KA, MacIntyre, DM, McLean, A, VanBeck, M, McQuillin, A, Bass, NJ, Robinson, M, Lawrence, J, Anjorin, A, Curtis, D, Scolnick, EM, Daly, MJ, Blackwood, DH, Gurling, HM, Purcell, SM
出版 2008

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia

由 Rees, E, Kirov, G, Walters, J T, Richards, A L, Howrigan, D, Kavanagh, D H, Pocklington, A J, Fromer, M, Ruderfer, D M, Georgieva, L, Carrera, N, 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, Neale, B M, Palotie, A, Sklar, P, Purcell, S M, McCarroll, S A, Holmans, P, Owen, M J, O'Donovan, M C
發表在 Transl Psychiatry (2015)

Evidence that duplications of 22q11.2 protect against schizophrenia

由 Rees, E, Kirov, G, Sanders, A, Walters, J T R, Chambert, K D, Shi, J, Szatkiewicz, J, O'Dushlaine, C, Richards, A L, Green, E K, Jones, I, Davies, G, Legge, S E, Moran, J L, Pato, C, Pato, M, Genovese, G, Levinson, D, Duan, J, Moy, W, Göring, H H H, Morris, D, Cormican, P, Kendler, K S, O'Neill, F A, Riley, B, Gill, M, Corvin, A, Craddock, N, Sklar, P, Hultman, C, Sullivan, P F, Gejman, P V, McCarroll, S A, O'Donovan, M C, Owen, M J
出版 2014

Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder

由 Charney, A W, Ruderfer, D M, Stahl, E A, Moran, J L, Chambert, K, Belliveau, R A, Forty, L, Gordon-Smith, K, Di Florio, A, Lee, P H, Bromet, E J, Buckley, P F, Escamilla, M A, Fanous, A H, Fochtmann, L J, Lehrer, D S, Malaspina, D, Marder, S R, Morley, C P, Nicolini, H, Perkins, D O, Rakofsky, J J, Rapaport, M H, Medeiros, H, Sobell, J L, Green, E K, Backlund, L, Bergen, S E, Juréus, A, Schalling, M, Lichtenstein, P, Roussos, P, Knowles, J A, Jones, I, Jones, L A, Hultman, C M, Perlis, R H, Purcell, S M, McCarroll, S A, Pato, C N, Pato, M T, Craddock, N, Landén, M, Smoller, J W, Sklar, P
發表在 Transl Psychiatry (2017)

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

由 Chen, X, Lee, G, Maher, BS, Fanous, AH, Chen, J, Zhao, Z, Guo, A, van den Oord, E, Sullivan, PF, Shi, J, Levinson, DF, Gejman, PV, Sanders, A, Duan, J, Owen, MJ, Craddock, NJ, O’Donovan, MC, Blackman, J, Lewis, D, Kirov, GK, Qin, W, Schwab, S, Wildenauer, D, Chowdari, K, Nimgaonkar, V, Straub, RE, Weinberger, DR, O’Neill, FA, Walsh, D, Bronstein, M, Darvasi, A, Lencz, T, Malhotra, AK, Rujescu, D, Giegling, I, Werge, T, Hansen, T, Ingason, A, Nöethen, MM, Rietschel, M, Cichon, S, Djurovic, S, Andreassen, OA, Cantor, RM, Ophoff, R, Corvin, A, Morris, DW, Gill, M, Pato, CN, Pato, MT, Macedo, A, Gurling, HMD, McQuillin, A, Pimm, J, Hultman, C, Lichtenstein, P, Sklar, P, Purcell, SM, Scolnick, E, St Clair, D, Blackwood, DHR, Kendler, KS
出版 2010

Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder

由 Song, J, Bergen, S E, Di Florio, A, Karlsson, R, Charney, A, Ruderfer, D M, Stahl, E A, Chambert, K D, Moran, J L, Gordon-Smith, K, Forty, L, Green, E K, Jones, I, Jones, L, Scolnick, E M, Sklar, P, Smoller, J W, Lichtenstein, P, Hultman, C, Craddock, N, Landén, M, Smoller, Jordan W, Perlis, Roy H, Lee, Phil Hyoun, Castro, Victor M, Hoffnagle, Alison G, Sklar, Pamela, Stahl, Eli A, Purcell, Shaun M, Ruderfer, Douglas M, Charney, Alexander W, Roussos, Panos, Michele Pato, Carlos Pato, Medeiros, Helen, Sobel, Janet, Craddock, Nick, Jones, Ian, Forty, Liz, Florio, Arianna Di, Green, Elaine, Jones, Lisa, Gordon-Smith, Katherine, Landen, Mikael, Hultman, Christina, Jureus, Anders, Bergen, Sarah, McCarroll, Steven, Moran, Jennifer, Smoller, Jordan W, Chambert, Kimberly, Belliveau, Richard A
發表在 Mol Psychiatry (2016)