| Year |
Citation |
Score |
| 2023 |
Lo T, Kushima I, Kimura H, Aleksic B, Okada T, Kato H, Inada T, Nawa Y, Torii Y, Yamamoto M, Kimura R, Funabiki Y, Kosaka H, Numata S, Kasai K, et al. Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case-control study. Neuropsychopharmacology Reports. PMID 37915257 DOI: 10.1002/npr2.12370 |
0.345 |
|
| 2022 |
Furuta S, Aleksic B, Nawa Y, Kimura H, Kushima I, Ishizuka K, Kato H, Toyama M, Arioka Y, Mori D, Morikawa M, Inada T, Ozaki N. Investigation of as a candidate gene for schizophrenia and autism spectrum disorder. Nagoya Journal of Medical Science. 84: 260-268. PMID 35967956 DOI: 10.18999/nagjms.84.2.260 |
0.323 |
|
| 2022 |
Kato H, Kimura H, Kushima I, Takahashi N, Aleksic B, Ozaki N. The genetic architecture of schizophrenia: review of large-scale genetic studies. Journal of Human Genetics. PMID 35821406 DOI: 10.1038/s10038-022-01059-4 |
0.327 |
|
| 2022 |
Chen CH, Cheng MC, Hu TM, Ping LY, Kushima I, Aleksic B. Identification of rare mutations of the vasoactive intestinal peptide receptor 2 gene in schizophrenia. Psychiatric Genetics. 32: 125-130. PMID 35353798 DOI: 10.1097/YPG.0000000000000313 |
0.314 |
|
| 2020 |
Nawa Y, Kimura H, Mori D, Kato H, Toyama M, Furuta S, Yu Y, Ishizuka K, Kushima I, Aleksic B, Arioka Y, Morikawa M, Okada T, Inada T, Kaibuchi K, et al. Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility. Human Genome Variation. 7: 37. PMID 33298905 DOI: 10.1038/s41439-020-00125-7 |
0.335 |
|
| 2020 |
Kato H, Kushima I, Mori D, Yoshimi A, Aleksic B, Nawa Y, Toyama M, Furuta S, Yu Y, Ishizuka K, Kimura H, Arioka Y, Tsujimura K, Morikawa M, Okada T, et al. Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder. Translational Psychiatry. 10: 421. PMID 33279929 DOI: 10.1038/s41398-020-01107-7 |
0.312 |
|
| 2020 |
Sekiguchi M, Sobue A, Kushima I, Wang C, Arioka Y, Kato H, Kodama A, Kubo H, Ito N, Sawahata M, Hada K, Ikeda R, Shinno M, Mizukoshi C, Tsujimura K, ... ... Aleksic B, et al. ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk. Translational Psychiatry. 10: 247. PMID 32699248 DOI: 10.1038/S41398-020-00917-Z |
0.403 |
|
| 2020 |
Suzuki T, Suzuki T, Raveau M, Miyake N, Sudo G, Tsurusaki Y, Watanabe T, Sugaya Y, Tatsukawa T, Mazaki E, Shimohata A, Kushima I, Aleksic B, Shiino T, Toyota T, et al. A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders. Annals of Clinical and Translational Neurology. PMID 32530565 DOI: 10.1002/Acn3.51093 |
0.36 |
|
| 2020 |
Sawahata M, Mori D, Arioka Y, Kubo H, Kushima I, Kitagawa K, Sobue A, Shishido E, Sekiguchi M, Kodama A, Ikeda R, Aleksic B, Kimura H, Ishizuka K, Nagai T, et al. Generation and analysis of novel Reln-deleted mouse model corresponding to exonic Reln deletion in schizophrenia. Psychiatry and Clinical Neurosciences. PMID 32065683 DOI: 10.1111/Pcn.12993 |
0.429 |
|
| 2020 |
Arioka Y, Hirata A, Kushima I, Aleksic B, Mori D, Ozaki N. Characterization of a schizophrenia patient with a rare RELN deletion by combining genomic and patient-derived cell analyses. Schizophrenia Research. 216: 511-515. DOI: 10.1016/J.Schres.2019.10.038 |
0.385 |
|
| 2019 |
Kubota C, Inada T, Shiino T, Ando M, Aleksic B, Yamauchi A, Sato M, Ohara M, Murase S, Morikawa M, Nakamura Y, Okada T, Goto S, Kanai A, Ozaki N. Relation Between Perinatal Depressive Symptoms, Harm Avoidance, and a History of Major Depressive Disorder: A Cohort Study of Pregnant Women in Japan. Frontiers in Psychiatry. 10: 515. PMID 31404277 DOI: 10.3389/Fpsyt.2019.00515 |
0.302 |
|
| 2019 |
Novakovic N, Milovancevic MP, Dejanovic SD, Aleksic B. Effects of Snoezelen-Multisensory environment on CARS scale in adolescents and adults with autism spectrum disorder. Research in Developmental Disabilities. 89: 51-58. DOI: 10.1016/J.Ridd.2019.03.007 |
0.319 |
|
| 2019 |
Nawa Y, Kimura H, Ishizuka K, Kushima I, Aleksic B, Ozaki N. S98Investigation Of Rare Single-Nucleotide Dab1 Variants And Its Contribution To Schizophrenia And Autism Spectrum Disorder Susceptibility European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.08.099 |
0.451 |
|
| 2019 |
Kimura H, Aleksic B, Ishizuka K, Wang C, Kushima I, Ozaki N. Su126Target Sequencing Of Genes Involved In Neurodevelopment From Whole Genome Copy Number Variation Analysis Of Japanese Schizophrenia European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.490 |
0.382 |
|
| 2019 |
Kimura H, Ishizuka K, Wang C, Kushima I, Morikawa M, Uno Y, Okada T, Inanda T, Aleksic B, Mori D, Ozaki N. A Novel Rare Variant R292H In Rtn4R Affects Growth Cone Formation And Possibly Contributes To Schizophrenia Susceptibility European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.415 |
0.427 |
|
| 2019 |
Ishizuka K, Aleksic B, Ozaki N. Investigation Of Novel Rare Variants In Nrxn1 Contributes To The Increased Risk Of Autism Spectrum Disorders And Schizophrenia European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.085 |
0.473 |
|
| 2018 |
Ikeda M, Takahashi A, Kamatani Y, Momozawa Y, Saito T, Kondo K, Shimasaki A, Kawase K, Sakusabe T, Iwayama Y, Toyota T, Wakuda T, Kikuchi M, Kanahara N, Yamamori H, ... ... Aleksic B, et al. Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. Schizophrenia Bulletin. PMID 30285260 DOI: 10.1093/Schbul/Sby140 |
0.411 |
|
| 2018 |
Kushima I, Aleksic B, Nakatochi M, Shimamura T, Okada T, Uno Y, Morikawa M, Ishizuka K, Shiino T, Kimura H, Arioka Y, Yoshimi A, Takasaki Y, Yu Y, Nakamura Y, et al. Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights. Cell Reports. 24: 2838-2856. PMID 30208311 DOI: 10.1016/J.Celrep.2018.08.022 |
0.435 |
|
| 2018 |
Sobue A, Kushima I, Nagai T, Shan W, Kohno T, Aleksic B, Aoyama Y, Mori D, Arioka Y, Kawano N, Yamamoto M, Hattori M, Nabeshima T, Yamada K, Ozaki N. Genetic and animal model analyses reveal the pathogenic role of a novel deletion of RELN in schizophrenia. Scientific Reports. 8: 13046. PMID 30158644 DOI: 10.1038/S41598-018-31390-W |
0.379 |
|
| 2018 |
Ishizuka K, Kimura H, Kushima I, Inada T, Okahisa Y, Ikeda M, Iwata N, Mori D, Aleksic B, Ozaki N. Assessment of a glyoxalase I frameshift variant, p.P122fs, in Japanese patients with schizophrenia. Psychiatric Genetics. PMID 29975244 DOI: 10.1097/Ypg.0000000000000204 |
0.444 |
|
| 2018 |
Yu Y, Lin Y, Takasaki Y, Wang C, Kimura H, Xing J, Ishizuka K, Toyama M, Kushima I, Mori D, Arioka Y, Uno Y, Shiino T, Nakamura Y, Okada T, ... ... Aleksic B, et al. Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility. Translational Psychiatry. 8: 12. PMID 29317596 DOI: 10.1038/S41398-017-0061-Y |
0.359 |
|
| 2017 |
Ogasawara K, Nakamura Y, Kimura H, Aleksic B, Ozaki N. Issues on the diagnosis and etiopathogenesis of mood disorders: reconsidering DSM-5. Journal of Neural Transmission (Vienna, Austria : 1996). PMID 29275445 DOI: 10.1007/S00702-017-1828-2 |
0.349 |
|
| 2017 |
Kimura H, Kushima I, Yohimi A, Aleksic B, Ozaki N. Copy number variant in the region of adenosine kinase (ADK) and its possible contribution to schizophrenia susceptibility. The International Journal of Neuropsychopharmacology. PMID 29126171 DOI: 10.1093/Ijnp/Pyx103 |
0.383 |
|
| 2017 |
Ishizuka K, Tabata H, Ito H, Kushima I, Noda M, Yoshimi A, Usami M, Watanabe K, Morikawa M, Uno Y, Okada T, Mori D, Aleksic B, Ozaki N, Nagata KI. Possible involvement of a cell adhesion molecule, Migfilin, in brain development and pathogenesis of autism spectrum disorders. Journal of Neuroscience Research. PMID 29114925 DOI: 10.1002/Jnr.24194 |
0.347 |
|
| 2017 |
Ishizuka K, Fujita Y, Kawabata T, Kimura H, Iwayama Y, Inada T, Okahisa Y, Egawa J, Usami M, Kushima I, Uno Y, Okada T, Ikeda M, Aleksic B, Mori D, et al. Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders. Translational Psychiatry. 7: e1184. PMID 28763059 DOI: 10.1038/Tp.2017.173 |
0.422 |
|
| 2017 |
Lim ET, Uddin M, De Rubeis S, Chan Y, Kamumbu AS, Zhang X, D'Gama AM, Kim SN, Hill RS, Goldberg AP, Poultney C, Minshew NJ, Kushima I, Aleksic B, Ozaki N, et al. Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nature Neuroscience. PMID 28714951 DOI: 10.1038/Nn.4598 |
0.331 |
|
| 2017 |
Aleksic B, Ozaki N. Schizophrenia polygenic risk score and prepubertal developmental impairments The Lancet Psychiatry. 4: 7-8. PMID 27932232 DOI: 10.1016/S2215-0366(16)30409-6 |
0.383 |
|
| 2017 |
Fujioi J, Iwamoto K, Banno M, Kikuchi T, Aleksic B, Ozaki N. Effect of Adjunctive Aripiprazole on Sexual Dysfunction in Schizophrenia: A Preliminary Open-Label Study. Pharmacopsychiatry. 50: 74-78. PMID 27656915 DOI: 10.1055/S-0042-116323 |
0.33 |
|
| 2016 |
Ishizuka K, Kimura H, Yoshimi A, Banno M, Kushima I, Uno Y, Okada T, Mori D, Aleksic B, Ozaki N. Investigation of single-nucleotide variants in MBD5 associated with autism spectrum disorders and schizophrenia phenotypes. Nagoya Journal of Medical Science. 78: 465-474. PMID 28008202 DOI: 10.18999/Nagjms.78.4.465 |
0.447 |
|
| 2016 |
Takasaki Y, Koide T, Wang C, Kimura H, Xing J, Kushima I, Ishizuka K, Mori D, Sekiguchi M, Ikeda M, Aizawa M, Tsurumaru N, Iwayama Y, Yoshimi A, Arioka Y, ... ... Aleksic B, et al. Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population. Scientific Reports. 6: 33311. PMID 27616045 DOI: 10.1038/Srep33311 |
0.377 |
|
| 2016 |
Kimura H, Wang C, Ishizuka K, Xing J, Takasaki Y, Kushima I, Aleksic B, Uno Y, Okada T, Ikeda M, Mori D, Inada T, Iwata N, Ozaki N. Identification of a rare variant in CHD8 that contributes to schizophrenia and autism spectrum disorder susceptibility. Schizophrenia Research. PMID 27595554 DOI: 10.1016/J.Schres.2016.08.023 |
0.447 |
|
| 2016 |
Kuroki T, Ishitobi M, Kamio Y, Sugihara G, Murai T, Motomura K, Ogasawara K, Kimura H, Aleksic B, Ozaki N, Nakao T, Yamada K, Yoshiuchi K, Kiriike N, Ishikawa T, et al. Current Viewpoints on DSM-5 in Japan. Psychiatry and Clinical Neurosciences. PMID 27414748 DOI: 10.1111/Pcn.12421 |
0.347 |
|
| 2016 |
Xing J, Kimura H, Wang C, Ishizuka K, Kushima I, Arioka Y, Yoshimi A, Nakamura Y, Shiino T, Oya-Ito T, Takasaki Y, Uno Y, Okada T, Iidaka T, Aleksic B, et al. Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders. Scientific Reports. 6: 27491. PMID 27271353 DOI: 10.1038/Srep27491 |
0.444 |
|
| 2016 |
Kushima I, Aleksic B, Nakatochi M, Shimamura T, Shiino T, Yoshimi A, Kimura H, Takasaki Y, Wang C, Xing J, Ishizuka K, Oya-Ito T, Nakamura Y, Arioka Y, Maeda T, et al. High-resolution copy number variation analysis of schizophrenia in Japan. Molecular Psychiatry. PMID 27240532 DOI: 10.1038/Mp.2016.88 |
0.389 |
|
| 2016 |
Isles AR, Ingason A, Lowther C, Walters J, Gawlick M, Stöber G, Rees E, Martin J, Little RB, Potter H, Georgieva L, Pizzo L, Ozaki N, Aleksic B, Kushima I, et al. Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. Plos Genetics. 12: e1005993. PMID 27153221 DOI: 10.1371/Journal.Pgen.1005993 |
0.339 |
|
| 2016 |
Ishizuka K, Kimura H, Wang C, Xing J, Kushima I, Arioka Y, Oya-Ito T, Uno Y, Okada T, Mori D, Aleksic B, Ozaki N. Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders. Plos One. 11: e0153224. PMID 27058588 DOI: 10.1371/Journal.Pone.0153224 |
0.429 |
|
| 2016 |
Higashiyama R, Ohnuma T, Takebayashi Y, Hanzawa R, Shibata N, Yamamori H, Yasuda Y, Kushima I, Aleksic B, Kondo K, Ikeda M, Hashimoto R, Iwata N, Ozaki N, Arai H. Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 171: 447-57. PMID 26852906 DOI: 10.1002/Ajmg.B.32426 |
0.441 |
|
| 2016 |
Higashiyama R, Ohnuma T, Takebayashi Y, Hanzawa R, Shibata N, Yamamori H, Yasuda Y, Kushima I, Aleksic B, Kondo K, Ikeda M, Hashimoto R, Iwata N, Ozaki N, Arai H. Association of copy number polymorphisms at the promoter and translated region of COMT with Japanese patients with schizophrenia American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. DOI: 10.1002/ajmg.b.32426 |
0.316 |
|
| 2015 |
Tanaka S, Yoshida K, Katayama H, Kohmura K, Kawano N, Imaeda M, Kato S, Ando M, Aleksic B, Nishioka K, Ozaki N. Association of Beck Depression Inventory score and Temperament and Character Inventory-125 in patients with eating disorders and severe malnutrition. Journal of Eating Disorders. 3: 36. PMID 26550476 DOI: 10.1186/S40337-015-0077-8 |
0.334 |
|
| 2015 |
Kimura H, Tanaka S, Kushima I, Koide T, Banno M, Kikuchi T, Nakamura Y, Shiino T, Yoshimi A, Oya-Ito T, Xing J, Wang C, Takasaki Y, Aleksic B, Okada T, et al. Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population. Scientific Reports. 5: 15705. PMID 26494551 DOI: 10.1038/Srep15705 |
0.425 |
|
| 2015 |
Wang C, Aleksic B, Ozaki N. Glia-related genes and their contribution to schizophrenia. Psychiatry and Clinical Neurosciences. PMID 25759284 DOI: 10.1111/Pcn.12290 |
0.434 |
|
| 2015 |
Kimura H, Tsuboi D, Wang C, Kushima I, Koide T, Ikeda M, Iwayama Y, Toyota T, Yamamoto N, Kunimoto S, Nakamura Y, Yoshimi A, Banno M, Xing J, Takasaki Y, ... ... Aleksic B, et al. Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility. Schizophrenia Bulletin. 41: 744-53. PMID 25332407 DOI: 10.1093/Schbul/Sbu147 |
0.41 |
|
| 2015 |
Takahashi T, Nakamura M, Nakamura Y, Aleksic B, Kido M, Sasabayashi D, Takayanagi Y, Furuichi A, Nishikawa Y, Noguchi K, Ozaki N, Suzuki M. The Disrupted-in-Schizophrenia-1 Ser704Cys polymorphism and brain neurodevelopmental markers in schizophrenia and healthy subjects. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 56: 11-7. PMID 25092219 DOI: 10.1016/J.Pnpbp.2014.07.005 |
0.431 |
|
| 2014 |
Xing J, Wang C, Kimura H, Takasaki Y, Kunimoto S, Yoshimi A, Nakamura Y, Koide T, Banno M, Kushima I, Uno Y, Okada T, Aleksic B, Ikeda M, Iwata N, et al. Resequencing and association analysis of PTPRA, a possible susceptibility gene for schizophrenia and autism spectrum disorders. Plos One. 9: e112531. PMID 25393624 DOI: 10.1371/Journal.Pone.0112531 |
0.48 |
|
| 2014 |
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 515: 209-15. PMID 25363760 DOI: 10.1038/Nature13772 |
0.301 |
|
| 2014 |
Kido M, Nakamura Y, Nemoto K, Takahashi T, Aleksic B, Furuichi A, Nakamura Y, Ikeda M, Noguchi K, Kaibuchi K, Iwata N, Ozaki N, Suzuki M. The polymorphism of YWHAE, a gene encoding 14-3-3epsilon, and brain morphology in schizophrenia: a voxel-based morphometric study. Plos One. 9: e103571. PMID 25105667 DOI: 10.1371/Journal.Pone.0103571 |
0.41 |
|
| 2014 |
Katayama H, Kohmura K, Tanaka S, Imaeda M, Kawano N, Noda Y, Nishioka K, Ando M, Aleksic B, Iidaka T, Ozaki N. Social insecurity in relation to orbitofrontal activity in patients with eating disorders: a near-infrared spectroscopy study. Bmc Psychiatry. 14: 173. PMID 24924100 DOI: 10.1186/1471-244X-14-173 |
0.307 |
|
| 2014 |
Saito T, Kondo K, Iwayama Y, Shimasaki A, Aleksic B, Yamada K, Toyota T, Hattori E, Esaki K, Ujike H, Inada T, Kunugi H, Kato T, Yoshikawa T, Ozaki N, et al. Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: support for association of MHC region with psychosis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 421-7. PMID 24888570 DOI: 10.1002/Ajmg.B.32246 |
0.407 |
|
| 2014 |
Wang C, Koide T, Kimura H, Kunimoto S, Yoshimi A, Nakamura Y, Kushima I, Banno M, Kawano N, Takasaki Y, Xing J, Noda Y, Mouri A, Aleksic B, Ikeda M, et al. Novel rare variants in F-box protein 45 (FBXO45) in schizophrenia. Schizophrenia Research. 157: 149-56. PMID 24878430 DOI: 10.1016/J.Schres.2014.04.032 |
0.432 |
|
| 2014 |
Takahashi T, Nakamura Y, Nakamura Y, Aleksic B, Takayanagi Y, Furuichi A, Kido M, Nakamura M, Sasabayashi D, Ikeda M, Noguchi K, Kaibuchi K, Iwata N, Ozaki N, Suzuki M. The polymorphism of YWHAE, a gene encoding 14-3-3epsilon, and orbitofrontal sulcogyral pattern in patients with schizophrenia and healthy subjects. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 51: 166-71. PMID 24561237 DOI: 10.1016/J.Pnpbp.2014.02.005 |
0.427 |
|
| 2014 |
Shishido E, Aleksic B, Ozaki N. Copy-number variation in the pathogenesis of autism spectrum disorder. Psychiatry and Clinical Neurosciences. 68: 85-95. PMID 24372918 DOI: 10.1111/Pcn.12128 |
0.374 |
|
| 2014 |
Kajio Y, Kondo K, Saito T, Iwayama Y, Aleksic B, Yamada K, Toyota T, Hattori E, Ujike H, Inada T, Kunugi H, Kato T, Yoshikawa T, Ozaki N, Ikeda M, et al. Genetic association study between the detected risk variants based upon type II diabetes GWAS and psychotic disorders in the Japanese population. Journal of Human Genetics. 59: 54-6. PMID 24196380 DOI: 10.1038/Jhg.2013.116 |
0.401 |
|
| 2014 |
Suzuki M, Nakamura Y, Nakamura Y, Aleksic B, Takayanagi Y, Furuichi A, Kido M, Noguchi K, Kaibuchi K, Ozaki N, Takahashi T. Poster #S66 THE POLYMORPHISM OF YWHAE, A GENE ENCODING 14-3-3EPSILON, AND ORBITOFRONTAL SULCOGYRAL PATTERN IN SCHIZOPHRENIA AND HEALTHY SUBJECTS Schizophrenia Research. 153. DOI: 10.1016/S0920-9964(14)70345-7 |
0.391 |
|
| 2013 |
Aleksic B, Kushima I, Ohye T, Ikeda M, Kunimoto S, Nakamura Y, Yoshimi A, Koide T, Iritani S, Kurahashi H, Iwata N, Ozaki N. Definition and refinement of the 7q36.3 duplication region associated with schizophrenia. Scientific Reports. 3: 2587. PMID 24002029 DOI: 10.1038/Srep02587 |
0.417 |
|
| 2013 |
Kondo K, Ikeda M, Kajio Y, Saito T, Iwayama Y, Aleksic B, Yamada K, Toyota T, Hattori E, Ujike H, Inada T, Kunugi H, Kato T, Yoshikawa T, Ozaki N, et al. Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study. Plos One. 8: e70964. PMID 23967141 DOI: 10.1371/Journal.Pone.0070964 |
0.415 |
|
| 2013 |
Ukai K, Kimura H, Arao M, Aleksic B, Yamauchi A, Ishihara R, Iritani S, Kurita K, Ozaki N. Effectiveness of low-dose milnacipran for a patient suffering from pain disorder with delusional disorder (somatic type) in the orofacial region. Psychogeriatrics : the Official Journal of the Japanese Psychogeriatric Society. 13: 99-102. PMID 23909967 DOI: 10.1111/J.1479-8301.2012.00430.X |
0.305 |
|
| 2013 |
Hashimoto R, Ikeda M, Ohi K, Yasuda Y, Yamamori H, Fukumoto M, Umeda-Yano S, Dickinson D, Aleksic B, Iwase M, Kazui H, Ozaki N, Weinberger DR, Iwata N, Takeda M. Genome-wide association study of cognitive decline in schizophrenia. The American Journal of Psychiatry. 170: 683-4. PMID 23732972 DOI: 10.1176/Appi.Ajp.2013.12091228 |
0.369 |
|
| 2013 |
Ikeda M, Okahisa Y, Aleksic B, Won M, Kondo N, Naruse N, Aoyama-Uehara K, Sora I, Iyo M, Hashimoto R, Kawamura Y, Nishida N, Miyagawa T, Takeda M, Sasaki T, et al. Evidence for shared genetic risk between methamphetamine-induced psychosis and schizophrenia. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 38: 1864-70. PMID 23594818 DOI: 10.1038/Npp.2013.94 |
0.442 |
|
| 2013 |
Ikeda M, Aleksic B, Yamada K, Iwayama-Shigeno Y, Matsuo K, Numata S, Watanabe Y, Ohnuma T, Kaneko T, Fukuo Y, Okochi T, Toyota T, Hattori E, Shimodera S, Itakura M, et al. Genetic evidence for association between NOTCH4 and schizophrenia supported by a GWAS follow-up study in a Japanese population. Molecular Psychiatry. 18: 636-8. PMID 22641179 DOI: 10.1038/Mp.2012.74 |
0.41 |
|
| 2013 |
Aleksic B, Kushima I, Hashimoto R, Ohi K, Ikeda M, Yoshimi A, Nakamura Y, Ito Y, Okochi T, Fukuo Y, Yasuda Y, Fukumoto M, Yamamori H, Ujike H, Suzuki M, et al. Analysis of the VAV3 as candidate gene for schizophrenia: evidences from voxel-based morphometry and mutation screening. Schizophrenia Bulletin. 39: 720-8. PMID 22416266 DOI: 10.1093/Schbul/Sbs038 |
0.47 |
|
| 2012 |
Banno M, Koide T, Aleksic B, Okada T, Kikuchi T, Kohmura K, Adachi Y, Kawano N, Iidaka T, Ozaki N. Wisconsin Card Sorting Test scores and clinical and sociodemographic correlates in Schizophrenia: multiple logistic regression analysis. Bmj Open. 2. PMID 23135537 DOI: 10.1136/Bmjopen-2012-001340 |
0.38 |
|
| 2012 |
Matsunaga S, Ikeda M, Kishi T, Fukuo Y, Aleksic B, Yoshimura R, Okochi T, Yamanouchi Y, Kinoshita Y, Kawashima K, Umene-Nakano W, Inada T, Kunugi H, Kato T, Yoshikawa T, et al. An evaluation of polymorphisms in casein kinase 1 delta and epsilon genes in major psychiatric disorders. Neuroscience Letters. 529: 66-9. PMID 22981886 DOI: 10.1016/J.Neulet.2012.08.070 |
0.425 |
|
| 2012 |
Koide T, Aleksic B, Kikuchi T, Banno M, Kohmura K, Adachi Y, Kawano N, Iidaka T, Ozaki N. Evaluation of factors affecting continuous performance test identical pairs version score of schizophrenic patients in a Japanese clinical sample. Schizophrenia Research and Treatment. 2012: 970131. PMID 22966454 DOI: 10.1155/2012/970131 |
0.382 |
|
| 2012 |
Koide T, Banno M, Aleksic B, Yamashita S, Kikuchi T, Kohmura K, Adachi Y, Kawano N, Kushima I, Nakamura Y, Okada T, Ikeda M, Ohi K, Yasuda Y, Hashimoto R, et al. Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients. Plos One. 7: e36836. PMID 22649501 DOI: 10.1371/Journal.Pone.0036836 |
0.456 |
|
| 2012 |
Adachi Y, Aleksic B, Nobata R, Suzuki T, Yoshida K, Ono Y, Ozaki N. Combination use of Beck Depression Inventory and two-question case-finding instrument as a screening tool for depression in the workplace. Bmj Open. 2. PMID 22566608 DOI: 10.1136/Bmjopen-2011-000596 |
0.3 |
|
| 2012 |
Kitazawa M, Ohnuma T, Takebayashi Y, Shibata N, Baba H, Ohi K, Yasuda Y, Nakamura Y, Aleksic B, Yoshimi A, Okochi T, Ikeda M, Naitoh H, Hashimoto R, Iwata N, et al. No associations found between the genes situated at 6p22.1, HIST1H2BJ, PRSS16, and PGBD1 in Japanese patients diagnosed with schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 456-64. PMID 22488895 DOI: 10.1002/Ajmg.B.32049 |
0.455 |
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| 2012 |
Kikuchi T, Iwamoto K, Sasada K, Aleksic B, Yoshida K, Ozaki N. Sexual dysfunction and hyperprolactinemia in Japanese schizophrenic patients taking antipsychotics. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 37: 26-32. PMID 22172534 DOI: 10.1016/J.Pnpbp.2011.11.016 |
0.303 |
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| 2012 |
Kushima I, Nakamura Y, Aleksic B, Ikeda M, Ito Y, Shiino T, Okochi T, Fukuo Y, Ujike H, Suzuki M, Inada T, Hashimoto R, Takeda M, Kaibuchi K, Iwata N, et al. Resequencing and association analysis of the KALRN and EPHB1 genes and their contribution to schizophrenia susceptibility. Schizophrenia Bulletin. 38: 552-60. PMID 21041834 DOI: 10.1093/Schbul/Sbq118 |
0.431 |
|
| 2011 |
Banno M, Koide T, Aleksic B, Yamada K, Kikuchi T, Kohmura K, Adachi Y, Kawano N, Kushima I, Ikeda M, Inada T, Yoshikawa T, Iwata N, Ozaki N. A case control association study and cognitive function analysis of neuropilin and tolloid-like 1 gene and schizophrenia in the Japanese population. Plos One. 6: e28929. PMID 22205981 DOI: 10.1371/Journal.Pone.0028929 |
0.337 |
|
| 2011 |
Takahashi N, Nielsen KS, Aleksic B, Petersen S, Ikeda M, Kushima I, Vacaresse N, Ujike H, Iwata N, Dubreuil V, Mirza N, Sakurai T, Ozaki N, Buxbaum JD, Sap J. Loss of function studies in mice and genetic association link receptor protein tyrosine phosphatase α to schizophrenia. Biological Psychiatry. 70: 626-35. PMID 21831360 DOI: 10.1016/J.Biopsych.2011.06.016 |
0.417 |
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| 2011 |
Yoshimura T, Usui H, Takahashi N, Yoshimi A, Saito S, Aleksic B, Ujike H, Inada T, Yamada M, Uchimura N, Iwata N, Sora I, Iyo M, Ozaki N. Association analysis of the GDNF gene with methamphetamine use disorder in a Japanese population. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 35: 1268-72. PMID 21514351 DOI: 10.1016/J.Pnpbp.2011.04.003 |
0.327 |
|
| 2011 |
Ikeda M, Aleksic B, Kinoshita Y, Okochi T, Kawashima K, Kushima I, Ito Y, Nakamura Y, Kishi T, Okumura T, Fukuo Y, Williams HJ, Hamshere ML, Ivanov D, Inada T, et al. Genome-wide association study of schizophrenia in a Japanese population. Biological Psychiatry. 69: 472-8. PMID 20832056 DOI: 10.1016/J.Biopsych.2010.07.010 |
0.457 |
|
| 2010 |
Nakamura Y, Ito Y, Aleksic B, Kushima I, Yasui-Furukori N, Inada T, Ono Y, Ozaki N. Influence of HTR2A polymorphisms and parental rearing on personality traits in healthy Japanese subjects. Journal of Human Genetics. 55: 838-41. PMID 20827275 DOI: 10.1038/Jhg.2010.110 |
0.311 |
|
| 2010 |
Yoshimi A, Aleksic B, Kawamura Y, Takahashi N, Yamada S, Usui H, Saito S, Ito Y, Iwata N, Inada T, Noda Y, Yamada K, Ozaki N. Gene-wide association study between the methylenetetrahydrofolate reductase gene (MTHFR) and schizophrenia in the Japanese population, with an updated meta-analysis on currently available data. Schizophrenia Research. 124: 216-22. PMID 20692813 DOI: 10.1016/J.Schres.2010.07.011 |
0.426 |
|
| 2010 |
Koide T, Aleksic B, Ito Y, Usui H, Yoshimi A, Inada T, Suzuki M, Hashimoto R, Takeda M, Iwata N, Ozaki N. A two-stage case-control association study of the dihydropyrimidinase-like 2 gene (DPYSL2) with schizophrenia in Japanese subjects. Journal of Human Genetics. 55: 469-72. PMID 20414250 DOI: 10.1038/Jhg.2010.38 |
0.402 |
|
| 2010 |
Aleksic B, Kushima I, Ito Y, Nakamura Y, Ujike H, Suzuki M, Inada T, Hashimoto R, Takeda M, Iwata N, Ozaki N. Genetic association study of KREMEN1 and DKK1 and schizophrenia in a Japanese population. Schizophrenia Research. 118: 113-7. PMID 20153141 DOI: 10.1016/J.Schres.2010.01.014 |
0.454 |
|
| 2010 |
Kushima I, Aleksic B, Ito Y, Nakamura Y, Nakamura K, Mori N, Kikuchi M, Inada T, Kunugi H, Nanko S, Kato T, Yoshikawa T, Ujike H, Suzuki M, Iwata N, et al. Association study of ubiquitin-specific peptidase 46 (USP46) with bipolar disorder and schizophrenia in a Japanese population. Journal of Human Genetics. 55: 133-6. PMID 20111060 DOI: 10.1038/Jhg.2009.139 |
0.465 |
|
| 2010 |
Kushima I, Aleksic B, Ikeda M, Yamanouchi Y, Kinoshita Y, Ito Y, Nakamura Y, Inada T, Iwata N, Ozaki N. Association study of bromodomain-containing 1 gene with schizophrenia in Japanese population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 786-91. PMID 19908236 DOI: 10.1002/Ajmg.B.31048 |
0.456 |
|
| 2010 |
Ikeda M, Aleksic B, Kirov G, Kinoshita Y, Yamanouchi Y, Kitajima T, Kawashima K, Okochi T, Kishi T, Zaharieva I, Owen MJ, O'Donovan MC, Ozaki N, Iwata N. Copy number variation in schizophrenia in the Japanese population. Biological Psychiatry. 67: 283-6. PMID 19880096 DOI: 10.1016/J.Biopsych.2009.08.034 |
0.366 |
|
| 2009 |
Kawashima K, Ikeda M, Kishi T, Kitajima T, Yamanouchi Y, Kinoshita Y, Okochi T, Aleksic B, Tomita M, Okada T, Kunugi H, Inada T, Ozaki N, Iwata N. BDNF is not associated with schizophrenia: data from a Japanese population study and meta-analysis. Schizophrenia Research. 112: 72-9. PMID 19406621 DOI: 10.1016/J.Schres.2009.03.040 |
0.408 |
|
| 2009 |
Ito Y, Koide T, Aleksic B, Inada T, Iwata N, Ozaki N. Dense association mapping of dihydropyrimidinase-like 2 (DPYSL2) gene in susceptibility to schizophrenia in a Japanese population Neuroscience Research. 65. DOI: 10.1016/J.Neures.2009.09.1441 |
0.395 |
|
| 2008 |
Kinoshita Y, Ikeda M, Ujike H, Kitajima T, Yamanouchi Y, Aleksic B, Kishi T, Kawashima K, Ohkouchi T, Ozaki N, Inada T, Harano M, Komiyama T, Hori T, Yamada M, et al. Association study of the calcineurin A gamma subunit gene (PPP3CC) and methamphetamine-use disorder in a Japanese population. Annals of the New York Academy of Sciences. 1139: 57-62. PMID 18991849 DOI: 10.1196/Annals.1432.021 |
0.465 |
|
| 2008 |
Aleksic B, Ikeda M, Ishihara R, Saito S, Inada T, Iwata N, Ozaki N. No association between the oligodendrocyte-related gene PLP1 and schizophrenia in the Japanese population. Journal of Human Genetics. 53: 863-6. PMID 18604471 DOI: 10.1007/S10038-008-0318-7 |
0.419 |
|
| 2008 |
Ito Y, Nakamura Y, Takahashi N, Saito S, Aleksic B, Iwata N, Inada T, Ozaki N. A genetic association study of the FXYD domain containing ion transport regulator 6 (FXYD6) gene, encoding phosphohippolin, in susceptibility to schizophrenia in a Japanese population. Neuroscience Letters. 438: 70-5. PMID 18455306 DOI: 10.1016/J.Neulet.2008.04.010 |
0.426 |
|
| 2008 |
Saito S, Takahashi N, Maeno N, Ito Y, Aleksic B, Usui H, Iidaka T, Inada T, Ozaki N. An association study of tachykinin receptor 3 gene with schizophrenia in the Japanese population. Neuroreport. 19: 471-3. PMID 18287949 DOI: 10.1097/Wnr.0B013E3282F600B4 |
0.409 |
|
| 2008 |
Ikeda M, Takahashi N, Saito S, Aleksic B, Watanabe Y, Nunokawa A, Yamanouchi Y, Kitajima T, Kinoshita Y, Kishi T, Kawashima K, Hashimoto R, Ujike H, Inada T, Someya T, et al. Failure to replicate the association between NRG1 and schizophrenia using Japanese large sample. Schizophrenia Research. 101: 1-8. PMID 18282690 DOI: 10.1016/J.Schres.2008.01.010 |
0.409 |
|
| 2008 |
Yoshimi A, Takahashi N, Saito S, Ito Y, Aleksic B, Usui H, Kawamura Y, Waki Y, Yoshikawa T, Kato T, Iwata N, Inada T, Noda Y, Ozaki N. Genetic analysis of the gene coding for DARPP-32 (PPP1R1B) in Japanese patients with schizophrenia or bipolar disorder. Schizophrenia Research. 100: 334-41. PMID 18055181 DOI: 10.1016/J.Schres.2007.10.028 |
0.471 |
|
| 2007 |
Aleksic B, Ishihara R, Takahashi N, Maeno N, Ji X, Saito S, Inada T, Ozaki N. Gap junction coding genes and schizophrenia: a genetic association study. Journal of Human Genetics. 52: 498-501. PMID 17427027 DOI: 10.1007/S10038-007-0142-5 |
0.461 |
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