Similar articles for PMID: 29385606

Year	Number of Results
2009	1
2011	1
2012	2
2013	6
2014	3
2015	7
2016	13
2017	15
2018	16
2019	21
2020	20
2021	18
2022	8
2023	4
2024	0

1

Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis.

John J, Sharma A, Kukshal P, Bhatia T, Nimgaonkar VL, Deshpande SN, Thelma BK. John J, et al. Schizophr Bull. 2019 Jan 1;45(1):256-263. doi: 10.1093/schbul/sbx196. Schizophr Bull. 2019. PMID: 29385606 Free PMC article.

2

Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study.

John J, Kukshal P, Sharma A, Bhatia T, Nimgaonkar VL, Deshpande SN, Thelma BK. John J, et al. Schizophr Res. 2019 Apr;206:75-81. doi: 10.1016/j.schres.2018.12.012. Epub 2018 Dec 27. Schizophr Res. 2019. PMID: 30594456 Free PMC article.

3

Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia.

John J, Kukshal P, Bhatia T, Chowdari KV, Nimgaonkar VL, Deshpande SN, Thelma BK. John J, et al. Schizophr Res. 2017 Nov;189:190-195. doi: 10.1016/j.schres.2017.02.020. Epub 2017 Feb 24. Schizophr Res. 2017. PMID: 28242106 Free PMC article.

4

Multiple rare inherited variants in a four generation schizophrenia family offer leads for complex mode of disease inheritance.

John J, Bhattacharyya U, Yadav N, Kukshal P, Bhatia T, Nimgaonkar VL, Deshpande SN, Thelma BK. John J, et al. Schizophr Res. 2020 Feb;216:288-294. doi: 10.1016/j.schres.2019.11.041. Epub 2019 Dec 5. Schizophr Res. 2020. PMID: 31813803 Free PMC article.

5

Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.

Egawa J, Hoya S, Watanabe Y, Nunokawa A, Shibuya M, Ikeda M, Inoue E, Okuda S, Kondo K, Saito T, Kaneko N, Muratake T, Igeta H, Iwata N, Someya T. Egawa J, et al. Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):797-805. doi: 10.1002/ajmg.b.32444. Epub 2016 Mar 14. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 26990377

6

An examination of multiple classes of rare variants in extended families with bipolar disorder.

Toma C, Shaw AD, Allcock RJN, Heath A, Pierce KD, Mitchell PB, Schofield PR, Fullerton JM. Toma C, et al. Transl Psychiatry. 2018 Mar 13;8(1):65. doi: 10.1038/s41398-018-0113-y. Transl Psychiatry. 2018. PMID: 29531218 Free PMC article.

7

Exome Sequencing of Familial Bipolar Disorder.

Goes FS, Pirooznia M, Parla JS, Kramer M, Ghiban E, Mavruk S, Chen YC, Monson ET, Willour VL, Karchin R, Flickinger M, Locke AE, Levy SE, Scott LJ, Boehnke M, Stahl E, Moran JL, Hultman CM, Landén M, Purcell SM, Sklar P, Zandi PP, McCombie WR, Potash JB. Goes FS, et al. JAMA Psychiatry. 2016 Jun 1;73(6):590-7. doi: 10.1001/jamapsychiatry.2016.0251. JAMA Psychiatry. 2016. PMID: 27120077 Free PMC article.

8

Rare Pathogenic Variants in Genes Implicated in Glutamatergic Neurotransmission Pathway Segregate with Schizophrenia in Pakistani Families.

Fatima A, Abdullah U, Farooq M, Mang Y, Mehrjouy MM, Asif M, Ali Z, Tommerup N, Baig SM. Fatima A, et al. Genes (Basel). 2021 Nov 26;12(12):1899. doi: 10.3390/genes12121899. Genes (Basel). 2021. PMID: 34946848 Free PMC article.

9

Co-Occurrence of Familial Non-Medullary Thyroid Cancer (FNMTC) and Hereditary Non-Polyposis Colorectal Cancer (HNPCC) Associated Tumors-A Cohort Study.

Aswath K, Welch J, Gubbi S, Veeraraghavan P, Avadhanula S, Gara SK, Dikoglu E, Merino M, Raffeld M, Xi L, Kebebew E, Klubo-Gwiezdzinska J. Aswath K, et al. Front Endocrinol (Lausanne). 2021 Jul 13;12:653401. doi: 10.3389/fendo.2021.653401. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34326811 Free PMC article.

10

Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families.

Timms AE, Dorschner MO, Wechsler J, Choi KY, Kirkwood R, Girirajan S, Baker C, Eichler EE, Korvatska O, Roche KW, Horwitz MS, Tsuang DW. Timms AE, et al. JAMA Psychiatry. 2013 Jun;70(6):582-90. doi: 10.1001/jamapsychiatry.2013.1195. JAMA Psychiatry. 2013. PMID: 23553203

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