Similar articles for PMID: 28527622

Year	Number of Results
2001	2
2003	1
2007	1
2008	2
2009	5
2010	22
2011	30
2012	19
2013	33
2014	36
2015	31
2016	32
2017	34
2018	29
2019	27
2020	33
2021	34
2022	17
2023	7

1

Genome-wide copy number analysis reveals candidate gene loci that confer susceptibility to high-grade prostate cancer.

Poniah P, Mohd Zain S, Abdul Razack AH, Kuppusamy S, Karuppayah S, Sian Eng H, Mohamed Z. Poniah P, et al. Urol Oncol. 2017 Sep;35(9):545.e1-545.e11. doi: 10.1016/j.urolonc.2017.04.017. Epub 2017 May 17. Urol Oncol. 2017. PMID: 28527622

2

A genome-wide association study of copy-number variation identifies putative loci associated with osteoarthritis in Koreans.

Moon S, Keam B, Hwang MY, Lee Y, Park S, Oh JH, Kim YJ, Lee HS, Kim NH, Kim YJ, Kim DH, Han BG, Kim BJ, Lee J. Moon S, et al. BMC Musculoskelet Disord. 2015 Apr 4;16:76. doi: 10.1186/s12891-015-0531-4. BMC Musculoskelet Disord. 2015. PMID: 25880085 Free PMC article.

3

Copy number variation of urine exfoliated cells by low-coverage whole genome sequencing for diagnosis of prostate adenocarcinoma: a prospective cohort study.

Guan Y, Wang X, Guan K, Wang D, Bi X, Xiao Z, Xiao Z, Shan X, Hu L, Ma J, Li C, Zhang Y, Shou J, Wang B, Qian Z, Xing N. Guan Y, et al. BMC Med Genomics. 2022 May 5;15(Suppl 2):104. doi: 10.1186/s12920-022-01253-5. BMC Med Genomics. 2022. PMID: 35513884 Free PMC article.

4

The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.

Wain LV, Pedroso I, Landers JE, Breen G, Shaw CE, Leigh PN, Brown RH, Tobin MD, Al-Chalabi A. Wain LV, et al. PLoS One. 2009 Dec 4;4(12):e8175. doi: 10.1371/journal.pone.0008175. PLoS One. 2009. PMID: 19997636 Free PMC article.

5

Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.

Saadati HR, Wittig M, Helbig I, Häsler R, Anderson CA, Mathew CG, Kupcinskas L, Parkes M, Karlsen TH, Rosenstiel P, Schreiber S, Franke A. Saadati HR, et al. BMC Med Genet. 2016 Apr 1;17:26. doi: 10.1186/s12881-016-0289-z. BMC Med Genet. 2016. PMID: 27037036 Free PMC article.

6

Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries.

Costain G, Lionel AC, Ogura L, Marshall CR, Scherer SW, Silversides CK, Bassett AS. Costain G, et al. Int J Cardiol. 2016 Feb 1;204:115-21. doi: 10.1016/j.ijcard.2015.11.127. Epub 2015 Nov 22. Int J Cardiol. 2016. PMID: 26655555

7

Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.

Uebe S, Ehrlicher M, Ekici AB, Behrens F, Böhm B, Homuth G, Schurmann C, Völker U, Jünger M, Nauck M, Völzke H, Traupe H, Krawczak M, Burkhardt H, Reis A, Hüffmeier U. Uebe S, et al. BMC Med Genet. 2017 Aug 23;18(1):92. doi: 10.1186/s12881-017-0447-y. BMC Med Genet. 2017. PMID: 28835222 Free PMC article.

8

A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci.

Low JS, Chin YM, Mushiroda T, Kubo M, Govindasamy GK, Pua KC, Yap YY, Yap LF, Subramaniam SK, Ong CA, Tan TY, Khoo AS; Malaysian NPC Study Group; Ng CC. Low JS, et al. PLoS One. 2016 Jan 5;11(1):e0145774. doi: 10.1371/journal.pone.0145774. eCollection 2016. PLoS One. 2016. PMID: 26730743 Free PMC article.

9

Genome-wide association study of germline copy number variations reveals an association with prostate cancer aggressiveness.

Brezina S, Feigl M, Gumpenberger T, Staudinger R, Baierl A, Gsur A. Brezina S, et al. Mutagenesis. 2020 Jul 11;35(3):283-290. doi: 10.1093/mutage/geaa010. Mutagenesis. 2020. PMID: 32255470

10

Identification of rare germline copy number variations over-represented in five human cancer types.

Park RW, Kim TM, Kasif S, Park PJ. Park RW, et al. Mol Cancer. 2015 Feb 3;14:25. doi: 10.1186/s12943-015-0292-6. Mol Cancer. 2015. PMID: 25644941 Free PMC article.

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