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Items: 1 to 20 of 121

1.

[Genome-wide copy number scan in Chinese patients with premature ovarian failure].

Zhen XM, Sun YM, Qiao J, Li R, Wang LN, Liu P.

Beijing Da Xue Xue Bao Yi Xue Ban. 2013 Dec 18;45(6):841-7. Chinese.

2.

Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure.

McGuire MM, Bowden W, Engel NJ, Ahn HW, Kovanci E, Rajkovic A.

Fertil Steril. 2011 Apr;95(5):1595-600. doi: 10.1016/j.fertnstert.2010.12.052. Epub 2011 Jan 22.

3.

Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.

Yin CL, Chen HI, Li LH, Chien YL, Liao HM, Chou MC, Chou WJ, Tsai WC, Chiu YN, Wu YY, Lo CZ, Wu JY, Chen YT, Gau SS.

Mol Autism. 2016 Apr 1;7:23. doi: 10.1186/s13229-016-0087-7. eCollection 2016.

4.

Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases.

Tšuiko O, Nõukas M, Žilina O, Hensen K, Tapanainen JS, Mägi R, Kals M, Kivistik PA, Haller-Kikkatalo K, Salumets A, Kurg A.

Hum Reprod. 2016 Aug;31(8):1913-25. doi: 10.1093/humrep/dew142. Epub 2016 Jun 14.

5.

Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform.

Norling A, Hirschberg AL, Rodriguez-Wallberg KA, Iwarsson E, Wedell A, Barbaro M.

Hum Reprod. 2014 Aug;29(8):1818-27. doi: 10.1093/humrep/deu149. Epub 2014 Jun 17.

6.

Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies.

Goldmuntz E, Paluru P, Glessner J, Hakonarson H, Biegel JA, White PS, Gai X, Shaikh TH.

Congenit Heart Dis. 2011 Nov-Dec;6(6):592-602. doi: 10.1111/j.1747-0803.2011.00582.x. Epub 2011 Oct 20.

7.

Rare copy number variants in the genome of Chinese female children and adolescents with Turner syndrome.

Li L, Li Q, Wang Q, Liu L, Li R, Liu H, He Y, Lash GE.

Biosci Rep. 2019 Jan 11;39(1). pii: BSR20181305. doi: 10.1042/BSR20181305. Print 2019 Jan 31.

8.

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.

Jarick I, Volckmar AL, Pütter C, Pechlivanis S, Nguyen TT, Dauvermann MR, Beck S, Albayrak Ö, Scherag S, Gilsbach S, Cichon S, Hoffmann P, Degenhardt F, Nöthen MM, Schreiber S, Wichmann HE, Jöckel KH, Heinrich J, Tiesler CM, Faraone SV, Walitza S, Sinzig J, Freitag C, Meyer J, Herpertz-Dahlmann B, Lehmkuhl G, Renner TJ, Warnke A, Romanos M, Lesch KP, Reif A, Schimmelmann BG, Hebebrand J, Scherag A, Hinney A.

Mol Psychiatry. 2014 Jan;19(1):115-21. doi: 10.1038/mp.2012.161. Epub 2012 Nov 20.

9.

Genetic analysis of BMP4 gene in Chinese Han female population with premature ovarian insufficiency.

Bai T, Yang J, Chen B, Wang B, Ma X, Cao Y.

Climacteric. 2014 Jun;17(3):304-6. doi: 10.3109/13697137.2013.876619. Epub 2014 Feb 23.

PMID:
24559233
10.

Genome-wide analysis of CNV (copy number variation) and their associations with narcolepsy in a Japanese population.

Yamasaki M, Miyagawa T, Toyoda H, Khor SS, Koike A, Nitta A, Akiyama K, Sasaki T, Honda Y, Honda M, Tokunaga K.

J Hum Genet. 2014 May;59(5):235-40. doi: 10.1038/jhg.2014.13. Epub 2014 Apr 3.

PMID:
24694762
11.

Chromosomal instability in women with primary ovarian insufficiency.

Katari S, Aarabi M, Kintigh A, Mann S, Yatsenko SA, Sanfilippo JS, Zeleznik AJ, Rajkovic A.

Hum Reprod. 2018 Mar 1;33(3):531-538. doi: 10.1093/humrep/dey012.

12.

A genome-wide survey of copy number variations in Han Chinese residing in Taiwan.

Lin CH, Lin YC, Wu JY, Pan WH, Chen YT, Fann CS.

Genomics. 2009 Oct;94(4):241-6. doi: 10.1016/j.ygeno.2009.06.004. Epub 2009 Jun 25.

13.

High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.

Bestetti I, Castronovo C, Sironi A, Caslini C, Sala C, Rossetti R, Crippa M, Ferrari I, Pistocchi A, Toniolo D, Persani L, Marozzi A, Finelli P.

Hum Reprod. 2019 Mar 1;34(3):574-583. doi: 10.1093/humrep/dey389.

14.

Genetics of primary ovarian insufficiency: new developments and opportunities.

Qin Y, Jiao X, Simpson JL, Chen ZJ.

Hum Reprod Update. 2015 Nov-Dec;21(6):787-808. doi: 10.1093/humupd/dmv036. Epub 2015 Aug 4. Review.

15.

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.

BMC Med Genet. 2016 Apr 1;17:26. doi: 10.1186/s12881-016-0289-z.

16.

Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure.

Aboura A, Dupas C, Tachdjian G, Portnoï MF, Bourcigaux N, Dewailly D, Frydman R, Fauser B, Ronci-Chaix N, Donadille B, Bouchard P, Christin-Maitre S.

J Clin Endocrinol Metab. 2009 Nov;94(11):4540-6. doi: 10.1210/jc.2009-0186. Epub 2009 Oct 16.

PMID:
19837940
17.

Deletion variants of RABGAP1L, 10q21.3, and C4 are associated with the risk of systemic lupus erythematosus in Korean women.

Kim JH, Jung SH, Bae JS, Lee HS, Yim SH, Park SY, Bang SY, Hu HJ, Shin HD, Bae SC, Chung YJ.

Arthritis Rheum. 2013 Apr;65(4):1055-63. doi: 10.1002/art.37854.

18.

Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese.

Li Z, Chen J, Xu Y, Yi Q, Ji W, Wang P, Shen J, Song Z, Wang M, Yang P, Wang Q, Feng G, Liu B, Sun W, Xu Q, Li B, He L, He G, Li W, Wen Z, Liu K, Huang F, Zhou J, Ji J, Li X, Shi Y.

Biol Psychiatry. 2016 Aug 15;80(4):331-337. doi: 10.1016/j.biopsych.2015.11.012. Epub 2015 Nov 26.

PMID:
26795442
19.

Analysis of Chinese women with primary ovarian insufficiency by high resolution array-comparative genomic hybridization.

Liao C, Fu F, Yang X, Sun YM, Li DZ.

Chin Med J (Engl). 2011 Jun;124(11):1739-42.

PMID:
21740789
20.

Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population.

Zhao Q, Li T, Zhao X, Huang K, Wang T, Li Z, Ji J, Zeng Z, Zhang Z, Li K, Feng G, St Clair D, He L, Shi Y.

Schizophr Bull. 2013 May;39(3):712-9. doi: 10.1093/schbul/sbr197. Epub 2012 Feb 8.

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