Zhang F - Search Results

1

Assessing genome-wide copy number variation in the Han Chinese population.

Lu J, Lou H, Fu R, Lu D, Zhang F, Wu Z, Zhang X, Li C, Fang B, Pu F, Wei J, Wei Q, Zhang C, Wang X, Lu Y, Yan S, Yang Y, Jin L, Xu S. Lu J, et al. Among authors: zhang c, zhang f, zhang x. J Med Genet. 2017 Oct;54(10):685-692. doi: 10.1136/jmedgenet-2017-104613. Epub 2017 Jul 13. J Med Genet. 2017. PMID: 28705883

2

EIF4ENIF1 variants in two patients with non-syndromic premature ovarian insufficiency.

Shang L, Ren S, Yang X, Zhang F, Jin L, Zhang X, Wu Y. Shang L, et al. Among authors: zhang f, zhang x. Eur J Med Genet. 2022 Oct;65(10):104597. doi: 10.1016/j.ejmg.2022.104597. Epub 2022 Aug 25. Eur J Med Genet. 2022. PMID: 36030004

3

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Verbitsky M, Westland R, Perez A, Kiryluk K, Liu Q, Krithivasan P, Mitrotti A, Fasel DA, Batourina E, Sampson MG, Bodria M, Werth M, Kao C, Martino J, Capone VP, Vivante A, Shril S, Kil BH, Marasà M, Zhang JY, Na YJ, Lim TY, Ahram D, Weng PL, Heinzen EL, Carrea A, Piaggio G, Gesualdo L, Manca V, Masnata G, Gigante M, Cusi D, Izzi C, Scolari F, van Wijk JAE, Saraga M, Santoro D, Conti G, Zamboli P, White H, Drozdz D, Zachwieja K, Miklaszewska M, Tkaczyk M, Tomczyk D, Krakowska A, Sikora P, Jarmoliński T, Borszewska-Kornacka MK, Pawluch R, Szczepanska M, Adamczyk P, Mizerska-Wasiak M, Krzemien G, Szmigielska A, Zaniew M, Dobson MG, Darlow JM, Puri P, Barton DE, Furth SL, Warady BA, Gucev Z, Lozanovski VJ, Tasic V, Pisani I, Allegri L, Rodas LM, Campistol JM, Jeanpierre C, Alam S, Casale P, Wong CS, Lin F, Miranda DM, Oliveira EA, Simões-E-Silva AC, Barasch JM, Levy B, Wu N, Hildebrandt F, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Zhang F, Hakonarson H, Papaioannou VE, Mendelsohn CL, Gharavi AG, Sanna-Cherchi S. Verbitsky M, et al. Among authors: zhang f, zhang jy. Nat Genet. 2019 Jan;51(1):117-127. doi: 10.1038/s41588-018-0281-y. Epub 2018 Dec 21. Nat Genet. 2019. PMID: 30578417 Free PMC article.

4

The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

Liu J, Zhou Y, Liu S, Song X, Yang XZ, Fan Y, Chen W, Akdemir ZC, Yan Z, Zuo Y, Du R, Liu Z, Yuan B, Zhao S, Liu G, Chen Y, Zhao Y, Lin M, Zhu Q, Niu Y, Liu P, Ikegawa S, Song YQ, Posey JE, Qiu G; DISCO (Deciphering disorders Involving Scoliosis and COmorbidities) Study; Zhang F, Wu Z, Lupski JR, Wu N. Liu J, et al. Among authors: zhang f. Hum Genet. 2018 Jul;137(6-7):553-567. doi: 10.1007/s00439-018-1910-3. Epub 2018 Jul 17. Hum Genet. 2018. PMID: 30019117 Free PMC article.

5

Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause.

Chen Q, Ke H, Luo X, Wang L, Wu Y, Tang S, Li J, Jin L, Zhang F, Qin Y, Chen X. Chen Q, et al. Among authors: zhang f. Hum Mol Genet. 2020 Sep 29;29(16):2698-2707. doi: 10.1093/hmg/ddaa153. Hum Mol Genet. 2020. PMID: 32716490

6

A preliminary study of copy number variation in Tibetans.

Zhang YB, Li X, Zhang F, Wang DM, Yu J. Zhang YB, et al. Among authors: zhang f. PLoS One. 2012;7(7):e41768. doi: 10.1371/journal.pone.0041768. Epub 2012 Jul 23. PLoS One. 2012. PMID: 22844521 Free PMC article.

7

A heterozygous hypomorphic mutation of Fanca causes impaired follicle development and subfertility in female mice.

Pan Y, Yang X, Zhang F, Chen S, Zhou Z, Yin H, Ma H, Shang L, Yang J, Li G, Wang Y, Jin L, Shi Q, Wu Y. Pan Y, et al. Among authors: zhang f. Mol Genet Genomics. 2021 Jan;296(1):103-112. doi: 10.1007/s00438-020-01730-5. Epub 2020 Oct 6. Mol Genet Genomics. 2021. PMID: 33025164

8

A novel multiplex fluorescent competitive PCR for copy number variation detection.

Chen K, Dong SS, Wu N, Wu ZH, Zhou YX, Li K, Zhang F, Xiao JH. Chen K, et al. Among authors: zhang f. Genomics. 2019 Dec;111(6):1745-1751. doi: 10.1016/j.ygeno.2018.11.029. Epub 2018 Dec 5. Genomics. 2019. PMID: 30529537 Free article.

9

Whole exome sequencing identified a rare WT1 loss-of-function variant in a non-syndromic POI patient.

Wang Y, Chen Q, Zhang F, Yang X, Shang L, Ren S, Pan Y, Zhou Z, Li G, Fang Y, Jin L, Wu Y, Zhang X. Wang Y, et al. Among authors: zhang f, zhang x. Mol Genet Genomic Med. 2022 Jan;10(1):e1820. doi: 10.1002/mgg3.1820. Epub 2021 Nov 29. Mol Genet Genomic Med. 2022. PMID: 34845858 Free PMC article.

10

Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis.

Guo Y, Tan LJ, Lei SF, Yang TL, Chen XD, Zhang F, Chen Y, Pan F, Yan H, Liu X, Tian Q, Zhang ZX, Zhou Q, Qiu C, Dong SS, Xu XH, Guo YF, Zhu XZ, Liu SL, Wang XL, Li X, Luo Y, Zhang LS, Li M, Wang JT, Wen T, Drees B, Hamilton J, Papasian CJ, Recker RR, Song XP, Cheng J, Deng HW. Guo Y, et al. Among authors: zhang ls, zhang f, zhang zx. PLoS Genet. 2010 Jan 8;6(1):e1000806. doi: 10.1371/journal.pgen.1000806. PLoS Genet. 2010. PMID: 20072603 Free PMC article.

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