王文强1
; 张 琪 1; 谭 龙 1; 唐彩云 1; 刘圣美1; 陈 雯1 ; 沈 钧2; 张万起1(天津医科大学公共卫生学院1.营养与食品卫生学系;2. 卫生化学教研室,天津300070)
[1]Connor S E, Penney C C. MRI in the differential diagnosis of a sellar mass[J].Clin Radiol,2003,58(1):20
[2]张文礼,马建华. 66例甲状腺功能减退症患者的特殊临床表现及误诊漏诊分析[J].重庆医学,2010,24(24):3380
[3]Almandoz J P, Gharib H. Hypothyroidism: etiology, diagnosis, and management[J].Med Clin North Am,2012,96(2):203
[4]Burch H B, Burman K D, Cooper D S. A 2013 survey of clinical practice patterns in the management of primary hypothyroidism[J].J Clin Endocrinol Metab,2014,99(6):2077
[5]翟彪,郭海.原发性甲状腺功能减退症的病因分析[J].中国现代药物应用,2009,3(8):85
[6]Hindorff L A, Sethupathy P, Junkins H A, et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits[J].Proc Natl Acad Sci U S A,2009,106(23):9362
[7]Malinowski J R, Denny J C, Bielinski S J, et al. Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European americans and African americans from the eMERGE network[J].PLoS One,2014,9(12):e111301
[8]Mccarty C A, Chisholm R L, Chute C G, et al. The eMERGE network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies[J].BMC Med Genomics,2011,4(1):13
[9]Pathak J, Kiefer R C, Bielinski S J. Applying semantic web technologies for phenome-wide scan using an electronic health record linked Biobank[J].J Biomed Semantics,2012,3(1):10
[10]Joshua C. Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions:using Electronic Medical Records for Genome-and Phenome-wide studies[J].Clin Genet,2011,63(6):529
[11]Korzeniewski S J, Kleyn M, Young W I, et al. Screening for congenital hypothyroidism in newborns transferred to neonatal intensive care[J].Arch Dis Child Fetal Neonatal Ed,2013,98(4):F310
[12]Frost M, Petersen I, Hegedüs L, et al. Regulation of the Pituitary-Thyroid axis in adulthood is not related to birth weight:evidence from extremely birth weight–discordant monozygotic Danish twin pairs[J].Thyroid,2013,23(7):785
[13]Jyt N E, Kiefer A K, David A H, et al. Novel associations for hypothyroidism include KnownAutoimmune risk loci[J].PLoS One, 2012, 23(7):785
[14]Criswell L A, Pfeiffer K A, Lum R F, et al. Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes[J].Am J Hum Genet,2005,76(4):561
[15]Simmonds M J, Gough S C L. The search for the genetic contribution to autoimmune thyroid disease:the never ending story[J].Brief Funct Genomics,2011,10(2):77
[16]Tomer Y. Genetic susceptibility to autoimmune thyroid disease: past, present,and future[J].Thyroid,2010,20(7):715
基金项目 国家自然科学基金资助项目(81330064, 81273057),天津科委科技支撑项目(14ZCZDSY00022)
作者简介 王文强(1987-),男,硕士在读,研究方向:营养与食品卫生学;通信作者:张万起,E-mail:wqzhang126@126.com。
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