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乳腺癌
乳腺癌
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乳腺癌
26 个讨论
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有大神帮忙分析结果么？
微胖的TUSC3基因
• 最后回复
微胖的TUSC3基因
•
2016-10-26 08:24
2883
2
• 来自相关小组
不解：为什么直接查看乳腺癌的结果，和分享到微信的结果，不太一样？
flatfoosie
• 最后回复
不羁的PKP2基因
•
2016-09-29 12:26
3355
3
• 来自相关小组
我的报告乳腺癌风险高于平均风险，而我又高龄未育，就更危险了吧，该如何预防哪？
Tgerbear
• 最后回复
安静的NEB基因
•
2016-08-05 08:12
3692
5
• 来自相关小组
乳腺癌 BRCA2 rs11571746 相同人数百分比只有0.45%
ww2272
• 2016-05-15 11:31
3242
0
• 来自相关小组
乳腺癌基因
nasreddin
• 最后回复
flyboyleo
•
2016-03-25 11:12
6188
4
• 来自相关小组
脂联素分泌水平对乳腺癌的影响
zhengqiang
• 最后回复
wq
•
2015-01-17 23:31
4438
1
• 来自相关小组
发起讨论
乳腺癌
26 个讨论
相关基因
BRCA1
位点：I4000377
位点：I4000378
位点：RS16942
位点：RS1799950
位点：RS1799966
位点：RS2227945
位点：RS4986850
位点：RS55770810
BRCA2
位点：I4000379
位点：RS11571833
位点：RS144848
位点：RS28897756
位点：RS4987117
位点：RS766173
TP53
位点：RS1042522
CASP8
位点：RS1045485
ZNF276
位点：RS1061646
VTCN1
位点：RS10754339
位点：RS10801935
位点：RS3738414
FGFR2
位点：RS11200014
位点：RS1219648
位点：RS2420946
位点：RS2981578
位点：RS2981579
位点：RS3750817
位点：RS7895676
EPCAM
位点：RS1126497
TNFSF10
位点：RS1131532
DMBT1
位点：RS11523871
位点：RS2981745
PALB2
位点：RS118203997
位点：RS118203998
位点：RS180177083
位点：RS180177084
位点：RS180177091
位点：RS180177092
位点：RS180177097
位点：RS180177098
位点：RS180177099
位点：RS180177100
位点：RS180177102
位点：RS180177103
位点：RS180177110
位点：RS180177111
位点：RS180177112
位点：RS180177116
位点：RS180177121
位点：RS180177122
位点：RS180177124
位点：RS180177126
位点：RS180177127
位点：RS249954
CYP2C19
位点：RS12248560
TCF7L2
位点：RS12255372
BMPR1B
位点：RS1434536
THEMIS2
位点：RS1467465
ADIPOQ-AS1
位点：RS1501299
CHEK2
位点：RS17879961
ICAM1
位点：RS1799969
ATM
位点：RS1800054
位点：RS1800056
位点：RS1800057
位点：RS1800058
位点：RS4986761
CXCL12
位点：RS1801157
NCOA3
位点：RS2230782
ADIPOQ
位点：RS2241766
LUM
位点：RS2268578
SIPA1
位点：RS2448490
XRCC1
位点：RS25489
BARD1
位点：RS28997576
CDKN1A
位点：RS3176336
CDKN2B-AS1
位点：RS3218005
XRCC2
位点：RS3218536
CDKN1B
位点：RS34330
CDKN2A
位点：RS3731239
CASC16
位点：RS3803662
SLC4A7
位点：RS4973768
CCND1
位点：RS603965
ADIPOR1
位点：RS7539542
RRP1B
位点：RS9306160
CCNE1
位点：RS997669
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Reiling E, et al. Codon 72 polymorphism (rs1042522) of TP53 is associated with changes in diastolic blood pressure over time. 2012
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Cotignola J, et al. Investigation of the effect of MDM2 SNP309 and TP53 Arg72Pro polymorphisms on the age of onset of cutaneous melanoma. 2012
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Toyama T, et al. Association of TP53 codon 72 polymorphism and the outcome of adjuvant therapy in breast cancer patients. 2015
Gaudet MM, et al. Genetic variation of TP53, polycyclic aromatic hydrocarbon-related exposures, and breast cancer risk among women on Long Island, New York. 2008
Zhu Y, et al. Correlating observed odds ratios from lung cancer case-control studies to SNP functional scores predicted by bioinformatic tools. 2008
Rosenberger A, et al. Do genetic factors protect for early onset lung cancer? A case control study before the age of 50 years. 2008
Bittenbring J, et al. MDM2 gene SNP309 T/G and p53 gene SNP72 G/C do not influence diffuse large B-cell non-Hodgkin lymphoma onset or survival in central European Caucasians. 2008
Dai Z, et al. Genotyping panel for assessing response to cancer chemotherapy. 2008
Israni AK, et al. Association of donor inflammation- and apoptosis-related genotypes and delayed allograft function after kidney transplantation. 2008
Shi J, et al. Genetic associations with schizophrenia: meta-analyses of 12 candidate genes. 2008
Pangilinan F, et al. Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population. 2008
Tempfer CB, et al. Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis. 2009
Hamaguchi M, et al. Possible difference in frequencies of genetic polymorphisms of estrogen receptor alpha, estrogen metabolism and P53 genes between estrogen receptor-positive and -negative breast cancers. 2008
Wu X, et al. Germline genetic variations in drug action pathways predict clinical outcomes in advanced lung cancer treated with platinum-based chemotherapy. 2008
Lan Q, et al. Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity. 2009
Hung RJ, et al. International Lung Cancer Consortium: pooled analysis of sequence variants in DNA repair and cell cycle pathways. 2008
Polakova V, et al. Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic. 2009
Hirata H, et al. Bcl2 -938C/A polymorphism carries increased risk of biochemical recurrence after radical prostatectomy. 2009
Schildkraut JM, et al. Single nucleotide polymorphisms in the TP53 region and susceptibility to invasive epithelial ovarian cancer. 2009
Gallì P, et al. A case-control study on the combined effects of p53 and p73 polymorphisms on head and neck cancer risk in an Italian population. 2009
Kang HJ, et al. Single-nucleotide polymorphisms in the p53 pathway regulate fertility in humans. 2009
Zhou X, et al. Polymorphisms in HPV E6/E7 protein interacted genes and risk of cervical cancer in Chinese women: a case-control analysis. 2009
Marcel V, et al. TP53 PIN3 and MDM2 SNP309 polymorphisms as genetic modifiers in the Li-Fraumeni syndrome: impact on age at first diagnosis. 2009
Klug SJ, et al. TP53 codon 72 polymorphism and cervical cancer: a pooled analysis of individual data from 49 studies. 2009
Scacchi R, et al. Association study between P53 and P73 gene polymorphisms and the sporadic late-onset form of Alzheimer's disease. 2009
Imboden M, et al. Decreased PM10 exposure attenuates age-related lung function decline: genetic variants in p53, p21, and CCND1 modify this effect. 2009
Daugherty CL, et al. Primary open angle glaucoma in a Caucasian population is associated with the p53 codon 72 polymorphism. 2009
Zhu F, et al. Genetic factors associated with intestinal metaplasia in a high risk Singapore-Chinese population: a cohort study. 2009
Doi N, et al. Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint. 2009
Maia AT, et al. Extent of differential allelic expression of candidate breast cancer genes is similar in blood and breast. 2009
Lee EB, et al. TP53 mutations in Korean patients with non-small cell lung cancer. 2010
Grochola LF, et al. Single-nucleotide polymorphisms in the p53 signaling pathway. 2010
Robertson LB, et al. Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation. 2010
Huang YJ, et al. A novel functional DEC1 promoter polymorphism -249T>C reduces risk of squamous cell carcinoma of the head and neck. 2010
Di Pietro F, et al. Genomic DNA extraction from whole blood stored from 15- to 30-years at -20 °C by rapid phenol-chloroform protocol: a useful tool for genetic epidemiology studies. 2011
Jha P, et al. TP53 polymorphisms in gliomas from Indian patients: Study of codon 72 genotype, rs1642785, rs1800370 and 16 base pair insertion in intron-3. 2011
Qu L, et al. Association between polymorphisms in RAPGEF1, TP53, NRF1 and type 2 diabetes in Chinese Han population. 2011
Caamaño J, et al. TP53 codon 72 polymorphism is associated with coronary artery disease in Chilean subjects. 2011
Burgdorf KS, et al. Studies of the association of Arg72Pro of tumor suppressor protein p53 with type 2 diabetes in a combined analysis of 55,521 Europeans. 2011
Savage SA, et al. Using epidemiology and genomics to understand osteosarcoma etiology. 2011
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Denisov EV, et al. Coordination of TP53 abnormalities in breast cancer: data from analysis of TP53 polymorphisms, loss of heterozygosity, methylation, and mutations. 2011
Liu L, et al. Combined effect of genetic polymorphisms in P53, P73, and MDM2 on non-small cell lung cancer survival. 2011
von Keyserling H, et al. Analysis of 4 single-nucleotide polymorphisms in relation to cervical dysplasia and cancer development using a high-throughput ligation-detection reaction procedure. 2011
Lin HY, et al. Polymorphisms of TP53 are markers of bladder cancer vulnerability and prognosis. 2013
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Bonfigli AR, et al. The p53 codon 72 (Arg72Pro) polymorphism is associated with the degree of insulin resistance in type 2 diabetic subjects: a cross-sectional study. 2013
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Chansaenroj J, et al. Polymorphisms in TP53 (rs1042522), p16 (rs11515 and rs3088440) and NQO1 (rs1800566) genes in Thai cervical cancer patients with HPV 16 infection. 2015
Son MS, et al. Promoter polymorphisms of pri-miR-34b/c are associated with hepatocellular carcinoma. 2013
de Lourdes Perim A, et al. CXCL12 and TP53 genetic polymorphisms as markers of susceptibility in a Brazilian children population with acute lymphoblastic leukemia (ALL). 2013
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Molina E, et al. The GSTM1null (deletion) and MGMT84 rs12917 (Phe/Phe) haplotype are associated with bulky DNA adduct levels in human leukocytes. 2013
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Shephard ND, et al. A breast cancer risk haplotype in the caspase-8 gene. 2009
Enjuanes A, et al. Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia. 2008
Ramus SJ, et al. Consortium analysis of 7 candidate SNPs for ovarian cancer. 2008
Pittman AM, et al. CASP8 variants D302H and -652 6N ins/del do not influence the risk of colorectal cancer in the United Kingdom population. 2008
Couch FJ, et al. Association of breast cancer susceptibility variants with risk of pancreatic cancer. 2009
Lubahn J, et al. Association of CASP8 D302H polymorphism with reduced risk of aggressive prostate carcinoma. 2010
Srivastava K, et al. Caspase-8 polymorphisms and risk of gallbladder cancer in a northern Indian population. 2010
Campa D, et al. Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium. 2011
Abnet CC, et al. Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies. 2012
Pharoah PD, et al. Association between common variation in 120 candidate genes and breast cancer risk. 2007
Sigurdson AJ, et al. Polymorphisms in apoptosis- and proliferation-related genes, ionizing radiation exposure, and risk of breast cancer among U.S. Radiologic Technologists. 2007
Loza MJ, et al. Assembly of inflammation-related genes for pathway-focused genetic analysis. 2007
Li C, et al. Genetic variants and haplotypes of the caspase-8 and caspase-10 genes contribute to susceptibility to cutaneous melanoma. 2008
Gail MH, et al. Discriminatory accuracy from single-nucleotide polymorphisms in models to predict breast cancer risk. 2008
Smith AK, et al. Association of polymorphisms in CASP10 and CASP8 with FEV(1)/FVC and bronchial hyperresponsiveness in ethnically diverse asthmatics. 2008
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Tapper W, et al. The influence of genetic variation in 30 selected genes on the clinical characteristics of early onset breast cancer. 2008
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Lan Q, et al. Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies. 2009
Gaudet MM, et al. Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium. 2009
Sergentanis TN, et al. Association of two CASP8 polymorphisms with breast cancer risk: a meta-analysis. 2010
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Grochola LF, et al. Single-nucleotide polymorphisms in the p53 signaling pathway. 2010
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Srivastava K, et al. Gallbladder cancer predisposition: a multigenic approach to DNA-repair, apoptotic and inflammatory pathway genes. 2011
Broeks A, et al. Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium. 2011
Bye H, et al. Population-specific genetic associations with oesophageal squamous cell carcinoma in South Africa. 2011
Nell EM, et al. The apoptosis pathway and the genetic predisposition to Achilles tendinopathy. 2012
Guan YP, et al. Breast cancer association studies in a Han Chinese population using 10 European-ancestry-associated breast cancer susceptibility SNPs. 1009
Rihani A, et al. CASP8 SNP D302H (rs1045485) is associated with worse survival in MYCN-amplified neuroblastoma patients. 2014
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Zhu X, et al. Histone-acetylated control of fibroblast growth factor receptor 2 intron 2 polymorphisms and isoform splicing in breast cancer. 2009
Nan H, et al. Genetic variants in FGFR2 and FGFR4 genes and skin cancer risk in the Nurses' Health Study. 2009
Barnholtz-Sloan JS, et al. FGFR2 and other loci identified in genome-wide association studies are associated with breast cancer in African-American and younger women. 2010
Chan M, et al. Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population. 2012
Zhou L, et al. Three novel functional polymorphisms in the promoter of FGFR2 gene and breast cancer risk: a HuGE review and meta-analysis. 2012
Jiang L, et al. A non-synonymous polymorphism Thr115Met in the EpCAM gene is associated with an increased risk of breast cancer in Chinese population. 2011
Hu M, et al. Functional polymorphism in the EpCAM gene is associated with occurrence and advanced disease status of cervical cancer in Chinese population. 2012
Yang Y, et al. Polymorphisms of EpCAM gene and prognosis for non-small-cell lung cancer in Han Chinese. 2014
Jung JH, et al. TNF superfamily gene polymorphism as prognostic factor in early breast cancer. 2010
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Schnabel RB, et al. The relation of genetic and environmental factors to systemic inflammatory biomarker concentrations. 2009
Tchatchou S, et al. Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity. 2010
Johnson N, et al. Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility. 2007
Won HH, et al. Cataloging coding sequence variations in human genome databases. 2008
Garcia-Closas M, et al. Genome-wide association studies identify four ER negative-specific breast cancer risk loci. 2013
Michailidou K, et al. Large-scale genotyping identifies 41 new loci associated with breast cancer risk. 2013
Wang Y, et al. Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. 2014
Casadei S, et al. Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer. 2011
Rahman N, et al. PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. 2007
Hofstatter EW, et al. PALB2 mutations in familial breast and pancreatic cancer. 2011
Hunter DJ, et al. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. 2007
Zhao ZZ, et al. Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk. 2008
Raskin L, et al. FGFR2 is a breast cancer susceptibility gene in Jewish and Arab Israeli populations. 2008
Liang J, et al. Genetic variants in fibroblast growth factor receptor 2 (FGFR2) contribute to susceptibility of breast cancer in Chinese women. 2008
Gates MA, et al. Breast cancer susceptibility alleles and ovarian cancer risk in 2 study populations. 2009
Rebbeck TR, et al. Hormone-dependent effects of FGFR2 and MAP3K1 in breast cancer susceptibility in a population-based sample of post-menopausal African-American and European-American women. 2009
Hunter DJ, et al. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. 2007
Zheng W, et al. Evaluation of 11 breast cancer susceptibility loci in African-American women. 2009
Chen XH, et al. Risk of aggressive breast cancer in women of Han nationality carrying TGFB1 rs1982073 C allele and FGFR2 rs1219648 G allele in North China. 2011
Long J, et al. Evaluation of breast cancer susceptibility loci in Chinese women. 2010
Li J, et al. A combined analysis of genome-wide association studies in breast cancer. 2011
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[PMID 25784121] Associations between breast density and a panel of single nucleotide polymorphisms linked to breast cancer risk: a cohort study with digital mammography
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[PMID 25784121] Associations between breast density and a panel of single nucleotide polymorphisms linked to breast cancer risk: a cohort study with digital mammography
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Rrp1B gene polymorphism (1307T>C) in metastatic progression of breast cancer
Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population
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