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Publication Listing for the MeSH term polymorphisms. Found 13 abstracts

Myers RE, Manne SL, Wilfond B, Sifri R, Ziring B, Wolf TA, Cocroft J, Ueland A, Petrich A, Swan H, DiCarlo M, Weinberg DS. A randomized trial of genetic and environmental risk assessment (GERA) for colorectal cancer risk in primary care: Trial design and baseline findings. Contemporary clinical trials. 2011 Jan;32(1):25-31.   PMCID: PMC3006063
Osorio A, Milne RL, Pita G, Peterlongo P, Heikkinen T, Simard J, Chenevix-Trench G, Spurdle AB, Beesley J, Chen X, Healey S, Neuhausen SL, Ding YC, Couch FJ, Wang X, Lindor N, Manoukian S, Barile M, Viel A, Tizzoni L, Szabo CI, Foretova L, Zikan M, Claes K, Greene MH, Mai P, Rennert G, Lejbkowicz F, Barnett-Griness O, Andrulis IL, Ozcelik H, Weerasooriya N, Gerdes AM, Thomassen M, Cruger DG, Caligo MA, Friedman E, Kaufman B, Laitman Y, Cohen S, Kontorovich T, Gershoni-Baruch R, Dagan E, Jernstrom H, Askmalm MS, Arver B, Malmer B, Domchek SM, Nathanson KL, Brunet J, Cajal TR, Yannoukakos D, Hamann U, Hogervorst FB, Verhoef S, Garcia EB, Wijnen JT, van den Ouweland A, Easton DF, Peock S, Cook M, Oliver CT, Frost D, Luccarini C, Evans DG, Lalloo F, Eeles R, Pichert G, Cook J, Hodgson S, Morrison PJ, Douglas F, Godwin AK, Sinilnikova OM, Barjhoux L, Stoppa-Lyonnet D, Moncoutier V, Giraud S, Cassini C, Olivier-Faivre L, Revillion F, Peyrat JP, Muller D, Fricker JP, Lynch HT, John EM, Buys S, Daly M, Hopper JL, Terry MB, Miron A, Yassin Y, Goldgar D, Singer CF, Gschwantler-Kaulich D, Pfeiler G, Spiess AC, Hansen TV, Johannsson OT, Kirchhoff T, Offit K, Kosarin K, Piedmonte M, Rodriguez GC, Wakeley K, Boggess JF, Basil J, Schwartz PE, Blank SV, Toland AE, Montagna M, Casella C, Imyanitov EN, Allavena A, Schmutzler RK, Versmold B, Engel C, Meindl A, Ditsch N, Arnold N, Niederacher D, Deissler H, Fiebig B, Varon-Mateeva R, Schaefer D, Froster UG, Caldes T, de la Hoya M, McGuffog L, Antoniou AC, Nevanlinna H, Radice P, Benitez J. Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA). British Journal of Cancer. 2009 Dec;101(12):2048-54.   PMCID: PMC2795432
Whittemore AS, Stearman B, Venne V, Halpern J, Felberg A, McGuire V, Daly M, Buys SS. No evidence of familial correlation in breast cancer metastasis. Breast Cancer Research and Treatment. 2009 Dec;118(3):575-81.   PMCID: PMC 2783315
Kittles RA, Baffoe-Bonnie AB, Moses TY, Robbins CM, Ahaghotu C, Huusko P, Pettaway C, Vijayakumar S, Bennett J, Hoke G, Mason T, Weinrich S, Trent JM, Collins FS, Mousses S, Bailey-Wilson J, Furbert-Harris P, Dunston G, Powell IJ, Carpten JD. A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history. JOURNAL OF MEDICAL GENETICS. 2006 Jun;43(6):507-11.
Walker C, Ahmed SA, Brown T, Ho SM, Hodges L, Lucier G, Russo J, Weigel N, Weise T, Vandenbergh J. Species, interindividual, and tissue specificity in endocrine signaling. Environmental Health Perspectives. 1999 Aug;107:619-24.
ShattuckEidens D, Oliphant A, McClure M, McBride C, Gupte J, Rubano T, Pruss D, Tavtigian SV, Teng DH, Adey N, Staebell M, Gumpper K, Lundstrom R, Hulick M, Kelly M, Holmen J, Lingenfelter B, Manley S, Fujimura F, Luce M, Ward B, CannonAlbright L, Steele L, Offit K, Gilewski T, Norton L, Brown K, Schulz C, Hampel H, Schluger A, Giulotto E, Zoli W, Ravaioli A, Nevanlinna H, Pyrhonen S, Rowley P, Loader S, Osborne MP, Daly M, Tepler I, Weinstein PL, Scalia JL, Michaelson R, Scott RJ, Radice P, Pierotti MA, Garber JE, Isaacs C, Peshkin B, Lippman ME, Dosik MH, Caligo MA, Greenstein RM, Pilarski R, Weber B, Burgemeister R, Frank TS, Skolnick MH, Thomas A. BRCA 1 sequence analysis in women at high risk for susceptibility mutations - Risk factor analysis and implications for genetic testing. JAMA-Journal of the American Medical Association. 1997 Oct 15;278(15):1242-50.
Rebbeck TR, Godwin AK, Buetow KH. Variability in loss of constitutional heterozygosity across loci and among individuals: Association with candidate genes in ductal breast carcinoma. Molecular Carcinogenesis. 1996 Nov;17(3):117-25.
Gastier JM, Pulido JC, Sunden S, Brody T, Buetow KH, Murray JC, Weber JL, Hudson TJ, Sheffield VC, Duyk GM. Survey of Trinucleotide Repeats in the Human Genome - Assessment of Their Utility as Genetic-Markers. Human molecular genetics. 1995 Oct;4(10):1829-36.
Sheffield VC, Weber JL, Buetow KH, Murray JC, Even DA, Wiles K, Gastier JM, Pulido JC, Yandava C, Sunden SL, Mattes G, Businga T, McClain A, Beck J, Scherpier T, Gilliam J, Zhong J, Duyk GM. A Collection of Trinucleotide and Tetranucleotide Repeat Markers Used to Generate High-Quality, High-Resolution Human Genome-Wide Linkage Maps. Human molecular genetics. 1995 Oct;4(10):1837-44.
Hino O, Testa JR, Buetow KH, Taguchi T, Zhou JY, Bremer M, Bruzel A, Yeung R, Levan G, Levan KK, Knudson AG, Tartof KD. Universal Mapping Probes and the Origin of Human Chromosome-3. Proceedings of the National Academy of Sciences of the United States of America. 1993 Jan 15;90(2):730-4.
Mills KA, Buetow KH, Xu Y, Weber JL, Altherr MR, Wasmuth JJ, Murray JC. Genetic and Physical Maps of Human Chromosome-4 Based on Dinucleotide Repeats. Genomics. 1992 Oct;14(2):209-19.
Murray JC, Bennett SR, Kwitek AE, Small KW, Schinzel A, Alward WL, Weber JL, Bell GI, Buetow KH. Linkage of Rieger Syndrome to the Region of the Epidermal Growth-Factor Gene on Chromosome-4. Nature genetics. 1992 Sep;2(1):46-9.
Stadler HS, Padanilam BJ, Buetow K, Murray JC, Solursh M. Identification and Genetic-Mapping of a Homeobox Gene to the 4p16.1 Region of Human Chromosome-4. Proceedings of the National Academy of Sciences of the United States of America. 1992 Dec;89(23):11579-83.
The above publications are sorted by year, faculty last name, and first author. Click on any highlighted author listed to find all publications attributed to that individual. Click on the publication title to see the abstract. First authors who are faculty are highlighted like this. Last authors who are faculty are highlighted like this. Other authors who are faculty are highlighted like this.

MeSH cloud from publications including the MeSH term polymorphisms

polymorphisms expression markers construction susceptibility hybridization dna breast-cancer linkage polymerase chain-reaction heterogeneity cancer human genome excision-repair term-follow-up ovarian- Colorectal neoplasms Decision making-Mass screening-Risk assessment-Genetic screening identification hormone-binding globulin independent activation strong candidate admixture dynamics organization amplification oxidoreductase colon-cancer in- germline mutations invitro transcriptional activity BRCA2 BRCA1-ERCC4-breast cancer carcinogen metabolism women receptor gene cag tooth tandem complex breast-cancer families prostate androgen receptor chromosomes vitro craniofacial interventions huntington disease gene regions steroid-receptors triplet repeat somatic mutation rodent model genes progression linkage disequilibrium p450 genetic-variation african-americans survival reproductive-tract leiomyomata 4q oligonucleotide Breast cancer region Familial correlation srd5a2 gene dna-sequence genetic susceptibility Metastatic potential panel-2 colorectal-cancer frequency drosophila antennapedia breast neoplasms deletion endocrine disruptor participation disease nucleotide synteny locus ovarian-cancer regression population stratification protein truncation test progesterone-receptor allele loss arm steroid hormone receptors recombination model chromosome-17 systematic reviews albumin sequence single-stranded conformational polymorphism egf metabolizing enzymes homeodomain sequences impact instability animal models dystrophy mouse reproductive tract degenerate serum
Last updated on Friday, January 03, 2020