299 related articles for article (PubMed ID: 23531357)
21. Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.
Yang R; Chen B; Pfütze K; Buch S; Steinke V; Holinski-Feder E; Stöcker S; von Schönfels W; Becker T; Schackert HK; Royer-Pokora B; Kloor M; Schmiegel WH; Büttner R; Engel C; Lascorz Puertolas J; Försti A; Kunkel N; Bugert P; Schreiber S; Krawczak M; Schafmayer C; Propping P; Hampe J; Hemminki K; Burwinkel B
Carcinogenesis; 2014 Feb; 35(2):315-23. PubMed ID: 24127187
[TBL] [Abstract][Full Text] [Related]
22. Challenges in the diagnosis and management of Lynch Syndrome in an Indigenous family living in a remote West Australian community.
Schofield L; Goldblatt J; Iacopetta B
Rural Remote Health; 2011; 11(4):1836. PubMed ID: 22188021
[TBL] [Abstract][Full Text] [Related]
23. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
Sokolowski M; Wasserman J; Wasserman D
PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
[TBL] [Abstract][Full Text] [Related]
24. Identification of genome-wide copy number variations and a family-based association study of Avellino corneal dystrophy.
Bae JS; Cheong HS; Chun JY; Park TJ; Kim JO; Kim EM; Park M; Kim DJ; Lee EJ; Kim EK; Lee JY; Shin HD
Ophthalmology; 2010 Jul; 117(7):1306-12.e4. PubMed ID: 20202685
[TBL] [Abstract][Full Text] [Related]
25. Association of a let-7 miRNA binding region of TGFBR1 with hereditary mismatch repair proficient colorectal cancer (MSS HNPCC).
Xicola RM; Bontu S; Doyle BJ; Rawson J; Garre P; Lee E; de la Hoya M; Bessa X; Clofent J; Bujanda L; Balaguer F; Castellví-Bel S; Alenda C; Jover R; Ruiz-Ponte C; Syngal S; Andreu M; Carracedo A; Castells A; Newcomb PA; Lindor N; Potter JD; Baron JA; Ellis NA; Caldes T; LLor X
Carcinogenesis; 2016 Aug; 37(8):751-8. PubMed ID: 27234654
[TBL] [Abstract][Full Text] [Related]
26. MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer.
Reeves SG; Meldrum C; Groombridge C; Spigelman AD; Suchy J; Kurzawski G; Lubinski J; McElduff P; Scott RJ
Eur J Hum Genet; 2009 May; 17(5):629-35. PubMed ID: 19156174
[TBL] [Abstract][Full Text] [Related]
27. Hereditary non-polyposis colorectal cancer/Lynch syndrome in three dimensions.
Kravochuck SE; Church JM
ANZ J Surg; 2017 Dec; 87(12):1006-1010. PubMed ID: 26990828
[TBL] [Abstract][Full Text] [Related]
28. HaplotypeCN: copy number haplotype inference with Hidden Markov Model and localized haplotype clustering.
Lin YJ; Chen YT; Hsu SN; Peng CH; Tang CY; Yen TC; Hsieh WP
PLoS One; 2014; 9(5):e96841. PubMed ID: 24849202
[TBL] [Abstract][Full Text] [Related]
29. The effect of algorithms on copy number variant detection.
Tsuang DW; Millard SP; Ely B; Chi P; Wang K; Raskind WH; Kim S; Brkanac Z; Yu CE
PLoS One; 2010 Dec; 5(12):e14456. PubMed ID: 21209939
[TBL] [Abstract][Full Text] [Related]
30. A population-based study of hereditary non-polyposis colorectal cancer: evidence of pathologic and genetic heterogeneity.
Warden G; Harnett D; Green J; Wish T; Woods MO; Green R; Dicks E; Rahman P; Zhai G; Parfrey P
Clin Genet; 2013 Dec; 84(6):522-30. PubMed ID: 23278430
[TBL] [Abstract][Full Text] [Related]
31. Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data.
Marenne G; Real FX; Rothman N; Rodríguez-Santiago B; Pérez-Jurado L; Kogevinas M; García-Closas M; Silverman DT; Chanock SJ; Génin E; Malats N
BMC Genomics; 2012 Jul; 13():326. PubMed ID: 22817656
[TBL] [Abstract][Full Text] [Related]
32. Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.
Degenhardt F; Priebe L; Herms S; Mattheisen M; Mühleisen TW; Meier S; Moebus S; Strohmaier J; Groß M; Breuer R; Lange C; Hoffmann P; Meyer-Lindenberg A; Heinz A; Walter H; Lucae S; Wolf C; Müller-Myhsok B; Holsboer F; Maier W; Rietschel M; Nöthen MM; Cichon S
Am J Med Genet B Neuropsychiatr Genet; 2012 Apr; 159B(3):263-73. PubMed ID: 22344817
[TBL] [Abstract][Full Text] [Related]
33. Analysis of the oxidative damage repair genes NUDT1, OGG1, and MUTYH in patients from mismatch repair proficient HNPCC families (MSS-HNPCC).
Garre P; Briceño V; Xicola RM; Doyle BJ; de la Hoya M; Sanz J; Llovet P; Pescador P; Puente J; Díaz-Rubio E; Llor X; Caldés T
Clin Cancer Res; 2011 Apr; 17(7):1701-12. PubMed ID: 21355073
[TBL] [Abstract][Full Text] [Related]
34. The spectrum of Lynch syndrome-associated germ-line mutations in Russia.
Yanus GA; Akhapkina TA; Iyevleva AG; Kornilov AV; Suspitsin EN; Kuligina ES; Ivantsov AO; Aleksakhina SN; Sokolova TN; Sokolenko AP; Togo AV; Imyanitov EN
Eur J Med Genet; 2020 Mar; 63(3):103753. PubMed ID: 31491536
[TBL] [Abstract][Full Text] [Related]
35. Women with synchronous primary cancers of the endometrium and ovary: do they have Lynch syndrome?
Soliman PT; Broaddus RR; Schmeler KM; Daniels MS; Gonzalez D; Slomovitz BM; Gershenson DM; Lu KH
J Clin Oncol; 2005 Dec; 23(36):9344-50. PubMed ID: 16361634
[TBL] [Abstract][Full Text] [Related]
36. Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort.
Zhao L; Bracken MB; DeWan AT
Ann Hum Genet; 2013 Jul; 77(4):277-87. PubMed ID: 23551011
[TBL] [Abstract][Full Text] [Related]
37. Biological relevance of CNV calling methods using familial relatedness including monozygotic twins.
Castellani CA; Melka MG; Wishart AE; Locke ME; Awamleh Z; O'Reilly RL; Singh SM
BMC Bioinformatics; 2014 Apr; 15():114. PubMed ID: 24750645
[TBL] [Abstract][Full Text] [Related]
38. Genome-wide algorithm for detecting CNV associations with diseases.
Xu Y; Peng B; Fu Y; Amos CI
BMC Bioinformatics; 2011 Aug; 12():331. PubMed ID: 21827692
[TBL] [Abstract][Full Text] [Related]
39. Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.
Veerappa AM; Suresh RV; Vishweswaraiah S; Lingaiah K; Murthy M; Manjegowda DS; Padakannaya P; Ramachandra NB
Genet Res (Camb); 2015 Sep; 97():e18. PubMed ID: 26390810
[TBL] [Abstract][Full Text] [Related]
40. MDM2 SNP309 T>G alone or in combination with the TP53 R72P polymorphism does not appear to influence disease expression and age of diagnosis of colorectal cancer in HNPCC patients.
Talseth BA; Meldrum C; Suchy J; Kurzawski G; Lubinski J; Scott RJ
Int J Cancer; 2007 Feb; 120(3):563-5. PubMed ID: 17096342
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
