Phelan CM - Search Results

1

Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas.

Ruttledge MH, Sarrazin J, Rangaratnam S, Phelan CM, Twist E, Merel P, Delattre O, Thomas G, Nordenskjöld M, Collins VP, et al. Ruttledge MH, et al. Among authors: phelan cm. Nat Genet. 1994 Feb;6(2):180-4. doi: 10.1038/ng0294-180. Nat Genet. 1994. PMID: 8162072

2

Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus.

Phelan CM, Rebbeck TR, Weber BL, Devilee P, Ruttledge MH, Lynch HT, Lenoir GM, Stratton MR, Easton DF, Ponder BA, Cannon-Albright L, Larsson C, Goldgar DE, Narod SA. Phelan CM, et al. Nat Genet. 1996 Mar;12(3):309-11. doi: 10.1038/ng0396-309. Nat Genet. 1996. PMID: 8589723

3

Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease.

Ruttledge MH, Andermann AA, Phelan CM, Claudio JO, Han FY, Chretien N, Rangaratnam S, MacCollin M, Short P, Parry D, Michels V, Riccardi VM, Weksberg R, Kitamura K, Bradburn JM, Hall BD, Propping P, Rouleau GA. Ruttledge MH, et al. Among authors: phelan cm. Am J Hum Genet. 1996 Aug;59(2):331-42. Am J Hum Genet. 1996. PMID: 8755919 Free PMC article.

4

Chromosome 17 abnormalities and lack of TP53 mutations in paediatric central nervous system tumours.

Phelan CM, Liu L, Ruttledge MH, Müntzning K, Ridderheim PA, Collins VP. Phelan CM, et al. Hum Genet. 1995 Dec;96(6):684-90. doi: 10.1007/BF00210300. Hum Genet. 1995. PMID: 8522328

5

The human mammary-derived growth inhibitor (MDGI) gene: genomic structure and mutation analysis in human breast tumors.

Phelan CM, Larsson C, Baird S, Futreal PA, Ruttledge MH, Morgan K, Tonin P, Hung H, Korneluk RG, Pollak MN, Narod SA. Phelan CM, et al. Genomics. 1996 May 15;34(1):63-8. doi: 10.1006/geno.1996.0241. Genomics. 1996. PMID: 8661024

6

Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families.

Phelan CM, Lancaster JM, Tonin P, Gumbs C, Cochran C, Carter R, Ghadirian P, Perret C, Moslehi R, Dion F, Faucher MC, Dole K, Karimi S, Foulkes W, Lounis H, Warner E, Goss P, Anderson D, Larsson C, Narod SA, Futreal PA. Phelan CM, et al. Nat Genet. 1996 May;13(1):120-2. doi: 10.1038/ng0596-120. Nat Genet. 1996. PMID: 8673090

7

Exclusion of the phosphoinositide-specific phospholipase C beta 3 (PLCB3) gene as a candidate for multiple endocrine neoplasia type 1.

Weber G, Grimmond S, Lagercrantz J, Friedman E, Phelan C, Carson E, Hayward N, Jacobovitz O, Nordenskjöld M, Larsson C. Weber G, et al. Hum Genet. 1997 Jan;99(1):130-2. doi: 10.1007/s004390050326. Hum Genet. 1997. PMID: 9003510

8

Analysis of microsatellite repeats in pediatric brain tumors.

Amariglio N, Friedman E, Mor O, Stiebel H, Phelan C, Collins P, Nordenskjold M, Brok-Simoni F, Rechavi G. Amariglio N, et al. Cancer Genet Cytogenet. 1995 Oct 1;84(1):56-9. doi: 10.1016/0165-4608(95)00085-2. Cancer Genet Cytogenet. 1995. PMID: 7497444

9

Candidate genes for multiple endocrine neoplasia type 1.

Lagercrantz J, Larsson C, Grimmond S, Skogseid B, Gobl A, Friedman E, Carson E, Phelan C, Oberg K, Nordenskjöld M, et al. Lagercrantz J, et al. J Intern Med. 1995 Sep;238(3):245-8. doi: 10.1111/j.1365-2796.1995.tb00930.x. J Intern Med. 1995. PMID: 7673854

10

Identification of six new susceptibility loci for invasive epithelial ovarian cancer.

Kuchenbaecker KB, Ramus SJ, Tyrer J, Lee A, Shen HC, Beesley J, Lawrenson K, McGuffog L, Healey S, Lee JM, Spindler TJ, Lin YG, Pejovic T, Bean Y, Li Q, Coetzee S, Hazelett D, Miron A, Southey M, Terry MB, Goldgar DE, Buys SS, Janavicius R, Dorfling CM, van Rensburg EJ, Neuhausen SL, Ding YC, Hansen TV, Jønson L, Gerdes AM, Ejlertsen B, Barrowdale D, Dennis J, Benitez J, Osorio A, Garcia MJ, Komenaka I, Weitzel JN, Ganschow P, Peterlongo P, Bernard L, Viel A, Bonanni B, Peissel B, Manoukian S, Radice P, Papi L, Ottini L, Fostira F, Konstantopoulou I, Garber J, Frost D, Perkins J, Platte R, Ellis S; EMBRACE; Godwin AK, Schmutzler RK, Meindl A, Engel C, Sutter C, Sinilnikova OM; GEMO Study Collaborators; Damiola F, Mazoyer S, Stoppa-Lyonnet D, Claes K, De Leeneer K, Kirk J, Rodriguez GC, Piedmonte M, O'Malley DM, de la Hoya M, Caldes T, Aittomäki K, Nevanlinna H, Collée JM, Rookus MA, Oosterwijk JC; Breast Cancer Family Registry; Tihomirova L, Tung N, Hamann U, Isaccs C, Tischkowitz M, Imyanitov EN, Caligo MA, Campbell IG, Hogervorst FB; HEBON; Olah E, Diez O, Blanco I, Brunet J, Lazaro C, Pujana MA, Jakubowska A, Gronwald J, Lubinski J, Sukiennicki G, Barkardottir RB, Plante M, Sim… See abstract for full author list ➔ Kuchenbaecker KB, et al. Among authors: phelan cm. Nat Genet. 2015 Feb;47(2):164-71. doi: 10.1038/ng.3185. Epub 2015 Jan 12. Nat Genet. 2015. PMID: 25581431 Free PMC article.

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