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A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer geneticsJIANFENG XU; DIMITROV, Latchezar; GILES, Graham G et al.American journal of human genetics. 2005, Vol 77, Num 2, pp 219-229, issn 0002-9297, 11 p.Article

Age at first birth and the risk of breast cancer in BRCA1 and BRCA2 mutation carriersKOTSOPOULOS, Joanne; LUBINSKI, Jan; DOMCHEK, Susan et al.Breast cancer research and treatment. 2007, Vol 105, Num 2, pp 221-228, issn 0167-6806, 8 p.Article

Surveillance for familial breast cancer : Differences in outcome according to BRCA mutation statusMOLLER, Pal; GARETH EVANS, D; LUCASSEN, Anneke et al.International journal of cancer. 2007, Vol 121, Num 5, pp 1017-1020, issn 0020-7136, 4 p.Article

Effect of pregnancy as a risk factor for breast cancer in BRCA1/BRCA2 mutation carriersCULLINANE, Carey A; LUBINSKI, Jan; FRIEDMAN, Eitan et al.International journal of cancer. 2005, Vol 117, Num 6, pp 988-991, issn 0020-7136, 4 p.Article

Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriersNAROD, Steven A; DUBE, Marie-Pierre; OFFIT, Kenneth et al.Journal of the National Cancer Institute. 2002, Vol 94, Num 23, pp 1773-1779, issn 0027-8874, 7 p.Article

Compelling evidence for a prostate cancer gene at 22q12.3 by the international Consortium for Prostate Cancer GeneticsCAMP, Nicola J; CANNON-ALBRIGHT, Lisa A; SEVERI, Gianluca et al.Human molecular genetics (Print). 2007, Vol 16, Num 11, pp 1271-1278, issn 0964-6906, 8 p.Article

Breast cancer risk following bilateral oophorectomy in BRCA1 and BRCA2 mutation carriers : An international case-control studyEISEN, Andrea; LUBINSKI, Jan; FOULKES, William D et al.Journal of clinical oncology. 2005, Vol 23, Num 30, pp 7491-7496, issn 0732-183X, 6 p.Article

The impact of pregnancy on breast cancer survival in women who carry a BRCA1 or BRCA2 mutationVALENTINI, Adriana; LUBINSKI, Jan; OLOPADE, Olufunmilayo I et al.Breast cancer research and treatment. 2013, Vol 142, Num 1, pp 177-185, issn 0167-6806, 9 p.Article

Chromosomes 4 and 8 Implicated in a Genome Wide SNP Linkage Scan of 762 Prostate Cancer Families Collected by the ICPCGLINGYI LU; CANCEL-TASSIN, Geraldine; SCHLEUTKER, Johanna et al.The Prostate. 2012, Vol 72, Num 4, pp 410-426, issn 0270-4137, 17 p.Article

Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patientsDE LEEUW, Wiljo J. F; DIERSSEN, Janwillem; CORNELISSE, Cees J et al.Journal of pathology. 2000, Vol 192, Num 3, pp 328-335, issn 0022-3417Article

Genome-Wide Linkage Analysis of I,233 Prostate Cancer Pedigrees From the International Consortium for Prostate Cancer Genetics Using Novel sum LINK and sum LOD AnalysesBRYCE CHRISTENSEN, G; BAFFOE-BONNIE, Agnes B; FOULKES, William D et al.The Prostate. 2010, Vol 70, Num 7, pp 735-744, issn 0270-4137, 10 p.Article

Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindredsGRINDEDAL, Eli Marie; RENKONEN-SINISALO, Laura; SAMPSON, Julian et al.Journal of medical genetics. 2010, Vol 47, Num 2, pp 99-102, issn 0022-2593, 4 p.Article

Smoking and the risk of breast cancer in BRCA1 and BRCA2 carriers : an updateGINSBURG, Ophira; GHADIRIAN, Parviz; KLIJN, Jan et al.Breast cancer research and treatment. 2009, Vol 114, Num 1, pp 127-135, issn 0167-6806, 9 p.Article

Hormone Therapy and the Risk of Breast Cancer in BRCA1 Mutation CarriersEISEN, Andrea; LUBINSKI, Jan; MANOUKIAN, Siranoush et al.Journal of the National Cancer Institute. 2008, Vol 100, Num 19, pp 1361-1367, issn 0027-8874, 7 p.Article

International variation in rates of uptake of preventive options in BRCA1 and BRCA2 mutation carriersMETCALFE, Kelly A; BIRENBAUM-CARMELI, Daphna; KIM-SING, Charmaine et al.International journal of cancer. 2008, Vol 122, Num 9, pp 2017-2022, issn 0020-7136, 6 p.Article

Prophylactic bilateral salpingo-oophorectomy (PBSO) with or without prophylactic bilateral mastectomy (PBM) or no intervention in BRCA1 mutation carriers : A cost-effectiveness analysisNORUM, Jan; HAGEN, Anne Irene; MOEHLE, Lovise et al.European journal of cancer (1990). 2008, Vol 44, Num 7, pp 963-971, issn 0959-8049, 9 p.Article

Fanconi anaemia, BRCA2 and familial considerations: follow up on a previous case reportBODD, Trine Levin; VAN GHELUE, Marijke; EIKLID, Kristin et al.Acta paediatrica (Oslo). 2010, Vol 99, Num 11, pp 1741-1743, issn 0803-5253, 3 p.Article

Prevention of colorectal cancer by colonoscopic surveillance in families with hereditary colorectal cancerSTORMORKEN, Astrid T; CLARK, Neal; GRINDEDAL, Eli et al.Scandinavian journal of gastroenterology. 2007, Vol 42, Num 5, pp 611-617, issn 0036-5521, 7 p.Article

Genetic epidemiology of brca mutations - : family history detects less than 50% of the mutation carriersMØLLER, Pal; HAGEN, Anne Irene; APOLD, Jaran et al.European journal of cancer (1990). 2007, Vol 43, Num 11, pp 1713-1717, issn 0959-8049, 5 p.Article

Estimated prevalence of hereditary cancers and the need for surveillance in a Norwegian county, TelemarkSTORMORKEN, Astrid T; HOFF, Geir; NORSTEIN, Jarle et al.Scandinavian journal of gastroenterology. 2006, Vol 41, Num 1, pp 71-79, issn 0036-5521, 9 p.Article

High Risk for Ovarian Cancer in a Prospective Series Is Restricted to BRCA1/2 Mutation CarriersMAEHLE, Lovise; APOLD, Jaran; PAULSEN, Torbjørn et al.Clinical cancer research (Print). 2008, Vol 14, Num 22, pp 7569-7573, issn 1078-0432, 5 p.Article

Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer familiesVALLON-CHRISTERSSON, Johan; CAYANAN, Charmagne; BORG, Ake et al.Human molecular genetics (Print). 2001, Vol 10, Num 4, pp 353-360, issn 0964-6906Article

Survival of patients with BRCA1-associated breast cancer diagnosed in an MRI-based surveillance programMØLLER, Pål; STORMORKEN, Astrid; JONSRUD, Christoffer et al.Breast cancer research and treatment. 2013, Vol 139, Num 1, pp 155-161, issn 0167-6806, 7 p.Article

Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancerSTORMORKEN, Astrid T; BOWITZ-LOTHE, Inger Marie; NOREN, Tove et al.Journal of clinical oncology. 2005, Vol 23, Num 21, pp 4705-4712, issn 0732-183X, 8 p.Article

Germ-Line Mutations in Mismatch Repair Genes Associated with Prostate CancerGRINDEDAL, Eli Marie; MØLLER, Pal; EELES, Ros et al.Cancer epidemiology, biomarkers & prevention. 2009, Vol 18, Num 9, pp 2460-2467, issn 1055-9965, 8 p.Article

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