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Lone Sunde
Lone Sunde
MD, PhD, Professor, Institute of Biomedicine, Aarhus University
Verified email at rm.dk
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Cited by
Year
The risk of extra‐colonic, extra‐endometrial cancer in the Lynch syndrome
P Watson, HFA Vasen, JP Mecklin, I Bernstein, M Aarnio, HJ Järvinen, ...
International journal of cancer 123 (2), 444-449, 2008
7122008
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
TR Rebbeck, N Mitra, F Wan, OM Sinilnikova, S Healey, L McGuffog, ...
Jama 313 (13), 1347-1361, 2015
5422015
Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database
P Møller, TT Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 67 (7), 1306-1316, 2018
5362018
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database
P Møller, T Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 66 (3), 464-472, 2017
5342017
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
M Dominguez-Valentin, JR Sampson, TT Seppälä, SW Ten Broeke, ...
Genetics in Medicine 22 (1), 15-25, 2020
4832020
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general …
AC Antoniou, X Wang, ZS Fredericksen, L McGuffog, R Tarrell, ...
Nature genetics 42 (10), 885-892, 2010
4062010
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
KB Kuchenbaecker, SJ Ramus, J Tyrer, A Lee, HC Shen, J Beesley, ...
Nature genetics 47 (2), 164-171, 2015
3062015
High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome
S Aretz, D Stienen, S Uhlhaas, M Stolte, MM Entius, S Loff, W Back, ...
Journal of medical genetics 44 (11), 702-709, 2007
2682007
Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction
AC Antoniou, J Beesley, L McGuffog, OM Sinilnikova, S Healey, ...
Cancer research 70 (23), 9742-9754, 2010
2542010
Does fetal antigen 1 (FA1) identify cells with regenerative, endocrine and neuroendocrine potentials? A study of FA1 in embryonic, fetal, and placental tissue and in maternal …
C Floridon, CH Jensen, P Thorsen, O Nielsen, L Sunde, JG Westergaard, ...
Differentiation 66 (1), 49-59, 2000
1932000
Prediction of breast and prostate cancer risks in male BRCA1 and BRCA2 mutation carriers using polygenic risk scores
J Lecarpentier, V Silvestri, KB Kuchenbaecker, D Barrowdale, J Dennis, ...
Journal of Clinical Oncology 35 (20), 2240, 2017
1912017
Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database
P Møller, T Seppälä, I Bernstein, E Holinski-Feder, P Sala, DG Evans, ...
Gut 66 (9), 1657-1664, 2017
1492017
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
AC Antoniou, OM Sinilnikova, L McGuffog, S Healey, H Nevanlinna, ...
Human molecular genetics 18 (22), 4442-4456, 2009
1462009
Localization of E-cadherin in villous, extravillous and vascular trophoblasts during intrauterine, ectopic and molar pregnancy
C Floridon, O Nielsen, B Hølund, L Sunde, JG Westergaard, SG Thomsen, ...
MHR: Basic science of reproductive medicine 6 (10), 943-950, 2000
1422000
Risk‐reducing mastectomy and salpingo‐oophorectomy in unaffected BRCA mutation carriers: uptake and timing*
AB Skytte, AM Gerdes, MK Andersen, L Sunde, K Brøndum‐Nielsen, ...
Clinical genetics 77 (4), 342-349, 2010
1192010
Von Hippel-Lindau disease (vHL)
ML Binderup, ML Bisgaard, V Harbud, HU Møller, S Gimsing, ...
National clinical guideline for diagnosis and surveillance in Denmark. 3rd …, 2013
1162013
A genome-wide scan in affected sibling pairs with idiopathic recurrent miscarriage suggests genetic linkage
AM Kolte, HS Nielsen, I Moltke, B Degn, B Pedersen, L Sunde, ...
Molecular human reproduction 17 (6), 379-385, 2011
1162011
Evaluation of the risk of persistent trophoblastic disease after twin pregnancy with diploid hydatidiform mole and coexisting normal fetus
I Niemann, L Sunde, LK Petersen
American Journal of Obstetrics and Gynecology 197 (1), 45. e1-45. e5, 2007
1112007
A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma
KAW Wadt, LG Aoude, P Johansson, A Solinas, A Pritchard, O Crainic, ...
Clinical genetics 88 (3), 267-272, 2015
992015
Genotype–phenotype correlations in L1 syndrome: a guide for genetic counselling and mutation analysis
YJ Vos, HEK De Walle, KK Bos, JA Stegeman, AM Ten Berge, M Bruining, ...
Journal of medical genetics 47 (3), 169-175, 2010
952010
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