Search Results - "Kraan, Jaennelle"

Intronic variants in BRCA1 and BRCA2 that affect RNA splicing can be reliably selected by splice-site prediction programs by Vreeswijk, Maaike P.G, Kraan, Jaennelle N, van der Klift, Heleen M, Vink, Geraldine R, Cornelisse, Cees J, Wijnen, Juul T, Bakker, Egbert, van Asperen, Christi J, Devilee, Peter

“…A large number of sequence variants identified in BRCA1 and BRCA2 cannot be distinguished as either disease-causing mutations or neutral variants. These…”
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Characterization of Familial Non-BRCA1/2 Breast Tumors by Loss of Heterozygosity and Immunophenotyping by OLDENBURG, Rogier A, KROEZE-JANSEMA, Karin, MORREAU, Hans, CORNELISSE, Cees J, DEVILEE, Peter, MEIJERS-HEIJBOER, Hanne, VAN ASPEREN, Cristi J, HOOGERBRUGGE, Nicoline, VAN LEEUWEN, Inge, VASEN, Hans F. A, CLETON-JANSEN, Anne-Marie, KRAAN, Jaennelle, HOUWING-DUISTERMAAT, Jeanine J

“…Purpose: Since the identification of BRCA1 and BRCA2 , there has been no major breast cancer susceptibility gene discovered by linkage analysis in breast…”
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A genome wide linkage search for breast cancer susceptibility genes by Smith, Paula, McGuffog, Lesley, Easton, Douglas F., Mann, Graham J., Pupo, Gulietta M., Newman, Beth, Chenevix-Trench, Georgia, Szabo, Csilla, Southey, Melissa, Renard, Hélène, Odefrey, Fabrice, Lynch, Henry, Stoppa-Lyonnet, Dominique, Couch, Fergus, Hopper, John L., Giles, Graham G., McCredie, Margaret R. E., Buys, Saundra, Andrulis, Irene, Senie, Ruby, Goldgar, David E., Oldenburg, Rogier, Kroeze-Jansema, Karin, Kraan, Jaennelle, Meijers-Heijboer, Hanne, Klijn, Jan G. M., van Asperen, Christi, van Leeuwen, Inge, Vasen, Hans F. A., Cornelisse, Cees J., Devilee, Peter, Baskcomb, Linda, Seal, Sheila, Barfoot, Rita, Mangion, Jon, Hall, Anita, Edkins, Sarah, Rapley, Elizabeth, Wooster, Richard, Chang-Claude, Jenny, Eccles, Diana, Evans, D. Gareth, Futreal, P. Andrew, Nathanson, Katherine L., Weber, Barbara L., Rahman, Nazneen, Stratton, Michael R.

“…Mutations in known breast cancer susceptibility genes account for a minority of the familial aggregation of the disease. To search for further breast cancer…”
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The CHEK21100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families by OLDENBURG, Rogier A, KROEZE-JANSEMA, Karin, MEIJERS-HEIJBOER, Hanne, DE BOCK, Truuske H, CORNELISSE, Cees J, DEVILEE, Peter, KRAAN, Jaennelle, MORREAU, Hans, KLIJN, Jan G. M, HOOGERBRUGGE, Nicoline, LIGTENBERG, Marjolein J. L, VAN ASPEREN, Christi J, VASEN, Hans F. A, MEIJERS, Carel

“…The frame-shifting mutation 1100delC in the cell-cycle-checkpoint kinase 2 gene (CHEK2) has been reported to be associated with familial breast cancer in…”
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Are ATM mutations 7271T→G and IVS10-6T→G really high-risk breast cancer-susceptibility alleles? by SZABO, Csilla I, SCHUTTE, Mieke, FLOORE, Arno N, KRAAN, Jaennelle, KLIJN, Jan G. M, VAN DEN OUWELAND, Ans M. W, WAGNER, Teresa M. U, DEVILEE, Peter, SIMARD, Jacques, VAN'T VEER, Laura J, GOLDGAR, David E, MEIJERS-HEIJBOER, Hanne, BROEKS, Annegien, HOUWING-DUISTERMAAT, Jeanine J, THORSTENSON, Yvonne R, DUROCHER, Francine, OLDENBURG, Rogier A, WASIELEWSKI, Marijke, ODEFREY, Fabrice, THOMPSON, Deborah

“…Two mutations of the ATM gene were recently suggested to confer breast cancer risks similar to mutations of BRCA1 or BRCA2. Here, we set out to confirm these…”
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Multicolor Fiber FISH by Kraan, Jaennelle, von Bergh, Anne R M, Kleiverda, Karin, Vaandrager, Jan-Willem, Jordanova, Ekaterina S, Raap, Anton K, Kluin, Philip M, Schuuring, Ed

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