Search Results - "Rantala, Johanna"

Antimicrobial prophylaxis is considered sufficient to preserve an acceptable surgical site infection rate in clean orthopaedic and neurosurgeries in dogs by Välkki, Kirsi Johanna, Thomson, Katariina Hanne, Grönthal, Thomas Sven Christer, Junnila, Jouni Juho Tapio, Rantala, Merja Hilma Johanna, Laitinen-Vapaavuori, Outi Maria, Mölsä, Sari Helena

“…Surgical site infections (SSI) are associated with increased morbidity and mortality. To lower the incidence of SSI, antimicrobial prophylaxis is given…”
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Description of two Serratia marcescens associated mastitis outbreaks in Finnish dairy farms and a review of literature by Friman, Mari Johanna, Eklund, Marjut Hannele, Pitkälä, Anna Helena, Rajala-Schultz, Päivi Johanna, Rantala, Merja Hilma Johanna

“…Infection with Serratia spp. have been associated with mastitis outbreaks in dairy cattle herds. Environmental contamination or a point source, like a teat dip…”
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Risk perception after genetic counseling in patients with increased risk of cancer by Rantala, Johanna, Platten, Ulla, Lindgren, Gunilla, Nilsson, Bo, Arver, Brita, Lindblom, Annika, Brandberg, Yvonne

“…Counselees are more aware of genetics and seek information, reassurance, screening and genetic testing. Risk counseling is a key component of genetic…”
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Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer by Stacey, Simon N, Stefansson, Kari, Manolescu, Andrei, Sulem, Patrick, Thorlacius, Steinunn, Gudjonsson, Sigurjon A, Jonsson, Gudbjörn F, Jakobsdottir, Margret, Bergthorsson, Jon T, Gudmundsson, Julius, Aben, Katja K, Strobbe, Luc J, Swinkels, Dorine W, van Engelenburg, K C Anton, Henderson, Brian E, Kolonel, Laurence N, Le Marchand, Loic, Millastre, Esther, Andres, Raquel, Saez, Berta, Lambea, Julio, Godino, Javier, Polo, Eduardo, Tres, Alejandro, Picelli, Simone, Rantala, Johanna, Margolin, Sara, Jonsson, Thorvaldur, Sigurdsson, Helgi, Jonsdottir, Thora, Hrafnkelsson, Jon, Johannsson, Jakob, Sveinsson, Thorarinn, Myrdal, Gardar, Grimsson, Hlynur Niels, Sveinsdottir, Steinunn G, Alexiusdottir, Kristin, Saemundsdottir, Jona, Sigurdsson, Asgeir, Kostic, Jelena, Gudmundsson, Larus, Kristjansson, Kristleifur, Masson, Gisli, Fackenthal, James D, Adebamowo, Clement, Ogundiran, Temidayo, Olopade, Olufunmilayo I, Haiman, Christopher A, Lindblom, Annika, Mayordomo, Jose I, Kiemeney, Lambertus A, Gulcher, Jeffrey R, Rafnar, Thorunn, Thorsteinsdottir, Unnur, Johannsson, Oskar T, Kong, Augustine

“…We carried out a genome-wide association study of breast cancer predisposition with replication and refinement studies involving 6,145 cases and 33,016…”
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Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) by Silvestri, Valentina, Leslie, Goska, Barnes, Daniel R, Agnarsson, Bjarni A, Aittomäki, Kristiina, Alducci, Elisa, Andrulis, Irene L, Barkardottir, Rosa B, Barroso, Alicia, Barrowdale, Daniel, Benitez, Javier, Bonanni, Bernardo, Borg, Ake, Buys, Saundra S, Caldés, Trinidad, Caligo, Maria A, Capalbo, Carlo, Campbell, Ian, Chung, Wendy K, Claes, Kathleen B M, Colonna, Sarah V, Cortesi, Laura, Couch, Fergus J, de la Hoya, Miguel, Diez, Orland, Ding, Yuan Chun, Domchek, Susan, Easton, Douglas F, Ejlertsen, Bent, Engel, Christoph, Evans, D Gareth, Feliubadalò, Lidia, Foretova, Lenka, Fostira, Florentia, Géczi, Lajos, Gerdes, Anne-Marie, Glendon, Gord, Godwin, Andrew K, Goldgar, David E, Hahnen, Eric, Hogervorst, Frans B L, Hopper, John L, Hulick, Peter J, Isaacs, Claudine, Izquierdo, Angel, James, Paul A, Janavicius, Ramunas, Jensen, Uffe Birk, John, Esther M, Joseph, Vijai, Konstantopoulou, Irene, Kurian, Allison W, Kwong, Ava, Landucci, Elisabetta, Lesueur, Fabienne, Loud, Jennifer T, Machackova, Eva, Mai, Phuong L, Majidzadeh-A, Keivan, Manoukian, Siranoush, Montagna, Marco, Moserle, Lidia, Mulligan, Anna Marie, Nathanson, Katherine L, Nevanlinna, Heli, Ngeow, Joanne, Nikitina-Zake, Liene, Offit, Kenneth, Olah, Edith, Olopade, Olufunmilayo I, Osorio, Ana, Papi, Laura, Park, Sue K, Pedersen, Inge Sokilde, Perez-Segura, Pedro, Petersen, Annabeth H, Pinto, Pedro, Porfirio, Berardino, Pujana, Miquel Angel, Radice, Paolo, Rantala, Johanna, Rashid, Muhammad U, Rosenzweig, Barak, Rossing, Maria, Santamariña, Marta, Schmutzler, Rita K, Senter, Leigha, Simard, Jacques, Singer, Christian F, Solano, Angela R, Southey, Melissa C, Steele, Linda, Steinsnyder, Zoe, Stoppa-Lyonnet, Dominique, Tan, Yen Yen, Teixeira, Manuel R, Teo, Soo H, Terry, Mary Beth, Thomassen, Mads, Toland, Amanda E

“…The limited data on cancer phenotypes in men with germline BRCA1 and BRCA2 pathogenic variants (PVs) have hampered the development of evidence-based…”
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Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study by Schrijver, Lieske, Antoniou, Antonis, Olsson, Håkan, Mooij, Thea, Roos-Blom, Marie-José, Azarang, Leyla, Adlard, Julian, Ahmed, Munaza, Barrowdale, Daniel, Davidson, Rosemarie, Donaldson, Alan, Eeles, Ros, Evans, D. Gareth, Frost, Debra, Henderson, Alex, Izatt, Louise, Ong, Kai-Ren, Bonadona, Valérie, Coupier, Isabelle, Faivre, Laurence, Fricker, Jean-Pierre, Gesta, Paul, van Engelen, Klaartje, Jager, Agnes, Menko, Fred, Mourits, Marian J.E., Singer, Christian, Tan, Yen, Foretova, Lenka, Navratilova, Marie, Schmutzler, Rita, Ellberg, Carolina, Gerdes, Anne-Marie, Caldes, Trinidad, Simard, Jacques, Olah, Edith, Jakubowska, Anna, Rantala, Johanna, Osorio, Ana, Hopper, John, Phillips, Kelly-Anne, Milne, Roger, Beth Terry, Mary, Noguès, Catherine, Engel, Christoph, Kast, Karin, Goldgar, David, van Leeuwen, Flora, Easton, Douglas, Andrieu, Nadine, Rookus, Matti, Noguès, Catherine, Laborde, Lilian, Pontois, Pauline, Breysse, Emanuelle, Berline, Margot, Stoppa-Lyonnet, Dominique, Gauthier-Villars, Marion, Buecher, Bruno, Colas, Chrystelle, Caron, Olivier, Mouret-Fourme, Emmanuelle, Saule, Claire, Lasset, Christine, Dussard, Sophie, Berthet, Pascaline, Luporsi, Elisabeth, Mari, Véronique, Gladieff, Laurence, Chieze-Valéro, Stéphanie, Moretta, Jessica, Sobol, Hagay, Eisinger, François, Popovici, Cornel, Longy, Michel, Grivelli, Louise, Soubrier, Florent, Benusiglio, Patrick, Pujol, Pascal, Corsini, Carole, Morin-Meschin, Marie-Emmanuelle, Lortholary, Alain, Adenis, Claude, Maillez, Audrey, Nguyen, Tan Dat, Delnatte, Capucine, Abadie, Caroline, Tinat, Julie, Tennevet, Isabelle, Maugard, Christine, Bignon, Yves-Jean, Gay Bellile, Mathilde, Penet, Clotilde, Dreyfus, Hélène, Cohen-Haguenauer, Odile, Gilbert, Brigitte, Venat-Bouvet, Laurence, Leroux, Dominique, Legrand, Clémentine, Zattara-Cannoni, Hélène

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An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers by Madorsky-Feldman, Dana, Sklair-Levy, Miri, Perri, Tamar, Laitman, Yael, Paluch-Shimon, Shani, Schmutzler, Rita, Rhiem, Kerstin, Lester, Jenny, Karlan, Beth Y., Singer, Christian F., Van Maerken, Tom, Claes, Kathleen, Brunet, Joan, Izquierdo, Angel, Teulé, Alex, Lee, Jong Won, Kim, Sung-Won, Arun, Banu, Jakubowska, Anna, Lubinski, Jan, Tucker, Katherine, Poplawski, Nicola K., Varesco, Liliana, Bonelli, Luigina Ada, Buys, Saundra S., Mitchell, Gillian, Tischkowitz, Marc, Gerdes, Anne-Marie, Seynaeve, Caroline, Robson, Mark, Kwong, Ava, Tung, Nadine, Tessa, Nalven, Domchek, Susan M., Godwin, Andrew K., Rantala, Johanna, Arver, Brita, Friedman, Eitan

“…Female BRCA1 / BRCA2 mutation carriers are at substantially increased risk for developing breast and/or ovarian cancer, and are offered enhanced surveillance…”
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The use of telephone in genetic counseling versus in-person counseling: a randomized study on counselees’ outcome by Platten, Ulla, Rantala, Johanna, Lindblom, Annika, Brandberg, Yvonne, Lindgren, Gunilla, Arver, Brita

“…Increased demand for genetic counseling services necessitates exploring alternatives to in-person counseling. Telephone counseling is a less time-consuming and…”
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Whole-genome Linkage Analysis and Sequence Analysis of Candidate Loci in Familial Breast Cancer by Marikkannu, Rajeshwari, Aravidis, Christos, Rantala, Johanna, Picelli, Simone, Adamovic, Tatjana, Keihas, Markku, Liu, Tao, Kontham, Vinaykumar, Nilsson, Daniel, Lindblom, Annika

“…Known breast cancer-predisposing genes account for fewer than 25% of all familial breast cancer cases and further studies are required to find the remaining…”
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Genetic Predisposition for Cancer; Genes and Genetic Counseling by Rantala, Johanna

“…Breast cancer accounts for one third of all female cancer cases worldwide. A hereditary component accounts for 10-15% of all breast and ovarian cancer cases…”
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The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers by Laitman, Yael, Kuchenbaecker, Karoline B., Rantala, Johanna, Hogervorst, Frans, Peock, Susan, Godwin, Andrew K., Arason, Adalgeir, Kirchhoff, Tomas, Offit, Kenneth, Isaacs, Claudine, Schmutzler, Rita K., Wappenschmidt, Barbara, Nevanlinna, Heli, Chen, Xiaoqing, Chenevix-Trench, Georgia, Healey, Sue, Couch, Fergus, Peterlongo, Paolo, Radice, Paolo, Nathanson, Katherine L., Caligo, Maria Adelaide, Neuhausen, Susan L., Ganz, Patricia, Sinilnikova, Olga M., McGuffog, Lesley, Easton, Douglas F., Antoniou, Antonis C., Wolf, Ido, Friedman, Eitan

“…Klotho (KL) is a putative tumor suppressor gene in breast and pancreatic cancers located at chromosome 13q12. A functional sequence variant of Klotho (KL-VS)…”
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Common variants on chromosome 5pl2 confer susceptibility to estrogen receptor-positive breast cancer by STACEY, Simon N, MANOLESCU, Andrei, STROBBE, Luc J, SWINKELS, Dorine W, VAN ENGELENBURG, K. C. Anton, HENDERSON, Brian E, KOLONEL, Laurence N, LE MARCHAND, Loic, MILLASTRE, Esther, ANDRES, Raquel, SAEZ, Berta, LAMBEA, Julio, SULEM, Patrick, GODINO, Javier, POLO, Eduardo, TRES, Alejandro, PICELLI, Simone, RANTALA, Johanna, MARGOLIN, Sara, JONSSON, Thorvaldur, SIGURDSSON, Helgi, JONSDOTTIR, Thora, HRAFNHKELSSON, Jon, THORLACIUS, Steinunn, JOHANNSSON, Jakob, SVEINSSON, Thorarinn, MYRDAL, Gardar, NIELS GRIMSSON, Hlynur, SVEINSDOTTIR, Steinunn G, ALEXIUSDOTTIR, Kristin, SAEMUNDSDOTTIR, Jona, SIGURDSSON, Asgeir, KOSTIC, Jelena, GUDMUNDSSON, Larus, GUDJONSSON, Sigurjon A, KRISTJANSSON, Kristleifur, MASSON, Gisli, FACKENTHAL, James D, ADEBAMOWO, Clement, OGUNDIRAN, Temidayo, OLOPADE, Olufunmilayo I, HAIMAN, Christopher A, LINDBLOM, Annika, MAYORDOMO, Jose I, KIEMENEY, Lambertus A, JONSSON, Gudbjorn F, GULCHER, Jeffrey R, RAFHAR, Thorunn, THORSTEINSDOTTIR, Unnur, JOHANNSSON, Oskar T, KONG, Augustine, STEFANSSON, Kari, JAKOBSDOTTIR, Margret, BERGTHORSSON, Jon T, GUDMUNDSSON, Julius, ABEN, Katja K

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Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith–Magenis syndrome minimum deletion to ~650 kb by Schoumans, Jacqueline, Staaf, Johan, Jönsson, Göran, Rantala, Johanna, Zimmer, Kerstin Sars, Borg, Åke, Nordenskjöld, Magnus, Anderlid, Britt-Marie

“…Smith–Magenis syndrome (SMS) is a multiple congenital anomaly/mental retardation syndrome and it is characterized by an interstitial deletion of chromosome…”
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From chromosomes to molecular karyotyping : Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith-Magenis syndrome minimum deletion to ∼650 kb by SCHOUMANS, Jacqueline, STAAF, Johan, JÖNSSON, Göran, RANTALA, Johanna, ZIMMER, Kerstin Sars, BORG, Ake, NORDENSKJÖLD, Magnus, ANDERLID, Britt-Marie

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Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith-Magenis syndrome minimum deletion to approximately 650 kb by Schoumans, Jacqueline, Staaf, Johan, Jönsson, Göran, Rantala, Johanna, Zimmer, Kerstin Sars, Borg, Ake, Nordenskjöld, Magnus, Anderlid, Britt-Marie

“…Smith-Magenis syndrome (SMS) is a multiple congenital anomaly/mental retardation syndrome and it is characterized by an interstitial deletion of chromosome…”
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