Pre‐ and postnatal growth failure with microcephaly due to two novel heterozygous IGF1R mutations and response to growth hormone treatment by Gkourogianni, Alexandra, Andrade, Anenisia C., Jonsson, Björn‐Anders, Segerlund, Emma, Werner‐Sperker, Antje, Horemuzova, Eva, Dahlgren, Jovanna, Burstedt, Magnus, Nilsson, Ola

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A Missense Mutation in the Aggrecan C-type Lectin Domain Disrupts Extracellular Matrix Interactions and Causes Dominant Familial Osteochondritis Dissecans by Stattin, Eva-Lena, Wiklund, Fredrik, Lindblom, Karin, Önnerfjord, Patrik, Jonsson, Björn-Anders, Tegner, Yelverton, Sasaki, Takako, Struglics, André, Lohmander, Stefan, Dahl, Niklas, Heinegård, Dick, Aspberg, Anders

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Genetic screening in sudden cardiac death in the young can save future lives by Stattin, Eva-Lena, Westin, Ida Maria, Cederquist, Kristina, Jonasson, Jenni, Jonsson, Björn-Anders, Mörner, Stellan, Norberg, Anna, Krantz, Peter, Wisten, Aase

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Characterization of a Recurrent Germ Line Mutation of the E-Cadherin Gene: Implications for Genetic Testing and Clinical Management by SURIANO, Gianpaolo, YEW, Sandie, OLIVEIRA, Maria J, MACGILLIVRAY, Barbara, RAO, Arundhati, SEARS, Dawn, JACKSON, Charles E, BOYD, Jeff, YEE, Cindy, DETERS, Carolyn, PAI, G. Shashidhar, HAMMOND, Lyn S, FERREIRA, Paulo, MCGIVERN, Bobbi J, MEDGYESY, Diane, SARTZ, Denise, ARUN, Banu, OELSCHLAGER, Brant K, UPTON, Mellisa P, NEUFELD-KAISER, Whitney, SILVA, Orlando E, DONENBERG, Talia R, KOOBY, David A, SENZ, Janine, SHARMA, Shobha, JONSSON, Bjorn-Anders, GRONBERG, Henrik, GALLINGER, Steve, SERUCA, Raquel, LYNCH, Henry, HUNTSMAN, David G, KAURAH, Pardeep, FORD, James M, LONGACRE, Teri A, NORTON, Jeffrey A, CHUN, Nicki, YOUNG, Sean

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Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing by Stattin, Eva-Lena, Boström, Ida Maria, Winbo, Annika, Cederquist, Kristina, Jonasson, Jenni, Jonsson, Björn-Anders, Diamant, Ulla-Britt, Jensen, Steen M, Rydberg, Annika, Norberg, Anna

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Genetic Analysis of the RNASEL Gene in Hereditary, Familial, and Sporadic Prostate Cancer by WIKLUND, Fredrik, JONSSON, Björn-Anders, BROOKES, Anthony J, STRÖMQVIST, Linda, ADOLFSSON, Jan, EMANUELSSON, Monica, ADAMI, Hans-Olov, AUGUSTSSON-BÄLTER, Katarina, GRÖNBERG, Henrik

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Systematic replication study of reported genetic associations in prostate cancer: Strong support for genetic variation in the androgen pathway by Lindström, Sara, Zheng, S. Lilly, Wiklund, Fredrik, Jonsson, Björn-Anders, Adami, Hans-Olov, Bälter, Katarina Augustsson, Brookes, Anthony J., Sun, Jielin, Chang, Bao-Li, Liu, Wennuan, Li, Ge, Isaacs, William B., Adolfsson, Jan, Grönberg, Henrik, Xu, Jianfeng

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160C/A polymorphism in the E‐cadherin gene promoter and risk of hereditary, familial and sporadic prostate cancer by Jonsson, Björn‐Anders, Adami, Hans‐Olov, Hägglund, Maria, Bergh, Anders, Göransson, Ingela, Stattin, Pär, Wiklund, Fredrik, Grönberg, Henrik

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Germline mutations in E‐cadherin do not explain association of hereditary prostate cancer, gastric cancer and breast cancer by Jonsson, Björn‐Anders, Bergh, Anders, Stattin, Pär, Emmanuelsson, Monika, Grönberg, Henrik

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Linkage analysis of prostate cancer susceptibility: confirmation of linkage at 8p22-23 by WIKLUND, Fredrik, JONSSON, Björn-Anders, GÖRANSSON, Ingela, BERGH, Anders, GRÖNBERG, Henrik

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Comprehensive genetic evaluation of common E-cadherin sequence variants and prostate cancer risk : strong confirmation of functional promoter snp by LINDSTRÖM, Sara, WIKLUND, Fredrik, GRÖNBERG, Henrik, JONSSON, Björn-Anders, ADAMI, Hans-Olov, BÄLTER, Katarina, BROOKES, Anthony J, JIANFENG XU, ZHENG, S. Lilly, ISAACS, William B, ADOLFSSON, Jan

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Genome-wide scan of Swedish families with hereditary prostate cancer: Suggestive evidence of linkage at 5q11.2 and 19p13.3 by Wiklund, Fredrik, Gillanders, Elizabeth M., Albertus, Julie A., Bergh, Anders, Damber, Jan-Erik, Emanuelsson, Monica, Freas-Lutz, Diana L., Gildea, Derek E., Göransson, Ingela, Jones, MaryPat S., Jonsson, Björn-Anders, Lindmark, Fredrik, Markey, Carol J., Riedesel, Erica L., Stenman, Elisabeth, Trent, Jeffry M., Grönberg, Henrik

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Low frequency of allelic imbalance at the prostate cancer susceptibility loci HPC1 and 1p36 in Swedish men with hereditary prostate cancer by Åhman, Anna-Karin, Jonsson, Björn-Anders, Damber, Jan-Erik, Bergh, Anders, Emanuelsson, Monica, Grönberg, Henrik

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In Swedish Families with Hereditary Prostate Cancer, Linkage to the HPC1 Locus on Chromosome 1q24-25 Is Restricted to Families with Early-Onset Prostate Cancer by Grönberg, Henrik, Smith, Jeffrey, Emanuelsson, Monika, Jonsson, Björn-Anders, Bergh, Anders, Carpten, John, Isaacs, William, Xu, Jianfeng, Meyers, Deborah, Trent, Jeffrey, Damber, Jan-Erik

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Analysis of the macrophage scavenger receptor I gene in Swedish hereditary and sporadic prostate cancer by LINDMARK, Fredrik, JONSSON, Björn-Anders, BERGH, Anders, STATTIN, Pär, ZHENG, S. Lilly, MEYERS, Deborah A, JIANFENG XU, GRÖNBERG, Henrik

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The prognostic role of KRAS, BRAF, PIK3CA and PTEN in colorectal cancer by Eklöf, V, Wikberg, M L, Edin, S, Dahlin, A M, Jonsson, B-A, Öberg, Å, Rutegård, J, Palmqvist, R

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Analysis of the macrophage scavenger receptor 1 gene in Swedish hereditary and sporadic prostate cancer by Lindmark, Fredrik, Jonsson, Björn-Anders, Bergh, Anders, Stattin, Pär, Zheng, S. Lilly, Meyers, Deborah A., Xu, Jianfeng, Grönberg, Henrik

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Microsatellite Instability, PTEN and p53 Germline Mutations in Glioma Families by Beatrice Malmer, Henrik Grönberg, Ulrika Andersson, Björn-Anders Jonsson, Roger Henriksson

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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 Genetics by Xu, Jianfeng, Dimitrov, Latchezar, Chang, Bao-Li, Adams, Tamara S., Turner, Aubrey R., Meyers, Deborah A., Eeles, Rosalind A., Easton, Douglas F., Foulkes, William D., Simard, Jacques, Giles, Graham G., Hopper, John L., Mahle, Lovise, Moller, Pal, Bishop, Tim, Evans, Chris, Edwards, Steve, Meitz, Julia, Bullock, Sarah, Hope, Questa, Hsieh, Chih-lin, Halpern, Jerry, Balise, Raymond N., Oakley-Girvan, Ingrid, Whittemore, Alice S., Ewing, Charles M., Gielzak, Marta, Isaacs, Sarah D., Walsh, Patrick C., Wiley, Kathleen E., Isaacs, William B., Thibodeau, Stephen N., McDonnell, Shannon K., Cunningham, Julie M., Zarfas, Katherine E., Hebbring, Scott, Schaid, Daniel J., Friedrichsen, Danielle M., Deutsch, Kerry, Kolb, Suzanne, Badzioch, Michael, Jarvik, Gail P., Janer, Marta, Hood, Leroy, Ostrander, Elaine A., Stanford, Janet L., Lange, Ethan M., Beebe-Dimmer, Jennifer L., Mohai, Caroline E., Cooney, Kathleen A., Ikonen, Tarja, Baffoe-Bonnie, Agnes, Fredriksson, Henna, Matikainen, Mika P., Tammela, Teuvo LJ, Bailey-Wilson, Joan, Schleutker, Johanna, Maier, Christiane, Herkommer, Kathleen, Hoegel, Josef J., Vogel, Walther, Paiss, Thomas, Wiklund, Fredrik, Emanuelsson, Monica, Stenman, Elisabeth, Jonsson, Björn-Anders, Grönberg, Henrik, Camp, Nicola J., Farnham, James, Cannon-Albright, Lisa A., Seminara, Daniela

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Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families by Bailey-Wilson, Joan E, Childs, Erica J, Cropp, Cheryl D, Schaid, Daniel J, Xu, Jianfeng, Camp, Nicola J, Cannon-Albright, Lisa A, Farnham, James M, George, Asha, Powell, Isaac, Carpten, John D, Giles, Graham G, Hopper, John L, Severi, Gianluca, English, Dallas R, Foulkes, William D, Mæhle, Lovise, Møller, Pål, Eeles, Rosalind, Easton, Douglas, Guy, Michelle, Edwards, Steve, Badzioch, Michael D, Whittemore, Alice S, Oakley-Girvan, Ingrid, Hsieh, Chih-Lin, Dimitrov, Latchezar, Stanford, Janet L, Karyadi, Danielle M, Deutsch, Kerry, McIntosh, Laura, Ostrander, Elaine A, Wiley, Kathleen E, Isaacs, Sarah D, Walsh, Patrick C, Thibodeau, Stephen N, McDonnell, Shannon K, Hebbring, Scott, Lange, Ethan M, Cooney, Kathleen A, Tammela, Teuvo L J, Schleutker, Johanna, Maier, Christiane, Bochum, Sylvia, Hoegel, Josef, Grönberg, Henrik, Wiklund, Fredrik, Emanuelsson, Monica, Cancel-Tassin, Geraldine, Valeri, Antoine, Cussenot, Olivier, Isaacs, William B

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