Juvenile selective vitamin B(12) malabsorption: 50 years after its description – 10 years of genetic testing

od Gräsbeck, Ralph, Tanner, Stephan M.
Izdano 2011

Vitamin B(12) deficiency in a 15-year old boy due to mutations in the intrinsic factor gene

od Overgaard, Ulrik M., Tanner, Stephan M., Birgens, Henrik S.
Izdano 2010

Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns

od Tanner Stephan M, Sturm Amy C, Baack Elizabeth C, Liyanarachchi Sandya, de la Chapelle Albert
Izdano 2012-08-01

Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns

od Tanner, Stephan M, Sturm, Amy C, Baack, Elizabeth C, Liyanarachchi, Sandya, de la Chapelle, Albert
Izdano 2012

Juvenile Cobalamin Deficiency in a 17 Year Old Child with Autonomic Dysfunction and Skin Changes

od Siddiqui, Abdul Hafeez, Ansari, Aamir, Beech, Cameron M., Shah, Nidhi P., Tanner, Stephan M., Sarnaik, Sharada A.
Izdano 2012

Allele-specific expression of TGFBR1 in colon cancer patients

od Tomsic, Jerneja, Guda, Kishore, Liyanarachchi, Sandya, Hampel, Heather, Natale, Leanna, Markowitz, Sanford D., Tanner, Stephan M., de la Chapelle, Albert
Izdano 2010

Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF

od Ament, Andrea E., Li, Zhongyuan, Sturm, Amy C., Perko, James D., Lawson, Sarah, Masterson, Margaret, Quadros, Edward V., Tanner, Stephan M.
Izdano 2008

Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities

od Beech, Cameron M, Liyanarachchi, Sandya, Shah, Nidhi P, Sturm, Amy C, Sadiq, May F, de la Chapelle, Albert, Tanner, Stephan M
Izdano 2011

Hereditary Intrinsic Factor Deficiency in Chaldeans

od Sturm, Amy C., Baack, Elizabeth C., Armstrong, Michael B., Schiff, Deborah, Zia, Ayesha, Savasan, Sureyya, de la Chapelle, Albert, Tanner, Stephan M.
Izdano 2012

RelA/p65 functions to maintain cellular senescence by regulating genomic stability and DNA repair

od Wang, Jingxin, Jacob, Naduparambil K, Ladner, Katherine J, Beg, Amer, Perko, James D, Tanner, Stephan M, Liyanarachchi, Sandya, Fishel, Richard, Guttridge, Denis C
Izdano 2009

Expression profiling reveals fundamental biological differences in acute myeloid leukemia with isolated trisomy 8 and normal cytogenetics

od Virtaneva, Kimmo, Wright, Fred A., Tanner, Stephan M., Yuan, Bo, Lemon, William J., Caligiuri, Michael A., Bloomfield, Clara D., de la Chapelle, Albert, Krahe, Ralf
Izdano 2001

Germline Allele-Specific Expression of DAPK1 in Chronic Lymphocytic Leukemia

od Wei, Quan-Xiang, Claus, Rainer, Hielscher, Thomas, Mertens, Daniel, Raval, Aparna, Oakes, Christopher C., Tanner, Stephan M., de la Chapelle, Albert, Byrd, John C., Stilgenbauer, Stephan, Plass, Christoph
Izdano 2013

Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene

od Tanner, Stephan M., Li, Zhongyuan, Perko, James D., Öner, Cihan, Çetin, Mualla, Altay, Çiğdem, Yurtsever, Zekiye, David, Karen L., Faivre, Laurence, Ismail, Essam A., Gräsbeck, Ralph, de la Chapelle, Albert
Izdano 2005

Infrequent Detection of Germline Allele-Specific Expression of TGFBR1 in Lymphoblasts and Tissues of Colon Cancer Patients

od Guda, Kishore, Natale, Leanna, Lutterbaugh, James, Wiesner, Georgia L., Lewis, Susan, Tanner, Stephan M., Tomsic, Jerneja, Valle, Laura, de la Chapelle, Albert, Elston, Robert C., Willis, Joseph, Markowitz, Sanford D.
Izdano 2009

Heritable polymorphism predisposes to high BAALC expression in acute myeloid leukemia

od Eisfeld, Ann-Kathrin, Marcucci, Guido, Liyanarachchi, Sandya, Döhner, Konstanze, Schwind, Sebastian, Maharry, Kati, Leffel, Benjamin, Döhner, Hartmut, Radmacher, Michael D., Bloomfield, Clara D., Tanner, Stephan M., de la Chapelle, Albert
Izdano 2012

Acute myeloid leukemia with complex karyotypes and abnormal chromosome 21: Amplification discloses overexpression of APP, ETS2, and ERG genes

od Baldus, Claudia D., Liyanarachchi, Sandya, Mrózek, Krzysztof, Auer, Herbert, Tanner, Stephan M., Guimond, Martin, Ruppert, Amy S., Mohamed, Nehad, Davuluri, Ramana V., Caligiuri, Michael A., Bloomfield, Clara D., de la Chapelle, Albert
Izdano 2004

Germline Allele-Specific Expression of TGFBR1 Confers an Increased Risk of Colorectal Cancer

od Valle, Laura, Serena-Acedo, Tarsicio, Liyanarachchi, Sandya, Hampel, Heather, Comeras, Ilene, Li, Zhongyuan, Zeng, Qinghua, Zhang, Hong-Tao, Pennison, Michael J., Sadim, Maureen, Pasche, Boris, Tanner, Stephan M., de la Chapelle, Albert
Izdano 2008

Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B(12)) absorption in vivo

od He, Qianchuan, Madsen, Mette, Kilkenney, Adam, Gregory, Brittany, Christensen, Erik I., Vorum, Henrik, Højrup, Peter, Schäffer, Alejandro A., Kirkness, Ewen F., Tanner, Stephan M., de la Chapelle, Albert, Giger, Urs, Moestrup, Søren K., Fyfe, John C.
Izdano 2005

BAALC, the human member of a novel mammalian neuroectoderm gene lineage, is implicated in hematopoiesis and acute leukemia

od Tanner, Stephan M., Austin, Jamie L., Leone, Gustavo, Rush, Laura J., Plass, Christoph, Heinonen, Kristiina, Mrózek, Krzysztof, Sill, Heinz, Knuutila, Sakari, Kolitz, Jonathan E., Archer, Kellie J., Caligiuri, Michael A., Bloomfield, Clara D., de la Chapelle, Albert
Izdano 2001

Variants in the Netrin-1 Receptor UNC5C Prevent Apoptosis and Increase Risk for Familial Colorectal Cancer

od Coissieux, Marie-May, Tomsic, Jerneja, Castets, Marie, Hampel, Heather, Tuupanen, Sari, Andrieu, Nadine, Comeras, Ilene, Drouet, Youenn, Lasset, Christine, Liyanarachchi, Sandya, Mazelin, Laetitia, Puisieux, Alain, Saurin, Jean-Christophe, Scoazec, Jean-Yves, Wang, Qing, Aaltonen, Lauri, Tanner, Stephan M, de la Chapelle, Albert, Bernet, Agnès, Mehlen, Patrick
Izdano 2011