Acute Lymphoblastic Leukemia in Children: Treatment Planning via Minimal Residual Disease Assessment

Por Bartram, Claus R, Schrauder, André, Köhler, Rolf, Schrappe, Martin
Publicado em 2012

Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Evaluation of Genotype-Phenotype Correlation in Patients Detected by Newborn Screening

Por Gramer, Gwendolyn, Haege, Gisela, Fang-Hoffmann, Junmin, Hoffmann, Georg F., Bartram, Claus R., Hinderhofer, Katrin, Burgard, Peter, Lindner, Martin
Publicado no JIMD Rep (2015)

Clinical Significance of Aberrant DNA Methylation in Childhood Acute Lymphoblastic Leukemia

Por Takeuchi, Seisho, Matsushita, Masahide, Zimmermann, Martin, Ikezoe, Takayuki, Komatsu, Naoki, Seriu, Taku, Schrappe, Martin, Bartram, Claus R., Koeffler, H. Phillip
Publicado em 2011

BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study

Por Bugert Peter, Kiechle Marion, Sutter Christian, Wappenschmidt Barbara, Hemminki Kari, Meindl Alfons, Frank Bernd, Schmutzler Rita K, Bartram Claus R, Burwinkel Barbara
Publicado em 2007-05-01

Transcription factor 7-like 2 (TCF7L2) variant is associated with familial breast cancer risk: a case-control study

Por Burwinkel, Barbara, Shanmugam, Kalai S, Hemminki, Kari, Meindl, Alfons, Schmutzler, Rita K, Sutter, Christian, Wappenschmidt, Barbara, Kiechle, Marion, Bartram, Claus R, Frank, Bernd
Publicado em 2006

BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study

Por Frank, Bernd, Hemminki, Kari, Meindl, Alfons, Wappenschmidt, Barbara, Sutter, Christian, Kiechle, Marion, Bugert, Peter, Schmutzler, Rita K, Bartram, Claus R, Burwinkel, Barbara
Publicado em 2007

Functional analysis of a novel DNA polymorphism of a tandem repeated sequence in the asparagine synthetase gene in acute lymphoblastic leukemia cells

Por Akagi, Tadayuki, Yin, Dong, Kawamata, Norihiko, Bartram, Claus R., Hofmann, Wolf-K., Song, Jee Hoon, Miller, Carl W., den Boer, Monique L., Koeffler, H. Phillip
Publicado em 2008

So rare we need to hunt for them: reframing the ethical debate on incidental findings

Por Schuol, Sebastian, Schickhardt, Christoph, Wiemann, Stefan, Bartram, Claus R., Tanner, Klaus, Eils, Roland, Meder, Benjamin, Richter, Daniela, Glimm, Hanno, von Kalle, Christof, Winkler, Eva C.
Publicado no Genome Med (2015)

IKZF1 deletion is an independent predictor of outcome in pediatric acute lymphoblastic leukemia treated according to the ALL-BFM 2000 protocol

Por Dörge, Petra, Meissner, Barbara, Zimmermann, Martin, Möricke, Anja, Schrauder, André, Bouquin, Jean-Pierre, Schewe, Denis, Harbott, Jochen, Teigler-Schlegel, Andrea, Ratei, Richard, Ludwig, Wolf-Dieter, Koehler, Rolf, Bartram, Claus R., Schrappe, Martin, Stanulla, Martin, Cario, Gunnar
Publicado em 2013

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

Por Kawamata, Norihiko, Ogawa, Seishi, Zimmermann, Martin, Kato, Motohiro, Sanada, Masashi, Hemminki, Kari, Yamatomo, Go, Nannya, Yasuhito, Koehler, Rolf, Flohr, Thomas, Miller, Carl W., Harbott, Jochen, Ludwig, Wolf-Dieter, Stanulla, Martin, Schrappe, Martin, Bartram, Claus R., Koeffler, H. Phillip
Publicado em 2008

Cloning of genes involved in chromosomal translocations by high-resolution single nucleotide polymorphism genomic microarray

Por Kawamata, Norihiko, Ogawa, Seishi, Zimmermann, Martin, Niebuhr, Birte, Stocking, Carol, Sanada, Masashi, Hemminki, Kari, Yamatomo, Go, Nannya, Yasuhito, Koehler, Rolf, Flohr, Thomas, Miller, Carl W., Harbott, Jochen, Ludwig, Wolf-Dieter, Stanulla, Martin, Schrappe, Martin, Bartram, Claus R., Koeffler, H. Phillip
Publicado em 2008

Low platelet counts after induction therapy for childhood acute lymphoblastic leukemia are strongly associated with poor early response to treatment as measured by minimal residual...

Por Zeidler, Lutz, Zimmermann, Martin, Möricke, Anja, Meissner, Barbara, Bartels, Dorothee, Tschan, Christoph, Schrauder, André, Cario, Gunnar, Goudeva, Lilia, Jäger, Sarah, Ratei, Richard, Ludwig, Wolf-Dieter, Teigler-Schlegel, Andrea, Skokowa, Julia, Koehler, Rolf, Bartram, Claus R., Riehm, Hansjörg, Schrappe, Martin, Welte, Karl, Stanulla, Martin
Publicado em 2012

DNA methylation array analysis identifies breast cancer associated RPTOR, MGRN1 and RAPSN hypomethylation in peripheral blood DNA

Por Tang, Qiuqiong, Holland-Letz, Tim, Slynko, Alla, Cuk, Katarina, Marme, Frederik, Schott, Sarah, Heil, Jörg, Qu, Bin, Golatta, Michael, Bewerunge-Hudler, Melanie, Sutter, Christian, Surowy, Harald, Wappenschmidt, Barbara, Schmutzler, Rita, Hoth, Markus, Bugert, Peter, Bartram, Claus R., Sohn, Christof, Schneeweiss, Andreas, Yang, Rongxi, Burwinkel, Barbara
Publicado no Oncotarget (2016)

Nuclear receptor coregulator SNP discovery and impact on breast cancer risk

Por Varon-Mateeva Raymonda, Arnold Norbert, Niederacher Dieter, Weber Bernhard HF, Bugert Peter, Ditsch Nina, Sutter Christian, Hemminki Kari, Rae Jimmy M, Skaar Todd C, McGuire Sean E, Wang Jay, Richter Alexandra S, Tchatchou Sandrine, Hartmaier Ryan J, Wappenschmidt Barbara, Schmutzler Rita K, Meindl Alfons, Bartram Claus R, Burwinkel Barbara, Oesterreich Steffi
Publicado em 2009-12-01

Nuclear receptor coregulator SNP discovery and impact on breast cancer risk

Por Hartmaier, Ryan J, Tchatchou, Sandrine, Richter, Alexandra S, Wang, Jay, McGuire, Sean E, Skaar, Todd C, Rae, Jimmy M, Hemminki, Kari, Sutter, Christian, Ditsch, Nina, Bugert, Peter, Weber, Bernhard HF, Niederacher, Dieter, Arnold, Norbert, Varon-Mateeva, Raymonda, Wappenschmidt, Barbara, Schmutzler, Rita K, Meindl, Alfons, Bartram, Claus R, Burwinkel, Barbara, Oesterreich, Steffi
Publicado em 2009

Mutations in ROGDI Cause Kohlschütter-Tönz Syndrome

Por Schossig, Anna, Wolf, Nicole I., Fischer, Christine, Fischer, Maria, Stocker, Gernot, Pabinger, Stephan, Dander, Andreas, Steiner, Bernhard, Tönz, Otmar, Kotzot, Dieter, Haberlandt, Edda, Amberger, Albert, Burwinkel, Barbara, Wimmer, Katharina, Fauth, Christine, Grond-Ginsbach, Caspar, Koch, Martin J., Deichmann, Annette, von Kalle, Christof, Bartram, Claus R., Kohlschütter, Alfried, Trajanoski, Zlatko, Zschocke, Johannes
Publicado em 2012

The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A

Por Vijayakrishnan, Jayaram, Henrion, Marc, Moorman, Anthony V., Fiege, Bettina, Kumar, Rajiv, Inacio da Silva Filho, Miguel, Holroyd, Amy, Koehler, Rolf, Thomsen, Hauke, Irving, Julie A., Allan, James M., Lightfoot, Tracy, Roman, Eve, Kinsey, Sally E., Sheridan, Eamonn, Thompson, Pamela D., Hoffmann, Per, Nöthen, Markus M., Mühleisen, Thomas W., Eisele, Lewin, Bartram, Claus R., Schrappe, Martin, Greaves, Mel, Hemminki, Kari, Harrison, Christine J., Stanulla, Martin, Houlston, Richard S.
Publicado no Sci Rep (2015)

A non-enzymatic function of 17β-hydroxysteroid dehydrogenase type 10 is required for mitochondrial integrity and cell survival

Por Rauschenberger, Katharina, Schöler, Katja, Sass, Jörn Oliver, Sauer, Sven, Djuric, Zdenka, Rumig, Cordula, Wolf, Nicole I, Okun, Jürgen G, Kölker, Stefan, Schwarz, Heinz, Fischer, Christine, Grziwa, Beate, Runz, Heiko, Nümann, Astrid, Shafqat, Naeem, Kavanagh, Kathryn L, Hämmerling, Günter, Wanders, Ronald J A, Shield, Julian P H, Wendel, Udo, Stern, David, Nawroth, Peter, Hoffmann, Georg F, Bartram, Claus R, Arnold, Bernd, Bierhaus, Angelika, Oppermann, Udo, Steinbeisser, Herbert, Zschocke, Johannes
Publicado em 2010

Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia

Por Sherborne, Amy L., Hemminki, Kari, Kumar, Rajiv, Bartram, Claus R., Stanulla, Martin, Schrappe, Martin, Petridou, Eleni, Semsei, Ágnes F., Szalai, Csaba, Sinnett, Daniel, Krajinovic, Maja, Healy, Jasmine, Lanciotti, Marina, Dufour, Carlo, Indaco, Stefania, El-Ghouroury, Eman A, Sawangpanich, Ruchchadol, Hongeng, Suradej, Pakakasama, Samart, Gonzalez-Neira, Anna, Ugarte, Evelia L., Leal, Valeria P., Espinoza, Juan P.M., Kamel, Azza M., Ebid, Gamal T.A., Radwan, Eman R., Yalin, Serap, Yalin, Erdinc, Berkoz, Mehmet, Simpson, Jill, Roman, Eve, Lightfoot, Tracy, Hosking, Fay J., Vijayakrishnan, Jayaram, Greaves, Mel, Houlston, Richard S.
Publicado em 2011

Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk

Por Sherborne, Amy L, Hosking, Fay J, Prasad, Rashmi B, Kumar, Rajiv, Koehler, Rolf, Vijayakrishnan, Jayaram, Papaemmanuil, Elli, Bartram, Claus R, Stanulla, Martin, Schrappe, Martin, Gast, Andreas, Dobbins, Sara E, Ma, Yussanne, Sheridan, Eamonn, Taylor, Malcolm, Kinsey, Sally E, Lightfoot, Tracey, Roman, Eve, Irving, Julie A E, Allan, James M, Moorman, Anthony V, Harrison, Christine J, Tomlinson, Ian P, Richards, Sue, Zimmermann, Martin, Szalai, Csaba, Semsei, Ágnes F, Erdelyi, Daniel J, Krajinovic, Maja, Sinnett, Daniel, Healy, Jasmine, Neira, Anna Gonzalez, Kawamata, Norihiko, Ogawa, Seishi, Koeffler, H Phillip, Hemminki, Kari, Greaves, Mel, Houlston, Richard S
Publicado em 2010