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Claus Bartram

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Disorders

Chemicals & Drugs

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Molecular Sequence Data

Physiology

Living Beings

Infant

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Genes & Molecular Sequences

Single Nucleotide Polymorphism

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Publications

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Yang Rongxi; Chen Bowang; Hemminki Kari; Wappenschmidt Barbara; Engel Christoph; Sutter Christian; Ditsch Nina; Weber Bernhard H F; Niederacher Dieter; Arnold Norbert; Meindl Alfons; Bartram Claus R; Schmutzler Rita K; Burwinkel Barbara
Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk.
Schwarz Arne Kristian; Stanulla Martin; Cario Gunnar; Flohr Thomas; Sutton Rosemary; Möricke Anja; Anker Philippe; Stroun Maurice; Welte Karl; Bartram Claus R; Schrappe Martin; Schrauder André
Quantification of free total plasma DNA and minimal residual disease detection in the plasma of children with acute lymphoblastic leukemia.
Remke Marc; Pfister Stefan; Kox Corinne; Toedt Grischa; Becker Natalia; Benner Axel; Werft Wiebke; Breit Stephen; Liu Shuangyou; Engel Felix; Wittmann Andrea; Zimmermann Martin; Stanulla Martin; Schrappe Martin; Ludwig Wolf-Dieter; Bartram Claus R; Radlwimmer Bernhard; Muckenthaler Martina U; Lichter Peter; Kulozik Andreas E
High-resolution genomic profiling of childhood T-ALL reveals frequent copy-number alterations affecting the TGF-beta and PI3K-AKT pathways and deletions at 6q15-16.1 as a genomic marker for unfavorable early treatment response.

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All Publications

2009: Yang Rongxi; Chen Bowang; Hemminki Kari; Wappenschmidt Barbara; Engel Christoph; Sutter Christian; Ditsch Nina; Weber Bernhard H F; Niederacher Dieter; Arnold Norbert; Meindl Alfons; Bartram Claus R; Schmutzler Rita K; Burwinkel Barbara
Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk.
Breast cancer research and treatment 2009;118(2):407-13.
2009: Schwarz Arne Kristian; Stanulla Martin; Cario Gunnar; Flohr Thomas; Sutton Rosemary; Möricke Anja; Anker Philippe; Stroun Maurice; Welte Karl; Bartram Claus R; Schrappe Martin; Schrauder André
Quantification of free total plasma DNA and minimal residual disease detection in the plasma of children with acute lymphoblastic leukemia.
Annals of hematology 2009;88(9):897-905.
2009: Remke Marc; Pfister Stefan; Kox Corinne; Toedt Grischa; Becker Natalia; Benner Axel; Werft Wiebke; Breit Stephen; Liu Shuangyou; Engel Felix; Wittmann Andrea; Zimmermann Martin; Stanulla Martin; Schrappe Martin; Ludwig Wolf-Dieter; Bartram Claus R; Radlwimmer Bernhard; Muckenthaler Martina U; Lichter Peter; Kulozik Andreas E
High-resolution genomic profiling of childhood T-ALL reveals frequent copy-number alterations affecting the TGF-beta and PI3K-AKT pathways and deletions at 6q15-16.1 as a genomic marker for unfavorable early treatment response.
Blood 2009;114(5):1053-62.
2009: Dai Liping; Gast Andreas; Horska Alexandra; Schrappe Martin; Bartram Claus R; Hemminki Kari; Kumar Rajiv; Bermejo Justo Lorenzo
A case-control study of childhood acute lymphoblastic leukaemia and polymorphisms in the TGF-beta and receptor genes.
Pediatric blood & cancer 2009;52(7):819-23.
2009: 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
Functional analysis of a novel DNA polymorphism of a tandem repeated sequence in the asparagine synthetase gene in acute lymphoblastic leukemia cells.
Leukemia research 2009;33(7):991-6.
2009: Kawamata Norihiko; Ogawa Seishi; Seeger Karl; Kirschner-Schwabe Renate; Huynh Thien; Chen John; Megrabian Nairi; Harbott Jochen; Zimmermann Martin; Henze Günter; Schrappe Martin; Bartram Claus R; Koeffler H Phillip
Molecular allelokaryotyping of relapsed pediatric acute lymphoblastic leukemia.
International journal of oncology 2009;34(6):1603-12.
2009: Tchatchou Sandrine; Jung Anke; Hemminki Kari; Sutter Christian; Wappenschmidt Barbara; Bugert Peter; Weber Bernhard H F; Niederacher Dieter; Arnold Norbert; Varon-Mateeva Raymonda; Ditsch Nina; Meindl Alfons; Schmutzler Rita K; Bartram Claus R; Burwinkel Barbara
A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women.
Carcinogenesis 2009;30(1):59-64.
2008: Frank Bernd; Rigas Sushila H; Bermejo Justo Lorenzo; Wiestler Miriam; Wagner Kerstin; Hemminki Kari; Reed Malcolm W; Sutter Christian; Wappenschmidt Barbara; Balasubramanian Sabapathy P; Meindl Alfons; Kiechle Marion; Bugert Peter; Schmutzler Rita K; Bartram Claus R; Justenhoven Christina; Ko Yon-Dschun; Brüning Thomas; Brauch Hiltrud; Hamann Ute; Pharoah Paul P D; Dunning Alison M; Pooley Karen A; Easton Douglas F; Cox Angela; Burwinkel Barbara
The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study.
Breast cancer research and treatment 2008;111(1):139-44.
2008: 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
Cloning of genes involved in chromosomal translocations by high-resolution single nucleotide polymorphism genomic microarray.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(33):11921-6.
2008: Burmeister Thomas; Schwartz Stefan; Bartram Claus R; Gökbuget Nicola; Hoelzer Dieter; Thiel Eckhard;
Patients' age and BCR-ABL frequency in adult B-precursor ALL: a retrospective analysis from the GMALL study group.
Blood 2008;112(3):918-9.
2008: Hillengass Jens; Zechmann Christian M; Nadler Andreas; Hose Dirk; Cremer Friedrich W; Jauch Anna; Heiss Christiane; Benner Axel; Ho Anthony D; Bartram Claus R; Kauczor Hans-Ulrich; Delorme Stefan; Goldschmidt Hartmut; Moehler Thomas M
Gain of 1q21 and distinct adverse cytogenetic abnormalities correlate with increased microcirculation in multiple myeloma.
International journal of cancer. Journal international du cancer 2008;122(12):2871-5.
2008: Bochtler Tilmann; Hegenbart Ute; Cremer Friedrich W; Heiss Christiane; Benner Axel; Hose Dirk; Moos Marion; Bila Jelena; Bartram Claus R; Ho Anthony D; Goldschmidt Hartmut; Jauch Anna; Schonland Stefan O
Evaluation of the cytogenetic aberration pattern in amyloid light chain amyloidosis as compared with monoclonal gammopathy of undetermined significance reveals common pathways of karyotypic instability.
Blood 2008;111(9):4700-5.
2008: Yang Rongxi; Frank Bernd; Hemminki Kari; Bartram Claus R; Wappenschmidt Barbara; Sutter Christian; Kiechle Marion; Bugert Peter; Schmutzler Rita K; Arnold Norbert; Weber Bernhard H F; Niederacher Dieter; Meindl Alfons; Burwinkel Barbara
SNPs in ultraconserved elements and familial breast cancer risk.
Carcinogenesis 2008;29(2):351-5.
2008: 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
Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray.
Blood 2008;111(2):776-84.
2007: Vaclavicek Annika; Bermejo Justo Lorenzo; Wappenschmidt Barbara; Meindl Alfons; Sutter Christian; Schmutzler Rita K; Kiechle Marion; Bugert Peter; Burwinkel Barbara; Bartram Claus R; Hemminki Kari; Försti Asta
Genetic variation in the major mitotic checkpoint genes does not affect familial breast cancer risk.
Breast cancer research and treatment 2007;106(2):205-13.
2007: Helgesson Gert; Dillner Joakim; Carlson Joyce; Bartram Claus R; Hansson Mats G
Ethical framework for previously collected biobank samples.
Nature biotechnology 2007;25(9):973-6.
2007: Frank Bernd; Bermejo Justo Lorenzo; Hemminki Kari; Sutter Christian; Wappenschmidt Barbara; Meindl Alfons; Kiechle-Bahat Marion; Bugert Peter; Schmutzler Rita K; Bartram Claus R; Burwinkel Barbara
Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk.
Carcinogenesis 2007;28(7):1442-5.
2007: Vaclavicek Annika; Bermejo Justo Lorenzo; Schmutzler Rita K; Sutter Christian; Wappenschmidt Barbara; Meindl Alfons; Kiechle Marion; Arnold Norbert; Weber Bernhard H F; Niederacher Dieter; Burwinkel Barbara; Bartram Claus R; Hemminki Kari; Försti Asta
Polymorphisms in the Janus kinase 2 (JAK)/signal transducer and activator of transcription (STAT) genes: putative association of the STAT gene region with familial breast cancer.
Endocrine-related cancer 2007;14(2):267-77.
2007: Brecht Marcus; Steenvoorden Agatha C M; Luf Susanne; Bartram Claus R; Janssen Johannes W G
Rearrangement and expression of myeov and hst in NIH/3T3 transfectants: a caveat for the interpretation of DNA transfection analyses.
Oncology reports 2007;17(5):1127-31.
2007: Tchatchou Sandrine; Wirtenberger Michael; Hemminki Kari; Sutter Christian; Meindl Alfons; Wappenschmidt Barbara; Kiechle Marion; Bugert Peter; Schmutzler Rita K; Bartram Claus R; Burwinkel Barbara
Aurora kinases A and B and familial breast cancer risk.
Cancer letters 2007;247(2):266-72.
2007: Gast A; Bermejo J L; Flohr T; Stanulla M; Burwinkel B; Schrappe M; Bartram C R; Hemminki K; Kumar R
Folate metabolic gene polymorphisms and childhood acute lymphoblastic leukemia: a case-control study.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2007;21(2):320-5.
2007: Wirtenberger Michael; Schmutzhard Julia; Hemminki Kari; Meindl Alfons; Sutter Christian; Schmutzler Rita K; Wappenschmidt Barbara; Kiechle Marion; Arnold Norbert; Weber Bernhard H F; Niederacher Dieter; Bartram Claus R; Burwinkel Barbara
The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancer.
Carcinogenesis 2007;28(2):423-6.
2007: Frank Bernd; Hemminki Kari; Meindl Alfons; Wappenschmidt Barbara; Sutter Christian; Kiechle Marion; Bugert Peter; Schmutzler Rita K; Bartram Claus R; Burwinkel Barbara
BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study.
BMC cancer 2007;7():83.
2006: Wirtenberger Michael; Tchatchou Sandrine; Hemminki Kari; Schmutzhard Julia; Sutter Christian; Schmutzler Rita K; Meindl Alfons; Wappenschmidt Barbara; Kiechle Marion; Arnold Norbert; Weber Bernhard H F; Niederacher Dieter; Bartram Claus R; Burwinkel Barbara
Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer.
Carcinogenesis 2006;27(11):2201-8.
2006: Wirtenberger Michael; Frank Bernd; Hemminki Kari; Klaes Rüdiger; Schmutzler Rita K; Wappenschmidt Barbara; Meindl Alfons; Kiechle Marion; Arnold Norbert; Weber Bernhard H F; Niederacher Dieter; Bartram Claus R; Burwinkel Barbara
Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer.
Carcinogenesis 2006;27(8):1655-60.
2006: Frank Bernd; Hemminki Kari; Wappenschmidt Barbara; Klaes Rüdiger; Meindl Alfons; Schmutzler Rita K; Bugert Peter; Untch Michael; Bartram Claus R; Burwinkel Barbara
Variable number of tandem repeats polymorphism in the SMYD3 promoter region and the risk of familial breast cancer.
International journal of cancer. Journal international du cancer 2006;118(11):2917-8.
2006: Frank Bernd; Hemminki Kari; Meindl Alfons; Wappenschmidt Barbara; Klaes Rüdiger; Schmutzler Rita K; Untch Michael; Bugert Peter; Bartram Claus R; Burwinkel Barbara
Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk.
International journal of cancer. Journal international du cancer 2006;118(10):2505-8.
2006: Vaclavicek Annika; Hemminki Kari; Bartram Claus R; Wagner Kerstin; Wappenschmidt Barbara; Meindl Alfons; Schmutzler Rita K; Klaes Rüdiger; Untch Michael; Burwinkel Barbara; Försti Asta
Association of prolactin and its receptor gene regions with familial breast cancer.
The Journal of clinical endocrinology and metabolism 2006;91(4):1513-9.
2006: Hansson Mats G; Dillner Joakim; Bartram Claus R; Carlson Joyce A; Helgesson Gert
Should donors be allowed to give broad consent to future biobank research?
The lancet oncology 2006;7(3):266-9.
2006: Frank Bernd; Hemminki Kari; Wappenschmidt Barbara; Meindl Alfons; Klaes Rüdiger; Schmutzler Rita K; Bugert Peter; Untch Michael; Bartram Claus R; Burwinkel Barbara
Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant.
Carcinogenesis 2006;27(3):606-9.
2006: Wirtenberger Michael; Tchatchou Sandrine; Hemminki Kari; Klaes Rüdiger; Schmutzler Rita K; Bermejo Justo L; Chen Bowang; Wappenschmidt Barbara; Meindl Alfons; Bartram Claus R; Burwinkel Barbara
Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer.
Carcinogenesis 2006;27(3):593-8.
2006: Tsukasaki Kunihiro; Lohr Dirk; Sugahara Kazuyuki; Kamihira Shimeru; Tomonaga Masao; Bartram Claus R; Jauch Anna
Comparative genomic hybridization analysis of Japanese B-cell chronic lymphocytic leukemia: correlation with clinical course.
Leukemia & lymphoma 2006;47(2):261-6.
2006: Brüggemann Monika; Raff Thorsten; Flohr Thomas; Gökbuget Nicola; Nakao Makoto; Droese Jo; Lüschen Silke; Pott Christiane; Ritgen Matthias; Scheuring Urban; Horst Heinz-August; Thiel Eckhard; Hoelzer Dieter; Bartram Claus R; Kneba Michael;
Clinical significance of minimal residual disease quantification in adult patients with standard-risk acute lymphoblastic leukemia.
Blood 2006;107(3):1116-23.
2006: Wilkening Stefan; Bermejo Justo Lorenzo; Burwinkel Barbara; Klaes Rüdiger; Bartram Claus R; Meindl Alfons; Bugert Peter; Schmutzler Rita K; Wappenschmidt Barbara; Untch Michael; Hemminki Kari; Försti Asta
The single nucleotide polymorphism IVS1+309 in mouse double minute 2 does not affect risk of familial breast cancer.
Cancer research 2006;66(2):646-8.
2006: de Almeida Rogério Alves; Heuser Tanja; Blaschke Rüdiger; Bartram Claus R; Janssen Johannes W G
Control of MYEOV protein synthesis by upstream open reading frames.
The Journal of biological chemistry 2006;281(2):695-704.
2006: Yang Yang; Takeuchi Seisho; Hofmann Wolf K; Ikezoe Takayuki; van Dongen Jacques J M; Szczepanski Tomasz; Bartram Claus R; Yoshino Norihide; Taguchi Hirokuni; Koeffler H Phillip
Aberrant methylation in promoter-associated CpG islands of multiple genes in acute lymphoblastic leukemia.
Leukemia research 2006;30(1):98-102.
2006: Burwinkel Barbara; Shanmugam Kalai S; Hemminki Kari; Meindl Alfons; Schmutzler Rita K; Sutter Christian; Wappenschmidt Barbara; Kiechle Marion; Bartram Claus R; Frank Bernd
Transcription factor 7-like 2 (TCF7L2) variant is associated with familial breast cancer risk: a case-control study.
BMC cancer 2006;6():268.
2005: Gleissner Beate; Goekbuget Nicola; Rieder Harald; Arnold Renate; Schwartz Stefan; Diedrich Helmut; Schoch Claudia; Heinze Barbara; Fonatsch Christa; Bartram Claus R; Hoelzer Dieter; Thiel Eckhard;
CD10- pre-B acute lymphoblastic leukemia (ALL) is a distinct high-risk subgroup of adult ALL associated with a high frequency of MLL aberrations: results of the German Multicenter Trials for Adult ALL (GMALL).
Blood 2005;106(13):4054-6.
2005: Frank Bernd; Hemminki Kari; Shanmugam Kalai S; Meindl Alfons; Klaes Rüdiger; Schmutzler Rita K; Wappenschmidt Barbara; Untch Michael; Bugert Peter; Bartram Claus R; Burwinkel Barbara
Association of death receptor 4 haplotype 626C-683C with an increased breast cancer risk.
Carcinogenesis 2005;26(11):1975-7.
2005: Wirtenberger Michael; Hemminki Kari; Försti Asta; Klaes Rüdiger; Schmutzler Rita K; Grzybowska Ewa; Bermejo Justo L; Wappenschmidt Barbara; Bugert Peter; Butkiewicz Dorota; Pamula Jolanta; Pekala Wioletta; Zientek Helena; Bartram Claus R; Burwinkel Barbara
c-MYC Asn11Ser is associated with increased risk for familial breast cancer.
International journal of cancer. Journal international du cancer 2005;117(4):638-42.
2005: D'Haese Jan G; Tsukasaki Kunihiro; Cremer Friedrich W; Fischer Christine; Bartram Claus R; Jauch Anna
Chromosomal aberrations in follicular non-Hodgkin lymphomas of Japanese patients, detected with comparative genomic hybridization and polymerase chain reaction analysis.
Cancer genetics and cytogenetics 2005;162(2):107-14.
2005: Cremer Friedrich W; Bila Jelena; Buck Isabelle; Kartal Mutlu; Hose Dirk; Ittrich Carina; Benner Axel; Raab Marc S; Theil Ann-Cathrin; Moos Marion; Goldschmidt Hartmut; Bartram Claus R; Jauch Anna
Delineation of distinct subgroups of multiple myeloma and a model for clonal evolution based on interphase cytogenetics.
Genes, chromosomes & cancer 2005;44(2):194-203.
2005: Cremer Friedrich W; Kartal Mutlu; Hose Dirk; Bila Jelena; Buck Isabelle; Bellos Frauke; Raab Marc-Steffen; Brough Michaela; Moebus Anke; Hager Hans-Dieter; Goldschmidt Hartmut; Moos Marion; Bartram Claus R; Jauch Anna
High incidence and intraclonal heterogeneity of chromosome 11 aberrations in patients with newly diagnosed multiple myeloma detected by multiprobe interphase FISH.
Cancer genetics and cytogenetics 2005;161(2):116-24.
2005: Janssen Bart; Hohenadel Daniela; Brinkkoetter Paul; Peters Verena; Rind Nina; Fischer Christine; Rychlik Ivan; Cerna Marie; Romzova Marianna; de Heer Emile; Baelde Hans; Bakker Stephan J L; Zirie Mahmoud; Rondeau Eric; Mathieson Peter; Saleem Moin A; Meyer Jochen; Köppel Hannes; Sauerhoefer Sibylle; Bartram Claus R; Nawroth Peter; Hammes Hans-Peter; Yard Benito A; Zschocke Johannes; van der Woude Fokko J
Carnosine as a protective factor in diabetic nephropathy: association with a leucine repeat of the carnosinase gene CNDP1.
Diabetes 2005;54(8):2320-7.
2005: Burwinkel Barbara; Wirtenberger Michael; Klaes Rüdiger; Schmutzler Rita K; Grzybowska Ewa; Försti Asta; Frank Bernd; Bermejo Justo Lorenzo; Bugert Peter; Wappenschmidt Barbara; Butkiewicz Dorota; Pamula Jolanta; Pekala Wioletta; Zientek Helena; Mielzynska Danuta; Siwinska Ewa; Bartram Claus R; Hemminki Kari
Association of NCOA3 polymorphisms with breast cancer risk.
Clinical cancer research : an official journal of the American Association for Cancer Research 2005;11(6):2169-74.
2005: Stanulla Martin; Schaeffeler Elke; Flohr Thomas; Cario Gunnar; Schrauder André; Zimmermann Martin; Welte Karl; Ludwig Wolf-Dieter; Bartram Claus R; Zanger Ulrich M; Eichelbaum Michel; Schrappe Martin; Schwab Matthias
Thiopurine methyltransferase (TPMT) genotype and early treatment response to mercaptopurine in childhood acute lymphoblastic leukemia.
JAMA : the journal of the American Medical Association 2005;293(12):1485-9.
2005: Frank Bernd; Hemminki Kari; Wirtenberger Michael; Bermejo Justo Lorenzo; Bugert Peter; Klaes Rüdiger; Schmutzler Rita K; Wappenschmidt Barbara; Bartram Claus R; Burwinkel Barbara
The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk.
Carcinogenesis 2005;26(3):643-7.
2005: Schaaf Christian P; Benzing Jörg; Schmitt Thomas; Erz Dorothee H R; Tewes Magdalena; Bartram Claus R; Janssen Johannes W G
Novel interaction partners of the TPR/MET tyrosine kinase.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2005;19(2):267-9.
2005: Brecht Marcus; Steenvoorden Agatha C M; Collard John G; Luf Susanne; Erz Dorothee; Bartram Claus R; Janssen Johannes W G
Activation of gef-h1, a guanine nucleotide exchange factor for RhoA, by DNA transfection.
International journal of cancer. Journal international du cancer 2005;113(4):533-40.
2005: Cario Gunnar; Stanulla Martin; Fine Bernard M; Teuffel Oliver; Neuhoff Nils V; Schrauder André; Flohr Thomas; Schäfer Beat W; Bartram Claus R; Welte Karl; Schlegelberger Brigitte; Schrappe Martin
Distinct gene expression profiles determine molecular treatment response in childhood acute lymphoblastic leukemia.
Blood 2005;105(2):821-6.
2005: Götte Karl; Tremmel Susanne C; Popp Susanne; Weber Susanne; Hörmann Karl; Bartram Claus R; Jauch Anna
Intratumoral genomic heterogeneity in advanced head and neck cancer detected by comparative genomic hybridization.
Advances in oto-rhino-laryngology 2005;62():38-48.
2004: Hartmann Carolin; John Anika L; Klaes Rüdiger; Hofmann Wera; Bielen Rainer; Koehler Rolf; Janssen Bart; Bartram Claus R; Arnold Norbert; Zschocke Johannes
Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families.
Human mutation 2004;24(6):534.
2004: Grünig Ekkehard; Koehler Rolf; Miltenberger-Miltenyi Gabriel; Zimmermann Rainer; Gorenflo Matthias; Mereles Derliz; Arnold Karlin; Naust Barbara; Wilkens Heinrike; Benz Andreas; von Hippel Albrecht; Ulmer Herbert E; Kübler Wolfgang; Katus Hugo A; Bartram Claus R; Schranz Dietmar; Janssen Bart
Primary pulmonary hypertension in children may have a different genetic background than in adults.
Pediatric research 2004;56(4):571-8.
2004: Matsushita Chise; Yang Yang; Takeuchi Seisho; Matsushita Masahide; Van Dongen Jacques J M; Szczepanski Tomasz; Bartram Claus R; Seo Hiromi; Koeffler H Phillip; Taguchi Hirokuni
Aberrant methylation in promoter-associated CpG islands of multiple genes in relapsed childhood acute lymphoblastic leukemia.
Oncology reports 2004;12(1):97-9.
2004: Tsukasaki Kunihiro; Tanosaki Sakae; DeVos Sven; Hofmann Wolf K; Wachsman William; Gombart Adrian F; Krebs Johannes; Jauch Anna; Bartram Claus R; Nagai Kazuhiro; Tomonaga Masao; Said Jonathan W; Koeffler H Phillip
Identifying progression-associated genes in adult T-cell leukemia/lymphoma by using oligonucleotide microarrays.
International journal of cancer. Journal international du cancer 2004;109(6):875-81.
2004: Gökbuget N; Raff R; Brügge-Mann M; Flohr T; Scheuring U; Pfeifer H; Bartram C R; Kneba M; Hoelzer D
Risk/MRD adapted GMALL trials in adult ALL.
Annals of hematology 2004;83 Suppl 1():S129-31.
2003: Weber-Mangal Susanne; Sinn Hans-Peter; Popp Susanne; Klaes Rüdiger; Emig Robert; Bentz Martin; Mansmann Ulrich; Bastert Gunther; Bartram Claus R; Jauch Anna
Breast cancer in young women (< or = 35 years): Genomic aberrations detected by comparative genomic hybridization.
International journal of cancer. Journal international du cancer 2003;107(4):583-92.
2003: Takeuchi Seisho; Seriu Taku; van Dongen Jacques J M; Szczepanski Tomasz; Tsukasaki Kunihiro; Takeuchi Naoko; Fermin Anthony C; Seo Hiromi; Bartram Claus R; Koeffler H Phillip
Allelotype analysis in relapsed childhood acute lymphoblastic leukemia.
Oncogene 2003;22(44):6970-6.
2003: Meyer Peter; Voigtlaender Theda; Bartram Claus R; Klaes Ruediger
Twenty-three novel BRCA1 and BRCA2 sequence alterations in breast and/or ovarian cancer families in Southern Germany.
Human mutation 2003;22(3):259.
2003: Tremmel Susanne C; Götte Karl; Popp Susanne; Weber Susanne; Hörmann Karl; Bartram Claus R; Jauch Anna
Intratumoral genomic heterogeneity in advanced head and neck cancer detected by comparative genomic hybridization.
Cancer genetics and cytogenetics 2003;144(2):165-74.
2003: Rindermann Matthias; Grünig Ekkehard; von Hippel Albrecht; Koehler Rolf; Miltenberger-Miltenyi Gabriel; Mereles Derliz; Arnold Karlin; Pauciulo Michael; Nichols William; Olschewski Horst; Hoeper Marius M; Winkler Jörg; Katus Hugo A; Kübler Wolfgang; Bartram Claus R; Janssen Bart
Primary pulmonary hypertension may be a heterogeneous disease with a second locus on chromosome 2q31.
Journal of the American College of Cardiology 2003;41(12):2237-44.
2003: Seriu Taku; Stark Yvonne; Erz Dorothee; Bartram Claus R
Size and composition of T-cell receptor delta (TCRD) junctional sequences are not predictive of the sensitivity of clonospecific oligonucleotides designed for detection of minimal residual disease in acute lymphoblastic leukemia.
International journal of hematology 2003;77(4):371-5.
2003: Krämer Alwin; Fruehauf Stefan; Ho Anthony D; Hager Hans-Dieter; Bartram Claus R; Hochhaus Andreas
Novel constitutional t(2;12)(q21;q22) in a patient with t(9;22)-negative chronic myelocytic leukemia.
Cancer genetics and cytogenetics 2003;142(2):162-4.
2003: Takeuchi S; Tsukasaki K; Bartram C R; Seriu T; Zimmermann M; Schrappe M; Takeuchi N; Park S; Taguchi H; Koeffler H P
Long-term study of the clinical significance of loss of heterozygosity in childhood acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2003;17(1):149-54.
2002: Takeuchi Seisho; Takeuchi Naoko; Tsukasaki Kunihiro; Bartram Claus R; Zimmermann Martin; Schrappe Martin; Taguchi Hirokuni; Koeffler H Phillip
Genetic polymorphisms in the tumour necrosis factor locus in childhood acute lymphoblastic leukaemia.
British journal of haematology 2002;119(4):985-7.
2002: Janssen Johannes W G; Cuny Marguerite; Orsetti Béatrice; Rodriguez Carmen; Vallés Hélène; Bartram Claus R; Schuuring Ed; Theillet Charles
MYEOV: a candidate gene for DNA amplification events occurring centromeric to CCND1 in breast cancer.
International journal of cancer. Journal international du cancer 2002;102(6):608-14.
2002: Vardarli Irfan; Baier Leslie J; Hanson Robert L; Akkoyun Imren; Fischer Christine; Rohmeiss Peter; Basci Ali; Bartram Claus R; Van Der Woude Fokko J; Janssen Bart
Gene for susceptibility to diabetic nephropathy in type 2 diabetes maps to 18q22.3-23.
Kidney international 2002;62(6):2176-83.
2002: Hansen-Hagge T E; Schäfer M; Kiyoi H; Morris S W; Whitlock J A; Koch P; Bohlmann I; Mahotka C; Bartram C R; Janssen J W G
Disruption of the RanBP17/Hox11L2 region by recombination with the TCRdelta locus in acute lymphoblastic leukemias with t(5;14)(q34;q11).
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2002;16(11):2205-12.
2002: Hoelzer D; Arnold R; Bartram C R; Böhme A; Freund M; Ganser A; Kneba M; Lipp T; Ludwig W D; Maschmeyer G; Rieder H; Thiel E; Messerer D; Weiss A; Gökbuget N
[Acute lymphatic leukemia in the adult. Diagnosis, risk groups and therapy]
Der Internist 2002;43(10):1212-6, 1219-22, 1224-7.
2002: Xie Dong; Jauch Anna; Miller Carl W; Bartram Claus R; Koeffler H Phillip
Discovery of over-expressed genes and genetic alterations in breast cancer cells using a combination of suppression subtractive hybridization, multiplex FISH and comparative genomic hybridization.
International journal of oncology 2002;21(3):499-507.
2002: Willemse Marja J; Seriu Taku; Hettinger Klaudia; d'Aniello Elisabetta; Hop Wim C J; Panzer-Grümayer E Renate; Biondi Andrea; Schrappe Martin; Kamps Willem A; Masera Guiseppe; Gadner Helmut; Riehm Hansjoerg; Bartram Claus R; van Dongen Jacques J M
Detection of minimal residual disease identifies differences in treatment response between T-ALL and precursor B-ALL.
Blood 2002;99(12):4386-93.
2002: Szczepanski Tomasz; Flohr Thomas; van der Velden Vincent H J; Bartram Claus R; van Dongen Jacques J M
Molecular monitoring of residual disease using antigen receptor genes in childhood acute lymphoblastic leukaemia.
Best practice & research. Clinical haematology 2002;15(1):37-57.
2002: Grünig E; Mereles D; Arnold K; Benz A; Olschewski Horst; Miltenberger-Miltenyi G; Borst M M; Abushi A; Seeger W; Winkler J; Höper M M; Bartram C R; Kübler W; Janssen B
Primary pulmonary hypertension is predominantly a hereditary disease.
Chest 2002;121(3 Suppl):81S-82S.
2002: Janssen Bart; Rindermann Matthias; Barth Ulrike; Miltenberger-Miltenyi Gabriel; Mereles Derliz; Abushi Adel; Seeger Werner; Kübler Wolfgang; Bartram Claus R; Grünig Ekkehard
Linkage analysis in a large family with primary pulmonary hypertension: genetic heterogeneity and a second primary pulmonary hypertension locus on 2q31-32.
Chest 2002;121(3 Suppl):54S-56S.
2002: Gleissner Beate; Gökbuget Nicola; Bartram Claus R; Janssen Bart; Rieder Harald; Janssen Johannes W G; Fonatsch Christa; Heyll Axel; Voliotis Dimitris; Beck Joachim; Lipp Thomas; Munzert Gerd; Maurer Jürgen; Hoelzer Dieter; Thiel Eckhard;
Leading prognostic relevance of the BCR-ABL translocation in adult acute B-lineage lymphoblastic leukemia: a prospective study of the German Multicenter Trial Group and confirmed polymerase chain reaction analysis.
Blood 2002;99(5):1536-43.
2002: Janssen Johannes W G; Imoto Issei; Inoue Jun; Shimada Yutaka; Ueda Masakazu; Imamura Masayuki; Bartram Claus R; Inazawa Johji
MYEOV, a gene at 11q13, is coamplified with CCND1, but epigenetically inactivated in a subset of esophageal squamous cell carcinomas.
Journal of human genetics 2002;47(9):460-4.
2001: Gleissner B; Rieder H; Thiel E; Fonatsch C; Janssen L A; Heinze B; Janssen J W; Schoch C; Goekbuget N; Maurer J; Hoelzer D; Bartram C R
Prospective BCR-ABL analysis by polymerase chain reaction (RT-PCR) in adult acute B-lineage lymphoblastic leukemia: reliability of RT-nested-PCR and comparison to cytogenetic data.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2001;15(12):1834-40.
2001: Tsukasaki K; Krebs J; Nagai K; Tomonaga M; Koeffler H P; Bartram C R; Jauch A
Comparative genomic hybridization analysis in adult T-cell leukemia/lymphoma: correlation with clinical course.
Blood 2001;97(12):3875-81.
2001: Trautmann K; Thakker R V; Ellison D W; Ibrahim A; Lees P D; Harding B; Fischer C; Popp S; Bartram C R; Jauch A
Chromosomal aberrations in sporadic pituitary tumors.
International journal of cancer. Journal international du cancer 2001;91(6):809-14.
2001: Scholz I; Popp S; Granzow M; Schoell B; Holtgreve-Grez H; Takeuchi S; Schrappe M; Harbott J; Teigler-Schlegel A; Zimmermann M; Fischer C; Koeffler H P; Bartram C R; Jauch A
Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis.
Cancer genetics and cytogenetics 2001;124(2):89-97.
2000: Gökbuget N; Hoelzer D; Arnold R; Böhme A; Bartram C R; Freund M; Ganser A; Kneba M; Langer W; Lipp T; Ludwig W D; Maschmeyer G; Rieder H; Thiel E; Weiss A; Messerer D
Treatment of Adult ALL according to protocols of the German Multicenter Study Group for Adult ALL (GMALL).
Hematology/oncology clinics of North America 2000;14(6):1307-25, ix.
2000: Koch P; Bohlmann I; Schäfer M; Hansen-Hagge T E; Kiyoi H; Wilda M; Hameister H; Bartram C R; Janssen J W
Identification of a novel putative Ran-binding protein and its close homologue.
Biochemical and biophysical research communications 2000;278(1):241-9.
2000: Biondi A; Valsecchi M G; Seriu T; D'Aniello E; Willemse M J; Fasching K; Pannunzio A; Gadner H; Schrappe M; Kamps W A; Bartram C R; van Dongen J J; Panzer-Grümayer E R
Molecular detection of minimal residual disease is a strong predictive factor of relapse in childhood B-lineage acute lymphoblastic leukemia with medium risk features. A case control study of the International BFM study group.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2000;14(11):1939-43.
2000: Nakao M; Janssen J W; Flohr T; Bartram C R
Rapid and reliable quantification of minimal residual disease in acute lymphoblastic leukemia using rearranged immunoglobulin and T-cell receptor loci by LightCycler technology.
Cancer research 2000;60(12):3281-9.
2000: Seriu T; Hansen-Hagge T E; Stark Y; Bartram C R
Immunoglobulin kappa gene rearrangements between the kappa deleting element and Jkappa recombination signal sequences in acute lymphoblastic leukemia and normal hematopoiesis.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2000;14(4):671-4.
2000: Janssen J W; Vaandrager J W; Heuser T; Jauch A; Kluin P M; Geelen E; Bergsagel P L; Kuehl W M; Drexler H G; Otsuki T; Bartram C R; Schuuring E
Concurrent activation of a novel putative transforming gene, myeov, and cyclin D1 in a subset of multiple myeloma cell lines with t(11;14)(q13;q32).
Blood 2000;95(8):2691-8.
2000: Nakao M; Janssen J W; Erz D; Seriu T; Bartram C R
Tandem duplication of the FLT3 gene in acute lymphoblastic leukemia: a marker for the monitoring of minimal residual disease.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2000;14(3):522-4.
2000: Nakao M; Janssen J W; Seriu T; Bartram C R
Rapid and reliable detection of N-ras mutations in acute lymphoblastic leukemia by melting curve analysis using LightCycler technology.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2000;14(2):312-5.
2000: Komatsu N; Takeuchi S; Ikezoe T; Tasaka T; Hatta Y; Machida H; Williamson I K; Bartram C R; Koeffler H P; Taguchi H
Mutations of the E2F4 gene in hematological malignancies having microsatellite instability.
Blood 2000;95(4):1509-10.
1999: Takeuchi S; Cho S K; Seriu T; Koike M; Bartram C R; Reiter A; Schrappe M; Takeuchi C; Taguchi H; Koeffler H P
Identification of three distinct regions of deletion on the long arm of chromosome 11 in childhood acute lymphoblastic leukemia.
Oncogene 1999;18(51):7387-8.
1999: Janssen J W; Braunger J; Ballas K; Faust M; Siebers U; Steenvoorden A C; Bartram C R
Spectrum of transforming sequences detected by tumorigenicity assay in a large series of human neoplasms.
International journal of cancer. Journal international du cancer 1999;80(6):857-62.
1999: Pongers-Willemse M J; Seriu T; Stolz F; d'Aniello E; Gameiro P; Pisa P; Gonzalez M; Bartram C R; Panzer-Grümayer E R; Biondi A; San Miguel J F; van Dongen J J
Primers and protocols for standardized detection of minimal residual disease in acute lymphoblastic leukemia using immunoglobulin and T cell receptor gene rearrangements and TAL1 deletions as PCR targets: report of the BIOMED-1 CONCERTED ACTION: investigation of minimal residual disease in acute leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1999;13(1):110-8.
1998: van Dongen J J; Seriu T; Panzer-Grümayer E R; Biondi A; Pongers-Willemse M J; Corral L; Stolz F; Schrappe M; Masera G; Kamps W A; Gadner H; van Wering E R; Ludwig W D; Basso G; de Bruijn M A; Cazzaniga G; Hettinger K; van der Does-van den Berg A; Hop W C; Riehm H; Bartram C R
Prognostic value of minimal residual disease in acute lymphoblastic leukaemia in childhood.
Lancet 1998;352(9142):1731-8.
1998: Takeuchi S; Koike M; Park S; Seriu T; Bartram C R; Taub H E; Williamson I K; Grewal J; Taguchi H; Koeffler H P
The ATM gene and susceptibility to childhood T-cell acute lymphoblastic leukaemia.
British journal of haematology 1998;103(2):536-8.
1998: Schrappe M; Aricò M; Harbott J; Biondi A; Zimmermann M; Conter V; Reiter A; Valsecchi M G; Gadner H; Basso G; Bartram C R; Lampert F; Riehm H; Masera G
Philadelphia chromosome-positive (Ph+) childhood acute lymphoblastic leukemia: good initial steroid response allows early prediction of a favorable treatment outcome.
Blood 1998;92(8):2730-41.
1998: Rieder H; Bonwetsch C; Janssen L A; Maurer J; Janssen J W; Schwartz S; Ludwig W D; Gassmann W; Bartram C R; Thiel E; Löffler H; Gökbuget N; Hoelzer D; Fonatsch C
High rate of chromosome abnormalities detected by fluorescence in situ hybridization using BCR and ABL probes in adult acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1998;12(9):1473-81.
1998: Ludwig W D; Rieder H; Bartram C R; Heinze B; Schwartz S; Gassmann W; Löffler H; Hossfeld D; Heil G; Handt S; Heyll A; Diedrich H; Fischer K; Weiss A; Völkers B; Aydemir U; Fonatsch C; Gökbuget N; Thiel E; Hoelzer D
Immunophenotypic and genotypic features, clinical characteristics, and treatment outcome of adult pro-B acute lymphoblastic leukemia: results of the German multicenter trials GMALL 03/87 and 04/89.
Blood 1998;92(6):1898-909.
1998: Takeuchi S; Koike M; Seriu T; Bartram C R; Schrappe M; Reiter A; Park S; Taub H E; Kubonishi I; Miyoshi I; Koeffler H P
Frequent loss of heterozygosity on the long arm of chromosome 6: identification of two distinct regions of deletion in childhood acute lymphoblastic leukemia.
Cancer research 1998;58(12):2618-23.
1998: Hansen-Hagge T E; Janssen J W; Hameister H; Papa F R; Zechner U; Seriu T; Jauch A; Becke D; Hochstrasser M; Bartram C R
An evolutionarily conserved gene on human chromosome 5q33-q34, UBH1, encodes a novel deubiquitinating enzyme.
Genomics 1998;49(3):411-8.
1998: Janssen J W; Schleithoff L; Bartram C R; Schulz A S
An oncogenic fusion product of the phosphatidylinositol 3-kinase p85beta subunit and HUMORF8, a putative deubiquitinating enzyme.
Oncogene 1998;16(13):1767-72.
1997: Takeuchi S; Koike M; Seriu T; Bartram C R; Slater J; Park S; Miyoshi I; Koeffler H P
Homozygous deletions at 9p21 in childhood acute lymphoblastic leukemia detected by microsatellite analysis.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(10):1636-40.
1997: Liptay S; Seriu T; Bartram C R; Schmid R M
Germline configuration of nfkb2, c-rel and bcl3 in childhood acute lymphoblastic leukemia (ALL).
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(8):1364-6.
1997: Takeuchi S; Seriu T; Bartram C R; Golub T R; Reiter A; Miyoshi I; Gilliland D G; Koeffler H P
TEL is one of the targets for deletion on 12p in many cases of childhood B-lineage acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(8):1220-3.
1997: Takeuchi S; Seriu T; Tasaka T; Koike M; Cho S K; Park S; Slater J; Mufti I; Hatta Y; Miyoshi I; Bartram C R; Koeffler H P
Microsatellite instability and other molecular abnormalities in childhood acute lymphoblastic leukaemia.
British journal of haematology 1997;98(1):134-9.
1997: Braunger J; Schleithoff L; Schulz A S; Kessler H; Lammers R; Ullrich A; Bartram C R; Janssen J W
Intracellular signaling of the Ufo/Axl receptor tyrosine kinase is mediated mainly by a multi-substrate docking-site.
Oncogene 1997;14(22):2619-31.
1997: Seriu T; Erz D; Stark Y; Bartram C R
T cell receptor Ddelta2Ddelta3 rearrangement: a suitable allele-specific marker for the detection of minimal residual disease in childhood acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(5):759-61.
1997: Kawamata N; Seriu T; Bartram C R; Koeffler H P
Molecular analysis of the secretory phospholipase A2 gene, a candidate of Mom1 gene, in neuroblastomas.
Cancer letters 1997;111(1-2):71-5.
1996: Rieder H; Ludwig W D; Gassmann W; Maurer J; Janssen J W; Gökbuget N; Schwartz S; Thiel E; Löffler H; Bartram C R; Hoelzer D; Fonatsch C
Prognostic significance of additional chromosome abnormalities in adult patients with Philadelphia chromosome positive acute lymphoblastic leukaemia.
British journal of haematology 1996;95(4):678-91.
1996: McLean T W; Ringold S; Neuberg D; Stegmaier K; Tantravahi R; Ritz J; Koeffler H P; Takeuchi S; Janssen J W; Seriu T; Bartram C R; Sallan S E; Gilliland D G; Golub T R
TEL/AML-1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia.
Blood 1996;88(11):4252-8.
1996: Pannicke U; Tuchschmid P; Friedrich W; Bartram C R; Schwarz K
Two novel missense and frameshift mutations in exons 5 and 6 of the purine nucleoside phosphorylase (PNP) gene in a severe combined immunodeficiency (SCID) patient.
Human genetics 1996;98(6):706-9.
1996: Schwarz K; Gauss G H; Ludwig L; Pannicke U; Li Z; Lindner D; Friedrich W; Seger R A; Hansen-Hagge T E; Desiderio S; Lieber M R; Bartram C R
RAG mutations in human B cell-negative SCID.
Science (New York, N.Y.) 1996;274(5284):97-9.
1996: Morosetti R; Grignani F; Liberatore C; Pelicci P G; Schiller G J; Kizaki M; Bartram C R; Miller C W; Koeffler H P
Infrequent alterations of the RAR alpha gene in acute myelogenous leukemias, retinoic acid-resistant acute promyelocytic leukemias, myelodysplastic syndromes, and cell lines.
Blood 1996;87(10):4399-403.
1996: Bartram C R
Molecular genetic aspects of myelodysplastic syndromes.
Seminars in hematology 1996;33(2):139-49.
1996: Takeuchi S; Bartram C R; Miller C W; Reiter A; Seriu T; Zimmerann M; Schrappe M; Mori N; Slater J; Miyoshi I; Koeffler H P
Acute lymphoblastic leukemia of childhood: identification of two distinct regions of deletion on the short arm of chromosome 12 in the region of TEL and KIP1.
Blood 1996;87(8):3368-74.
1996: Stegmaier K; Takeuchi S; Golub T R; Bohlander S K; Bartram C R; Koeffler H P
Mutational analysis of the candidate tumor suppressor genes TEL and KIP1 in childhood acute lymphoblastic leukemia.
Cancer research 1996;56(6):1413-7.
1996: Seriu T; Erz D; Bartram C R
Germline configuration of the p27(Kip1) gene in childhood acute lymphoblastic leukemia (ALL).
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(2):345.
1996: Kawamata N; Seriu T; Koeffler H P; Bartram C R
Molecular analysis of the cyclin-dependent kinase inhibitor family: p16(CDKN2/MTS1/INK4A), p18(INK4C) and p27(Kip1) genes in neuroblastomas.
Cancer 1996;77(3):570-5.
1996: Schwarz K; Bartram C R
V(D)J recombination pathology.
Advances in immunology 1996;61():285-326.
1995: Takeuchi S; Bartram C R; Wada M; Reiter A; Hatta Y; Seriu T; Lee E; Miller C W; Miyoshi I; Koeffler H P
Allelotype analysis of childhood acute lymphoblastic leukemia.
Cancer research 1995;55(22):5377-82.
1995: Raghavachar A; Janssen J W; Schrezenmeier H; Wagner B; Bartram C R; Schulz A S; Hein C; Cowling G; Mubarik A; Testa N G; Dexter T M; Hows J M; Marsh J C
Clonal hematopoiesis as defined by polymorphic X-linked loci occurs infrequently in aplastic anemia.
Blood 1995;86(8):2938-47.
1995: Mahotka C; Hansen-Hagge T E; Bartram C R
Alternative splicing of T cell receptor (TCR) alpha chain transcripts containing V alpha 1 or V alpha 14 elements.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(10):1700-3.
1995: Takeuchi S; Bartram C R; Seriu T; Miller C W; Tobler A; Janssen J W; Reiter A; Ludwig W D; Zimmermann M; Schwaller J
Analysis of a family of cyclin-dependent kinase inhibitors: p15/MTS2/INK4B, p16/MTS1/INK4A, and p18 genes in acute lymphoblastic leukemia of childhood.
Blood 1995;86(2):755-60.
1995: Janssen J W; Ridge S A; Papadopoulos P; Cotter F; Ludwig W D; Fonatsch C; Rieder H; Ostertag W; Bartram C R; Wiedemann L M
The fusion of TEL and ABL in human acute lymphoblastic leukaemia is a rare event.
British journal of haematology 1995;90(1):222-4.
1995: Ludwig L; Janssen J W; Bartram C R
Exon trap analysis of a NF1 splice-site mutation in a chronic myelomonocytic leukemia patient.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(5):922-4.
1995: Hansen-Hagge T E; Mahotka C; Panzer-Grümayer R E; Reuter H J; Schwarz K; van Dongen J J; Bartram C R
Alternative splicing restricts translation of rearrangements at the T-cell receptor delta/alpha locus.
Blood 1995;85(7):1888-96.
1995: Seriu T; Hansen-Hagge T E; Erz D H; Bartram C R
Improved detection of minimal residual leukemia through modifications of polymerase chain reaction analyses based on clonospecific T cell receptor junctions.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(2):316-20.
1994: Whitlock J A; Raimondi S C; Harbott J; Morris S W; McCurley T L; Hansen-Hagge T E; Ludwig W D; Weimann G; Bartram C R
t(5;14)(q33-34;q11), a new recurring cytogenetic abnormality in childhood acute leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1994;8(9):1539-43.
1994: Schwarz K; Hameister H; Gessler M; Grzeschik K H; Hansen-Hagge T E; Bartram C R
Confirmation of the localization of the human recombination activating gene 1 (RAG1) to chromosome 11p13.
Human genetics 1994;93(2):215-7.
1993: Wada M; Bartram C R; Nakamura H; Hachiya M; Chen D L; Borenstein J; Miller C W; Ludwig L; Hansen-Hagge T E; Ludwig W D
Analysis of p53 mutations in a large series of lymphoid hematologic malignancies of childhood.
Blood 1993;82(10):3163-9.
1993: Janssen J W; Ludwig W D; Sterry W; Bartram C R
SIL-TAL1 deletion in T-cell acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1993;7(8):1204-10.
1993: Ludwig L; Janssen J W; Schulz A S; Bartram C R
Mutations within the FLR exon of NF1 are rare in myelodysplastic syndromes and acute myelocytic leukemias.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1993;7(7):1058-60.
1993: Arnold R; Janssen J W; Heinze B; Bunjes D; Hertenstein B; Wiesneth M; Kubanek B; Heimpel H; Bartram C R
Influence of graft-versus-host disease on the eradication of minimal residual leukemia detected by polymerase chain reaction in chronic myeloid leukemia patients after bone marrow transplantation.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1993;7(5):747-51.
1993: Linz U; Schleithoff L; Janssen J W; Bartram C R; Müller C R
A PvuII-polymorphism within the AXL gene on chromosome 19q13.1.
Human molecular genetics 1993;2(4):492.
1993: Schulz A S; Schleithoff L; Faust M; Bartram C R; Janssen J W
The genomic structure of the human UFO receptor.
Oncogene 1993;8(2):509-13.
1993: Ludwig W D; Harbott J; Bartram C R; Komischke B; Sperling C; Teichmann J V; Seibt-Jung H; Notter M; Odenwald E; Nehmer A
Incidence and prognostic significance of immunophenotypic subgroups in childhood acute lymphoblastic leukemia: experience of the BFM study 86.
Recent results in cancer research. Fortschritte der Krebsforschung. Progrès dans les recherches sur le cancer 1993;131():269-82.
1993: Bartram C R
Molecular genetic techniques for detection of minimal residual disease in acute lymphoblastic leukemia: possibilities and limitations.
Recent results in cancer research. Fortschritte der Krebsforschung. Progrès dans les recherches sur le cancer 1993;131():149-55.
1993: Schwarz K; Hansen-Hagge T E; Bartram C R
Recombinase deficiency in mouse and man.
Immunodeficiency 1993;4(1-4):249-52.
1992: Ludwig L; Schulz A S; Janssen J W; Grünewald K; Bartram C R
P53 mutations in myelodysplastic syndromes.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1992;6(12):1302-4.
1992: Hansen-Hagge T E; Yokota S; Reuter H J; Schwarz K; Bartram C R
Human common acute lymphoblastic leukemia-derived cell lines are competent to recombine their T-cell receptor delta/alpha regions along a hierarchically ordered pathway.
Blood 1992;80(9):2353-62.
1992: Lindner M; Wolf A; Moh B; Steinbach P; Kleihauer E; Bartram C R; Kulozik A E
The spectrum of CFTR mutations in south-west German cystic fibrosis patients.
Human genetics 1992;90(3):267-9.
1992: Faust M; Ebensperger C; Schulz A S; Schleithoff L; Hameister H; Bartram C R; Janssen J W
The murine ufo receptor: molecular cloning, chromosomal localization and in situ expression analysis.
Oncogene 1992;7(7):1287-93.
1992: Bartram C R
Molecular genetic aspects of myelodysplastic syndromes.
Hematology/oncology clinics of North America 1992;6(3):557-70.
1992: Soekarman D; von Lindern M; van der Plas D C; Selleri L; Bartram C R; Martiat P; Culligan D; Padua R A; Hasper-Voogt K P; Hagemeijer A
Dek-can rearrangement in translocation (6;9)(p23;q34).
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1992;6(6):489-94.
1992: Janssen J W; Fonatsch C; Ludwig W D; Rieder H; Maurer J; Bartram C R
Polymerase chain reaction analysis of BCR-ABL sequences in adult Philadelphia chromosome-negative acute lymphoblastic leukemia patients.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1992;6(5):463-4.
1991: Schwarz K; Hansen-Hagge T E; Knobloch C; Friedrich W; Kleihauer E; Bartram C R
Severe combined immunodeficiency (SCID) in man: B cell-negative (B-) SCID patients exhibit an irregular recombination pattern at the JH locus.
The Journal of experimental medicine 1991;174(5):1039-48.
1991: Janssen J W; Schulz A S; Steenvoorden A C; Schmidberger M; Strehl S; Ambros P F; Bartram C R
A novel putative tyrosine kinase receptor with oncogenic potential.
Oncogene 1991;6(11):2113-20.
1991: Wahn V; Yokota S; Meyer K L; Janssen J W; Hansen-Hagge T E; Knobloch C; Koletzko S; Stein H; Friedrich W; Bartram C R
Expansion of a maternally derived monoclonal T cell population with CD3+/CD8+/T cell receptor-gamma/delta+ phenotype in a child with severe combined immunodeficiency.
Journal of immunology (Baltimore, Md. : 1950) 1991;147(9):2934-41.
1991: Kulozik A E; Bail S; Bellan-Koch A; Bartram C R; Kohne E; Kleihauer E
The proximal element of the beta globin locus control region is not functionally required in vivo.
The Journal of clinical investigation 1991;87(6):2142-6.
1991: Heil G; Gunsilius E; Raghavachar A; Bartram C R; Ganser A; Kurrle E; Aydemir U; Löffler H; Hoelzer D; Thiel E
Ultrastructural demonstration of peroxidase expression in acute unclassified leukemias: correlation to immunophenotype and treatment outcome.
Blood 1991;77(6):1305-12.
1991: Yokota S; Hansen-Hagge T E; Bartram C R
T-cell receptor delta gene recombination in common acute lymphoblastic leukemia: preferential usage of V delta 2 and frequent involvement of the J alpha cluster.
Blood 1991;77(1):141-8.
1991: Yokota S; Hansen-Hagge T E; Ludwig W D; Reiter A; Raghavachar A; Kleihauer E; Bartram C R
Use of polymerase chain reactions to monitor minimal residual disease in acute lymphoblastic leukemia patients.
Blood 1991;77(2):331-9.
1990: Bartram C R; Yokota S; Hansen-Hagge T E; Janssen J W
Detection of minimal residual leukemia by polymerase chain reactions.
Bone marrow transplantation 1990;6 Suppl 1():4-8.
1990: Janssen J W; Anger B R; Drexler H G; Bartram C R; Heimpel H
Essential thrombocythemia in two sisters originating from different stem cell levels.
Blood 1990;75(8):1633-6.
1990: Anger B; Janssen J W; Schrezenmeier H; Hehlmann R; Heimpel H; Bartram C R
Clonal analysis of chronic myeloproliferative disorders using X-linked DNA polymorphisms.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1990;4(4):258-61.
1990: Janssen O; Heinze B; Bartram C R; Pawlita M; Binder T; Heimpel H; Diehl K; Kabelitz D
Establishment and characterization of a new Epstein-Barr virus transformed cell line from a human B cell lymphoma.
Blut 1990;60(3):206-12.
1990: Ludwig W D; Thiel E; Köller U; Bartram C R; Harbott J; Teichmann J V; Seibt-Jung H; Creutzig U; Ritter J; Riehm H
Incidence and clinical implications of acute hybrid leukemia in childhood.
Haematology and blood transfusion 1990;33():516-22.
1990: Ludwig W D; Thiel E; Bartram C R; Kranz B R; Raghavachar A; Löffler H; Ganser A; Büchner T; Hiddemann W; Heil G
Clinical importance of T-ALL subclassification according to thymic or prethymic maturation stage.
Haematology and blood transfusion 1990;33():419-27.
1990: Bartram C R; Janssen J W
Clonal analysis of human leukemias by molecular genetic approaches.
Haematology and blood transfusion 1990;33():17-22.
1989: Köller U; Haas O A; Ludwig W D; Bartram C R; Harbott J; Panzer-Grümayer R; Hansen-Hagge T; Ritter J; Creutzig U; Knapp W
Phenotypic and genotypic heterogeneity in infant acute leukemia. II. Acute nonlymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(10):708-14.
1989: Hansen-Hagge T E; Yokota S; Bartram C R
Detection of minimal residual disease in acute lymphoblastic leukemia by in vitro amplification of rearranged T-cell receptor delta chain sequences.
Blood 1989;74(5):1762-7.
1989: Arnold R; Bartram C R; Heinze B; Carbonell F; Wiesneth M; Hertenstein B; Schmeiser T; Heit W; Kubanek B; Heimpel H
Evaluation of remission state in chronic myeloid leukemia patients after bone marrow transplantation using cytogenetic and molecular genetic approaches.
Bone marrow transplantation 1989;4(4):389-92.
1989: Ludwig W D; Bartram C R; Harbott J; Köller U; Haas O A; Hansen-Hagge T; Heil G; Seibt-Jung H; Teichmann J V; Ritter J
Phenotypic and genotypic heterogeneity in infant acute leukemia. I. Acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(6):431-9.
1989: Grünewald K; Lyons J; Fröhlich A; Feichtinger H; Weger R A; Schwab G; Janssen J W; Bartram C R
High frequency of Ki-ras codon 12 mutations in pancreatic adenocarcinomas.
International journal of cancer. Journal international du cancer 1989;43(6):1037-41.
1989: Raghavachar A; Thiel E; Hansen-Hagge T E; Kranz B; Bartram C R
Rearrangement of T cell receptor beta, gamma, and delta gene loci in human pre-T cell acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(6):413-8.
1989: Bartram C R; Ludwig W D; Hiddemann W; Lyons J; Buschle M; Ritter J; Harbott J; Fröhlich A; Janssen J W
Acute myeloid leukemia: analysis of ras gene mutations and clonality defined by polymorphic X-linked loci.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(4):247-56.
1989: Thiel E; Kranz B R; Raghavachar A; Bartram C R; Löffler H; Messerer D; Ganser A; Ludwig W D; Büchner T; Hoelzer D
Prethymic phenotype and genotype of pre-T (CD7+/ER-)-cell leukemia and its clinical significance within adult acute lymphoblastic leukemia.
Blood 1989;73(5):1247-58.
1989: Janssen J W; Bartram C R
Silent mutation at codon 15 interferes with the detection of a mutated N-ras codon 12 allele by oligonucleotide hybridization.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(3):235.
1989: Panzer S; Kiefel V; Bartram C R; Haas O A; Hinterberger W; Mueller-Eckhardt C; Lechner K
Immune thrombocytopenia more than a year after allogeneic marrow transplantation due to antibodies against donor platelets with anti-PlA1 specificity: evidence for a host-derived immune reaction.
British journal of haematology 1989;71(2):259-64.
1989: Janssen J W; Buschle M; Layton M; Lyons J; Bartram C R
ras gene mutations and clonal analysis using RFLPs of X-chromosome genes in myelodysplastic syndromes.
Haematology and blood transfusion 1989;32():386-9.
1988: Kulozik A E; Lyons J; Kohne E; Bartram C R; Kleihauer E
Rapid and non-radioactive prenatal diagnosis of beta thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR).
British journal of haematology 1988;70(4):455-8.
1988: Buschle M; Janssen J W; Drexler H; Lyons J; Anger B; Bartram C R
Evidence for pluripotent stem cell origin of idiopathic myelofibrosis: clonal analysis of a case characterized by a N-ras gene mutation.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(10):658-60.
1988: Raghavachar A; Binder T; Bartram C R
Immunoglobulin and T-cell receptor gene rearrangements in Hodgkin's disease.
Cancer research 1988;48(13):3591-4.
1988: Raghavachar A; Ludwig W D; Bartram C R
Clonal variation in childhood acute lymphoblastic leukaemia at early and late relapse detected by analyses of phenotype and genotype.
European journal of pediatrics 1988;147(5):503-7.
1988: Ludwig W D; Bartram C R; Ritter J; Raghavachar A; Hiddemann W; Heil G; Harbott J; Seibt-Jung H; Teichmann J V; Riehm H
Ambiguous phenotypes and genotypes in 16 children with acute leukemia as characterized by multiparameter analysis.
Blood 1988;71(6):1518-28.
1988: Steenvoorden A C; Janssen J W; Drexler H G; Lyons J; Tesch H; Binder T; Jones D B; Bartram C R
Ras mutations in Hodgkin's disease.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(5):325-6.
1988: Janssen J W; Steenvoorden A C; Schmidtberger M; Bartram C R
Activation of the mas oncogene during transfection of monoblastic cell line DNA.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(5):318-20.
1988: Valent P; Bartram C R; Radaszkiewicz T; Hinterberger W; Lechner K; Bettelheim P
T cell receptor alpha mRNA transcription in T-lymphoblastic transformation of chronic myelocytic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(3):144-7.
1988: Bartram C R
Rearrangement of the c-abl and bcr genes in Ph-negative CML and Ph-positive acute leukemias.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(1):63-4.
1987: Bartram C R; Bross-Bach U; Schmidt H; Waller H D
Philadelphia-positive chronic myelogenous leukemia with breakpoint 5' of the breakpoint cluster region but within the bcr gene.
Blut 1987;55(6):505-11.
1987: Janssen J W; Steenvoorden A C; Lyons J; Anger B; Böhlke J U; Bos J L; Seliger H; Bartram C R
RAS gene mutations in acute and chronic myelocytic leukemias, chronic myeloproliferative disorders, and myelodysplastic syndromes.
Proceedings of the National Academy of Sciences of the United States of America 1987;84(24):9228-32.
1987: Raghavachar A; Thiel E; Bartram C R
Analyses of phenotype and genotype in acute lymphoblastic leukemias at first presentation and in relapse.
Blood 1987;70(4):1079-83.
1987: Janssen J W; Lyons J; Steenvoorden A C; Seliger H; Bartram C R
Concurrent mutations in two different ras genes in acute myelocytic leukemias.
Nucleic acids research 1987;15(14):5669-80.
1987: Janssen J W; Steenvoorden A C; Losekoot M; Bartram C R
Novel transforming sequences in human acute myelocytic leukemia cell lines.
Oncogene 1987;1(2):175-9.
1987: Porzsolt F; Raghavachar A; Digel W; Raghavachar A; Bartram C R; Heimpel H
Strategy for the treatment of hairy cell leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1987;1(4):334-7.
1987: Bartram C R; Böhlke J V; Adolph S; Hameister H; Ganser A; Anger B; Heisterkamp N; Groffen J
Deletion of c-fms sequences in the 5q- syndrome.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1987;1(2):146-9.
1987: Bartram C R
Rearrangement of bcr and c-abl sequences in Ph-positive acute leukemias and Ph-negative CML--an update.
Haematology and blood transfusion 1987;31():160-2.
1987: Bartram C R; Janssen J W; Becher R
Persistence of CML despite deletion of rearranged bcr/c-abl sequences.
Haematology and blood transfusion 1987;31():145-8.

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