Sutter, Christian Dr. rer. nat.Universität HeidelbergHeidelberg
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Co-Autoren (Uni Heidelberg)
- Marmé, Frederik (7)
- Schott, Sarah (7)
- Bugert, Peter (6)
- Deimling, Andreas von (6)
- Milde, Till (6)
- Chang-Claude, Jenny (6)
- Moog, Ute (6)
- Jones, David T. W. (6)
- Hirsch, Steffen (6)
- Witt, Olaf (6)
- Brenner, Hermann (5)
- Sahm, Felix (5)
- Sturm, Dominik (5)
- Tilburg, Cornelis M. van (5)
- Yang, Rongxi (5)
- Pajtler, Kristian Wilfried (4)
- Grund, Kerstin (4)
- Surowy, Harald (4)
- Arndt, Volker (4)
- Cuk, Katarina (4)
- Kloor, Matthias (4)
- Golatta, Michael (4)
- Heil, Jörg (4)
- Evers, Christina (4)
- Sill, Martin (3)
- Knebel Doeberitz, Magnus von (3)
- Janssen, Johannes W. G. (3)
- Rudolph, Anja (3)
- Gebert, Johannes (3)
- Selt, Florian (3)
- Maas, Bianca (3)
- Jones, Barbara Christine (3)
- Ecker, Jonas (3)
- (weitere Einträge vorhanden...)
Co-Autoren (extern)
- Hauke, Jan (3)
- Hahnen, Eric (3)
- Gehrig, Andrea (3)
- Niehues, Tim (2)
- Korshunov, Andrey (2)
- Kuchenbaecker, Karoline (2)
- Silvestri, Valentina (2)
- Blein, Sophie (2)
- Peterlongo, Paolo (2)
- Rebbeck, Timothy (2)
- Faust, Ulrike (2)
- Kast, Karin (2)
- Borde, Julika (2)
- Hentschel, Julia (2)
- Schwab, Matthias (1)
- Hein, Rebecca (1)
- Schweinitz, Dietrich von (1)
- Cook, Margaret (1)
- Schroeder, Christopher (1)
- Schramm, Kathrin (1)
- Seitz, Stephan (1)
- Seibold, Petra Beate (1)
- Milne, Roger L. (1)
- Schneider, Dominik T. (1)
- Schmid, Irene (1)
- Nickels, Stefan (1)
- Bojesen, Stig Egil (1)
- D'Amato, Mauro (1)
- Wörner, Stefan M. (1)
- Maxwell, Chris (1)
- Busch, Elena (1)
- Osorio, Ana (1)
- Benner, Axel (1)
- (weitere Einträge vorhanden...)
Publikationen in heiBIB
- Ahmad, Olfat: BRCA1/2 potential founder variants in the Jordanian population : an opportunity for a customized screening panel / Olfat Ahmad, Christian Sutter, Steffen Hirsch, Stefan M. Pfister and Christian P. Schaaf, 2023. - 9 S. : Illustrationen
In: Hereditary cancer in clinical practice, ISSN 1897-4287. 21(2023), Artikel-ID 11, Seite 1-9
DOI: 10.1186/s13053-023-00256-2
- Ecker, Jonas: Corrigendum to ‘Molecular diagnostics enables detection of actionable targets: the Pediatric Targeted Therapy 2.0 registry’ [Eur J Cancer 180 (2023) 71-84] / Jonas Ecker, Florian Selt, Dominik Sturm, Martin Sill, Andrey Korshunov, Steffen Hirsch, David Cappe… , May 2023. - 2 S.
In: European journal of cancer, ISSN 1879-0852. 184(2023) vom: Mai, Seite 200-201
DOI: 10.1016/j.ejca.2023.02.024
- Ecker, Jonas: Molecular diagnostics enables detection of actionable targets : the Pediatric Targeted Therapy 2.0 registry / Jonas Ecker, Florian Selt, Dominik Sturm, Martin Sill, Andrey Korshunov, Steffen Hirsch, David Cappe… , February 2023. - 14 S. : Illustrationen
In: European journal of cancer, ISSN 1879-0852. 180(2023) vom: Feb., Seite 71-84
DOI: 10.1016/j.ejca.2022.11.015
- Sturm, Dominik: Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology / Dominik Sturm, David Capper, Felipe Andreiuolo, Marco Gessi, Christian Kölsche, Annekathrin Reinhard… , 16 March 2023. - 10 S.
In: Nature medicine, ISSN 1546-170X. 29(2023), 4, Seite 917-926
DOI: 10.1038/s41591-023-02255-1
- Barnes, Daniel R.: Breast and prostate cancer risks for male BRCA1 and BRCA2 pathogenic variant carriers using polygenic risk scores / Daniel R. Barnes, PhD, Ute Hamann, PhD, PhD, on behalf of the Consortium of Investigators of Modifie… , 2022. - 14 S.
In: Journal of the National Cancer Institute, ISSN 1460-2105. 114(2022), 1 vom: Jan., Seite 109-122
DOI: 10.1093/jnci/djab147
- Li, Shuai: Cancer risks associated with BRCA1 and BRCA2 pathogenic variants / Shuai Li, MD, PhD; Valentina Silvestri, PhD; Goska Leslie, MEng; Timothy R. Rebbeck, PhD; Susan L. N… , January 25, 2022. - 14 S.
In: Journal of clinical oncology, ISSN 1527-7755. 40(2022), 14, Seite 1529-1541
DOI: 10.1200/JCO.21.02112
- Dumont, Martine: Uncovering the contribution of moderate-penetrance susceptibility genes to breast cancer by whole-exome sequencing and targeted enrichment sequencing of candidate genes in women of european ancestry / Martine Dumont, Nana Weber-Lassalle, Charles Joly-Beauparlant, Corinna Ernst, Arnaud Droit, Bing-Jia… , 11 July 2022. - 23 S.
In: Cancers, ISSN 2072-6694. 14(2022), 14, Artikel-ID 3363, Seite 1-23
DOI: 10.3390/cancers14143363
- Borde, Julika: Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers / Julika Borde, Yael Laitman, Britta Blümcke, Dieter Niederacher, Konstantin Weber-Lassalle, Christian… , 27 June 2022. - 9 S.
In: BMC cancer, ISSN 1471-2407. 22(2022), Artikel-ID 706, Seite 1-9
DOI: 10.1186/s12885-022-09780-1
- Rolfes, Muriel: Prevalence of cancer predisposition germline variants in male breast cancer patients : results of the German Consortium for Hereditary Breast and Ovarian Cancer / Muriel Rolfes, Julika Borde, Kathrin Möllenhoff, Mohamad Kayali, Corinna Ernst, Andrea Gehrig, Chris… , 5 July 2022. - 13 S.
In: Cancers, ISSN 2072-6694. 14(2022), 13, Artikel-ID 3292, Seite 1-13
DOI: 10.3390/cancers14133292
- Rempel, Eugen: Pan-cancer analysis of genomic scar patterns caused by homologous repair deficiency (HRD) / E. Rempel, K. Kluck, S. Beck, I. Ourailidis, D. Kazdal, O. Neumann, A.L. Volckmar, M. Kirchner, H. G… , 09 June 2022. - 13 S.
In: npj precision oncology, ISSN 2397-768X. 6(2022), Artikel-ID 36, Seite 1-13
DOI: 10.1038/s41698-022-00276-6
- Rippinger, Nathalie: Breast cancer characteristics and surgery among women with Li-Fraumeni syndrome in Germany : a retrospective cohort study / Nathalie Rippinger, Christine Fischer, Hans-Peter Sinn, Nicola Dikow, Christian Sutter, Kerstin Rhie… , 2021. - 12 S.
In: Cancer medicine, ISSN 2045-7634. 10(2021), 21, Seite 7747-7758
DOI: 10.1002/cam4.4300
- Borde, Julika: Performance of breast cancer polygenic risk scores in 760 female CHEK2 germline mutation carrier / Julika Borde, MSc, Corinna Ernst, MSc, Barbara Wappenschmidt, PhD, Dieter Niederacher, PhD, Konstant… , 2021. - 7 S.
In: Journal of the National Cancer Institute, ISSN 1460-2105. 113(2021), 7 vom: Juli, Seite 893-899
DOI: 10.1093/jnci/djaa203
- Hirsch, Steffen: Germline testing for homologous recombination repair genes : opportunities and challenges / Steffen Hirsch, Laura Gieldon, Christian Sutter, Nicola Dikow, Christian P. Schaaf, 2021. - 12 S.
In: Genes, chromosomes & cancer, ISSN 1098-2264. 60(2021), 5, Seite 332-343
DOI: 10.1002/gcc.22900
- Tilburg, Cornelis M. van: The pediatric precision oncology INFORM registry : clinical outcome and benefit for patients with very high-evidence targets / Cornelis M. van Tilburg, Elke Pfaff, Kristian W. Pajtler, Karin P. S. Langenberg, Petra Fiesel, Barb… , August 9, 2021. - 16 S.
In: Cancer discovery, ISSN 2159-8290. 11(2021), 11, Seite 2764-2779
DOI: 10.1158/2159-8290.CD-21-0094
- Rippinger, Nathalie: Cancer surveillance and distress among adult pathogenic TP53 germline variant carriers in Germany : a multicenter feasibility and acceptance survey / Nathalie Rippinger, Christine Fischer, Markus W. Haun, Kerstin Rhiem, Sabine Grill, Marion Kiechle, … , September 1, 2020. - 10 S.
In: Cancer, ISSN 1097-0142. 126(2020), 17 vom: 1. Sept., Seite 4032-4041
DOI: 10.1002/cncr.33004
- Wappenschmidt, Barbara: Criteria of the German konsortium for hereditary breast and ovarian cancer for the classification of germline sequence variants in risk Genes for hereditary breast and ovarian cancer / Barbara Wappenschmidt, Jan Hauke, Ulrike Faust, Dieter Niederacher, Lisa Wiesmüller, Gunnar Schmidt,… , 21. April 2020. - 20 S.
In: Geburtshilfe und Frauenheilkunde, ISSN 1438-8804. 80(2020), 04, Seite 410-429
DOI: 10.1055/a-1110-0909
- Patel, Vivek L.: Association of genomic domains in BRCA1 and BRCA2 with prostate cancer risk and aggressiveness / Vivek L. Patel, Ute Hamann, Christian Sutter [und viele weitere], 2020. - 16 S.
In: Cancer research, ISSN 1538-7445. 80(2020), 3, Seite 624-638
DOI: 10.1158/0008-5472.CAN-19-1840
- Parsons, Michael T.: Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants : an ENIGMA resource to support clinical variant classification / Michael T. Parsons, Emma Tudini, Hongyan Li, Eric Hahnen, Barbara Wappenschmidt, Lidia Feliubadaló, … , 27 May 2019. - 22 S.
In: Human mutation, ISSN 1098-1004. 40(2019), 9, Seite 1557-1578
DOI: 10.1002/humu.23818
- Sepahi, Ilnaz: Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women / Ilnaz Sepahi, Ulrike Faust, Marc Sturm, Kristin Bosse, Martin Kehrer, Tilman Heinrich, Kathrin Grund… . -
London: BioMed Central ; Springer, 2019. - 1 Online-Ressource
DOI: 10.1186/s12885-019-5946-0
- Böck, Julia: Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation-negative early-onset and high-risk breast cancer patients / Julia Böck, Silke Appenzeller, Larissa Haertle, Tamara Schneider, Andrea Gehrig, Jörg Schröder, Simo… , 16 April 2018. - 10 S.
In: International journal of cancer, ISSN 1097-0215. 143(2018), 6, Seite 1416-1425
DOI: 10.1002/ijc.31526
- Bächli, Heidi: Molecular diagnostics in pediatric brain tumors : impact on diagnosis and clinical decision-making - a selected case series / Heidi Bächli, Jonas Ecker, Cornelis van Tilburg, Dominik Sturm, Florian Selt, Felix Sahm, Christian … , 11. Juli 2018. - 9 S.
In: Klinische Pädiatrie, ISSN 1439-3824. 230(2018), 06, Seite 305-313
DOI: 10.1055/a-0637-9653
- Qian, Frank: Height and body mass index as modifiers of breast cancer risk in BRCA1/2 mutation carriers : a mendelian randomization study / Frank Qian, Shengfeng Wang, Jonathan Mitchell, Lesley McGuffog, Daniel Barrowdale, Goska Leslie, Jan… , 2019. - 15 S.
In: Journal of the National Cancer Institute, ISSN 1460-2105. 111(2019), 4, Seite 350-364
DOI: 10.1093/jnci/djy132
- Hauke, Jan: Gene panel testing of 5589 BRCA1/2-negative index patients with breast cancer in a routine diagnostic setting : results of the German Consortium for Hereditary Breast and Ovarian Cancer / Jan Hauke, Judit Horvath, Eva Groß, Andrea Gehrig, Ellen Honisch, Karl Hackmann, Gunnar Schmidt, Nor… , 09 March 2018. - 10 S.
In: Cancer medicine, ISSN 2045-7634. 7(2018), 4, Seite 1349-1358
DOI: 10.1002/cam4.1376
- Klaschik, Kristina: The GPRC5A frameshift variant c.183del is not associated with increased breast cancer risk in BRCA1 mutation carriers / Kristina Klaschik, Jan Hauke, Guido Neidhardt, Christian Tränkle, Harald M. Surowy, Stefanie Heilman… , 2019. - 4 S.
In: International journal of cancer, ISSN 1097-0215. 144(2019), 7, Seite 1761-1763
DOI: 10.1002/ijc.32016
- Rebbeck, Timothy: Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations / Timothy R. Rebbeck, Tara M. Friebel, Eitan Friedman, Ute Hamann, Dezheng Huo, Ava Kwong, Edith Olah,… , 15 February 2018. - 28 S.
In: Human mutation, ISSN 1098-1004. 39(2018), 5, Seite 593-620
DOI: 10.1002/humu.23406
- Waszak, Sebastian Martin: Spectrum and prevalence of genetic predisposition in medulloblastoma : a retrospective genetic study and prospective validation in a clinical trial cohort / Sebastian M. Waszak, Paul A. Northcott, Ivo Buchhalter, Giles W. Robinson, Christian Sutter, Susanne… , 2018. - 14 S.
In: The lancet, ISSN 1474-5488. 19(2018), 6, Seite 785-798
DOI: 10.1016/S1470-2045(18)30242-0
- Yang, Rongxi: The association between breast cancer and S100P methylation in peripheral blood by multicenter case-control studies / Rongxi Yang, Sarah Stöcker, Sarah Schott, Jörg Heil, Frederik Marme, Katarina Cuk, Bowang Chen, Mich… , 2017. - 9 S.
In: Carcinogenesis, ISSN 1460-2180. 38(2017), 3, Seite 312-320
DOI: 10.1093/carcin/bgx004
- Busch, Elena: Successful immune checkpoint blockade in a patient with advanced stage microsatellite-unstable biliary tract cancer / Elena Czink, Matthias Kloor, Benjamin Goeppert, Stefan Fröhling, Sebastian Uhrig, Tim F. Weber, Jörn… , June 15, 2017. - 12 S.
In: Cold Spring Harbor molecular case studies, ISSN 2373-2873. 3(2017,5) Artikel-Nummer a001974, 12 Seiten
DOI: 10.1101/mcs.a001974
- Lecarpentier, Julie: Prediction of breast and prostate cancer risks in Male BRCA1and BRCA2 mutation carriers using polygenic risk scores / Julie Lecarpentier, Christian Sutter [und weitere]. - 17 S.
In: Journal of clinical oncology, ISSN 1527-7755. 35(2017), 20, S. 2240-2250
DOI: 10.1200/JCO.2016.69.4935
- Milne, Roger L.: Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer / Roger L Milne, Karoline B Kuchenbaecker, Kyriaki Michailidou, Jonathan Beesley, Siddhartha Kar, Sara… , 23 October 2017. - 12 S.
In: Nature genetics, ISSN 1546-1718. 49(2017), 12, Seite 1767-1778
DOI: 10.1038/ng.3785
- Silvestri, Valentina: Male breast cancer in BRCA1 and BRCA2 mutation carriers : pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 / Valentina Silvestri, Daniel Barrowdale, Anna Marie Mulligan, Susan L. Neuhausen, Stephen Fox, Beth Y… , 09 February 2016. - 13 S.
In: Breast cancer research, ISSN 1465-542X. 18(2016), Artikel-Nummer 15, 13 Seiten
DOI: 10.1186/s13058-016-0671-y
- Schäfer, Matthias: Neonatal Gardner fibroma leads to detection of familial adenomatous polyposis : two case reports / Mattias Schäfer, Martina Kadmon, Wolfgang Schmidt, Irmgard Treiber, Ute Moog, Christian Sutter, Maxi… , 2016. - 5 S.
In: European journal of pediatric surgery reports, ISSN 2194-7627. 4(2016), 1, Seite 17-21
DOI: 10.1055/s-0036-1582443
- Vigorito, Elena: Fine-scale mapping at 9p22.2 identifies candidate causal variants that modify ovarian cancer risk in BRCA1 and BRCA2 mutation carriers / Elena Vigorito, Karoline B. Kuchenbaecker, Jonathan Beesley, Julian Adlard, Bjarni A. Agnarsson, Ire…
In: PLOS ONE, ISSN 1932-6203. 11(2016,7) Artikel-Nummer e0158801, 19 Seiten
DOI: 10.1371/journal.pone.0158801
- Göhringer, Caroline: Double germline mutations in APC and BRCA2 in an individual with a pancreatic tumor / Caroline Goehringer, Christian Sutter, Matthias Kloor, Johannes Gebert, Emily P. Slater, Monika Kell… . - 7 S.
In: Familial cancer, ISSN 1573-7292. 16(2017), 2, S. 303-309
DOI: 10.1007/s10689-016-9952-y
- Sutter, Christian: Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression : identification of a modifier of breast cancer risk at locus 11q22.3 / Yosr Hamdi, Penny Soucy, Karoline B. Kuchenbaeker, Tomi Pastinen, Arnaud Droit, Audrey Lemaçon, Juli… . - 18 S.
In: Breast cancer research and treatment, ISSN 1573-7217. 161(2017), 1, S. 117-134
DOI: 10.1007/s10549-016-4018-2
- Jones, Barbara Christine: Next-generation personalised medicine for high-risk paediatric cancer patients - The INFORM pilot study / Barbara C. Worst, Cornelis M. van Tilburg, Gnana Prakash Balasubramanian, Petra Fiesel, Ruth Witt, A… , 29 July 2016. - 11 S.
In: European journal of cancer, ISSN 1879-0852. 65(2016), Seite 91-101
DOI: 10.1016/j.ejca.2016.06.009
- Tang, Qiuqiong: DNA methylation array analysis identifies breast cancer associated RPTOR , MGRN1 and RAPSN hypomethylation in peripheral blood DNA / Qiuqiong Tang, Tim Holland-Letz, Alla Slynko, Katarina Cuk, Frederik Marme, Sarah Schott, Jörg Heil,… , 26 August 2016. - 12 S.
In: OncoTarget, ISSN 1949-2553. 7(2016), 39, Seite 64191-64202
DOI: 10.18632/oncotarget.11640
- Lawrenson, Kate: Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus / Kate Lawrenson, Siddhartha Kar, Karen McCue, Karoline Kuchenbaeker, Kyriaki Michailidou, Jonathan Ty… , September 07, 2016. - 22 S.
In: Nature Communications, ISSN 2041-1723. 7(2016) Artikel-Nr. 12675, 22 S.
DOI: 10.1038/ncomms12675
- Antoniou, Antonis C.: Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers / Antonis C. Antoniou, Karoline B. Kuchenbaecker, Penny Soucy, Jonathan Beesley, Xiaoqing Chen, Lesley… . -
London: BioMed Central, 20 February 2012. - 1 Online-Ressource (18 Seiten)
DOI: 10.1186/bcr3121
- Silvestri, Valentina: Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 / Valentina Silvestri, Daniel Barrowdale, Anna Marie Mulligan, Susan L. Neuhausen, Stephen Fox, Beth Y… . -
London: BioMed Central, 2016. - 1 Online-Ressource (13 Seiten)
- Peterlongo, Paolo: Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers / Paolo Peterlongo, Jenny Chang-Claude, Anja Rudolph, Ute Hamann, Stefan Wilkening, Bowang Chen, Sutte… , 2015. - 9 S.
In: Cancer epidemiology, biomarkers & prevention, ISSN 1538-7755. 24(2015), 1, Seite 308-316
DOI: 10.1158/1055-9965.EPI-14-0532
- Rebbeck, Timothy: Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer / Timothy R. Rebbeck, Ute H amann, Christian Sutter, C.R. Bartram, Nicola Dikow [und 253 weitere], April 7, 2015. - 15 S.
In: The journal of the American Medical Association, ISSN 1538-3598. 313(2015), 13, Seite 1347-1361
DOI: 10.1001/jama.2014.5985
- Mavaddat, Nasim: Prediction of breast cancer risk based on profiling with common genetic variants / Nasim Mavaddat, Jenny Chang-Claude, Anja Rudolph, Petra Seibold, Barbara Burwinkel, Frederik Marme, … , April 2, 2015
In: Journal of the National Cancer Institute, ISSN 1460-2105. 107(2015,5) Artikel-Nummer djv036, 15 Seiten
DOI: 10.1093/jnci/djv036
- Blanco, Ignacio: Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers / Ignacio Blanco, Karoline Kuchenbaecker, Daniel Cuadras, Xianshu Wang, Daniel Barrowdale, Gorka Ruiz …
In: PLOS ONE, ISSN 1932-6203. 10(2015,4) Artikel-Nummer e0120020, 18 Seiten
DOI: 10.1371/journal.pone.0120020
- Blein, Sophie: An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers / Sophie Blein, Claire Bardel, Vincent Danjean, Lesley McGuffog, Sue Healey, Daniel Barrowdale, Andrew…
In: Breast cancer research, ISSN 1465-542X. 17(2015) Artikel-Nummer 61, 15 Seiten
DOI: 10.1186/s13058-015-0567-2
- Kuchenbaecker, Karoline: Identification of six new susceptibility loci for invasive epithelial ovarian cancer / Karoline B. Kuchenbaecker, Susan J. Ramus, Jonathan Tyrer, Andrew Lee, Howard C. Shen, Jonathan Bees… . - 8 S.
In: Nature genetics, ISSN 1546-1718. 47(2015), 2, S. 164-171
DOI: 10.1038/ng.3185
- Peterlongo, Paolo: FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity, and is a familial breast cancer risk factor / Paolo Peterlongo, Irene Catucci, Mara Colombo, Laura Caleca, Eliseos Mucaki, Massimo Bogliolo, Maria… . - 39 S.
In: Human molecular genetics, ISSN 1460-2083. 24(2015), 18, S. 5345-5383
DOI: 10.1093/hmg/ddv251
- Blein, Sophie: An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers / Sophie Blein, Claire Bardel, Vincent Danjean, Lesley McGuffog, Sue Healey, Daniel Barrowdale, Andrew… . -
London: BioMed Central, 2016. - 1 Online-Ressource (15 Seiten)
DOI: 10.1186/s13058-015-0567-2
- Yang, Rongxi: DNA methylation array analyses identified breast cancer-associated HYAL2 methylation in peripheral blood / Rongxi Yang, Katrin Pfütze, Manuela Zucknick, Christian Sutter, Barbara Wappenschmidt, Frederik Marm… , 2015. - 11 S.
In: International journal of cancer, ISSN 1097-0215. 136(2015), 8, Seite 1845-1855
DOI: 10.1002/ijc.29205
- Kaiser, Ann-Sophie: Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontia / Ann-Sophie Kaiser, Bianca Maas, Anna Wolff, Christian Sutter, Johannes WG Janssen, Katrin Hinderhofe… , 2015. - 4 S.
In: European journal of human genetics, ISSN 1476-5438. 23(2015), 5, Seite 704-707
DOI: 10.1038/ejhg.2014.163
- Spurdle, Amanda B.: Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia / Amanda B. Spurdle, Fergus J. Couch, Michael T. Parsons, Lesley McGuffog, Daniel Barrowdale, Manjeet … . -
London: BioMed Central, 2016. - 1 Online-Ressource (16 Seiten)
DOI: 10.1186/s13058-014-0474-y
- Kuchenbaecker, Karoline: Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers / Karoline B. Kuchenbäcker, Susan L. Neuhausen, Mark Robson, Daniel Barrowdale, Lesley McGuffog, Anna … . -
London: BioMed Central, [2015]. - 1 Online-Ressource (30 Seiten)
- Osorio, Ana: DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers / Ana Osorio, Roger L. Milne, Karoline Kuchenbaecker, Tereza Vaclová, Guillermo Pita, Rosario Alonso, …
In: PLoS Genetics, ISSN 1553-7404. 10(2014,4) Artikel-Nr. e1004256, 12 Seiten
DOI: 10.1371/journal.pgen.1004256
- Surowy, Harald: Clinical and molecular characterization of the BRCA2 p.Asn3124Ile variant reveals substantial evidence for pathogenic significance / Harald Martin Surowy, Christian Sutter, Max Mittnacht, Ruediger Klaes, Dieter Schaefer, Christina Ev… , 2014. - 10 S.
In: Breast cancer research and treatment, ISSN 1573-7217. 145(2014), 2, Seite 451-460
DOI: 10.1007/s10549-014-2943-5
- Evers, Christina: Mosaic deletion of EXOC6B : further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability / Christina Evers, Bianca Maas, Karin A. Koch, Anna Jauch, Johannes W.G. Janssen, Christian Sutter, Mi… . - 7 S.
In: American journal of medical genetics, ISSN 1552-4833. 164(2014), 12, S. 3088-3094
DOI: 10.1002/ajmg.a.36770
- Dikow, Nicola: 3p25.3 Microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behavior / Nicola Dikow, Bianca Maas, Stephanie Karch, Martin Granzow, Johannes W. G. Janssen, Anna Jauch, Katr… . - 8 S.
In: American journal of medical genetics, ISSN 1552-4833. 164(2014), 12, S. 3061-3068
DOI: 10.1002/ajmg.a.36761
- Bojesen, Stig Egil: Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer / Stig E. Bojesen, Jenny Chang-Claude, Barbara Burwinkel, Frederik Marme, Rebecca Hein, Hermann Brenn… , 27 March 2013. - 14 S.
In: Nature genetics, ISSN 1546-1718. 45(2013), 4, Seite 371-384
DOI: 10.1038/ng.2566
- Rath, Michèlle Geneviève: Association of death receptor 4 variant (683A>C) with ovarian cancer risk in BRCA1 mutation carriers / Michelle G. Dick, Beatrix Versmold, Christoph Engel, Alfons Meindl, Norbert Arnold, Raymonda Varon‐M… , 15 March 2012. - 5 S.
In: International journal of cancer, ISSN 1097-0215. 130(2012), 6, Seite 1314-1318
DOI: 10.1002/ijc.26134
- Evers, Christina: Hepatoblastoma in two siblings and familial adenomatous polyposis : causal nexus or coincidence? / Christina Evers, Harald Gaspar, Matthias Kloor, Gergana Bozukova, Martina Kadmon, Monika Keller, Chr… , September 2012. - 5 S.
In: Familial cancer, ISSN 1573-7292. 11(2012), 3, Seite 529-533
DOI: 10.1007/s10689-012-9538-2
- Mavaddat, Nasim: Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers : results from the consortium of investigators of modifiers of BRCA1/2 (CIMBA) / Nasim Mavaddat, Daniel Barrowdale, Irene L. Andrulis, Susan M. Domchek, Diana Eccles, Heli Nevanlinn… , January 2012. - 14 S.
In: Cancer epidemiology, biomarkers & prevention, ISSN 1538-7755. 21(2012), 1, Seite 134-147
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