heiBIB: Hemminki, Kari

Hemminki, Kari Prof. Dr.Universität HeidelbergHeidelberg

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englisch (122)

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Publikationen in heiBIB

Thomsen, Hauke: Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance / Hauke Thomsen, Subhayan Chattopadhyay, Niels Weinhold, Pavel Vodicka, Ludmila Vodickova, Per Hoffman… , 2024. - 12 S. : Illustrationen
In: Blood cancer journal, ISSN 2044-5385. 14(2024), Artikel-ID 140, Seite 1-12
DOI: 10.1038/s41408-024-01121-8
Macauda, Angelica: Identification of novel genetic loci for risk of multiple myeloma by functional annotation / Angelica Macauda, Klara Briem, Alyssa Clay-Gilmour, Wendy Cozen, Asta Försti, Matteo Giaccherini, Ch… , 18 September 2023. - 4 S. : Illustrationen
In: Leukemia, ISSN 1476-5551. 37(2023), 11, Seite 2326-2329
DOI: 10.1038/s41375-023-02022-8
Clavero, Esther: Polymorphisms within autophagy-related genes as susceptibility biomarkers for multiple myeloma : a meta-analysis of three large cohorts and functional characterization / Esther Clavero, José Manuel Sanchez-Maldonado, Angelica Macauda, Rob Ter Horst, Belém Sampaio-Marque… , 2023. - 20 S. : Illustrationen
In: International journal of molecular sciences, ISSN 1422-0067. 24(2023), 10, Artikel-ID 8500, Seite 1-20
DOI: 10.3390/ijms24108500
Krämer, Alwin: Cancer of unknown primary : ESMO clinical practice guideline for diagnosis, treatment and follow-up / A. Krämer, T. Bochtler, C. Pauli, G. Baciarello, S. Delorme, K. Hemminki, L. Mileshkin, H. Moch, K. … , March 2023. - 19 S.
In: Annals of oncology, ISSN 1569-8041. 34(2023), 3 vom: März, Seite 228-246
DOI: 10.1016/j.annonc.2022.11.013
Ajore, Ram: Functional dissection of inherited non-coding variation influencing multiple myeloma risk / Ram Ajore, Abhishek Niroula, Maroulio Pertesi, Caterina Cafaro, Malte Thodberg, Molly Went, Erik L. … , 10 January 2022. - 15 S.
In: Nature Communications, ISSN 2041-1723. 13(2022), Artikel-ID 151, Seite 1-15
DOI: 10.1038/s41467-021-27666-x
Clay-Gilmour, Alyssa: Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6 / Alyssa Clay-Gilmour, Subhayan Chattopadhyay, Michelle A.T. Hildebrandt, Hauke Thomsen, Niels Weinhol… , 13 April 2022. - 5 S.
In: Blood cancer journal, ISSN 2044-5385. 12(2022), 4, Artikel-ID 60, Seite 1-5
DOI: 10.1038/s41408-022-00658-w
Miao, Beiping: Whole-exome sequencing identifies a novel germline variant in PTK7 gene in familial colorectal cancer / Beiping Miao, Diamanto Skopelitou, Aayushi Srivastava, Sara Giangiobbe, Dagmara Dymerska, Nagarajan … , 24 January 2022. - 20 S.
In: International journal of molecular sciences, ISSN 1422-0067. 23(2022), 3, Artikel-ID 1295, Seite 1-20
DOI: 10.3390/ijms23031295
Zhu, Lizhen: Germline variants of CYBA and TRPM4 predispose to familial colorectal cancer / Lizhen Zhu, Beiping Miao, Dagmara Dymerska, Magdalena Kuswik, Elena Bueno-Martínez, Lara Sanoguera-M… , 28 January 2022. - 15 S.
In: Cancers, ISSN 2072-6694. 14(2022), 3, Artikel-ID 670, Seite 1-15
DOI: 10.3390/cancers14030670
Khandanpour, Cyrus: Prevalence of the GFI1-36N SNP in multiple myeloma patients and its impact on the prognosis / Cyrus Khandanpour, Christine Eisfeld, Subbaiah Chary Nimmagadda, Marc S. Raab, Niels Weinhold, Anja … , 25 October 2021. - 8 S.
In: Frontiers in oncology, ISSN 2234-943X. 11(2021) vom: 25. Okt., Artikel-ID 757664, Seite 1-8
DOI: 10.3389/fonc.2021.757664
Srivastava, Aayushi: Whole genome sequencing prioritizes CHEK2, EWSR1, and TIAM1 as possible predisposition genes for familial non-medullary thyroid cancer / Aayushi Srivastava, Sara Giangiobbe, Diamanto Skopelitou, Beiping Miao, Nagarajan Paramasivam, Chiar… , 22 February 2021. - 10 S.
In: Frontiers in endocrinology, ISSN 1664-2392. 12(2021) vom: 22. Feb., Artikel-ID 600682, Seite 1-10
DOI: 10.3389/fendo.2021.600682
Slater, Emily P.: Combinations of low-frequency genetic variants might predispose to familial pancreatic cancer / Emily P. Slater, Lisa M. Wilke, Lutz Benedikt Böhm, Konstantin Strauch, Manuel Lutz, Norman Gercke, … , 2 July 2021. - 14 S.
In: Journal of Personalized Medicine, ISSN 2075-4426. 11(2021), 7, Artikel-ID 631, Seite 1-14
DOI: 10.3390/jpm11070631
Skopelitou, Diamanto: A novel low-risk germline variant in the SH2 domain of the SRC gene affects multiple pathways in familial colorectal cancer / Diamanto Skopelitou, Beiping Miao, Aayushi Srivastava, Abhishek Kumar, Magdalena Kuświk, Dagmara Dym… , 1 April 2021. - 15 S.
In: Journal of Personalized Medicine, ISSN 2075-4426. 11(2021), 4, Artikel-ID 262, Seite 1-15
DOI: 10.3390/jpm11040262
Sainz, Juan: Polymorphisms within autophagy-related genes influence the risk of developing colorectal cancer : a meta-analysis of four large cohorts / Juan Sainz, Francisco José García-Verdejo, Manuel Martínez-Bueno, Abhishek Kumar, José Manuel Sánche… , 2 March 2021. - 16 S.
In: Cancers, ISSN 2072-6694. 13(2021), 6, Artikel-ID 1258, Seite 1-16
DOI: 10.3390/cancers13061258
Skopelitou, Diamanto: Whole exome sequencing identifies APCDD1 and HDAC5 genes as potentially cancer predisposing in familial colorectal cancer / Diamanto Skopelitou, Beiping Miao, Aayushi Srivastava, Abhishek Kumar, Magdalena Kuswick, Dagmara Dy… , 2 February 2021. - 21 S.
In: International journal of molecular sciences, ISSN 1422-0067. 22(2021), 4, Artikel-ID 1837, Seite 1-21
DOI: 10.3390/ijms22041837
Zheng, Guoqiao: Second primary cancers after kidney cancers, and kidney cancers as second primary cancers / Guoqiao Zheng, Kristina Sundquist, Jan Sundquist, Tianhui Chen, Asta Försti, Otto Hemminki, Kari Hem… , 9 January 2021. - 8 S.
In: European urology open science, ISSN 2666-1683. 24(2021), Seite 52-59
DOI: 10.1016/j.euros.2020.12.007
Catalano, Calogerina: Characterization of rare germline variants in familial multiple myeloma / Calogerina Catalano, Nagarajan Paramasivam, Joanna Blocka, Sara Giangiobbe, Stefanie Huhn, Matthias … , 13 February 2021. - 4 S.
In: Blood cancer journal, ISSN 2044-5385. 11(2021), Artikel-ID 33, Seite 1-4
DOI: 10.1038/s41408-021-00422-6
Kumar, Abhishek: A rare large duplication of MLH1 identified in Lynch syndrome / Abhishek Kumar, Nagarajan Paramasivam, Obul Reddy Bandapalli, Matthias Schlesner, Tianhui Chen, Rolf… , 19 January 2021. - 7 S.
In: Hereditary cancer in clinical practice, ISSN 1897-4287. 19(2021), Artikel-ID 10, Seite 1-7
DOI: 10.1186/s13053-021-00167-0
Went, Molly: Search for multiple myeloma risk factors using Mendelian randomization / Molly Went, Alex J. Cornish, Philip J. Law, Ben Kinnersley, Mark van Duin, Niels Weinhold, Asta Förs… , 20 May 2020. - 8 S.
In: Blood advances, ISSN 2473-9537. 4(2020), 10 vom: Mai, Seite 2172-2179
DOI: 10.1182/bloodadvances.2020001502
Zheng, Guoqiao: Association between tumor characteristics and second primary cancers with cutaneous melanoma survival : a nationwide cohort study / Guoqiao Zheng, Subhayan Chattopadhyay, Kristina Sundquist, Jan Sundquist, Asta Försti, Akseli Hemmin… , 03 February 2020. - 8 S.
In: Pigment cell & melanoma research, ISSN 1755-148X. 33(2020), 4, Seite 625-632
DOI: 10.1111/pcmr.12868
Zheng, Guoqiao: Cancer predisposition genes in cancer-free families / Guoqiao Zheng, Calogerina Catalano, Obul Reddy Bandapalli, Nagarajan Paramasivam, Subhayan Chattopad… , 27 September 2020. - 13 S.
In: Cancers, ISSN 2072-6694. 12(2020,10) Artikel-Nummer 2770, 13 Seiten
DOI: 10.3390/cancers12102770
Zheng, Guoqiao: Incidence differences between first primary cancers and second primary cancers following skin squamous cell Carcinoma as etiological clues / Guoqiao Zheng, Kristina Sundquist, Jan Sundquist, Asta Försti, Akseli Hemminki, Kari Hemminki, 6 August 2020. - 8 S.
In: Clinical epidemiology, ISSN 1179-1349. 12(2020), Seite 857-864
DOI: 10.2147/CLEP.S256662
Srivastava, Aayushi: A germline mutation in the POT1 gene is a candidate for familial non-medullary thyroid cancer / Aayushi Srivastava, Beiping Miao, Diamanto Skopelitou, Varun Kumar, Abhishek Kumar, Nagarajan Parama… , 1 June 2020. - 13 S.
In: Cancers, ISSN 2072-6694. 12(2020,6) Artikel-Nummer 1441, 13 Seiten
DOI: 10.3390/cancers12061441
Thomsen, Hauke: Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1 / Hauke Thomsen, Subhayan Chattopadhyay, Per Hoffmann, Markus M. Noethen, Helen Kalirai, Sarah E. Coup… , 2020. - 7 S.
In: Melanoma research, ISSN 1473-5636. 30(2020), 2, Seite 166-172
DOI: 10.1097/CMR.0000000000000641
Zheng, Guoqiao: Second primary cancers in melanoma patients critically shorten survival / Guoqiao Zheng, Subhayan Chattopadhyay, Kristina Sundquist, Jan Sundquist, Asta Försti, Akseli Hemmin… , 23 January 2020. - 8 S.
In: Clinical epidemiology, ISSN 1179-1349. 12(2020), Seite 105-112
DOI: 10.2147/CLEP.S230149
Srivastava, Aayushi: Identification of familial Hodgkin lymphoma predisposing genes using whole genome sequencing / Aayushi Srivastava, Sara Giangiobbe, Abhishek Kumar, Nagarajan Paramasivam, Dagmara Dymerska, Wolfga… , 06 March 2020. - 11 S.
In: Frontiers in Bioengineering and Biotechnology, ISSN 2296-4185. 8(2020) Artikel-Nummer 179, 11 Seiten
DOI: 10.3389/fbioe.2020.00179
Zhang, Luyao: Familial clustering, second primary cancers and causes of death in penile, vulvar and vaginal cancers / Luyao Zhang, Otto Hemminki, Tianhui Chen, Guoqiao Zheng, Asta Försti, Kristina Sundquist, Jan Sundqu… , 14 August 2019. - 9 S.
In: Scientific reports, ISSN 2045-2322. 9(2019), Artikel-ID 11804, Seite 1-9
DOI: 10.1038/s41598-019-48399-4
Chattopadhyay, Subhayan: Second primary cancers in non-Hodgkin lymphoma : family history and survival / Subhayan Chattopadhyay, Guoqiao Zheng, Amit Sud, Kristina Sundquist, Jan Sundquist, Asta Försti, Ric… , 2020. - 7 S.
In: International journal of cancer, ISSN 1097-0215. 146(2020), 4, Seite 970-976
DOI: 10.1002/ijc.32391
Schmidt, Amand F.: Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9 / Amand F. Schmidt, Michael V. Holmes, David Preiss, Daniel I. Swerdlow, Spiros Denaxas, Ghazaleh Fate… , 29 October 2019. - 10 S.
In: BMC cardiovascular disorders, ISSN 1471-2261. 19(2019,1) Artikel-Nummer 240, 10 Seiten
DOI: 10.1186/s12872-019-1187-z
Chattopadhyay, Subhayan: Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance / Subhayan Chattopadhyay, Hauke Thomsen, Niels Weinhold, Iman Meziane, Stefanie Huhn, Miguel Inacio da… , 2020. - 5 S.
In: Leukemia, ISSN 1476-5551. 34(2020), 4, Seite 1187-1191
DOI: 10.1038/s41375-019-0619-1
Chattopadhyay, Subhayan: Influence of family history on risk of second primary cancers and survival in patients with squamous cell skin cancer / S. Chattopadhyay, G. Zheng, A. Hemminki, A. Försti, K. Sundquist, J. Sundquist, K. Hemminki, 2020
In: British journal of dermatology, ISSN 1365-2133. 183(2020), 3, Seite 488-494
DOI: 10.1111/bjd.18809
Srivastava, Aayushi: Whole genome aequencing of familial non-medullary thyroid cancer identifies germline alterations in MAPK/ERK and PI3K/AKT aignaling pathways / Aayushi Srivastava, Abhishek Kumar, Sara Giangiobbe, Elena Bonora, Kari Hemminki, Asta Försti and Ob… , 13 October 2019. - 20 S.
In: Biomolecules, ISSN 2218-273X. 9(2019,9) Artikel-Nummer 605, 20 Seiten
DOI: 10.3390/biom9100605
Zhang, Luyao: Comparison of familial clustering of anogenital and skin cancers between in situ and invasive types / Luyao Zhang, Otto Hemminki, Guoqiao Zheng, Asta Försti, Kristina Sundquist, Jan Sundquist & Kari Hem… , 06 November 2019. - 6 S.
In: Scientific reports, ISSN 2045-2322. 9(2019), Artikel-ID 16151, Seite 1-6
DOI: 10.1038/s41598-019-51651-6
Zheng, Guoqiao: Second primary cancers in patients with acute lymphoblastic, chronic lymphocytic and hairy cell leukaemia / Guoqiao Zheng, Subhayan Chattopadhyay, Amit Sud, Kristina Sundquist, Jan Sundquist, Asta Försti, Ric… , 31 January 2019. - 8 S.
In: British journal of haematology, ISSN 1365-2141. 185(2019), 2, Seite 232-239
DOI: 10.1111/bjh.15777
Sud, Amit: Analysis of 153 115 patients with hematological malignancies refines the spectrum of familial risk / Amit Sud, Subhayan Chattopadhyay, Hauke Thomsen, Kristina Sundquist, Jan Sundquist, Richard S. Houls… , 8 August 2019. - 10 S.
In: Blood, ISSN 1528-0020. 134(2019), 12, Seite 960-969
DOI: 10.1182/blood.2019001362
Went, Molly: Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes / Molly Went, Ben Kinnersley, Amit Sud, David C. Johnson, Niels Weinhold, Asta Försti, Mark van Duin, … . -
London: Henry Stewart Publ., 2019. - 1 Online-Ressource
Thomsen, Hauke: Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS) : comparison with multiple myeloma / Hauke Thomsen, Subhayan Chattopadhyay, Niels Weinhold, Pavel Vodicka, Ludmila Vodickova, Per Hoffman… , 08 February 2019. - 5 S.
In: Leukemia, ISSN 1476-5551. 33(2019), 7, Seite 1817-1821
DOI: 10.1038/s41375-019-0396-x
Lu, Shun: Single nucleotide polymorphisms within MUC4 are associated with colorectal cancer survival / Shun Lu, Calogerina Catalano, Stefanie Huhn, Barbara Pardini, Linda Partu, Veronika Vymetalkova, Lud… , May 15, 2019. - 13 S.
In: PLOS ONE, ISSN 1932-6203. 14(2019,5) Artikel-Nummer e0216666, 13 Seiten
DOI: 10.1371/journal.pone.0216666
Zheng, Guoqiao: Types of second primary cancers influence survival in chronic lymphocytic and hairy cell leukemia patients / Guoqiao Zheng, Subhayan Chattopadhyay, Amit Sud, Kristina Sundquist, Jan Sundquist, Asta Försti, Ric… , 26 March 2019. - 4 S.
In: Blood cancer journal, ISSN 2044-5385. 9(2019,4) Artikel-Nummer 40, 4 Seiten
DOI: 10.1038/s41408-019-0201-0
Sud, Amit: Author correction : Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility / Amit Sud et al.#, 08 January 2019. - 3 S.
In: Nature Communications, ISSN 2041-1723. 10(2019) Artikel-Nummer 157, 3 Seiten
DOI: 10.1038/s41467-018-08105-w
Went, Molly: Author correction : identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma / Molly Went et al., 10 January 2019. - 3 S.
In: Nature Communications, ISSN 2041-1723. 10(2019) Artikel-Nummer 213, 3 Seiten
DOI: 10.1038/s41467-018-08107-8
Vijayakrishnan, Jayaram: Author correction : genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia / Jayaram Vijayakrishnan et al.#, 21 January 2019. - 3 S.
In: Nature Communications, ISSN 2041-1723. 10(2019) Artikel-Nummer 419, 3 Seiten
DOI: 10.1038/s41467-018-08106-9
Chattopadhyay, Subhayan: Risk of second primary cancer following myeloid neoplasia and risk of myeloid neoplasia as second primary cancer : a nationwide, observational follow up study in Sweden / Subhayan Chattopadhyay, Guoqiao Zheng, Amit Sud, Hongyao Yu, Kristina Sundquist, Jan Sundquist, Asta… , August 2018. - 10 S.
In: The lancet, ISSN 2352-3026. 5(2018), 8, Seite e368-e377
DOI: 10.1016/S2352-3026(18)30108-X
Chattopadhyay, Subhayan: Prostate cancer survivors : risk and mortality in second primary cancers / Subhayan Chattopadhyay, Guoqiao Zheng, Otto Hemminki, Asta Försti, Kristina Sundquist, Kari Hemminki, 01 October 2018. - 8 S.
In: Cancer medicine, ISSN 2045-7634. 7(2018), 11, Seite 5752-5759
DOI: 10.1002/cam4.1764
Chattopadhyay, Subhayan: Multiple myeloma : family history and mortality in second primary cancers / Subhayan Chattopadhyay, Hongyao Yu, Amit Sud, Jan Sundquist, Asta Försti, Akseli Hemminki and Kari H… , 07 August 2018. - 4 S.
In: Blood cancer journal, ISSN 2044-5385. 8(2018), 8, Seite 1-4
DOI: 10.1038/s41408-018-0108-1
Ali, Mina: The multiple myeloma risk allele at 5q15 lowers ELL2 expression and increases ribosomal gene expression / Mina Ali, Ram Ajore, Anna-Karin Wihlborg, Abhishek Niroula, Bhairavi Swaminathan, Ellinor Johnsson, … , 25 April 2018. - 9 S.
In: Nature Communications, ISSN 2041-1723. 9(2018) Artikel-Nummer 1649, 9 Seiten
DOI: 10.1038/s41467-018-04082-2
Yadav, Pankaj: Cytogenetic aberrations in multiple myeloma are associated with shifts in serum immunoglobulin isotypes distribution and levels / Pankaj Yadav, Maximilian Merz, Elias K. Mai, Asta Försti, Anna Jauch, Hartmut Goldschmidt, Kari Hemm… , 2018. - 3 S.
In: Haematologica, ISSN 1592-8721. 103(2018), 4, Seite e162-e164
DOI: 10.3324/haematol.2017.184226
Zheng, Guoqiao: Borderline ovarian tumors share familial risks with themselves and invasive cancers / Guoqiao Zheng, Hongyao Yu, Anna Kanerva, Asta Försti, Kristina Sundquist, and Kari Hemminki, July 17, 2018. - 7 S.
In: Cancer epidemiology, biomarkers & prevention, ISSN 1538-7755. 27(2018), 11, Seite 1358-1363
DOI: 10.1158/1055-9965.EPI-18-0503
Zheng, Guoqiao: Familial ovarian cancer clusters with other cancers / Guoqiao Zheng, Hongyao Yu, Anna Kanerva, Asta Försti, Kristina Sundquist, & Kari Hemminki, 01 August 2018. - 10 S.
In: Scientific reports, ISSN 2045-2322. 8(2018) Artikel-Nummer 11561, 10 Seiten
DOI: 10.1038/s41598-018-29888-4
Zheng, Guoqiao: Familial risks of second primary cancers and mortality in ovarian cancer patients / Guoqiao Zheng, Subhayan Chattopadhyay, Asta Försti, Kristina Sundquist, Kari Hemminki, 11 October 2018. - 14 S.
In: Clinical epidemiology, ISSN 1179-1349. 10(2018), Seite 1457-1466
DOI: 10.2147/CLEP.S174173
Went, Molly: Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology / Molly Went, Amit Sud, Helen Speedy, Nicola J. Sunter, Asta Försti, Philip J. Law, David C. Johnson, … , 2019. - 9 S.
In: Blood cancer journal, ISSN 2044-5385. 9(2019) Artikel-Nummer 1, 9 Seiten
DOI: 10.1038/s41408-018-0162-8
Bandapalli, Obul Reddy: Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma / Obul Reddy Bandapalli, Nagarajan Paramasivam, Sara Giangiobbe, Abhishek Kumar, Wolfgang Benisch, And… , 30 April 2018. - 3 S.
In: International journal of cancer, ISSN 1097-0215. 143(2018), 8, Seite 2076-2078
DOI: 10.1002/ijc.31576
Kumar, Abhishek: Familial cancer variant prioritization pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family / Abhishek Kumar, Obul Reddy Bandapalli, Nagarajan Paramasivam, Sara Giangiobbe, Chiara Diquigiovanni,… , 02 August 2018. - 12 S.
In: Scientific reports, ISSN 2045-2322. 8(2018) Artikel-Nummer 11635, 12 Seiten
DOI: 10.1038/s41598-018-29952-z
Kharazmi, Elham: Importance of tumor location and histology in familial risk of upper gastrointestinal cancers : a nationwide cohort study / Elham Kharazmi, Masoud Babaei, Mahdi Fallah, Tianhui Chen, Kristina Sundquist, Kari Hemminki, 4 September 2018. - 11 S.
In: Clinical epidemiology, ISSN 1179-1349. 10(2018), Seite 1169-1179
DOI: 10.2147/CLEP.S168152
Kharazmi, Elham: Familial risk of pleural mesothelioma increased drastically in certain occupations : a nationwide prospective cohort study / Elham Kharazmi, Tianhui Chen, Mahdi Fallah, Kristina Sundquist, Jan Sundquist, Maria Albin, Elisabet… , 6 September 2018. - 6 S.
In: European journal of cancer, ISSN 1879-0852. 103(2018), Seite 1-6
DOI: 10.1016/j.ejca.2018.07.139
Niazi, Yasmeen: Genetic variation associated with chromosomal aberration frequency : a genome-wide association study / Yasmeen Niazi, Hauke Thomsen, Bozena Smolkova, Ludmila Vodickova, Sona Vodenkova, Michal Kroupa, Ver… , 2019. - 12 S.
In: Environmental and molecular mutagenesis, ISSN 1098-2280. 60(2019), 1, Seite 17-28
DOI: 10.1002/em.22236
Went, Molly: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma / Molly Went, Amit Sud, Asta Försti, Britt-Marie Halvarsson, Niels Weinhold et al.#, 13 September 2018. - 10 S.
In: Nature Communications, ISSN 2041-1723. 9(2018) Artikel-Nummer 3707, 10 Seiten
DOI: 10.1038/s41467-018-04989-w
Mahmoudpour, Seyed Hamidreza: Chemotherapy-induced peripheral neuropathy : evidence from genome-wide association studies and replication within multiple myeloma patients / Seyed Hamidreza Mahmoudpour; Obul Reddy Bandapalli; Miguel Inácio da Silva Filho; Chiara Campo; Kari… . -
London ; Berlin ; Heidelberg: BioMed Central ; Springer, 2018. - 1 Online-Ressource (9 Seiten)
DOI: 10.1186/s12885-018-4728-4
Hemminki, Kari: Calculation of population attributable fraction familial relative risk and statistical power / Kari Hemminki, Justo Lorenzo Bermejo. -
Heidelberg: Universität, 2018-10-05. - 1 Online-Ressource (1 File)
DOI: 10.11588/data/1KJEDB
Chattopadhyay, Subhayan: Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance : a genome-wide genetic interaction study / Subhayan Chattopadhyay; Hauke Thomsen; Miguel Inacio da Silva Filho; Niels Weinhold; Per Hoffmann; M… . -
London ; New York: BioMed Central ; Springer, 11 June 2018. - 1 Online-Ressource (13 Seiten)
DOI: 10.1186/s10020-018-0031-8
Huhn, Stefanie: Coding variants in NOD-like receptors : an association study on risk and survival of colorectal cancer / Stefanie Huhn, Miguel I. da Silva Filho, Tharmila Sanmuganantham, Tica Pichulik, Calogerina Catalano… , June 21, 2018. - 16 S.
In: PLOS ONE, ISSN 1932-6203. 13(2018,6) Artikel-Nummer e0199350, 16 Seiten
DOI: 10.1371/journal.pone.0199350
Vijayakrishnan, Jayaram: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia / Jayaram Vijayakrishnan, James Studd, Peter Broderick, Ben Kinnersley, Amy Holroyd, Philip J. Law, Ra… , 2018. - 9 S.
In: Nature Communications, ISSN 2041-1723. 9(2018) Artikel-Nummer 1340, 9 Seiten
DOI: 10.1038/s41467-018-03178-z
Went, Molly: Assessing the effect of obesity-related traits on multiple myeloma using a Mendelian randomisation approach : letter to the editor / M. Went, A. Sud, P.J. Law, D.C. Johnson, N. Weinhold, A. Försti, M. van Duin, J.S. Mitchell, B. Chen… , 16 June 2017. - 3 S.
In: Blood cancer journal, ISSN 2044-5385. 7(2017), 6, Artikel-ID e573, Seite 1-3
DOI: 10.1038/bcj.2017.48
Vijayakrishnan, Jayaram: A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1 / J. Vijayakrishnan, R. Kumar, M.Y.R. Henrion, A.V. Moorman, P S. Rachakonda, I. Hosen, M.I. da Silva … , 2017. - 7 S.
In: Leukemia, ISSN 1476-5551. 31(2017), 3, Seite 573-579
DOI: 10.1038/leu.2016.271
Li, Lily: Genetic predisposition to multiple myeloma at 5q15 is mediated by an ELL2 enhancer polymorphism / Ni Li, David C. Johnson, Niels Weinhold, Scott Kimber, Sara E. Dobbins, Jonathan S. Mitchell, Ben Ki… , September 12, 2017. - 9 S.
In: Cell reports, ISSN 2211-1247. 20(2017), 11, Seite 2556-2564
DOI: 10.1016/j.celrep.2017.08.062
Thomsen, Hauke: Genomewide association study on monoclonal gammopathy of unknown significance (MGUS) / Hauke Thomsen, Chiara Campo, Niels Weinhold, Miguel Inacio da Silva Filho, Luděk Pour, Evžen Gregora… , 04 April 2017. - 10 S.
In: European journal of haematology, ISSN 1600-0609. 99(2017), 1, Seite 70-79
DOI: 10.1111/ejh.12892
Law, Philip J.: Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci / Philip J. Law, Amit Sud, Jonathan S. Mitchell, Marc Henrion, Giulia Orlando, Oleg Lenive, Peter Brod… , 23 January 2017. - 11 S.
In: Scientific reports, ISSN 2045-2322. 7(2017) Artikel-Nummer 41071, 11 Seiten
DOI: 10.1038/srep41071
Sud, Amit: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility / Amit Sud, Hauke Thomsen, Philip J. Law, Asta Försti, Miguel Inacio da Silva Filho, Amy Holroyd, Pete… , 2017 Dec 1. - 11 S.
In: Nature Communications, ISSN 2041-1723. 8(2017) Artikel-Nummer 1892, 11 Seiten
DOI: 10.1038/s41467-017-00320-1
Li, Lily: Multiple myeloma risk variant at 7p15.3 creates an IRF4-binding site and interferes with CDCA7L expression / Ni Li, David C. Johnson, Niels Weinhold, James B. Studd, Giulia Orlando, Fabio Mirabella, Jonathan S… , 24 Nov 2016. - 9 S.
In: Nature Communications, ISSN 2041-1723. 7(2016), Artikel-ID 13656, Seite 1-9
DOI: 10.1038/ncomms13656
Försti, Asta: Pedigree based DNA sequencing pipeline for germline genomes of cancer families / Asta Försti, Abhishek Kumar, Nagarajan Paramasivam, Matthias Schlesner, Calogerina Catalano, Dagmara… , 09 August 2016. - 9 S.
In: Hereditary cancer in clinical practice, ISSN 1897-4287. 14(2016), Artikel-ID 16, Seite 1-9
DOI: 10.1186/s13053-016-0058-1
Hemminki, Kari: Germline genetics of cancer of unknown primary (CUP) and its specific subtypes / Kari Hemminki, Bowang Chen, Abhishek Kumar, Olle Melander, Jonas Manjer, Göran Hallmans, Ulrika Pett… , March 03, 2016. - 10 S.
In: OncoTarget, ISSN 1949-2553. 7(2016), 16, Seite 22140-22149
DOI: 10.18632/oncotarget.7903
Chen, Tianhui: Risk of second primary cancers in multiple myeloma survivors in German and Swedish cancer registries / Tianhui Chen, Mahdi Fallah, Hermann Brenner, Lina Jansen, Elias K. Mai, Felipe A. Castro, Alexander … , 24 February 2016. - 8 S.
In: Scientific reports, ISSN 2045-2322. 6(2016) Artikel-Nummer 22084, 8 Seiten
DOI: 10.1038/srep22084
Hemminki, Kari: The incidence of senile cataract and glaucoma is increased in patients with plasma cell dyscrasias : etiologic implications / Kari Hemminki, Asta Försti, Raimo Tuuminen, Otto Hemminki, Hartmut Goldschmidt, Kristina Sundquist, … , 22 June 2016. - 7 S.
In: Scientific reports, ISSN 2045-2322. 6(2016), Artikel-ID 28500
DOI: 10.1038/srep28500
Macauda, Angelica: Identification of miRSNPs associated with the risk of multiple myeloma / Angelica Macauda, Diego Calvetti, Giuseppe Maccari, Kari Hemminki, Asta Försti, Hartmut Goldschmidt,… , 2017. - 9 S.
In: International journal of cancer, ISSN 1097-0215. 140(2017), 3, Seite 526-534
DOI: 10.1002/ijc.30465
Fallah, Mahdi: Familial risk of non-Hodgkin lymphoma by sex, relationship, age at diagnosis and histology : a joint study from five Nordic countries / M. Fallah, E. Kharazmi, E. Pukkala, S. Tretli, J.H. Olsen, L. Tryggvadottir, K. Sundquist and K. Hem… , 2016. - 6 S.
In: Leukemia, ISSN 1476-5551. 30(2016), 2, Seite 373-378
DOI: 10.1038/leu.2015.272
Hemminki, Kari: Cyclin D1 splice site variant triggers chromosomal aberrations in healthy humans / K Hemminki, L Musak, V Vymetalkova, Z Smerhovsky, E Halasova, O Osina, L Letkova, A Försti, L Vodick… , 2014. - 2 S.
In: Leukemia, ISSN 1476-5551. 28(2014), 3, Seite 721-722
DOI: 10.1038/leu.2013.353
Weinhold, Niels: Inherited genetic susceptibility to monoclonal gammopathy of unknown significance / Niels Weinhold, David C. Johnson, Andrew C. Rawstron, Asta Försti, Chi Doughty, Jayaram Vijayakrishn… , January 21, 2014. - 5 S.
In: Blood, ISSN 1528-0020. 123(2014), 16, Seite 2513-2517
DOI: 10.1182/blood-2013-10-532283
Rachakonda, P. Sivaramakrishna: Somatic mutations in exocrine pancreatic tumors : association with patient survival / P. Sivaramakrishna Rachakonda, Andrea S. Bauer, Huaping Xie, Daniele Campa, Cosmeri Rizzato, Federic… , April 2, 2013. - 8 S.
In: PLOS ONE, ISSN 1932-6203. 8(2013), 4, Artikel-ID e60870, Seite 1-8
DOI: 10.1371/journal.pone.0060870
Weinhold, Niels: The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma / Niels Weinhold, David C. Johnson, Daniel Chubb, Bowang Chen, Asta Försti, Fay J. Hosking, Peter Brod… , 17 March 2013. - 5 S.
In: Nature genetics, ISSN 1546-1718. 45(2013), 5, Seite 522-526
DOI: 10.1038/ng.2583
Musak, Ludovit: Chromosomal damage among medical staff occupationally exposed to volatile anesthetics, antineoplastic drugs, and formaldehyde / by Ludovit Musak, PhD, Zdenek Smerhovsky, PhD, Erika Halasova, PhD, Oto Osina, PhD, Lucia Letkova, M… , 2013. - 13 S.
In: Scandinavian journal of work, environment & health, ISSN 1795-990X. 39(2013), 6, Seite 618-630
DOI: 10.5271/sjweh.3358
Maccioni, Livia: Variants at the 9p21 locus and melanoma risk / Livia Maccioni, Panduranga Sivaramakrishna Rachakonda, Justo Lorenzo Bermejo, Dolores Planelles, Cel… , 2 Juli 2013. - 15 S.
In: BMC cancer, ISSN 1471-2407. 13(2013), Artikel-ID 325, Seite 1-15
DOI: 10.1186/1471-2407-13-325
Maccioni, Livia: Variants at chromosome 20 (ASIP locus) and melanoma risk / Livia Maccioni, P. Sivaramakrishna Rachakonda, Dominique Scherer, Justo Lorenzo Bermejo, Dolores Pla… , 2013. - 13 S.
In: International journal of cancer, ISSN 1097-0215. 132(2013), 1, Seite 42-54
DOI: 10.1002/ijc.27648
Migliorini, Gabriele: Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype / Gabriele Migliorini, Bettina Fiege, Fay J. Hosking, Yussanne Ma, Rajiv Kumar, Amy L. Sherborne, Migu… , August 30, 2013. - 10 S.
In: Blood, ISSN 1528-0020. 122(2013), 19, Seite 3298-3307
DOI: 10.1182/blood-2013-03-491316
Frampton, Matthew: Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin’s lymphoma / Matthew Frampton, Miguel Inacio da Silva Filho, Peter Broderick, Hauke Thomsen, Asta Försti, Jayaram… , 22 October 2013. - 7 S.
In: Nature Communications, ISSN 2041-1723. 4(2013), Artikel-ID 2549, Seite 1-7
DOI: 10.1038/ncomms3549
Klimosch, Sascha Niclas: Functional TLR5 genetic variants affect human colorectal cancer survival / Sascha N. Klimosch, Asta Försti, Jana Eckert, Jelena Knežević, Melanie Bevier, Witigo von Schönfels,… , October 23, 2013. - 12 S.
In: Cancer research, ISSN 1538-7445. 73(2013), 24, Seite 7232-7242
DOI: 10.1158/0008-5472.CAN-13-1746
Castro, Felipe A.: Increased risk of hepatobiliary cancers after hospitalization for autoimmune disease / Felipe A. Castro, Xiangdong Liu, Asta Försti, Jianguang Ji, Jan Sundquist, Kristina Sundquist, Jill … , 2014. - 8 S.
In: Clinical gastroenterology and hepatology, ISSN 1542-7714. 12(2014), 6, Seite 1038-1045.e7
DOI: 10.1016/j.cgh.2013.11.007
Liu, Hao: Second primary cancers after cancer of unknown primary in Sweden and Germany : efficacy of the modern work-up / Liu, Hao; Hemminki, Karia; Sundquist, Jan; Holleczek, Bernd; Katalinic, Alexander; Emrich, Katharina… , 2013. - 5 S.
In: European journal of cancer prevention, ISSN 1473-5709. 22(2013), 3, Seite 210-214
DOI: 10.1097/CEJ.0b013e3283592c62
Lenci, Romina Elizabeth: Influence of genetic variants in type I interferon genes on melanoma survival and therapy / Romina Elizabeth Lenci, Melanie Bevier, Andreas Brandt, Justo Lorenzo Bermejo, Antje Sucker, Iris Mo… , November 27, 2012. - 15 S.
In: PLOS ONE, ISSN 1932-6203. 7(2012, 11) Artikel-Nummer e50692, 15 Seiten
DOI: 10.1371/journal.pone.0050692
Hemminki, Kari: Site-specific survival rates for cancer of unknown primary according to location of metastases / Kari Hemminki, Matias Riihimäki, Kristina Sundquist and Akseli Hemminki, 2013. - 8 S.
In: Epidemiology, ISSN 1531-5487. 133(2013), 1, Seite 182-189
DOI: 10.1002/ijc.27988
Gast, Andreas: Association of inherited variation in Toll-like receptor genes with malignant melanoma susceptibility and survival / Andreas Gast, Justo Lorenzo Bermejo, Rainer Claus, Andreas Brandt, Marianne Weires, Alexander Weber,… , September 9, 2011. - 7 S.
In: PLOS ONE, ISSN 1932-6203. 6(2011), 9, Artikel-ID e24370, Seite 1-7
DOI: 10.1371/journal.pone.0024370
Sherborne, Amy: Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia / Amy L. Sherborne, Kari Hemminki, Rajiv Kumar, Claus R. Bartram, Martin Stanulla, Martin Schrappe, El… , July, 2011. - 6 S. : Diagramme
In: Haematologica, the hematology journal, ISSN 1592-8721. 96(2011), 7, Seite 1049-1054
DOI: 10.3324/haematol.2011.040121
Weires, Marianne: Clustering of concordant and discordant cancer types in Swedish couples is rare / Marianne Weires, Justo Lorenzo Bermejo, Jan Sundquist, Kari Hemminki, 2011. - 9 S.
In: European journal of cancer, ISSN 1879-0852. 47(2011), 1 vom: Jan., Seite 98-106
DOI: 10.1016/j.ejca.2010.06.125
Ott, Katja: DNA repair gene and MTHFR gene polymorphisms as prognostic markers in locally advanced adenocarcinoma of the esophagus or stomach treated with cisplatin and 5-fluorouracil-based neoadjuvant chemotherapy / Katja Ott, MD, P. Sivaramakrishna Rachakonda, PhD, Benjamin Panzram, PhD, Gisela Keller, MD, Florian… , 24 February 2011. - 11 S.
In: Annals of surgical oncology, ISSN 1534-4681. 18(2011), 9, Seite 2688-2698
DOI: 10.1245/s10434-011-1601-y
Hemminki, Kari: Searching for the missing heritability of complex diseases / Kari Hemminki, Asta Försti, Richard Houlston, and Justo Lorenzo Bermejo, [February 2011]. - 4 S. : Diagramme
In: Human mutation, ISSN 1098-1004. 32(2011), 2 vom: Feb., Seite 259-262
DOI: 10.1002/humu.21392
Hemminki, Kari: Familial bladder cancer and the related genes / Kari Hemminki, Justo L. Bermejo, Jianguang Ji and Rajiv Kumar, [September 2011]. - 7 S. : Diagramme
In: Current opinion in urology, ISSN 1473-6586. 21(2011), 5 vom: Sept., Seite 386-392
DOI: 10.1097/MOU.0b013e32834958ff
Pardini, Barbara: 5-Fluorouracil-based chemotherapy for colorectal cancer and MTHFR/MTRR genotypes / Barbara Pardini, Rajiv Kumar, Alessio Naccarati, Jan Novotny, Rashmi B. Prasad, Asta Forsti, Kari He… , 2011. - 2 S.
In: British journal of clinical pharmacology, ISSN 1365-2125. 72(2011), 1, Seite 162-163
DOI: 10.1111/j.1365-2125.2010.03892.x
Carrai, Maura: Association between TAS2R38 gene polymorphisms and colorectal cancer risk : a case-control study in two independent populations of caucasian origin / Maura Carrai, Verena Steinke, Pavel Vodicka, Barbara Pardini, Nils Rahner, Elke Holinski-Feder, Moni… , June 2, 2011. - 7 S.
In: PLOS ONE, ISSN 1932-6203. 6(2011), 6, Artikel-ID e20464, Seite 1-7
DOI: 10.1371/journal.pone.0020464
Lorenzo Bermejo, Justo: Comparison of six statistics of genetic association regarding their ability to discriminate between causal variants and genetically linked markers / Justo Lorenzo Bermejo, Alfonso Garcia Perez, Andreas Brandt, Kari Hemminki, Abigail G. Matthews, October 19, 2011. - 11 S.
In: Human heredity, ISSN 1423-0062. 72(2011), 2, Seite 142-152
DOI: 10.1159/000332006
Angelini, Sabrina: Exposure to low environmental levels of benzene : Evaluation of micronucleus frequencies and S-phenylmercapturic acid excretion in relation to polymorphisms in genes encoding metabolic enzymes / Sabrina Angelini, Rajiv Kumar, Justo Lorenzo Bermejo, Francesca Maffei, Anna Barbieri, Francesca Gra… , 2011. - 7 S.
In: Mutation research, ISSN 1388-2120. 719(2011), 1, Seite 7-13
DOI: 10.1016/j.mrgentox.2010.10.002
Broderick, Peter: Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk / Peter Broderick, Daniel Chubb, David C. Johnson, Niels Weinhold, Asta Försti, Amy Lloyd, Bianca Olve… , 2012. - 4 S.
In: Nature genetics, ISSN 1546-1718. 44(2012), 1, Seite 58-61
DOI: 10.1038/ng.993
Yang, Rongxi: A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer risk / Rongxi Yang, Bettina Schlehe, Kari Hemminki, Christian Sutter, Peter Bugert, Barbara Wappenschmidt, … , 2010. - 10 S.
In: Breast cancer research and treatment, ISSN 1573-7217. 121(2010), 3, Seite 693-702
DOI: 10.1007/s10549-009-0633-5
Tchatchou, Sandrine: Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity / Sandrine Tchatchou, Angela Riedel, Stefan Lyer, Julia Schmutzhard, Olga Strobel-Freidekind, Sabine G… , 2010. - 7 S.
In: Human mutation, ISSN 1098-1004. 31(2010), 1, Seite 60-66
DOI: 10.1002/humu.21134
Verdier, Petra J. de: Genotypes, haplotypes and diplotypes of three XPC polymorphisms in urinary-bladder cancer patients / Petra J. de Verdier, Somali Sanyal, Justo Lorenzo Bermejo, Gunnar Steineck, Kari Hemminki, Rajiv Kum… , 29 September 2010. - 6 S.
In: Mutation research, ISSN 1879-2871. 694(2010), 1/2 vom: Dez., Seite 39-44
DOI: 10.1016/j.mrfmmm.2010.09.003
Sherborne, Amy: Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk / Amy L. Sherborne, Fay J. Hosking, Rashmi B. Prasad, Rajiv Kumar, Rolf Koehler, Jayaram Vijayakrishna… , 9 May 2010. - 3 S.
In: Nature genetics, ISSN 1546-1718. 42(2010), 6, Seite 492-494
DOI: 10.1038/ng.585
Bokkasa, Rashmi Prasad: Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood / Rashmi B. Prasad, Fay J. Hosking, Jayaram Vijayakrishnan, Elli Papaemmanuil, Rolf Koehler, Mel Greav… , March 4, 2010. - 3 S.
In: Blood, ISSN 1528-0020. 115(2010), 9 vom: März, Seite 1765-1767
DOI: 10.1182/blood-2009-09-241513
Hemminki, Kari: Tumor location and patient characteristics of colon and rectal adenocarcinomas in relation to survival and TNM classes / Kari Hemminki, Irene Santi, Marianne Weires, Hauke Thomsen, Jan Sundquist, Justo Lorenzo Bermejo, 21 December 2010. - 6 S.
In: BMC cancer, ISSN 1471-2407. 10(2010), Artikel-ID 688, Seite 1-6
DOI: 10.1186/1471-2407-10-688
Hemminki, Kari: Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients / Kari Hemminki, Bertram Müller-Myhsok, Peter Lichtner, Christoph Engel, Bowang Chen, Barbara Burwinke… , [15 June 2010]. - 5 S.
In: International journal of cancer, ISSN 1097-0215. 126(2010), 12 vom: Juni, Seite 2858-2862
DOI: 10.1002/ijc.24986
Hemminki, Kari: Re "Underlying genetic models of inheritance in established type 2 diabetes associations" / Kari Hemminki, Asta Försti, and Justo Lorenzo Bermejo, 13 April 2010. - 2 S.
In: American journal of epidemiology, ISSN 1476-6256. 171(2010), 10 vom: Apr., Seite 1153-1154
DOI: 10.1093/aje/kwq058
Campa, Daniele: Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk : a two-step gene-wide case-control study / Daniele Campa, Barbara Pardini, Alessio Naccarati, Ludmila Vodickova, Jan Novotny, Verena Steinke, N… , 28 September 2010. - 6 S.
In: BMC gastroenterology, ISSN 1471-230X. 10(2010), 1, Artikel-ID 112, Seite 1-6
DOI: 10.1186/1471-230X-10-112
Lascorz Puértolas, Jesús: Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility / Jesús Lascorz, Asta Försti, Bowang Chen, Stephan Buch, Verena Steinke, Nils Rahner, Elke Holinski-Fe… , 07 July 2010. - 8 S.
In: Carcinogenesis, ISSN 1460-2180. 31(2010), 9 vom: Juli, Seite 1612-1619
DOI: 10.1093/carcin/bgq146
Brandt, Andreas: Breast cancer risk in women who fulfill high-risk criteria : at what age should surveillance start? / Andreas Brandt, Justo Lorenzo Bermejo, Jan Sundquist, Kari Hemminki, 2010. - 9 S.
In: Breast cancer research and treatment, ISSN 1573-7217. 121(2010), Seite 133-141
DOI: 10.1007/s10549-009-0486-y
Brandt, Andreas: Age-specific risk of incident prostate cancer and risk of death from prostate cancer defined by the number of affected family members / Andreas Brandt, Justo Lorenzo Bermejo, Jan Sundquist, Kari Hemminki, 13 February 2010. - 6 S.
In: European urology, ISSN 1873-7560. 58(2010), 2, Seite 275-280
DOI: 10.1016/j.eururo.2010.02.002
Brandt, Andreas: Familial risks of breast and prostate cancers : does the definition of the at risk period matter? / Andreas Brandt, Justo Lorenzo Bermejo, Jan Sundquist, Kari Hemminki, 2010. - 6 S.
In: European journal of cancer, ISSN 1879-0852. 46(2010), 4, Seite 752-757
DOI: 10.1016/j.ejca.2009.11.016
Brandt, Andreas: Age of onset in familial breast cancer as background data for medical surveillance / A Brandt, J Lorenzo Bermejo, J Sundquist and K Hemminki, 2010. - 6 S.
In: British journal of cancer, ISSN 1532-1827. 102(2010), Seite 42-47
DOI: 10.1038/sj.bjc.6605421
Bouwhuis, Marna G.: Polymorphisms in the CD28/CTLA4/ICOS genes: role in malignant melanoma susceptibility and prognosis? / Marna G. Bouwhuis, Andreas Gast, Adina Figl, Alexander M.M. Eggermont, Kari Hemminki, Dirk Schadendo… , 2010. - 10 S.
In: Cancer immunology immunotherapy, ISSN 1432-0851. 59(2010), 2, Seite 303-312
DOI: 10.1007/s00262-009-0751-2
Försti, Asta: Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility / Jesús Lascorz, Asta Försti, Bowang Chen, Stephan Buch, Verena Steinke, Nils Rahner, Elke Holinski-Fe… , 2010. - 8 S.
In: Carcinogenesis, ISSN 0143-3334. 31(2010), Seite 1612-1619
Lorenzo Bermejo, Justo: Representation of genetic association via attributable familial relative risks in order to identify polymorphisms functionally relevant to rheumatoid arthritis / Justo Lorenzo Bermejo, Christine Fischer, Anke Schulz, Nadine Cremer, Rebecca Hein, Lars Beckmann, J… . -
London: BioMed Central, 2009. - 1 Online-Ressource (6 Seiten)
Ugurel, Selma: B-RAF and N-RAS mutations are preserved during short time in vitro propagation and differentially impact prognosis / Selma Ugurel, Ranjit K. Thirumaran, Sandra Bloethner, Andreas Gast, Antje Sucker, Jan Mueller-Bergha… , February 21, 2007. - 13 S.
In: PLOS ONE, ISSN 1932-6203. 2(2007,2) Artikel-Nummer e236, 13 Seiten
DOI: 10.1371/journal.pone.0000236
Figl, Adina: Multiple melanomas after treatment for Hodgkin lymphoma in a non-Dutch p16-Leiden mutation carrier with 2 MC1R high-risk variants / Adina Figl, Ranjit K. Thirumaran, Selma Ugurel, Andreas Gast, Kari Hemminki, Rajiv Kumar, Dirk Schad… , 2007. - 5 S.
In: Archives of dermatology, ISSN 1538-3652. 143(2007), 4, Seite 495-499
DOI: 10.1001/archderm.143.4.495
Hemminki, Kari: Constraints for genetic association studies imposed by attributable fraction and familial risk / Kari Hemminki and Justo Lorenzo Bermejo, 01 March 2007. - 9 S.
In: Carcinogenesis, ISSN 1460-2180. 28(2007), 3, Seite 648-656
DOI: 10.1093/carcin/bgl182
Blöthner, Sandra: Differences in global gene expression in melanoma cell lines with and without homozygous deletion of the CDKN2A locus genes / Sandra Bloethner, Kari Hemminki, Ranjit K. Thirumaran, Bowang Chen, Jan Mueller-Berghaus, Selma Ugur… , August 2006. - 11 S.
In: Melanoma research, ISSN 1473-5636. 16(2006), 4, Seite 297-307
DOI: 10.1097/01.cmr.0000222597.50309.05
Thirumaran, Ranjit Kumar: Re: Association between endothelin receptor B nonsynonymous variants and melanoma risk / Ranjit K. Thirumaran, Adina Thoelke, Selma Ugurel, Kari Hemminki, Dirk Schadendorf, Rajiv Kumar, 06 September 2006. - 2 S.
In: Journal of the National Cancer Institute, ISSN 1460-2105. 98(2006), 17, Seite 1252-1253
DOI: 10.1093/jnci/djj336
Blöthner, Sandra: Effect of common B-RAF and N-RAS mutations on global gene expression in melanoma cell lines / Sandra Bloethner, Bowang Chen, Kari Hemminki, Jan Müller-Berghaus, Selma Ugurel, Dirk Schadendorf an… , 10 March 2005. - 9 S.
In: Carcinogenesis, ISSN 1460-2180. 26(2005), 7, Seite 1224-1232
DOI: 10.1093/carcin/bgi066

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