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2023
Mark Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel
Levi, Hagai ; Michailidou, Kyriaki ; Ahearn, Thomas ; Andrulis, Irene L ; Anton-Culver, Hoda ; Antoniou, Antonis C ; Arndt, Volker ; Augustinsson, Annelie ^LU ; Bermisheva, Marina and Bodelon, Clara , et al. (2023) In Journal of Medical Genetics 60(12). p.1186-1197
- Contribution to journal › Article
2022
Mark Genotype-phenotype correlation in arrhythmogenic right ventricular cardiomyopathy-risk of arrhythmias and heart failure
Christensen, Alex Hørby ; Platonov, Pyotr G. ^LU ; Jensen, Henrik Kjærulf ; Chivulescu, Monica ; Svensson, Anneli ^LU ; Dahlberg, Pia ^LU ; Madsen, Trine ; Frederiksen, Tanja Charlotte ; Heliö, Tiina and Lie, Øyvind Haugen , et al. (2022) In Journal of Medical Genetics 59(9). p.858-864
- Contribution to journal › Article
2020
Mark Efficacy of novel immunotherapy regimens in patients with metastatic melanoma with germline CDKN2A mutations
Helgadottir, Hildur ; Ghiorzo, Paola ; van Doorn, Remco ; Puig, Susana ; Levin, Max ; Kefford, Richard ; Lauss, Martin ^LU ; Queirolo, Paola ; Pastorino, Lorenza and Kapiteijn, Ellen , et al. (2020) In Journal of Medical Genetics 57(5). p.316-321
- Contribution to journal › Article
2019
Mark Progression from islet autoimmunity to clinical type 1 diabetes is influenced by genetic factors : Results from the prospective TEDDY study
Beyerlein, Andreas ; Bonifacio, Ezio ; Vehik, Kendra ^LU ; Hippich, Markus ; Winkler, Christiane ; Frohnert, Brigitte I. ; Steck, Andrea K. ; Hagopian, William A. ; Krischer, Jeffrey P. and Lernmark, Åke ^LU , et al. (2019) In Journal of Medical Genetics 56(9). p.602-605
- Contribution to journal › Article
Mark Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants : An ENIGMA report
Lopez-Perolio, Irene ; Leman, Raphaël ; Behar, Raquel ; Lattimore, Vanessa ; Pearson, John F. ; Castéra, Laurent ; Martins, Alexandra ; Vaur, Dominique ; Goardon, Nicolas and Davy, Grégoire , et al. (2019) In Journal of Medical Genetics 56(7). p.453-460
- Contribution to journal › Article
2018
Mark The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant : Breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium
Moghadasi, Setareh ; Meeks, Huong D. ; Vreeswijk, Maaike P G ; Janssen, Linda A.M. ; Borg, Åke ^LU ; Ehrencrona, Hans ^LU ; Paulsson-Karlsson, Ylva ; Wappenschmidt, Barbara ; Engel, Christoph and Gehrig, Andrea , et al. (2018) In Journal of Medical Genetics 55(1). p.15-20
- Contribution to journal › Article
Mark CM-Score : A validated scoring system to predict CDKN2A germline mutations in melanoma families from Northern Europe
Potjer, Thomas P. ; Helgadottir, Hildur ; Leenheer, Mirjam ; Van Der Stoep, Nienke ; Gruis, Nelleke A. ; Höiom, Veronica ; Olsson, Håkan ^LU ; Van Doorn, Remco ; Vasen, Hans F.A. and Van Asperen, Christi J. , et al. (2018) In Journal of Medical Genetics 55(10). p.661-668
- Contribution to journal › Article
2017
Mark Common cancers share familial susceptibility : Implications for cancer genetics and counselling
Yu, Hongyao ; Frank, Christoph ^LU ; Sundquist, Jan ^LU ; Hemminki, Akseli and Hemminki, Kari ^LU (2017) In Journal of Medical Genetics 54. p.248-253
- Contribution to journal › Article
Mark Regulating the advertising of genetic tests in Europe : a balancing act
Kalokairinou, Louiza ; Borry, Pascal and Howard, Heidi Carmen ^LU (2017) In Journal of Medical Genetics 54(10). p.651-656
- Contribution to journal › Article
2014
Mark High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families.
Helgadottir, Hildur ; Höiom, Veronica ; Jönsson, Göran B ^LU ; Tuominen, Rainer ; Ingvar, Christian ^LU ; Borg, Åke ^LU ; Olsson, Håkan ^LU and Hansson, Johan (2014) In Journal of Medical Genetics 51(8). p.545-552
- Contribution to journal › Article

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