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2019
Mark Germline variants in oculocutaneous albinism genes and predisposition to familial cutaneous melanoma
Nathan, Vaishnavi ; Johansson, Peter A. ; Palmer, Jane M. ; Howlie, Madeleine ; Hamilton, Hayley R. ; Wadt, Karin ; Jönsson, Göran ^LU ; Brooks, Kelly M. ; Pritchard, Antonia L. and Hayward, Nicholas K. (2019) In Pigment Cell and Melanoma Research 32(6). p.854-863
- Contribution to journal › Article
Mark Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma
Johansson, Peter A. ; Nathan, Vaishnavi ; Bourke, Lauren M. ; Palmer, Jane M. ; Zhang, Tongwu ; Symmons, Judith ; Howlie, Madeleine ; Patch, Ann Marie ; Read, Jazlyn and Holland, Elizabeth A. , et al. (2019) In Melanoma Research 29(5). p.483-490
- Contribution to journal › Article
Mark Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT
Taylor, Nicholas J ; Mitra, Nandita ; Qian, Lu ; Avril, Marie-Françoise ; Bishop, D Timothy ; Paillerets, Brigitte Bressac-de ; Bruno, William ; Calista, Donato ; Cuellar, Francisco and Cust, Anne E , et al. (2019) In Journal of the American Academy of Dermatology 81(2). p.386-394
- Contribution to journal › Article
2017
Mark Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families
Taylor, Nicholas J. ; Mitra, Nandita ; Goldstein, Alisa M. ; Tucker, Margaret A. ; Avril, Marie Françoise ; Azizi, Esther ; Bergman, Wilma ; Bishop, D. Timothy ; Bressac-de Paillerets, Brigitte and Bruno, William , et al. (2017) In Journal of Investigative Dermatology 137(12). p.2606-2612
- Contribution to journal › Article
2016
Mark Deep sequencing of uveal melanoma identifies a recurrent mutation in PLCB4.
Johansson, Peter ; Aoude, Lauren G ; Wadt, Karin ; Glasson, William J ; Warrier, Sunil K ; Hewitt, Alex W ; Kiilgaard, Jens Folke ; Heegaard, Steffen ; Isaacs, Tim and Franchina, Maria , et al. (2016) In Oncotarget 7(4). p.4624-4631
- Contribution to journal › Article
Mark Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families.
Taylor, Nicholas J ; Handorf, Elizabeth A ; Mitra, Nandita ; Avril, Marie-Françoise ; Azizi, Esther ; Bergman, Wilma ; Bianchi-Scarrà, Giovanna ; Bishop, D Timothy ; Bressac-de Paillerets, Brigitte and Calista, Donato , et al. (2016) In Journal of Investigative Dermatology 136(5). p.1066-1069
- Contribution to journal › Article
2015
Mark Nonsense Mutations in the Shelterin Complex Genes ACD and TERF2IP in Familial Melanoma.
Aoude, Lauren G ; Pritchard, Antonia L ; Robles-Espinoza, Carla Daniela ; Wadt, Karin ; Harland, Mark ; Choi, Jiyeon ; Gartside, Michael ; Quesada, Víctor ; Johansson, Peter and Palmer, Jane M , et al. (2015) In Journal of the National Cancer Institute 107(2). p.408-408
- Contribution to journal › Article
2014
Mark Primary Melanoma Tumors from CDKN2A Mutation Carriers do not Belong to a Distinct Molecular Subclass.
Staaf, Johan ^LU ; Harbst, Katja ^LU ; Lauss, Martin ^LU ; Ringnér, Markus ^LU ; Måsbäck, Anna ^LU ; Howlin, Jillian ^LU ; Jirström, Karin ^LU ; Harland, Mark ; Zebary, Abdlsattar and Palmer, Jane M , et al. (2014) In Journal of Investigative Dermatology 134(12). p.3000-3003
- Contribution to journal › Article
Mark Somatic BRAF and NRAS Mutations in Familial Melanomas with Known Germline CDKN2A Status: A GenoMEL Study
Zebary, Abdlsattar ; Omholt, Katarina ; van Doorn, Remco ; Ghiorzo, Paola ; Harbst, Katja ^LU ; Johansson, Carolina Hertzman ; Hoiom, Veronica ; Jönsson, Göran B ^LU ; Pjanova, Dace and Puig, Susana , et al. (2014) In Journal of Investigative Dermatology 134(1). p.287-290
- Contribution to journal › Letter
2007
Mark Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents
Goldstein, Alisa M ; Chan, May ; Harland, Mark ; Hayward, Nicholas K ; Demenais, Florence ; Bishop, D Timothy ; Azizi, Esther ; Bergman, Wilma ; Bianchi-Scarra, Giovanna and Bruno, William , et al. (2007) In Journal of Medical Genetics 44(2). p.99-106
- Contribution to journal › Article

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