Publications | Lund University Publications

1 – 10 of 14

show: 10
|
sort: year (new to old)

News feed Embed this list Save this search Mark all Export

Cancel

Embed this list

copy and paste the html snippet below into your own page:

<iframe src="https://lup.lub.lu.se/search/publication?embed=1&q=author%3D%22Tham%2C+Emma%22+or+(documentType+any+%22bookEditor+conferenceEditor%22+and+editor%3D%22Tham%2C+Emma%22)&amp;hide_pagination=1&amp;hide_info=1&amp;hide_options=1"
  width="100%"
  height="400"
  allowtransparency="true"
  frameborder="0">
</iframe>

« previous
1
2
next »

2025
Mark Characterisation of heritable TP53-related cancer syndrome in Sweden—a nationwide study of genotype-phenotype correlations in 90 families
Omran, Meis ; Liu, Yaxuan ; Sun Zhang, Alexander ; Poluha, Anna ; Stenmark-Askmalm, Marie ^LU ; Persson, Fredrik ; Hallbeck, Anna Lotta ; Rosén, Anna ; Helgadottir, Hafdis T. and Tham, Emma , et al. (2025) In European Journal of Human Genetics
- Contribution to journal › Article
2024
Mark Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors—a nationwide, prospective Swedish study
Tesi, Bianca ; Robinson, Kristina Lagerstedt ; Abel, Frida ; Díaz de Ståhl, Teresita ; Orrsjö, Sara ; Poluha, Anna ; Hellberg, Maria ^LU ; Wessman, Sandra ; Samuelsson, Sofie and Frisk, Tony , et al. (2024) In The Lancet Regional Health - Europe 39.
- Contribution to journal › Article
Mark Germline copy number variants and endometrial cancer risk
Stylianou, Cassie E. ; Wiggins, George A.R. ; Lau, Vanessa L. ; Dennis, Joe ; Shelling, Andrew N. ; Wilson, Michelle ; Sykes, Peter ; Amant, Frederic ; Annibali, Daniela and De Wispelaere, Wout , et al. (2024) In Human Genetics 143(12). p.1481-1498
- Contribution to journal › Article
2023
Mark Whole-body MRI surveillance in TP53 carriers is perceived as beneficial with no increase in cancer worry regardless of previous cancer : Data from the Swedish TP53 Study
Omran, Meis ; Johansson, Hemming ; Lundgren, Claudia ; Silander, Gustav ; Stenmark-Askmalm, Marie ^LU ; Loman, Niklas ^LU ; Baan, Annika ; Adra, Jamila ; Kuchinskaya, Ekaterina and Blomqvist, Lennart , et al. (2023) In Cancer 129(6). p.946-955
- Contribution to journal › Article
Mark Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer
Öfverholm, Anna ; Törngren, Therese ^LU ; Rosén, Anna ; Arver, Brita ; Einbeigi, Zakaria ; Haraldsson, Karin ^LU ; Ståhlbom, Anne Kinhult ; Kuchinskaya, Ekaterina ; Lindblom, Annika and Melin, Beatrice , et al. (2023) In BMC Cancer 23. p.1-12
- Contribution to journal › Article
2022
Mark Whole-Body MRI Surveillance—Baseline Findings in the Swedish Multicentre Hereditary TP53-Related Cancer Syndrome Study (SWEP53)
Omran, Meis ; Tham, Emma ; Brandberg, Yvonne ; Ahlström, Håkan ; Lundgren, Claudia ; Paulsson-Karlsson, Ylva ; Kuchinskaya, Ekaterina ; Silander, Gustav ; Rosén, Anna and Persson, Fredrik , et al. (2022) In Cancers 14(2).
- Contribution to journal › Article
2021
Mark A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients
Wendt, Camilla ; Muranen, Taru A ; Mielikäinen, Lotta ; Thutkawkorapin, Jessada ; Blomqvist, Carl ; Jiao, Xiang ; Ehrencrona, Hans ^LU ; Tham, Emma ; Arver, Brita and Melin, Beatrice , et al. (2021) In Scientific Reports 11. p.1-9
- Contribution to journal › Article
2020
Mark Public support for healthcare-mediated disclosure of hereditary cancer risk information : Results from a population-based survey in Sweden
Andersson, Andreas ; Hawranek, Carolina ; Öfverholm, Anna ; Ehrencrona, Hans ^LU ; Grill, Kalle ; Hajdarevic, Senada ; Melin, Beatrice ; Tham, Emma ; Hellquist, Barbro Numan and Rosén, Anna (2020) In Hereditary Cancer in Clinical Practice 18(1).
- Contribution to journal › Article
2019
Mark Functional characterization of novel germline TP53 variants in Swedish families
Kharaziha, Pedram ; Ceder, Sophia ; Axell, Olga ; Krall, Moritz ; Fotouhi, Omid ; Böhm, Stefanie ; Lain, Sonia ; Borg, Åke ^LU ; Larsson, Catharina and Wiman, Klas G. , et al. (2019) In Clinical Genetics 96(3). p.216-225
- Contribution to journal › Article
2018
Mark Expanding the Clinical Spectrum of Phenotypes Caused by Pathogenic Variants in PLOD2
Leal, Gabriela Ferraz ; Nishimura, Gen ; Voss, Ulrika ; Bertola, Débora Romeo ; Åström, Eva ; Svensson, Johan ^LU ; Yamamoto, Guilherme Lopes ; Hammarsjö, Anna ; Horemuzova, Eva and Papadiogannakis, Nikos , et al. (2018) In Journal of Bone and Mineral Research 33(4). p.753-760
- Contribution to journal › Article

« previous
1
2
next »

your query:: Remove author: Tham, Emma