Hans Ehrencrona

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2026
Mark Priority European strategies for sustainable access to high-quality genetic counselling in cancer: A Delphi study
McCrary, J.M. ; Ehrencrona, H. ^LU and Bergmann, A.K. (2026) In European Journal of Human Genetics
- Contribution to journal › Article
2025
Mark Precision Omics Initiative Sweden (PROMISE) will integrate research with healthcare
Kämpe, Anders ; Gudmundsson, Sanna ; Walsh, Colum P ; Lindblad-Toh, Kerstin ^LU ; Johansson, Åsa ; Clareborn, Anna ; Ameur, Adam ; Edsjö, Anders ^LU ; Fioretos, Thoas ^LU and Ehrencrona, Hans ^LU , et al. (2025) In Nature Medicine 31(6).
- Contribution to journal › Letter
Mark Whole genome sequencing in early onset advanced heart failure
Linnér, Erik ^LU ; Czuba, Tomasz ^LU ; Gidlöf, Olof ^LU ; Lundgren, Jakob ^LU ; Bollano, Entela ; Hellberg, Maria ; Celik, Selvi ^LU ; Pimpalwar, Neha ^LU ; Rentzsch, Philipp ^LU and Martorella, Molly ^LU , et al. (2025) In Scientific Reports 15(1).
- Contribution to journal › Article
Mark Implementing electronic informed consent in rare disease genomics
Ekholm, Katja ; Augustinsson, Annelie ^LU ; Sundström, Johan ; Johansen, Christian ; Storgärds, Maria ; Ljöstad, Lena ; Taylan, Fulya ; Ekblom, Eva ; Juran, Stephanie and Ek, Marlene , et al. (2025) In Scientific Reports 15(1).
- Contribution to journal › Article
Mark Direct letters to relatives at risk of hereditary cancer—a randomised trial on healthcare-assisted versus family-mediated risk disclosure
Ehrencrona, Hans ^LU ; Öfverholm, Anna ; Hawranek, Carolina ; Lovmar, Lovisa ; Svensson, Sara ^LU ; Wennstedt, Sigrid ; Hellquist, Barbro and Rosén, Anna (2025) In European Journal of Human Genetics 33(10). p.1359-1367
- Contribution to journal › Article
Mark Diagnostic Yield and Genetic Variation in 85 Swedish Patients with Mild to Profound Hearing Loss Analyzed by Whole Genome Sequencing
Elander, Johanna ^LU ; Ullmark, Tove ^LU ; Löwgren, Karolina ^LU ; Stenfeldt, Karin ^LU ; Falkenius-Schmidt, Karolina ^LU ; Löfgren, Maria ; Castiglione, Alessandro ^LU ; Busi, Micol ; Jonson, Tord ^LU and Ivarsson, Sofie ^LU , et al. (2025) In Journal of otolaryngology - head & neck surgery = Le Journal d'oto-rhino-laryngologie et de chirurgie cervico-faciale 54. p.19160216251345471-19160216251345471
- Contribution to journal › Article
2024
Mark Genetic counselling legislation and practice in cancer in EU Member States
McCrary, J. Matt ; Van Valckenborgh, Els ; Poirel, Hélène A. ; de Putter, Robin ; van Rooij, Jeroen ; Horgan, Denis ; Dierks, Marie Luise ; Antonova, Olga ; Brunet, Joan and Chirita-Emandi, Adela , et al. (2024) In European Journal of Public Health 34(4). p.666-675
- Contribution to journal › Article
Mark Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4 : A poly-glycine disease
Wallenius, Joel ^LU ; Kafantari, Efthymia ^LU ; Jhaveri, Emma ; Gorcenco, Sorina ^LU ; Ameur, Adam ; Karremo, Christin ^LU ; Dobloug, Sigurd ^LU ; Karrman, Kristina ^LU ; de Koning, Tom ^LU and Ilinca, Andreea ^LU , et al. (2024) In American Journal of Human Genetics 111(1). p.82-95
- Contribution to journal › Article
Mark Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia
Gorcenco, Sorina ^LU ; Kafantari, Efthymia ^LU ; Wallenius, Joel ^LU ; Karremo, Christin ^LU ; Alinder, Erik ; Dobloug, Sigurd ^LU ; Landqvist Waldö, Maria ^LU ; Englund, Elisabet ^LU ; Ehrencrona, Hans ^LU and Wictorin, Klas ^LU , et al. (2024) In Journal of Neurology 271(1). p.526-542
- Contribution to journal › Article
Mark A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities
Eisfeldt, Jesper ; Ameur, Adam ; Lenner, Felix ; Berk de Boer, Esmee Ten ; Ek, Marlene ; Wincent, Josephine ; Vaz, Raquel ; Ottosson, Jesper ; Jonson, Tord ^LU and Ivarsson, Sofie , et al. (2024) In Genome Research 34(11). p.1774-1784
- Contribution to journal › Article

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