How to do genetic counseling in psychiatry?
Johansson Soller, M., Moldovan, R., Ingvoldstad Malmgren, C., Cuthbert, A., Rietschel, M.
Published in EUROPEAN PSYCHIATRY (01.04.2021)
Published in EUROPEAN PSYCHIATRY (01.04.2021)
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Conference Proceeding
A retrospective two centre study of Birt-Hogg-Dubé syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population
Lagerstedt-Robinson, Kristina, Baranowska Körberg, Izabella, Tsiaprazis, Stefanos, Björck, Erik, Tham, Emma, Poluha, Anna, Hellström Pigg, Maritta, Paulsson-Karlsson, Ylva, Nordenskjöld, Magnus, Johansson-Soller, Maria, Aravidis, Christos
Published in PloS one (17.02.2022)
Published in PloS one (17.02.2022)
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Psychiatric genetic counseling: A mapping exercise
Moldovan, Ramona, McGhee, Kevin A., Coviello, Domenico, Hamang, Anniken, Inglis, Angela, Ingvoldstad Malmgren, Charlotta, Johansson‐Soller, Maria, Laurino, Mercy, Meiser, Bettina, Murphy, Lauren, Paneque, Milena, Papsuev, Oleg, Pawlak, Joanna, Rovira Moreno, Eulàlia, Serra‐Juhe, Clara, Shkedi‐Rafid, Shiri, Laing, Nakita, Voelckel, Marie‐Antoinette, Watson, Melanie, Austin, Jehannine C.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2019)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2019)
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The utility of whole genome sequencing in rare disease diagnostics
Johansson Soller, Maria, Nordgren, Ann, Ehrencrona, Hans, Lovmar, Lovisa, Wedell, Anna, Lindstrand, Anna
Published in Läkartidningen (10.05.2021)
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Published in Läkartidningen (10.05.2021)
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From cytogenetics to cytogenomics: whole genome sequencing as a comprehensive genetic test in rare disease diagnostics
Nilsson, D., Eisfeldt, J., Lundin, J., Pettersson, M., Kvarnung, M., Lieden, A., Sahlin, E., Lagerstedt, K., Martin, M., Ygberg, S., Bjerin, O., Stranneheim, H., Wedell, A., Nordenskjold, M., Soller, M. Johansson, Nordgren, A., Wirta, Valtteri, Lindstrand, A.
Published in EUROPEAN JOURNAL OF HUMAN GENETICS (2019)
Published in EUROPEAN JOURNAL OF HUMAN GENETICS (2019)
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Conference Proceeding
Integration of genome sequencing into health care - experiences from 3211 rare disease patients show high diagnostic rates across multiple clinical entities
Lindstrand, A., Laaksonen, Mikael, Magnusson, Måns, Wirta, Valtteri, Wedell, A.
Published in EUROPEAN JOURNAL OF HUMAN GENETICS (2020)
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Published in EUROPEAN JOURNAL OF HUMAN GENETICS (2020)
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Conference Proceeding
HIGH FREQUENCY OF THE TMPRSS2/ERG FUSION GENE IN PROSTATE CANCER
Soller, W., Johansson Soller, M., Isaksson, M., Elfving, P., Abrahamsson, P.A., Lundgren, R., Panagopoulos, I.
Published in European urology supplements : official journal of the European Association of Urology (01.09.2006)
Published in European urology supplements : official journal of the European Association of Urology (01.09.2006)
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