Medverkande i utredning : Eva Stattin

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Dlamini, Senanile B., Saunders, Colleen J., Cieszczyk, Paweł, Ficek, Krzysztof, Hager, Charlotte K., Stattin, Eva-Lena, Nilsson, Kjell G., Eynon, Nir, Feller, Julian A., Tirosh, Oren, Bope, Christian D., Chimusa, Emile R., Laguette, Mary-Jessica N., Collins, Malcolm, September, Alison V. och Stattin, Evalena, A novel combination of genomic loci in ITGB2, COL5A1 and VEGFA associated with anterior cruciate ligament rupture susceptibility : insights From Australian, Polish, Swedish, And South African Cohorts, Biology of Sport, 2026, 43, s. 3–20, : Institute of Sport

Sundblom, Jimmy, Bergdahl, Ingvar, Stattin, Eva-Lena och Niemelä, Valter, Lifetime risk of cancer in carriers of intermediate alleles in the HTT gene, Scientific Reports, 2026, 16 nr 1, : Springer Nature

Frisk Torell, Matilda, Svennblad, Bodil, Wisten, Aase, Börjesson, Erik, Bergfeldt, Lennart, Stattin, Eva Lena, Börjesson, Mats och Stattin, Evalena, Sudden Arrhythmic Death Syndrome in the Young: Risk Factors are Identifiable Prior to Sudden Cardiac Arrest, American Journal of Cardiology, 2025, 257, s. 193–199, : Elsevier

Galos, Emma, Christersson, Christina, Baron, Tomasz, Svennblad, Bodil, Wisten, Aase och Stattin, Eva-Lena, Autopsy results and factors associated with sudden cardiac death in young individuals with congenital heart disease – a nationwide study, Scandinavian Cardiovascular Journal, 2025, 59 nr 1, : Taylor & Francis

Lif, Hanna, Characterisation of unicoronal synostosis for improved surgical outcomes, 2025, Acta Universitatis Upsaliensis, Uppsala

van Roey, Victor L., Ombashi, Saranda, Mathijssen, Irene M.J., Munkhammar, Åsa A., Åsten, Pamela M., Bouzariouh, Anouar, Célérier, Charlotte, Dana, Caroline, van Dooren, Marieke, Faasse, Mariët, Fauroux, Brigitte, Frykholm, Peter, Heinen, Arnoud, Heliövaara, Arja, Joosten, Koen F.M., Kljajic, Marizela, Larsson, Eva, Loudon, Sjoukje, Marinac, Ivana, Munill Ferrer, Montserrat, Poldermans, Henriette, Stattin, Eva-Lena, Streppel, Marloes, Svensson, Malin, Thierry, Briac, Tjoa, Stephen T.H., Topa, Alexandra, Weissbach, Elin, Wolvius, Eppo B., Zafra Vallejo, Víctor och Versnel, Sarah L., The Development of a European Registry for Facial Dysostosis Syndromes : A Delphi-Guided Approach, The Journal of Craniofacial Surgery, 2025, 36 nr 8, s. 2712–2716, : Wolters Kluwer

van Roey, Victor L, Ombashi, Saranda, Mathijssen, Irene M J, Munkhammar, Åsa A, Åsten, Pamela M, Bouzariouh, Anouar, Célérier, Charlotte, Dana, Caroline, van Dooren, Marieke, Faasse, Mariët, Fauroux, Brigitte, Frykholm, Peter, Heinen, Arnoud, Heliövaara, Arja, Joosten, Koen F M, Kljajic, Marizela, Larsson, Eva, Loudon, Sjoukje, Marinac, Ivana, Munill Ferrer, Montserrat, Poldermans, Henriette, Stattin, Eva-Lena, Streppel, Marloes, Svensson, Malin, Thierry, Briac, Tjoa, Stephen T H, Topa, Alexandra, Weissbach, Elin, Wolvius, Eppo B, Zafra Vallejo, Víctor och Versnel, Sarah L, The Development of a European Registry for Facial Dysostosis Syndromes: A Delphi-Guided Approach., The Journal of craniofacial surgery, 2025, 36 nr 8, s. 2712–2716

Delgado-Vega, Angelica Maria, Cederroth, Helene, Taylan, F, Ekholm, K, Ek, M, Thonberg, H, Jemt, A, Nilsson, D, Eisfeldt, J, Bilgrav Saether, Kristine, Hoeijer, Ida, Akgun-Dogan, Ozlem, Asano, Yui, Barakat, Tahsin Stefan, Batkovskyte, Dominyka, Baynam, Gareth, Bodamer, Olaf, Chetruengchai, Wanna, Corcoran, Pádraic, Couse, Madeline, Botto, Lorenzo D., Demidov, German, Dohi, Eisuke, Erhardsson, Mattias, Fernandez-Luna, Luis, Fujiwara, Toyofumi, Garg, Neha, Giugliani, Roberto, Gonzaga-Jauregui, Claudia, van Zelst-Stams, Wendy A. G., Groza, Tudor, Gunnarsson, Cecilia, Hammarsjoe, Anna, Hammond, Charles Kumi, Hatirnaz Ng, OEzden, Hesketh, Sirisha, Hettiarachchi, Dineshani, Johansson Soller, Maria, Kirmani, Umn Ahmed, Kjellberg, Martin, Kvarnung, Malin, Kvlividze, Oleg, Lagerstedt-Robinson, Kristina, Lasko, Paul, Lassmann, Timo, Lau, Lynette Y. S., Laurie, Steven, Lim, Weng Khong, Liu, Zhandong, Lysenkova Wiklander, Mariya, Makay, Prince, Maiga, Alassane Baneye, Maya-Gonzalez, Carolina, Meyn, M. Stephen, Neethiraj, Ramprasad, Nigro, Vincenzo, Nordgren, Felix, Nordlund, Jessica, Orrsjö, Sara, Ottosson, Jesper, Ozbek, Ugur, Özdemir, Özkan, Partin, Clyde, Pearce, David A., Peck, Raquel, Pedersen, Annie, Pettersson, Maria, Pongpanich, Monnat, Posada de la Paz, Manuel, Ramani, Arun, Romero, Juan Andres, Romero, Vanessa I., Rosenquist, Richard, Saw, Aung Min, Spencer, Matthew, Stattin, Eva-Lena, Srichomthong, Chalurmpon, Tapia-Paez, Isabel, Taruscio, Domenica, Taylor, Julie P., Tkemaladze, Tinatin, Tully, Ian, Tuemer, Zeynep, van Zelst-Stams, Wendy A. G., Verloes, Alain, Vaesterviga, Emma, Wang, Sailan, Yang, Rachel, Yamamoto, Shinya, Yepez, Vicente A., Zhang, Qing, Shotelersuk, Vorasuk, Wiafe, Samuel Agyei, Alanay, Yasemin, Botto, Lorenzo D., Kirmani, Salman, Lumaka, Aime, Palmer, Elizabeth Emma, Puri, Ratna Dua, Wirta, Valtteri, Lindstrand, Anna, Buske, Orion J., Cederroth, Mikk, Nordgren, Ann och Stattin, Evalena, Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon, Nature Genetics, 2024, 56 nr 11, s. 2287–2294, : NATURE PORTFOLIO

Eisfeldt, J, Ameur, Adam, Lenner, Felix, Berk de Boer, Esmee Ten, Ek, M, Wincent, J, Vaz, Raquel, Ottosson, Jesper, Jonson, Tord, Ivarsson, Sofie, Thunström, Sofia, Topa, Alexandra, Stenberg, Simon, Rohlin, Anna, Sandestig, Anna, Nordling, Margareta, Palmebäck, Pia, Burstedt, Magnus, Nordin, Frida, Stattin, Eva-Lena, Sobol, Maria, Baliakas, Panagiotis, Bondeson, Marie-Louise, Höijer, Ida, Saether, Kristine Bilgrav, Lovmar, Lovisa, Ehrencrona, Hans, Melin, Malin, Feuk, Lars och Lindstrand, Anna, A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities, Genome Research, 2024, 34 nr 11, s. 1774–1784, : Cold Spring Harbor Laboratory

ten Berk de Boer, Esmee, Lindstrand, A, Bunikis, Ignas, Ek, Marlene, Stattin, Eva-Lena, Feuk, Lars, Eisfeldt, Jesper och Lindstrand, Anna, Long-read sequencing and optical mapping generates near T2T assemblies that resolves a centromeric translocation, SCIENTIFIC REPORTS, 2024, 14 nr 1, : Springer Science and Business Media LLC

Eriksson, Daniel, Gyll, David, Virtanen, Marie, Dahl, Niklas, Klar, Joakim och Stattin, Eva Lena, Palmoplantar keratoderma and digital clubbing in 2 sisters with hypertrophic osteoarthropathy, Jaad Case Reports, 2023, 31, s. 133–136, : Elsevier

Janhager Stier, Jenny, Stattin, Eva och Larsen, Katarina, Innovation ecosystem challenges : – Experiences from socially critical digitalization projects, Proceedings of the XXXIV ISPIM Innovation Conference, 2023

Börjesson, Erik, Svennblad, Bodil, Wisten, Aase, Börjesson, Mats, Stattin, Eva-Lena och Stattin, Evalena, Symptoms and ECG changes precede sudden cardiac death in hypertrophic cardiomyopathy-A nationwide study among the young in Sweden., PloS one, 2022, 17 nr 9, : Public Library of Science (PLoS)

Delgado-Vega, Angelica Maria, Kommata, Varvara, Svennblad, Bodil, Wisten, Aase, Hagström, Emil, Stattin, Evalena och Stattin, Eva-Lena, Family History and Warning Symptoms Precede Sudden Cardiac Death in Arrhythmogenic Right Ventricular Cardiomyopathy (From A Nationwide Study in Sweden), American Journal of Cardiology, 2022, 178, s. 124–130, : Elsevier

Eisfeldt, J, Schuy, J, Stattin, Eva-Lena, Kvarnung, M, Falk, Anna, Feuk, Lars och Lindstrand, A, Multi-Omic Investigations of a 17–19 Translocation Links MINK1 Disruption to Autism, Epilepsy and Osteoporosis, International Journal of Molecular Sciences, 2022, 23 nr 16, : MDPI

Hopfgarten, Johan, Christersson, Christina, Forsblad, Johan, Stattin, Eva-Lena och Albåge, Anders, Spontaneous Coronary Artery Dissection and Papillary Muscle Rupture in Patient With Undiagnosed Vascular Ehler-Danlos Syndrome., JACC, 2022, 4 nr 14, s. 902–905, : Elsevier

Stattin, Evalena, Hagström, Emil, Dahl, Niklas, Strömsöe, Anneli, Delgado-Vega, Angelica Maria, Klar, Joakim, Svennblad, Bodil, Börjesson, Mats, Wisten, Aase och Stattin, Eva-Lena, Cohort profile: the Swedish study of SUDden cardiac Death in the Young (SUDDY) 2000–2010: a complete nationwide cohort of SCDs, Bmj Open, 2022, 12 nr 5, : BMJ

Stattin, Eva-Lena, Hagström, Emil, Dahl, Niklas, Strömsöe, Anneli, Delgado-Vega, Angelica Maria, Klar, Joakim, Svennblad, Bodil, Börjesson, Mats och Wisten, Aase, Cohort profile : the Swedish study of SUDden cardiac Death in the Young (SUDDY) 2000–2010, BMJ Open, 2022, 12 nr 5, : BMJ Publishing Group Ltd

Stattin, Eva-Lena, Lindblom, Karin, Struglics, André, Önnerfjord, Patrik, Goldblatt, Jack, Dixit, Abhijit, Sarkar, Ajoy, Randell, Tabitha, Suri, Mohnish, Raggio, Cathleen, Davis, Jessica, Carter, Erin, Aspberg, Anders och Stattin, Evalena, Novel missense ACAN gene variants linked to familial osteochondritis dissecans cluster in the C-terminal globular domain of aggrecan, Scientific Reports, 2022, 12, s. 1–13, : Nature Publishing Group

Boberg, Nils, De Jong, Annelise, Emilsson, Erik och Stattin, Eva, Digitaliseringens möjligheter inom avfallsanläggningar – System som optimerar och skapar nya värden och smart teknik banar väg för effektiva lösningar, 2021, IVL Svenska Miljöinstitutet

Lennartsson, Otto, Lodefalk, Maria, Wehtje, Henrik, Stattin, Eva-Lena, Sävendahl, Lars, Nilsson, Ola och Stattin, Evalena, Case Report : Bilateral Epiphysiodesis Due to Extreme Tall Stature in a Girl With a De Novo DNMT3A Variant Associated With Tatton-Brown-Rahman Syndrome, Frontiers in Endocrinology, 2021, 12, : Frontiers Media S.A.

Ahlm, Maria, Stattin, Eva och Wohlén, Mattias, Digitala informationsflöden i byggprocessen – Vilka värden kan ett obrutet informationsflöde mellan material, tillverkare och fastighetsägare skapa?, 2020, IVL Svenska Miljöinstitutet

Green, Jeanette, Ejlertsson, Anders, Görman, Frida, Sandkvist, Filip, Stattin, Eva och Wohlén, Mattias, Loggbok för ett obrutet flöde av miljöinformation – Nya arbetssätt genom digitala ekosystem, blockkedja och digitala tvillingar., 2020, IVL Svenska Miljöinstitutet

Sundblom, Jimmy, Niemelä, Valter, Ghazarian, Maria, Strand, Ann-Sofi, Bergdahl, Ingvar A., Jansson, Jan-Håkan, Söderberg, Stefan och Stattin, Eva-Lena, High frequency of intermediary alleles in the HTT gene in Northern Sweden – The Swedish Huntingtin Alleles and Phenotype (SHAPE) study, Scientific Reports, 2020, 10 nr 1, : Nature Publishing Group

Clewemar, Pantelis, Hailer, Nils P., Hailer, Yasmin, Klar, Joakim, Kindmark, Andreas, Ljunggren, Östen och Stattin, Eva-Lena, Expanding the phenotypic spectrum of osteogenesis imperfecta type V including heterotopic ossification of muscle origins and attachments, Molecular Genetics & Genomic Medicine, 2019, 7 nr 7, : Wiley