Erik Björck

Publikationer
CV
Populärvetenskap och samverkan

Artiklar

Article: GENOME MEDICINE. 2026;18(1):30
The genomic medicine center Karolinska 10-year report on genome sequencing for rare diseases and a strategy for stepwise clinical implementation
Lindstrand A; Lagerstedt-Robinson K; Jemt A; Kvarnung M; Ygberg S; Vonlanthen S; Oscarson M; Nilsson D; Lesko N; Mantero AS; Anderlid B-M; Arnell H; Arthur C; Bajalica-Lagercrantz S; Barbaro M; Bergman P; Bjorck E; Picard OB; Bruhn H; Carlsten J; Correia SP; De Geer K; Delgado Vega AM; Ehn E; Eisfeldt J; Ek M; Elvers I; Engvall M; Freyer C; Frisk S; Graff C; Grigelioniene G; Gustafsson P; Hammarsjo A; Helgadottir HT; Hellstrom Pigg M; Henry OJ; Hagglund M; Iwarsson E; Janvid V; Soller MJ; Sundin L; Kuchinskaya E; Kampe A; Leinfelt A; Lieden A; Lindelof H; Lyander A; Malmgren H; Mannila M; Marits P; Naess K; Neethiraj R; Nyren K; Pappas C; Paucar M; Pekkola Pacheco N; Pena Perez L; Pettersson M; Pruisscher P; Rasi C; Renevey A; Rossner S; Sahlin E; Stenund E; Stodberg T; Sundin M; Svard K; Tesi B; Tham E; Thonberg H; Tohonen V; Ueberschar M; Wallander K; Westenius E; Winberg J; Winblad N; Wincent J; Winerdal M; Wredenberg A; Zetterlund A; Zetterstrom RH; Ofverholm I; Nordgren A; Stranneheim H; Wirta V; Wedell A
Article: ACTA OPHTHALMOLOGICA. 2025;103(3):327-338
The value of age of onset and family history as predictors of molecular diagnosis in a Swedish cohort of inherited retinal disease
De Geer K; Lofgren S; Lindstrand A; Kvarnung M; Bjorck E
Article: BMC OPHTHALMOLOGY. 2023;23(1):394
Unraveling mucolipidosis type III gamma through whole genome sequencing in late-onset retinitis pigmentosa: a case report
De Geer K; Mascianica K; Naess K; Sardh E; Lindstrand A; Bjoerck E
Article: ADVANCES IN HEALTH SCIENCES EDUCATION. 2023;28(3):811-826
How workplace learning is put into practice: contrasting the medical and nursing contexts from the perspective of teaching and learning regimes
Liljedahl M; Bjorck E; Laksov KB
Article: MEDICAL EDUCATION. 2023;57(7):679-688
Faculty development participants' experiences of working with change in clinical settings
Elmberger A; Blitz J; Bjorck E; Nieminen J; Laksov KB
Article: FRONTIERS IN GENETICS. 2023;14:1136339
Non-oral manifestations in adults with a clinical and molecularly confirmed diagnosis of periodontal Ehlers-Danlos syndrome
Angwin C; Zschocke J; Kammin T; Bjorck E; Bowen J; Brady AF; Burns H; Cummings C; Gardner R; Ghali N; Groebner R; Harris J; Higgins M; Johnson D; Lepperdinger U; Milnes D; Pope FM; Sehra R; Kapferer-Seebacher I; Sobey G; Van Dijk FS
Article: EUROPEAN JOURNAL OF MEDICAL GENETICS. 2023;66(1):104673
HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD). A statement from the HTAD working group of VASCERN
Caruana M; Baars MJ; Bashiardes E; Benke K; Bjorck E; Codreanu A; de Moya Rubio E; Dumfarth J; Evangelista A; Groenink M; Kallenbach K; Kempers M; Keravnou A; Loeys B; Muino-Mosquera L; Nagy E; Milleron O; Nistri S; Pepe G; Roos-Hesselink J; Szabolcs Z; Teixido-Tura G; Timmermans J; Van de Laar I; van Kimmenade R; Verstraeten A; Von Kodolitsch Y; De Backer J; Jondeau G
Article: GENETICS IN MEDICINE. 2022;24(11):2296-2307
Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disability
Lindstrand A; Ek M; Kvarnung M; Anderlid B-M; Bjoerck E; Carlsten J; Eisfeldt J; Grigelioniene G; Gustavsson P; Hammarsjoe A; Helgadottir HT; Hellstroem-Pigg M; Kuchinskaya E; Lagerstedt-Robinson K; Levin L-A; Lieden A; Lindeloef H; Malmgren H; Nilsson D; Svensson E; Paucar M; Sahlin E; Tesi B; Tham E; Winberg J; Winerdal M; Wincent J; Soller MJ; Pettersson M; Nordgren A
Article: GENES CHROMOSOMES & CANCER. 2022;61(10):585-591
Merged testing for colorectal cancer syndromes and re-evaluation of genetic variants improve diagnostic yield: Results from a nationwide prospective cohort
Svensson S; Zagoras T; Aravidis C; Askmalm MS; Bjorck E; Borg A; Kuchinskaya E; Nilbert M; Nordling M; Rohlin A; Silander G; Lagerstedt-Robinson K; Gebre-Medhin S
Article: HIGHER EDUCATION RESEARCH & DEVELOPMENT. 2022;41(2):269-283
Shifting to team-based faculty development: a programme designed to facilitate change in medical education
Bolander Laksov K; Elmberger A; Liljedahl M; Bjorck E
Article: PLOS ONE. 2022;17(2):e0264056
A retrospective two centre study of Birt-Hogg-Dube syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population
Lagerstedt-Robinson K; Korberg IB; Tsiaprazis S; Bjorck E; Tham E; Poluha A; Pigg MH; Paulsson-Karlsson Y; Nordenskjold M; Johansson-Soller M; Aravidis C
Article: VOCATIONS AND LEARNING. 2022;15(3):427-448
Navigating Affordances for Learning in Clinical Workplaces: A Qualitative Study of General Practitioners' Continued Professional Development
Stabel LS; McGrath C; Bjorck E; Elmberger A; Laksov KB
Article: MOLECULAR CYTOGENETICS. 2021;14(1):30
Discordant structural chromosomal aberrations in chorionic villi and amniotic fluid leading to a formation of an isochromosome 21: a case report
Westenius E; Pettersson M; Bjorck E
Article: GENOME MEDICINE. 2021;13(1):40
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients
Stranneheim H; Lagerstedt-Robinson K; Magnusson M; Kvarnung M; Nilsson D; Lesko N; Engvall M; Anderlid B-M; Arnell H; Johansson CB; Barbaro M; Bjorck E; Bruhn H; Eisfeldt J; Freyer C; Grigelioniene G; Gustavsson P; Hammarsjo A; Hellstrom-Pigg M; Iwarsson E; Jemt A; Laaksonen M; Enoksson SL; Malmgren H; Naess K; Nordenskjold M; Oscarson M; Pettersson M; Rasi C; Rosenbaum A; Sahlin E; Sardh E; Stodberg T; Tesi B; Tham E; Thonberg H; Tohonen V; von Dobeln U; Vassiliou D; Vonlanthen S; Wikstrom A-C; Wincent J; Winqvist O; Wredenberg A; Ygberg S; Zetterstrom RH; Marits P; Soller MJ; Nordgren A; Wirta V; Lindstrand A; Wedell A
Article: HEREDITARY CANCER IN CLINICAL PRACTICE. 2021;19(1):18
Room for improvement: One third of Lynch syndrome patients presenting for genetic testing in a highly specialised centre in Stockholm already have cancer
Bernstedt SW; Bjork J; Fritzell K; Spigelman AD; Bjorck E; Backman A-S
Article: BMC MEDICAL EDUCATION. 2020;20(1):497
Collaborative knotworking - transforming clinical teaching practice through faculty development
Elmberger A; Bjorck E; Nieminen J; Liljedahl M; Bolander Laksov K
Article: ORPHANET JOURNAL OF RARE DISEASES. 2019;14(1):264
European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants
van de laar IMBH; Arbustini E; Loeys B; Bjorck E; Murphy L; Groenink M; Kempers M; Timmermans J; Roos-Hesselink J; Benke K; Pepe G; Mulder B; Szabolcs Z; Teixido-Tura G; Robert L; Emmanuel Y; Evangelista A; Pini A; von Kodolitsch Y; Jondeau G; De Backer J
Article: FRONTIERS IN IMMUNOLOGY. 2019;10:2537
C1R Mutations Trigger Constitutive Complement 1 Activation in Periodontal Ehlers-Danlos Syndrome
Groebner R; Kapferer-Seebacher I; Amberger A; Redolfi R; Dalonneau F; Bjorck E; Milnes D; Bally I; Rossi V; Thielens N; Stoiber H; Gaboriaud C; Zschocke J
Article: ADVANCES IN HEALTH SCIENCES EDUCATION. 2019;24(1):125-140
Contradictions in clinical teachers' engagement in educational development: an activity theory analysis
Elmberger A; Bjorck E; Liljedahl M; Nieminen J; Laksov KB
Article: STUDIES IN HIGHER EDUCATION. 2019;44(2):275-286
Navigating without a map: how medical students interact with clinical learning environments
Liljedahl M; Bjorck E; Ponzer S; Laksov KB
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Alla övriga publikationer

Review: DISEASES. 2026;14(3):91
First Reported Use of Recombinant Parathyroid Hormone in Kenny-Caffey Syndrome Type 2: A Case Report and Literature Review
Djordjevic Milosevic M; Skakic A; Andjelkovic M; Delgado-Vega AM; Thonberg H; Klaassen K; Komazec J; Kecman B; Jocic N; Bjorck E; Lindstrand A; Stojiljkovic M
Review: LAKARTIDNINGEN. 2021;118:21126
[Medical doctor specialists - an overview of the research on formal and informal continued professional development].
Sturesson Stabel L; McGrath C; Elmberger A; Bolander Laksov K; Björck E
Letter: INTERNATIONAL JOURNAL OF DERMATOLOGY. 2021;60(5):641-642
Schopf-Schulz-Passarge syndrome with multiple angiomas on the tongue: a new feature?
Trocoli Drakensjo I; Bjorck E; Bradley M; Hedblad M-A
Corrigendum: FRONTIERS IN IMMUNOLOGY. 2019;10:2837
C1R Mutations Trigger Constitutive Complement 1 Activation in Periodontal Ehlers-Danlos Syndrome (vol 10, 2537, 2019)
Grobner R; Kapferer-Seebacher I; Amberger A; Redolfi R; Dalonneau F; Bjorck E; Milnes D; Bally I; Rossi V; Thielens N; Stoiber H; Gaboriaud C; Zschocke J
Letter: AMERICAN JOURNAL OF HEMATOLOGY. 2018;93(8):E213-E215
Congenital dyserythropoietic anemia type 1: A case with novel compound heterozygous mutations in the C15orf41 gene
Palmblad J; Sander B; Bain B; Klimkowska M; Bjoerck E
Other: LAKARTIDNINGEN. 2018;115:E7MI
Replik gällande Lynchs syndrom: - Syftet var att öka medvetenheten.
Björck E; Walton Bernstedt S; Mints M; Björk J; Backman A-S
Review: LAKARTIDNINGEN. 2018;115:EY3C
[
Lynch syndrome is a major cause of monogenetic familial colorectal cancer
].
Walton Bernstedt S; Björk J; Mints M; Björck E; Backman A-S
Letter: JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY. 2015;29(1):185-187
Impaired wound healing and cheilitis in a Pachyonychia Congenita K6a family
Winge MCG; Bradley M; Bjorck E
Letter: BLOOD. 2013;121(23):4807
Development of Hodgkin lymphoma in homozygotic triplets with constitutional deletion in MKL1
Bjorkholm M; Sjoberg J; Nygell UA; Porwit A; Bjorck E
Review: LAKARTIDNINGEN. 2011;108(50):2657-2659
[Birth-Hogg-Dube syndrome--a neglected condition that increases the risk of kidney cancer and pneumothorax].
Bradley M; Hedblad M-A; Björck E; Nordenskjöld M
Letter: LEUKEMIA. 2011;25(5):868-872
HAX-1 expression in human B lymphoma
Kwiecinska A; Ottosson-Wadlund A; Ceder R; Grafstrom RC; Bjorck E; Nordenskjold M; Porwit A; Fadeel B
Published conference paper: JOURNAL OF INVESTIGATIVE DERMATOLOGY SYMPOSIUM PROCEEDINGS. 2005;10(1):21-30
The genetic basis of pachyonychia congenita
Smith FJD; Liao HH; Cassidy AJ; Stewart A; Hamill KJ; Wood P; Joval I; van Steensel MAM; Björck E; Callif-Daley F; Pals G; Collins P; Leachman SA; Munro CS; McLean WHI
Doctoral thesis: 2005
Genetic studies of follicular and mantle cell lymphoma
Björck E
Letter: EUROPEAN JOURNAL OF HAEMATOLOGY. 1996;56(5):323-325
Syndrome of inappropriate secretion of antidiuretic hormone (SIADH) after treatment with cyclophosphamide, alpha-interferon and betamethasone in a patient with multiple myeloma
Bjorck E; Samuelsson J

Anställningar

Adjungerad Lektor, Molekylär medicin och kirurgi, Karolinska Institutet, 2024-2028

Examina och utbildning

Docent, Medicinsk genetik, Karolinska Institutet, 2014
MEDICINE DOKTORSEXAMEN, Institutionen för molekylär medicin och kirurgi, Karolinska Institutet, 2005
Läkarexamen, Karolinska Institutet, 1993

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