Erik Björck

Publikationer
CV
Populärvetenskap och samverkan

Artiklar

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: 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: 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: 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: 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: 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: 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: 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
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: HEREDITARY CANCER IN CLINICAL PRACTICE. 2018;16:16

A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families

Karimi M; von Salome J; Aravidis C; Silander G; Askmalm MS; Henriksson I; Gebre-Medhin S; Frodin J-E; Bjorck E; Lagerstedt-Robinson K; Lindblom A; Tham E
Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2016;99(5):1005-1014

Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement

Kapferer-Seebacher I; Pepin M; Werner R; Aitman TJ; Nordgren A; Stoiber H; Thielens N; Gaboriaud C; Amberger A; Schossig A; Gruber R; Giunta C; Bamshad M; Bjorck E; Chen C; Chitayat D; Dorschner M; Schmitt-Egenolf M; Hale CJ; Hanna D; Hennies HC; Heiss-Kisielewsky I; Lindstrand A; Lundberg P; Mitchell AL; Nickerson DA; Reinstein E; Rohrbach M; Romani N; Schmuth M; Silver R; Taylan F; Vandersteen A; Vandrovcova J; Weerakkody R; Yang M; Pope FM; Byers PH; Zschocke J
Article: BMC MEDICAL EDUCATION. 2016;16:197

To belong or not to belong: nursing students' interactions with clinical learning environments - an observational study

Liljedahl M; Bjorck E; Kalen S; Ponzer S; Laksov KB
Article: ANTICANCER RESEARCH. 2015;35(9):4813-4819

Predicting Outcome in Colonoscopic High-risk Surveillance

Forsberg AM; Hagel E; Jaramillo E; Rubio CA; Bjorck E; Lindblom A
Article: CLINICAL TEACHER. 2015;12(4):284-285

Participation in a clinical learning environment.

Liljedahl M; Boman LE; Björck E; Laksov KB
Article: SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY. 2015;50(7):866-874

Colonoscopy findings in high-risk individuals compared to an average-risk control population

Forsberg A; Kjellstrom L; Andreasson A; Jaramillo E; Rubio CA; Bjorck E; Agreus L; Talley NJ; Lindblom A
Article: JOURNAL OF INTERPROFESSIONAL CARE. 2015;29(2):156-158

Identifying keys to success in clinical learning: a study of two interprofessional learning environments

Laksov KB; Boman LE; Liljedahl M; Bjorck E
Article: FAMILIAL CANCER. 2012;11(3):355-362

Molecular characterization of parathyroid tumors from two patients with hereditary colorectal cancer syndromes

Andreasson A; Sulaiman L; do Vale S; Martins JM; Ferreira F; Miltenberger-Miltenyi G; Batista L; Haglund F; Bjorck E; Nilsson I-L; Hoog A; Larsson C; Juhlin CC
Article: LAKARTIDNINGEN. 2012;109(23-24):1167-1169

[Integrated teaching of ethics of value in the medical education].

Björck E; Juth N; Marions L
Article: SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY. 2012;47(2):184-190

Prevalence of colonic neoplasia and advanced lesions in the normal population: a prospective population-based colonoscopy study

Forsberg AM; Kjellstrom L; Agreus L; Andreasson AN; Nyhlin H; Talley NJ; Bjorck E
Article: JOURNAL OF OROFACIAL PAIN. 2012;26(4):307-314

Women with Ehlers-Danlos Syndrome Experience Low Oral Health Related Quality of Life

Berglund B; Bjorck E
Article: GYNECOLOGIC ONCOLOGY. 2011;121(3):462-465

Ovarian cancer linked to lynch syndrome typically presents as early-onset, non-serous epithelial tumors

Ketabi Z; Bartuma K; Bernstein I; Malander S; Gronberg H; Bjorck E; Holck S; Nilbert M
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2010;18(8):872-880

Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients

Hoornaert KP; Vereecke I; Dewinter C; Rosenberg T; Beemer FA; Leroy JG; Bendix L; Bjorck E; Bonduelle M; Boute O; Cormier-Daire V; De Die-Smulders C; Dieux-Coeslier A; Dollfus H; Elting M; Green A; Guerci VI; Hennekam RCM; Hilhorts-Hofstee Y; Holder M; Hoyng C; Jones KJ; Josifova D; Kaitila I; Kjaergaard S; Kroes YH; Lagerstedt K; Lees M; LeMerrer M; Magnani C; Marcelis C; Martorell L; Mathieu M; McEntagart M; Mendicino A; Morton J; Orazio G; Paquis V; Reish O; Simola KOJ; Smithson SF; Temple KI; Van Aken E; Van Bever Y; van den Ende J; Van Hagen JM; Zelante L; Zordania R; De Paepe A; Leroy BP; De Buyzere M; Coucke PJ; Mortier GR
Article: FAMILIAL CANCER. 2010;9(2):245-251

No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome

Vahteristo P; Koski TA; Naatsaari L; Kiuru M; Karhu A; Herva R; Sallinen S-L; Vierimaa O; Bjorck E; Richard S; Gardie B; Bessis D; Van Glabeke E; Blanco I; Houlston R; Senter L; Hietala M; Aittomaki K; Aaltonen LA; Launonen V; Lehtonen R
Article: ACTA OPHTHALMOLOGICA. 2009;87(6):659-665

Dystrophia Helsinglandica: a new type of hereditary corneal recurrent erosions with late subepithelial fibrosis

Hammar B; Bjorck E; Lind H; Lagerstedt K; Dellby A; Fagerholm P
Article: ACTA OPHTHALMOLOGICA. 2008;86(7):758-763

A new corneal disease with recurrent erosive episodes and autosomal-dominant inheritance

Hammar B; Bjorck E; Lagerstedt K; Dellby A; Fagerholm P
Article: CANCER GENETICS. 2008;183(2):83-88

Mutation screening of fumarate hydratase by multiplex ligation-dependent probe amplification:: detection of exonic deletion in a patient with leiomyomatosis and renal cell cancer

Ahvenainen T; Lehtonen HJ; Lehtonen R; Vahteristo P; Aittomaki K; Baynam G; Dommering C; Eng C; Gruber SB; Gronberg H; Harvima R; Herva R; Hietala M; Kujala M; Kaariainen H; Sunde L; Vierimaa O; Pollard PJ; Tomlinson IPM; Bjorck E; Aaltonen LA; Launonen V
Article: ARCHIVES OF NEUROLOGY. 2007;64(5):706-713

Hereditary spastic paraplegia 3A associated with axonal neuropathy

Ivanova N; Claeys KG; Deconinck T; Litvinenko I; Jordanova A; Auer-Grumbach M; Haberlova J; Lofgren A; Smeyers G; Nelis E; Mercelis R; Plecko B; Priller J; Zamecnik J; Ceulemans B; Erichsen AK; Bjorck E; Nicholson G; Sereda MW; Seeman P; Kremensky I; Mitev V; De Jonghe P
Article: INTERNATIONAL JOURNAL OF CANCER. 2006;118(8):2092-2097

Mantle cell lymphomas acquire increased expression of CCL4, CCL5 and 4-1BB-L implicated in cell survival

Ek S; Björck E; Högerkorp CM; Nordenskjöld M; Porwit-MacDonald A; Borrebaeck CAK
Article: BLOOD. 2005;105(7):2908-2915

High expression of cyclin B1 predicts a favorable outcome in patients with follicular lymphoma

Björck E; Ek S; Landgren O; Jerkeman M; Ehinger M; Björkholm M; Borrebaeck CAK; Porwit-MacDonald A; Nordenskjöld M
Article: EUROPEAN JOURNAL OF ENDOCRINOLOGY. 2005;152(3):459-470

Distinction in gene expression profiles demonstrated in parathyroid adenomas by high-density oligoarray technology

Forsberg L; Björck E; Hashemi J; Zedenius J; Höög A; Farnebo LO; Reimers M; Larsson C
Article: GENOME RESEARCH. 2004;14(9):1696-1703

Recurrent sites for new centromere seeding

Ventura M; Weigl S; Carbone L; Cardone MF; Misceo D; Teti M; D'Addabbo P; Wandall A; Björck E; de Jong PJ; She XW; Eichler EE; Archidiacono N; Rocchi M
Article: HAEMATOLOGICA. 2004;89(6):686-695

Increased expression of Ki-67 in mantle cell lymphoma is associated with de-regulation of several cell cycle regulatory components, as identified by global gene expression analysis

Ek S; Björck E; Porwit-MacDonald A; Nordenskjöld M; Borrebaeck CAK
Article: LEUKEMIA & LYMPHOMA. 2003;44(7):1229-1234

Molecular cytogenetic approach to the diagnosis of splenic lymphoma:: A case report of blastoid mantle cell lymphoma

Björck E; Landgren O; Schoumans J; Christensson B; Björkholm M; MacDonald AP; Nordenskjöld M
Article: BLOOD. 2003;101(10):4047-4054

Mutated V_H genes and preferential V_H3-21 use define new subsets of mantle cell lymphoma

Walsh SH; Thorsélius M; Johnson A; Söderberg O; Jerkernan M; Björck E; Eriksson I; Thunberg U; Landgren O; Ehinger M; Löfvenberg E; Wallman K; Enblad G; Sander B; Porwit-MacDonald A; Dictor M; Olofsson T; Sundström C; Roos G; Rosenquist R
Article: HUMAN MUTATION. 2000;16(6):509-517

Genetic variation in ICF syndrome:: Evidence for genetic heterogeneity

Wijmenga C; Hansen RS; Gimelli G; Björck EJ; Davies EG; Valentine D; Belohradsky BH; van Dongen JJ; Smeets DFCM; van den Heuvel LPWJ; Luyten JAFM; Strengman E; Weemaes C; Pearson PL
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2000;8(12):918-922

Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia

Jonasson J; Juvonen V; Sistonen P; Ignatius J; Johansson D; Björck EJ; Wahlström J; Melberg A; Holmgren G; Forsgren L; Holmberg M
Article: PRENATAL DIAGNOSIS. 2000;20(10):828-831

Early prenatal diagnosis of the ICF syndrome

Björck EJ; Bui TH; Wijmenga C; Grandell U; Nordenskjöld M
Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 1999;87(1):49-52

Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes:: i(9p) and i(9q)

Björck EJ; Anderlid BM; Blennow E
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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
Thesis / dissertation: 2005

Genetic studies of follicular and mantle cell lymphoma

Björck, Erik
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, 2024-2026

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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