Charlotta Ingvoldstad Malmgren

Publikationer
CV
Populärvetenskap och samverkan

Utvalda publikationer

Conference publication: EUROPEAN NEUROPSYCHOPHARMACOLOGY. 2022;63:E314
STATE-OF-THE-ART OF GENETIC TESTING, COUNSELLING AND TRAINING IN PSYCHIATRY IN EUROPE: OPPORTUNITIES AND PITFALLS OF THE IMPLEMENTATION OF PSYCHIATRIC GENETICS IN MEDICAL PRACTICE
Koido K; Ingvoldstad-Malmgren C; Pojskic L; Soller MJ; Van Assche E; Borg I; Jensen UB; Coviello D; Rietschel M; Grigoroiu-Serbanescu M; McQuillin A; Degenhardt F; Tammimies K; Chaumette B
Article: PRENATAL DIAGNOSIS. 2022;42(7):934-946
Factor's that impact on women's decision-making around prenatal genomic tests: An international discrete choice survey
Buchanan J; Hill M; Vass CM; Hammond J; Riedijk S; Klapwijk JE; Harding E; Lou S; Vogel I; Hui L; Ingvoldstad-Malmgren C; Soller MJ; Ormond KE; Choolani M; Zheng Q; Chitty LS; Lewis C
Article: PLOS ONE. 2022;17(1):e0261898
Assessing women's preferences towards tests that may reveal uncertain results from prenatal genomic testing: Development of attributes for a discrete choice experiment, using a mixed-methods design
Hammond J; Klapwijk JE; Riedijk S; Lou S; Ormond KE; Vogel I; Hui L; Sziepe E-J; Buchanan J; Ingvoldstad-Malmgren C; Soller MJ; Harding E; Hill M; Lewis C
Article: GENOME MEDICINE. 2021;13(1):92
Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries
Milne R; Morley KI; Almarri MA; Anwer S; Atutornu J; Baranova EE; Bevan P; Cerezo M; Cong Y; Costa A; Critchley C; Fernow J; Goodhand P; Hasan Q; Hibino A; Houeland G; Howard HC; Hussain SZ; Malmgren CI; Izhevskaya VL; Jedrzejak A; Jinhong C; Kimura M; Kleiderman E; Leach B; Liu K; Mascalzoni D; Mendes A; Minari J; Nicol D; Niemiec E; Patch C; Pollard J; Prainsack B; Riviere M; Robarts L; Roberts J; Romano V; Sheerah HA; Smith J; Soulier A; Steed C; Stefansdottir V; Tandre C; Thorogood A; Voigt TH; Wang N; West AV; Yoshizawa G; Middleton A
Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2020;107(4):743-752
Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?
Middleton A; Milne R; Almarri MA; Anwer S; Atutornu J; Baranova EE; Bevan P; Cerezo M; Cong Y; Critchley C; Fernow J; Goodhand P; Hasan Q; Hibino A; Houeland G; Howard HC; Hussain SZ; Malmgren CI; Izhevskaya VL; Jedrzejak A; Cao J; Kimura M; Kleiderman E; Leach B; Liu K; Mascalzoni D; Mendes A; Minari J; Wang N; Nicol D; Niemiec E; Patch C; Pollard J; Prainsack B; Riviere M; Robarts L; Roberts J; Romano V; Sheerah HA; Smith J; Soulier A; Steed C; Stefansdottir V; Tandre C; Thorogood A; Voigt TH; West AV; Yoshizawa G; Morley KI
Article: JOURNAL OF COMMUNITY GENETICS. 2020;11(1):113-117
Developing a national certification pathway for genetic counselors in Sweden-a short report
Pestoff R; Svensson K; Paneque M; Malmgren CI
Review: AMERICAN JOURNAL OF MEDICAL GENETICS, PART B: NEUROPSYCHIATRIC GENETICS. 2019;180(8):523-532
Psychiatric genetic counseling: A mapping exercise
Moldovan R; McGhee KA; Coviello D; Hamang A; Inglis A; Ingvoldstad Malmgren C; Johansson-Soller M; Laurino M; Meiser B; Murphy L; Paneque M; Papsuev O; Pawlak J; Rovira Moreno E; Serra-Juhe C; Shkedi-Rafid S; Laing N; Voelckel M-A; Watson M; Austin JC
Review: EUROPEAN JOURNAL OF HUMAN GENETICS. 2019;27(2):183-197
The Global State of the Genetic Counseling Profession
Abacan M; Alsubaie L; Barlow-Stewart K; Caanen B; Cordier C; Courtney E; Davoine E; Edwards J; Elackatt NJ; Gardiner K; Guan Y; Huang L-H; Malmgren CI; Kejriwal S; Kim HJ; Lambert D; Lantigua-Cruz PA; Lee JMH; Lodahl M; Lunde A; Macaulay S; Macciocca I; Margarit S; Middleton A; Moldovan R; Ngeow J; Obregon-Tito AJ; Ormond KE; Paneque M; Powell K; Sanghavi K; Scotcher D; Scott J; Juhe CS; Shkedi-Rafid S; Wessels T-M; Yoon S-Y; Wicklund C
Article: CLINICAL GENETICS. 2018;93(4):891-898
How practical experiences, educational routes and multidisciplinary teams influence genetic counselors' clinical practice in Europe
Pestoff R; Moldovan R; Cordier C; Serra-Juhe C; Paneque M; Ingvoldstad CM
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2017;25(8):918-923
Complementarity between medical geneticists and genetic counsellors: its added value in genetic services in Europe
Paneque M; Serra-Juhe C; Pestoff R; Cordier C; Silva J; Moldovan R; Ingvoldstad C
Article: JOURNAL OF COMMUNITY GENETICS. 2016;7(3):237-242
Why do pregnant women accept or decline prenatal diagnosis for Down syndrome?
Ternby E; Axelsson O; Annerén G; Lindgren P; Ingvoldstad C

Artiklar

Journal article: JOURNAL OF COMMUNITY GENETICS. 2024;:1-11
Factors influencing pregnant women's decision to accept or decline prenatal screening and diagnosis - a qualitative study
Ternby E; Axelsson O; Malmgren CI; Georgsson S
Article: PRENATAL DIAGNOSIS. 2024;44(4):480-491
Pregnant women's informational needs prior to decisions about prenatal diagnosis for chromosomal anomalies-A Q methodological study
Ternby E; Axelsson O; Georgsson S; Malmgren CI
Article: EUROPEAN JOURNAL OF MEDICAL GENETICS. 2023;66(8):104805
Lack of guidelines and translational knowledge is hindering the implementation of psychiatric genetic counseling and testing within Europe-A multi-professional survey study
Koido K; Malmgren CI; Pojskic L; Almos PZ; Bergen SE; Borg I; Bozina N; Coviello DA; Degenhardt F; Ganoci L; Jensen UB; Durand-Lennad L; Laurent-Levinson C; McQuillin A; Navickas A; Pace NP; Paneque M; Rietschel M; Grigoroiu-Serbanescu M; Soller MJ; Suvisaari J; Utkus A; Van Assche E; Vissouze L; Zuckerman S; Chaumette B; Tammimies K
Journal article: EUROPEAN NEUROPSYCHOPHARMACOLOGY. 2022;63:e271-e272
STATE-OF-THE-ART IN EUROPEAN-WIDE GENETIC TESTING AND COUNSELLING IN PSYCHIATRY
Malmgren CI; Chaumette B; Pojskic L; Koido K; Soller MJ; Tammimies K
Article: GENETICS IN MEDICINE. 2022;24(5):1120-1129
Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries
Milne R; Morley KI; Almarri MA; Atutornu J; Baranova EE; Bevan P; Cerezo M; Cong Y; Costa A; Feijao C; de Freitas C; Fernow J; Goodhand P; Hasan Q; Hibino A; Houeland G; Howard HC; Sheikh ZH; Malmgren CI; Izhevskaya VL; Jedrzejak A; Cao J; Kimura M; Kleiderman E; Liu K; Mascalzoni D; Mendes A; Minari J; Nicol D; Niemiec E; Patch C; Prainsack B; Riviere M; Robarts L; Roberts J; Romano V; Sheerah HA; Smith J; Soulier A; Steed C; Stefansdottir V; Tandre C; Thorogood A; Voigt TH; Wang N; Yoshizawa G; Middleton A
Article: PRENATAL DIAGNOSIS. 2021;41(6):720-732
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionals
Lewis C; Hammond J; Klapwijk JE; Harding E; Lou S; Vogel I; Szepe EJ; Hui L; Ingvoldstad-Malmgren C; Soller MJ; Ormond KE; Choolani M; Hill M; Riedijk S
Journal article: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2019;54(S1):98
OP05.01: High risk: what's next? Decisional conflict, regret and satisfaction among pregnant women making choices about further prenatal testing
Hartwig TS; Miltoft CB; Ingvoldstad C; Tabor A; Joergensen FS
Article: PRENATAL DIAGNOSIS. 2019;39(8):635-642
High risk-What's next? A survey study on decisional conflict, regret, and satisfaction among high-risk pregnant women making choices about further prenatal testing for fetal aneuploidy.
Hartwig TS; Borregaard Miltoft C; Malmgren CI; Tabor A; Jørgensen FS
Article: ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. 2017;96(10):1243-1250
Information about first-trimester screening and self-reported distress among pregnant women and partners - comparing two methods of information giving in Sweden
Lindgren P; Stadin M; Blomberg I; Nordin K; Sahlgren H; Malmgren CI
Article: NURSING AND HEALTH SCIENCES. 2017;19(3):294-300
Educational needs of nurses to provide genetic services in prenatal care: A cross-sectional study from Turkey
Seven M; Eroglu K; Akyuz A; Ingvoldstad C
Article: LAKARTIDNINGEN. 2017;114:EHTE
[NIPT – implentation, counselling and ethical issues].
Ingvoldstad Malmgren C; Iwarsson E; Juth N; Lindgren P
Journal article: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2016;48(S1):167-168
P01.03: Reasons for pregnant women to accept or decline prenatal diagnosis for Down's syndrome
Ingvoldstad C; Ternby E; Axelsson O; Lindgren P; Anneren G
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2016;24(3):350-355
Genetic counsellors in Sweden: their role and added value in the clinical setting
Pestoff R; Ingvoldstad C; Skirton H
Article: JOURNAL OF GENETIC COUNSELING. 2016;25(1):146-156
Swedish University Students' Opinion Regarding Information About Soft Markers
Roshanai AH; Lindgren P; Nordin K; Ingvoldstad C
Article: PRENATAL DIAGNOSIS. 2015;35(12):1202-1207
Midwives and information on prenatal testing with focus on Down syndrome
Ternby E; Ingvoldstad C; Anneren G; Axelsson O
Article: ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. 2015;94(3):329-332
Information and knowledge about Down syndrome among women and partners after first trimester combined testing
Ternby E; Ingvoldstad C; Anneren G; Lindgren P; Axelsson O
Article: ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. 2015;94(2):141-147
Fetal ultrasound examination and assessment of genetic soft markers in Sweden: are ethical principles respected?
Roshanai AH; Ingvoldstad C; Lindgren P
Article: ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. 2014;93(9):868-873
Implementation of combined ultrasound and biochemistry for risk evaluation of chromosomal abnormalities during the first trimester in Sweden
Ingvoldstad C; Ohman SG; Lindgren P
Journal article: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2014;44(S1):181
P01.03: Women and partners coming for a first trimester combined (CUB) test; why they choose it, how are they informed, knowledge about Down's syndrome and their plans if Down's syndrome is diagnosed
Ingvoldstad C; Ternby E; Lindgren P; Anneren G; Axelsson O
Journal article: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2014;44(S1):176-177
OP35.03: Information, handling and documentation of soft markers; does lack of national guidelines hampers the equality of health in Sweden?
Ingvoldstad C; Roshanai AH; Lindgren P
Journal article: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2014;44(S1):177
OP35.04: Swedish university students' opinion regarding information about soft markers: which information do they wish?
Ingvoldstad C; Roshanai AH; Nordin K; Lindgren P
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2013;21(10):1060-1066
A Delphi study to determine the European core curriculum for Master programmes in genetic counselling.
Skirton H; Barnoy S; Ingvoldstad C; van Kessel I; Patch C; O'Connor A; Serra-Juhe C; Stayner B; Voelckel M-A
Article: JOURNAL OF COMMUNITY GENETICS. 2012;3(4):323-329
Suggested components of the curriculum for nurses and midwives to enable them to develop essential knowledge and skills in genetics.
Skirton H; Barnoy S; Erdem Y; Ingvoldstad C; Pestoff R; Teksen F; Williams J
Article: JOURNAL OF GENETIC COUNSELING. 2012;21(4):510-526
What Information Do Cancer Genetic Counselees Prioritize?
Roshanai AH; Lampic C; Ingvoldstad C; Askmalm MS; Bjorvatn C; Rosenquist R; Nordin K
Article: RNA: A PUBLICATION OF THE RNA SOCIETY. 2000;6(3):311-324
An unusual structure formed by antisense-target RNA binding involves an extended kissing complex with a four-way junction and a side-by-side helical alignment.
Kolb FA; Malmgren C; Westhof E; Ehresmann C; Ehresmann B; Wagner EG; Romby P
Article: JOURNAL OF BIOLOGICAL CHEMISTRY. 1997;272(19):12508-12512
Antisense RNA control of plasmid R1 replication. The dominant product of the antisense rna-mrna binding is not a full RNA duplex.
Malmgren C; Wagner EG; Ehresmann C; Ehresmann B; Romby P
Journal article: MOLECULAR MICROBIOLOGY. 1994;12(1):49-60
Replication control of plasmid R1: disruption of an inhibitory RNA structure that sequesters the repA ribosome-binding site permits tap-independent RepA synthesis.
Blomberg P; Engdahl HM; Malmgren C; Romby P; Wagner EG
Journal article: GENOME RESEARCH. 1992;2(2):175-176
Reliable typing of DNA amplified from formalin-fixed tissue biopsies.
Malmgren C; Gustavsson I; Hurte I; Saldeen T; Gyllensten U
Visa fler

Alla övriga publikationer

Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2022;30(SUPPL 1):53
Women's preferences for receiving uncertain results from prenatal genomic testing: An international discrete choice experiment
Lewis C; Buchanan J; Hammond J; Riedijk S; Klapwijk J; Harding E; Lou S; Vogel I; Szepe EJ; Hui L; Ingvoldstad-Malmgren C; Soller MJ; Ormond KE; Choolani M; Hill M
Meeting abstract: EUROPEAN PSYCHIATRY. 2021;64:S50
How to do genetic counseling in psychiatry?
Soller MJ; Moldovan R; Malmgren CI; Cuthbert A; Rietschel M
Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2020;28(SUPPL 1):768-769
Creating an Master of Science in Genetic counselling in Sweden that fulfils EBMG-criteria
Pestoff R; Soderkvist P; Malmgren CI
Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2019;27:670
An alternative pathway for countries without a training program for genetic counsellors: the Swedish experience
Svensson K; Pestoff R; Paneque M; Ingvoldstad CM
Other: LAKARTIDNINGEN. 2017;114:ERHT
Replik från SFOG: - Ultraljud och NIPT till alla är önskvärt, men inte realistiskt.
Lindgren P; Ingvoldstad Malmgren C; Juth N; Iwarsson E; Herbst A; Jacobsson B
Review: JOURNAL OF COMMUNITY GENETICS. 2016;7(2):107-118
Components of genetic counsellor education: A systematic review of the peer-reviewed literature.
Ingvoldstad C; Seven M; Taris N; Cordier C; Paneque M; Skirton H
Review: EUROPEAN JOURNAL OF HUMAN GENETICS. 2015;23(4):452-458
The role of the genetic counsellor: a systematic review of research evidence.
Skirton H; Cordier C; Ingvoldstad C; Taris N; Benjamin C

Anställningar

Affiliated to research, Centrum för bioetik och forskningsetik, Centrum för bioetik och forskningsetik, Inst för folkhälso- och vårdvetenskap, Uppsala University, 2020-
genetisk vägledare, Center for Rare diseases, Clinical genetics, Karolinska University Hospital, 2019-
Genetisk Vägledare, Fosterdiagnostik, Karolinska university hospital, Center for fetal medicine, 2014-
Anknuten till Forskning, Molekylär medicin och kirurgi, Karolinska Institutet, 2022-2025

Examina och utbildning

Docent, medicinsk genetik, Karolinska Institutet, 2024
Certifierad genetisk vägledare enligt SFMG, Swedish Society for genetics and genomics, SFMG, 2020
Certifierad handledare i sorgebearbetning, Sorgebearbetning, Svenska institutet för sorgebearbetning, 2016
Magisterexamen i Genetisk vägledning, Genetisk vägledning, Inst. för folkhälso- och vårdvetenskap, Uppsala University, 2005
PhD, Mikrobiologi, The involvement of the structures of antisense RNA, target RNA, and their complexes in plasmid R1 copy number control, Dept of cell and molecular biology, Uppsala University, 2000
Fil. Kand, Biologi/Mikrobiologi, Uppsala University, 1995

Uppdrag i kommitté

Medlem, Program committee for the World congress of genetic counselling, https://coursesandconferences.wellcomeconnectingscience.org/event/world-congress-on-genetic-counselling-20231025/, 2020-
Ordförande, Etik och policygruppen inom SFMG, Svensk förening för medicinsk genetik och genomik, SFMG, 2020-
Ordförande, Snif- Svenskt nätverk för information kring fosterdiagnostik, http://www.snif.one/, 2015-
Ordförande, Utbildningsgruppen inom svensk förening för genetik och genomik, SFMG, https://sfmg.se/sfmg/utbildningsgrupp/, 2015-
Vice ordförande, Svensk förening för genetiska vägledare, Svensk förening för genetiska vägledare, SFGV, https://sfgv.n.nu/, 2007-

Utvalda publikationer

Artiklar

Alla övriga publikationer

Anställningar

Examina och utbildning

Uppdrag i kommitté

Nyheter från KI

Kalenderhändelser från KI