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

Factors 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; Jędrzejak A; Jinhong C; Kimura M; Kleiderman E; Leach B; Liu K; Mascalzoni D; Mendes Á; Minari J; Nicol D; Niemiec E; Patch C; Pollard J; Prainsack B; Rivière M; Robarts L; Roberts J; Romano V; Sheerah HA; Smith J; Soulier A; Steed C; Stefànsdóttir 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; Jędrzejak A; Jinhong C; Kimura M; Kleiderman E; Leach B; Liu K; Mascalzoni D; Mendes Á; Minari J; Wang N; Nicol D; Niemiec E; Patch C; Pollard J; Prainsack B; Rivière M; Robarts L; Roberts J; Romano V; Sheerah HA; Smith J; Soulier A; Steed C; Stefànsdóttir 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 Å; 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; Juhé 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-Juhé 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-Juhé 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

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; Božina 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; Hussain Sheikh Z; Malmgren CI; Izhevskaya VL; Jędrzejak A; Jinhong C; Kimura M; Kleiderman E; Liu K; Mascalzoni D; Mendes Á; Minari J; Nicol D; Niemiec E; Patch C; Prainsack B; Rivière M; Robarts L; Roberts J; Romano V; Sheerah HA; Smith J; Soulier A; Steed C; Stefànsdóttir 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 & 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; Ingvoldstad Malmgren C
Article: NURSING & 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; Akyüz 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 & 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; Annerén 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; Annerén 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?

Hayat Roshanai A; 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; Georgsson Öhman S; Lindgren P
Journal article: ULTRASOUND IN OBSTETRICS & 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
Journal article: ULTRASOUND IN OBSTETRICS & 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 & 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
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?

Hayat Roshanai A; Lampic C; Ingvoldstad C; Askmalm MS; Bjorvatn C; Rosenquist R; Nordin K
Journal article: RNA. 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
Journal 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
Letter: 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

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

Ordförande, Etik och policygruppen inom SFMG, Svensk förening för medicinsk genetik och genomik, SFMG, 2020
Medlem, Program committee for the World congress of genetic counselling, https://coursesandconferences.wellcomeconnectingscience.org/event/world-congress-on-genetic-counselling-20231025/, 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