̽»¨¾«Ñ¡

Charlotta Ingvoldstad Malmgren

Charlotta Ingvoldstad Malmgren

Affiliated to Research | Docent
Visiting address: ̽»¨¾«Ñ¡, BioClinicum J10:20, Visionsgatan 4, 17164 Solna
Postal address: K1 Molekylär medicin och kirurgi, K1 MMK Sällsynta diagnoser, 171 76 Stockholm
Part of:

About me

  • I work in the field of genetic counselling which is the process of helping people understand and adapt to the ̽»¨¾«Ñ¡, psychological and familial implications of genetic contributions to disease as well as helping individuals to reflect about the ethical aspects and own values related to genetics and genomics and the genetic conditions, thereby facilitating for individuals to make informed choices about i.e. genetic testing, manangement of results and coping with the situation. I meet patients mostly in the process of prenatal diagnosis and decisions on pregnancy, when a diagnosis of genetic condition is known. In summary, ethical aspects of genetics, genomics and genetic counselling are in main area of interest, together with patient engagemang, public awareness and education. Besides my clinical work as a Genetic counsellor, I work with education/teaching and research in different areas related to genetics, genetic counselling and ethics.
    I am also the chair of the Swedish network on information about prenatal diagnosis, Snif (www.snif.one) who’s aim is to create high quality information about prenatal diagnosis and conditions looked for and to increase the ethical awareness and discussions around prenatal diagnosis in society. I am also chair if the Ethic and policy group of the Swedish Society of genetics and genomics, SFMG.

    In combination with my background with a PhD in molecular biology my passion is human genetics and how the genetics might affect individuals and their families both genetically, relationally and psychosocially.

Research

  • One of my main focuses of research is the field of prenatal diagnosis- informational needs, genetic counselling, informed choice, uncertainties and ethics. Another of my main areas of research is related to the definition, education, role and implementation of the role of genetic counsellors in various settings. I am also involved in research related to psychiatric genetic counselling and ethics.
    An additional field of research is related to patient and public attitudes towards genetics and genomics as well as genomic data sharing.

Teaching

  • I teach many different subjects within the the field of genetic counselling in various settings, both at University courses in Genetic counselling as well as CDP courses for healthcare professionals (Doctors, Midwives and genetic counsellors)
    I have developed and co-developed courses at Uppsala University and Lund University in genetic counselling. I was also part of a small group who developed a ST-course in genetic counselling for becoming interns to be specialists in Clinical genetics.

Selected publications

  • Conference publication: EUROPEAN NEUROPSYCHOPHARMACOLOGY. 2022;63:E314
    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
    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
    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
    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
    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
    Pestoff R; Svensson K; Paneque M; Malmgren CI
  • Review: AMERICAN JOURNAL OF MEDICAL GENETICS, PART B: NEUROPSYCHIATRIC GENETICS. 2019;180(8):523-532
    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
    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
    Pestoff R; Moldovan R; Cordier C; Serra-Juhe C; Paneque M; Ingvoldstad CM
  • Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2017;25(8):918-923
    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
    Ternby E; Axelsson O; Annerén G; Lindgren P; Ingvoldstad C

Articles

  • Journal article: JOURNAL OF COMMUNITY GENETICS. 2024;15(6):711-721
    Ternby E; Axelsson O; Malmgren CI; Georgsson S
  • Article: PRENATAL DIAGNOSIS. 2024;44(4):480-491
    Ternby E; Axelsson O; Georgsson S; Malmgren CI
  • Article: EUROPEAN JOURNAL OF MEDICAL GENETICS. 2023;66(8):104805
    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
    Malmgren CI; Chaumette B; Pojskic L; Koido K; Soller MJ; Tammimies K
  • Article: GENETICS IN MEDICINE. 2022;24(5):1120-1129
    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
    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
    Hartwig TS; Miltoft CB; Ingvoldstad C; Tabor A; Joergensen FS
  • Article: PRENATAL DIAGNOSIS. 2019;39(8):635-642
    Hartwig TS; Borregaard Miltoft C; Malmgren CI; Tabor A; Jørgensen FS
  • Article: ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. 2017;96(10):1243-1250
    Lindgren P; Stadin M; Blomberg I; Nordin K; Sahlgren H; Malmgren CI
  • Article: NURSING AND HEALTH SCIENCES. 2017;19(3):294-300
    Seven M; Eroglu K; Akyuz A; Ingvoldstad C
  • Article: LAKARTIDNINGEN. 2017;114:EHTE
    Ingvoldstad Malmgren C; Iwarsson E; Juth N; Lindgren P
  • Journal article: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2016;48(S1):167-168
    Ingvoldstad C; Ternby E; Axelsson O; Lindgren P; Anneren G
  • Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2016;24(3):350-355
    Pestoff R; Ingvoldstad C; Skirton H
  • Article: JOURNAL OF GENETIC COUNSELING. 2016;25(1):146-156
    Roshanai AH; Lindgren P; Nordin K; Ingvoldstad C
  • Article: PRENATAL DIAGNOSIS. 2015;35(12):1202-1207
    Ternby E; Ingvoldstad C; Anneren G; Axelsson O
  • Article: ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. 2015;94(3):329-332
    Ternby E; Ingvoldstad C; Anneren G; Lindgren P; Axelsson O
  • Article: ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. 2015;94(2):141-147
    Roshanai AH; Ingvoldstad C; Lindgren P
  • Article: ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. 2014;93(9):868-873
    Ingvoldstad C; Ohman SG; Lindgren P
  • Journal article: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2014;44(S1):181
    Ingvoldstad C; Ternby E; Lindgren P; Anneren G; Axelsson O
  • Journal article: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2014;44(S1):176-177
    Ingvoldstad C; Roshanai AH; Lindgren P
  • Show more

All other publications

  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2022;30(SUPPL 1):53
    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
    Soller MJ; Moldovan R; Malmgren CI; Cuthbert A; Rietschel M
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2020;28(SUPPL 1):768-769
    Pestoff R; Soderkvist P; Malmgren CI
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2019;27:670
    Svensson K; Pestoff R; Paneque M; Ingvoldstad CM
  • Other: LAKARTIDNINGEN. 2017;114:ERHT
    Lindgren P; Ingvoldstad Malmgren C; Juth N; Iwarsson E; Herbst A; Jacobsson B
  • Review: JOURNAL OF COMMUNITY GENETICS. 2016;7(2):107-118
    Ingvoldstad C; Seven M; Taris N; Cordier C; Paneque M; Skirton H
  • Review: EUROPEAN JOURNAL OF HUMAN GENETICS. 2015;23(4):452-458
    Skirton H; Cordier C; Ingvoldstad C; Taris N; Benjamin C

Employments

  • Affiliated to research, Center for research ethics and bioethics, Center for research ethics and bioethics, dept. of public health and caring science, Uppsala University, 2020-
  • Genetic counsellor at center for Rare diseases, Center for Rare diseases, Clinical genetics, Karolinska University Hospital, 2019-
  • Genetic counsellor at Center for fetal medicine, Prenatal diagnosis, Karolinska university hospital, Center for fetal medicine, 2014-
  • Affiliated to Research, Department of Molecular Medicine and Surgery, ̽»¨¾«Ñ¡, 2022-2025

Degrees and Education

  • Docent, Medical Genetics, ̽»¨¾«Ñ¡, 2024
  • Certified genetic counsellor by SFMG, Swedish Society for genetics and genomics, SFMG, 2020
  • Certified supervisor in grief bereavment, Grief bereavment, Swedish institute for grief bereavment, 2016
  • Master degree in genetic counselling, Genetic counselling, Department of public health and caring Science, Uppsala University, 2005
  • PhD, Microbiology, 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
  • Bachelor of Science, Science in Biology/Microbiology, Uppsala University, 1995

Committee work

  • Chair, Ethics and policy group (EoP) of Swedish society for ̽»¨¾«Ñ¡ genetics and genomics, SFMG, Swedish Society for ̽»¨¾«Ñ¡ genetics and genomics, SFMG, 2020-
  • Member, Program committee for the World congress of genetic counselling, , 2020-
  • Chair, Snif- Swedish network for information about prental diagnosis, , 2015-
  • Chair, Educational group within the Swedish Society for ̽»¨¾«Ñ¡ genetics and genomics, SFMG, , 2015-
  • Vice chair, Swedish Society for genetic counsellors, SFGV, Swedish Society for genetic counsellors. SFGV, , 2007-

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