Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Christian Liebst Frisk Toft"'
Autor:
Line Dahl Jeppesen, Dorte Launholt Lildballe, Lotte Hatt, Jakob Hedegaard, Ripudaman Singh, Christian Liebst Frisk Toft, Palle Schelde, Anders Sune Pedersen, Michael Knudsen, Ida Vogel
Publikováno v:
Jeppesen, L D, Lildballe, D L, Hatt, L, Hedegaard, J, Singh, R, Toft, C L F, Schelde, P, Pedersen, A S, Knudsen, M & Vogel, I 2023, ' Noninvasive prenatal screening for cystic fibrosis using circulating trophoblasts : Detection of the 50 most common disease-causing variants ', Prenatal Diagnosis, vol. 43, no. 1, pp. 3-13 . https://doi.org/10.1002/pd.6276
OBJECTIVES: Cystic fibrosis (CF) is one of the most common severe autosomal recessive disorders. Prenatal or preconception CF screening is offered in some countries. A maternal blood sample in early pregnancy can provide circulating trophoblasts and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65c69e4474a5ec00a55d1968248f3fff
https://vbn.aau.dk/ws/files/510206222/Jeppesen_et_al_2023_Noninvasive_prenatal_screening_for_cystic_fibrosis_using_circulating_trophoblasts.pdf
https://vbn.aau.dk/ws/files/510206222/Jeppesen_et_al_2023_Noninvasive_prenatal_screening_for_cystic_fibrosis_using_circulating_trophoblasts.pdf
Autor:
Lotte Hatt, Bolette Hestbek Nicolaisen, Helle Mogensen, Steffen Sommer, Palle Schelde, Ida Vogel, Inge Søkilde Pedersen, Mathias Kølvraa, Henrik Okkels, Christian Liebst Frisk Toft, Ulrik Schiøler Kesmodel, Richard Farlie, Line Dahl Jeppesen, Anja Ernst, Inga Baasch Christensen, Birte Degn, Katarina Ravn, Hans Jakob Ingerslev, Kristín Rós Kjartansdóttir, Marianne Louise Vang Østergård, Niels Uldbjerg, Ripudaman Singh, Ann Nygaard Jensen
Publikováno v:
Toft, C L F, Ingerslev, H J, Kesmodel, U S, Hatt, L, Singh, R, Ravn, K, Nicolaisen, B H, Christensen, I B, Kølvraa, M, Jeppesen, L D, Schelde, P, Vogel, I, Uldbjerg, N, Farlie, R, Sommer, S, Østergård, M L V, Jensen, A N, Mogensen, H, Kjartansdóttir, K R, Degn, B, Okkels, H, Ernst, A & Pedersen, I S 2021, ' Cell-based non-invasive prenatal testing for monogenic disorders : confirmation of unaffected fetuses following preimplantation genetic testing ', Journal of Assisted Reproduction and Genetics, vol. 38, no. 8, pp. 1959-1970 . https://doi.org/10.1007/s10815-021-02104-5
Journal of Assisted Reproduction and Genetics
Journal of Assisted Reproduction and Genetics
Purpose Proof of concept of the use of cell-based non-invasive prenatal testing (cbNIPT) as an alternative to chorionic villus sampling (CVS) following preimplantation genetic testing for monogenic disorders (PGT-M). Method PGT-M was performed by com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2edcf80da04180683417130d568d9cb
https://doi.org/10.1007/s10815-021-02104-5
https://doi.org/10.1007/s10815-021-02104-5
Autor:
Christian Liebst Frisk Toft, Nehal Adel, Caroline Nørgaard-Pedersen, SUJAN CHATTERJEE, Ulla Christensen, Luís Crisóstomo, Fereshteh Dardmeh, Julie Forman, Zorana Jovanovic Andersen, Malene Møller Jørgensen
Publikováno v:
Human Reproduction. 35:i1-i522
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98ae82383147a6e0676de211920257df
https://doi.org/10.1093/humrep/35.supplement_1.1
https://doi.org/10.1093/humrep/35.supplement_1.1
Autor:
Kristina, Løssl, Jane Gasseholm, Bentzen, Morten Rønn, Petersen, Laura Sønderberg, Roos, Kristín Rós, Kjartansdóttir, Marie Louise, Grøndahl, Bettina, Troest, Christian Liebst Frisk, Toft, Inge Søkilde, Pedersen, Tue, Diemer, Hans Jakob, Ingerslev
Publikováno v:
Ugeskrift for laeger. 183(48)
Preimplantation genetic testing (PGT) for known familial monogenetic disease (PGT-M) or structural chromosomal rearrangements (PGT-SR) has evolved into a well-established alternative to prenatal diagnosis. PGT significantly reduces the risk of a preg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::11810a02d1be2a953a08a80186dcf873
https://pubmed.ncbi.nlm.nih.gov/34852911
https://pubmed.ncbi.nlm.nih.gov/34852911
Autor:
Kristine Løssl, Janne Gasseholm Bentzen, Morten Rønn Petersen, Laura Kirstine Sønderberg Roos, Kristín Rós Kjartansdóttir, Marie Louise Grøndahl, Bettina Troest, Christian Liebst Frisk Toft, Inge Søkilde Pedersen, Tue Diemer, Hans Jakob Ingerslev
Publikováno v:
Løssl, K, Bentzen, J G, Petersen, M R, Roos, L K S, Kjartansdóttir, K R, Grøndahl, M L, Troest, B, Toft, C L F, Pedersen, I S, Diemer, T & Ingerslev, H J 2021, ' Præimplantationsgenetisk testning ', Ugeskrift for Laeger, bind 183, V04210378 . < https://ugeskriftet-dk.auh.aub.aau.dk/videnskab/praeimplantationsgenetisk-testning >
Løssl, K, Bentzen, J G, Petersen, M R, Roos, L S, Kjartansdóttir, K R, Grøndahl, M L, Troest, B, Toft, C L F, Pedersen, I S, Diemer, T & Ingerslev, H J 2021, ' Præimplantationsgenetisk testning ', Ugeskrift for Laeger, bind 183, nr. 23, V04210378 .
Aalborg University
Løssl, K, Bentzen, J G, Petersen, M R, Roos, L S, Kjartansdóttir, K R, Grøndahl, M L, Troest, B, Toft, C L F, Pedersen, I S, Diemer, T & Ingerslev, H J 2021, ' Præimplantationsgenetisk testning ', Ugeskrift for Laeger, bind 183, nr. 23, V04210378 .
Aalborg University
Preimplantation genetic testing (PGT) for known familial monogenetic disease (PGT-M) or structural chromosomal rearrangements (PGT-SR) has evolved into a well-established alternative to prenatal diagnosis. PGT significantly reduces the risk of a preg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::76e671b279632613f83c9663b692a8df
https://vbn.aau.dk/da/publications/b51df972-1ee8-4791-81bc-58cf6878fbeb
https://vbn.aau.dk/da/publications/b51df972-1ee8-4791-81bc-58cf6878fbeb
Autor:
Tue Diemer, Inge Søkilde Pedersen, Ulrik Schiøler Kesmodel, Henrik Okkels, Kristín Rós Kjartansdóttir, Birte Degn, Anja Ernst, Hans Jakob Ingerslev, Christian Liebst Frisk Toft
Publikováno v:
Toft, C L F, Ingerslev, H J, Kesmodel, U S, Diemer, T, Degn, B, Ernst, A, Okkels, H, Kjartansdóttir, K R & Pedersen, I S 2020, ' A systematic review on concurrent aneuploidy screening and preimplantation genetic testing for hereditary disorders : What is the prevalence of aneuploidy and is there a clinical effect from aneuploidy screening? ', Acta Obstetricia et Gynecologica Scandinavica, vol. 99, no. 6, pp. 696-706 . https://doi.org/10.1111/aogs.13823
INTRODUCTION: In assisted reproductive technology, aneuploidy is considered a primary cause of failed embryo implantation. This has led to the implementation of preimplantation genetic testing for aneuploidy in some clinics. The prevalence of aneuplo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::535cc618940dc7f3e864e92020f6a09a
https://vbn.aau.dk/da/publications/8b6be070-88fe-4cdc-866e-f3cea9e28d66
https://vbn.aau.dk/da/publications/8b6be070-88fe-4cdc-866e-f3cea9e28d66
Autor:
Viktoria, Holmqvist, Laura Kristine Soenderberg, Roos, Kristin Ros, Kjartansdottir, Morten, Dunø, Morten Rønn, Petersen, Christina, Hnida, Inge Søkilde, Pedersen, Anja, Ernst, Christian Liebst Frisk, Toft, Tue, Diemer, Hans Jakob, Ingerslev, Anja, Pinborg, Kristine, Løssl
Publikováno v:
Ugeskrift for laeger. 181(20)
This review summarises the current knowledge on preimplantation genetic testing for aneuploidy (PGT-A). Selection and transfer of euploid embryos aim to improve live birth rate (LBR) per embryo transfer, but fluorescence in situ hybridisation-based P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f117b0d125471414d5de6db2d6ea9c2d
https://pubmed.ncbi.nlm.nih.gov/31124451
https://pubmed.ncbi.nlm.nih.gov/31124451
Autor:
Viktoria Holmqvist, Laura Kristine Soenderberg Roos, Kristin Ros Kjartansdottir, Morten Dunø, Christina Hnida, Inge Søkilde Pedersen, Anja Ernst, Christian Liebst Frisk Toft, Tue Diemer, Hans Jakob Ingerslev, Anja Pinborg, Kristine Løssl
Publikováno v:
Holmqvist, V, Roos, L K S, Kjartansdottir, K R, Dunø, M, Hnida, C, Pedersen, I S, Ernst, A, Toft, C L F, Diemer, T, Ingerslev, H J, Pinborg, A & Løssl, K 2019, ' Præimplantationsgenetisk testning for aneuploidi ', Ugeskrift for Laeger, bind 181, nr. 20, V12180849 . < https://ugeskriftet.dk/videnskab/praeimplantationsgenetisk-testning-aneuploidi >
Aalborg University
Aalborg University
This review summarises the current knowledge on preimplantation genetic testing for aneuploidy (PGT-A). Selection and transfer of euploid embryos aim to improve live birth rate (LBR) per embryo transfer, but fluorescence in situ hybridisation-based P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::95b07aade039c23fe8e570946fdfdc64
https://vbn.aau.dk/da/publications/93496bcc-6440-4fa1-9e5e-975212249395
https://vbn.aau.dk/da/publications/93496bcc-6440-4fa1-9e5e-975212249395
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Linneberg, C, Toft, C L F, Kjaer-Sorensen, K & Laursen, L S 2019, ' L1cam-mediated developmental processes of the nervous system are differentially regulated by proteolytic processing ', Scientific Reports, vol. 9, 3716 . https://doi.org/10.1038/s41598-019-39884-x
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Linneberg, C, Toft, C L F, Kjaer-Sorensen, K & Laursen, L S 2019, ' L1cam-mediated developmental processes of the nervous system are differentially regulated by proteolytic processing ', Scientific Reports, vol. 9, 3716 . https://doi.org/10.1038/s41598-019-39884-x
Normal brain development depends on tight temporal and spatial regulation of connections between cells. Mutations in L1cam, a member of the immunoglobulin (Ig) superfamily that mediate cell-cell contacts through homo- and heterophilic interactions, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f9501353627a74c7af58fd3f0ad98c8
https://pubmed.ncbi.nlm.nih.gov/30842511
https://pubmed.ncbi.nlm.nih.gov/30842511
Autor:
Christian Liebst Frisk Toft, Hans Jakob Ingerslev, Henrik Okkels, Christina Hnida, Inge Søkilde Pedersen, Tue Diemer, Anja Ernst, Birte Degn
Publikováno v:
Reproductive BioMedicine Online. 39:e52
Introduction Preimplantation genetic testing (PGT) is divided into three categories based on the indication: PGT-M (Monogenic), PGT-SR (Structural rearrangements) and PGT-A (Aneuploidy). A large study of more than 15000 trophectoderm biopsies found t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60d00390a31b85ae10208d9b1dd33737
https://doi.org/10.1016/j.rbmo.2019.04.094
https://doi.org/10.1016/j.rbmo.2019.04.094