Ellika Sahlin

Publications
CV
Public outreach and news

Articles

Article: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2024;63(5):658-663
Whole-genome sequencing in prenatally detected congenital malformations: prospective cohort study in clinical setting
Westenius E; Conner P; Pettersson M; Sahlin E; Papadogiannakis N; Lindstrand A; Iwarsson E
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: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2022;60(4):487-493
Diagnostic yield using whole-genome sequencing and in-silico panel of 281 genes associated with non-immune hydrops fetalis in clinical setting
Westenius E; Sahlin E; Conner P; Lindstrand A; Iwarsson E
Article: HEREDITARY CANCER IN CLINICAL PRACTICE. 2021;19(1):23
Massive parallel sequencing in a family with rectal cancer
Wallander K; Thutkawkorapin J; Sahlin E; Lindblom A; Lagerstedt-Robinson K
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: EBIOMEDICINE. 2020;59:102872
Fetal HLA-G mediated immune tolerance and interferon response in preeclampsia
Wedenoja S; Yoshihara M; Teder H; Sariola H; Gissler M; Katayama S; Wedenoja J; Hakkinen IM; Ezer S; Linder N; Lundin J; Skoog T; Sahlin E; Iwarsson E; Pettersson K; Kajantie E; Mokkonen M; Heinonen S; Laivuori H; Krjutskov K; Kere J
Article: MOLECULAR GENETICS & GENOMIC MEDICINE. 2020;8(2):e1084
Pathogenic copy number variants are detected in a subset of patients with gastrointestinal malformations
Winberg J; Gustavsson P; Sahlin E; Larsson M; Ehren H; Fossum M; Wester T; Nordgren A; Nordenskjold A
Article: GENOME MEDICINE. 2019;11(1):68
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability
Lindstrand A; Eisfeldt J; Pettersson M; Carvalho CMB; Kvarnung M; Grigelioniene G; Anderlid B-M; Bjerin O; Gustavsson P; Hammarsjo A; Georgii-Hemming P; Iwarsson E; Johansson-Soller M; Lagerstedt-Robinson K; Lieden A; Magnusson M; Martin M; Malmgren H; Nordenskjold M; Norling A; Sahlin E; Stranneheim H; Tham E; Wincent J; Ygberg S; Wedell A; Wirta V; Nordgren A; Lundin J; Nilsson D
Article: PLOS ONE. 2019;14(1):e0210017
Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirth
Sahlin E; Green A; Gustavsson P; Lieden A; Nordenskjold M; Papadogiannakis N; Pettersson K; Nilsson D; Jonasson J; Iwarsson E
Article: JOURNAL OF GENETIC COUNSELING. 2017;26(3):447-454
Knowledge and Attitudes Regarding Non-Invasive Prenatal Testing (NIPT) and Preferences for Risk Information among High School Students in Sweden
Georgsson S; Sahlin E; Iwarsson M; Nordenskjold M; Gustavsson P; Iwarsson E
Article: PLOS ONE. 2016;11(5):e0156088
Positive Attitudes towards Non-Invasive Prenatal Testing (NIPT) in a Swedish Cohort of 1,003 Pregnant Women
Sahlin E; Nordenskjold M; Gustavsson P; Wincent J; Georgsson S; Iwarsson E
Article: ACTA PAEDIATRICA, INTERNATIONAL JOURNAL OF PAEDIATRICS. 2015;104(6):610-618
Rare copy number variants are common in young children with autism spectrum disorder
Eriksson MA; Lieden A; Westerlund J; Bremer A; Wincent J; Sahlin E; Gillberg C; Fernell E; Anderlid B-M
Article: GENOMICS. 2015;105(3):150-158
Amplification-free sequencing of cell-free DNA for prenatal non-invasive diagnosis of chromosomal aberrations
Karlsson K; Sahlin E; Iwarsson E; Westgren M; Nordenskjold M; Linnarsson S
Article: PLOS ONE. 2015;10(4):e0123343
Fetal Calcifications Are Associated with Chromosomal Abnormalities
Sahlin E; Sirotkina M; Marnerides A; Iwarsson E; Papadogiannakis N
Article: AMERICAN JOURNAL OF MEDICAL GENETICS, PART A. 2014;164(12):3083-3087
Intragenic Duplication-A Novel Causative Mechanism for SATB2-Associated Syndrome
Lieden A; Kvarnung M; Nilssson D; Sahlin E; Lundberg ES
Article: FETAL DIAGNOSIS AND THERAPY. 2014;36(4):326-332
Molecular and Cytogenetic Analysis in Stillbirth: Results from 481 Consecutive Cases
Sahlin E; Gustavsson P; Lieden A; Papadogiannakis N; Bjareborn L; Pettersson K; Nordenskjold M; Iwarsson E
Article: PLOS ONE. 2014;9(1):e85313
Mutation Screening and Array Comparative Genomic Hybridization Using a 180K Oligonucleotide Array in VACTERL Association
Winberg J; Gustavsson P; Papadogiannakis N; Sahlin E; Bradley F; Nordenskjold E; Svensson P-J; Anneren G; Iwarsson E; Nordgren A; Nordenskjold A

All other publications

Letter: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2022;60(4):586
Prenatal diagnosis of non-immune hydrops fetalis: whole-exome sequencing or whole-genome sequencing? Reply
Westenius E; Sahlin E; Conner P; Lindstrand A; Iwarsson E
Letter: ULTRASOUND IN OBSTETRICS AND GYNECOLOGY. 2022;60(4):585-586
Prenatal diagnosis of non-immune hydrops fetalis: whole-exome sequencing or whole-genome sequencing?
Westenius E; Sahlin E; Conner P; Lindstrand A; Iwarsson E
Thesis / dissertation: 2016
New molecular tools for prenatal diagnosis
Sahlin, Ellika

Employments

Affiliated to Research, Department of Molecular Medicine and Surgery, Karolinska Institutet, 2022-2025

Degrees and Education

Degree Of Doctor Of Philosophy, Department of Molecular Medicine and Surgery, Karolinska Institutet, 2016
Degree Of Bachelor Of Medical Science, Karolinska Institutet, 2010

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