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Sahlin, Ellika
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1

Genome sequencing is a sensitive first-line test to diagnos..:

Lindstrand, Anna ; Ek, Marlene ; Kvarnung, Malin...
Pathology.  55 (2023)  - p. S19-S20 , 2023
Link: https://doi.org/10.1016/..
 
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2

Genome sequencing is a sensitive first-line test to diagnos..:

Lindstrand, Anna ; Ek, Marlene ; Kvarnung, Malin...
Genetics in Medicine.  24 (2022)  11 - p. 2296-2307 , 2022
Link: https://doi.org/10.1016/..
 
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3

Massive parallel sequencing in a family with rectal cancer:

Wallander, Karin ; Thutkawkorapin, Jessada ; Sahlin, Ellika..
Hereditary Cancer in Clinical Practice.  19 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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4

Fetal HLA-G mediated immune tolerance and interferon respon..:

Wedenoja, Satu ; Yoshihara, Masahito ; Teder, Hindrek...
eBioMedicine.  59 (2020)  - p. 102872 , 2020
Link: https://doi.org/10.1016/..
 
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5

Identification of putative pathogenic single nucleotide var..:

Sahlin, Ellika ; Gréen, Anna ; Gustavsson, Peter...
PLOS ONE.  14 (2019)  1 - p. e0210017 , 2019
Link: https://doi.org/10.1371/..
 
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6

From cytogenetics to cytogenomics: whole-genome sequencing ..:

Lindstrand, Anna ; Eisfeldt, Jesper ; Pettersson, Maria...
Genome Medicine.  11 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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7

Pathogenic copy number variants are detected in a subset of..:

Winberg, Johanna ; Gustavsson, Peter ; Sahlin, Ellika...
Molecular Genetics & Genomic Medicine.  8 (2019)  2 - p. , 2019
Link: https://doi.org/10.1002/..
 
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8

Positive Attitudes towards Non-Invasive Prenatal Testing (N..:

Sahlin, Ellika ; Nordenskjöld, Magnus ; Gustavsson, Peter...
PLOS ONE.  11 (2016)  5 - p. e0156088 , 2016
Link: https://doi.org/10.1371/..
 
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9

Knowledge and Attitudes Regarding Non‐Invasive Prenatal Tes..:

Georgsson, Susanne ; Sahlin, Ellika ; Iwarsson, Moa...
Journal of Genetic Counseling.  26 (2016)  3 - p. 447-454 , 2016
Link: https://doi.org/10.1007/..
 
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10

Amplification-free sequencing of cell-free DNA for prenatal..:

Karlsson, Kasper ; Sahlin, Ellika ; Iwarsson, Erik...
Genomics.  105 (2015)  3 - p. 150-158 , 2015
Link: https://doi.org/10.1016/..
 
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11

Rare copy number variants are common in young children with..:

Eriksson, Mats Anders ; Liedén, Agne ; Westerlund, Joakim...
Acta Paediatrica.  104 (2015)  6 - p. 610-618 , 2015
Link: https://doi.org/10.1111/..
 
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12

Fetal Calcifications Are Associated with Chromosomal Abnorm..:

Sahlin, Ellika ; Sirotkina, Meeli ; Marnerides, Andreas...
PLOS ONE.  10 (2015)  4 - p. e0123343 , 2015
Link: https://doi.org/10.1371/..
 
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13

Intragenic duplication—A novel causative mechanism for SATB..:

Liedén, Agne ; Kvarnung, Malin ; Nilssson, Daniel..
American Journal of Medical Genetics Part A.  164 (2014)  12 - p. 3083-3087 , 2014
Link: https://doi.org/10.1002/..
 
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14

Mutation Screening and Array Comparative Genomic Hybridizat..:

Winberg, Johanna ; Gustavsson, Peter ; Papadogiannakis, Nikos...
PLoS ONE.  9 (2014)  1 - p. e85313 , 2014
Link: https://doi.org/10.1371/..
 
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15

Genome sequencing is a sensitive first-line test to diagnos..:

Lindstrand, Anna ; Ek, Marlene ; Kvarnung, Malin...
Genetics in Medicine, 1098-3600, 2022, 24:11, s. 2296-2307.  , 2022
Link: http://urn.kb.se/resolve..
 
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