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Liedén, Agne
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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

DNA Methylation Signature for JARID2-Neurodevelopmental Syn..:

Verberne, Eline A. ; van der Laan, Liselot ; Haghshenas, Sadegheh...
International Journal of Molecular Sciences.  23 (2022)  14 - p. 8001 , 2022
Link: https://doi.org/10.3390/..
 
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4

Cell-free tumour DNA analysis detects copy number alteratio..:

Wallander, Karin ; Eisfeldt, Jesper ; Lindblad, Mats...
PLOS ONE.  16 (2021)  2 - p. e0245488 , 2021
Link: https://doi.org/10.1371/..
 
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5

Ataxia in Patients With Bi-Allelic NFASC Mutations and Abse..:

Kvarnung, Malin ; Shahsavani, Mansoureh ; Taylan, Fulya...
Frontiers in Genetics.  10 (2019)  - p. , 2019
Link: https://doi.org/10.3389/..
 
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6

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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7

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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8

Replicative and non-replicative mechanisms in the formation..:

Nazaryan-Petersen, Lusine ; Eisfeldt, Jesper ; Pettersson, Maria...
PLOS Genetics.  14 (2018)  11 - p. e1007780 , 2018
Link: https://doi.org/10.1371/..
 
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9

TSHZ3 deletion causes an autism syndrome and defects in cor..:

Caubit, Xavier ; Gubellini, Paolo ; Andrieux, Joris...
Nature Genetics.  48 (2016)  11 - p. 1359-1369 , 2016
Link: https://doi.org/10.1038/..
 
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10

Deletion of Wiskott–Aldrich syndrome protein triggers Rac2 ..:

Baptista, Marisa A. P. ; Keszei, Marton ; Oliveira, Mariana...
Nature Communications.  7 (2016)  1 - p. , 2016
Link: https://doi.org/10.1038/..
 
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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

Whole-exome sequencing of Ethiopian patients with ichthyosi..:

Taylan, Fulya ; Nilsson, Daniel ; Asad, Samina...
Journal of Allergy and Clinical Immunology.  136 (2015)  2 - p. 507-509.e19 , 2015
Link: https://doi.org/10.1016/..
 
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13

Skin Barrier Function and Staphylococcus aureus Colonizatio..:

Berents, Teresa Løvold ; Carlsen, Karin Cecilie Lødrup ; Mowinckel, Petter...
PLOS ONE.  10 (2015)  6 - p. e0130145 , 2015
Link: https://doi.org/10.1371/..
 
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14

No evidence for mosaic pathogenic copy number variations in..:

Winberg, Johanna ; Berggren, Håkan ; Malm, Torsten...
European Journal of Medical Genetics.  58 (2015)  3 - p. 129-133 , 2015
Link: https://doi.org/10.1016/..
 
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15

Characterization of Stem-Like Cells in Mucoepidermoid Trach..:

Lim, Mei Ling ; Ooi, Brandon Nick Sern ; Jungebluth, Philipp...
PLoS ONE.  9 (2014)  9 - p. e107712 , 2014
Link: https://doi.org/10.1371/..
 
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