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Sofie Samuelsson

Showing results (1-10 of 7) with videos related to

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European Journal of Human Genetics : EJHG|October 26, 2018
A stroke gene panel for whole-exome sequencingAndreea Ilinca, Sofie Samuelsson, Paul Piccinelli, et al.
Neurology. Genetics|March 17, 2021
<i>MAP3K6</i> Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and TremorAndreea Ilinca, Elisabet Englund, Sofie Samuelsson, et al.
International Journal of Pediatric Otorhinolaryngology|July 2, 2022
Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementationJohanna Elander, Tove Ullmark, Hans Ehrencrona, et al.
Stroke|March 17, 2020
Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of StrokeAndreea Ilinca, Nicolas Martinez-Majander, Sofie Samuelsson, et al.
European Journal of Medical Genetics|February 24, 2019
Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinismHenrik Thybo Christesen, Lene Gaarsmand Christensen, Åsa Mattsson Löfgren, et al.
JCO Precision Oncology|June 29, 2023
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With CancerElisabeth Wadensten, Sandra Wessman, Frida Abel, et al.
The Lancet Regional Health. Europe|May 28, 2024
Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors-a nationwide, prospective Swedish studyBianca Tesi, Kristina Lagerstedt Robinson, Frida Abel, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
European Journal of Human Genetics : EJHG|October 26, 2018
A stroke gene panel for whole-exome sequencingAndreea Ilinca, Sofie Samuelsson, Paul Piccinelli, et al.
Neurology. Genetics|March 17, 2021
<i>MAP3K6</i> Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and TremorAndreea Ilinca, Elisabet Englund, Sofie Samuelsson, et al.
International Journal of Pediatric Otorhinolaryngology|July 2, 2022
Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementationJohanna Elander, Tove Ullmark, Hans Ehrencrona, et al.
Stroke|March 17, 2020
Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of StrokeAndreea Ilinca, Nicolas Martinez-Majander, Sofie Samuelsson, et al.
European Journal of Medical Genetics|February 24, 2019
Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinismHenrik Thybo Christesen, Lene Gaarsmand Christensen, Åsa Mattsson Löfgren, et al.
JCO Precision Oncology|June 29, 2023
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With CancerElisabeth Wadensten, Sandra Wessman, Frida Abel, et al.
The Lancet Regional Health. Europe|May 28, 2024
Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors-a nationwide, prospective Swedish studyBianca Tesi, Kristina Lagerstedt Robinson, Frida Abel, et al.
Pageof 1