Julia Stellmachova

Affiliations

Department of Medical Genetics, Faculty of Medicine and Dentistry, Palacký University Olomouc, Olomouc, Czechia.

Publications (6)

Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development.

Frontiers in neuroscience

Avec: Kristyna Kolarikova , Radek Vodicka , Radek Vrtel , Julia Stellmachova , Martin Prochazka , Katerina Mensikova , Petr Kanovsky

Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms.

Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia

Avec: Petr Vrtel , Radek Vrtel , Eva Klaskova , Dita Vrbicka , Katerina Adamova , Jan Pavlicek , Vaclav Hana , Vaclav Hana , Ondrej Soucek , Veronika Stara , Jan Lebl , Marta Snajdrova , Jirina Zapletalova , Tomas Furst , Sabina Kapralova , Zdenek Tauber , Eva Krejcirikova , Marketa Routilova , Julia Stellmachova , Radek Vodicka , Martin Prochazka

High-Throughput Sequencing Haplotype Analysis Indicates in

Life (Basel, Switzerland)

Avec: Kristyna Kolarikova , Radek Vodicka , Radek Vrtel , Julia Stellmachova , Martin Prochazka , Katerina Mensikova , Tereza Bartonikova , Tomas Furst , Petr Kanovsky , Jan Geryk

SPG11: clinical and genetic features of seven Czech patients and literature review.

Neurological research

Avec: Kristyna Doleckova , Jan Roth , Julia Stellmachova , Tomas Gescheidt , Vladimir Sigut , Pavel Houska , Robert Jech , Michael Zech , Martin Vyhnalek , Emilie Vyhnalkova , Pavel Seeman , Anna Uhrova Meszarosova

Two types of recessive hereditary spastic paraplegia in Roma patients in compound heterozygous state; no ethnically prevalent variant found.

Neuroscience letters

Avec: Anna Uhrova Meszarosova , Pavel Seeman , Jan Jencik , Jana Drabova , Renata Cibochova , Julia Stellmachova , Dana Safka Brozkova

Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing.

Diagnostics (Basel, Switzerland)

Avec: Petr Vrtel , Ludek Slavik , Radek Vodicka , Julia Stellmachova , Martin Prochazka , Jana Prochazkova , Jana Ulehlova , Peter Rohon , Tomas Simurda , Jan Stasko , Ivana Martinkova , Radek Vrtel

Réseau de co-auteurs

Radek Vodicka 4 collaborations

Radek Vrtel 4 collaborations

Martin Prochazka 4 collaborations

Kristyna Kolarikova 2 collaborations

Katerina Mensikova 2 collaborations

Petr Kanovsky 2 collaborations

Petr Vrtel 2 collaborations

Vaclav Hana 2 collaborations

Tomas Furst 2 collaborations

Pavel Seeman 2 collaborations

Anna Uhrova Meszarosova 2 collaborations

Eva Klaskova 1 collaboration

Dita Vrbicka 1 collaboration

Katerina Adamova 1 collaboration

Jan Pavlicek 1 collaboration

Ondrej Soucek 1 collaboration

Veronika Stara 1 collaboration

Jan Lebl 1 collaboration

Marta Snajdrova 1 collaboration

Jirina Zapletalova 1 collaboration

Sabina Kapralova 1 collaboration

Zdenek Tauber 1 collaboration

Eva Krejcirikova 1 collaboration

Marketa Routilova 1 collaboration

Tereza Bartonikova 1 collaboration

Jan Geryk 1 collaboration

Kristyna Doleckova 1 collaboration

Jan Roth 1 collaboration

Tomas Gescheidt 1 collaboration

Vladimir Sigut 1 collaboration

Pavel Houska 1 collaboration

Robert Jech 1 collaboration

Michael Zech 1 collaboration

Martin Vyhnalek 1 collaboration

Emilie Vyhnalkova 1 collaboration

Jan Jencik 1 collaboration

Jana Drabova 1 collaboration

Renata Cibochova 1 collaboration

Dana Safka Brozkova 1 collaboration

Ludek Slavik 1 collaboration

Jana Prochazkova 1 collaboration

Jana Ulehlova 1 collaboration

Peter Rohon 1 collaboration

Tomas Simurda 1 collaboration

Jan Stasko 1 collaboration

Ivana Martinkova 1 collaboration