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Reka Kovacs-Nagy

Showing results (1-10 of 21) with videos related to

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Electrophoresis|May 11, 2011
Haplotyping of putative microRNA-binding sites in the SNAP-25 geneReka Kovacs-Nagy, Peter Sarkozy, Jimmy Hu, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 8, 2013
Association of aggression with a novel microRNA binding site polymorphism in the wolframin geneReka Kovacs-Nagy, Zsuzsanna Elek, Anna Szekely, et al.
Neuropediatrics|September 11, 2018
A De Novo Missense Variant in POU3F2 Identified in a Child with Global Developmental DelayDominik Sebastian Westphal, Korbinian Maria Riedhammer, Reka Kovacs-Nagy, et al.
Frontiers in Pediatrics|December 12, 2017
Identification of a Novel Heterozygous <i>De Novo</i> 7-bp Frameshift Deletion in <i>PBX1</i> by Whole-Exome Sequencing Causing a Multi-Organ Syndrome Including Bilateral Dysplastic Kidneys and Hypoplastic ClaviclesKorbinian Maria Riedhammer, Corinna Siegel, Bader Alhaddad, et al.
Neuropediatrics|November 24, 2020
Thiamine Pyrophosphokinase Deficiency due to Mutations in the TPK1 Gene: A Rare, Treatable Neurodegenerative DisorderChristina T Rüsch, Saskia B Wortmann, Reka Kovacs-Nagy, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 29, 2014
Glycogen synthase kinase 3 beta gene structural variants as possible risk factors of bipolar depressionZsolt Ronai, Reka Kovacs-Nagy, Eszter Szantai, et al.
The International Journal of Clinical and Experimental Hypnosis|May 29, 2010
Association between hypnotizability and the catechol-O-methyltransferase (COMT) polymorphismAnna Szekely, Reka Kovacs-Nagy, Eva I Bányai, et al.
BMC Medical Genetics|August 21, 2009
Association of hypoxia inducible factor-1 alpha gene polymorphism with both type 1 and type 2 diabetes in a Caucasian (Hungarian) sampleGeza Nagy, Reka Kovacs-Nagy, Eva Kereszturi, et al.
Neuropediatrics|September 16, 2017
Biallelic Mutations in SLC1A2; an Additional Mode of Inheritance for SLC1A2-Related EpilepsyMatias Wagner, Mirjana Gusic, Roman Günthner, et al.
Neuropediatrics|August 17, 2018
HTRA2 Defect: A Recognizable Inborn Error of Metabolism with 3-Methylglutaconic Aciduria as Discriminating Feature Characterized by Neonatal Movement Disorder and Epilepsy-Report of 11 PatientsReka Kovacs-Nagy, Gilles Morin, Maria Al Nouri, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Electrophoresis|May 11, 2011
Haplotyping of putative microRNA-binding sites in the SNAP-25 geneReka Kovacs-Nagy, Peter Sarkozy, Jimmy Hu, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 8, 2013
Association of aggression with a novel microRNA binding site polymorphism in the wolframin geneReka Kovacs-Nagy, Zsuzsanna Elek, Anna Szekely, et al.
Neuropediatrics|September 11, 2018
A De Novo Missense Variant in POU3F2 Identified in a Child with Global Developmental DelayDominik Sebastian Westphal, Korbinian Maria Riedhammer, Reka Kovacs-Nagy, et al.
Frontiers in Pediatrics|December 12, 2017
Identification of a Novel Heterozygous <i>De Novo</i> 7-bp Frameshift Deletion in <i>PBX1</i> by Whole-Exome Sequencing Causing a Multi-Organ Syndrome Including Bilateral Dysplastic Kidneys and Hypoplastic ClaviclesKorbinian Maria Riedhammer, Corinna Siegel, Bader Alhaddad, et al.
Neuropediatrics|November 24, 2020
Thiamine Pyrophosphokinase Deficiency due to Mutations in the TPK1 Gene: A Rare, Treatable Neurodegenerative DisorderChristina T Rüsch, Saskia B Wortmann, Reka Kovacs-Nagy, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 29, 2014
Glycogen synthase kinase 3 beta gene structural variants as possible risk factors of bipolar depressionZsolt Ronai, Reka Kovacs-Nagy, Eszter Szantai, et al.
The International Journal of Clinical and Experimental Hypnosis|May 29, 2010
Association between hypnotizability and the catechol-O-methyltransferase (COMT) polymorphismAnna Szekely, Reka Kovacs-Nagy, Eva I Bányai, et al.
BMC Medical Genetics|August 21, 2009
Association of hypoxia inducible factor-1 alpha gene polymorphism with both type 1 and type 2 diabetes in a Caucasian (Hungarian) sampleGeza Nagy, Reka Kovacs-Nagy, Eva Kereszturi, et al.
Neuropediatrics|September 16, 2017
Biallelic Mutations in SLC1A2; an Additional Mode of Inheritance for SLC1A2-Related EpilepsyMatias Wagner, Mirjana Gusic, Roman Günthner, et al.
Neuropediatrics|August 17, 2018
HTRA2 Defect: A Recognizable Inborn Error of Metabolism with 3-Methylglutaconic Aciduria as Discriminating Feature Characterized by Neonatal Movement Disorder and Epilepsy-Report of 11 PatientsReka Kovacs-Nagy, Gilles Morin, Maria Al Nouri, et al.
Pageof 3