Jorune Balciuniene - Concepedia

Concepedia

Author

Jorune Balciuniene

Children's Hospital of Philadelphia ORCID

Also Known As

Caleb Bupp, J Balciuniene, J. Balciuniene, Jorune Balciuniene

67

Publications

1.8K

Citations

26

H-Index

118

Concepts

All Affiliations

Children's Hospital of Philadelphia Temple University University of Pennsylvania Uppsala University University of Minnesota

JB

About

Jorune Balciuniene is an author at Children's Hospital of Philadelphia specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	24	1.2K
2	Arts	3	3	159
3	Engineering	1	1	69
4	Health Sciences	1	1	13
5	Natural Sciences	1	1	26

Jorune Balciuniene

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37

Publications

1.8K

Citations

26

H-Index

	Year	Citations
Investigation of the functional effect of monoamine oxidase polymorphisms in human brain Jorune Balciuniene, Lina Emilsson, Lars Oreland, Human Genetics NeuropsychologyPsychiatryNeurophysiologyFunctional EffectNeuropharmacology	2001	163
Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities Jorune Balciuniene, Ningping Feng, Kelly Iyadurai, The American Journal of Human Genetics Genomic DisorderPsychiatryPsychiatric DisordersMedicineGenetics	2007	105
Increased monoamine oxidase messenger RNA expression levels in frontal cortex of Alzheimer's disease patients Lina Emilsson, Peter Saetre, Jorune Balciuniene, Neuroscience Letters NeuropsychologyAlzheimer's DiseaseBrain FunctionDementiaNeurochemical Biomarkers	2002	97
Automated Clinical Exome Reanalysis Reveals Novel Diagnoses Samuel W. Baker, Jill R. Murrell, Addie I. Nesbitt, Journal of Molecular Diagnostics	2018	84
Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior Holly K. Harris, Tojo Nakayama, Jenny Lai, Genetics in Medicine Neurodevelopmental DisordersSyndromic AutismMedicineGeneticsGenetic Disorder	2021	79
A Gene for Autosomal Dominant Progressive Cone Dystrophy (CORD5) Maps to Chromosome 17p12–p13 Jorune Balciuniene, Kent Johansson, Ola Sandgren, Genomics Mendelian DisorderGenetic DisorderGeneticsPathologyDegenerative Disease	1995	78
Targeted transgene integration overcomes variability of position effects in zebrafish Jennifer Roberts, Irene Miguel-Escalada, Katherine J. Slovik, Development EngineeringGene Regulatory NetworkOptogeneticsCell SpecializationGene Transfer	2014	69
Alpha-tectorin involvement in hearing disabilities: one gene - two phenotypes Jorune Balciuniene, Niklas Dahl, Paula Jalonen, Human Genetics Developmental BiologyGeneticsAlpha-tectorin InvolvementAudiologyAuditory Physiology	1999	67
The phenotype of recurrent 10q22q23 deletions and duplications Bregje W.M. van Bon, Jorune Balciuniene, Gary Fruhman, European Journal of Human Genetics Genetic DisorderGeneticsRecurrent 10Q22q23Molecular GeneticsGenomics	2011	64
Mice Mutant in the DM Domain Gene <i>Dmrt4</i> Are Viable and Fertile but Have Polyovular Follicles Jorune Balciuniene, Vivian J. Bardwell, David Zarkower Molecular and Cellular Biology Dm DomainGeneticsDm Domain GenesReproductive BiologyEpigenetics	2006	64

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