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V. Tasic · SciRah

Researcher profile · Semantic Scholar

V. Tasic

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V. Tasic — researcher profile on SciRah

h-index: 44
Works: 274
Citations: 7,155

Most-cited papers

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
Jillian K. Warejko, Wei-Zhen Tan, Ankana Daga, D. Schapiro +57 more
2018American Society of Nephrology. Clinical Journal209 citations Open access
Semantic Scholar
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
M. Verbitsky, R. Westland, Alejandra Pérez, K. Kiryluk +86 more
2018Nature Genetics195 citations Open access
Semantic Scholar
Treatment and long-term outcome in primary distal renal tubular acidosis.
S. Lopez-Garcia, F. Emma, S. Walsh, M. Fila +83 more
2019Nephrology, Dialysis and Transplantation109 citations Open access
Semantic Scholar
Functional rare and low frequency variants in BLK and BANK1 contribute to human lupus
Simon H. Jiang, V. Athanasopoulos, J. Ellyard, Aaron Chuah +37 more
2019Nature Communications103 citations Open access
Semantic Scholar
Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome
Joost Kummeling, Diante E. Stremmelaar, Nicholas Raun, M. Reijnders +39 more
2019bioRxiv72 citations Open access
Semantic Scholar
Distal Renal Tubular Acidosis: ERKNet/ESPN Clinical Practice Points.
F. Trepiccione, S. Walsh, G. Ariceta, O. Boyer +15 more
2021Nephrology, Dialysis and Transplantation59 citations Open access
Semantic Scholar
COVID-19 in children treated with immunosuppressive medication for kidney diseases
M. Marlais, Tanja Wlodkowski, S. Al-Akash, P. Ananin +27 more
2020Archives of Disease in Childhood54 citations Open access
Semantic Scholar
GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome.
Tobias Hermle, Ronen Schneider, D. Schapiro, Daniela A. Braun +24 more
2018Journal of the American Society of Nephrology53 citations Open access
Semantic Scholar
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Alexandra Barry, M. McNulty, Xiaoyuan Jia, Y. Gupta +66 more
2023Nature Communications49 citations Open access
Semantic Scholar
Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies.
K. Riedhammer, M. Braunisch, R. Günthner, M. Wagner +16 more
2020American Journal of Kidney Diseases46 citations Open access
Semantic Scholar
Clinical, biochemical, and pathophysiological analysis of SLC34A1 mutations
A. Fearn, Benjamin Allison, S. Rice, Noel Edwards +9 more
2018Physiological Reports42 citations Open access
Semantic Scholar
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
D. Connaughton, R. Dai, D. Owen, Jonathan Marquez +95 more
2020American Journal of Human Genetics39 citations Open access
Semantic Scholar
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT
Steve Seltzsam, Chunyan Wang, B. Zheng, Nina Mann +41 more
2021Genetics in Medicine38 citations Open access
Semantic Scholar
Metabolic Profiles in Obese Children and Adolescents with Insulin Resistance
M. Kostovski, V. Simeonovski, K. Mironska, V. Tasic +1 more
2018Open Access Macedonian Journal of Medical Sciences36 citations Open access
Semantic Scholar
Treatment and long-term outcome in primary nephrogenic diabetes insipidus.
S. Lopez-Garcia, M. Downie, Ji Soo Kim, O. Boyer +73 more
2020Nephrology, Dialysis and Transplantation22 citations Open access
Semantic Scholar
Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)
C. Wu, Nina Mann, Makiko Nakayama, D. Connaughton +18 more
2020Genetics in Medicine22 citations Open access
Semantic Scholar
COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans
T. Kitzler, Ronen Schneider, Stefan Kohl, Caroline M. Kolvenbach +18 more
2019Human Genetics21 citations Open access
Semantic Scholar
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.
M. Verbitsky, Priya Krithivasan, Ekaterina Batourina, Atlas Khan +75 more
2021Journal of the American Society of Nephrology20 citations Open access
Semantic Scholar
CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor Mutations.
Nina Mann, Franziska Kause, Erik Henze, A. Gharpure +29 more
2019American Journal of Human Genetics19 citations Open access
Semantic Scholar
Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience
K. Riedhammer, Jasmina Ćomić, V. Tasic, J. Putnik +8 more
2023European Journal of Human Genetics18 citations Open access
Semantic Scholar
Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population
B. Stibůrková, J. Bohata, K. Pavelcová, V. Tasic +4 more
2021Biomedicines18 citations Open access
Semantic Scholar
Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important
T. Eggermann, Johanna Brück, C. Knopp, G. Fekete +6 more
2020Journal of molecular medicine18 citations Open access
Semantic Scholar
Duplication of The SOX3 Gene in an Sry-negative 46,XX Male with Associated Congenital Anomalies of Kidneys and the Urinary Tract: Case Report and Review of the Literature
V. Tasic, A. Mitrotti, F. Riepe, AE Kulle +6 more
2019Balkan Journal of Medical Genetics16 citations Open access
Semantic Scholar
Trio Clinical Exome Sequencing in a Patient With Multicentric Carpotarsal Osteolysis Syndrome: First Case Report in the Balkans
Aleksandra Stajkovska, S. Mehandziska, Margarita Stavrevska, K. Jakovleva +6 more
2018Frontiers in Genetics15 citations Open access
Semantic Scholar
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis
D. Ahram, Tze Y. Lim, J. Ke, G. Jin +78 more
2023Journal of the American Society of Nephrology12 citations Open access
Semantic Scholar
Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 2
Y. Toyoda, S. Cho, V. Tasic, K. Pavelcová +11 more
2023Frontiers in Genetics12 citations Open access
Semantic Scholar
DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes
Jonathan Marquez, Nina Mann, Kathya Arana, E. Deniz +16 more
2020Journal of Medical Genetics12 citations Open access
Semantic Scholar
NEUTROPHIL GELATINASE-ASSOCIATED LIPOCALIN AS AN EARLY BIOMARKER OF ACUTE KIDNEY INJURY IN NEWBORNS
S. Naunova-Timovska, S. Cekovska, E. Sahpazova, V. Tasic
2020Acta Clinica Croatica12 citations Open access
Semantic Scholar
Pathogenic Variants in RNPC3 are Associated with Hypopituitarism and Primary Ovarian Insufficiency
L. Akın, K. Rizzoti, L. Gregory, B. Corredor +26 more
2021Genetics in Medicine10 citations Open access
Semantic Scholar
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract
C. Wu, Tze Y. Lim, Chunyan Wang, Steve Seltzsam +32 more
2022European Urology Open Science9 citations Open access
Semantic Scholar
Rare heterozygous GDF6 variants in patients with renal anomalies
Helge Martens, Imke Hennies, M. Getwan, A. Christians +13 more
2020European Journal of Human Genetics9 citations Open access
Semantic Scholar
Is there a dominant‐negative effect in individuals with heterozygous disease‐causing variants in COL4A3/COL4A4?
K. Riedhammer, H. Simmendinger, V. Tasic, J. Putnik +11 more
2024Clinical Genetics8 citations Open access
Semantic Scholar
IGF1R Gene Alterations in Children Born Small for Gestitional Age (SGA)
A. Janchevska, M. Krstevska-Konstantinova, Heike Pfäffle, Marina Schlicke +8 more
2018Open Access Macedonian Journal of Medical Sciences8 citations Open access
Semantic Scholar
Homeostasis Model Assessment - Insulin Resistance and Sensitivity (HOMA-IR and IS) Index in Overweight Children Born Small for Gestational Age (SGA)
A. Janchevska, Z. Gucev, V. Tasic, M. Polenaković
2018PRILOZI8 citations Open access
Semantic Scholar
Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract
Esra Kesdiren, Helge Martens, Frank Brand, Lina Werfel +15 more
2024European Journal of Human Genetics7 citations Open access
Semantic Scholar
Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes–Brocks syndrome 2
A. Christians, Esra Kesdiren, Imke Hennies, A. Hofmann +16 more
2022Human Genetics7 citations Open access
Semantic Scholar
Severe digital malformations in a rare variant of fibrodysplasia ossificans progressiva
Z. Gucev, V. Tasic, D. Plaseska-Karanfilska, M. Dimishkovska +8 more
2019American Journal of Medical Genetics. Part A7 citations
Semantic Scholar
Trio exome sequencing in individuals with CAKUT identifies de novo variants in potential novel candidate genes in 19.62%
L. M. Merz, Caroline M. Kolvenbach, Chunyan Wang, N. D. Mertens +50 more
2025Genetics in Medicine6 citations Open access
Semantic Scholar
Pathogenic PHIP Variants are Variably Associated With CAKUT
Jonathan de Fallois, T. Sieckmann, Ria Schönauer, Friederike Petzold +16 more
2024Kidney International Reports6 citations Open access
Semantic Scholar
Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies
J. Martino, Qingxue Liu, K. Vukojević, J. Ke +27 more
2023Genetics in Medicine6 citations Open access
Semantic Scholar
The Rationale of Complement Blockade of the MCPggaac Haplotype following Atypical Hemolytic Uremic Syndrome of Three Southeastern European Countries with a Literature Review
D. Turudić, D. Pokrajac, V. Tasic, Dino Kasumović +2 more
2023International Journal of Molecular Sciences6 citations Open access
Semantic Scholar
Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models
Chunyan Wang, Steve Seltzsam, B. Zheng, C. Wu +24 more
2022American Journal of Medical Genetics. Part A6 citations Open access
Semantic Scholar
Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age
R. Günthner, Lea Knipping, Stefanie Jeruschke, Robin Satanoskij +22 more
2022Frontiers in Medicine6 citations Open access
Semantic Scholar
The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy—A human genetics department experience
Jasmina Ćomić, K. Riedhammer, R. Günthner, C. Schaaf +16 more
2022Frontiers in Medicine6 citations Open access
Semantic Scholar
A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tract
B. Zheng, Chunyan Wang, Steve Seltzsam, Sophia Schneider +12 more
2021American Journal of Medical Genetics. Part A6 citations Open access
Semantic Scholar
Mutations in Collagen Genes in the Context of an Isolated Population
Andrej Zupan, Alenka Matjašič, Gašper Grubelnik, V. Tasic +1 more
2020Genes6 citations Open access
Semantic Scholar
Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutation.
Z. Gucev, V. Tasic, Ivona Bogevska, N. Laban +9 more
2019European Journal of Medical Genetics6 citations
Semantic Scholar
The Spectrum of Kidney Diseases in Children Associated with Low Molecular Weight Proteinuria
Shpetim Salihu, K. Tosheska, N. Aluloska, Z. Gucev +2 more
2018Open Access Macedonian Journal of Medical Sciences6 citations Open access
Semantic Scholar
A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux
A. T. van der Ven, B. Kobbe, Stefan Kohl, S. Shril +24 more
2018PLoS ONE6 citations Open access
Semantic Scholar
COL4A5-p.Gly624Asp is the Predominant Variant in Europe Associated With a Mild Alport Syndrome Phenotype
Bastian M. Krüger, Annika Jens, A. Neuhaus, Jasmina Ćomić +24 more
2025Kidney International Reports5 citations Open access
Semantic Scholar

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