Iren Haltrich
Semmelweis Egyetem
H-index: 12
Europe-Hungary
Top articles of Iren Haltrich
Next-Generation Sequencing–Based Genomic Profiling of Children with Acute Myeloid Leukemia
The Journal of Molecular Diagnostics
2023/8/1
Hypodiploidy has unfavorable impact on survival in pediatric acute myeloid leukemia: an I-BFM Study Group collaboration
Blood advances
2023/3/28
Iren Haltrich
H-Index: 8
Gábor Kovács
H-Index: 16
PersonALL: a genetic scoring guide for personalized risk assessment in pediatric B-cell precursor acute lymphoblastic leukemia
British Journal of Cancer
2023/8/24
PB1699: GENOMIC AND TRANSCRIPTOMIC PROFILING REVEALS NOVEL GENE FUSIONS AND MARKERS OF CLINICAL RESPONSE IN PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA
HemaSphere
2023/8/1
Clinical evaluation of rare copy number variations identified by chromosomal microarray in a Hungarian neurodevelopmental disorder patient cohort
Molecular Cytogenetics
2022/11/1
An ultra-rare manifestation of an X-linked recessive disorder: Duchenne muscular dystrophy in a female patient
International Journal of Molecular Sciences
2022/10/28
Pre-and perinatal aspects of sex chromosome abnormalities and other gonadal dysgeneses
2022/5/20
Anna Lengyel
H-Index: 2
Iren Haltrich
H-Index: 8
A 22q11. 2-microdeletiós szindróma klinikai jellemzői
Orvosi Hetilap
2022/1/2
Diagnostic difficulties and possibilities of NF1-like syndromes in childhood
BMC pediatrics
2021/12
Anna Lengyel
H-Index: 2
Iren Haltrich
H-Index: 8
Chromosome 2q14.3 microdeletion encompassing CNTNAP5 gene in a patient carrying a complex chromosomal rearrangement
Journal of Genetics
2021/10
Deletion of 16q22. 2q23. 3 in a Boy with a Phenotype Reminiscent of Silver-Russell Syndrome
Molecular Syndromology
2021/8/31
A lizoszomális tárolási megbetegedések okozta szisztémás immunológiai eltérések.
2021
Generation of multiple iPSC clones from a male schizophrenia patient carrying de novo mutations in genes KHSRP, LRRC7, and KIR2DL1, and his parents
Stem Cell Research
2021/3/1
What should we consider in the case of combined Down-and 47, XY,+ i (X)(q10) Klinefelter syndromes? The unique case of a male newborn and review of the literature
2020/12
Anna Lengyel
H-Index: 2
Iren Haltrich
H-Index: 8
Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature
2020/10/1
Comprehensive profiling of disease-relevant copy number aberrations for advanced clinical diagnostics of pediatric acute lymphoblastic leukemia
Modern Pathology
2020/5/1
Similar cause, different phenotype: SOX9 enhancer duplication in a family
Hormone Research in Paediatrics
2020/4/29
