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O

Olga Tšuiko

KU Leuven

H指数:19

被引数:1,072

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Prevalence and mechanistic origins of genome-wide ploidy abnormalities in ICSI derived human preimplantation embryos

人囊胚中全基因组倍性异常的流行率及其机制起源

Human Molecular Genetics

IF3.2

2026-09-080

PRE

1q gain bypasses the selective barrier against aneuploidy in RPE differentiation via wild-type co-culture rescue

1q获得通过野生型共培养拯救的方式绕过了RPE分化中对非整倍体的选择性屏障。

Nature Communications

IF15.7

2025-11-250

OAAI

Analytical capability and clinical utility of WGS in PGT

WGS在PGT中的分析能力与临床应用价值

HUMAN REPRODUCTION

IF6.1

2025-06-010

OAAI

High aneuploidy rate in embryos of young female BRCA carriers

年轻女性BRCA携带者胚胎的高非整倍体率

HUMAN REPRODUCTION

IF6.1

2025-06-010

OA

Origin and development of uniparental and polyploid blastomeres

单亲源和多倍体分裂球的起源与发展

IF4.1

2025-05-010

OAAI

Long-read whole-genome sequencing-based concurrent haplotyping and aneuploidy profiling of single cells

基于长读长全基因组测序的单细胞联合分型与非整倍性分析

NUCLEIC ACIDS RESEARCH

IF13.1

2025-04-010

OA

Perspectives of preimplantation genetic testing patients in Belgium on the ethics of polygenic embryo screening

比利时植入前基因检测患者对多基因胚胎筛查伦理学的看法

REPRODUCTIVE BIOMEDICINE ONLINE

IF3.5

2024-09-014

PRE

Polygenic embryo screening: quo vadis?

多基因胚胎筛查: quo vadis？

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

IF2.7

2024-06-151

PRE

Are we not going too far?: Socio-ethical considerations of preimplantation genetic testing using polygenic risk scores according to healthcare professionals

SOCIAL SCIENCE & MEDICINE

IF5

2024-02-016

PRE

Genome-wide equine preimplantation genetic testing enabled by simultaneous haplotyping and copy number detection

SCIENTIFIC REPORTS

IF3.9

2024-01-233

OAAI

TET2-Driver and NLRC4-Passenger Variants in Adult-Onset Autoinflammation

NEW ENGLAND JOURNAL OF MEDICINE

IF78.5

2023-04-276

OA

Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores

局限性，担忧和潜力: 医疗保健专业人员对使用多基因风险评分进行植入前基因检测的态度

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2023-03-2015

OA

Preclinical workup using long-read amplicon sequencing provides families with de novo pathogenic variants access to universal preimplantation genetic testing

HUMAN REPRODUCTION

IF6.1

2023-01-108

PRE

Parental genomes segregate into distinct blastomeres during multipolar zygotic divisions leading to mixoploid and chimeric blastocysts

IF9.4

2022-10-0311

OAAI

Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2022-07-2725

OA

A review of normative documents on preimplantation genetic testing: Recommendations for PGT-P

GENETICS IN MEDICINE

IF6.2

2022-06-0112

OAAI

Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing

NUCLEIC ACIDS RESEARCH

IF13.1

2022-02-2520

OAAI

Polygenic risk scoring of human embryos: a qualitative study of media coverage

人类胚胎的多基因风险评分: 媒体报道的定性研究

BMC MEDICAL ETHICS

IF3.1

2021-09-1818

OAAI

Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA

GENETICS IN MEDICINE

IF6.2

2020-05-0123

OAAI

Identity-by-state-based haplotyping expands the application of comprehensive preimplantation genetic testing

HUMAN REPRODUCTION

IF6.1

2020-03-214

PREAI