Publications by authors named "A Pasanen"

Article Synopsis
  • Acute viral bronchiolitis is a leading cause of hospitalizations in infants and may increase the risk of developing asthma later in life, indicating a potential genetic link between the two.
  • A genome-wide association study analyzed over 1,400 infants with bronchiolitis and identified significant genetic variants in GSDMB and CDHR3, both associated with respiratory issues and asthma.
  • Findings suggest that these genetic variants may increase susceptibility to bronchiolitis caused by various viruses, and severe cases in infancy could either lead to asthma or indicate a genetic predisposition for developing it.
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Introduction: MicroRNAs regulate post-transcriptional gene expression. Their expression has been linked to many pregnancy complications, including preterm birth. Placental microRNA levels differ between preterm and term pregnancies.

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Background: Repeat leiomyoma occurrence or even reintervention is common after myomectomy. Little is known about the factors related to repeat interventions.

Objective: This study aimed to determine the frequency of leiomyoma-related reintervention after an initial laparoscopic or abdominal myomectomy and to analyze both clinical and molecular risk factors for reinterventions.

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Objective: Prognostic stratification of endometrial cancer involves the assessment of stage, uterine risk factors, and molecular classification. This process can be further refined through annotation of prognostic biomarkers, notably L1 cell adhesion molecule (L1CAM) and hormonal receptors. Loss of asparaginase-like protein 1 (ASRGL1) has been shown to correlate with poor outcome in endometrial cancer.

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Objective: To assess the risk stratification of clinicopathologically and molecularly classified endometrial cancer based on estrogen receptor (ER) and L1 cell adhesion molecule (L1CAM) expression.

Methods: This was a retrospective study of patients who underwent primary treatment at a single tertiary center. Carcinomas were classified into 5 clinicopathological risk groups, as per European guidelines.

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