PIEZO1 is the most common monogenic etiology of non‐immune hydrops fetalis detected by prenatal exome sequencing

Diagnostic yield from prenatal exome sequencing for non‐immune hydrops fetalis: A systematic review and meta‐analysis

(2023) Huda B. Al‐Kouatly et al.   CLINICAL GENETICS

Piezo1-Regulated Mechanotransduction Controls Flow-Activated Lymphatic Expansion

(2022) Dongwon Choi et al.   CIRCULATION RESEARCH

Structural Designs and Mechanogating Mechanisms of the Mechanosensitive Piezo Channels

(2021) Yan Jiang et al.   TRENDS IN BIOCHEMICAL SCIENCES

Recent advances in the pathophysiology of PIEZO1 ‐related hereditary xerocytosis

(2021) Nicolas Jankovsky et al.   AMERICAN JOURNAL OF HEMATOLOGY

Value of Exome Sequencing in Diagnosis and Management of Recurrent Non-immune Hydrops Fetalis: A Retrospective Analysis

(2021) Xinyao Zhou et al.   Frontiers in Genetics

The many etiologies of nonimmune hydrops fetalis diagnosed by exome sequencing

(2021) Tova Wagner et al.   PRENATAL DIAGNOSIS

Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalis

(2021) Alec Reginald Errol Correa et al.   PRENATAL DIAGNOSIS

Implementation of fetal clinical exome sequencing: Comparing prospective and retrospective cohorts

(2021) Martina Marangoni et al.   GENETICS IN MEDICINE

Evolving fetal phenotypes and clinical impact of progressive prenatal exome sequencing pathways: cohort study

(2021) F. Mone et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

Hereditary Xerocytosis: Differential Behavior of PIEZO1 Mutations in the N-Terminal Extracellular Domain Between Red Blood Cells and HEK Cells

(2021) Yohei Yamaguchi et al.   Frontiers in Physiology

Non‐immune hydrops fetalis was rare in Sweden during 1997‐2015, but cases were associated with complications and poor prognosis

(2020) Catharina Whybra et al.   ACTA PAEDIATRICA

Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis

(2020) Teresa N. Sparks et al.   NEW ENGLAND JOURNAL OF MEDICINE

Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes

(2020) Qingwei Qi et al.   Genes

Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos-channelopathy: A retrospective series of 126 patients

(2019) Véronique Picard et al.   HAEMATOLOGICA

Trio‐whole‐exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations

(2019) Wei Guo et al.   HUMAN MUTATION

Molecular autopsy in maternal–fetal medicine

(2017) Hanan E Shamseldin et al.   GENETICS IN MEDICINE

Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal development

(2017) Carin L Yates et al.   GENETICS IN MEDICINE

Structure of the mechanically activated ion channel Piezo1

(2017) Kei Saotome et al.   NATURE

Society for Maternal-Fetal Medicine (SMFM) Clinical Guideline #7: nonimmune hydrops fetalis

(2015) Mary E. Norton et al.   AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Piezo1 integration of vascular architecture with physiological force

(2014) Jing Li et al.   NATURE

Piezo1, a mechanically activated ion channel, is required for vascular development in mice

(2014) S. S. Ranade et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA