Hila Milo Rasouly

Assistant Professor

Columbia University

United States

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About

Hila Milo Rasouly is an Assistant Professor at Columbia University in the United States. Her research focuses on genetic aspects of nephrology, particularly regarding kidney malformations, chronic kidney disease, and genetic counseling practices. Recent publications highlight her contributions to understanding the role of genetic testing in clinical settings and its implications for pediatric and adult nephrology. She is dedicated to improving genetic education and referral processes among nephrologists.

Articles (20)

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2025

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2025

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2025

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2023

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2021

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2021

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2020

Collaborators (21)

Wayne Liang

Assistant Professor

Emory University

UNITED STATES

Hila Milo Rasouly

Research Interests

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About

Articles (20)

Pediatric nephrologists’ perspectives and clinical practices related to genetic testing and education

Exome analysis links kidney malformations to developmental disorders and reveals causal genes.

The Art and Science of Genetic Counseling in Nephrology

Genetic evaluation of living kidney donor candidates: A review and recommendations for best practices

The Clinical Utility of Genetic Testing in the Diagnosis and Management of Adults with Chronic Kidney Disease

The effect of genetic education on the referral of patients to genetic evaluation: Findings from a national survey of nephrologists.

ZEB2 controls kidney stromal progenitor differentiation and inhibits abnormal myofibroblast expansion and kidney fibrosis

Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.

The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network

Genetics of Kidney Disease: The Unexpected Role of Rare Disorders.

Incorporating genetics services into adult kidney disease care.

Diagnostic sequencing to support genetically stratified medicine in a tertiary care setting.

Longitudinal Outcomes of COVID-19-Associated Collapsing Glomerulopathy and Other Podocytopathies.

Do research participants share genomic screening results with family members?

Neptune: an environment for the delivery of genomic medicine.

GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing

Cases in Precision Medicine: Genetic Testing to Predict Future Risk for Disease in a Healthy Patient.

Cases in Precision Medicine: Genetic Testing to Predict Future Risk for Disease in a Healthy Patient

An electronic health record (EHR) log analysis shows limited clinician engagement with unsolicited genetic test results.

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.

Collaborators (21)

Wayne Liang

Christopher T. Gordon

Mark Elliott

Adam Gordon

Eleni Giannoulatou

Robert Daniel Blank

Suzette Bielinski

Sudhir Kumar

Jordan Nestor

Weining Lu

Johannes Schlondorff

Albertien M. van Eerde

Krista L. Lentine

Emilie CORNEC-LE GALL

Elisabet Ars

Michael Wagner

Hilda Fernandez

Melanie Myers

Beata S. Lipska-Ziętkiewicz

Oliver Gross

Maria Szczepanska

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