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Author Details

Hila Milo Rasouly
Center for Precision Medicine and Genomics, Columbia University Irving Medical Center
2008
38
14
PMIDPaper TitleJournal TitlePublished Year
36375470Genetics of Kidney Disease: The Unexpected Role of Rare Disorders.Annu Rev Med2023
38057357The diagnostic yield of exome sequencing in liver diseases from a curated gene panel.Sci Rep2023
36789889The effect of genetic education on the referral of patients to genetic evaluation: Findings from a national survey of nephrologists.Genet Med2023
36445780ZEB2 controls kidney stromal progenitor differentiation and inhibits abnormal myofibroblast expansion and kidney fibrosis.JCI Insight2023
36868514Genetic evaluation of living kidney donor candidates: A review and recommendations for best practices.Am J Transplant2023
36758113Clinical and Genetic Characteristics of CKD Patients with High-Risk APOL1 Genotypes.J Am Soc Nephrol2023
34665896Do research participants share genomic screening results with family members?J Genet Couns2022
36161695Incorporating genetics services into adult kidney disease care.Am J Med Genet C Semin Med Genet2022
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
35078725Diagnostic sequencing to support genetically stratified medicine in a tertiary care setting.Genet Med2022
33368851GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing.J Genet Couns2021
36046768Returning negative results from large-scale genomic screening: Experiences from the eMERGE III network.Am J Med Genet A2021
34670811Longitudinal Outcomes of COVID-19-Associated Collapsing Glomerulopathy and Other Podocytopathies.J Am Soc Nephrol2021
33460345Cases in Precision Medicine: Genetic Testing to Predict Future Risk for Disease in a Healthy Patient.Ann Intern Med2021
32220420Loss of Roundabout Guidance Receptor 2 (Robo2) in Podocytes Protects Adult Mice from Glomerular Injury by Maintaining Podocyte Foot Process Structure.Am J Pathol2020
33276377Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.Hum Mol Genet2020
32891193Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.Am J Hum Genet2020
32555418Ethical conflicts in translational genetic research: lessons learned from the eMERGE-III experience.Genet Med2020
32358593The ethics of genetic testing for kidney diseases.Nat Rev Nephrol2020
32413979Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.J Pers Med2020
32349224Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.J Pers Med2020
30476936The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing.Ann Intern Med2019
31040387Correction: Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study.Genet Med2019
30930462Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study.Genet Med2019
29301385Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.J Pers Med2018
30014107Whole-Exome Sequencing in Adults With Chronic Kidney Disease.Ann Intern Med2018
30450447Pitfalls and Challenges of Consenting to Genetic Research Studies.Kidney Int Rep2018
29307893Genomic medicine for kidney disease.Nat Rev Nephrol2018
29204651Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.Ann Intern Med2018
29220675Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.Am J Hum Genet2017
29100090Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.Am J Hum Genet2017
27272550Response to 'Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects': reply from the authors.Br J Dermatol2016
26471493Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects.Br J Dermatol2016
27882344SLIT2/ROBO2 signaling pathway inhibits nonmuscle myosin IIA activity and destabilizes kidney podocyte adhesion.JCI Insight2016
27591083Loss of Zeb2 in mesenchyme-derived nephrons causes primary glomerulocystic disease.Kidney Int2016
23408557Lower urinary tract development and disease.Wiley Interdiscip Rev Syst Biol Med2013
22840396Inhibitory effects of Robo2 on nephrin: a crosstalk between positive and negative signals regulating podocyte structure.Cell Rep2012
18637884Cholesteryl ester transfer protein (CETP) genetic variation and early onset of non-fatal myocardial infarction.Ann Hum Genet2008
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Collaborators

Ali G Gharavi
Columbia University College of Physicians and Surgeons
Co-authored papers 21
Maddalena Marasa
Columbia University College of Physicians and Surgeons
Co-authored papers 14
Julia Wynn
Vagelos College of Physicians and Surgeons, Columbia University
Co-authored papers 10
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
Co-authored papers 9
Krzysztof Kiryluk
Columbia University
Co-authored papers 8
Kathleen A Leppig
Kaiser Permanente Washington
Co-authored papers 7
Richard R Sharp
Biomedical Ethics, Mayo Clinic and Foundation
Co-authored papers 6
Ingrid A Holm
Harvard Medical School
Co-authored papers 6
Paul S Appelbaum
Center for Law, Columbia University Irving Medical Center
Co-authored papers 6
Melanie F Myers
Cincinnati Children's Hospital Medical Center
Co-authored papers 6
Maureen E Smith
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
Co-authored papers 6
Janet L Williams
Genomic Medicine Institute
Co-authored papers 6
Iftikhar J Kullo
Mayo Clinic
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Cynthia A Prows
Cincinnati Children's Hospital Medical Center
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Christin Hoell
Northwestern University, Center for Genetic Medicine
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Margaret Harr
Center for Applied Genomics, Children's Hospital of Philadelphia
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Sharon Aufox
Northwestern University, Center for Genetic Medicine
Co-authored papers 5
Georgia L Wiesner
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
Co-authored papers 5
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 5
E Clayton
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 4
Chunhua Weng
Columbia University Irving Medical Center
Co-authored papers 4
Jordan G Nestor
Columbia University
Co-authored papers 4
Alanna Kulchak Rahm
Research Institute
Co-authored papers 4
David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 4
Eric B Larson
University of Washington
Co-authored papers 3
Colin Halverson
Indiana University Center for Bioethics.
Co-authored papers 3
Richard P Lifton
The Rockefeller University
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Robert C Green
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Release 1.2