Ghaleb H. Daouk, MD, SM
Nephrologist, Division of Nephrology; Director, Extramural Programs
Assistant Professor of Pediatrics, Harvard Medical School
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Ghaleb H. Daouk, MD, SM
Nephrologist, Division of Nephrology; Director, Extramural Programs
Assistant Professor of Pediatrics, Harvard Medical School
Medical Services
Languages
Arabic
English
Education
Undergraduate School
Syracuse University
1979
Syracuse
NY
Medical School
American University of Beirut
1984
Beirut
Lebanon
Graduate School
MIT Sloan School - Management of Technology
1991
Boston
MA
Internship
Massachusetts General Hospital
1988
Boston
MA
Residency
Pediatrics
Massachusetts General Hospital
1990
Boston
MA
Fellowship
Pediatric Nephrology
Massachusetts General Hospital
1994
Boston
MA
Certifications
American Board of Pediatrics (General)
Publications
Trio exome sequencing in individuals with CAKUT identifies de novo variants in potential novel candidate genes in 19.62. View Abstract
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT. View Abstract
Beyond the tubule: pathological variants of LRP2, encoding the megalin receptor, result in glomerular loss and early progressive chronic kidney disease. View Abstract
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. View Abstract
Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome. View Abstract
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients. View Abstract
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. View Abstract
A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes. View Abstract
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ˜43% of 35 Families With Midaortic Syndrome. View Abstract
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome. View Abstract
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. View Abstract
Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center. View Abstract
Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract. View Abstract
Recent advances in the pathogenesis of hypertension in children. View Abstract
Tuberous sclerosis complex and renal angiomyolipoma: case report and review of the literature. View Abstract
Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 11-2004. A boy with rash, edema, and hypertension. View Abstract
Postnatal transient renal insufficiency in the feto-fetal transfusion syndrome. View Abstract
Inhibition of proteinase 3 by ANCA and its correlation with disease activity in Wegener's granulomatosis. View Abstract
Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombination. View Abstract
Induction of a cellular enzyme for energy metabolism by transforming domains of adenovirus E1a. View Abstract
Isolation of a functional human gene for brain creatine kinase. View Abstract
Regulation of coenzyme utilization by the dual nucleotide-specific glucose 6-phosphate dehydrogenase from Leuconostoc mesenteroids. View Abstract
Simultaneous analysis of NAD- and NADP-linked activities of dual nucleotide-specific dehydrogenases. Application to Leuconostoc mesenteroides glucose-6-phosphate dehydrogenase. View Abstract
Locations